Item | Value |
---|---|
geneid | 121536 |
ensemblid | ENSG00000139154.16 |
hgncid | 24051 |
symbol | AEBP2 |
name | AE binding protein 2 |
refseq_nuc | NM_153207.5 |
refseq_prot | NP_694939.2 |
ensembl_nuc | ENST00000266508.14 |
ensembl_prot | ENSP00000266508.9 |
mane_status | MANE Select |
chr | chr12 |
start | 19439492 |
end | 19522227 |
strand | + |
ver | v1.2 |
region | chr12:19439492-19522227 |
region5000 | chr12:19434492-19527227 |
regionname0 | AEBP2_chr12_19439492_19522227 |
regionname5000 | AEBP2_chr12_19434492_19527227 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 503 | 403 | 96 | 74 | 181 | 10 | 40 | 139 | AEBP2_chr12_19434492_19527227 | AEBP2 | MAAAI others(498): Show |
chr12 | 19434492 | 19527227 |
a0002 | 0/0 | 495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | MAAAI others(490): Show |
chr12 | 19434492 | 19527227 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1509 | 343 | 81 | 69 | 142 | 10 | 39 | AEBP2_chr12_19434492_19527227 | AEBP2 | ATGGC others(1504): Show |
chr12 | 19434492 | 19527227 | ||
a0001c0002 | 0/0 | 1509 | 53 | 13 | 3 | 37 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | ATGGC others(1504): Show |
chr12 | 19434492 | 19527227 | ||
a0001c0003 | 0/0 | 1509 | 3 | 2 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | ATGGC others(1504): Show |
chr12 | 19434492 | 19527227 | ||
a0001c0004 | 0/0 | 1509 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | ATGGC others(1504): Show |
chr12 | 19434492 | 19527227 | ||
a0001c0005 | 0/0 | 1509 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | ATGGC others(1504): Show |
chr12 | 19434492 | 19527227 | ||
a0001c0006 | 0/0 | 1509 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | ATGGC others(1504): Show |
chr12 | 19434492 | 19527227 | ||
a0002c0007 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | ATGGC others(1480): Show |
chr12 | 19434492 | 19527227 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5833 | 41 | 20 | 4 | 15 | 0 | 2 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0002 | 1/0 | 5830 | 59 | 2 | 20 | 27 | 1 | 8 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0003 | 0/1 | 5828 | 52 | 1 | 12 | 30 | 4 | 4 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0004 | 0/0 | 5827 | 41 | 10 | 3 | 21 | 0 | 7 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5822): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0005 | 0/0 | 5830 | 28 | 7 | 11 | 9 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0006 | 0/0 | 5832 | 20 | 3 | 5 | 1 | 1 | 10 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5827): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0007 | 0/0 | 5828 | 14 | 11 | 0 | 1 | 1 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0008 | 0/0 | 5827 | 10 | 0 | 3 | 4 | 1 | 2 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5822): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0009 | 0/0 | 5829 | 7 | 0 | 4 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5824): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0010 | 0/0 | 5832 | 4 | 1 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5827): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0011 | 0/0 | 5826 | 7 | 1 | 0 | 5 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5821): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0012 | 0/0 | 5829 | 6 | 0 | 1 | 5 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5824): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0013 | 0/0 | 5830 | 5 | 5 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0014 | 0/0 | 5831 | 5 | 0 | 4 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5826): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0015 | 0/0 | 5829 | 4 | 4 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5824): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0016 | 0/0 | 5831 | 4 | 0 | 0 | 4 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5826): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0017 | 0/0 | 5829 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5824): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0018 | 0/0 | 5830 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0019 | 0/0 | 5831 | 3 | 0 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5826): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0020 | 0/0 | 5834 | 3 | 3 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5829): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0021 | 0/0 | 5827 | 2 | 0 | 0 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5822): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0022 | 0/0 | 5829 | 2 | 1 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5824): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0023 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5829): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0024 | 0/0 | 5826 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5821): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0025 | 0/0 | 5828 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0026 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5829): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0027 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0028 | 0/0 | 5828 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0029 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0030 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0031 | 0/0 | 5828 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0032 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5824): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0034 | 0/0 | 5830 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0035 | 0/0 | 5830 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0036 | 0/0 | 5831 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5826): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0037 | 0/0 | 5830 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0039 | 0/0 | 5832 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5827): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0041 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0042 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0046 | 0/0 | 5834 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5829): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0047 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0001t0048 | 0/0 | 5828 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5823): Show |
chr12 | 19434492 | 19527227 |
a0001c0002t0001 | 0/0 | 5833 | 35 | 12 | 3 | 20 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0002t0002 | 0/0 | 5830 | 10 | 0 | 0 | 10 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0002t0010 | 0/0 | 5832 | 4 | 0 | 0 | 4 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5827): Show |
chr12 | 19434492 | 19527227 |
a0001c0002t0038 | 0/0 | 5832 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5827): Show |
chr12 | 19434492 | 19527227 |
a0001c0002t0040 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0002t0043 | 0/0 | 5833 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0002t0045 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0003t0001 | 0/0 | 5833 | 2 | 1 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0003t0044 | 0/0 | 5833 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5828): Show |
chr12 | 19434492 | 19527227 |
a0001c0004t0002 | 0/0 | 5830 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0001c0004t0009 | 0/0 | 5829 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5824): Show |
chr12 | 19434492 | 19527227 |
a0001c0005t0023 | 0/0 | 5834 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5829): Show |
chr12 | 19434492 | 19527227 |
a0001c0006t0033 | 0/0 | 5830 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5825): Show |
chr12 | 19434492 | 19527227 |
a0002c0007t0002 | 0/0 | 5806 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | AGTCT others(5801): Show |
chr12 | 19434492 | 19527227 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0219 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0374 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0383 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0003g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0004g0394 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0387 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0007g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0008g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0009g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0009g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0011g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0011g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0011g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0011g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0011g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0011g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0011g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0012g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0012g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0012g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0012g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0012g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0012g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0013g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0013g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0013g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0014g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0014g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0014g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0014g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0015g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0015g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0015g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0016g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0016g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0017g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0018g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0018g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0018g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0019g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0019g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0019g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0020g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0020g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0020g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0021g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0021g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0022g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0022g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0023g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0024g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0025g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0026g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0027g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0028g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0029g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0030g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0031g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0032g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0034g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0035g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0036g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0037g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0039g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0041g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0042g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0046g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0047g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0001t0048g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0010g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0010g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0038g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0040g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0043g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0002t0045g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0003t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0003t0044g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0004t0009g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0005t0023g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0001c0006t0033g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
a0002c0007t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | GBR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0338 | EUR | GBR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0383 | EUR | FIN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00323 | hp2 | a0001 | c0001 | t0014 | g0030 | EUR | FIN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00438 | hp1 | a0001 | c0001 | t0030 | g0349 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00558 | hp2 | a0001 | c0002 | t0010 | g0110 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00639 | hp1 | a0001 | c0001 | t0014 | g0023 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0154 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0339 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0184 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01069 | hp2 | a0001 | c0001 | t0014 | g0028 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0029 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0359 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0252 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0325 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0276 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0052 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0155 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01167 | hp2 | a0001 | c0001 | t0014 | g0033 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01168 | hp2 | a0001 | c0001 | t0009 | g0165 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01169 | hp2 | a0001 | c0001 | t0014 | g0034 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0153 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01243 | hp2 | a0001 | c0001 | t0025 | g0290 | AMR | PUR | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01256 | hp2 | a0001 | c0001 | t0009 | g0170 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0307 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0379 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0240 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0354 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01433 | hp2 | a0001 | c0001 | t0009 | g0211 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01496 | hp1 | a0001 | c0001 | t0006 | g0022 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01496 | hp2 | a0001 | c0001 | t0012 | g0337 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0372 | EUR | IBS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0013 | EUR | IBS | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01884 | hp1 | a0001 | c0001 | t0041 | g0253 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01891 | hp1 | a0001 | c0001 | t0013 | g0164 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0254 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0152 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0017 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01934 | hp2 | a0001 | c0006 | t0033 | g0044 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0138 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0137 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01975 | hp1 | a0001 | c0001 | t0022 | g0131 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0341 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02004 | hp1 | a0001 | c0001 | t0005 | g0136 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02015 | hp2 | a0001 | c0002 | t0040 | g0053 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02027 | hp1 | a0001 | c0001 | t0012 | g0361 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02040 | hp1 | a0001 | c0002 | t0010 | g0104 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0347 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02055 | hp1 | a0001 | c0001 | t0017 | g0047 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02071 | hp1 | a0001 | c0002 | t0043 | g0066 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02074 | hp1 | a0001 | c0001 | t0027 | g0351 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02083 | hp1 | a0001 | c0002 | t0010 | g0069 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02132 | hp2 | a0001 | c0001 | t0007 | g0348 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0163 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0293 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0395 | EAS | CDX | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02258 | hp1 | a0001 | c0003 | t0044 | g0251 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02258 | hp2 | a0001 | c0001 | t0020 | g0265 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02280 | hp2 | a0001 | c0001 | t0015 | g0233 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0376 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0378 | AMR | PEL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02523 | hp1 | a0001 | c0001 | t0011 | g0295 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | KHV | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02572 | hp2 | a0001 | c0001 | t0017 | g0045 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0014 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0396 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02622 | hp2 | a0001 | c0001 | t0015 | g0235 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0317 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0316 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02735 | hp1 | a0001 | c0001 | t0036 | g0264 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02735 | hp2 | a0001 | c0005 | t0023 | g0036 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0279 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02809 | hp1 | a0001 | c0001 | t0035 | g0162 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0236 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02818 | hp2 | a0001 | c0001 | t0024 | g0234 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02886 | hp1 | a0001 | c0001 | t0042 | g0244 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02886 | hp2 | a0001 | c0001 | t0015 | g0237 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0315 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02922 | hp1 | a0001 | c0001 | t0018 | g0232 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02922 | hp2 | a0001 | c0001 | t0020 | g0266 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02965 | hp2 | a0001 | c0001 | t0022 | g0239 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02970 | hp1 | a0001 | c0001 | t0018 | g0231 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02976 | hp1 | a0001 | c0001 | t0020 | g0229 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0256 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0274 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0018 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0394 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03098 | hp1 | a0001 | c0001 | t0034 | g0049 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0319 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0119 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03195 | hp1 | a0001 | c0002 | t0045 | g0123 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0302 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0004 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0020 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0313 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03486 | hp1 | a0001 | c0001 | t0013 | g0160 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0331 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0015 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03492 | hp1 | a0001 | c0001 | t0011 | g0301 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0016 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03516 | hp2 | a0001 | c0001 | t0007 | g0389 | AFR | ESN | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03579 | hp1 | a0001 | c0001 | t0018 | g0230 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0280 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0024 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0364 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0019 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0305 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03834 | hp2 | a0001 | c0001 | t0007 | g0385 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0139 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03942 | hp1 | a0001 | c0001 | t0028 | g0308 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04115 | hp1 | a0001 | c0001 | t0006 | g0031 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0321 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0026 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0381 | SAS | BEB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0286 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0284 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0021 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG04228 | hp2 | a0001 | c0001 | t0039 | g0027 | SAS | STU | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0392 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18612 | hp1 | a0001 | c0001 | t0008 | g0366 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0296 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18906 | hp2 | a0001 | c0001 | t0013 | g0159 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18942 | hp1 | a0001 | c0001 | t0009 | g0188 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0367 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18946 | hp1 | a0001 | c0001 | t0026 | g0344 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18948 | hp1 | a0001 | c0001 | t0029 | g0326 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18948 | hp2 | a0001 | c0001 | t0021 | g0272 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0132 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18950 | hp2 | a0001 | c0001 | t0012 | g0324 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18953 | hp2 | a0001 | c0001 | t0019 | g0037 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18957 | hp1 | a0001 | c0002 | t0038 | g0062 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0003 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18960 | hp1 | a0001 | c0001 | t0011 | g0299 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18960 | hp2 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18962 | hp2 | a0002 | c0007 | t0002 | g0202 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18963 | hp1 | a0001 | c0001 | t0021 | g0271 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0380 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18965 | hp2 | a0001 | c0001 | t0011 | g0277 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18966 | hp2 | a0001 | c0004 | t0009 | g0225 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0388 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18968 | hp1 | a0001 | c0001 | t0008 | g0384 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18972 | hp1 | a0001 | c0001 | t0019 | g0040 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18974 | hp1 | a0001 | c0001 | t0032 | g0181 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18974 | hp2 | a0001 | c0001 | t0008 | g0382 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0375 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18979 | hp2 | a0001 | c0004 | t0002 | g0226 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0363 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18982 | hp1 | a0001 | c0001 | t0046 | g0035 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18983 | hp1 | a0001 | c0001 | t0009 | g0260 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18988 | hp1 | a0001 | c0001 | t0048 | g0377 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18988 | hp2 | a0001 | c0002 | t0010 | g0113 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18989 | hp1 | a0001 | c0001 | t0012 | g0335 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18992 | hp1 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0373 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18998 | hp1 | a0001 | c0001 | t0016 | g0038 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0369 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19004 | hp2 | a0001 | c0001 | t0016 | g0041 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19005 | hp1 | a0001 | c0001 | t0008 | g0332 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19006 | hp2 | a0001 | c0001 | t0047 | g0126 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19054 | hp2 | a0001 | c0001 | t0016 | g0042 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19057 | hp2 | a0001 | c0001 | t0011 | g0288 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19060 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19066 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0102 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19070 | hp2 | a0001 | c0001 | t0012 | g0333 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19079 | hp1 | a0001 | c0001 | t0019 | g0043 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19081 | hp2 | a0001 | c0001 | t0012 | g0365 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19085 | hp2 | a0001 | c0001 | t0009 | g0176 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19086 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19091 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0360 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19240 | hp1 | a0001 | c0001 | t0017 | g0046 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | YRI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ASW | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ASW | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0370 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20752 | hp2 | a0001 | c0001 | t0037 | g0205 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0387 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20805 | hp2 | a0001 | c0001 | t0008 | g0371 | EUR | TSI | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0386 | SAS | GIH | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0327 | SAS | GIH | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG01123 | hp2 | a0001 | c0001 | t0008 | g0350 | AMR | CLM | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02109 | hp1 | a0001 | c0001 | t0013 | g0161 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0362 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0393 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | ACB | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG06807 | hp1 | a0001 | c0001 | t0007 | g0390 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
HG06807 | hp2 | a0001 | c0001 | t0031 | g0032 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA18955 | hp2 | a0001 | c0001 | t0023 | g0309 | EAS | JPT | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0320 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0391 | AFR | USA | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | LWK | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0374 | REF | REF | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0219 | REF | REF | AEBP2_chr12_19434492_19527227 | AEBP2 | chr12 | 19434492 | 19527227 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:19439879 | CGGCGGCA others(17): Show |
C | 1 | a0002 | 1 | NA18962.hp2 | conservative_inframe_deletion | MODERATE | c.187_210delAGCGGTGG others(16): Show |
p.Ser63_Gly70del | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 395/5830 | 187/1512 | 63/503 | INFO_REALIGN_3_PRIME | chr12 | 19439879 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:19439864 | G | C | 1 | a0001c0004 | 2 | NA18966.hp2 NA18979.hp2 |
synonymous_variant | LOW | c.165G>C | p.Ala55Ala | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 373/5830 | 165/1512 | 55/503 | chr12 | 19439864 | |||
chr12:19439966 | C | T | 1 | a0001c0006 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.267C>T | p.Ser89Ser | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 475/5830 | 267/1512 | 89/503 | chr12 | 19439966 | |||
chr12:19440158 | C | T | 1 | a0001c0003 | 3 | HG01081.hp2 HG01891.hp2 HG02258.hp1 |
synonymous_variant | LOW | c.459C>T | p.Asp153Asp | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 667/5830 | 459/1512 | 153/503 | chr12 | 19440158 | |||
chr12:19473271 | T | C | 1 | a0001c0002 | 53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
synonymous_variant | LOW | c.903T>C | p.Gly301Gly | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/8 | 1111/5830 | 903/1512 | 301/503 | chr12 | 19473271 | |||
chr12:19500128 | A | G | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.1206A>G | p.Thr402Thr | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/8 | 1414/5830 | 1206/1512 | 402/503 | chr12 | 19500128 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:19439507 | G | T | 1 | a0001c0001t0048 | 1 | NA18988.hp1 | 5_prime_UTR_variant | MODIFIER | c.-193G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 193 | chr12 | 19439507 | ||||||
chr12:19439666 | G | GGGA | 22 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(19): Show |
133 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(130): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-12dupGAG | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 11 | INFO_REALIGN_3_PRIME | chr12 | 19439666 | |||||
chr12:19439666 | GGGA | G | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(12): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
5_prime_UTR_variant | MODIFIER | c.-14_-12delGAG | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/8 | 12 | INFO_REALIGN_3_PRIME | chr12 | 19439666 | |||||
chr12:19518206 | A | T | 1 | a0001c0001t0037 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 89 | chr12 | 19518206 | ||||||
chr12:19518218 | C | CT | 12 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0020 others(9): Show |
77 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*121dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 122 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | |||||
chr12:19518218 | C | CTT | 1 | a0001c0001t0012 | 6 | HG01496.hp2 HG02027.hp1 NA18950.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*121dupTT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 122 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | |||||
chr12:19518218 | CT | C | 13 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0010 others(10): Show |
56 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*121delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 121 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | |||||
chr12:19518218 | CTT | C | 2 | a0001c0001t0014 a0001c0001t0031 |
6 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*121delTT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 120 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | |||||
chr12:19518218 | CTTT | C | 2 | a0001c0001t0016 a0001c0001t0019 |
7 | NA18953.hp2 NA18972.hp1 NA18998.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*119_*121delTTT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 119 | INFO_REALIGN_3_PRIME | chr12 | 19518218 | |||||
chr12:19518878 | C | T | 1 | a0001c0001t0035 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*761C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 761 | chr12 | 19518878 | ||||||
chr12:19518967 | T | C | 1 | a0001c0001t0019 | 3 | NA18953.hp2 NA18972.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*850T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 850 | chr12 | 19518967 | ||||||
chr12:19519518 | A | G | 1 | a0001c0001t0047 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1401A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1401 | chr12 | 19519518 | ||||||
chr12:19519651 | C | T | 1 | a0001c0001t0030 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1534C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1534 | chr12 | 19519651 | ||||||
chr12:19519830 | A | C | 3 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0046 |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1713A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1713 | chr12 | 19519830 | ||||||
chr12:19519884 | A | T | 1 | a0001c0001t0021 | 2 | NA18948.hp2 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1767A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1767 | chr12 | 19519884 | ||||||
chr12:19519973 | T | G | 1 | a0001c0001t0032 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1856T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 1856 | chr12 | 19519973 | ||||||
chr12:19520427 | T | G | 1 | a0001c0001t0017 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2310T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2310 | chr12 | 19520427 | ||||||
chr12:19520644 | T | A | 1 | a0001c0002t0040 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2527T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2527 | chr12 | 19520644 | ||||||
chr12:19520678 | ACAAGCAT others(19): Show |
A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2562_*2587delCAAG others(22): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2562 | chr12 | 19520678 | ||||||
chr12:19520740 | G | A | 1 | a0001c0001t0041 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2623G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2623 | chr12 | 19520740 | ||||||
chr12:19520764 | C | T | 2 | a0001c0001t0013 a0001c0001t0035 |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2647C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2647 | chr12 | 19520764 | ||||||
chr12:19521067 | T | A | 1 | a0001c0001t0042 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2950T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 2950 | chr12 | 19521067 | ||||||
chr12:19521164 | T | C | 3 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0046 |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3047T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3047 | chr12 | 19521164 | ||||||
chr12:19521228 | T | A | 1 | a0001c0001t0017 | 3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3111T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3111 | chr12 | 19521228 | ||||||
chr12:19521235 | A | T | 2 | a0001c0001t0015 a0001c0001t0024 |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3118A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3118 | chr12 | 19521235 | ||||||
chr12:19521247 | G | C | 11 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(8): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3130G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3130 | chr12 | 19521247 | ||||||
chr12:19521284 | T | C | 1 | a0001c0002t0038 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3167T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3167 | chr12 | 19521284 | ||||||
chr12:19521301 | A | G | 1 | a0001c0001t0018 | 3 | HG02922.hp1 HG02970.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3184A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3184 | chr12 | 19521301 | ||||||
