Item | Value |
---|---|
geneid | 55780 |
ensemblid | ENSG00000130023.16 |
hgncid | 21056 |
symbol | ERMARD |
name | ER membrane associated RNA degradation |
refseq_nuc | NM_018341.3 |
refseq_prot | NP_060811.1 |
ensembl_nuc | ENST00000366773.8 |
ensembl_prot | ENSP00000355735.3 |
mane_status | MANE Select |
chr | chr6 |
start | 169751622 |
end | 169781600 |
strand | + |
ver | v1.2 |
region | chr6:169751622-169781600 |
region5000 | chr6:169746622-169786600 |
regionname0 | ERMARD_chr6_169751622_169781600 |
regionname5000 | ERMARD_chr6_169746622_169786600 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 678 | 219 | 46 | 45 | 88 | 9 | 31 | 67 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0002 | 0/1 | 678 | 105 | 27 | 24 | 44 | 4 | 5 | 37 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0003 | 0/0 | 678 | 39 | 10 | 4 | 22 | 1 | 2 | 16 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0004 | 0/0 | 678 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | MVVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0005 | 0/0 | 678 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0006 | 0/0 | 678 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0007 | 0/0 | 678 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0008 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0009 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0010 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0011 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
a0012 | 0/0 | 678 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | MEVLI others(673): Show |
chr6 | 169746622 | 169786600 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2034 | 187 | 36 | 43 | 77 | 9 | 22 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0001c0005 | 0/0 | 2034 | 19 | 0 | 2 | 10 | 0 | 7 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0001c0007 | 0/0 | 2034 | 5 | 5 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0001c0009 | 0/0 | 2034 | 3 | 3 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0001c0013 | 0/0 | 2034 | 2 | 0 | 0 | 0 | 0 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0001c0015 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0001c0017 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0001c0019 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0002c0002 | 0/1 | 2034 | 54 | 9 | 12 | 28 | 1 | 3 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0002c0003 | 0/0 | 2034 | 45 | 13 | 11 | 16 | 3 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0002c0006 | 0/0 | 2034 | 6 | 5 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0003c0004 | 0/0 | 2034 | 36 | 8 | 3 | 22 | 1 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0003c0012 | 0/0 | 2034 | 2 | 1 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0003c0020 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0004c0008 | 0/0 | 2034 | 4 | 4 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGT others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0005c0011 | 0/0 | 2034 | 3 | 3 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0006c0010 | 0/0 | 2034 | 3 | 0 | 0 | 3 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0007c0022 | 0/0 | 2034 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0008c0023 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0009c0021 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0010c0016 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0011c0018 | 0/0 | 2034 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 | ||
a0012c0014 | 0/0 | 2034 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | ATGGA others(2029): Show |
chr6 | 169746622 | 169786600 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2160 | 186 | 36 | 43 | 76 | 9 | 22 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0001t0002 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0005t0001 | 0/0 | 2160 | 19 | 0 | 2 | 10 | 0 | 7 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0007t0001 | 0/0 | 2160 | 5 | 5 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0009t0001 | 0/0 | 2160 | 3 | 3 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0013t0001 | 0/0 | 2160 | 2 | 0 | 0 | 0 | 0 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0015t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0017t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0001c0019t0001 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0002c0002t0001 | 0/1 | 2160 | 54 | 9 | 12 | 28 | 1 | 3 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0002c0003t0001 | 0/0 | 2160 | 45 | 13 | 11 | 16 | 3 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0002c0006t0001 | 0/0 | 2160 | 6 | 5 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0003c0004t0001 | 0/0 | 2160 | 36 | 8 | 3 | 22 | 1 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0003c0012t0001 | 0/0 | 2160 | 2 | 1 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0003c0020t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0004c0008t0001 | 0/0 | 2160 | 4 | 4 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0005c0011t0001 | 0/0 | 2160 | 3 | 3 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0006c0010t0001 | 0/0 | 2160 | 3 | 0 | 0 | 3 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0007c0022t0001 | 0/0 | 2160 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0008c0023t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0009c0021t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0010c0016t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0011c0018t0001 | 0/0 | 2160 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
a0012c0014t0001 | 0/0 | 2160 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | GTCAT others(2155): Show |
chr6 | 169746622 | 169786600 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 24 | 0 | 0 | 22 | 0 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0003 | 0/0 | 21 | 3 | 8 | 1 | 1 | 8 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0005 | 0/0 | 10 | 0 | 8 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0007 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0011 | 0/0 | 7 | 0 | 2 | 3 | 2 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0014 | 0/0 | 6 | 1 | 0 | 0 | 1 | 4 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0012 | 0/0 | 6 | 0 | 1 | 2 | 0 | 3 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0007t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0007t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0009t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0009t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0013t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0015t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0017t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0001c0019t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0001 | 0/0 | 28 | 4 | 9 | 12 | 0 | 3 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0047 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0006 | 0/0 | 7 | 1 | 2 | 3 | 1 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0010 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0013 | 0/0 | 7 | 0 | 3 | 2 | 1 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0006t0001g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0006t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0006t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0006t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0002c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0004 | 0/0 | 12 | 0 | 1 | 8 | 1 | 2 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0021 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0012t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0012t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0003c0020t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0004c0008t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0004c0008t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0005c0011t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0005c0011t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0005c0011t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0006c0010t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0007c0022t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0008c0023t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0009c0021t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0010c0016t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0011c0018t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
a0012c0014t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0144 | EUR | GBR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | FIN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00558 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00609 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00621 | hp2 | a0003 | c0004 | t0001 | g0050 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00639 | hp1 | a0001 | c0005 | t0001 | g0012 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00735 | hp2 | a0003 | c0004 | t0001 | g0021 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01070 | hp2 | a0002 | c0003 | t0001 | g0041 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0041 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01074 | hp1 | a0002 | c0003 | t0001 | g0133 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01081 | hp1 | a0007 | c0022 | t0001 | g0154 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01099 | hp1 | a0002 | c0006 | t0001 | g0051 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01099 | hp2 | a0003 | c0004 | t0001 | g0004 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01257 | hp2 | a0003 | c0012 | t0001 | g0167 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0109 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01496 | hp1 | a0002 | c0003 | t0001 | g0113 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01496 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | CLM | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01516 | hp1 | a0002 | c0003 | t0001 | g0006 | EUR | IBS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0108 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01934 | hp2 | a0001 | c0005 | t0001 | g0033 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01943 | hp1 | a0002 | c0003 | t0001 | g0107 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01952 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02004 | hp2 | a0003 | c0004 | t0001 | g0155 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02055 | hp1 | a0002 | c0006 | t0001 | g0162 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02071 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02132 | hp2 | a0003 | c0004 | t0001 | g0165 | EAS | KHV | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02145 | hp2 | a0008 | c0023 | t0001 | g0040 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02155 | hp2 | a0001 | c0019 | t0001 | g0066 | EAS | CDX | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02165 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | CDX | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0130 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02258 | hp2 | a0005 | c0011 | t0001 | g0055 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02273 | hp2 | a0002 | c0003 | t0001 | g0013 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02572 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02602 | hp2 | a0001 | c0005 | t0001 | g0012 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02622 | hp2 | a0003 | c0020 | t0001 | g0152 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02630 | hp2 | a0001 | c0009 | t0001 | g0044 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02647 | hp1 | a0003 | c0004 | t0001 | g0153 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02683 | hp1 | a0001 | c0005 | t0001 | g0012 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02683 | hp2 | a0001 | c0005 | t0001 | g0081 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02717 | hp1 | a0003 | c0004 | t0001 | g0166 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02723 | hp1 | a0001 | c0009 | t0001 | g0044 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02738 | hp1 | a0001 | c0013 | t0001 | g0034 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02809 | hp1 | a0001 | c0009 | t0001 | g0124 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02809 | hp2 | a0001 | c0015 | t0001 | g0115 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02818 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02886 | hp2 | a0003 | c0012 | t0001 | g0168 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02895 | hp2 | a0004 | c0008 | t0001 | g0006 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02896 | hp1 | a0009 | c0021 | t0001 | g0150 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02896 | hp2 | a0003 | c0004 | t0001 | g0049 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02897 | hp1 | a0003 | c0004 | t0001 | g0049 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02922 | hp1 | a0010 | c0016 | t0001 | g0040 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02922 | hp2 | a0011 | c0018 | t0001 | g0009 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02965 | hp1 | a0005 | c0011 | t0001 | g0054 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02965 | hp2 | a0002 | c0006 | t0001 | g0161 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02970 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02976 | hp1 | a0003 | c0004 | t0001 | g0021 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02976 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03098 | hp2 | a0002 | c0003 | t0001 | g0149 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0035 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03225 | hp2 | a0004 | c0008 | t0001 | g0006 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03453 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03486 | hp1 | a0002 | c0006 | t0001 | g0163 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03486 | hp2 | a0003 | c0004 | t0001 | g0021 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03491 | hp1 | a0003 | c0004 | t0001 | g0004 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03516 | hp1 | a0002 | c0006 | t0001 | g0164 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0039 | AFR | ESN | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03579 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03669 | hp2 | a0002 | c0003 | t0001 | g0013 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0112 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03710 | hp1 | a0001 | c0005 | t0001 | g0076 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04115 | hp1 | a0001 | c0013 | t0001 | g0034 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04184 | hp1 | a0003 | c0004 | t0001 | g0004 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04199 | hp1 | a0001 | c0005 | t0001 | g0069 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0080 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04228 | hp1 | a0001 | c0005 | t0001 | g0012 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18522 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | YRI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | CHB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | CHB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18906 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | YRI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18906 | hp2 | a0004 | c0008 | t0001 | g0110 | AFR | YRI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18940 | hp1 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18940 | hp2 | a0001 | c0005 | t0001 | g0075 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18944 | hp2 | a0006 | c0010 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18945 | hp1 | a0003 | c0004 | t0001 | g0158 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18947 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18948 | hp1 | a0002 | c0003 | t0001 | g0131 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18949 | hp1 | a0003 | c0004 | t0001 | g0156 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18954 | hp2 | a0001 | c0005 | t0001 | g0082 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18956 | hp1 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18957 | hp1 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18961 | hp1 | a0012 | c0014 | t0001 | g0012 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18961 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18963 | hp1 | a0001 | c0005 | t0001 | g0078 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18966 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18970 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18978 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18979 | hp2 | a0006 | c0010 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18986 | hp2 | a0001 | c0005 | t0001 | g0074 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18987 | hp1 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18993 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18995 | hp1 | a0001 | c0005 | t0001 | g0033 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18999 | hp2 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19001 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19003 | hp2 | a0006 | c0010 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19030 | hp2 | a0005 | c0011 | t0001 | g0053 | AFR | LWK | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19043 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | LWK | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19056 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19057 | hp2 | a0001 | c0005 | t0001 | g0077 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19065 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19066 | hp2 | a0003 | c0004 | t0001 | g0050 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19068 | hp1 | a0003 | c0004 | t0001 | g0159 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19072 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19077 | hp1 | a0003 | c0004 | t0001 | g0004 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19078 | hp2 | a0003 | c0004 | t0001 | g0160 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19080 | hp2 | a0002 | c0003 | t0001 | g0132 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19082 | hp2 | a0002 | c0003 | t0001 | g0006 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19084 | hp1 | a0001 | c0005 | t0001 | g0079 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19085 | hp2 | a0001 | c0005 | t0001 | g0097 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19087 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19090 | hp1 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19090 | hp2 | a0001 | c0005 | t0001 | g0012 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19091 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | YRI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ASW | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0010 | EUR | TSI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0013 | EUR | TSI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20805 | hp1 | a0003 | c0004 | t0001 | g0004 | EUR | TSI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02109 | hp2 | a0001 | c0007 | t0001 | g0016 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02486 | hp1 | a0001 | c0007 | t0001 | g0056 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02559 | hp1 | a0003 | c0004 | t0001 | g0169 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03471 | hp1 | a0001 | c0017 | t0001 | g0125 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG03471 | hp2 | a0004 | c0008 | t0001 | g0006 | AFR | MSL | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG06807 | hp1 | a0002 | c0006 | t0001 | g0051 | AFR | USA | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | USA | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | USA | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
NA20300 | hp2 | a0003 | c0004 | t0001 | g0021 | AFR | USA | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0139 | REF | REF | ERMARD_chr6_169746622_169786600 | ERMARD | chr6 | 169746622 | 169786600 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169751662 | A | T | 1 | a0004 | 4 | HG02895.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.5A>T | p.Glu2Val | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/18 | 41/2160 | 5/2037 | 2/678 | chr6 | 169751662 | |||
chr6:169753917 | A | G | 1 | a0008 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.60A>G | p.Ile20Met | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/18 | 96/2160 | 60/2037 | 20/678 | chr6 | 169753917 | |||
chr6:169755364 | C | A | 1 | a0005 | 3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.257C>A | p.Thr86Asn | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 3/18 | 293/2160 | 257/2037 | 86/678 | chr6 | 169755364 | |||
chr6:169760687 | A | G | 1 | a0006 | 3 | NA18944.hp2 NA18979.hp2 NA19003.hp2 |
missense_variant | MODERATE | c.788A>G | p.Lys263Arg | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/18 | 824/2160 | 788/2037 | 263/678 | chr6 | 169760687 | |||
chr6:169760692 | G | A | 1 | a0012 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.793G>A | p.Ala265Thr | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/18 | 829/2160 | 793/2037 | 265/678 | chr6 | 169760692 | |||
chr6:169769592 | A | G | 1 | a0007 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1112A>G | p.His371Arg | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/18 | 1148/2160 | 1112/2037 | 371/678 | chr6 | 169769592 | |||
chr6:169776050 | G | A | 3 | a0003 a0006 a0007 |
43 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
missense_variant | MODERATE | c.1505G>A | p.Arg502His | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/18 | 1541/2160 | 1505/2037 | 502/678 | chr6 | 169776050 | |||
chr6:169776058 | A | G | 1 | a0011 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1513A>G | p.Thr505Ala | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/18 | 1549/2160 | 1513/2037 | 505/678 | chr6 | 169776058 | |||
chr6:169776523 | T | C | 2 | a0008 a0010 |
2 | HG02145.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.1589T>C | p.Leu530Pro | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/18 | 1625/2160 | 1589/2037 | 530/678 | chr6 | 169776523 | |||
chr6:169776552 | A | G | 9 | a0002 a0003 a0004 others(6): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
missense_variant | MODERATE | c.1618A>G | p.Ser540Gly | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/18 | 1654/2160 | 1618/2037 | 540/678 | chr6 | 169776552 | |||
chr6:169781498 | T | G | 1 | a0009 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.2022T>G | p.Ser674Arg | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 18/18 | 2058/2160 | 2022/2037 | 674/678 | chr6 | 169781498 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169753866 | A | C | 2 | a0001c0007 a0005c0011 |
8 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.9A>C | p.Val3Val | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/18 | 45/2160 | 9/2037 | 3/678 | chr6 | 169753866 | |||
chr6:169755299 | C | T | 1 | a0001c0013 | 2 | HG02738.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.192C>T | p.Tyr64Tyr | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 3/18 | 228/2160 | 192/2037 | 64/678 | chr6 | 169755299 | |||
chr6:169760718 | A | G | 1 | a0001c0007 | 5 | HG02109.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.819A>G | p.Pro273Pro | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/18 | 855/2160 | 819/2037 | 273/678 | chr6 | 169760718 | |||
