Item | Value |
---|---|
geneid | 51676 |
ensemblid | ENSG00000100628.12 |
hgncid | 16012 |
symbol | ASB2 |
name | ankyrin repeat and SOCS box containing 2 |
refseq_nuc | NM_001202429.2 |
refseq_prot | NP_001189358.1 |
ensembl_nuc | ENST00000555019.6 |
ensembl_prot | ENSP00000451575.1 |
mane_status | MANE Select |
chr | chr14 |
start | 93934166 |
end | 93976570 |
strand | - |
ver | v1.2 |
region | chr14:93934166-93976570 |
region5000 | chr14:93929166-93981570 |
regionname0 | ASB2_chr14_93934166_93976570 |
regionname5000 | ASB2_chr14_93929166_93981570 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 635 | 351 | 89 | 54 | 152 | 15 | 40 | 119 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0002 | 0/0 | 635 | 5 | 0 | 4 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0003 | 0/0 | 635 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MAMQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0004 | 0/0 | 635 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0005 | 0/0 | 635 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0006 | 0/0 | 635 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0007 | 0/0 | 635 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MAMQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0008 | 0/0 | 635 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0009 | 0/0 | 635 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0010 | 0/0 | 635 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0011 | 0/0 | 635 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
a0012 | 0/0 | 635 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | MATQI others(630): Show |
chr14 | 93929166 | 93981570 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1905 | 213 | 32 | 31 | 113 | 10 | 27 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0002 | 0/0 | 1905 | 68 | 34 | 8 | 16 | 2 | 8 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0003 | 0/1 | 1905 | 59 | 16 | 12 | 22 | 3 | 5 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0005 | 0/0 | 1905 | 4 | 4 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0008 | 0/0 | 1905 | 2 | 0 | 1 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0013 | 0/0 | 1905 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0015 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0016 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0018 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0001c0020 | 0/0 | 1905 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0002c0004 | 0/0 | 1905 | 5 | 0 | 4 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0003c0010 | 0/0 | 1905 | 2 | 2 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0003c0011 | 0/0 | 1905 | 2 | 0 | 2 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0003c0022 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0004c0006 | 0/0 | 1905 | 2 | 0 | 1 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0005c0007 | 0/0 | 1905 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0006c0009 | 0/0 | 1905 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0007c0023 | 0/0 | 1905 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0008c0021 | 0/0 | 1905 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0009c0014 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0010c0012 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0011c0017 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 | ||
a0012c0019 | 0/0 | 1905 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | ATGGC others(1900): Show |
chr14 | 93929166 | 93981570 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2608 | 135 | 32 | 26 | 50 | 10 | 17 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0001t0002 | 0/0 | 2607 | 76 | 0 | 4 | 63 | 0 | 9 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0001t0005 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0001t0006 | 0/0 | 2607 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0002t0001 | 0/0 | 2608 | 10 | 10 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0002t0002 | 0/0 | 2607 | 55 | 21 | 8 | 16 | 2 | 8 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0002t0003 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0002t0004 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0003t0001 | 0/1 | 2608 | 57 | 16 | 12 | 20 | 3 | 5 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0003t0002 | 0/0 | 2607 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0005t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0005t0002 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0005t0003 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0005t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0008t0002 | 0/0 | 2607 | 2 | 0 | 1 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0001c0013t0001 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0015t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0016t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0018t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0001c0020t0001 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0002c0004t0001 | 0/0 | 2608 | 5 | 0 | 4 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0003c0010t0004 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0003c0011t0001 | 0/0 | 2608 | 2 | 0 | 2 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0003c0022t0003 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0004c0006t0003 | 0/0 | 2607 | 2 | 0 | 1 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0005c0007t0001 | 0/0 | 2608 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0006c0009t0003 | 0/0 | 2607 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0007c0023t0001 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0008c0021t0001 | 0/0 | 2608 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0009c0014t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
a0010c0012t0002 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0011c0017t0003 | 0/0 | 2607 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2602): Show |
chr14 | 93929166 | 93981570 |
a0012c0019t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | GAACT others(2603): Show |
chr14 | 93929166 | 93981570 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0001t0006g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0002t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0139 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0005t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0005t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0005t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0008t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0008t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0013t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0015t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0016t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0018t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0001c0020t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0002c0004t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0002c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0002c0004t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0002c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0003c0010t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0003c0010t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0003c0011t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0003c0011t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0003c0022t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0004c0006t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0004c0006t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0005c0007t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0006c0009t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0006c0009t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0007c0023t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0008c0021t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0009c0014t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0010c0012t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0011c0017t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
a0012c0019t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | GBR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | GBR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0331 | EUR | FIN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0260 | EUR | FIN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0202 | EUR | FIN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00438 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | CHS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00735 | hp1 | a0007 | c0023 | t0001 | g0349 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00738 | hp2 | a0002 | c0004 | t0001 | g0190 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG00741 | hp2 | a0003 | c0011 | t0001 | g0348 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0194 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0335 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0243 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0345 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01109 | hp2 | a0004 | c0006 | t0003 | g0056 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01167 | hp1 | a0001 | c0013 | t0001 | g0334 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0105 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0073 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01255 | hp2 | a0001 | c0008 | t0002 | g0156 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0183 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01257 | hp1 | a0003 | c0011 | t0001 | g0350 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0195 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0209 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01358 | hp1 | a0002 | c0004 | t0001 | g0058 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01361 | hp2 | a0002 | c0004 | t0001 | g0009 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0336 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01516 | hp2 | a0008 | c0021 | t0001 | g0208 | EUR | IBS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01517 | hp2 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01943 | hp2 | a0001 | c0020 | t0001 | g0131 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0303 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02071 | hp2 | a0001 | c0003 | t0001 | g0280 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02145 | hp2 | a0001 | c0005 | t0004 | g0293 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0216 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | CDX | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0102 | EAS | CDX | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | CDX | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0123 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02280 | hp1 | a0001 | c0016 | t0001 | g0032 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02293 | hp2 | a0001 | c0003 | t0001 | g0002 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0308 | AMR | PEL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0154 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0124 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0317 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0304 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02622 | hp1 | a0003 | c0010 | t0004 | g0351 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0287 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02647 | hp2 | a0003 | c0022 | t0003 | g0219 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0040 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0328 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0305 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02809 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02818 | hp1 | a0001 | c0015 | t0001 | g0315 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0301 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0213 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0300 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0288 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02965 | hp2 | a0001 | c0002 | t0004 | g0344 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02970 | hp2 | a0010 | c0012 | t0002 | g0155 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0346 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0125 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0224 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03209 | hp1 | a0011 | c0017 | t0003 | g0291 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0309 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03453 | hp2 | a0012 | c0019 | t0001 | g0034 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0233 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0319 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03491 | hp1 | a0001 | c0001 | t0006 | g0353 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0296 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0281 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0232 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0306 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0330 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0307 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0145 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0220 | SAS | BEB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0181 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0329 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0245 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0141 | AFR | YRI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0313 | AFR | YRI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18944 | hp2 | a0005 | c0007 | t0001 | g0010 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18947 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18951 | hp1 | a0005 | c0007 | t0001 | g0010 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18952 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18959 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18961 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0110 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18968 | hp2 | a0001 | c0003 | t0002 | g0098 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18977 | hp2 | a0006 | c0009 | t0003 | g0338 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18979 | hp1 | a0006 | c0009 | t0003 | g0337 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19009 | hp1 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | LWK | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19043 | hp1 | a0001 | c0005 | t0003 | g0297 | AFR | LWK | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0290 | AFR | LWK | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19056 | hp1 | a0001 | c0003 | t0001 | g0120 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19066 | hp1 | a0001 | c0008 | t0002 | g0116 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19067 | hp2 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19082 | hp2 | a0004 | c0006 | t0003 | g0186 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19088 | hp1 | a0001 | c0003 | t0002 | g0265 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0273 | AFR | YRI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | YRI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0289 | AFR | ASW | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0314 | AFR | ASW | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0341 | EUR | TSI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02109 | hp2 | a0001 | c0018 | t0001 | g0267 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02559 | hp1 | a0009 | c0014 | t0001 | g0049 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG02559 | hp2 | a0001 | c0005 | t0002 | g0037 | AFR | ACB | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG03471 | hp2 | a0003 | c0010 | t0004 | g0347 | AFR | MSL | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | USA | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | USA | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0139 | REF | REF | ASB2_chr14_93929166_93981570 | ASB2 | chr14 | 93929166 | 93981570 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:93934756 | C | T | 1 | a0004 | 2 | HG01109.hp2 NA19082.hp2 |
missense_variant | MODERATE | c.1808G>A | p.Arg603Gln | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 10/10 | 2018/2608 | 1808/1908 | 603/635 | chr14 | 93934756 | |||
chr14:93937716 | C | T | 2 | a0011 a0012 |
2 | HG03209.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1753G>A | p.Val585Ile | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/10 | 1963/2608 | 1753/1908 | 585/635 | chr14 | 93937716 | |||
chr14:93939473 | C | T | 1 | a0005 | 2 | NA18944.hp2 NA18951.hp1 |
missense_variant | MODERATE | c.1252G>A | p.Ala418Thr | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/10 | 1462/2608 | 1252/1908 | 418/635 | chr14 | 93939473 | |||
chr14:93939485 | C | G | 1 | a0006 | 2 | NA18977.hp2 NA18979.hp1 |
missense_variant | MODERATE | c.1240G>C | p.Ala414Pro | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/10 | 1450/2608 | 1240/1908 | 414/635 | chr14 | 93939485 | |||
chr14:93951101 | C | T | 1 | a0009 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.778G>A | p.Gly260Arg | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/10 | 988/2608 | 778/1908 | 260/635 | chr14 | 93951101 | |||
chr14:93951133 | T | C | 1 | a0011 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.746A>G | p.Asn249Ser | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/10 | 956/2608 | 746/1908 | 249/635 | chr14 | 93951133 | |||
chr14:93951185 | T | C | 2 | a0002 a0007 |
6 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(3): Show |
missense_variant | MODERATE | c.694A>G | p.Asn232Asp | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/10 | 904/2608 | 694/1908 | 232/635 | chr14 | 93951185 | |||
chr14:93953475 | G | T | 1 | a0010 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.511C>A | p.Gln171Lys | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/10 | 721/2608 | 511/1908 | 171/635 | chr14 | 93953475 | |||
chr14:93964365 | G | A | 1 | a0008 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.175C>T | p.Arg59Cys | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/10 | 385/2608 | 175/1908 | 59/635 | chr14 | 93964365 | |||
chr14:93964532 | G | A | 2 | a0003 a0007 |
6 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(3): Show |
missense_variant | MODERATE | c.8C>T | p.Thr3Met | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/10 | 218/2608 | 8/1908 | 3/635 | chr14 | 93964532 | |||
chr14:93976435 | T | C | 1 | a0001 | 1 | HG03491.hp1 | splice_region_variant | LOW | c.-75A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/10 | chr14 | 93976435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:93939195 | G | A | 1 | a0011c0017 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1530C>T | p.Tyr510Tyr | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/10 | 1740/2608 | 1530/1908 | 510/635 | chr14 | 93939195 | |||
chr14:93939260 | G | A | 1 | a0001c0016 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1465C>T | p.Leu489Leu | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/10 | 1675/2608 | 1465/1908 | 489/635 | chr14 | 93939260 | |||
chr14:93939525 | G | C | 18 | a0001c0001 a0001c0002 a0001c0005 others(15): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
synonymous_variant | LOW | c.1200C>G | p.Ala400Ala | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/10 | 1410/2608 | 1200/1908 | 400/635 | chr14 | 93939525 | |||
chr14:93947393 | G | A | 1 | a0001c0020 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.1008C>T | p.Asp336Asp | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/10 | 1218/2608 | 1008/1908 | 336/635 | chr14 | 93947393 | |||
chr14:93947417 | G | C | 1 | a0006c0009 | 2 | NA18977.hp2 NA18979.hp1 |
synonymous_variant | LOW | c.984C>G | p.Ala328Ala | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/10 | 1194/2608 | 984/1908 | 328/635 | chr14 | 93947417 | |||
chr14:93951075 | G | A | 10 | a0001c0001 a0001c0013 a0001c0018 others(7): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
synonymous_variant | LOW | c.804C>T | p.Asn268Asn | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/10 | 1014/2608 | 804/1908 | 268/635 | chr14 | 93951075 | |||