chr12:19521310 | C | T | 1 | a0001c0001t0034 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3193C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3193 | chr12 | 19521310 | ||||||
chr12:19521354 | C | T | 5 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0022 others(2): Show |
37 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3237C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3237 | chr12 | 19521354 | ||||||
chr12:19521407 | T | G | 1 | a0001c0002t0043 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3290T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3290 | chr12 | 19521407 | ||||||
chr12:19521462 | G | A | 1 | a0001c0001t0027 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3345G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3345 | chr12 | 19521462 | ||||||
chr12:19521558 | G | A | 1 | a0001c0003t0044 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3441G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3441 | chr12 | 19521558 | ||||||
chr12:19521577 | T | C | 3 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0046 |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3460T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3460 | chr12 | 19521577 | ||||||
chr12:19521821 | A | G | 2 | a0001c0001t0034 a0001c0006t0033 |
2 | HG01934.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3704A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3704 | chr12 | 19521821 | ||||||
chr12:19521831 | T | A | 1 | a0001c0002t0045 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3714T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3714 | chr12 | 19521831 | ||||||
chr12:19521873 | T | C | 6 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0015 others(3): Show |
32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3756T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3756 | chr12 | 19521873 | ||||||
chr12:19521950 | T | G | 1 | a0001c0001t0028 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3833T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3833 | chr12 | 19521950 | ||||||
chr12:19522067 | A | AT | 4 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0025 others(1): Show |
9 | HG01243.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3962dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3963 | INFO_REALIGN_3_PRIME | chr12 | 19522067 | |||||
chr12:19522067 | A | T | 2 | a0001c0001t0034 a0001c0006t0033 |
2 | HG01934.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3950A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3950 | chr12 | 19522067 | ||||||
chr12:19522079 | T | G | 6 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0015 others(3): Show |
32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3962T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3962 | chr12 | 19522079 | ||||||
chr12:19522092 | C | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3975C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3975 | chr12 | 19522092 | ||||||
chr12:19522094 | T | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3977T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3977 | chr12 | 19522094 | ||||||
chr12:19522101 | G | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3984G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3984 | chr12 | 19522101 | ||||||
chr12:19522103 | T | TCTGTTAA others(25): Show |
1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3986_*3987insCTGT others(28): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 3987 | chr12 | 19522103 | ||||||
chr12:19522122 | C | A | 1 | a0001c0001t0026 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4005C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 4005 | chr12 | 19522122 | ||||||
chr12:19522190 | C | T | 3 | a0001c0001t0013 a0001c0001t0035 a0001c0001t0039 |
7 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4073C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 4073 | chr12 | 19522190 | ||||||
chr12:19522191 | G | A | 3 | a0001c0001t0016 a0001c0001t0019 a0001c0001t0046 |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4074G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 8/8 | 4074 | chr12 | 19522191 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:19440394 | C | T | 1 | a0001c0001t0007g0396 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.671+24C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440394 | |||||||
chr12:19440405 | C | T | 1 | a0001c0001t0003g0006 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.671+35C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440405 | |||||||
chr12:19440539 | C | T | 94 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(91): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.671+169C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440539 | |||||||
chr12:19440579 | C | A | 1 | a0001c0001t0004g0007 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.671+209C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440579 | |||||||
chr12:19440582 | A | G | 42 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(39): Show |
42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.671+212A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440582 | |||||||
chr12:19440631 | C | T | 2 | a0001c0001t0020g0265 a0001c0001t0020g0266 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.671+261C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440631 | |||||||
chr12:19440779 | A | T | 1 | a0001c0001t0004g0305 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.671+409A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440779 | |||||||
chr12:19440818 | G | C | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+448G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440818 | |||||||
chr12:19440861 | C | G | 1 | a0001c0001t0004g0304 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.671+491C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19440861 | |||||||
chr12:19441021 | G | A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+651G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441021 | |||||||
chr12:19441045 | G | A | 1 | a0001c0001t0004g0267 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.671+675G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441045 | |||||||
chr12:19441089 | CAA | C | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0036g0264 |
3 | HG00735.hp2 HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.671+722_671+723del others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19441089 | ||||||
chr12:19441208 | T | G | 98 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(95): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.671+838T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441208 | |||||||
chr12:19441212 | T | C | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+842T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441212 | |||||||
chr12:19441262 | A | G | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+892A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441262 | |||||||
chr12:19441317 | TATC | T | 3 | a0001c0001t0002g0261 a0001c0001t0003g0395 a0001c0001t0009g0260 |
3 | HG02165.hp2 NA18983.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.671+950_671+952del others(3): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19441317 | ||||||
chr12:19441377 | A | G | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+1007A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441377 | |||||||
chr12:19441443 | A | G | 6 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0390 others(3): Show |
7 | HG02559.hp1 HG03041.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.671+1073A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441443 | |||||||
chr12:19441580 | A | T | 1 | a0001c0001t0005g0259 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.671+1210A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441580 | |||||||
chr12:19441605 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.671+1235G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441605 | |||||||
chr12:19441687 | G | T | 2 | a0001c0001t0004g0302 a0001c0001t0004g0303 |
2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.671+1317G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441687 | |||||||
chr12:19441840 | A | G | 18 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
18 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.671+1470A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441840 | |||||||
chr12:19441897 | A | T | 1 | a0001c0002t0001g0240 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.671+1527A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19441897 | |||||||
chr12:19442306 | G | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.671+1936G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442306 | |||||||
chr12:19442322 | C | T | 2 | a0001c0001t0005g0238 a0001c0001t0022g0239 |
2 | HG02257.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.671+1952C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442322 | |||||||
chr12:19442455 | T | C | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2085T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442455 | |||||||
chr12:19442509 | G | A | 104 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(101): Show |
104 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.671+2139G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442509 | |||||||
chr12:19442538 | T | G | 1 | a0001c0001t0017g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.671+2168T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442538 | |||||||
chr12:19442674 | C | T | 136 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(133): Show |
136 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.671+2304C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442674 | |||||||
chr12:19442679 | G | A | 323 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(320): Show |
325 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.671+2309G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442679 | |||||||
chr12:19442685 | T | A | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+2315T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442685 | |||||||
chr12:19442696 | T | G | 42 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(39): Show |
42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.671+2326T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442696 | |||||||
chr12:19442726 | T | G | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 |
3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.671+2356T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442726 | |||||||
chr12:19442785 | A | G | 3 | a0001c0001t0018g0230 a0001c0001t0018g0231 a0001c0001t0018g0232 |
3 | HG02922.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.671+2415A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19442785 | |||||||
chr12:19443026 | G | A | 1 | a0001c0002t0040g0053 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.671+2656G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443026 | |||||||
chr12:19443037 | G | A | 1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.671+2667G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443037 | |||||||
chr12:19443103 | CT | C | 323 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(320): Show |
325 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.671+2745delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19443103 | ||||||
chr12:19443133 | A | G | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2763A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443133 | |||||||
chr12:19443190 | GGGTT | G | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+2821_671+2824d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443190 | |||||||
chr12:19443266 | T | G | 31 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(28): Show |
31 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.671+2896T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443266 | |||||||
chr12:19443332 | A | G | 148 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(145): Show |
148 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.671+2962A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443332 | |||||||
chr12:19443416 | C | G | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3046C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443416 | |||||||
chr12:19443438 | G | T | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.671+3068G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443438 | |||||||
chr12:19443448 | G | T | 1 | a0001c0001t0002g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.671+3078G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443448 | |||||||
chr12:19443485 | G | A | 3 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 |
3 | HG01346.hp1 HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.671+3115G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443485 | |||||||
chr12:19443553 | T | C | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.671+3183T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443553 | |||||||
chr12:19443669 | G | A | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+3299G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443669 | |||||||
chr12:19443813 | T | C | 1 | a0001c0001t0006g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.671+3443T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443813 | |||||||
chr12:19443839 | C | G | 4 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0129 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+3469C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443839 | |||||||
chr12:19443859 | AT | A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3496delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19443859 | ||||||
chr12:19443866 | T | C | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3496T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443866 | |||||||
chr12:19443868 | C | A | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+3498C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443868 | |||||||
chr12:19443893 | C | G | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.671+3523C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19443893 | |||||||
chr12:19443966 | CTTTGGTT others(23): Show |
C | 1 | a0001c0001t0004g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.671+3629_671+3658d others(32): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19443966 | ||||||
chr12:19444043 | G | A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3673G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444043 | |||||||
chr12:19444144 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.671+3774G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444144 | |||||||
chr12:19444160 | A | T | 3 | a0001c0001t0005g0156 a0001c0001t0005g0157 a0001c0001t0005g0158 |
3 | HG02647.hp1 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.671+3790A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444160 | |||||||
chr12:19444162 | T | A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+3792T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444162 | |||||||
chr12:19444163 | T | A | 145 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(142): Show |
147 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.671+3793T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444163 | |||||||
chr12:19444421 | A | G | 32 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(29): Show |
32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.671+4051A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444421 | |||||||
chr12:19444559 | G | C | 322 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(319): Show |
324 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.671+4189G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444559 | |||||||
chr12:19444587 | C | A | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.671+4217C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444587 | |||||||
chr12:19444626 | A | G | 1 | a0001c0001t0004g0305 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.671+4256A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444626 | |||||||
chr12:19444736 | C | T | 104 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(101): Show |
104 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.671+4366C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444736 | |||||||
chr12:19444933 | C | T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.671+4563C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444933 | |||||||
chr12:19444936 | G | A | 1 | a0001c0001t0003g0307 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.671+4566G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19444936 | |||||||
chr12:19445013 | G | A | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+4643G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445013 | |||||||
chr12:19445168 | A | G | 1 | a0001c0002t0002g0125 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.671+4798A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445168 | |||||||
chr12:19445201 | A | G | 323 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(320): Show |
325 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.671+4831A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445201 | |||||||
chr12:19445303 | A | G | 1 | a0001c0001t0007g0389 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.671+4933A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445303 | |||||||
chr12:19445308 | C | T | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+4938C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445308 | |||||||
chr12:19445337 | T | A | 1 | a0001c0001t0003g0307 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.671+4967T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445337 | |||||||
chr12:19445354 | G | A | 323 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(320): Show |
325 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.671+4984G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445354 | |||||||
chr12:19445364 | C | T | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+4994C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445364 | |||||||
chr12:19445370 | C | CT | 17 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0002g0223 others(14): Show |
17 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.671+5017dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445370 | ||||||
chr12:19445370 | CT | C | 28 | a0001c0001t0002g0166 a0001c0001t0002g0167 a0001c0001t0003g0388 others(25): Show |
28 | HG00438.hp2 HG00621.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.671+5017delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445370 | ||||||
chr12:19445370 | CTT | C | 106 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(103): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.671+5016_671+5017d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445370 | ||||||
chr12:19445525 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.671+5155A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445525 | |||||||
chr12:19445798 | C | A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+5428C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445798 | |||||||
chr12:19445887 | ATAAC | A | 28 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(25): Show |
28 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.671+5520_671+5523d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19445887 | ||||||
chr12:19445967 | A | G | 1 | a0001c0001t0019g0043 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.671+5597A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445967 | |||||||
chr12:19445970 | A | C | 1 | a0001c0001t0015g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.671+5600A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19445970 | |||||||
chr12:19446004 | C | T | 1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.671+5634C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446004 | |||||||
chr12:19446011 | T | A | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.671+5641T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446011 | |||||||
chr12:19446022 | C | A | 94 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(91): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.671+5652C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446022 | |||||||
chr12:19446067 | A | G | 40 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(37): Show |
40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.671+5697A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446067 | |||||||
chr12:19446100 | A | AATGGCTA others(3): Show |
107 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(104): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.671+5735_671+5736i others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446100 | ||||||
chr12:19446151 | T | C | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+5781T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446151 | |||||||
chr12:19446194 | C | T | 1 | a0001c0001t0004g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.671+5824C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446194 | |||||||
chr12:19446457 | C | T | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.671+6087C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446457 | |||||||
chr12:19446467 | C | T | 1 | a0001c0002t0045g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.671+6097C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446467 | |||||||
chr12:19446516 | T | C | 1 | a0001c0001t0022g0131 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.671+6146T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446516 | |||||||
chr12:19446546 | G | A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+6176G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446546 | |||||||
chr12:19446556 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.671+6186C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446556 | |||||||
chr12:19446599 | G | A | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+6229G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446599 | |||||||
chr12:19446600 | C | G | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+6230C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446600 | |||||||
chr12:19446601 | G | A | 10 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(7): Show |
10 | HG02735.hp2 HG03942.hp1 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.671+6231G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446601 | |||||||
chr12:19446605 | A | C | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.671+6235A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446605 | |||||||
chr12:19446621 | A | G | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.671+6251A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446621 | |||||||
chr12:19446671 | G | A | 136 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(133): Show |
136 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.671+6301G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446671 | |||||||
chr12:19446718 | C | T | 2 | a0001c0002t0001g0118 a0001c0002t0001g0119 |
2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.671+6348C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446718 | |||||||
chr12:19446732 | C | CAAA | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+6379_671+6381d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446732 | ||||||
chr12:19446732 | CA | C | 44 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0120 others(41): Show |
44 | HG00323.hp2 HG00609.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.671+6381delA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446732 | ||||||
chr12:19446732 | CAA | C | 268 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0064 others(265): Show |
270 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.671+6380_671+6381d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19446732 | ||||||
chr12:19446794 | T | G | 323 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(320): Show |
325 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(322): Show |
intron_variant | MODIFIER | c.671+6424T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446794 | |||||||
chr12:19446837 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.671+6467G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446837 | |||||||
chr12:19446872 | A | G | 1 | a0001c0001t0011g0299 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.671+6502A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446872 | |||||||
chr12:19446912 | A | G | 1 | a0001c0001t0031g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671+6542A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446912 | |||||||
chr12:19446967 | T | G | 1 | a0001c0001t0006g0012 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.671+6597T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19446967 | |||||||
chr12:19447097 | A | G | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.671+6727A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447097 | |||||||
chr12:19447247 | T | G | 379 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(376): Show |
385 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(382): Show |
intron_variant | MODIFIER | c.671+6877T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447247 | |||||||
chr12:19447298 | T | C | 99 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(96): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.671+6928T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447298 | |||||||
chr12:19447325 | C | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+6955C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447325 | |||||||
chr12:19447326 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.671+6956G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447326 | |||||||
chr12:19447489 | A | G | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+7119A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447489 | |||||||
chr12:19447536 | A | G | 1 | a0001c0001t0003g0313 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.671+7166A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447536 | |||||||
chr12:19447618 | A | G | 1 | a0001c0001t0004g0297 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.671+7248A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447618 | |||||||
chr12:19447687 | TTA | T | 322 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(319): Show |
324 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(321): Show |
intron_variant | MODIFIER | c.671+7323_671+7324d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19447687 | ||||||
chr12:19447744 | G | A | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+7374G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447744 | |||||||
chr12:19447985 | G | A | 8 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0315 others(5): Show |
9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+7615G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19447985 | |||||||
chr12:19448203 | T | G | 108 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(105): Show |
110 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.671+7833T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448203 | |||||||
chr12:19448258 | A | G | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+7888A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448258 | |||||||
chr12:19448310 | G | A | 1 | a0001c0001t0004g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.671+7940G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448310 | |||||||
chr12:19448422 | T | A | 94 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(91): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.671+8052T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448422 | |||||||
chr12:19448447 | T | G | 1 | a0001c0002t0002g0060 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.671+8077T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448447 | |||||||
chr12:19448498 | A | G | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+8128A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448498 | |||||||
chr12:19448500 | T | G | 140 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(137): Show |
140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+8130T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448500 | |||||||
chr12:19448572 | A | G | 1 | a0001c0001t0031g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671+8202A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448572 | |||||||
chr12:19448607 | A | T | 82 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(79): Show |
83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.671+8237A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448607 | |||||||
chr12:19448640 | A | G | 11 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(8): Show |
11 | HG01934.hp2 HG02735.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.671+8270A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448640 | |||||||
chr12:19448666 | A | G | 2 | a0001c0001t0020g0265 a0001c0001t0020g0266 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.671+8296A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448666 | |||||||
chr12:19448744 | G | A | 41 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(38): Show |
41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.671+8374G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448744 | |||||||
chr12:19448790 | C | A | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.671+8420C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448790 | |||||||
chr12:19448832 | A | G | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.671+8462A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448832 | |||||||
chr12:19448846 | C | A | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.671+8476C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448846 | |||||||
chr12:19448895 | G | A | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+8525G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448895 | |||||||
chr12:19448977 | G | A | 4 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0129 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+8607G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19448977 | |||||||
chr12:19449034 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.671+8664T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449034 | |||||||
chr12:19449265 | C | A | 1 | a0001c0002t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.671+8895C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449265 | |||||||
chr12:19449478 | T | C | 1 | a0001c0001t0031g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.671+9108T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449478 | |||||||
chr12:19449505 | G | T | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.671+9135G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449505 | |||||||
chr12:19449516 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+9146A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449516 | |||||||
chr12:19449553 | T | C | 140 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(137): Show |
140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+9183T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449553 | |||||||
chr12:19449681 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+9311A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449681 | |||||||
chr12:19449754 | T | C | 1 | a0001c0001t0002g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.671+9384T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449754 | |||||||
chr12:19449825 | T | C | 4 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.671+9455T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449825 | |||||||
chr12:19449921 | G | A | 326 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(323): Show |
328 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.671+9551G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19449921 | |||||||
chr12:19450016 | G | C | 326 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(323): Show |
328 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.671+9646G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450016 | |||||||
chr12:19450130 | C | A | 74 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(71): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.671+9760C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450130 | |||||||
chr12:19450160 | A | AAGACCAG others(49): Show |
1 | a0001c0001t0002g0174 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.671+9792_671+9847d others(58): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450160 | ||||||
chr12:19450192 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671+9822C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450192 | |||||||
chr12:19450318 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.671+9948C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450318 | |||||||
chr12:19450322 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.671+9952C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450322 | |||||||
chr12:19450349 | A | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.671+9979A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450349 | |||||||
chr12:19450355 | A | T | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+9985A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450355 | |||||||
chr12:19450458 | T | C | 140 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(137): Show |
140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+10088T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450458 | |||||||
chr12:19450469 | A | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG00735.hp2 HG01074.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+10099A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450469 | |||||||
chr12:19450474 | G | C | 1 | a0001c0002t0001g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671+10104G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450474 | |||||||
chr12:19450567 | T | C | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.671+10197T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450567 | |||||||
chr12:19450574 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.671+10204A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450574 | |||||||
chr12:19450655 | T | G | 140 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(137): Show |
140 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(137): Show |
intron_variant | MODIFIER | c.671+10285T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450655 | |||||||
chr12:19450667 | C | CA | 133 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(130): Show |
135 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.671+10311dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450667 | ||||||
chr12:19450668 | AAAAAAAA others(7): Show |
A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.671+10309_671+1032 others(18): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450668 | ||||||
chr12:19450685 | A | T | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.671+10315A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450685 | |||||||
chr12:19450709 | G | T | 1 | a0001c0001t0005g0153 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.671+10339G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450709 | |||||||