chr6:169762441 | C | T | 7 | a0002c0002 a0002c0006 a0003c0004 others(4): Show |
101 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
synonymous_variant | LOW | c.870C>T | p.Cys290Cys | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/18 | 906/2160 | 870/2037 | 290/678 | chr6 | 169762441 | |||
chr6:169762531 | G | A | 1 | a0001c0009 | 3 | HG02630.hp2 HG02723.hp1 HG02809.hp1 |
splice_region_variant&synonymous_variant | LOW | c.960G>A | p.Glu320Glu | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/18 | 996/2160 | 960/2037 | 320/678 | chr6 | 169762531 | |||
chr6:169768126 | T | C | 1 | a0002c0006 | 6 | HG01099.hp1 HG02055.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.1014T>C | p.Asp338Asp | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/18 | 1050/2160 | 1014/2037 | 338/678 | chr6 | 169768126 | |||
chr6:169775281 | T | C | 1 | a0001c0015 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.1329T>C | p.Cys443Cys | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 14/18 | 1365/2160 | 1329/2037 | 443/678 | chr6 | 169775281 | |||
chr6:169775323 | A | G | 1 | a0001c0019 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.1371A>G | p.Glu457Glu | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 14/18 | 1407/2160 | 1371/2037 | 457/678 | chr6 | 169775323 | |||
chr6:169776551 | C | T | 13 | a0002c0002 a0002c0003 a0002c0006 others(10): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
synonymous_variant | LOW | c.1617C>T | p.Ile539Ile | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/18 | 1653/2160 | 1617/2037 | 539/678 | chr6 | 169776551 | |||
chr6:169779236 | G | A | 1 | a0003c0020 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1794G>A | p.Glu598Glu | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/18 | 1830/2160 | 1794/2037 | 598/678 | chr6 | 169779236 | |||
chr6:169781375 | C | T | 1 | a0001c0017 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1899C>T | p.Tyr633Tyr | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 18/18 | 1935/2160 | 1899/2037 | 633/678 | chr6 | 169781375 | |||
chr6:169781420 | A | G | 3 | a0001c0005 a0001c0013 a0012c0014 |
22 | HG00639.hp1 HG01934.hp2 HG02602.hp2 others(19): Show |
synonymous_variant | LOW | c.1944A>G | p.Thr648Thr | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 18/18 | 1980/2160 | 1944/2037 | 648/678 | chr6 | 169781420 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169781560 | G | A | 1 | a0001c0001t0002 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*47G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 18/18 | 47 | chr6 | 169781560 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:169751670 | C | T | 54 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(51): Show |
118 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(115): Show |
splice_region_variant&intron_variant | LOW | c.6+7C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169751670 | |||||||
chr6:169751734 | G | A | 1 | a0002c0003t0001g0045 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.6+71G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169751734 | |||||||
chr6:169751874 | G | GC | 5 | a0002c0003t0001g0010 a0002c0003t0001g0130 a0002c0003t0001g0131 others(2): Show |
12 | HG01074.hp1 HG02257.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.6+213dupC | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | 169751874 | ||||||
chr6:169751984 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.6+321T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169751984 | |||||||
chr6:169752006 | C | T | 1 | a0002c0002t0001g0170 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.6+343C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169752006 | |||||||
chr6:169752106 | A | G | 1 | a0003c0004t0001g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6+443A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169752106 | |||||||
chr6:169752316 | G | A | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.6+653G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169752316 | |||||||
chr6:169752599 | T | G | 5 | a0001c0007t0001g0016 a0001c0007t0001g0056 a0005c0011t0001g0053 others(2): Show |
8 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+936T>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169752599 | |||||||
chr6:169752600 | G | A | 5 | a0001c0007t0001g0016 a0001c0007t0001g0056 a0005c0011t0001g0053 others(2): Show |
8 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.6+937G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169752600 | |||||||
chr6:169752874 | T | C | 1 | a0002c0003t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7-990T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169752874 | |||||||
chr6:169752895 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
322 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(319): Show |
intron_variant | MODIFIER | c.7-969G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169752895 | |||||||
chr6:169753051 | C | T | 5 | a0001c0007t0001g0016 a0001c0007t0001g0056 a0005c0011t0001g0053 others(2): Show |
8 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.7-813C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169753051 | |||||||
chr6:169753077 | C | A | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.7-787C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169753077 | |||||||
chr6:169753606 | A | C | 16 | a0002c0003t0001g0006 a0002c0003t0001g0013 a0002c0003t0001g0025 others(13): Show |
34 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.7-258A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 1/17 | chr6 | 169753606 | |||||||
chr6:169754292 | TTGA | T | 5 | a0001c0007t0001g0016 a0001c0007t0001g0056 a0005c0011t0001g0053 others(2): Show |
8 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+266_175+268del others(3): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr6 | 169754292 | ||||||
chr6:169754360 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.175+328T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169754360 | |||||||
chr6:169754410 | G | A | 70 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(67): Show |
152 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.175+378G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169754410 | |||||||
chr6:169754652 | A | G | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.175+620A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169754652 | |||||||
chr6:169754749 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.176-534C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169754749 | |||||||
chr6:169754892 | G | T | 5 | a0001c0007t0001g0016 a0001c0007t0001g0056 a0005c0011t0001g0053 others(2): Show |
8 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-391G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169754892 | |||||||
chr6:169754973 | A | G | 1 | a0002c0002t0001g0026 | 3 | HG01975.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.176-310A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169754973 | |||||||
chr6:169755017 | G | C | 2 | a0002c0002t0001g0151 a0009c0021t0001g0150 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.176-266G>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169755017 | |||||||
chr6:169755142 | A | G | 5 | a0001c0007t0001g0016 a0001c0007t0001g0056 a0005c0011t0001g0053 others(2): Show |
8 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-141A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169755142 | |||||||
chr6:169755235 | A | T | 69 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(66): Show |
151 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.176-48A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 2/17 | chr6 | 169755235 | |||||||
chr6:169755538 | G | A | 18 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(15): Show |
50 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.315+116G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 3/17 | chr6 | 169755538 | |||||||
chr6:169755612 | G | A | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.315+190G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 3/17 | chr6 | 169755612 | |||||||
chr6:169755829 | G | A | 23 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(20): Show |
47 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.315+407G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 3/17 | chr6 | 169755829 | |||||||
chr6:169755876 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.315+454T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 3/17 | chr6 | 169755876 | |||||||
chr6:169756587 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0022 others(9): Show |
24 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.418-132T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 4/17 | chr6 | 169756587 | |||||||
chr6:169756675 | T | A | 2 | a0001c0001t0001g0067 a0001c0019t0001g0066 |
2 | HG02155.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.418-44T>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 4/17 | chr6 | 169756675 | |||||||
chr6:169756883 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.507+75A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169756883 | |||||||
chr6:169756918 | C | T | 1 | a0003c0012t0001g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.507+110C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169756918 | |||||||
chr6:169757124 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0104 others(1): Show |
7 | HG01109.hp1 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+316A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169757124 | |||||||
chr6:169757192 | C | T | 73 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(70): Show |
155 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.507+384C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169757192 | |||||||
chr6:169757554 | T | C | 1 | a0002c0003t0001g0039 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.507+746T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169757554 | |||||||
chr6:169757729 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0068 |
3 | NA18939.hp2 NA18979.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.507+921T>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169757729 | |||||||
chr6:169757737 | G | A | 70 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(67): Show |
152 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.507+929G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169757737 | |||||||
chr6:169757768 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.507+960C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169757768 | |||||||
chr6:169757858 | C | T | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.507+1050C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169757858 | |||||||
chr6:169758206 | A | G | 1 | a0003c0012t0001g0168 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.508-762A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758206 | |||||||
chr6:169758223 | C | T | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508-745C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758223 | |||||||
chr6:169758277 | C | T | 2 | a0003c0012t0001g0167 a0003c0012t0001g0168 |
2 | HG01257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.508-691C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758277 | |||||||
chr6:169758321 | C | T | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.508-647C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758321 | |||||||
chr6:169758606 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.508-362A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758606 | |||||||
chr6:169758697 | T | C | 1 | a0002c0002t0001g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.508-271T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758697 | |||||||