chr14:93951195 | A | G | 19 | a0001c0001 a0001c0002 a0001c0005 others(16): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
synonymous_variant | LOW | c.684T>C | p.Asn228Asn | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/10 | 894/2608 | 684/1908 | 228/635 | chr14 | 93951195 | |||
chr14:93951240 | G | A | 12 | a0001c0001 a0001c0005 a0001c0013 others(9): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
synonymous_variant | LOW | c.639C>T | p.Cys213Cys | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/10 | 849/2608 | 639/1908 | 213/635 | chr14 | 93951240 | |||
chr14:93953454 | A | G | 1 | a0001c0013 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.532T>C | p.Leu178Leu | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/10 | 742/2608 | 532/1908 | 178/635 | chr14 | 93953454 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:93934234 | C | A | 3 | a0001c0002t0004 a0001c0005t0004 a0003c0010t0004 |
5 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*422G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 10/10 | 422 | chr14 | 93934234 | ||||||
chr14:93934494 | TG | T | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0002t0002 others(10): Show |
146 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*161delC | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 10/10 | 161 | chr14 | 93934494 | ||||||
chr14:93934560 | G | A | 7 | a0001c0001t0002 a0001c0001t0006 a0001c0002t0002 others(4): Show |
138 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 10/10 | 96 | chr14 | 93934560 | ||||||
chr14:93934581 | G | A | 1 | a0001c0001t0005 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*75C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 10/10 | 75 | chr14 | 93934581 | ||||||
chr14:93976457 | A | G | 1 | a0001c0001t0005 | 1 | HG01070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-97T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/10 | 11918 | chr14 | 93976457 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:93934942 | A | G | 1 | a0001c0001t0002g0092 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1772-150T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93934942 | |||||||
chr14:93935010 | C | T | 128 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(125): Show |
138 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.1772-218G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935010 | |||||||
chr14:93935042 | G | A | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1772-250C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935042 | |||||||
chr14:93935050 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1772-258G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935050 | |||||||
chr14:93935240 | G | T | 1 | a0001c0002t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1772-448C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935240 | |||||||
chr14:93935288 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(293): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1772-496A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935288 | |||||||
chr14:93935423 | G | GTCAT | 201 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0021 others(198): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.1772-635_1772-632d others(6): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935423 | |||||||
chr14:93935423 | G | GTCATTCA others(1): Show |
71 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0020 others(68): Show |
73 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1772-639_1772-632d others(10): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935423 | |||||||
chr14:93935423 | G | GTCATTCA others(5): Show |
3 | a0001c0001t0001g0065 a0001c0001t0001g0236 a0001c0001t0005g0019 |
3 | HG01070.hp2 NA19030.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1772-643_1772-632d others(14): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935423 | |||||||
chr14:93935423 | GTCAT | G | 4 | a0001c0002t0004g0301 a0001c0005t0004g0293 a0003c0010t0004g0347 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1772-635_1772-632d others(6): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935423 | |||||||
chr14:93935601 | C | T | 6 | a0001c0002t0004g0301 a0001c0005t0003g0297 a0001c0005t0004g0293 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1772-809G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935601 | |||||||
chr14:93935646 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1772-854G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935646 | |||||||
chr14:93935778 | A | ACTGCCCT others(5): Show |
147 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(144): Show |
158 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1772-998_1772-987d others(14): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935778 | |||||||
chr14:93935861 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1772-1069A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935861 | |||||||
chr14:93935947 | C | T | 140 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(137): Show |
151 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.1772-1155G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935947 | |||||||
chr14:93935976 | T | C | 7 | a0001c0003t0001g0008 a0001c0003t0001g0105 a0001c0003t0001g0109 others(4): Show |
8 | HG00280.hp2 HG01192.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1772-1184A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93935976 | |||||||
chr14:93936041 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1772-1249T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93936041 | |||||||
chr14:93936535 | T | C | 6 | a0001c0002t0004g0301 a0001c0005t0004g0293 a0003c0010t0004g0347 others(3): Show |
6 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1771+1163A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93936535 | |||||||
chr14:93936590 | T | A | 132 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(129): Show |
142 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.1771+1108A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93936590 | |||||||
chr14:93936616 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1771+1082G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93936616 | |||||||
chr14:93936881 | C | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0144 a0001c0001t0001g0180 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1771+817G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93936881 | |||||||
chr14:93937049 | G | A | 5 | a0001c0001t0002g0012 a0001c0001t0002g0126 a0001c0001t0002g0171 others(2): Show |
6 | HG00558.hp1 NA18943.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1771+649C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937049 | |||||||
chr14:93937142 | G | C | 20 | a0001c0001t0001g0086 a0001c0001t0001g0095 a0001c0001t0001g0100 others(17): Show |
20 | HG00544.hp1 HG00597.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1771+556C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937142 | |||||||
chr14:93937182 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0316 |
2 | HG02258.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1771+516G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937182 | |||||||
chr14:93937236 | C | T | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1771+462G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937236 | |||||||
chr14:93937240 | C | T | 1 | a0001c0001t0002g0283 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1771+458G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937240 | |||||||
chr14:93937256 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1771+442C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937256 | |||||||
chr14:93937453 | C | T | 3 | a0001c0002t0002g0016 a0001c0002t0002g0313 a0001c0002t0002g0345 |
4 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1771+245G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937453 | |||||||
chr14:93937475 | A | G | 1 | a0011c0017t0003g0291 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1771+223T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937475 | |||||||
chr14:93937627 | C | T | 130 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(127): Show |
140 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1771+71G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937627 | |||||||
chr14:93937644 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1771+54G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 9/9 | chr14 | 93937644 | |||||||
chr14:93937871 | G | C | 134 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(131): Show |
144 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.1618-20C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93937871 | |||||||
chr14:93937901 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1618-50C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93937901 | |||||||
chr14:93938185 | C | T | 144 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(141): Show |
155 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.1618-334G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938185 | |||||||
chr14:93938233 | C | CT | 11 | a0001c0001t0001g0295 a0001c0001t0002g0083 a0001c0001t0002g0088 others(8): Show |
11 | HG01255.hp1 HG03098.hp2 NA18967.hp2 others(8): Show |
intron_variant | MODIFIER | c.1618-383dupA | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | C | CTTTTT | 8 | a0001c0001t0002g0024 a0001c0001t0002g0140 a0001c0001t0002g0178 others(5): Show |
8 | HG02451.hp2 HG02572.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.1618-387_1618-383d others(7): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | C | CTTTTTT | 60 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(57): Show |
67 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.1618-388_1618-383d others(8): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | C | CTTTTTTT | 35 | a0001c0001t0002g0012 a0001c0001t0002g0080 a0001c0001t0002g0082 others(32): Show |
37 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1618-389_1618-383d others(9): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | C | CTTTTTTT others(1): Show |
13 | a0001c0001t0002g0079 a0001c0001t0002g0108 a0001c0001t0002g0149 others(10): Show |