chr12:19450800 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.671+10430C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450800 | |||||||
chr12:19450818 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.671+10448A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450818 | |||||||
chr12:19450842 | C | CA | 116 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0241 others(113): Show |
118 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.671+10483dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450842 | ||||||
chr12:19450859 | A | AT | 19 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(16): Show |
19 | HG00438.hp2 HG01081.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.671+10500dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450859 | ||||||
chr12:19450859 | A | T | 1 | a0001c0001t0010g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.671+10489A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19450859 | |||||||
chr12:19450987 | GT | G | 324 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(321): Show |
326 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.671+10627delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19450987 | ||||||
chr12:19451147 | C | G | 4 | a0001c0001t0006g0029 a0001c0001t0006g0031 a0001c0001t0014g0028 others(1): Show |
4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.671+10777C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451147 | |||||||
chr12:19451199 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.671+10829C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451199 | |||||||
chr12:19451259 | G | A | 41 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(38): Show |
41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.671+10889G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451259 | |||||||
chr12:19451432 | G | C | 395 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(392): Show |
401 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(398): Show |
intron_variant | MODIFIER | c.671+11062G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451432 | |||||||
chr12:19451489 | G | A | 326 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(323): Show |
328 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.672-11021G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451489 | |||||||
chr12:19451520 | A | G | 2 | a0001c0001t0002g0207 a0001c0001t0037g0205 |
2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.672-10990A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451520 | |||||||
chr12:19451558 | G | A | 1 | a0001c0001t0018g0230 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.672-10952G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451558 | |||||||
chr12:19451573 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.672-10937G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451573 | |||||||
chr12:19451660 | G | A | 2 | a0001c0001t0021g0271 a0001c0001t0021g0272 |
2 | NA18948.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.672-10850G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451660 | |||||||
chr12:19451686 | A | AT | 137 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0058 others(134): Show |
137 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.672-10808dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19451686 | ||||||
chr12:19451686 | AT | A | 45 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(42): Show |
45 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.672-10808delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19451686 | ||||||
chr12:19451686 | ATT | A | 98 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(95): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.672-10809_672-1080 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19451686 | ||||||
chr12:19451753 | G | A | 106 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(103): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.672-10757G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451753 | |||||||
chr12:19451983 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.672-10527C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451983 | |||||||
chr12:19451993 | C | T | 1 | a0001c0001t0010g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.672-10517C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19451993 | |||||||
chr12:19452081 | G | C | 1 | a0001c0001t0003g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.672-10429G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452081 | |||||||
chr12:19452162 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.672-10348A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452162 | |||||||
chr12:19452327 | A | AC | 47 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(44): Show |
47 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.672-10182dupC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452327 | ||||||
chr12:19452512 | T | G | 11 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(8): Show |
11 | HG01934.hp2 HG02735.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-9998T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452512 | |||||||
chr12:19452515 | G | T | 1 | a0001c0001t0002g0174 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9995G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452515 | |||||||
chr12:19452516 | T | G | 1 | a0001c0001t0002g0174 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9994T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452516 | |||||||
chr12:19452672 | G | C | 1 | a0001c0001t0003g0322 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.672-9838G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452672 | |||||||
chr12:19452961 | C | CT | 143 | a0001c0001t0001g0058 a0001c0001t0001g0111 a0001c0001t0001g0117 others(140): Show |
145 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.672-9527dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | ||||||
chr12:19452961 | C | CTT | 13 | a0001c0001t0003g0311 a0001c0001t0003g0321 a0001c0001t0003g0376 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-9528_672-9527d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | ||||||
chr12:19452961 | CT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0242 a0001c0001t0002g0175 others(4): Show |
7 | HG00639.hp2 HG01256.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-9527delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | ||||||
chr12:19452961 | CTTTTT | C | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-9531_672-9527d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | ||||||
chr12:19452961 | CTTTTTTT others(4): Show |
C | 47 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(44): Show |
47 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.672-9537_672-9527d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19452961 | ||||||
chr12:19452988 | C | T | 1 | a0001c0001t0005g0152 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.672-9522C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19452988 | |||||||
chr12:19453004 | C | T | 99 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(96): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.672-9506C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453004 | |||||||
chr12:19453037 | C | T | 1 | a0001c0001t0003g0375 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.672-9473C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453037 | |||||||
chr12:19453114 | A | G | 326 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(323): Show |
328 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.672-9396A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453114 | |||||||
chr12:19453131 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-9379G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453131 | |||||||
chr12:19453169 | C | T | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-9341C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453169 | |||||||
chr12:19453228 | C | A | 1 | a0001c0001t0002g0174 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9282C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453228 | |||||||
chr12:19453230 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.672-9280A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453230 | |||||||
chr12:19453232 | G | A | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02735.hp2 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-9278G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453232 | |||||||
chr12:19453259 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.672-9251G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453259 | |||||||
chr12:19453279 | A | T | 109 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(106): Show |
111 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.672-9231A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453279 | |||||||
chr12:19453323 | G | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-9187G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453323 | |||||||
chr12:19453335 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-9175C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453335 | |||||||
chr12:19453424 | C | CT | 48 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0267 others(45): Show |
48 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.672-9083dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19453424 | ||||||
chr12:19453424 | C | CTT | 94 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(91): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.672-9084_672-9083d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19453424 | ||||||
chr12:19453424 | C | CTTT | 3 | a0001c0001t0003g0375 a0001c0001t0003g0381 a0001c0001t0004g0284 |
3 | HG04184.hp2 HG04199.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.672-9085_672-9083d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19453424 | ||||||
chr12:19453428 | C | T | 297 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(294): Show |
299 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(296): Show |
intron_variant | MODIFIER | c.672-9082C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453428 | |||||||
chr12:19453506 | C | T | 5 | a0001c0001t0001g0058 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | NA18944.hp1 NA18973.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-9004C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453506 | |||||||
chr12:19453554 | G | C | 1 | a0001c0001t0009g0170 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.672-8956G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453554 | |||||||
chr12:19453578 | C | T | 4 | a0001c0001t0006g0029 a0001c0001t0006g0031 a0001c0001t0014g0028 others(1): Show |
4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-8932C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453578 | |||||||
chr12:19453815 | A | G | 1 | a0001c0002t0001g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.672-8695A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19453815 | |||||||
chr12:19454036 | T | A | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.672-8474T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454036 | |||||||
chr12:19454039 | C | T | 45 | a0001c0001t0003g0310 a0001c0001t0003g0373 a0001c0001t0004g0003 others(42): Show |
45 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.672-8471C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454039 | |||||||
chr12:19454201 | A | G | 1 | a0001c0001t0005g0153 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.672-8309A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454201 | |||||||
chr12:19454265 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.672-8245C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454265 | |||||||
chr12:19454359 | CCA | C | 3 | a0001c0001t0002g0174 a0001c0002t0001g0105 a0001c0002t0038g0062 |
3 | NA18952.hp2 NA18957.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.672-8139_672-8138d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19454359 | ||||||
chr12:19454360 | C | T | 31 | a0001c0001t0003g0321 a0001c0001t0003g0372 a0001c0001t0003g0379 others(28): Show |
31 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.672-8150C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454360 | |||||||
chr12:19454370 | C | A | 1 | a0001c0001t0005g0134 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.672-8140C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454370 | |||||||
chr12:19454454 | C | T | 1 | a0001c0001t0006g0012 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.672-8056C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454454 | |||||||
chr12:19454534 | G | A | 2 | a0001c0002t0002g0060 a0001c0002t0002g0125 |
2 | NA18991.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.672-7976G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454534 | |||||||
chr12:19454548 | C | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.672-7962C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454548 | |||||||
chr12:19454632 | A | G | 2 | a0001c0001t0013g0163 a0001c0001t0035g0162 |
2 | HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.672-7878A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454632 | |||||||
chr12:19454702 | C | T | 2 | a0001c0001t0017g0045 a0001c0001t0017g0047 |
2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.672-7808C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454702 | |||||||
chr12:19454764 | C | G | 34 | a0001c0001t0003g0313 a0001c0001t0003g0321 a0001c0001t0003g0370 others(31): Show |
34 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.672-7746C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454764 | |||||||
chr12:19454783 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0117 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.672-7727G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454783 | |||||||
chr12:19454858 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7652C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454858 | |||||||
chr12:19454858 | C | T | 1 | a0001c0001t0005g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.672-7652C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454858 | |||||||
chr12:19454942 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0008g0327 |
3 | HG02896.hp2 HG02897.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.672-7568G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454942 | |||||||
chr12:19454946 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7564A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19454946 | |||||||
chr12:19455002 | G | T | 1 | a0001c0002t0010g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.672-7508G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455002 | |||||||
chr12:19455003 | A | ATTT | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7495_672-7493d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455003 | ||||||
chr12:19455044 | C | T | 2 | a0001c0001t0002g0207 a0001c0001t0037g0205 |
2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.672-7466C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455044 | |||||||
chr12:19455067 | A | G | 1 | a0001c0001t0007g0389 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.672-7443A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455067 | |||||||
chr12:19455096 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-7414A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455096 | |||||||
chr12:19455105 | C | T | 54 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(51): Show |
54 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.672-7405C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455105 | |||||||
chr12:19455160 | A | AT | 31 | a0001c0001t0003g0313 a0001c0001t0003g0321 a0001c0001t0003g0372 others(28): Show |
31 | HG00323.hp2 HG00639.hp1 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.672-7336dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455160 | ||||||
chr12:19455160 | AT | A | 8 | a0001c0001t0003g0328 a0001c0001t0003g0329 a0001c0001t0005g0156 others(5): Show |
8 | HG01934.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.672-7336delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455160 | ||||||
chr12:19455185 | G | T | 8 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0315 others(5): Show |
9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.672-7325G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455185 | |||||||
chr12:19455267 | G | T | 1 | a0001c0002t0001g0091 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.672-7243G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455267 | |||||||
chr12:19455270 | G | A | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.672-7240G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455270 | |||||||
chr12:19455272 | C | T | 13 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(10): Show |
13 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.672-7238C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455272 | |||||||
chr12:19455460 | A | C | 38 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(35): Show |
38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-7050A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455460 | |||||||
chr12:19455504 | C | G | 24 | a0001c0002t0001g0059 a0001c0002t0001g0074 a0001c0002t0001g0075 others(21): Show |
24 | HG01358.hp1 HG01928.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.672-7006C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455504 | |||||||
chr12:19455570 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0004g0274 |
2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.672-6940G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455570 | |||||||
chr12:19455684 | A | G | 4 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.672-6826A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455684 | |||||||
chr12:19455695 | C | T | 1 | a0001c0001t0028g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.672-6815C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455695 | |||||||
chr12:19455730 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-6780A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455730 | |||||||
chr12:19455944 | C | CT | 39 | a0001c0001t0002g0174 a0001c0001t0003g0313 a0001c0001t0003g0321 others(36): Show |
39 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.672-6555dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455944 | ||||||
chr12:19455955 | T | C | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.672-6555T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19455955 | |||||||
chr12:19455955 | T | TC | 109 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.672-6553dupC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19455955 | ||||||
chr12:19456080 | C | G | 4 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0320 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-6430C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456080 | |||||||
chr12:19456082 | A | T | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-6428A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456082 | |||||||
chr12:19456162 | A | G | 1 | a0001c0002t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.672-6348A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456162 | |||||||
chr12:19456175 | A | G | 1 | a0001c0001t0002g0201 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.672-6335A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456175 | |||||||
chr12:19456227 | A | G | 1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.672-6283A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456227 | |||||||
chr12:19456330 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-6180A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456330 | |||||||
chr12:19456526 | A | G | 1 | a0001c0001t0020g0266 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672-5984A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456526 | |||||||
chr12:19456569 | A | G | 147 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(144): Show |
149 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.672-5941A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456569 | |||||||
chr12:19456619 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-5891C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456619 | |||||||
chr12:19456713 | A | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-5797A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456713 | |||||||
chr12:19456778 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-5732T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456778 | |||||||
chr12:19456791 | A | T | 112 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(109): Show |
112 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(109): Show |
intron_variant | MODIFIER | c.672-5719A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456791 | |||||||
chr12:19456819 | A | G | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-5691A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456819 | |||||||
chr12:19456945 | C | A | 32 | a0001c0001t0003g0321 a0001c0001t0003g0372 a0001c0001t0003g0379 others(29): Show |
32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.672-5565C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456945 | |||||||
chr12:19456995 | G | A | 329 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(326): Show |
331 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.672-5515G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19456995 | |||||||
chr12:19457018 | A | G | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.672-5492A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457018 | |||||||
chr12:19457019 | A | C | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.672-5491A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457019 | |||||||
chr12:19457093 | A | G | 1 | a0001c0001t0006g0025 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.672-5417A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457093 | |||||||
chr12:19457097 | T | C | 86 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(83): Show |
86 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.672-5413T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457097 | |||||||
chr12:19457279 | C | T | 149 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(146): Show |
149 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.672-5231C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457279 | |||||||
chr12:19457319 | T | G | 1 | a0001c0001t0003g0330 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.672-5191T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457319 | |||||||
chr12:19457324 | G | A | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.672-5186G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457324 | |||||||
chr12:19457358 | G | T | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.672-5152G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457358 | |||||||
chr12:19457803 | C | G | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.672-4707C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19457803 | |||||||
chr12:19458032 | A | C | 4 | a0001c0001t0002g0166 a0001c0001t0002g0200 a0001c0001t0002g0221 others(1): Show |
4 | NA18940.hp2 NA18967.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-4478A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458032 | |||||||
chr12:19458507 | T | C | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.672-4003T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458507 | |||||||
chr12:19458585 | C | G | 1 | a0001c0001t0007g0389 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.672-3925C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458585 | |||||||
chr12:19458593 | A | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-3917A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458593 | |||||||
chr12:19458765 | T | G | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3745T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458765 | |||||||
chr12:19458835 | G | A | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.672-3675G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458835 | |||||||
chr12:19458885 | G | A | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-3625G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458885 | |||||||
chr12:19458961 | G | T | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.672-3549G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19458961 | |||||||
chr12:19459028 | T | A | 4 | a0001c0001t0006g0029 a0001c0001t0006g0031 a0001c0001t0014g0028 others(1): Show |
4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.672-3482T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459028 | |||||||
chr12:19459076 | T | C | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.672-3434T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459076 | |||||||
chr12:19459131 | G | A | 1 | a0001c0002t0001g0118 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.672-3379G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459131 | |||||||
chr12:19459164 | T | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-3346T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459164 | |||||||
chr12:19459384 | A | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-3126A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459384 | |||||||
chr12:19459539 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-2971C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459539 | |||||||
chr12:19459560 | A | G | 38 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(35): Show |
38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-2950A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459560 | |||||||
chr12:19459561 | T | C | 6 | a0001c0001t0003g0313 a0001c0001t0003g0321 a0001c0001t0003g0372 others(3): Show |
6 | HG01261.hp1 HG01515.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.672-2949T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459561 | |||||||
chr12:19459567 | A | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-2943A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459567 | |||||||
chr12:19459755 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-2755T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19459755 | |||||||
chr12:19460050 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-2460T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460050 | |||||||
chr12:19460093 | C | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.672-2417C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460093 | |||||||
chr12:19460094 | G | A | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.672-2416G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460094 | |||||||
chr12:19460114 | T | G | 38 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(35): Show |
38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-2396T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460114 | |||||||
chr12:19460135 | G | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.672-2375G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460135 | |||||||
chr12:19460391 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.672-2119G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460391 | |||||||
chr12:19460443 | C | T | 1 | a0001c0001t0024g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.672-2067C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460443 | |||||||
chr12:19460459 | A | G | 1 | a0001c0001t0018g0232 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.672-2051A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460459 | |||||||
chr12:19460477 | C | T | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.672-2033C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460477 | |||||||
chr12:19460478 | C | G | 1 | a0001c0001t0003g0395 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.672-2032C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460478 | |||||||
chr12:19460542 | T | C | 300 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(297): Show |
302 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.672-1968T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460542 | |||||||
chr12:19460657 | G | GT | 11 | a0001c0001t0001g0092 a0001c0001t0001g0103 a0001c0001t0001g0255 others(8): Show |
11 | HG02074.hp2 HG02615.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.672-1838dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | 19460657 | ||||||
chr12:19460678 | A | G | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.672-1832A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460678 | |||||||
chr12:19460780 | G | A | 1 | a0001c0001t0008g0331 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.672-1730G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460780 | |||||||
chr12:19460886 | T | C | 150 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(147): Show |
152 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.672-1624T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460886 | |||||||
chr12:19460915 | A | G | 38 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(35): Show |
38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-1595A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460915 | |||||||
chr12:19460937 | C | T | 88 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(85): Show |
90 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.672-1573C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19460937 | |||||||
chr12:19461114 | A | G | 3 | a0001c0002t0001g0089 a0001c0002t0001g0240 a0001c0002t0010g0113 |
3 | HG01358.hp1 HG01928.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.672-1396A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461114 | |||||||
chr12:19461180 | G | A | 1 | a0001c0001t0004g0275 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.672-1330G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461180 | |||||||
chr12:19461226 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-1284A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461226 | |||||||
chr12:19461254 | T | G | 38 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(35): Show |
38 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.672-1256T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461254 | |||||||
chr12:19461270 | T | G | 5 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 others(2): Show |
5 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-1240T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461270 | |||||||
chr12:19461338 | C | G | 1 | a0001c0001t0004g0296 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.672-1172C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461338 | |||||||
chr12:19461338 | C | T | 28 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.672-1172C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461338 | |||||||
chr12:19461460 | T | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-1050T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461460 | |||||||
chr12:19461489 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-1021G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461489 | |||||||
chr12:19461590 | A | G | 1 | a0001c0001t0004g0394 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.672-920A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461590 | |||||||
chr12:19461704 | T | A | 94 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(91): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.672-806T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461704 | |||||||
chr12:19461728 | T | C | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.672-782T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461728 | |||||||
chr12:19461848 | T | G | 1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.672-662T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461848 | |||||||
chr12:19461861 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-649C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461861 | |||||||
chr12:19461940 | A | G | 2 | a0001c0001t0006g0014 a0001c0001t0006g0024 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.672-570A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19461940 | |||||||
chr12:19462140 | C | T | 5 | a0001c0001t0001g0250 a0001c0001t0041g0253 a0001c0003t0001g0252 others(2): Show |
5 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.672-370C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19462140 | |||||||
chr12:19462180 | A | G | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.672-330A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19462180 | |||||||
chr12:19462307 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.672-203C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 1/7 | chr12 | 19462307 | |||||||
chr12:19463019 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.879+302G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463019 | |||||||
chr12:19463087 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.879+370G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463087 | |||||||
chr12:19463100 | G | T | 109 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.879+383G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463100 | |||||||
chr12:19463150 | A | G | 1 | a0001c0001t0006g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.879+433A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463150 | |||||||
chr12:19463167 | G | C | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.879+450G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463167 | |||||||
chr12:19463228 | G | A | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 |
3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.879+511G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463228 | |||||||
chr12:19463317 | T | C | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.879+600T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463317 | |||||||
chr12:19463351 | A | G | 3 | a0001c0002t0001g0089 a0001c0002t0001g0240 a0001c0002t0010g0113 |
3 | HG01358.hp1 HG01928.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.879+634A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463351 | |||||||
chr12:19463621 | A | G | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.879+904A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463621 | |||||||
chr12:19463624 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+907G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463624 | |||||||
chr12:19463640 | C | T | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+923C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463640 | |||||||
chr12:19463667 | A | AT | 68 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(65): Show |
69 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.879+974dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | ||||||
chr12:19463667 | A | ATT | 68 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(65): Show |
69 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.879+973_879+974dup others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | ||||||
chr12:19463667 | A | ATTT | 16 | a0001c0001t0003g0312 a0001c0001t0003g0313 a0001c0001t0003g0314 others(13): Show |
16 | HG01361.hp2 HG02027.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.879+972_879+974dup others(3): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | ||||||
chr12:19463667 | AT | A | 88 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0005g0135 others(85): Show |