chr6:169758727 | T | C | 1 | a0002c0003t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.508-241T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758727 | |||||||
chr6:169758772 | A | G | 70 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(67): Show |
152 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.508-196A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758772 | |||||||
chr6:169758811 | T | C | 1 | a0001c0001t0001g0029 | 2 | NA18982.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.508-157T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758811 | |||||||
chr6:169758927 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
321 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.508-41G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 5/17 | chr6 | 169758927 | |||||||
chr6:169759163 | A | G | 16 | a0002c0003t0001g0006 a0002c0003t0001g0013 a0002c0003t0001g0025 others(13): Show |
34 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.605+98A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 6/17 | chr6 | 169759163 | |||||||
chr6:169759676 | C | G | 1 | a0002c0003t0001g0114 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.606-162C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 6/17 | chr6 | 169759676 | |||||||
chr6:169759815 | CAG | C | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.606-21_606-20delGA | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr6 | 169759815 | ||||||
chr6:169759822 | C | T | 1 | a0003c0004t0001g0166 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.606-16C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 6/17 | chr6 | 169759822 | |||||||
chr6:169760138 | C | T | 2 | a0003c0012t0001g0167 a0003c0012t0001g0168 |
2 | HG01257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.742+164C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760138 | |||||||
chr6:169760147 | GCCT | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
73 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.742+179_742+181del others(3): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr6 | 169760147 | ||||||
chr6:169760183 | T | A | 1 | a0001c0001t0001g0059 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.742+209T>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760183 | |||||||
chr6:169760253 | G | A | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.742+279G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760253 | |||||||
chr6:169760314 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743-328A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760314 | |||||||
chr6:169760335 | G | A | 6 | a0003c0004t0001g0021 a0003c0004t0001g0049 a0003c0004t0001g0153 others(3): Show |
10 | HG00735.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.743-307G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760335 | |||||||
chr6:169760337 | A | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0099 others(3): Show |
16 | HG00735.hp1 HG01168.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.743-305A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760337 | |||||||
chr6:169760462 | G | A | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.743-180G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760462 | |||||||
chr6:169760494 | A | G | 28 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0031 others(25): Show |
47 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.743-148A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 7/17 | chr6 | 169760494 | |||||||
chr6:169760828 | C | T | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.857+72C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169760828 | |||||||
chr6:169760861 | G | C | 1 | a0002c0003t0001g0039 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.857+105G>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169760861 | |||||||
chr6:169760903 | C | T | 1 | a0001c0005t0001g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.857+147C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169760903 | |||||||
chr6:169760938 | T | C | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.857+182T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169760938 | |||||||
chr6:169761025 | A | G | 2 | a0002c0002t0001g0048 a0002c0002t0001g0170 |
3 | HG02056.hp2 NA18612.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.857+269A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761025 | |||||||
chr6:169761070 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.857+314C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761070 | |||||||
chr6:169761071 | A | G | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.857+315A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761071 | |||||||
chr6:169761136 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.857+380A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761136 | |||||||
chr6:169761458 | C | T | 2 | a0002c0002t0001g0151 a0009c0021t0001g0150 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.857+702C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761458 | |||||||
chr6:169761459 | G | A | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.857+703G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761459 | |||||||
chr6:169761480 | G | A | 73 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(70): Show |
155 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.857+724G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761480 | |||||||
chr6:169761577 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.857+821C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761577 | |||||||
chr6:169761673 | G | GGTTTTGT others(3): Show |
104 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
236 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.858-740_858-731dup others(10): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 169761673 | ||||||
chr6:169761673 | G | GGTTTTGT others(8): Show |
44 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(41): Show |
81 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.858-745_858-731dup others(15): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 169761673 | ||||||
chr6:169761673 | G | GGTTTTGT others(13): Show |
1 | a0001c0001t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.858-750_858-731dup others(20): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr6 | 169761673 | ||||||
chr6:169761774 | C | G | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.858-655C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761774 | |||||||
chr6:169761774 | C | T | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.858-655C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761774 | |||||||
chr6:169761880 | G | A | 1 | a0001c0005t0001g0069 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.858-549G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761880 | |||||||
chr6:169761885 | A | G | 73 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(70): Show |
155 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.858-544A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761885 | |||||||
chr6:169761972 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.858-457T>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761972 | |||||||
chr6:169761997 | T | C | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.858-432T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169761997 | |||||||
chr6:169762072 | C | A | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.858-357C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169762072 | |||||||
chr6:169762180 | G | A | 1 | a0007c0022t0001g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.858-249G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169762180 | |||||||
chr6:169762207 | T | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
73 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.858-222T>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169762207 | |||||||
chr6:169762211 | G | T | 2 | a0003c0012t0001g0167 a0003c0012t0001g0168 |
2 | HG01257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.858-218G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169762211 | |||||||
chr6:169762418 | C | A | 1 | a0002c0003t0001g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.858-11C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169762418 | |||||||
chr6:169762418 | C | T | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.858-11C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169762418 | |||||||
chr6:169762419 | A | C | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
73 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.858-10A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 8/17 | chr6 | 169762419 | |||||||
chr6:169762761 | G | A | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.960+230G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169762761 | |||||||
chr6:169762766 | C | T | 14 | a0001c0005t0001g0012 a0001c0005t0001g0033 a0001c0005t0001g0069 others(11): Show |
21 | HG00639.hp1 HG01934.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.960+235C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169762766 | |||||||
chr6:169762767 | G | A | 1 | a0003c0020t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.960+236G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169762767 | |||||||
chr6:169762820 | G | A | 4 | a0002c0003t0001g0149 a0005c0011t0001g0053 a0005c0011t0001g0054 others(1): Show |
4 | HG02258.hp2 HG02965.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+289G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169762820 | |||||||
chr6:169762834 | C | A | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.960+303C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169762834 | |||||||
chr6:169762843 | C | T | 5 | a0002c0003t0001g0010 a0002c0003t0001g0130 a0002c0003t0001g0131 others(2): Show |
12 | HG01074.hp1 HG02257.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.960+312C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169762843 | |||||||
chr6:169763035 | C | T | 1 | a0002c0002t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.960+504C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763035 | |||||||
chr6:169763095 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
320 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.960+564G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763095 | |||||||
chr6:169763326 | A | G | 2 | a0003c0012t0001g0167 a0003c0012t0001g0168 |
2 | HG01257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.960+795A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763326 | |||||||
chr6:169763494 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.960+963C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763494 | |||||||
chr6:169763559 | C | T | 1 | a0001c0005t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.960+1028C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763559 | |||||||
chr6:169763571 | G | A | 2 | a0002c0002t0001g0151 a0009c0021t0001g0150 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.960+1040G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763571 | |||||||
chr6:169763591 | G | A | 71 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(68): Show |
154 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.960+1060G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763591 | |||||||
chr6:169763680 | A | G | 2 | a0001c0007t0001g0016 a0001c0007t0001g0056 |
5 | HG02109.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+1149A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763680 | |||||||
chr6:169763780 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
320 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.960+1249G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763780 | |||||||
chr6:169763804 | A | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0031 others(24): Show |