14 | HG01123.hp2 HG02486.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1618-390_1618-383d others(10): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0002g0249 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1618-393_1618-383d others(13): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0228 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1618-394_1618-383d others(14): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | CT | C | 134 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0018 others(131): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.1618-383delA | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938233 | CTT | C | 8 | a0001c0001t0001g0263 a0001c0001t0005g0019 a0001c0002t0001g0123 others(5): Show |
8 | HG01070.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1618-384_1618-383d others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938233 | |||||||
chr14:93938281 | C | T | 2 | a0001c0002t0001g0123 a0001c0002t0001g0132 |
2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1618-430G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938281 | |||||||
chr14:93938370 | C | G | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1618-519G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938370 | |||||||
chr14:93938494 | C | T | 136 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(133): Show |
147 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.1617+614G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938494 | |||||||
chr14:93938706 | T | TAGTTTGG others(1): Show |
12 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(9): Show |
13 | HG02145.hp2 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1617+394_1617+401d others(10): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938706 | |||||||
chr14:93938790 | T | G | 1 | a0001c0002t0002g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1617+318A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938790 | |||||||
chr14:93938809 | G | A | 1 | a0001c0001t0002g0271 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1617+299C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938809 | |||||||
chr14:93938944 | C | T | 1 | a0001c0002t0002g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1617+164G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93938944 | |||||||
chr14:93939025 | G | C | 1 | a0011c0017t0003g0291 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1617+83C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 8/9 | chr14 | 93939025 | |||||||
chr14:93939740 | C | G | 2 | a0001c0002t0003g0031 a0011c0017t0003g0291 |
2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1053-68G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93939740 | |||||||
chr14:93939750 | A | C | 293 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(290): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1053-78T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93939750 | |||||||
chr14:93939868 | G | GTC | 12 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(9): Show |
13 | HG02145.hp2 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1053-198_1053-197d others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93939868 | |||||||
chr14:93940008 | C | G | 1 | a0001c0003t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1053-336G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940008 | |||||||
chr14:93940025 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1053-353A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940025 | |||||||
chr14:93940060 | C | T | 2 | a0001c0002t0001g0217 a0009c0014t0001g0049 |
2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1053-388G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940060 | |||||||
chr14:93940168 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1053-496C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940168 | |||||||
chr14:93940207 | G | A | 1 | a0001c0001t0001g0321 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1053-535C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940207 | |||||||
chr14:93940226 | C | T | 1 | a0001c0002t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1053-554G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940226 | |||||||
chr14:93940307 | A | G | 130 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(127): Show |
140 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1053-635T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940307 | |||||||
chr14:93940381 | A | G | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1053-709T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940381 | |||||||
chr14:93940383 | T | G | 1 | a0003c0011t0001g0348 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1053-711A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940383 | |||||||
chr14:93940575 | C | A | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1053-903G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940575 | |||||||
chr14:93940615 | C | A | 3 | a0001c0001t0002g0207 a0001c0001t0002g0230 a0001c0001t0002g0261 |
3 | HG00438.hp2 HG00558.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1053-943G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940615 | |||||||
chr14:93940808 | G | A | 4 | a0001c0002t0004g0301 a0001c0005t0004g0293 a0003c0010t0004g0347 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053-1136C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940808 | |||||||
chr14:93940865 | T | C | 143 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(140): Show |
154 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.1053-1193A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940865 | |||||||
chr14:93940867 | C | T | 1 | a0011c0017t0003g0291 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1053-1195G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93940867 | |||||||
chr14:93941164 | G | C | 129 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(126): Show |
139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.1053-1492C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941164 | |||||||
chr14:93941533 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
13 | HG01081.hp1 HG02886.hp1 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.1053-1861G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941533 | |||||||
chr14:93941576 | G | C | 2 | a0001c0002t0002g0122 a0001c0002t0002g0346 |
2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1053-1904C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941576 | |||||||
chr14:93941647 | A | T | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1053-1975T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941647 | |||||||
chr14:93941648 | A | T | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1053-1976T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941648 | |||||||
chr14:93941653 | C | T | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1053-1981G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941653 | |||||||
chr14:93941654 | T | G | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1053-1982A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941654 | |||||||
chr14:93941681 | C | T | 2 | a0001c0001t0001g0205 a0001c0005t0001g0040 |
2 | HG02717.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.1053-2009G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941681 | |||||||
chr14:93941696 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1053-2024T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941696 | |||||||
chr14:93941757 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0198 |
2 | HG01106.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1053-2085C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941757 | |||||||
chr14:93941762 | C | T | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1053-2090G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941762 | |||||||
chr14:93941767 | G | A | 4 | a0001c0002t0004g0301 a0001c0005t0004g0293 a0003c0010t0004g0347 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053-2095C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941767 | |||||||
chr14:93941847 | C | T | 125 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(122): Show |
135 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.1053-2175G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93941847 | |||||||
chr14:93942244 | A | G | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1053-2572T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942244 | |||||||
chr14:93942315 | C | A | 1 | a0001c0003t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1053-2643G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942315 | |||||||
chr14:93942383 | G | A | 1 | a0011c0017t0003g0291 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1053-2711C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942383 | |||||||
chr14:93942574 | G | A | 138 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(135): Show |
148 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.1053-2902C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942574 | |||||||
chr14:93942644 | G | T | 1 | a0001c0016t0001g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1053-2972C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942644 | |||||||
chr14:93942673 | A | G | 1 | a0001c0005t0002g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1053-3001T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942673 | |||||||
chr14:93942680 | C | G | 71 | a0001c0001t0001g0246 a0001c0001t0002g0001 a0001c0001t0002g0006 others(68): Show |
77 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1053-3008G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942680 | |||||||
chr14:93942713 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1053-3041C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942713 | |||||||
chr14:93942743 | A | G | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1053-3071T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942743 | |||||||
chr14:93942773 | A | C | 6 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053-3101T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942773 | |||||||
chr14:93942849 | GTGA | G | 139 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(136): Show |
150 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(147): Show |