88 | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.879+974delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | ||||||
chr12:19463667 | ATT | A | 48 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(45): Show |
48 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.879+973_879+974del others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | ||||||
chr12:19463667 | ATTTT | A | 7 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(4): Show |
7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+971_879+974del others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19463667 | ||||||
chr12:19463890 | T | G | 1 | a0001c0001t0012g0333 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.879+1173T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463890 | |||||||
chr12:19463942 | A | T | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.879+1225A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19463942 | |||||||
chr12:19464102 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0016 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.879+1385G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464102 | |||||||
chr12:19464107 | C | T | 4 | a0001c0001t0003g0321 a0001c0001t0003g0379 a0001c0001t0003g0381 others(1): Show |
4 | HG01261.hp1 HG04115.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1390C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464107 | |||||||
chr12:19464145 | C | T | 1 | a0001c0001t0031g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+1428C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464145 | |||||||
chr12:19464248 | T | G | 1 | a0001c0002t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.879+1531T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464248 | |||||||
chr12:19464354 | G | T | 1 | a0001c0001t0008g0384 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.879+1637G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464354 | |||||||
chr12:19464355 | C | T | 1 | a0001c0001t0008g0384 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.879+1638C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464355 | |||||||
chr12:19464403 | T | C | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+1686T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464403 | |||||||
chr12:19464423 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.879+1706C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464423 | |||||||
chr12:19464437 | G | A | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+1720G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464437 | |||||||
chr12:19464458 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+1741C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464458 | |||||||
chr12:19464521 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.879+1804A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464521 | |||||||
chr12:19464551 | GATTTTTA others(4): Show |
G | 1 | a0001c0001t0004g0283 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.879+1846_879+1856d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19464551 | ||||||
chr12:19464592 | A | AT | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.879+1886dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19464592 | ||||||
chr12:19464667 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.879+1950A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464667 | |||||||
chr12:19464679 | C | T | 1 | a0001c0001t0014g0030 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.879+1962C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464679 | |||||||
chr12:19464770 | G | A | 1 | a0001c0001t0012g0335 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.879+2053G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464770 | |||||||
chr12:19464885 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.879+2168C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464885 | |||||||
chr12:19464916 | A | G | 2 | a0001c0001t0003g0383 a0001c0001t0008g0359 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.879+2199A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464916 | |||||||
chr12:19464953 | A | G | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+2236A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19464953 | |||||||
chr12:19465103 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+2386G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465103 | |||||||
chr12:19465221 | C | T | 1 | a0001c0001t0004g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.879+2504C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465221 | |||||||
chr12:19465309 | G | A | 4 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0173 others(1): Show |
4 | HG00140.hp1 HG01123.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+2592G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465309 | |||||||
chr12:19465404 | TAAATA | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+2696_879+2700d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465404 | ||||||
chr12:19465421 | G | A | 1 | a0001c0001t0022g0131 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.879+2704G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465421 | |||||||
chr12:19465441 | G | C | 48 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(45): Show |
48 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.879+2724G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465441 | |||||||
chr12:19465564 | T | G | 98 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(95): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.879+2847T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465564 | |||||||
chr12:19465614 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+2897A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465614 | |||||||
chr12:19465621 | G | A | 1 | a0001c0001t0003g0376 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.879+2904G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465621 | |||||||
chr12:19465781 | A | G | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.879+3064A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465781 | |||||||
chr12:19465791 | CT | C | 264 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0058 others(261): Show |
266 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.879+3092delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465791 | ||||||
chr12:19465791 | CTT | C | 10 | a0001c0001t0001g0054 a0001c0001t0001g0250 a0001c0001t0002g0222 others(7): Show |
10 | HG01081.hp2 HG01257.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+3091_879+3092d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465791 | ||||||
chr12:19465794 | T | TTC | 7 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0042 others(4): Show |
7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+3078_879+3079i others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19465794 | ||||||
chr12:19465796 | T | C | 1 | a0001c0001t0031g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.879+3079T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465796 | |||||||
chr12:19465813 | A | T | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.879+3096A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465813 | |||||||
chr12:19465844 | T | C | 1 | a0001c0001t0006g0025 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.879+3127T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465844 | |||||||
chr12:19465858 | C | T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.879+3141C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465858 | |||||||
chr12:19465869 | A | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.879+3152A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465869 | |||||||
chr12:19465878 | G | A | 2 | a0001c0001t0020g0265 a0001c0001t0020g0266 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.879+3161G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465878 | |||||||
chr12:19465934 | A | G | 37 | a0001c0002t0001g0056 a0001c0002t0001g0059 a0001c0002t0001g0065 others(34): Show |
37 | HG00558.hp2 HG01358.hp1 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.879+3217A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465934 | |||||||
chr12:19465967 | T | C | 1 | a0001c0001t0004g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.879+3250T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19465967 | |||||||
chr12:19466028 | G | T | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.879+3311G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466028 | |||||||
chr12:19466122 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.879+3405T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466122 | |||||||
chr12:19466202 | C | G | 1 | a0001c0001t0011g0295 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.879+3485C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466202 | |||||||
chr12:19466426 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+3709G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466426 | |||||||
chr12:19466450 | C | CA | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+3741dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19466450 | ||||||
chr12:19466533 | C | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.879+3816C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466533 | |||||||
chr12:19466537 | G | A | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.879+3820G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466537 | |||||||
chr12:19466593 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+3876C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466593 | |||||||
chr12:19466607 | T | C | 331 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(328): Show |
333 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.879+3890T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466607 | |||||||
chr12:19466608 | T | C | 331 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(328): Show |
333 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.879+3891T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466608 | |||||||
chr12:19466792 | G | A | 1 | a0001c0005t0023g0036 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.879+4075G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466792 | |||||||
chr12:19466968 | C | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG02738.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.879+4251C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466968 | |||||||
chr12:19466982 | T | C | 138 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(135): Show |
140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.879+4265T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19466982 | |||||||
chr12:19467091 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.879+4374A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467091 | |||||||
chr12:19467144 | G | A | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+4427G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467144 | |||||||
chr12:19467214 | C | CT | 74 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(71): Show |
75 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.879+4506dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19467214 | ||||||
chr12:19467358 | A | G | 1 | a0001c0001t0004g0270 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.879+4641A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467358 | |||||||
chr12:19467384 | C | T | 1 | a0001c0001t0005g0134 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.879+4667C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467384 | |||||||
chr12:19467507 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+4790T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467507 | |||||||
chr12:19467513 | C | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.879+4796C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467513 | |||||||
chr12:19467515 | A | T | 1 | a0001c0002t0001g0088 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.879+4798A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467515 | |||||||
chr12:19467575 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.879+4858T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467575 | |||||||
chr12:19467653 | A | G | 1 | a0001c0001t0004g0273 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.879+4936A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467653 | |||||||
chr12:19467665 | A | G | 11 | a0001c0001t0005g0136 a0001c0001t0005g0137 a0001c0001t0005g0138 others(8): Show |
11 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.879+4948A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467665 | |||||||
chr12:19467672 | G | C | 1 | a0001c0001t0020g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.879+4955G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467672 | |||||||
chr12:19467677 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.879+4960C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467677 | |||||||
chr12:19467764 | C | T | 1 | a0001c0001t0036g0264 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.879+5047C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19467764 | |||||||
chr12:19468126 | T | TGTGTGTG others(8): Show |
1 | a0001c0001t0008g0332 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.880-5122_880-5121i others(17): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468126 | |||||||
chr12:19468126 | T | TGTGTGTG others(10): Show |
1 | a0001c0001t0046g0035 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.880-5122_880-5121i others(19): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468126 | |||||||
chr12:19468126 | T | TTG | 3 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0037g0205 |
3 | HG01261.hp2 HG02622.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.880-5092_880-5091d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTG | 19 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(16): Show |
19 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.880-5094_880-5091d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(1): Show |
36 | a0001c0001t0003g0338 a0001c0001t0003g0339 a0001c0001t0003g0340 others(33): Show |
36 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.880-5098_880-5091d others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(3): Show |
16 | a0001c0001t0003g0312 a0001c0001t0003g0328 a0001c0001t0003g0341 others(13): Show |
16 | HG01106.hp2 HG01891.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.880-5100_880-5091d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(5): Show |
40 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(37): Show |
41 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.880-5102_880-5091d others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(7): Show |
66 | a0001c0001t0002g0208 a0001c0001t0003g0307 a0001c0001t0003g0310 others(63): Show |
66 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.880-5104_880-5091d others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(9): Show |
42 | a0001c0001t0003g0006 a0001c0001t0003g0329 a0001c0001t0003g0352 others(39): Show |
43 | HG00558.hp1 HG01074.hp1 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.880-5106_880-5091d others(18): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(11): Show |
7 | a0001c0001t0004g0294 a0001c0001t0014g0023 a0001c0001t0016g0038 others(4): Show |
7 | HG00639.hp1 HG02572.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-5108_880-5091d others(20): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(13): Show |
9 | a0001c0001t0003g0322 a0001c0001t0003g0330 a0001c0001t0003g0336 others(6): Show |
9 | HG00408.hp1 NA18944.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-5110_880-5091d others(22): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | T | TTGTGTGT others(19): Show |
1 | a0001c0001t0003g0378 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.880-5116_880-5091d others(28): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | TTG | T | 3 | a0001c0001t0002g0227 a0001c0001t0010g0063 a0001c0006t0033g0044 |
3 | HG01934.hp2 NA18960.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.880-5092_880-5091d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468126 | TTGTGTGT others(5): Show |
T | 52 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(49): Show |
52 | HG00558.hp2 HG01109.hp1 HG01358.hp1 others(49): Show |
intron_variant | MODIFIER | c.880-5102_880-5091d others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19468126 | ||||||
chr12:19468260 | T | G | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-4988T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468260 | |||||||
chr12:19468293 | C | G | 149 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(146): Show |
151 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.880-4955C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468293 | |||||||
chr12:19468316 | G | A | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-4932G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468316 | |||||||
chr12:19468464 | T | C | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-4784T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468464 | |||||||
chr12:19468553 | A | T | 1 | a0001c0003t0001g0254 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.880-4695A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468553 | |||||||
chr12:19468750 | T | G | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-4498T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19468750 | |||||||
chr12:19469045 | C | T | 49 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(46): Show |
49 | HG00558.hp2 HG01109.hp1 HG01358.hp1 others(46): Show |
intron_variant | MODIFIER | c.880-4203C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469045 | |||||||
chr12:19469060 | G | C | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-4188G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469060 | |||||||
chr12:19469135 | A | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0196 a0001c0001t0002g0199 others(4): Show |
9 | NA18955.hp1 NA18963.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-4113A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469135 | |||||||
chr12:19469169 | A | G | 8 | a0001c0002t0001g0065 a0001c0002t0001g0070 a0001c0002t0001g0071 others(5): Show |
8 | HG00558.hp2 HG02040.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-4079A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469169 | |||||||
chr12:19469180 | C | G | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.880-4068C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469180 | |||||||
chr12:19469262 | T | A | 57 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(54): Show |
57 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.880-3986T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469262 | |||||||
chr12:19469284 | G | A | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-3964G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469284 | |||||||
chr12:19469411 | C | A | 75 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(72): Show |
76 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.880-3837C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469411 | |||||||
chr12:19469451 | A | G | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.880-3797A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469451 | |||||||
chr12:19469547 | T | G | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.880-3701T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469547 | |||||||
chr12:19469557 | C | G | 1 | a0001c0001t0003g0310 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.880-3691C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469557 | |||||||
chr12:19469608 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-3640C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469608 | |||||||
chr12:19469680 | C | A | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-3568C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469680 | |||||||
chr12:19469751 | G | T | 2 | a0001c0001t0002g0208 a0001c0001t0004g0274 |
2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.880-3497G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469751 | |||||||
chr12:19469768 | T | G | 1 | a0001c0001t0017g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.880-3480T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19469768 | |||||||
chr12:19470024 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.880-3224C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470024 | |||||||
chr12:19470120 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.880-3128T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470120 | |||||||
chr12:19470151 | A | C | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-3097A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470151 | |||||||
chr12:19470164 | C | CT | 111 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(108): Show |
111 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.880-3072dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19470164 | ||||||
chr12:19470214 | A | G | 5 | a0001c0002t0001g0112 a0001c0002t0001g0127 a0001c0002t0001g0128 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-3034A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470214 | |||||||
chr12:19470244 | C | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-3004C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470244 | |||||||
chr12:19470294 | G | A | 2 | a0001c0002t0001g0105 a0001c0002t0038g0062 |
2 | NA18952.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.880-2954G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470294 | |||||||
chr12:19470327 | T | A | 97 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(94): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.880-2921T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470327 | |||||||
chr12:19470390 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.880-2858G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470390 | |||||||
chr12:19470405 | C | T | 10 | a0001c0001t0005g0136 a0001c0001t0005g0137 a0001c0001t0005g0138 others(7): Show |
10 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-2843C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470405 | |||||||
chr12:19470474 | C | A | 331 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(328): Show |
333 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.880-2774C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470474 | |||||||
chr12:19470481 | C | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.880-2767C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470481 | |||||||
chr12:19470599 | C | T | 110 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(107): Show |
112 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.880-2649C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470599 | |||||||
chr12:19470624 | A | G | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-2624A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470624 | |||||||
chr12:19470631 | A | G | 1 | a0001c0001t0003g0341 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.880-2617A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470631 | |||||||
chr12:19470743 | A | C | 3 | a0001c0001t0018g0230 a0001c0001t0018g0231 a0001c0001t0018g0232 |
3 | HG02922.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.880-2505A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470743 | |||||||
chr12:19470807 | T | G | 114 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(111): Show |
114 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.880-2441T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470807 | |||||||
chr12:19470859 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.880-2389T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470859 | |||||||
chr12:19470934 | C | G | 1 | a0001c0001t0002g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.880-2314C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470934 | |||||||
chr12:19470999 | C | T | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-2249C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19470999 | |||||||
chr12:19471053 | C | A | 1 | a0001c0002t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880-2195C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471053 | |||||||
chr12:19471064 | T | TCCTCCTC others(115): Show |
2 | a0001c0001t0003g0313 a0001c0005t0023g0036 |
2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.880-2063_880-2062i others(124): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19471064 | ||||||
chr12:19471090 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-2158G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471090 | |||||||
chr12:19471161 | G | C | 4 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0320 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-2087G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471161 | |||||||
chr12:19471194 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-2054T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471194 | |||||||
chr12:19471300 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.880-1948G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471300 | |||||||
chr12:19471300 | G | C | 5 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(2): Show |
5 | NA18982.hp1 NA18998.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1948G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471300 | |||||||
chr12:19471302 | A | G | 1 | a0001c0002t0002g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.880-1946A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471302 | |||||||
chr12:19471377 | A | C | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-1871A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471377 | |||||||
chr12:19471505 | A | T | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-1743A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471505 | |||||||
chr12:19471507 | G | GT | 28 | a0001c0001t0002g0195 a0001c0001t0006g0008 a0001c0001t0006g0009 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.880-1730dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr12 | 19471507 | ||||||
chr12:19471657 | C | G | 1 | a0001c0001t0047g0126 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.880-1591C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471657 | |||||||
chr12:19471666 | C | T | 30 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(27): Show |
30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.880-1582C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471666 | |||||||
chr12:19471680 | A | C | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.880-1568A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471680 | |||||||
chr12:19471868 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-1380C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19471868 | |||||||
chr12:19472055 | A | G | 1 | a0001c0001t0004g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.880-1193A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472055 | |||||||
chr12:19472115 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.880-1133G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472115 | |||||||
chr12:19472328 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-920T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472328 | |||||||
chr12:19472359 | A | T | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.880-889A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472359 | |||||||
chr12:19472482 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-766C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472482 | |||||||
chr12:19472581 | G | A | 1 | a0001c0002t0001g0074 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.880-667G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472581 | |||||||
chr12:19472587 | T | A | 3 | a0001c0001t0006g0025 a0001c0001t0014g0023 a0001c0001t0031g0032 |
3 | HG00639.hp1 HG01106.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-661T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472587 | |||||||
chr12:19472634 | T | C | 3 | a0001c0001t0003g0338 a0001c0001t0003g0339 a0001c0001t0012g0337 |
3 | HG00140.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.880-614T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472634 | |||||||
chr12:19472661 | A | G | 3 | a0001c0001t0002g0177 a0001c0001t0002g0192 a0001c0001t0002g0193 |
3 | HG00597.hp1 NA18747.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.880-587A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472661 | |||||||
chr12:19472758 | C | T | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.880-490C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472758 | |||||||
chr12:19472780 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.880-468A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19472780 | |||||||
chr12:19473137 | A | G | 1 | a0001c0002t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.880-111A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19473137 | |||||||
chr12:19473195 | A | T | 1 | a0001c0001t0002g0191 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.880-53A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 2/7 | chr12 | 19473195 | |||||||
chr12:19473375 | A | AAATT | 119 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(116): Show |
119 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.987+21_987+24dupAA others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473375 | ||||||
chr12:19473375 | A | AAATTAAT others(1): Show |
4 | a0001c0001t0001g0064 a0001c0001t0001g0097 a0001c0001t0001g0109 others(1): Show |
4 | HG01074.hp2 NA18944.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+24_987+25insAA others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473375 | ||||||
chr12:19473376 | A | AATTAATT others(1): Show |
6 | a0001c0001t0001g0248 a0001c0001t0001g0250 a0001c0001t0001g0257 others(3): Show |
6 | HG01081.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+24_987+25insAA others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473376 | A | AATTT | 7 | a0001c0001t0001g0249 a0001c0001t0002g0177 a0001c0001t0002g0186 others(4): Show |
7 | HG00621.hp2 HG01168.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+64_987+67dupTT others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473376 | A | AATTTATT others(1): Show |
9 | a0001c0001t0002g0169 a0001c0001t0002g0189 a0001c0001t0009g0188 others(6): Show |
9 | HG01884.hp1 NA18942.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+60_987+67dupTT others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473376 | A | AATTTATT others(5): Show |
5 | a0001c0001t0002g0190 a0001c0001t0002g0207 a0001c0001t0016g0038 others(2): Show |
5 | HG01192.hp1 HG02083.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+56_987+67dupTT others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473376 | A | AATTTATT others(9): Show |
1 | a0001c0001t0037g0205 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.987+52_987+67dupTT others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473376 | AATTT | A | 141 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(138): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+64_987+67delTT others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473376 | AATTTATT others(1): Show |
A | 12 | a0001c0001t0004g0268 a0001c0001t0004g0269 a0001c0001t0004g0304 others(9): Show |
12 | HG01109.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.987+60_987+67delTT others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473376 | AATTTATT others(5): Show |
A | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+56_987+67delTT others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473376 | ||||||
chr12:19473380 | T | A | 116 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(113): Show |
116 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.987+25T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473380 | |||||||
chr12:19473384 | T | A | 243 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(240): Show |
245 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.987+29T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473384 | |||||||
chr12:19473388 | T | A | 240 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0001t0001g0098 others(237): Show |
242 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.987+33T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473388 | |||||||
chr12:19473392 | T | A | 240 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(237): Show |
242 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.987+37T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473392 | |||||||
chr12:19473396 | T | A | 155 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(152): Show |
157 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.987+41T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473396 | |||||||
chr12:19473400 | T | A | 112 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0120 others(109): Show |
113 | HG00323.hp1 HG00438.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.987+45T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473400 | |||||||
chr12:19473404 | T | A | 57 | a0001c0001t0001g0122 a0001c0001t0004g0267 a0001c0001t0004g0282 others(54): Show |
57 | HG00735.hp1 HG01071.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.987+49T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473404 | |||||||
chr12:19473408 | T | A | 8 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(5): Show |
8 | HG01891.hp1 HG01934.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+53T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473408 | |||||||
chr12:19473412 | T | A | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987+57T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473412 | |||||||
chr12:19473416 | T | A | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987+61T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473416 | |||||||
chr12:19473440 | C | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.987+85C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473440 | |||||||
chr12:19473525 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+170T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473525 | |||||||
chr12:19473628 | A | T | 60 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(57): Show |
60 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.987+273A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473628 | |||||||
chr12:19473662 | A | G | 1 | a0001c0001t0004g0267 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.987+307A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473662 | |||||||
chr12:19473759 | TAA | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+407_987+408del others(2): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19473759 | ||||||
chr12:19473762 | A | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+407A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473762 | |||||||
chr12:19473763 | A | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+408A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473763 | |||||||
chr12:19473766 | T | G | 4 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0129 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.987+411T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473766 | |||||||
chr12:19473877 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.987+522G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473877 | |||||||
chr12:19473881 | A | G | 138 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(135): Show |