45 | HG00639.hp1 HG00639.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.960+1273A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763804 | |||||||
chr6:169763957 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(32): Show |
87 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.960+1426C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763957 | |||||||
chr6:169763975 | C | A | 1 | a0002c0002t0001g0136 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.960+1444C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169763975 | |||||||
chr6:169764025 | TC | T | 7 | a0002c0003t0001g0010 a0002c0003t0001g0035 a0002c0003t0001g0045 others(4): Show |
16 | HG01074.hp1 HG02257.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+1495delC | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764025 | |||||||
chr6:169764033 | T | C | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.960+1502T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764033 | |||||||
chr6:169764081 | C | T | 2 | a0003c0004t0001g0153 a0003c0004t0001g0166 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.960+1550C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764081 | |||||||
chr6:169764082 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.960+1551G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764082 | |||||||
chr6:169764107 | C | T | 1 | a0009c0021t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.960+1576C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764107 | |||||||
chr6:169764144 | T | C | 5 | a0002c0003t0001g0010 a0002c0003t0001g0130 a0002c0003t0001g0131 others(2): Show |
12 | HG01074.hp1 HG02257.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.960+1613T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764144 | |||||||
chr6:169764164 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.960+1633G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764164 | |||||||
chr6:169764172 | C | G | 1 | a0003c0004t0001g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.960+1641C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764172 | |||||||
chr6:169764175 | C | T | 1 | a0001c0005t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.960+1644C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764175 | |||||||
chr6:169764177 | GC | G | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.960+1649delC | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169764177 | ||||||
chr6:169764184 | C | T | 1 | a0002c0003t0001g0130 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.960+1653C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764184 | |||||||
chr6:169764225 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.960+1694C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764225 | |||||||
chr6:169764327 | C | T | 2 | a0002c0002t0001g0151 a0009c0021t0001g0150 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.960+1796C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764327 | |||||||
chr6:169764438 | A | AT | 14 | a0001c0005t0001g0012 a0001c0005t0001g0033 a0001c0005t0001g0069 others(11): Show |
21 | HG00639.hp1 HG01934.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.960+1917dupT | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169764438 | ||||||
chr6:169764603 | C | T | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.961-2035C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764603 | |||||||
chr6:169764614 | G | T | 14 | a0001c0005t0001g0012 a0001c0005t0001g0033 a0001c0005t0001g0069 others(11): Show |
21 | HG00639.hp1 HG01934.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.961-2024G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764614 | |||||||
chr6:169764684 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0117 a0001c0001t0001g0126 |
6 | NA18950.hp1 NA18951.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.961-1954G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764684 | |||||||
chr6:169764875 | A | C | 3 | a0001c0005t0001g0078 a0001c0005t0001g0079 a0001c0005t0001g0082 |
3 | NA18954.hp2 NA18963.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.961-1763A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764875 | |||||||
chr6:169764925 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.961-1713T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169764925 | |||||||
chr6:169765026 | T | C | 1 | a0001c0001t0001g0014 | 6 | HG00140.hp2 HG02698.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-1612T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765026 | |||||||
chr6:169765057 | G | A | 71 | a0001c0001t0001g0031 a0002c0002t0001g0001 a0002c0002t0001g0026 others(68): Show |
155 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.961-1581G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765057 | |||||||
chr6:169765144 | G | A | 3 | a0005c0011t0001g0053 a0005c0011t0001g0054 a0005c0011t0001g0055 |
3 | HG02258.hp2 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.961-1494G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765144 | |||||||
chr6:169765277 | A | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
320 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.961-1361A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765277 | |||||||
chr6:169765640 | C | G | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.961-998C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765640 | |||||||
chr6:169765683 | G | A | 2 | a0003c0012t0001g0167 a0003c0012t0001g0168 |
2 | HG01257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.961-955G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765683 | |||||||
chr6:169765730 | T | C | 5 | a0002c0003t0001g0010 a0002c0003t0001g0130 a0002c0003t0001g0131 others(2): Show |
12 | HG01074.hp1 HG02257.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.961-908T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765730 | |||||||
chr6:169765809 | C | T | 1 | a0001c0005t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.961-829C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765809 | |||||||
chr6:169765850 | A | G | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.961-788A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765850 | |||||||
chr6:169765858 | GCTGTCAA others(29): Show |
G | 2 | a0002c0006t0001g0051 a0002c0006t0001g0164 |
3 | HG01099.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.961-753_961-718del others(36): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169765858 | ||||||
chr6:169765858 | GCTGTCAA others(137): Show |
G | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.961-753_961-610del | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169765858 | ||||||
chr6:169765889 | G | GGCTGTCT others(29): Show |
34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
85 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.961-677_961-642dup others(36): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169765889 | ||||||
chr6:169765889 | GGCTGTCT others(29): Show |
G | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.961-677_961-642del others(36): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169765889 | ||||||
chr6:169765997 | T | C | 1 | a0001c0019t0001g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.961-641T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169765997 | |||||||
chr6:169766005 | GTCAAATC | G | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.961-629_961-623del others(7): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169766005 | ||||||
chr6:169766009 | A | C | 2 | a0002c0002t0001g0151 a0009c0021t0001g0150 |
2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.961-629A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766009 | |||||||
chr6:169766029 | G | A | 1 | a0001c0007t0001g0016 | 4 | HG02109.hp2 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-609G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766029 | |||||||
chr6:169766067 | G | T | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.961-571G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766067 | |||||||
chr6:169766104 | A | C | 1 | a0002c0002t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.961-534A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766104 | |||||||
chr6:169766176 | A | G | 1 | a0001c0005t0001g0077 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.961-462A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766176 | |||||||
chr6:169766194 | A | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
372 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(369): Show |
intron_variant | MODIFIER | c.961-444A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766194 | |||||||
chr6:169766234 | T | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(33): Show |
91 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.961-404T>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766234 | |||||||
chr6:169766336 | G | A | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.961-302G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766336 | |||||||
chr6:169766415 | C | G | 1 | a0005c0011t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.961-223C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766415 | |||||||
chr6:169766491 | C | T | 5 | a0002c0003t0001g0010 a0002c0003t0001g0130 a0002c0003t0001g0131 others(2): Show |
12 | HG01074.hp1 HG02257.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.961-147C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766491 | |||||||
chr6:169766493 | C | CA | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.961-144dupA | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | 169766493 | ||||||
chr6:169766602 | T | G | 1 | a0002c0002t0001g0137 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.961-36T>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 9/17 | chr6 | 169766602 | |||||||
chr6:169766860 | A | G | 1 | a0001c0005t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.990+193A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169766860 | |||||||
chr6:169767042 | G | A | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.990+375G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767042 | |||||||
chr6:169767077 | C | G | 1 | a0002c0002t0001g0145 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.990+410C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767077 | |||||||
chr6:169767088 | C | A | 1 | a0001c0001t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.990+421C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767088 | |||||||
chr6:169767096 | G | T | 1 | a0002c0003t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.990+429G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767096 | |||||||
chr6:169767129 | G | A | 2 | a0005c0011t0001g0054 a0005c0011t0001g0055 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.990+462G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767129 | |||||||
chr6:169767184 | C | T | 1 | a0002c0002t0001g0135 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.990+517C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767184 | |||||||
chr6:169767240 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.990+573G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767240 | |||||||
chr6:169767300 | T | C | 1 | a0003c0004t0001g0155 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.990+633T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767300 | |||||||
chr6:169767311 | T | C | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.990+644T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767311 | |||||||
chr6:169767371 | A | G | 1 | a0002c0003t0001g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.990+704A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767371 | |||||||
chr6:169767522 | C | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(27): Show |