intron_variant | MODIFIER | c.1053-3180_1053-317 others(7): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942849 | |||||||
chr14:93942870 | A | G | 3 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1053-3198T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942870 | |||||||
chr14:93942957 | T | C | 4 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(1): Show |
5 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1053-3285A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93942957 | |||||||
chr14:93943094 | G | A | 4 | a0001c0002t0004g0301 a0001c0005t0004g0293 a0003c0010t0004g0347 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1053-3422C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943094 | |||||||
chr14:93943094 | G | C | 1 | a0001c0001t0001g0282 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1053-3422C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943094 | |||||||
chr14:93943211 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1053-3539A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943211 | |||||||
chr14:93943215 | C | G | 1 | a0001c0001t0002g0107 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1053-3543G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943215 | |||||||
chr14:93943323 | C | G | 292 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(289): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1053-3651G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943323 | |||||||
chr14:93943343 | C | A | 69 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(66): Show |
75 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1053-3671G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943343 | |||||||
chr14:93943394 | G | C | 294 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(291): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1053-3722C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943394 | |||||||
chr14:93943426 | G | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(289): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1053-3754C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943426 | |||||||
chr14:93943496 | T | C | 2 | a0001c0001t0002g0226 a0001c0001t0002g0235 |
2 | NA18960.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1053-3824A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943496 | |||||||
chr14:93943634 | G | A | 1 | a0003c0011t0001g0348 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1052+3715C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943634 | |||||||
chr14:93943868 | C | T | 1 | a0001c0005t0004g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1052+3481G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943868 | |||||||
chr14:93943929 | CA | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0007 others(119): Show |
132 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1052+3419delT | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93943929 | |||||||
chr14:93944101 | T | C | 294 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(291): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1052+3248A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944101 | |||||||
chr14:93944116 | C | T | 6 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(3): Show |
7 | HG02258.hp2 HG02723.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052+3233G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944116 | |||||||
chr14:93944118 | G | T | 3 | a0001c0001t0002g0148 a0001c0001t0002g0255 a0001c0001t0002g0271 |
3 | NA18960.hp1 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1052+3231C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944118 | |||||||
chr14:93944276 | T | A | 129 | a0001c0001t0001g0246 a0001c0001t0002g0001 a0001c0001t0002g0006 others(126): Show |
139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.1052+3073A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944276 | |||||||
chr14:93944330 | C | G | 1 | a0001c0001t0001g0299 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1052+3019G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944330 | |||||||
chr14:93944443 | C | G | 3 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 |
4 | HG02895.hp1 HG02896.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1052+2906G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944443 | |||||||
chr14:93944479 | G | A | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1052+2870C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944479 | |||||||
chr14:93944545 | C | T | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1052+2804G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944545 | |||||||
chr14:93944667 | A | T | 1 | a0001c0001t0002g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1052+2682T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944667 | |||||||
chr14:93944668 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1052+2681C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944668 | |||||||
chr14:93944669 | C | G | 1 | a0001c0001t0002g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1052+2680G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944669 | |||||||
chr14:93944689 | C | G | 1 | a0001c0001t0001g0302 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1052+2660G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944689 | |||||||
chr14:93944833 | C | T | 1 | a0003c0011t0001g0350 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1052+2516G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944833 | |||||||
chr14:93944871 | G | T | 1 | a0001c0001t0002g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1052+2478C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944871 | |||||||
chr14:93944872 | C | G | 1 | a0001c0001t0002g0254 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1052+2477G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93944872 | |||||||
chr14:93945038 | C | G | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1052+2311G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945038 | |||||||
chr14:93945224 | C | T | 5 | a0001c0002t0004g0301 a0003c0010t0004g0347 a0003c0010t0004g0351 others(2): Show |
5 | HG01109.hp2 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1052+2125G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945224 | |||||||
chr14:93945229 | T | C | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1052+2120A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945229 | |||||||
chr14:93945344 | C | T | 3 | a0001c0002t0004g0301 a0003c0010t0004g0347 a0003c0010t0004g0351 |
3 | HG02622.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1052+2005G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945344 | |||||||
chr14:93945397 | C | A | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1052+1952G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945397 | |||||||
chr14:93945425 | A | G | 5 | a0001c0001t0001g0018 a0001c0001t0001g0068 a0001c0001t0001g0325 others(2): Show |
6 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052+1924T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945425 | |||||||
chr14:93945456 | C | T | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1052+1893G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945456 | |||||||
chr14:93945489 | C | T | 3 | a0001c0002t0002g0113 a0001c0002t0002g0135 a0001c0002t0002g0158 |
3 | HG02080.hp1 HG02155.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.1052+1860G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945489 | |||||||
chr14:93945490 | G | A | 8 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 others(5): Show |
8 | HG01109.hp2 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1052+1859C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945490 | |||||||
chr14:93945525 | A | G | 33 | a0001c0002t0002g0015 a0001c0002t0002g0026 a0001c0002t0002g0028 others(30): Show |
34 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1052+1824T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945525 | |||||||
chr14:93945536 | G | A | 1 | a0001c0002t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052+1813C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945536 | |||||||
chr14:93945619 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0275 |
2 | HG02129.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1052+1730G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945619 | |||||||
chr14:93945632 | C | G | 6 | a0001c0002t0002g0005 a0001c0002t0002g0191 a0001c0002t0002g0209 others(3): Show |
7 | HG01168.hp1 HG01261.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1052+1717G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945632 | |||||||
chr14:93945820 | T | C | 1 | a0001c0002t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1052+1529A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945820 | |||||||
chr14:93945853 | C | T | 3 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1052+1496G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945853 | |||||||
chr14:93945896 | G | C | 1 | a0001c0002t0002g0015 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1052+1453C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945896 | |||||||
chr14:93945968 | G | A | 6 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1052+1381C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945968 | |||||||
chr14:93945980 | G | A | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1052+1369C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93945980 | |||||||
chr14:93946044 | T | C | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1052+1305A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946044 | |||||||
chr14:93946268 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1052+1081C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946268 | |||||||
chr14:93946423 | T | C | 1 | a0002c0004t0001g0009 | 2 | HG00438.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1052+926A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946423 | |||||||
chr14:93946427 | T | C | 128 | a0001c0001t0001g0011 a0001c0001t0001g0246 a0001c0001t0001g0352 others(125): Show |
139 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.1052+922A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946427 | |||||||