140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.987+526A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473881 | |||||||
chr12:19473906 | G | A | 1 | a0001c0001t0003g0323 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.987+551G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473906 | |||||||
chr12:19473907 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+552G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473907 | |||||||
chr12:19473924 | T | C | 1 | a0001c0001t0020g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.987+569T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19473924 | |||||||
chr12:19474030 | T | C | 45 | a0001c0001t0002g0208 a0001c0001t0003g0362 a0001c0001t0003g0378 others(42): Show |
45 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.987+675T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474030 | |||||||
chr12:19474109 | T | G | 1 | a0001c0001t0004g0394 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.987+754T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474109 | |||||||
chr12:19474331 | A | G | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 |
3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.987+976A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474331 | |||||||
chr12:19474441 | G | A | 12 | a0001c0001t0003g0373 a0001c0001t0016g0038 a0001c0001t0016g0039 others(9): Show |
12 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+1086G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474441 | |||||||
chr12:19474539 | T | C | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+1184T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474539 | |||||||
chr12:19474548 | T | G | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+1193T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474548 | |||||||
chr12:19474625 | A | G | 43 | a0001c0001t0002g0208 a0001c0001t0003g0362 a0001c0001t0003g0378 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.987+1270A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474625 | |||||||
chr12:19474726 | A | C | 4 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0320 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+1371A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474726 | |||||||
chr12:19474793 | G | GT | 287 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(284): Show |
289 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.987+1447dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19474793 | ||||||
chr12:19474818 | A | T | 2 | a0001c0001t0003g0383 a0001c0001t0008g0359 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.987+1463A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474818 | |||||||
chr12:19474941 | C | T | 9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | NA18953.hp2 NA18957.hp1 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.987+1586C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19474941 | |||||||
chr12:19475019 | T | C | 3 | a0001c0001t0002g0177 a0001c0001t0002g0192 a0001c0001t0002g0193 |
3 | HG00597.hp1 NA18747.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.987+1664T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475019 | |||||||
chr12:19475027 | G | A | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+1672G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475027 | |||||||
chr12:19475052 | A | T | 1 | a0001c0001t0003g0314 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.987+1697A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475052 | |||||||
chr12:19475191 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1836C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475191 | |||||||
chr12:19475204 | G | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1849G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475204 | |||||||
chr12:19475295 | CTAATTA | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1944_987+1949d others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19475295 | ||||||
chr12:19475326 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+1971A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475326 | |||||||
chr12:19475356 | A | G | 18 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0243 others(15): Show |
18 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.987+2001A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475356 | |||||||
chr12:19475433 | G | GGTATGTA others(1): Show |
8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2089_987+2096d others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19475433 | ||||||
chr12:19475464 | G | GTGTATAT others(3): Show |
8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2110_987+2111i others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19475464 | ||||||
chr12:19475541 | A | G | 1 | a0001c0001t0007g0389 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.987+2186A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475541 | |||||||
chr12:19475583 | T | C | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+2228T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475583 | |||||||
chr12:19475626 | C | G | 1 | a0001c0001t0048g0377 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.987+2271C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475626 | |||||||
chr12:19475646 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2291A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475646 | |||||||
chr12:19475678 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+2323T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475678 | |||||||
chr12:19475683 | A | C | 143 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(140): Show |
145 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.987+2328A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475683 | |||||||
chr12:19475789 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2434T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475789 | |||||||
chr12:19475983 | T | C | 30 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(27): Show |
30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.987+2628T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19475983 | |||||||
chr12:19476021 | A | G | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.987+2666A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476021 | |||||||
chr12:19476045 | G | C | 1 | a0001c0002t0045g0123 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.987+2690G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476045 | |||||||
chr12:19476046 | T | C | 39 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(36): Show |
39 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.987+2691T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476046 | |||||||
chr12:19476187 | T | G | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+2832T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476187 | |||||||
chr12:19476257 | A | T | 2 | a0001c0004t0002g0226 a0001c0004t0009g0225 |
2 | NA18966.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.987+2902A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476257 | |||||||
chr12:19476338 | G | A | 48 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0166 others(45): Show |
52 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.987+2983G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476338 | |||||||
chr12:19476373 | G | A | 2 | a0001c0001t0004g0291 a0001c0001t0004g0292 |
2 | NA18992.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.987+3018G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476373 | |||||||
chr12:19476434 | C | T | 2 | a0001c0001t0007g0392 a0001c0001t0007g0393 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.987+3079C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476434 | |||||||
chr12:19476435 | G | A | 1 | a0001c0001t0012g0337 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.987+3080G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476435 | |||||||
chr12:19476521 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.987+3166T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476521 | |||||||
chr12:19476530 | CAG | C | 75 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(72): Show |
76 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.987+3178_987+3179d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19476530 | ||||||
chr12:19476585 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+3230G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476585 | |||||||
chr12:19476621 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+3266C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476621 | |||||||
chr12:19476622 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.987+3267G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476622 | |||||||
chr12:19476681 | G | A | 328 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(325): Show |
330 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(327): Show |
intron_variant | MODIFIER | c.987+3326G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476681 | |||||||
chr12:19476762 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+3407C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476762 | |||||||
chr12:19476844 | G | A | 109 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.987+3489G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476844 | |||||||
chr12:19476850 | A | G | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.987+3495A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476850 | |||||||
chr12:19476877 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+3522G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19476877 | |||||||
chr12:19477027 | A | T | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+3672A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477027 | |||||||
chr12:19477090 | A | G | 1 | a0001c0002t0001g0065 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.987+3735A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477090 | |||||||
chr12:19477149 | C | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.987+3794C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477149 | |||||||
chr12:19477263 | T | C | 331 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(328): Show |
333 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.987+3908T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477263 | |||||||
chr12:19477264 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.987+3909A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477264 | |||||||
chr12:19477273 | T | C | 141 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(138): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.987+3918T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477273 | |||||||
chr12:19477416 | C | G | 3 | a0001c0001t0004g0276 a0001c0001t0004g0281 a0001c0001t0004g0282 |
3 | HG01099.hp2 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.987+4061C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477416 | |||||||
chr12:19477445 | T | C | 2 | a0001c0001t0002g0178 a0001c0001t0002g0201 |
2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.987+4090T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477445 | |||||||
chr12:19477741 | T | A | 50 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(47): Show |
50 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.987+4386T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477741 | |||||||
chr12:19477741 | T | C | 3 | a0001c0001t0005g0156 a0001c0001t0005g0157 a0001c0001t0005g0158 |
3 | HG02647.hp1 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.987+4386T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477741 | |||||||
chr12:19477766 | A | T | 2 | a0001c0001t0003g0362 a0001c0001t0003g0378 |
2 | HG02300.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.987+4411A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477766 | |||||||
chr12:19477803 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+4448C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477803 | |||||||
chr12:19477818 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+4463C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477818 | |||||||
chr12:19477828 | G | C | 1 | a0001c0001t0002g0191 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.987+4473G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19477828 | |||||||
chr12:19478054 | G | A | 13 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(10): Show |
13 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.987+4699G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478054 | |||||||
chr12:19478101 | G | A | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+4746G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478101 | |||||||
chr12:19478319 | A | G | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.987+4964A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478319 | |||||||
chr12:19478465 | T | A | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.987+5110T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478465 | |||||||
chr12:19478539 | C | T | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.987+5184C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478539 | |||||||
chr12:19478570 | G | A | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.987+5215G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478570 | |||||||
chr12:19478842 | A | G | 93 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(90): Show |
95 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.987+5487A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478842 | |||||||
chr12:19478883 | C | T | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.987+5528C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478883 | |||||||
chr12:19478889 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+5534A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478889 | |||||||
chr12:19478959 | C | T | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+5604C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19478959 | |||||||
chr12:19479086 | G | C | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+5731G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479086 | |||||||
chr12:19479140 | C | G | 97 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(94): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.987+5785C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479140 | |||||||
chr12:19479218 | G | A | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+5863G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479218 | |||||||
chr12:19479258 | TTGTTACA others(3): Show |
T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.987+5907_987+5916d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479258 | ||||||
chr12:19479526 | T | C | 1 | a0001c0001t0017g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.987+6171T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479526 | |||||||
chr12:19479553 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+6198A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479553 | |||||||
chr12:19479584 | G | C | 2 | a0001c0001t0020g0265 a0001c0001t0020g0266 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.987+6229G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479584 | |||||||
chr12:19479609 | A | AATTATTT others(34): Show |
8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+6258_987+6298d others(43): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479609 | ||||||
chr12:19479640 | G | T | 97 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(94): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.987+6285G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479640 | |||||||
chr12:19479650 | T | A | 75 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(72): Show |
76 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.987+6295T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479650 | |||||||
chr12:19479705 | A | C | 329 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(326): Show |
331 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.987+6350A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479705 | |||||||
chr12:19479717 | G | GT | 30 | a0001c0001t0002g0001 a0001c0001t0002g0166 a0001c0001t0002g0169 others(27): Show |
32 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.987+6393dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | G | GTT | 39 | a0001c0001t0002g0185 a0001c0001t0002g0187 a0001c0001t0002g0215 others(36): Show |
40 | HG00408.hp1 HG00621.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.987+6392_987+6393d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | G | GTTT | 28 | a0001c0001t0003g0310 a0001c0001t0003g0311 a0001c0001t0003g0314 others(25): Show |
28 | HG00323.hp1 HG00609.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.987+6391_987+6393d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | G | GTTTT | 16 | a0001c0001t0003g0307 a0001c0001t0003g0312 a0001c0001t0003g0328 others(13): Show |
17 | HG00438.hp1 HG01257.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.987+6390_987+6393d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | G | GTTTTT | 6 | a0001c0001t0007g0393 a0001c0001t0008g0366 a0001c0001t0008g0384 others(3): Show |
6 | HG02074.hp1 HG02559.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+6389_987+6393d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | G | GTTTTTTT | 9 | a0001c0001t0006g0010 a0001c0001t0006g0011 a0001c0001t0006g0013 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+6387_987+6393d others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | G | GTTTTTTT others(1): Show |
15 | a0001c0001t0006g0008 a0001c0001t0006g0015 a0001c0001t0006g0016 others(12): Show |
15 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.987+6386_987+6393d others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GT | G | 6 | a0001c0001t0002g0221 a0001c0001t0005g0134 a0001c0001t0011g0319 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+6393delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTT | G | 24 | a0001c0001t0005g0135 a0001c0001t0005g0137 a0001c0001t0005g0139 others(21): Show |
24 | HG00609.hp2 HG00735.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.987+6392_987+6393d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTTT | G | 12 | a0001c0001t0005g0133 a0001c0001t0005g0136 a0001c0001t0005g0138 others(9): Show |
12 | HG01071.hp2 HG01167.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.987+6391_987+6393d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTTTTTT | G | 25 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0103 others(22): Show |
25 | HG00558.hp2 HG01109.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.987+6388_987+6393d others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTTTTTTT | G | 80 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(77): Show |
80 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.987+6387_987+6393d others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTTTTTTT others(4): Show |
G | 40 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(37): Show |
40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.987+6383_987+6393d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTTTTTTT others(5): Show |
G | 2 | a0001c0001t0005g0150 a0001c0001t0015g0236 |
2 | HG02818.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.987+6382_987+6393d others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTTTTTTT others(6): Show |
G | 2 | a0001c0001t0015g0235 a0001c0001t0015g0237 |
2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.987+6381_987+6393d others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479717 | GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0006g0012 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.987+6375_987+6393d others(21): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19479717 | ||||||
chr12:19479723 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+6368T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479723 | |||||||
chr12:19479830 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+6475A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479830 | |||||||
chr12:19479839 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.987+6484C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479839 | |||||||
chr12:19479918 | A | G | 97 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(94): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.987+6563A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479918 | |||||||
chr12:19479944 | C | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+6589C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19479944 | |||||||
chr12:19480002 | C | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+6647C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480002 | |||||||
chr12:19480137 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.987+6782C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480137 | |||||||
chr12:19480178 | C | T | 1 | a0001c0001t0016g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.987+6823C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480178 | |||||||
chr12:19480305 | A | T | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.987+6950A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480305 | |||||||
chr12:19480312 | C | G | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+6957C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480312 | |||||||
chr12:19480356 | C | T | 1 | a0001c0001t0007g0392 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.987+7001C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480356 | |||||||
chr12:19480357 | G | A | 3 | a0001c0001t0020g0229 a0001c0001t0020g0265 a0001c0001t0020g0266 |
3 | HG02258.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.987+7002G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480357 | |||||||
chr12:19480411 | G | A | 4 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0320 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+7056G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480411 | |||||||
chr12:19480431 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.987+7076G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480431 | |||||||
chr12:19480433 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.987+7078G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480433 | |||||||
chr12:19480435 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.987+7080T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480435 | |||||||
chr12:19480473 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.987+7118G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480473 | |||||||
chr12:19480507 | C | G | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.987+7152C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480507 | |||||||
chr12:19480508 | C | T | 1 | a0001c0001t0003g0345 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.987+7153C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480508 | |||||||
chr12:19480532 | C | G | 1 | a0001c0001t0003g0357 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.987+7177C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480532 | |||||||
chr12:19480557 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.987+7202T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480557 | |||||||
chr12:19480571 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7216T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480571 | |||||||
chr12:19480587 | A | ATT | 11 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.987+7233_987+7234d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19480587 | ||||||
chr12:19480844 | C | A | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.987+7489C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480844 | |||||||
chr12:19480939 | G | T | 53 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(50): Show |
53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.987+7584G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480939 | |||||||
chr12:19480978 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7623A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480978 | |||||||
chr12:19480987 | T | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7632T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480987 | |||||||
chr12:19480998 | T | G | 1 | a0001c0001t0002g0221 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.987+7643T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19480998 | |||||||
chr12:19481075 | A | G | 8 | a0001c0001t0002g0001 a0001c0001t0002g0175 a0001c0001t0002g0180 others(5): Show |
10 | HG00639.hp2 HG00738.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.987+7720A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481075 | |||||||
chr12:19481082 | G | C | 328 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(325): Show |
330 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(327): Show |
intron_variant | MODIFIER | c.987+7727G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481082 | |||||||
chr12:19481086 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.987+7731T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481086 | |||||||
chr12:19481092 | C | CT | 95 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0103 others(92): Show |
99 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.987+7763dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | C | CTT | 34 | a0001c0001t0002g0173 a0001c0001t0002g0182 a0001c0001t0002g0204 others(31): Show |
34 | HG00323.hp2 HG00621.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.987+7762_987+7763d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | C | CTTT | 6 | a0001c0001t0004g0269 a0001c0001t0005g0135 a0001c0001t0005g0141 others(3): Show |
6 | HG00639.hp1 HG01106.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+7761_987+7763d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.987+7750_987+7763d others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | C | CTTTTTTT others(8): Show |
3 | a0001c0001t0005g0143 a0001c0001t0005g0259 a0001c0001t0022g0239 |
3 | HG02559.hp2 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.987+7749_987+7763d others(17): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0005g0153 a0001c0001t0005g0238 |
2 | HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.987+7742_987+7763d others(24): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | CT | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG01167.hp1 HG01257.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+7763delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | CTT | C | 7 | a0001c0001t0012g0335 a0001c0001t0013g0159 a0001c0001t0013g0160 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.987+7762_987+7763d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | CTTT | C | 9 | a0001c0001t0003g0354 a0001c0001t0003g0363 a0001c0001t0003g0369 others(6): Show |
9 | HG01358.hp2 HG02630.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+7761_987+7763d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | CTTTT | C | 81 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(78): Show |
83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.987+7760_987+7763d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | CTTTTT | C | 9 | a0001c0001t0003g0347 a0001c0001t0003g0372 a0001c0001t0005g0156 others(6): Show |
9 | HG01346.hp1 HG01515.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.987+7759_987+7763d others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481092 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0024g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.987+7754_987+7763d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19481092 | ||||||
chr12:19481113 | T | C | 2 | a0001c0001t0003g0343 a0001c0001t0003g0345 |
2 | NA18945.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.987+7758T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481113 | |||||||
chr12:19481155 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7800T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481155 | |||||||
chr12:19481160 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+7805A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481160 | |||||||
chr12:19481165 | A | G | 1 | a0001c0001t0003g0336 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.987+7810A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481165 | |||||||
chr12:19481202 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0002g0192 |
2 | HG00597.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.987+7847G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481202 | |||||||
chr12:19481258 | A | G | 11 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.987+7903A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481258 | |||||||
chr12:19481422 | C | T | 2 | a0001c0001t0006g0018 a0001c0001t0006g0026 |
2 | HG03017.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.987+8067C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481422 | |||||||
chr12:19481503 | G | A | 1 | a0001c0001t0017g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.987+8148G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481503 | |||||||
chr12:19481563 | T | C | 148 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(145): Show |
150 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.987+8208T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481563 | |||||||
chr12:19481646 | A | T | 148 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(145): Show |
150 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.987+8291A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481646 | |||||||
chr12:19481679 | G | A | 2 | a0001c0001t0003g0313 a0001c0001t0003g0381 |
2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.987+8324G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481679 | |||||||
chr12:19481766 | A | G | 37 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(34): Show |
37 | HG00609.hp2 HG00735.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.987+8411A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481766 | |||||||
chr12:19481861 | G | A | 1 | a0001c0001t0004g0283 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.987+8506G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481861 | |||||||
chr12:19481925 | C | G | 136 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(133): Show |
136 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.987+8570C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19481925 | |||||||
chr12:19482061 | C | A | 109 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.987+8706C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482061 | |||||||
chr12:19482081 | C | T | 109 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
109 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.987+8726C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482081 | |||||||
chr12:19482344 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+8989C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482344 | |||||||
chr12:19482382 | A | G | 92 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(89): Show |
94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.987+9027A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482382 | |||||||
chr12:19482404 | T | C | 1 | a0001c0001t0007g0389 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.987+9049T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482404 | |||||||
chr12:19482455 | G | A | 1 | a0001c0001t0004g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.987+9100G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482455 | |||||||
chr12:19482476 | C | T | 6 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(3): Show |
6 | HG02486.hp1 HG02723.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.987+9121C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482476 | |||||||
chr12:19482529 | G | C | 60 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(57): Show |
60 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.987+9174G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482529 | |||||||
chr12:19482529 | G | T | 53 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(50): Show |
53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.987+9174G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482529 | |||||||
chr12:19482589 | G | A | 1 | a0001c0001t0031g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.987+9234G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482589 | |||||||
chr12:19482642 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+9287G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482642 | |||||||
chr12:19482805 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.987+9450G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482805 | |||||||
chr12:19482873 | G | T | 1 | a0001c0001t0005g0134 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.987+9518G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482873 | |||||||
chr12:19482912 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+9557T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482912 | |||||||
chr12:19482946 | T | G | 39 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(36): Show |
39 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.987+9591T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19482946 | |||||||
chr12:19483013 | G | A | 1 | a0001c0001t0007g0389 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.987+9658G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483013 | |||||||
chr12:19483070 | G | T | 1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.987+9715G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483070 | |||||||
chr12:19483171 | G | C | 1 | a0001c0001t0007g0393 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.987+9816G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483171 | |||||||
chr12:19483202 | T | C | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.987+9847T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483202 | |||||||
chr12:19483207 | G | A | 1 | a0001c0001t0004g0302 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.987+9852G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483207 | |||||||
chr12:19483220 | C | T | 1 | a0001c0001t0016g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.987+9865C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483220 | |||||||
chr12:19483408 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+10053T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483408 | |||||||
chr12:19483681 | A | T | 2 | a0001c0001t0005g0143 a0001c0001t0005g0153 |
2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.988-10119A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483681 | |||||||
chr12:19483932 | TGTC | T | 109 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(106): Show |
109 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.988-9865_988-9863d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19483932 | ||||||
chr12:19483933 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.988-9867G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483933 | |||||||
chr12:19483935 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.988-9865C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483935 | |||||||
chr12:19483936 | G | A | 1 | a0001c0001t0004g0317 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.988-9864G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483936 | |||||||
chr12:19483955 | G | A | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-9845G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19483955 | |||||||