77 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.991-581C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767522 | |||||||
chr6:169767525 | T | A | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.991-578T>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767525 | |||||||
chr6:169767563 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.991-540G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767563 | |||||||
chr6:169767572 | AAC | A | 2 | a0001c0007t0001g0016 a0001c0007t0001g0056 |
5 | HG02109.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.991-525_991-524del others(2): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767572 | ||||||
chr6:169767595 | T | TAC | 14 | a0003c0004t0001g0004 a0003c0004t0001g0008 a0003c0004t0001g0050 others(11): Show |
33 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.991-496_991-495dup others(2): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767595 | ||||||
chr6:169767692 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.991-411C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767692 | |||||||
chr6:169767754 | A | G | 1 | a0002c0003t0001g0041 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.991-349A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767754 | |||||||
chr6:169767756 | T | TAC | 21 | a0001c0001t0001g0119 a0001c0005t0001g0076 a0002c0002t0001g0143 others(18): Show |
39 | HG01081.hp1 HG01099.hp1 HG01361.hp2 others(36): Show |
intron_variant | MODIFIER | c.991-323_991-322dup others(2): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767756 | ||||||
chr6:169767756 | T | TACAC | 51 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(48): Show |
86 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.991-325_991-322dup others(4): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767756 | ||||||
chr6:169767756 | T | TACACAC | 29 | a0001c0001t0001g0070 a0002c0002t0001g0001 a0002c0002t0001g0026 others(26): Show |
79 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.991-327_991-322dup others(6): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767756 | ||||||
chr6:169767756 | T | TACACACA others(5): Show |
4 | a0003c0004t0001g0021 a0003c0004t0001g0153 a0003c0004t0001g0166 others(1): Show |
7 | HG00735.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-333_991-322dup others(12): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767756 | ||||||
chr6:169767756 | T | TACACACA others(7): Show |
1 | a0003c0004t0001g0049 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.991-335_991-322dup others(14): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767756 | ||||||
chr6:169767756 | TAC | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(30): Show |
85 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.991-323_991-322del others(2): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767756 | ||||||
chr6:169767756 | TACAC | T | 2 | a0001c0007t0001g0016 a0001c0007t0001g0056 |
5 | HG02109.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.991-325_991-322del others(4): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767756 | ||||||
chr6:169767780 | C | CACACACA others(7): Show |
1 | a0003c0020t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.991-322_991-321ins others(14): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr6 | 169767780 | ||||||
chr6:169767852 | C | G | 1 | a0002c0003t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.991-251C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169767852 | |||||||
chr6:169768080 | T | C | 1 | a0002c0003t0001g0107 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.991-23T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 10/17 | chr6 | 169768080 | |||||||
chr6:169768346 | C | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0022 others(9): Show |
24 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1059+175C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768346 | |||||||
chr6:169768440 | G | A | 21 | a0002c0003t0001g0006 a0002c0003t0001g0010 a0002c0003t0001g0013 others(18): Show |
46 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1059+269G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768440 | |||||||
chr6:169768460 | T | C | 2 | a0005c0011t0001g0054 a0005c0011t0001g0055 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1059+289T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768460 | |||||||
chr6:169768485 | C | T | 1 | a0001c0005t0001g0097 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1059+314C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768485 | |||||||
chr6:169768521 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1059+350G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768521 | |||||||
chr6:169768529 | G | T | 1 | a0005c0011t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1059+358G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768529 | |||||||
chr6:169768555 | A | G | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1059+384A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768555 | |||||||
chr6:169768648 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0022 others(9): Show |
24 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1059+477C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768648 | |||||||
chr6:169768757 | C | T | 1 | a0001c0001t0001g0036 | 2 | NA18964.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1059+586C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768757 | |||||||
chr6:169768760 | C | T | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+589C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169768760 | |||||||
chr6:169769077 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
86 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1060-463G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169769077 | |||||||
chr6:169769116 | A | T | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-424A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169769116 | |||||||
chr6:169769249 | G | A | 2 | a0002c0006t0001g0051 a0002c0006t0001g0164 |
3 | HG01099.hp1 HG03516.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1060-291G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169769249 | |||||||
chr6:169769457 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1060-83T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169769457 | |||||||
chr6:169769522 | CT | C | 6 | a0003c0004t0001g0008 a0003c0004t0001g0156 a0003c0004t0001g0159 others(3): Show |
13 | HG02132.hp2 NA18944.hp2 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.1060-17delT | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169769522 | |||||||
chr6:169769528 | A | G | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-12A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 11/17 | chr6 | 169769528 | |||||||
chr6:169769723 | A | G | 21 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(18): Show |
53 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1233+10A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169769723 | |||||||
chr6:169769784 | A | G | 1 | a0009c0021t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1233+71A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169769784 | |||||||
chr6:169769926 | C | T | 1 | a0002c0006t0001g0164 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1233+213C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169769926 | |||||||
chr6:169770118 | GTTA | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(74): Show |
163 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.1233+408_1233+410d others(5): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169770118 | ||||||
chr6:169770311 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1233+598A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169770311 | |||||||
chr6:169770465 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
86 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1233+752C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169770465 | |||||||
chr6:169770553 | C | T | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1233+840C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169770553 | |||||||
chr6:169770609 | T | A | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+896T>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169770609 | |||||||
chr6:169770650 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
320 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.1233+937T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169770650 | |||||||
chr6:169770845 | G | A | 74 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(71): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1233+1132G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169770845 | |||||||
chr6:169771077 | C | CT | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1233+1374dupT | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169771077 | ||||||
chr6:169771088 | G | GT | 9 | a0001c0017t0001g0125 a0002c0006t0001g0051 a0002c0006t0001g0161 others(6): Show |
10 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1233+1385dupT | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169771088 | ||||||
chr6:169771144 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1233+1431C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169771144 | |||||||
chr6:169771441 | G | A | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+1728G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169771441 | |||||||
chr6:169771709 | C | CTTCATAC others(121): Show |
1 | a0001c0001t0001g0031 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1234-1609_1234-148 others(132): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169771709 | ||||||
chr6:169771811 | G | A | 6 | a0003c0004t0001g0021 a0003c0004t0001g0049 a0003c0004t0001g0153 others(3): Show |
10 | HG00735.hp2 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1234-1508G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169771811 | |||||||
chr6:169771887 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1234-1432T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169771887 | |||||||
chr6:169771892 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0095 a0001c0005t0001g0069 |
11 | HG00597.hp2 HG00621.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1234-1427C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169771892 | |||||||
chr6:169771905 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1234-1414G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169771905 | |||||||
chr6:169771917 | TC | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0062 others(1): Show |
6 | HG01167.hp2 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1234-1400delC | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169771917 | ||||||
chr6:169772220 | C | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
72 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1234-1099C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772220 | |||||||
chr6:169772282 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1234-1037T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772282 | |||||||
chr6:169772302 | C | T | 2 | a0002c0003t0001g0035 a0002c0003t0001g0045 |
4 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1234-1017C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772302 | |||||||
chr6:169772306 | C | T | 5 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0093 others(2): Show |
5 | HG00609.hp2 HG02155.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-1013C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772306 | |||||||
chr6:169772333 | A | C | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-986A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772333 | |||||||
chr6:169772503 | C | T | 2 | a0005c0011t0001g0054 a0005c0011t0001g0055 |
2 | HG02258.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1234-816C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772503 | |||||||