chr14:93946566 | G | A | 1 | a0001c0016t0001g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1052+783C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946566 | |||||||
chr14:93946618 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
13 | HG01081.hp1 HG02886.hp1 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.1052+731G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946618 | |||||||
chr14:93946621 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1052+728G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946621 | |||||||
chr14:93946765 | T | A | 142 | a0001c0001t0001g0011 a0001c0001t0001g0246 a0001c0001t0001g0352 others(139): Show |
154 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.1052+584A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946765 | |||||||
chr14:93946916 | C | G | 1 | a0001c0005t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1052+433G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946916 | |||||||
chr14:93946971 | A | G | 1 | a0001c0002t0002g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1052+378T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946971 | |||||||
chr14:93946973 | G | A | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1052+376C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93946973 | |||||||
chr14:93947112 | T | C | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1052+237A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93947112 | |||||||
chr14:93947121 | G | T | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1052+228C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93947121 | |||||||
chr14:93947171 | T | C | 130 | a0001c0001t0001g0011 a0001c0001t0001g0246 a0001c0001t0001g0352 others(127): Show |
141 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1052+178A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 7/9 | chr14 | 93947171 | |||||||
chr14:93947617 | C | T | 1 | a0001c0002t0002g0220 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.881-97G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947617 | |||||||
chr14:93947642 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.881-122G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947642 | |||||||
chr14:93947652 | G | A | 1 | a0001c0002t0002g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.881-132C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947652 | |||||||
chr14:93947697 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.881-177T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947697 | |||||||
chr14:93947710 | G | A | 1 | a0003c0011t0001g0350 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.881-190C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947710 | |||||||
chr14:93947752 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.881-232C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947752 | |||||||
chr14:93947769 | G | A | 1 | a0001c0002t0002g0340 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.881-249C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947769 | |||||||
chr14:93947770 | G | T | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.881-250C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947770 | |||||||
chr14:93947886 | C | T | 63 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0065 others(60): Show |
64 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.881-366G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947886 | |||||||
chr14:93947977 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.881-457T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947977 | |||||||
chr14:93947991 | C | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(287): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.881-471G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947991 | |||||||
chr14:93947995 | G | GA | 7 | a0001c0002t0002g0141 a0001c0002t0002g0151 a0001c0002t0002g0154 others(4): Show |
7 | HG02451.hp2 HG02602.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.881-476dupT | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947995 | |||||||
chr14:93947995 | G | GAA | 61 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0001g0217 others(58): Show |
65 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.881-477_881-476dup others(2): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947995 | |||||||
chr14:93947995 | G | GAAA | 7 | a0001c0001t0001g0022 a0001c0001t0002g0160 a0001c0002t0002g0124 others(4): Show |
7 | HG02572.hp1 HG02818.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.881-478_881-476dup others(3): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947995 | |||||||
chr14:93947995 | G | GAAAA | 17 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0033 others(14): Show |
18 | HG00558.hp1 HG01081.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.881-479_881-476dup others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947995 | |||||||
chr14:93947995 | G | GAAAAA | 166 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0020 others(163): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.881-480_881-476dup others(5): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947995 | |||||||
chr14:93947995 | G | GAAAAAA | 35 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0070 others(32): Show |
37 | HG00438.hp1 HG00673.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.881-481_881-476dup others(6): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947995 | |||||||
chr14:93947995 | GAAAAAAA others(3): Show |
G | 1 | a0004c0006t0003g0056 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.881-485_881-476del others(10): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93947995 | |||||||
chr14:93948044 | A | G | 3 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881-524T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948044 | |||||||
chr14:93948106 | G | A | 62 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0001g0217 others(59): Show |
66 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.881-586C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948106 | |||||||
chr14:93948118 | G | T | 3 | a0001c0002t0004g0301 a0001c0016t0001g0032 a0003c0010t0004g0347 |
3 | HG02280.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.881-598C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948118 | |||||||
chr14:93948119 | T | C | 1 | a0001c0018t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.881-599A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948119 | |||||||
chr14:93948216 | C | A | 5 | a0001c0002t0002g0017 a0001c0002t0002g0300 a0001c0002t0002g0309 others(2): Show |
6 | HG01123.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.881-696G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948216 | |||||||
chr14:93948511 | C | T | 74 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(71): Show |
79 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.881-991G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948511 | |||||||
chr14:93948637 | CCAAGAAA others(89): Show |
C | 3 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881-1213_881-1118d others(98): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948637 | |||||||
chr14:93948671 | A | T | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.881-1151T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948671 | |||||||
chr14:93948734 | A | T | 3 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881-1214T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948734 | |||||||
chr14:93948935 | G | C | 2 | a0001c0002t0002g0146 a0001c0002t0002g0162 |
2 | NA19087.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.881-1415C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93948935 | |||||||
chr14:93949035 | T | C | 3 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881-1515A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949035 | |||||||
chr14:93949061 | G | C | 1 | a0001c0001t0002g0093 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.881-1541C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949061 | |||||||
chr14:93949158 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(293): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.881-1638A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949158 | |||||||
chr14:93949225 | C | T | 1 | a0011c0017t0003g0291 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.881-1705G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949225 | |||||||
chr14:93949226 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(293): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.881-1706A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949226 | |||||||
chr14:93949266 | G | A | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.880+1733C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949266 | |||||||
chr14:93949285 | C | T | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.880+1714G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949285 | |||||||
chr14:93949309 | C | T | 1 | a0001c0002t0002g0232 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.880+1690G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949309 | |||||||
chr14:93949485 | T | C | 1 | a0001c0016t0001g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.880+1514A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949485 | |||||||
chr14:93949511 | G | A | 1 | a0001c0002t0004g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.880+1488C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949511 | |||||||
chr14:93949691 | G | A | 63 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0001g0137 others(60): Show |
67 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.880+1308C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949691 | |||||||
chr14:93949767 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.880+1232C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949767 | |||||||
chr14:93949854 | C | G | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.880+1145G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949854 | |||||||
chr14:93949862 | A | G | 1 | a0001c0002t0002g0124 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.880+1137T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949862 | |||||||
chr14:93949913 | C | G | 6 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(3): Show |