chr12:19484042 | C | T | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-9758C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484042 | |||||||
chr12:19484250 | AT | A | 80 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0096 others(77): Show |
84 | HG00408.hp2 HG00597.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.988-9525delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19484250 | ||||||
chr12:19484250 | ATT | A | 245 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0092 others(242): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.988-9526_988-9525d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19484250 | ||||||
chr12:19484250 | ATTT | A | 43 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0001g0242 others(40): Show |
44 | HG00558.hp2 HG00735.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.988-9527_988-9525d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19484250 | ||||||
chr12:19484317 | C | T | 1 | a0001c0001t0003g0339 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.988-9483C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484317 | |||||||
chr12:19484340 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-9460C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484340 | |||||||
chr12:19484500 | G | A | 1 | a0001c0001t0003g0330 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.988-9300G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484500 | |||||||
chr12:19484615 | C | T | 1 | a0001c0001t0004g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988-9185C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484615 | |||||||
chr12:19484633 | A | G | 139 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(136): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.988-9167A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484633 | |||||||
chr12:19484663 | G | A | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-9137G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484663 | |||||||
chr12:19484664 | C | T | 139 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(136): Show |
139 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.988-9136C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484664 | |||||||
chr12:19484807 | G | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-8993G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484807 | |||||||
chr12:19484815 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-8985T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484815 | |||||||
chr12:19484947 | C | T | 1 | a0001c0001t0023g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.988-8853C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484947 | |||||||
chr12:19484949 | G | A | 5 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0019 others(2): Show |
5 | HG01934.hp1 HG03017.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-8851G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19484949 | |||||||
chr12:19485032 | C | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-8768C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485032 | |||||||
chr12:19485117 | G | T | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-8683G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485117 | |||||||
chr12:19485123 | A | G | 2 | a0001c0001t0004g0004 a0001c0001t0007g0004 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.988-8677A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485123 | |||||||
chr12:19485201 | G | A | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-8599G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485201 | |||||||
chr12:19485241 | C | G | 46 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0166 others(43): Show |
50 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.988-8559C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485241 | |||||||
chr12:19485485 | T | C | 2 | a0001c0002t0001g0072 a0001c0002t0010g0104 |
2 | HG02040.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.988-8315T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485485 | |||||||
chr12:19485708 | C | CA | 79 | a0001c0001t0001g0058 a0001c0001t0002g0208 a0001c0001t0004g0003 others(76): Show |
79 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.988-8076dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485708 | ||||||
chr12:19485708 | C | CAA | 202 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0064 others(199): Show |
204 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.988-8077_988-8076d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485708 | ||||||
chr12:19485708 | C | CAAA | 10 | a0001c0001t0001g0048 a0001c0001t0001g0103 a0001c0001t0001g0258 others(7): Show |
10 | HG01358.hp2 HG01515.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-8078_988-8076d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485708 | ||||||
chr12:19485740 | A | G | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-8060A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485740 | |||||||
chr12:19485948 | C | CT | 63 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0120 others(60): Show |
64 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.988-7832dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485948 | ||||||
chr12:19485948 | CT | C | 41 | a0001c0001t0001g0098 a0001c0001t0001g0107 a0001c0001t0002g0206 others(38): Show |
41 | HG00639.hp1 HG01106.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.988-7832delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485948 | ||||||
chr12:19485948 | CTT | C | 35 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(32): Show |
35 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.988-7833_988-7832d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19485948 | ||||||
chr12:19485952 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.988-7848T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485952 | |||||||
chr12:19485965 | TTTTC | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-7834_988-7831d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19485965 | |||||||
chr12:19486082 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-7718A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486082 | |||||||
chr12:19486101 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-7699C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486101 | |||||||
chr12:19486203 | G | A | 1 | a0001c0001t0023g0309 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.988-7597G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486203 | |||||||
chr12:19486262 | T | C | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-7538T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486262 | |||||||
chr12:19486277 | C | T | 48 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0166 others(45): Show |
52 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.988-7523C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486277 | |||||||
chr12:19486304 | A | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.988-7496A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486304 | |||||||
chr12:19486388 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.988-7412A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486388 | |||||||
chr12:19486529 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.988-7271T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486529 | |||||||
chr12:19486572 | A | G | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.988-7228A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486572 | |||||||
chr12:19486584 | C | T | 1 | a0001c0001t0004g0283 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.988-7216C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486584 | |||||||
chr12:19486742 | A | G | 1 | a0001c0002t0002g0082 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.988-7058A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486742 | |||||||
chr12:19486798 | C | G | 2 | a0001c0001t0003g0313 a0001c0005t0023g0036 |
2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.988-7002C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486798 | |||||||
chr12:19486808 | C | CT | 40 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(37): Show |
40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.988-6982dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19486808 | ||||||
chr12:19486813 | T | C | 2 | a0001c0001t0017g0046 a0001c0001t0017g0047 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.988-6987T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486813 | |||||||
chr12:19486909 | C | T | 113 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(110): Show |
113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.988-6891C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19486909 | |||||||
chr12:19487007 | T | C | 1 | a0001c0001t0004g0303 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.988-6793T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487007 | |||||||
chr12:19487102 | A | G | 1 | a0001c0001t0035g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.988-6698A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487102 | |||||||
chr12:19487166 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-6634A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487166 | |||||||
chr12:19487271 | G | A | 41 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(38): Show |
41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.988-6529G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487271 | |||||||
chr12:19487478 | G | T | 1 | a0001c0001t0004g0267 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.988-6322G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487478 | |||||||
chr12:19487544 | C | T | 2 | a0001c0001t0014g0033 a0001c0001t0014g0034 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.988-6256C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487544 | |||||||
chr12:19487576 | A | C | 31 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
31 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.988-6224A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487576 | |||||||
chr12:19487601 | T | C | 2 | a0001c0001t0004g0386 a0001c0001t0007g0385 |
2 | HG03834.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.988-6199T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487601 | |||||||
chr12:19487713 | C | T | 1 | a0001c0001t0024g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.988-6087C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487713 | |||||||
chr12:19487758 | T | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-6042T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487758 | |||||||
chr12:19487798 | A | G | 1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.988-6002A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487798 | |||||||
chr12:19487881 | A | C | 39 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(36): Show |
39 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.988-5919A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487881 | |||||||
chr12:19487965 | T | C | 1 | a0001c0002t0001g0072 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.988-5835T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19487965 | |||||||
chr12:19488126 | A | AT | 146 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(143): Show |
148 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.988-5659dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19488126 | ||||||
chr12:19488147 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-5653G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488147 | |||||||
chr12:19488204 | A | G | 1 | a0001c0001t0003g0340 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.988-5596A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488204 | |||||||
chr12:19488217 | G | A | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-5583G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488217 | |||||||
chr12:19488235 | C | T | 8 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0315 others(5): Show |
9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-5565C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488235 | |||||||
chr12:19488290 | A | AT | 47 | a0001c0001t0001g0103 a0001c0001t0001g0124 a0001c0001t0002g0204 others(44): Show |
47 | HG00323.hp2 HG00609.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.988-5492dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19488290 | ||||||
chr12:19488290 | AT | A | 9 | a0001c0001t0001g0054 a0001c0001t0016g0038 a0001c0001t0016g0039 others(6): Show |
9 | HG01257.hp1 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-5492delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19488290 | ||||||
chr12:19488319 | G | A | 3 | a0001c0002t0001g0057 a0001c0002t0001g0118 a0001c0002t0001g0119 |
3 | HG03139.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.988-5481G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488319 | |||||||
chr12:19488345 | C | T | 3 | a0001c0003t0001g0252 a0001c0003t0001g0254 a0001c0003t0044g0251 |
3 | HG01081.hp2 HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.988-5455C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488345 | |||||||
chr12:19488367 | A | G | 1 | a0001c0001t0003g0378 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.988-5433A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488367 | |||||||
chr12:19488453 | G | A | 21 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(18): Show |
21 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.988-5347G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488453 | |||||||
chr12:19488482 | A | G | 2 | a0001c0001t0003g0340 a0001c0001t0003g0369 |
2 | NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.988-5318A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488482 | |||||||
chr12:19488483 | G | A | 2 | a0001c0001t0003g0340 a0001c0001t0003g0369 |
2 | NA18999.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.988-5317G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488483 | |||||||
chr12:19488543 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-5257A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488543 | |||||||
chr12:19488551 | T | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-5249T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488551 | |||||||
chr12:19488553 | T | C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(2): Show |
5 | HG02486.hp1 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-5247T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488553 | |||||||
chr12:19488590 | T | C | 11 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-5210T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488590 | |||||||
chr12:19488651 | T | G | 30 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(27): Show |
30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.988-5149T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488651 | |||||||
chr12:19488829 | C | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-4971C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488829 | |||||||
chr12:19488910 | C | T | 1 | a0001c0001t0003g0353 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.988-4890C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488910 | |||||||
chr12:19488912 | C | T | 1 | a0001c0001t0007g0396 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.988-4888C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19488912 | |||||||
chr12:19489331 | GCAGGGGA others(6): Show |
G | 1 | a0001c0001t0004g0297 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.988-4466_988-4454d others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489331 | ||||||
chr12:19489352 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.988-4448A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489352 | |||||||
chr12:19489407 | A | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.988-4393A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489407 | |||||||
chr12:19489611 | G | A | 1 | a0001c0001t0003g0369 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.988-4189G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489611 | |||||||
chr12:19489731 | CTG | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-4065_988-4064d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489731 | ||||||
chr12:19489870 | G | GT | 58 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(55): Show |
59 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.988-3921dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489870 | ||||||
chr12:19489942 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-3858A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19489942 | |||||||
chr12:19489990 | C | CT | 130 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(127): Show |
130 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.988-3785dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | ||||||
chr12:19489990 | C | CTT | 40 | a0001c0001t0001g0096 a0001c0001t0001g0111 a0001c0001t0001g0124 others(37): Show |
40 | HG00323.hp2 HG00639.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.988-3786_988-3785d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | ||||||
chr12:19489990 | C | CTTT | 13 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0101 others(10): Show |
13 | HG02071.hp2 HG02280.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.988-3787_988-3785d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | ||||||
chr12:19489990 | CTTTTTT | C | 9 | a0001c0001t0002g0187 a0001c0001t0005g0140 a0001c0001t0005g0144 others(6): Show |
9 | HG00621.hp2 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.988-3790_988-3785d others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | ||||||
chr12:19489990 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.988-3795_988-3785d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | ||||||
chr12:19489990 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.988-3798_988-3785d others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19489990 | ||||||
chr12:19490045 | C | T | 58 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(55): Show |
58 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.988-3755C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490045 | |||||||
chr12:19490138 | A | G | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-3662A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490138 | |||||||
chr12:19490150 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-3650T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490150 | |||||||
chr12:19490166 | C | G | 1 | a0001c0001t0006g0025 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.988-3634C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490166 | |||||||
chr12:19490215 | T | C | 1 | a0001c0001t0004g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.988-3585T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490215 | |||||||
chr12:19490270 | A | C | 11 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(8): Show |
11 | HG02055.hp1 HG02572.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-3530A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490270 | |||||||
chr12:19490339 | T | G | 1 | a0001c0001t0003g0307 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.988-3461T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490339 | |||||||
chr12:19490416 | C | T | 2 | a0001c0001t0004g0270 a0001c0001t0004g0285 |
2 | HG00438.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.988-3384C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490416 | |||||||
chr12:19490456 | A | ACTG | 38 | a0001c0001t0003g0310 a0001c0001t0003g0312 a0001c0001t0003g0322 others(35): Show |
38 | HG00408.hp1 HG00438.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.988-3341_988-3339d others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19490456 | ||||||
chr12:19490537 | C | T | 1 | a0001c0001t0015g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.988-3263C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490537 | |||||||
chr12:19490707 | C | T | 1 | a0001c0001t0008g0371 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.988-3093C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490707 | |||||||
chr12:19490724 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-3076C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490724 | |||||||
chr12:19490995 | T | A | 5 | a0001c0002t0001g0112 a0001c0002t0001g0127 a0001c0002t0001g0128 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-2805T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19490995 | |||||||
chr12:19491069 | T | C | 1 | a0001c0001t0006g0025 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.988-2731T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491069 | |||||||
chr12:19491099 | G | C | 1 | a0001c0001t0005g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.988-2701G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491099 | |||||||
chr12:19491133 | C | T | 113 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(110): Show |
113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.988-2667C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491133 | |||||||
chr12:19491281 | A | T | 34 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(31): Show |
34 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.988-2519A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491281 | |||||||
chr12:19491290 | A | C | 1 | a0001c0001t0005g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.988-2510A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491290 | |||||||
chr12:19491317 | T | G | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.988-2483T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491317 | |||||||
chr12:19491455 | G | A | 1 | a0001c0002t0001g0114 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.988-2345G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491455 | |||||||
chr12:19491507 | C | A | 147 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(144): Show |
149 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(146): Show |
intron_variant | MODIFIER | c.988-2293C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491507 | |||||||
chr12:19491592 | G | A | 331 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(328): Show |
333 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(330): Show |
intron_variant | MODIFIER | c.988-2208G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491592 | |||||||
chr12:19491716 | A | AT | 37 | a0001c0001t0003g0375 a0001c0001t0004g0279 a0001c0001t0004g0280 others(34): Show |
37 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.988-2073dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19491716 | ||||||
chr12:19491849 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.988-1951G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491849 | |||||||
chr12:19491855 | T | TGA | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1944_988-1943d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19491855 | ||||||
chr12:19491858 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1942C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491858 | |||||||
chr12:19491866 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1934T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491866 | |||||||
chr12:19491989 | C | CACA | 8 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0315 others(5): Show |
9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-1810_988-1809i others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr12 | 19491989 | ||||||
chr12:19491991 | G | T | 8 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0315 others(5): Show |
9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-1809G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491991 | |||||||
chr12:19491992 | C | T | 8 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0315 others(5): Show |
9 | HG02559.hp1 HG02723.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-1808C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491992 | |||||||
chr12:19491998 | A | G | 6 | a0001c0001t0003g0313 a0001c0001t0003g0321 a0001c0001t0003g0372 others(3): Show |
6 | HG01261.hp1 HG01515.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.988-1802A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19491998 | |||||||
chr12:19492038 | A | G | 1 | a0001c0001t0006g0009 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.988-1762A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492038 | |||||||
chr12:19492040 | G | A | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.988-1760G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492040 | |||||||
chr12:19492088 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1712C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492088 | |||||||
chr12:19492262 | G | A | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.988-1538G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492262 | |||||||
chr12:19492313 | A | G | 53 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 others(50): Show |
53 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.988-1487A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492313 | |||||||
chr12:19492574 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.988-1226T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492574 | |||||||
chr12:19492585 | A | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0117 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.988-1215A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492585 | |||||||
chr12:19492604 | A | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1196A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492604 | |||||||
chr12:19492740 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-1060A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492740 | |||||||
chr12:19492859 | A | C | 91 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(88): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.988-941A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492859 | |||||||
chr12:19492859 | A | T | 1 | a0001c0001t0003g0336 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.988-941A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492859 | |||||||
chr12:19492927 | G | T | 3 | a0001c0001t0003g0338 a0001c0001t0003g0339 a0001c0001t0012g0337 |
3 | HG00140.hp2 HG00738.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.988-873G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492927 | |||||||
chr12:19492998 | C | G | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-802C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19492998 | |||||||
chr12:19493382 | T | C | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.988-418T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493382 | |||||||
chr12:19493423 | A | C | 1 | a0001c0002t0001g0056 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.988-377A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493423 | |||||||
chr12:19493475 | C | A | 1 | a0001c0001t0003g0322 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.988-325C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493475 | |||||||
chr12:19493595 | T | C | 11 | a0001c0001t0002g0167 a0001c0001t0002g0209 a0001c0001t0002g0210 others(8): Show |
11 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.988-205T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493595 | |||||||
chr12:19493598 | A | C | 114 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(111): Show |
114 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.988-202A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493598 | |||||||
chr12:19493632 | A | G | 41 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(38): Show |
41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.988-168A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493632 | |||||||
chr12:19493640 | C | T | 32 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(29): Show |
32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.988-160C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493640 | |||||||
chr12:19493641 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-159G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493641 | |||||||
chr12:19493663 | C | T | 36 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(33): Show |
36 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.988-137C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493663 | |||||||
chr12:19493755 | C | T | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.988-45C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 3/7 | chr12 | 19493755 | |||||||
chr12:19494009 | CTGGTGTA others(5): Show |
C | 137 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(134): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1174+28_1174+39del others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494009 | ||||||
chr12:19494259 | G | A | 1 | a0001c0001t0012g0335 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1174+273G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494259 | |||||||
chr12:19494320 | AAGTAATC others(3): Show |
A | 1 | a0001c0001t0001g0262 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1174+335_1174+344d others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494320 | |||||||
chr12:19494329 | A | G | 2 | a0001c0001t0003g0383 a0001c0001t0008g0359 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1174+343A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494329 | |||||||
chr12:19494399 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0004g0274 |
2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1174+413A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494399 | |||||||
chr12:19494498 | C | CT | 77 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0094 others(74): Show |
77 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.1174+533dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494498 | ||||||
chr12:19494498 | CT | C | 9 | a0001c0001t0002g0218 a0001c0001t0003g0356 a0001c0001t0004g0268 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174+533delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494498 | ||||||
chr12:19494498 | CTTTT | C | 7 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(4): Show |
7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1174+530_1174+533d others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19494498 | ||||||
chr12:19494521 | A | C | 1 | a0001c0001t0003g0353 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1174+535A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494521 | |||||||
chr12:19494542 | G | C | 145 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(142): Show |
147 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1174+556G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494542 | |||||||
chr12:19494590 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+604G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494590 | |||||||
chr12:19494627 | G | A | 1 | a0001c0001t0006g0025 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1174+641G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494627 | |||||||
chr12:19494662 | G | T | 1 | a0001c0001t0031g0032 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1174+676G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494662 | |||||||
chr12:19494679 | C | G | 1 | a0001c0001t0004g0283 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1174+693C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494679 | |||||||
chr12:19494694 | T | A | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1174+708T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494694 | |||||||
chr12:19494741 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+755T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494741 | |||||||
chr12:19494798 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+812G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494798 | |||||||
chr12:19494851 | G | C | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1174+865G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494851 | |||||||
chr12:19494932 | G | A | 395 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(392): Show |
401 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(398): Show |
intron_variant | MODIFIER | c.1174+946G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494932 | |||||||
chr12:19494978 | C | T | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1174+992C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19494978 | |||||||
chr12:19495052 | C | T | 1 | a0001c0001t0007g0315 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1174+1066C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495052 | |||||||
chr12:19495077 | T | C | 1 | a0001c0001t0005g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1174+1091T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495077 | |||||||
chr12:19495125 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1139G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495125 | |||||||
chr12:19495173 | G | A | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1174+1187G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495173 | |||||||
chr12:19495211 | A | G | 143 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(140): Show |
145 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1174+1225A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495211 | |||||||
chr12:19495257 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1271A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495257 | |||||||
chr12:19495481 | A | AT | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1503dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495481 | ||||||
chr12:19495481 | A | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174+1495A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495481 | |||||||
chr12:19495540 | A | G | 2 | a0001c0001t0003g0310 a0001c0001t0003g0373 |
2 | HG00609.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1174+1554A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495540 | |||||||
chr12:19495547 | C | CT | 33 | a0001c0001t0001g0122 a0001c0001t0004g0394 a0001c0001t0006g0008 others(30): Show |
34 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1174+1575dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | ||||||
chr12:19495547 | C | CTTTTTTT others(3): Show |
1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1174+1566_1174+157 others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | ||||||
chr12:19495547 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1174+1565_1174+157 others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | ||||||
chr12:19495547 | C | CTTTTTTT others(5): Show |
9 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(6): Show |
9 | HG02055.hp1 NA18953.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.1174+1564_1174+157 others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | ||||||
chr12:19495547 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0016g0042 a0001c0001t0017g0045 |
2 | HG02572.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1174+1563_1174+157 others(17): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | ||||||
chr12:19495547 | CT | C | 30 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(27): Show |
30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1174+1575delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | ||||||
chr12:19495547 | CTT | C | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174+1574_1174+157 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19495547 | ||||||