chr6:169772510 | A | G | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1234-809A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772510 | |||||||
chr6:169772595 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1234-724C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772595 | |||||||
chr6:169772630 | C | T | 1 | a0003c0004t0001g0158 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1234-689C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772630 | |||||||
chr6:169772725 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0100 |
3 | NA18970.hp1 NA19076.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1234-594G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772725 | |||||||
chr6:169772748 | CA | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0022 others(10): Show |
26 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.1234-566delA | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169772748 | ||||||
chr6:169772770 | C | CA | 9 | a0001c0001t0001g0042 a0001c0001t0001g0117 a0001c0001t0001g0118 others(6): Show |
11 | HG00741.hp2 HG01099.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1234-526dupA | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169772770 | ||||||
chr6:169772770 | CA | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0023 others(34): Show |
61 | HG00438.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1234-526delA | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169772770 | ||||||
chr6:169772770 | CAA | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(40): Show |
105 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.1234-527_1234-526d others(4): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169772770 | ||||||
chr6:169772770 | CAAA | C | 38 | a0001c0001t0001g0063 a0002c0002t0001g0001 a0002c0002t0001g0026 others(35): Show |
94 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1234-528_1234-526d others(5): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169772770 | ||||||
chr6:169772770 | CAAAA | C | 21 | a0002c0002t0001g0046 a0002c0002t0001g0143 a0002c0003t0001g0006 others(18): Show |
40 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.1234-529_1234-526d others(6): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169772770 | ||||||
chr6:169772770 | CAAAAA | C | 4 | a0001c0015t0001g0115 a0002c0003t0001g0010 a0002c0003t0001g0130 others(1): Show |
11 | HG01074.hp1 HG02257.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1234-530_1234-526d others(7): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr6 | 169772770 | ||||||
chr6:169772796 | G | A | 1 | a0002c0002t0001g0144 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1234-523G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772796 | |||||||
chr6:169772875 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
86 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1234-444G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772875 | |||||||
chr6:169772889 | T | C | 1 | a0001c0005t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1234-430T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772889 | |||||||
chr6:169772890 | G | T | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1234-429G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772890 | |||||||
chr6:169772891 | T | TTTA | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1234-428_1234-427i others(5): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772891 | |||||||
chr6:169772892 | G | A | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1234-427G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772892 | |||||||
chr6:169772966 | G | A | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
72 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1234-353G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772966 | |||||||
chr6:169772990 | A | G | 2 | a0001c0005t0001g0075 a0001c0005t0001g0077 |
2 | NA18940.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1234-329A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169772990 | |||||||
chr6:169773059 | A | G | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1234-260A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169773059 | |||||||
chr6:169773168 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0094 |
2 | HG00609.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1234-151C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169773168 | |||||||
chr6:169773181 | G | A | 41 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(38): Show |
72 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1234-138G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 12/17 | chr6 | 169773181 | |||||||
chr6:169773490 | T | C | 2 | a0001c0009t0001g0044 a0001c0009t0001g0124 |
3 | HG02630.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1317+88T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169773490 | |||||||
chr6:169773499 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1317+97C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169773499 | |||||||
chr6:169773818 | T | C | 74 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(71): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1317+416T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169773818 | |||||||
chr6:169773959 | T | G | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1317+557T>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169773959 | |||||||
chr6:169774101 | C | T | 1 | a0002c0002t0001g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1317+699C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774101 | |||||||
chr6:169774106 | C | T | 1 | a0002c0003t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1317+704C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774106 | |||||||
chr6:169774138 | A | ATCCTGGC others(14): Show |
1 | a0001c0001t0001g0061 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1317+737_1317+757d others(23): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 169774138 | ||||||
chr6:169774273 | A | G | 74 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(71): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1317+871A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774273 | |||||||
chr6:169774312 | C | T | 18 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(15): Show |
49 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1317+910C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774312 | |||||||
chr6:169774326 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1317+924C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774326 | |||||||
chr6:169774354 | C | T | 1 | a0002c0003t0001g0111 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1318-916C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774354 | |||||||
chr6:169774360 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1318-910C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774360 | |||||||
chr6:169774672 | A | G | 1 | a0001c0005t0001g0075 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1318-598A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774672 | |||||||
chr6:169774851 | AG | A | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1318-417delG | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 169774851 | ||||||
chr6:169774972 | C | T | 2 | a0001c0007t0001g0016 a0001c0007t0001g0056 |
5 | HG02109.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1318-298C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169774972 | |||||||
chr6:169775171 | T | TTTATAGA | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1318-98_1318-97ins others(7): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr6 | 169775171 | ||||||
chr6:169775175 | G | A | 2 | a0001c0005t0001g0080 a0001c0013t0001g0034 |
3 | HG02738.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1318-95G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 13/17 | chr6 | 169775175 | |||||||
chr6:169775589 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1394+243G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 14/17 | chr6 | 169775589 | |||||||
chr6:169775626 | TG | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0057 a0001c0001t0001g0062 others(1): Show |
6 | HG01167.hp2 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394+283delG | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr6 | 169775626 | ||||||
chr6:169775730 | T | C | 2 | a0002c0003t0001g0035 a0002c0003t0001g0045 |
4 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1395-210T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 14/17 | chr6 | 169775730 | |||||||
chr6:169775848 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1395-92G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 14/17 | chr6 | 169775848 | |||||||
chr6:169776250 | A | T | 1 | a0001c0001t0001g0030 | 2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1520+185A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776250 | |||||||
chr6:169776300 | T | C | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1521-155T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776300 | |||||||
chr6:169776301 | A | C | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1521-154A>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776301 | |||||||
chr6:169776310 | C | A | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1521-145C>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776310 | |||||||
chr6:169776311 | G | A | 74 | a0001c0001t0001g0061 a0002c0002t0001g0001 a0002c0002t0001g0026 others(71): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1521-144G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776311 | |||||||
chr6:169776312 | C | T | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1521-143C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776312 | |||||||
chr6:169776316 | T | C | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1521-139T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776316 | |||||||
chr6:169776343 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG01175.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1521-112C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776343 | |||||||
chr6:169776349 | G | A | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1521-106G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776349 | |||||||
chr6:169776371 | A | G | 67 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(64): Show |
149 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.1521-84A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776371 | |||||||
chr6:169776376 | G | A | 1 | a0002c0002t0001g0140 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1521-79G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 15/17 | chr6 | 169776376 | |||||||
chr6:169776691 | T | C | 20 | a0003c0004t0001g0004 a0003c0004t0001g0008 a0003c0004t0001g0021 others(17): Show |
43 | HG00558.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1739+18T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169776691 | |||||||
chr6:169776751 | C | T | 74 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(71): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1739+78C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169776751 | |||||||
chr6:169776770 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(31): Show |
86 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.1739+97C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169776770 | |||||||
chr6:169776786 | C | T | 66 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(63): Show |
148 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.1739+113C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169776786 | |||||||
chr6:169776842 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1739+169G>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169776842 | |||||||