7 | HG02280.hp1 HG02818.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.880+1086G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949913 | |||||||
chr14:93949978 | C | T | 3 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0001g0285 |
3 | HG02258.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.880+1021G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93949978 | |||||||
chr14:93950128 | C | A | 56 | a0001c0002t0001g0137 a0001c0002t0001g0217 a0001c0002t0001g0233 others(53): Show |
60 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.880+871G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950128 | |||||||
chr14:93950216 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.880+783C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950216 | |||||||
chr14:93950407 | T | G | 5 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(2): Show |
6 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.880+592A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950407 | |||||||
chr14:93950420 | C | T | 62 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0001g0137 others(59): Show |
66 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.880+579G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950420 | |||||||
chr14:93950537 | G | A | 62 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0001g0137 others(59): Show |
66 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.880+462C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950537 | |||||||
chr14:93950560 | G | A | 61 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0001g0137 others(58): Show |
65 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.880+439C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950560 | |||||||
chr14:93950602 | C | T | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.880+397G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950602 | |||||||
chr14:93950701 | T | C | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.880+298A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950701 | |||||||
chr14:93950718 | A | G | 222 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(219): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.880+281T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950718 | |||||||
chr14:93950755 | G | A | 3 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.880+244C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950755 | |||||||
chr14:93950812 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.880+187C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950812 | |||||||
chr14:93950973 | T | C | 2 | a0004c0006t0003g0056 a0004c0006t0003g0186 |
2 | HG01109.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.880+26A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 6/9 | chr14 | 93950973 | |||||||
chr14:93951265 | G | A | 1 | a0001c0002t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.635-21C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951265 | |||||||
chr14:93951329 | A | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(214): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.635-85T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951329 | |||||||
chr14:93951379 | C | T | 59 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(56): Show |
64 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.635-135G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951379 | |||||||
chr14:93951456 | C | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(219): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.635-212G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951456 | |||||||
chr14:93951480 | C | G | 2 | a0001c0005t0003g0297 a0003c0022t0003g0219 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.635-236G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951480 | |||||||
chr14:93951672 | C | G | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.635-428G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951672 | |||||||
chr14:93951679 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0310 others(2): Show |
5 | HG01109.hp1 HG01884.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-435G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951679 | |||||||
chr14:93951682 | G | T | 1 | a0001c0001t0002g0006 | 2 | NA18747.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.635-438C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951682 | |||||||
chr14:93951729 | T | C | 1 | a0001c0002t0004g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.635-485A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951729 | |||||||
chr14:93951758 | G | A | 22 | a0001c0002t0002g0047 a0001c0002t0002g0141 a0001c0002t0002g0154 others(19): Show |
22 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.635-514C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951758 | |||||||
chr14:93951781 | G | A | 94 | a0001c0002t0001g0004 a0001c0002t0001g0025 a0001c0002t0001g0027 others(91): Show |
99 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.635-537C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951781 | |||||||
chr14:93951800 | G | A | 26 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0038 others(23): Show |
27 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.635-556C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951800 | |||||||
chr14:93951909 | C | T | 4 | a0001c0005t0001g0040 a0001c0005t0004g0293 a0006c0009t0003g0337 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-665G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951909 | |||||||
chr14:93951928 | C | T | 2 | a0001c0005t0003g0297 a0003c0022t0003g0219 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.635-684G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93951928 | |||||||
chr14:93952065 | A | G | 2 | a0001c0005t0001g0040 a0001c0005t0004g0293 |
2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.635-821T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952065 | |||||||
chr14:93952113 | G | C | 91 | a0001c0001t0001g0299 a0001c0002t0001g0004 a0001c0002t0001g0025 others(88): Show |
96 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(93): Show |
intron_variant | MODIFIER | c.635-869C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952113 | |||||||
chr14:93952225 | T | C | 1 | a0001c0001t0002g0239 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.635-981A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952225 | |||||||
chr14:93952343 | A | G | 2 | a0001c0005t0003g0297 a0003c0022t0003g0219 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.634+1009T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952343 | |||||||
chr14:93952358 | C | T | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.634+994G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952358 | |||||||
chr14:93952402 | G | A | 1 | a0001c0003t0001g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.634+950C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952402 | |||||||
chr14:93952410 | C | T | 95 | a0001c0001t0001g0299 a0001c0002t0001g0004 a0001c0002t0001g0025 others(92): Show |
100 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.634+942G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952410 | |||||||
chr14:93952411 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.634+941C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952411 | |||||||
chr14:93952613 | C | T | 1 | a0001c0016t0001g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.634+739G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952613 | |||||||
chr14:93952755 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.634+597T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952755 | |||||||
chr14:93952765 | G | A | 9 | a0001c0005t0001g0040 a0001c0005t0003g0297 a0001c0005t0004g0293 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.634+587C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952765 | |||||||
chr14:93952902 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.634+450T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952902 | |||||||
chr14:93952914 | C | A | 4 | a0001c0005t0001g0040 a0001c0005t0004g0293 a0006c0009t0003g0337 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+438G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952914 | |||||||
chr14:93952964 | G | A | 2 | a0001c0002t0002g0141 a0001c0002t0002g0154 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.634+388C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93952964 | |||||||
chr14:93953253 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.634+99G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93953253 | |||||||
chr14:93953302 | A | G | 1 | a0001c0002t0002g0151 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.634+50T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93953302 | |||||||
chr14:93953317 | C | T | 1 | a0001c0002t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.634+35G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93953317 | |||||||
chr14:93953319 | G | T | 90 | a0001c0001t0001g0299 a0001c0002t0001g0004 a0001c0002t0001g0025 others(87): Show |
95 | HG00609.hp1 HG00673.hp2 HG00735.hp2 others(92): Show |
intron_variant | MODIFIER | c.634+33C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93953319 | |||||||
chr14:93953335 | C | T | 1 | a0001c0002t0003g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.634+17G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 5/9 | chr14 | 93953335 | |||||||
chr14:93953525 | G | A | 2 | a0001c0002t0002g0051 a0001c0002t0002g0220 |
2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.479-18C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953525 | |||||||
chr14:93953542 | A | G | 343 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(340): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.479-35T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953542 | |||||||
chr14:93953563 | A | G | 4 | a0001c0002t0001g0123 a0001c0002t0001g0132 a0001c0002t0002g0141 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-56T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953563 | |||||||
chr14:93953577 | G | A | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.479-70C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953577 | |||||||