chr12:19495567 | A | G | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1174+1581A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495567 | |||||||
chr12:19495885 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+1899C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495885 | |||||||
chr12:19495889 | G | A | 137 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(134): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1174+1903G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19495889 | |||||||
chr12:19496086 | G | A | 1 | a0001c0001t0022g0131 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1174+2100G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496086 | |||||||
chr12:19496132 | C | G | 2 | a0001c0001t0003g0312 a0001c0001t0003g0328 |
2 | NA18940.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1174+2146C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496132 | |||||||
chr12:19496160 | CTT | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+2176_1174+217 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19496160 | ||||||
chr12:19496162 | T | C | 95 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(92): Show |
97 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1174+2176T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496162 | |||||||
chr12:19496255 | C | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1174+2269C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496255 | |||||||
chr12:19496299 | G | A | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1174+2313G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496299 | |||||||
chr12:19496374 | G | T | 1 | a0001c0001t0004g0292 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1174+2388G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496374 | |||||||
chr12:19496664 | C | CTTTTTTT | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+2685_1174+269 others(11): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19496664 | ||||||
chr12:19496725 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1174+2739A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496725 | |||||||
chr12:19496939 | G | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+2953G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496939 | |||||||
chr12:19496961 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1174+2975C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19496961 | |||||||
chr12:19497032 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1174+3046T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497032 | |||||||
chr12:19497070 | G | A | 136 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(133): Show |
138 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1175-3027G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497070 | |||||||
chr12:19497144 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2953T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497144 | |||||||
chr12:19497148 | C | G | 1 | a0001c0002t0002g0068 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1175-2949C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497148 | |||||||
chr12:19497184 | T | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2913T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497184 | |||||||
chr12:19497326 | G | GT | 4 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0390 others(1): Show |
5 | HG03041.hp2 HG03471.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-2770dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497326 | ||||||
chr12:19497326 | GTGTTT | G | 7 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(4): Show |
7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-2769_1175-276 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497326 | ||||||
chr12:19497328 | G | GT | 126 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0166 others(123): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1175-2745dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | ||||||
chr12:19497328 | G | GTT | 37 | a0001c0001t0002g0001 a0001c0001t0002g0168 a0001c0001t0002g0173 others(34): Show |
37 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1175-2746_1175-274 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | ||||||
chr12:19497328 | G | GTTT | 27 | a0001c0001t0001g0121 a0001c0001t0002g0186 a0001c0001t0002g0194 others(24): Show |
27 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1175-2747_1175-274 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | ||||||
chr12:19497328 | G | GTTTT | 98 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(95): Show |
98 | HG00558.hp2 HG00597.hp2 HG01074.hp2 others(95): Show |
intron_variant | MODIFIER | c.1175-2748_1175-274 others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | ||||||
chr12:19497328 | G | GTTTTT | 52 | a0001c0001t0001g0048 a0001c0001t0001g0093 a0001c0001t0001g0096 others(49): Show |
52 | HG00558.hp1 HG00621.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1175-2749_1175-274 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | ||||||
chr12:19497328 | G | GTTTTTT | 19 | a0001c0001t0001g0098 a0001c0001t0001g0124 a0001c0001t0001g0243 others(16): Show |
19 | HG00609.hp2 HG01243.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1175-2750_1175-274 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | ||||||
chr12:19497328 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0004g0285 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1175-2754_1175-274 others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19497328 | ||||||
chr12:19497328 | G | T | 5 | a0001c0001t0004g0394 a0001c0001t0007g0005 a0001c0001t0007g0390 others(2): Show |
6 | HG02559.hp1 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-2769G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497328 | |||||||
chr12:19497378 | C | T | 1 | a0001c0001t0016g0039 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1175-2719C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497378 | |||||||
chr12:19497494 | A | C | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1175-2603A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497494 | |||||||
chr12:19497497 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2600A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497497 | |||||||
chr12:19497570 | G | A | 1 | a0001c0001t0008g0384 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1175-2527G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497570 | |||||||
chr12:19497628 | A | G | 2 | a0001c0001t0002g0174 a0001c0001t0002g0185 |
2 | NA18950.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1175-2469A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497628 | |||||||
chr12:19497684 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-2413C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497684 | |||||||
chr12:19497702 | T | C | 13 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(10): Show |
13 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1175-2395T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497702 | |||||||
chr12:19497713 | C | G | 4 | a0001c0001t0006g0029 a0001c0001t0006g0031 a0001c0001t0014g0028 others(1): Show |
4 | HG00323.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-2384C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497713 | |||||||
chr12:19497834 | C | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1175-2263C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497834 | |||||||
chr12:19497895 | A | C | 1 | a0001c0001t0002g0207 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1175-2202A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19497895 | |||||||
chr12:19498075 | C | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1175-2022C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498075 | |||||||
chr12:19498203 | A | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1175-1894A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498203 | |||||||
chr12:19498305 | G | C | 332 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(329): Show |
334 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.1175-1792G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498305 | |||||||
chr12:19498402 | T | C | 43 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(40): Show |
43 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1175-1695T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498402 | |||||||
chr12:19498555 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1175-1542A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498555 | |||||||
chr12:19498601 | C | T | 41 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(38): Show |
41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1175-1496C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498601 | |||||||
chr12:19498894 | C | T | 6 | a0001c0001t0002g0178 a0001c0001t0002g0183 a0001c0001t0002g0194 others(3): Show |
6 | HG01069.hp1 HG01168.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175-1203C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19498894 | |||||||
chr12:19499041 | A | G | 4 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0354 others(1): Show |
5 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175-1056A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499041 | |||||||
chr12:19499058 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-1039C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499058 | |||||||
chr12:19499171 | T | C | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1175-926T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499171 | |||||||
chr12:19499332 | G | A | 40 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(37): Show |
40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1175-765G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499332 | |||||||
chr12:19499353 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1175-744C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499353 | |||||||
chr12:19499378 | C | T | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1175-719C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499378 | |||||||
chr12:19499468 | G | T | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1175-629G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499468 | |||||||
chr12:19499613 | CT | C | 7 | a0001c0001t0005g0137 a0001c0001t0016g0041 a0001c0001t0016g0042 others(4): Show |
7 | HG01952.hp1 NA18953.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1175-482delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19499613 | ||||||
chr12:19499614 | T | TA | 74 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(71): Show |
74 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1175-483_1175-482i others(3): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499614 | |||||||
chr12:19499614 | T | TAA | 55 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(52): Show |
55 | HG00735.hp2 HG01074.hp2 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1175-483_1175-482i others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499614 | |||||||
chr12:19499614 | T | TAAA | 7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0246 others(4): Show |
7 | HG00597.hp2 HG01884.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175-483_1175-482i others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499614 | |||||||
chr12:19499615 | T | A | 325 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(322): Show |
327 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(324): Show |
intron_variant | MODIFIER | c.1175-482T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499615 | |||||||
chr12:19499632 | A | G | 1 | a0001c0001t0004g0306 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1175-465A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499632 | |||||||
chr12:19499660 | G | T | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1175-437G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499660 | |||||||
chr12:19499746 | G | GAT | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1175-345_1175-344d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr12 | 19499746 | ||||||
chr12:19499786 | T | G | 4 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0320 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1175-311T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499786 | |||||||
chr12:19499835 | G | T | 3 | a0001c0002t0001g0089 a0001c0002t0001g0240 a0001c0002t0010g0113 |
3 | HG01358.hp1 HG01928.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.1175-262G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499835 | |||||||
chr12:19499940 | A | G | 40 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(37): Show |
40 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1175-157A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499940 | |||||||
chr12:19499954 | C | G | 1 | a0001c0001t0002g0208 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1175-143C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 4/7 | chr12 | 19499954 | |||||||
chr12:19500478 | A | G | 1 | a0001c0001t0004g0197 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1299+257A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500478 | |||||||
chr12:19500633 | C | G | 1 | a0001c0001t0008g0327 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1299+412C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500633 | |||||||
chr12:19500767 | A | G | 170 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(167): Show |
172 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.1299+546A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500767 | |||||||
chr12:19500818 | A | G | 51 | a0001c0001t0002g0204 a0001c0002t0001g0050 a0001c0002t0001g0051 others(48): Show |
51 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1299+597A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500818 | |||||||
chr12:19500991 | C | G | 1 | a0001c0001t0001g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1299+770C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19500991 | |||||||
chr12:19501073 | T | TAACTCTA others(5): Show |
1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+854_1299+855i others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501073 | ||||||
chr12:19501077 | C | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+856C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501077 | |||||||
chr12:19501079 | C | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+858C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501079 | |||||||
chr12:19501084 | T | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+863T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501084 | |||||||
chr12:19501090 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+869G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501090 | |||||||
chr12:19501091 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+870A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501091 | |||||||
chr12:19501097 | A | G | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+876A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501097 | |||||||
chr12:19501100 | C | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+879C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501100 | |||||||
chr12:19501105 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1299+884G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501105 | |||||||
chr12:19501107 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+886A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501107 | |||||||
chr12:19501110 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+889A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501110 | |||||||
chr12:19501113 | T | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+892T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501113 | |||||||
chr12:19501114 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+893G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501114 | |||||||
chr12:19501115 | A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+894A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501115 | |||||||
chr12:19501116 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+895G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501116 | |||||||
chr12:19501117 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+896G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501117 | |||||||
chr12:19501120 | A | G | 3 | a0001c0001t0004g0386 a0001c0001t0007g0385 a0001c0001t0007g0387 |
3 | HG03834.hp2 NA20805.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1299+899A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501120 | |||||||
chr12:19501121 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+900G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501121 | |||||||
chr12:19501122 | G | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+901G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501122 | |||||||
chr12:19501134 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+913A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501134 | |||||||
chr12:19501135 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+914G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501135 | |||||||
chr12:19501139 | G | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+918G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501139 | |||||||
chr12:19501140 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+919G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501140 | |||||||
chr12:19501149 | G | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+928G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501149 | |||||||
chr12:19501151 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+930A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501151 | |||||||
chr12:19501152 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+931A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501152 | |||||||
chr12:19501153 | A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+932A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501153 | |||||||
chr12:19501154 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+933A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501154 | |||||||
chr12:19501157 | C | A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+936C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501157 | |||||||
chr12:19501165 | A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+944A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501165 | |||||||
chr12:19501168 | A | C | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+947A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501168 | |||||||
chr12:19501171 | AATACAAA others(4): Show |
A | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+951_1299+961d others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501171 | |||||||
chr12:19501184 | A | T | 1 | a0001c0001t0008g0382 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1299+963A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501184 | |||||||
chr12:19501279 | C | T | 120 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(117): Show |
120 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.1299+1058C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501279 | |||||||
chr12:19501288 | A | G | 13 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(10): Show |
13 | HG01934.hp2 HG02055.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1299+1067A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501288 | |||||||
chr12:19501331 | C | CA | 12 | a0001c0001t0002g0223 a0001c0001t0002g0228 a0001c0001t0004g0004 others(9): Show |
12 | HG01361.hp1 HG01934.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.1299+1128dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501331 | ||||||
chr12:19501331 | C | CAAA | 7 | a0001c0001t0016g0039 a0001c0001t0016g0041 a0001c0001t0016g0042 others(4): Show |
7 | HG02055.hp1 NA18953.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+1126_1299+112 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501331 | ||||||
chr12:19501331 | CA | C | 7 | a0001c0001t0008g0382 a0001c0001t0014g0030 a0001c0001t0015g0233 others(4): Show |
7 | HG00323.hp2 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1299+1128delA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501331 | ||||||
chr12:19501343 | A | G | 2 | a0001c0001t0015g0235 a0001c0001t0015g0236 |
2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1299+1122A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501343 | |||||||
chr12:19501562 | A | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+1341A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501562 | |||||||
chr12:19501647 | AATT | A | 72 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(69): Show |
72 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1299+1429_1299+143 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501647 | ||||||
chr12:19501648 | ATT | A | 91 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(88): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1299+1428_1299+142 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501648 | |||||||
chr12:19501658 | C | T | 3 | a0001c0002t0001g0067 a0001c0002t0002g0068 a0001c0002t0043g0066 |
3 | HG02071.hp1 HG02129.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1299+1437C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501658 | |||||||
chr12:19501767 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1299+1546A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501767 | |||||||
chr12:19501776 | G | A | 1 | a0001c0001t0015g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1299+1555G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501776 | |||||||
chr12:19501797 | G | GT | 8 | a0001c0001t0001g0098 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG00408.hp2 HG00609.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+1596dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | G | GTTTGT | 21 | a0001c0001t0002g0208 a0001c0001t0004g0267 a0001c0001t0004g0274 others(18): Show |
21 | HG00438.hp2 HG00621.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | G | GTTTGTT | 18 | a0001c0001t0004g0003 a0001c0001t0004g0007 a0001c0001t0004g0270 others(15): Show |
18 | HG00558.hp1 HG01106.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | G | GTTTTT | 66 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(63): Show |
68 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1299+1592_1299+159 others(9): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | G | GTTTTTT | 38 | a0001c0001t0003g0311 a0001c0001t0003g0321 a0001c0001t0003g0323 others(35): Show |
38 | HG00323.hp2 HG00438.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.1299+1591_1299+159 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | G | GTTTTTTG others(1): Show |
7 | a0001c0001t0016g0039 a0001c0001t0016g0041 a0001c0001t0016g0042 others(4): Show |
7 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1299+1582_1299+158 others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | G | GTTTTTTT | 13 | a0001c0001t0003g0352 a0001c0001t0003g0362 a0001c0001t0004g0320 others(10): Show |
13 | HG01106.hp1 HG01934.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.1299+1590_1299+159 others(11): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | G | T | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1299+1576G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501797 | |||||||
chr12:19501797 | GT | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(126): Show |
133 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.1299+1596delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501797 | GTT | G | 15 | a0001c0001t0001g0241 a0001c0001t0001g0243 a0001c0001t0001g0245 others(12): Show |
15 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1299+1595_1299+159 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501797 | ||||||
chr12:19501798 | T | TTTG | 6 | a0001c0001t0005g0139 a0001c0001t0005g0153 a0001c0001t0005g0158 others(3): Show |
6 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501798 | ||||||
chr12:19501799 | T | TTG | 30 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(27): Show |
30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1299+1579_1299+158 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19501799 | ||||||
chr12:19501802 | T | G | 1 | a0001c0001t0002g0214 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1299+1581T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501802 | |||||||
chr12:19501839 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+1618C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501839 | |||||||
chr12:19501840 | G | A | 1 | a0001c0001t0004g0289 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1299+1619G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501840 | |||||||
chr12:19501852 | C | T | 8 | a0001c0001t0001g0058 a0001c0001t0001g0093 a0001c0001t0001g0107 others(5): Show |
8 | NA18944.hp1 NA18960.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.1299+1631C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501852 | |||||||
chr12:19501866 | G | T | 4 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0320 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+1645G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501866 | |||||||
chr12:19501951 | G | A | 2 | a0001c0001t0015g0233 a0001c0001t0024g0234 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1299+1730G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19501951 | |||||||
chr12:19502101 | C | T | 30 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(27): Show |
30 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1299+1880C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502101 | |||||||
chr12:19502113 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1299+1892A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502113 | |||||||
chr12:19502128 | A | G | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1299+1907A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502128 | |||||||
chr12:19502237 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+2016C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502237 | |||||||
chr12:19502258 | C | T | 2 | a0001c0001t0003g0360 a0001c0001t0008g0332 |
2 | NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1299+2037C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502258 | |||||||
chr12:19502268 | G | A | 1 | a0001c0001t0004g0296 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1299+2047G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502268 | |||||||
chr12:19502302 | T | G | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1299+2081T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502302 | |||||||
chr12:19502397 | G | A | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1299+2176G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502397 | |||||||
chr12:19502429 | C | T | 1 | a0001c0001t0020g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1299+2208C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502429 | |||||||
chr12:19502439 | T | C | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1299+2218T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502439 | |||||||
chr12:19502569 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1299+2348A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502569 | |||||||
chr12:19502584 | A | G | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1299+2363A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502584 | |||||||
chr12:19502652 | C | CT | 42 | a0001c0001t0002g0169 a0001c0001t0002g0208 a0001c0001t0004g0003 others(39): Show |
42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1299+2444dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19502652 | ||||||
chr12:19502652 | CT | C | 9 | a0001c0001t0002g0166 a0001c0001t0016g0038 a0001c0001t0016g0039 others(6): Show |
9 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+2444delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19502652 | ||||||
chr12:19502705 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+2484A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502705 | |||||||
chr12:19502732 | T | C | 1 | a0001c0003t0044g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1299+2511T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502732 | |||||||
chr12:19502849 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1299+2628C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502849 | |||||||
chr12:19502851 | T | C | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1299+2630T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502851 | |||||||
chr12:19502930 | C | T | 1 | a0001c0001t0009g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1299+2709C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502930 | |||||||
chr12:19502969 | A | G | 1 | a0001c0001t0008g0325 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1299+2748A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19502969 | |||||||
chr12:19503017 | G | A | 1 | a0001c0001t0009g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1299+2796G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503017 | |||||||
chr12:19503139 | G | C | 5 | a0001c0002t0001g0112 a0001c0002t0001g0127 a0001c0002t0001g0128 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+2918G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503139 | |||||||
chr12:19503180 | G | A | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+2959G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503180 | |||||||
chr12:19503328 | G | GGT | 9 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0111 others(6): Show |
9 | HG02083.hp1 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+3124_1299+312 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19503328 | ||||||
chr12:19503329 | G | GTA | 40 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(37): Show |
40 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.1299+3109_1299+311 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19503329 | ||||||
chr12:19503347 | A | ATG | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+3140_1299+314 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19503347 | ||||||
chr12:19503373 | G | A | 1 | a0001c0001t0004g0280 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1299+3152G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503373 | |||||||
chr12:19503398 | C | T | 3 | a0001c0002t0001g0057 a0001c0002t0001g0118 a0001c0002t0001g0119 |
3 | HG03139.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1299+3177C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503398 | |||||||
chr12:19503416 | G | C | 4 | a0001c0001t0004g0317 a0001c0001t0004g0318 a0001c0001t0004g0320 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+3195G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503416 | |||||||
chr12:19503430 | A | C | 5 | a0001c0001t0015g0233 a0001c0001t0015g0235 a0001c0001t0015g0236 others(2): Show |
5 | HG02280.hp2 HG02622.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+3209A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503430 | |||||||
chr12:19503542 | T | C | 3 | a0001c0001t0004g0276 a0001c0001t0004g0281 a0001c0001t0004g0282 |
3 | HG01099.hp2 HG01106.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1299+3321T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503542 | |||||||
chr12:19503564 | C | A | 111 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(108): Show |
111 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1299+3343C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503564 | |||||||
chr12:19503626 | A | G | 1 | a0001c0001t0004g0297 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1299+3405A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503626 | |||||||
chr12:19503707 | A | G | 1 | a0001c0001t0007g0387 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1299+3486A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503707 | |||||||
chr12:19503872 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+3651T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503872 | |||||||
chr12:19503983 | T | C | 2 | a0001c0001t0002g0207 a0001c0001t0037g0205 |
2 | HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1299+3762T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19503983 | |||||||
chr12:19504020 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1299+3799G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504020 | |||||||
chr12:19504079 | C | T | 90 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(87): Show |
92 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.1299+3858C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504079 | |||||||
chr12:19504080 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+3859G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504080 | |||||||
chr12:19504213 | C | G | 1 | a0001c0002t0001g0061 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1299+3992C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504213 | |||||||
chr12:19504269 | C | G | 1 | a0002c0007t0002g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1299+4048C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504269 | |||||||
chr12:19504280 | G | A | 113 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(110): Show |
113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1299+4059G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504280 | |||||||
chr12:19504296 | G | A | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1299+4075G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504296 | |||||||
chr12:19504297 | C | T | 1 | a0001c0001t0003g0376 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1299+4076C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504297 | |||||||
chr12:19504308 | C | T | 1 | a0001c0001t0004g0275 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1299+4087C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504308 | |||||||
chr12:19504320 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1299+4099C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504320 | |||||||
chr12:19504380 | G | GC | 54 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(51): Show |
54 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1299+4167dupC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19504380 | ||||||
chr12:19504380 | GC | G | 136 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(133): Show |
138 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1299+4167delC | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19504380 | ||||||
chr12:19504388 | C | T | 3 | a0001c0002t0001g0057 a0001c0002t0001g0118 a0001c0002t0001g0119 |
3 | HG03139.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1299+4167C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504388 | |||||||
chr12:19504403 | AT | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+4189delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19504403 | ||||||
chr12:19504405 | T | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+4184T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504405 | |||||||
chr12:19504411 | G | A | 113 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(110): Show |
113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1299+4190G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504411 | |||||||
chr12:19504461 | C | T | 113 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(110): Show |
113 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1299+4240C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504461 | |||||||