chr6:169776931 | A | T | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1739+258A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169776931 | |||||||
chr6:169776950 | T | G | 1 | a0001c0007t0001g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1739+277T>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169776950 | |||||||
chr6:169777108 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0065 |
5 | HG01069.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1739+435C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777108 | |||||||
chr6:169777140 | G | C | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1739+467G>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777140 | |||||||
chr6:169777150 | G | A | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1739+477G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777150 | |||||||
chr6:169777236 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1739+563G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777236 | |||||||
chr6:169777264 | C | T | 1 | a0003c0004t0001g0050 | 2 | HG00621.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1739+591C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777264 | |||||||
chr6:169777301 | A | T | 74 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(71): Show |
157 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.1739+628A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777301 | |||||||
chr6:169777423 | A | T | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1739+750A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777423 | |||||||
chr6:169777424 | T | A | 1 | a0003c0004t0001g0156 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1739+751T>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777424 | |||||||
chr6:169777512 | C | T | 76 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0001 others(73): Show |
159 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1739+839C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777512 | |||||||
chr6:169777572 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1739+899C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777572 | |||||||
chr6:169777769 | C | T | 74 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0001 others(71): Show |
156 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.1739+1096C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777769 | |||||||
chr6:169777846 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0070 others(4): Show |
14 | HG00639.hp2 HG01884.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1739+1173C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777846 | |||||||
chr6:169777849 | T | C | 1 | a0002c0003t0001g0133 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1739+1176T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777849 | |||||||
chr6:169777922 | T | C | 1 | a0005c0011t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1739+1249T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777922 | |||||||
chr6:169777930 | C | G | 68 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0001 others(65): Show |
150 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.1740-1252C>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169777930 | |||||||
chr6:169778028 | C | T | 2 | a0003c0012t0001g0167 a0003c0012t0001g0168 |
2 | HG01257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1740-1154C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778028 | |||||||
chr6:169778100 | A | G | 20 | a0002c0002t0001g0001 a0002c0002t0001g0026 a0002c0002t0001g0046 others(17): Show |
52 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1740-1082A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778100 | |||||||
chr6:169778233 | A | G | 1 | a0001c0009t0001g0124 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1740-949A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778233 | |||||||
chr6:169778318 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1740-864G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778318 | |||||||
chr6:169778357 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1740-825A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778357 | |||||||
chr6:169778395 | G | A | 5 | a0002c0003t0001g0010 a0002c0003t0001g0130 a0002c0003t0001g0131 others(2): Show |
12 | HG01074.hp1 HG02257.hp1 NA18947.hp1 others(9): Show |
intron_variant | MODIFIER | c.1740-787G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778395 | |||||||
chr6:169778557 | G | T | 4 | a0001c0005t0001g0074 a0001c0005t0001g0078 a0001c0005t0001g0079 others(1): Show |
4 | NA18954.hp2 NA18963.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1740-625G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778557 | |||||||
chr6:169778564 | G | GTATCTGT others(46): Show |
1 | a0003c0004t0001g0160 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1740-618_1740-617i others(55): Show |
ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778564 | |||||||
chr6:169778565 | G | T | 1 | a0003c0004t0001g0160 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1740-617G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778565 | |||||||
chr6:169778605 | C | T | 9 | a0002c0003t0001g0006 a0002c0003t0001g0013 a0002c0003t0001g0041 others(6): Show |
24 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1740-577C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778605 | |||||||
chr6:169778769 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1740-413G>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778769 | |||||||
chr6:169778913 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1740-269G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778913 | |||||||
chr6:169778932 | G | A | 8 | a0002c0006t0001g0051 a0002c0006t0001g0161 a0002c0006t0001g0162 others(5): Show |
9 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1740-250G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169778932 | |||||||
chr6:169779085 | A | G | 1 | a0001c0015t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1740-97A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 16/17 | chr6 | 169779085 | |||||||
chr6:169779334 | G | A | 10 | a0002c0002t0001g0151 a0002c0006t0001g0051 a0002c0006t0001g0161 others(7): Show |
11 | HG01099.hp1 HG02055.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1853+39G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169779334 | |||||||
chr6:169779411 | C | T | 76 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0001 others(73): Show |
159 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1853+116C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169779411 | |||||||
chr6:169779503 | G | GT | 38 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(35): Show |
69 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1853+216dupT | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 169779503 | ||||||
chr6:169779602 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(149): Show |
321 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(318): Show |
intron_variant | MODIFIER | c.1853+307T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169779602 | |||||||
chr6:169779756 | G | T | 1 | a0004c0008t0001g0110 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1853+461G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169779756 | |||||||
chr6:169780061 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1853+766G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780061 | |||||||
chr6:169780094 | T | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(148): Show |
320 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.1853+799T>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780094 | |||||||
chr6:169780117 | A | AG | 76 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0001 others(73): Show |
159 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1853+825dupG | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr6 | 169780117 | ||||||
chr6:169780210 | G | T | 16 | a0002c0003t0001g0006 a0002c0003t0001g0013 a0002c0003t0001g0025 others(13): Show |
34 | HG01070.hp2 HG01071.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1853+915G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780210 | |||||||
chr6:169780333 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(153): Show |
327 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(324): Show |
intron_variant | MODIFIER | c.1854-997T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780333 | |||||||
chr6:169780487 | A | G | 7 | a0001c0007t0001g0016 a0001c0007t0001g0056 a0002c0006t0001g0051 others(4): Show |
11 | HG01099.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1854-843A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780487 | |||||||
chr6:169780511 | G | A | 62 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0032 others(59): Show |
130 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1854-819G>A | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780511 | |||||||
chr6:169780533 | A | T | 93 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0018 others(90): Show |
191 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.1854-797A>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780533 | |||||||
chr6:169780575 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1854-755C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780575 | |||||||
chr6:169780593 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1854-737C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780593 | |||||||
chr6:169780619 | A | G | 81 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0058 others(78): Show |
169 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1854-711A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780619 | |||||||
chr6:169780620 | T | C | 81 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0058 others(78): Show |
169 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.1854-710T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780620 | |||||||
chr6:169780682 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1854-648T>C | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780682 | |||||||
chr6:169780707 | C | T | 1 | a0002c0003t0001g0111 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1854-623C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780707 | |||||||
chr6:169780858 | A | G | 1 | a0009c0021t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1854-472A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780858 | |||||||
chr6:169780903 | C | T | 3 | a0002c0006t0001g0051 a0002c0006t0001g0162 a0002c0006t0001g0164 |
4 | HG01099.hp1 HG02055.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1854-427C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780903 | |||||||
chr6:169780935 | A | G | 77 | a0001c0001t0001g0093 a0001c0001t0001g0104 a0001c0001t0001g0105 others(74): Show |
160 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.1854-395A>G | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169780935 | |||||||
chr6:169781054 | C | T | 1 | a0002c0006t0001g0161 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1854-276C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169781054 | |||||||
chr6:169781084 | C | T | 76 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0001 others(73): Show |
159 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.1854-246C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169781084 | |||||||
chr6:169781107 | G | T | 1 | a0001c0001t0001g0027 | 2 | NA18945.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1854-223G>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169781107 | |||||||
chr6:169781109 | C | T | 2 | a0008c0023t0001g0040 a0010c0016t0001g0040 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1854-221C>T | ERMARD | ENSG00000130023.16 | transcript | ENST00000366773.8 | protein_coding | 17/17 | chr6 | 169781109 |