chr12:19504478 | G | A | 4 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0354 others(1): Show |
5 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+4257G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504478 | |||||||
chr12:19504483 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1299+4262A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504483 | |||||||
chr12:19504572 | A | G | 1 | a0001c0002t0002g0146 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1299+4351A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504572 | |||||||
chr12:19504606 | A | G | 3 | a0001c0001t0006g0025 a0001c0001t0014g0023 a0001c0001t0031g0032 |
3 | HG00639.hp1 HG01106.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1299+4385A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504606 | |||||||
chr12:19504645 | A | G | 172 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(169): Show |
174 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1299+4424A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504645 | |||||||
chr12:19504735 | T | C | 2 | a0001c0001t0012g0324 a0001c0001t0012g0361 |
2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1299+4514T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504735 | |||||||
chr12:19504795 | A | G | 137 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0307 others(134): Show |
139 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1299+4574A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504795 | |||||||
chr12:19504871 | T | C | 1 | a0001c0001t0005g0136 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1299+4650T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504871 | |||||||
chr12:19504872 | A | G | 4 | a0001c0001t0003g0347 a0001c0001t0003g0353 a0001c0001t0007g0348 others(1): Show |
4 | HG02040.hp2 HG02132.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1299+4651A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504872 | |||||||
chr12:19504873 | G | T | 2 | a0001c0001t0004g0289 a0001c0001t0025g0290 |
2 | HG01243.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1299+4652G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19504873 | |||||||
chr12:19505124 | C | G | 7 | a0001c0001t0002g0002 a0001c0001t0002g0196 a0001c0001t0002g0199 others(4): Show |
9 | NA18955.hp1 NA18963.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.1299+4903C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505124 | |||||||
chr12:19505169 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+4948G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505169 | |||||||
chr12:19505223 | A | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5002A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505223 | |||||||
chr12:19505337 | TTAAGGTG others(7): Show |
T | 1 | a0001c0001t0002g0166 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1299+5117_1299+513 others(18): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505337 | |||||||
chr12:19505397 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5176G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505397 | |||||||
chr12:19505445 | G | A | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1299+5224G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505445 | |||||||
chr12:19505527 | A | C | 1 | a0001c0002t0010g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1299+5306A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505527 | |||||||
chr12:19505533 | A | T | 1 | a0001c0001t0007g0396 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1299+5312A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505533 | |||||||
chr12:19505605 | C | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+5384C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505605 | |||||||
chr12:19505761 | T | TTTTG | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5560_1299+556 others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19505761 | ||||||
chr12:19505889 | C | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+5668C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505889 | |||||||
chr12:19505926 | C | A | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1299+5705C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505926 | |||||||
chr12:19505930 | G | C | 302 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(299): Show |
304 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1299+5709G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505930 | |||||||
chr12:19505969 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5748C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505969 | |||||||
chr12:19505979 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+5758T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19505979 | |||||||
chr12:19506040 | C | T | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+5819C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506040 | |||||||
chr12:19506144 | C | T | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+5923C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506144 | |||||||
chr12:19506167 | G | A | 1 | a0001c0001t0003g0375 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1299+5946G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506167 | |||||||
chr12:19506204 | C | G | 39 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(36): Show |
39 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1299+5983C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506204 | |||||||
chr12:19506222 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1299+6001T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19506222 | |||||||
chr12:19507013 | G | T | 1 | a0001c0001t0008g0325 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1300-5385G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507013 | |||||||
chr12:19507151 | A | C | 1 | a0001c0001t0009g0184 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1300-5247A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507151 | |||||||
chr12:19507220 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0101 |
3 | HG02056.hp1 HG02071.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1300-5178A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507220 | |||||||
chr12:19507508 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1300-4890A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507508 | |||||||
chr12:19507509 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1300-4889A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507509 | |||||||
chr12:19507577 | A | T | 179 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(176): Show |
179 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(176): Show |
intron_variant | MODIFIER | c.1300-4821A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507577 | |||||||
chr12:19507632 | C | CAGTT | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4765_1300-476 others(8): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19507632 | ||||||
chr12:19507636 | A | C | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4762A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507636 | |||||||
chr12:19507638 | G | GT | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4760_1300-475 others(5): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507638 | |||||||
chr12:19507640 | T | A | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1300-4758T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507640 | |||||||
chr12:19507726 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-4672G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507726 | |||||||
chr12:19507772 | A | G | 1 | a0001c0002t0002g0080 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1300-4626A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507772 | |||||||
chr12:19507905 | T | A | 1 | a0001c0001t0032g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-4493T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507905 | |||||||
chr12:19507906 | A | T | 1 | a0001c0001t0032g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-4492A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507906 | |||||||
chr12:19507924 | A | G | 1 | a0001c0002t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1300-4474A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19507924 | |||||||
chr12:19508046 | A | C | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1300-4352A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508046 | |||||||
chr12:19508063 | TGCTTGGT others(2): Show |
T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0093 a0001c0001t0001g0107 others(4): Show |
7 | NA18944.hp1 NA18960.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-4329_1300-432 others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19508063 | ||||||
chr12:19508104 | T | C | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-4294T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508104 | |||||||
chr12:19508123 | C | T | 1 | a0001c0001t0013g0160 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1300-4275C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508123 | |||||||
chr12:19508139 | T | C | 54 | a0001c0001t0002g0204 a0001c0002t0001g0050 a0001c0002t0001g0051 others(51): Show |
54 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.1300-4259T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508139 | |||||||
chr12:19508202 | T | C | 1 | a0001c0001t0006g0011 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1300-4196T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508202 | |||||||
chr12:19508223 | A | G | 4 | a0001c0001t0005g0142 a0001c0001t0005g0238 a0001c0001t0005g0259 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-4175A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508223 | |||||||
chr12:19508326 | G | A | 111 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(108): Show |
111 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.1300-4072G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508326 | |||||||
chr12:19508353 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(1): Show |
4 | HG00597.hp2 HG02056.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-4045G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508353 | |||||||
chr12:19508363 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1300-4035A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508363 | |||||||
chr12:19508438 | T | A | 1 | a0001c0002t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1300-3960T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508438 | |||||||
chr12:19508503 | C | T | 395 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(392): Show |
401 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(398): Show |
intron_variant | MODIFIER | c.1300-3895C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508503 | |||||||
chr12:19508632 | T | C | 1 | a0001c0001t0005g0133 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1300-3766T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508632 | |||||||
chr12:19508644 | T | C | 1 | a0001c0001t0034g0049 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1300-3754T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508644 | |||||||
chr12:19508772 | AACAAAT | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-3625_1300-362 others(10): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508772 | |||||||
chr12:19508840 | C | A | 1 | a0001c0001t0039g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1300-3558C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508840 | |||||||
chr12:19508872 | C | G | 1 | a0001c0001t0003g0358 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1300-3526C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508872 | |||||||
chr12:19508923 | A | G | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1300-3475A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19508923 | |||||||
chr12:19509121 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-3277A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509121 | |||||||
chr12:19509253 | G | A | 329 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(326): Show |
331 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(328): Show |
intron_variant | MODIFIER | c.1300-3145G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509253 | |||||||
chr12:19509404 | T | G | 1 | a0001c0001t0005g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1300-2994T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509404 | |||||||
chr12:19509520 | C | T | 91 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(88): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.1300-2878C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509520 | |||||||
chr12:19509570 | A | C | 1 | a0001c0001t0032g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-2828A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509570 | |||||||
chr12:19509793 | C | T | 1 | a0001c0001t0011g0301 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1300-2605C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509793 | |||||||
chr12:19509816 | CTTTCTTT others(8): Show |
C | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1300-2578_1300-256 others(19): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509816 | ||||||
chr12:19509820 | C | CT | 43 | a0001c0001t0001g0246 a0001c0001t0002g0179 a0001c0001t0002g0200 others(40): Show |
43 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.1300-2552dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | ||||||
chr12:19509820 | C | CTT | 6 | a0001c0001t0005g0134 a0001c0001t0005g0156 a0001c0001t0005g0157 others(3): Show |
6 | HG02148.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-2553_1300-255 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | ||||||
chr12:19509820 | CT | C | 128 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(125): Show |
128 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.1300-2552delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | ||||||
chr12:19509820 | CTT | C | 82 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(79): Show |
83 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1300-2553_1300-255 others(6): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | ||||||
chr12:19509820 | CTTT | C | 53 | a0001c0001t0002g0208 a0001c0001t0003g0006 a0001c0001t0003g0311 others(50): Show |
53 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1300-2554_1300-255 others(7): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | ||||||
chr12:19509820 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1300-2562_1300-255 others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19509820 | ||||||
chr12:19509977 | C | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1300-2421C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19509977 | |||||||
chr12:19510126 | T | A | 1 | a0001c0001t0002g0212 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1300-2272T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510126 | |||||||
chr12:19510285 | A | C | 32 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(29): Show |
32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1300-2113A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510285 | |||||||
chr12:19510288 | C | G | 1 | a0001c0001t0002g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1300-2110C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510288 | |||||||
chr12:19510508 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1300-1890C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510508 | |||||||
chr12:19510564 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-1834G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510564 | |||||||
chr12:19510568 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1300-1830G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510568 | |||||||
chr12:19510653 | A | G | 5 | a0001c0002t0001g0112 a0001c0002t0001g0127 a0001c0002t0001g0128 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-1745A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510653 | |||||||
chr12:19510800 | A | G | 32 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(29): Show |
32 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1300-1598A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19510800 | |||||||
chr12:19510865 | C | CT | 61 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0167 others(58): Show |
65 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1300-1516dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | ||||||
chr12:19510865 | C | CTTTTTTT | 18 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0247 others(15): Show |
18 | HG02055.hp2 HG02257.hp1 HG02647.hp2 others(15): Show |
intron_variant | MODIFIER | c.1300-1522_1300-151 others(11): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | ||||||
chr12:19510865 | C | CTTTTTTT others(1): Show |
142 | a0001c0001t0001g0054 a0001c0001t0001g0111 a0001c0001t0001g0116 others(139): Show |
144 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1300-1523_1300-151 others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | ||||||
chr12:19510865 | C | CTTTTTTT others(2): Show |
108 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0058 others(105): Show |
108 | HG00323.hp2 HG00558.hp2 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1300-1524_1300-151 others(13): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | ||||||
chr12:19510865 | C | CTTTTTTT others(3): Show |
45 | a0001c0001t0001g0098 a0001c0001t0001g0246 a0001c0001t0001g0250 others(42): Show |
45 | HG00609.hp2 HG01081.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.1300-1525_1300-151 others(14): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | ||||||
chr12:19510865 | C | CTTTTTTT others(4): Show |
13 | a0001c0001t0005g0134 a0001c0001t0005g0136 a0001c0001t0005g0137 others(10): Show |
13 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1300-1526_1300-151 others(15): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | ||||||
chr12:19510865 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0005g0148 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1300-1527_1300-151 others(16): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19510865 | ||||||
chr12:19511117 | G | A | 108 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(105): Show |
108 | HG00558.hp2 HG00597.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1300-1281G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511117 | |||||||
chr12:19511175 | T | C | 140 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0208 others(137): Show |
142 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1300-1223T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511175 | |||||||
chr12:19511176 | C | T | 1 | a0001c0001t0004g0283 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1300-1222C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511176 | |||||||
chr12:19511271 | G | A | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1300-1127G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511271 | |||||||
chr12:19511328 | T | G | 1 | a0001c0001t0002g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1300-1070T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511328 | |||||||
chr12:19511358 | T | G | 2 | a0001c0001t0007g0315 a0001c0001t0007g0316 |
2 | HG02723.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1300-1040T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511358 | |||||||
chr12:19511388 | T | A | 1 | a0001c0001t0005g0139 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1300-1010T>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511388 | |||||||
chr12:19511419 | G | GA | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1300-975dupA | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr12 | 19511419 | ||||||
chr12:19511923 | T | G | 5 | a0001c0001t0001g0058 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
5 | NA18944.hp1 NA18973.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300-475T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511923 | |||||||
chr12:19511984 | C | G | 6 | a0001c0001t0013g0159 a0001c0001t0013g0160 a0001c0001t0013g0161 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300-414C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19511984 | |||||||
chr12:19512193 | T | G | 1 | a0001c0001t0032g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1300-205T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 5/7 | chr12 | 19512193 | |||||||
chr12:19512479 | A | G | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1367+14A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512479 | |||||||
chr12:19512602 | A | G | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1367+137A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512602 | |||||||
chr12:19512651 | A | T | 1 | a0001c0001t0017g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1367+186A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512651 | |||||||
chr12:19512669 | CTT | C | 35 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(32): Show |
35 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.1367+214_1367+215d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19512669 | ||||||
chr12:19512738 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1367+273G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512738 | |||||||
chr12:19512818 | C | T | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1367+353C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19512818 | |||||||
chr12:19513206 | T | C | 330 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(327): Show |
332 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(329): Show |
intron_variant | MODIFIER | c.1367+741T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513206 | |||||||
chr12:19513322 | A | AT | 182 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0002g0208 others(179): Show |
184 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1367+864dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513322 | ||||||
chr12:19513329 | T | TTA | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1367+864_1367+865i others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513329 | |||||||
chr12:19513481 | G | T | 1 | a0001c0001t0032g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1367+1016G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513481 | |||||||
chr12:19513711 | C | T | 4 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0129 others(1): Show |
4 | HG02280.hp1 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-960C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513711 | |||||||
chr12:19513719 | T | G | 37 | a0001c0001t0002g0183 a0001c0001t0005g0132 a0001c0001t0005g0133 others(34): Show |
37 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.1368-952T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513719 | |||||||
chr12:19513788 | A | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-883A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513788 | |||||||
chr12:19513794 | A | G | 27 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(24): Show |
27 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1368-877A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513794 | |||||||
chr12:19513886 | G | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0103 a0001c0001t0010g0102 |
3 | NA18952.hp1 NA18978.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1368-785G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513886 | |||||||
chr12:19513892 | A | AT | 12 | a0001c0001t0002g0002 a0001c0001t0002g0196 a0001c0001t0002g0199 others(9): Show |
14 | HG00621.hp1 HG02055.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1368-762dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513892 | ||||||
chr12:19513892 | AT | A | 88 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(85): Show |
88 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.1368-762delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513892 | ||||||
chr12:19513892 | ATT | A | 71 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(68): Show |
71 | HG00609.hp2 HG01081.hp2 HG01109.hp1 others(68): Show |
intron_variant | MODIFIER | c.1368-763_1368-762d others(4): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513892 | ||||||
chr12:19513945 | C | CT | 11 | a0001c0001t0003g0353 a0001c0001t0003g0362 a0001c0001t0004g0279 others(8): Show |
11 | HG02486.hp2 HG02738.hp2 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1368-712dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513945 | ||||||
chr12:19513945 | CT | C | 18 | a0001c0001t0001g0121 a0001c0001t0001g0247 a0001c0001t0003g0360 others(15): Show |
19 | HG00558.hp1 HG01167.hp1 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.1368-712delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513945 | ||||||
chr12:19513973 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1368-698T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513973 | |||||||
chr12:19513989 | T | C | 1 | a0001c0001t0004g0300 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1368-682T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19513989 | |||||||
chr12:19513999 | G | GT | 5 | a0001c0001t0002g0166 a0001c0001t0003g0312 a0001c0001t0003g0388 others(2): Show |
5 | HG01433.hp1 NA18940.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368-665dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19513999 | ||||||
chr12:19514000 | T | G | 1 | a0001c0001t0004g0287 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-671T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514000 | |||||||
chr12:19514008 | G | GT | 7 | a0001c0001t0003g0336 a0001c0001t0004g0281 a0001c0001t0004g0287 others(4): Show |
7 | HG01192.hp2 HG03516.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-655dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19514008 | ||||||
chr12:19514008 | G | T | 1 | a0001c0001t0002g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1368-663G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514008 | |||||||
chr12:19514031 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-640A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514031 | |||||||
chr12:19514117 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1368-554G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514117 | |||||||
chr12:19514191 | G | GGGTTTCA others(3): Show |
1 | a0001c0001t0032g0181 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1368-479_1368-478i others(12): Show |
AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr12 | 19514191 | ||||||
chr12:19514278 | G | C | 1 | a0001c0001t0004g0287 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-393G>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514278 | |||||||
chr12:19514280 | A | C | 1 | a0001c0001t0004g0287 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-391A>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514280 | |||||||
chr12:19514285 | C | A | 1 | a0001c0001t0004g0287 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1368-386C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514285 | |||||||
chr12:19514289 | C | T | 6 | a0001c0001t0004g0275 a0001c0001t0004g0278 a0001c0001t0004g0283 others(3): Show |
6 | HG00621.hp1 HG02015.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-382C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514289 | |||||||
chr12:19514455 | C | T | 1 | a0001c0001t0012g0335 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1368-216C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514455 | |||||||
chr12:19514602 | T | G | 4 | a0001c0001t0006g0017 a0001c0001t0006g0018 a0001c0001t0006g0019 others(1): Show |
4 | HG01934.hp1 HG03017.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-69T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514602 | |||||||
chr12:19514640 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-31C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 6/7 | chr12 | 19514640 | |||||||
chr12:19514903 | A | T | 1 | a0001c0001t0002g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1481+119A>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19514903 | |||||||
chr12:19514912 | CT | C | 29 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(26): Show |
29 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.1481+140delT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 19514912 | ||||||
chr12:19514995 | T | C | 3 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0052 |
3 | HG01109.hp1 HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1481+211T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19514995 | |||||||
chr12:19515152 | A | AT | 111 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(108): Show |
111 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(108): Show |
intron_variant | MODIFIER | c.1481+376dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 19515152 | ||||||
chr12:19515184 | C | A | 1 | a0001c0001t0007g0390 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1481+400C>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515184 | |||||||
chr12:19515207 | T | C | 2 | a0001c0001t0004g0268 a0001c0001t0004g0269 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1481+423T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515207 | |||||||
chr12:19515333 | T | C | 2 | a0001c0001t0003g0313 a0001c0005t0023g0036 |
2 | HG02735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1481+549T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515333 | |||||||
chr12:19515558 | T | C | 41 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(38): Show |
41 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1481+774T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515558 | |||||||
chr12:19515592 | C | CT | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+814dupT | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr12 | 19515592 | ||||||
chr12:19515756 | C | T | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+972C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515756 | |||||||
chr12:19515769 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1481+985A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515769 | |||||||
chr12:19515829 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+1045G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515829 | |||||||
chr12:19515953 | C | T | 1 | a0001c0001t0003g0378 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1481+1169C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515953 | |||||||
chr12:19515964 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481+1180G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515964 | |||||||
chr12:19515996 | G | T | 1 | a0001c0001t0020g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1481+1212G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19515996 | |||||||
chr12:19516018 | G | A | 31 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(28): Show |
31 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.1481+1234G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516018 | |||||||
chr12:19516131 | T | C | 2 | a0001c0001t0034g0049 a0001c0006t0033g0044 |
2 | HG01934.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1481+1347T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516131 | |||||||
chr12:19516396 | A | G | 94 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(91): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1481+1612A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516396 | |||||||
chr12:19516397 | G | T | 94 | a0001c0001t0003g0006 a0001c0001t0003g0307 a0001c0001t0003g0310 others(91): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.1481+1613G>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516397 | |||||||
chr12:19516434 | C | G | 1 | a0001c0001t0007g0387 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1481+1650C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516434 | |||||||
chr12:19516517 | T | C | 48 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0166 others(45): Show |
52 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1482-1570T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516517 | |||||||
chr12:19516521 | A | G | 97 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0003g0006 others(94): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1482-1566A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516521 | |||||||
chr12:19516566 | A | G | 55 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0055 others(52): Show |
55 | HG00597.hp2 HG00735.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.1482-1521A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516566 | |||||||
chr12:19516623 | A | G | 3 | a0001c0001t0017g0045 a0001c0001t0017g0046 a0001c0001t0017g0047 |
3 | HG02055.hp1 HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1482-1464A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516623 | |||||||
chr12:19516699 | C | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482-1388C>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516699 | |||||||
chr12:19516710 | T | G | 42 | a0001c0001t0002g0208 a0001c0001t0004g0003 a0001c0001t0004g0007 others(39): Show |
42 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1482-1377T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19516710 | |||||||
chr12:19517162 | T | C | 1 | a0001c0001t0017g0045 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1482-925T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517162 | |||||||
chr12:19517241 | T | G | 36 | a0001c0001t0005g0132 a0001c0001t0005g0133 a0001c0001t0005g0134 others(33): Show |
36 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1482-846T>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517241 | |||||||
chr12:19517261 | C | T | 1 | a0001c0001t0009g0211 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1482-826C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517261 | |||||||
chr12:19517289 | A | G | 3 | a0001c0001t0015g0235 a0001c0001t0015g0236 a0001c0001t0015g0237 |
3 | HG02622.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1482-798A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517289 | |||||||
chr12:19517439 | A | G | 2 | a0001c0001t0003g0383 a0001c0001t0008g0359 |
2 | HG00323.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1482-648A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517439 | |||||||
chr12:19517468 | A | G | 1 | a0001c0001t0011g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1482-619A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517468 | |||||||
chr12:19517574 | G | A | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482-513G>A | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517574 | |||||||
chr12:19517686 | T | C | 1 | a0001c0001t0004g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1482-401T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517686 | |||||||
chr12:19517693 | C | T | 1 | a0001c0006t0033g0044 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1482-394C>T | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517693 | |||||||
chr12:19517914 | A | G | 8 | a0001c0001t0016g0038 a0001c0001t0016g0039 a0001c0001t0016g0041 others(5): Show |
8 | NA18953.hp2 NA18972.hp1 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482-173A>G | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19517914 | |||||||
chr12:19518010 | T | C | 30 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0010 others(27): Show |
30 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1482-77T>C | AEBP2 | ENSG00000139154.16 | transcript | ENST00000266508.14 | protein_coding | 7/7 | chr12 | 19518010 |