chr14:93953682 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.479-175C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953682 | |||||||
chr14:93953687 | C | T | 1 | a0004c0006t0003g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.479-180G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953687 | |||||||
chr14:93953735 | C | T | 1 | a0005c0007t0001g0010 | 2 | NA18944.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.479-228G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953735 | |||||||
chr14:93953764 | T | C | 316 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(313): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.479-257A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953764 | |||||||
chr14:93953782 | CCATTGCT others(1): Show |
C | 20 | a0001c0002t0002g0047 a0001c0002t0003g0031 a0001c0003t0001g0046 others(17): Show |
20 | HG01255.hp2 HG01884.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.479-283_479-276del others(8): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953782 | |||||||
chr14:93953835 | C | T | 1 | a0001c0002t0002g0234 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.479-328G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93953835 | |||||||
chr14:93954005 | T | C | 3 | a0001c0005t0003g0297 a0003c0010t0004g0347 a0003c0022t0003g0219 |
3 | HG02647.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.478+312A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93954005 | |||||||
chr14:93954103 | T | A | 1 | a0001c0001t0001g0253 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.478+214A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93954103 | |||||||
chr14:93954164 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.478+153G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93954164 | |||||||
chr14:93954225 | G | A | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.478+92C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 4/9 | chr14 | 93954225 | |||||||
chr14:93954650 | T | C | 99 | a0001c0001t0001g0144 a0001c0001t0001g0180 a0001c0001t0001g0278 others(96): Show |
104 | HG00280.hp1 HG00609.hp1 HG00735.hp2 others(101): Show |
intron_variant | MODIFIER | c.312-167A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93954650 | |||||||
chr14:93954681 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.312-198G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93954681 | |||||||
chr14:93954701 | C | G | 1 | a0001c0001t0001g0331 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.312-218G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93954701 | |||||||
chr14:93954764 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.312-281T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93954764 | |||||||
chr14:93954928 | C | T | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.312-445G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93954928 | |||||||
chr14:93954933 | G | GA | 5 | a0001c0001t0001g0018 a0001c0001t0001g0318 a0001c0001t0001g0325 others(2): Show |
6 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-451dupT | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93954933 | |||||||
chr14:93955142 | C | T | 35 | a0001c0001t0001g0200 a0001c0001t0001g0278 a0001c0001t0001g0331 others(32): Show |
40 | HG00280.hp1 HG01070.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.312-659G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955142 | |||||||
chr14:93955144 | A | G | 1 | a0001c0002t0002g0096 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.312-661T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955144 | |||||||
chr14:93955184 | T | C | 1 | a0001c0003t0002g0265 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.312-701A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955184 | |||||||
chr14:93955214 | G | A | 1 | a0001c0002t0002g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.312-731C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955214 | |||||||
chr14:93955259 | T | A | 4 | a0001c0002t0002g0141 a0001c0002t0002g0154 a0001c0005t0001g0040 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-776A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955259 | |||||||
chr14:93955321 | C | T | 65 | a0001c0001t0001g0159 a0001c0001t0001g0236 a0001c0001t0001g0279 others(62): Show |
71 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.312-838G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955321 | |||||||
chr14:93955367 | G | A | 20 | a0001c0002t0002g0047 a0001c0003t0001g0046 a0001c0003t0001g0048 others(17): Show |
20 | HG01255.hp2 HG01884.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.312-884C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955367 | |||||||
chr14:93955386 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.312-903G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955386 | |||||||
chr14:93955412 | C | T | 3 | a0001c0001t0001g0253 a0001c0002t0002g0141 a0001c0002t0002g0154 |
3 | HG00673.hp1 HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.312-929G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955412 | |||||||
chr14:93955610 | C | T | 1 | a0001c0003t0001g0181 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.312-1127G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955610 | |||||||
chr14:93955621 | C | T | 1 | a0001c0002t0002g0340 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.312-1138G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955621 | |||||||
chr14:93955630 | C | T | 7 | a0001c0001t0002g0081 a0001c0001t0002g0092 a0001c0001t0002g0093 others(4): Show |
7 | NA18955.hp1 NA18964.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.311+1136G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955630 | |||||||
chr14:93955836 | G | A | 1 | a0001c0001t0002g0076 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.311+930C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955836 | |||||||
chr14:93955846 | C | T | 88 | a0001c0001t0001g0020 a0001c0001t0001g0086 a0001c0001t0001g0090 others(85): Show |
90 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.311+920G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955846 | |||||||
chr14:93955851 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.311+915G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955851 | |||||||
chr14:93955852 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0326 a0001c0001t0001g0327 |
4 | HG01168.hp2 HG01169.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+914C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955852 | |||||||
chr14:93955933 | T | A | 201 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0030 others(198): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.311+833A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955933 | |||||||
chr14:93955985 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.311+781T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93955985 | |||||||
chr14:93956000 | A | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(268): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.311+766T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956000 | |||||||
chr14:93956058 | T | C | 4 | a0001c0002t0001g0132 a0001c0002t0002g0028 a0001c0002t0002g0029 others(1): Show |
4 | HG02809.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+708A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956058 | |||||||
chr14:93956121 | G | A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0163 others(8): Show |
11 | HG00099.hp2 HG00323.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.311+645C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956121 | |||||||
chr14:93956188 | G | A | 12 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0064 others(9): Show |
12 | HG00323.hp1 HG01496.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.311+578C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956188 | |||||||
chr14:93956189 | C | T | 1 | a0001c0013t0001g0334 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.311+577G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956189 | |||||||
chr14:93956225 | G | A | 4 | a0001c0001t0001g0299 a0001c0002t0002g0303 a0001c0002t0004g0301 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+541C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956225 | |||||||
chr14:93956237 | T | C | 4 | a0001c0001t0001g0114 a0001c0001t0001g0215 a0001c0001t0002g0268 others(1): Show |
4 | HG00597.hp2 HG02071.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+529A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956237 | |||||||
chr14:93956277 | A | T | 277 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0018 others(274): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.311+489T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956277 | |||||||
chr14:93956335 | G | A | 1 | a0001c0002t0004g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.311+431C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956335 | |||||||
chr14:93956398 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.311+368G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956398 | |||||||
chr14:93956522 | A | AG | 94 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0065 others(91): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.311+243dupC | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956522 | |||||||
chr14:93956551 | A | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(65): Show |
71 | HG00741.hp2 HG01081.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.311+215T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956551 | |||||||
chr14:93956571 | TCTGTGGC others(4): Show |
T | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.311+184_311+194del others(11): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956571 | |||||||
chr14:93956626 | C | G | 1 | a0008c0021t0001g0208 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.311+140G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956626 | |||||||
chr14:93956692 | C | T | 3 | a0001c0001t0001g0272 a0001c0002t0002g0273 a0001c0002t0004g0301 |
3 | HG02145.hp1 HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.311+74G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956692 | |||||||
chr14:93956722 | G | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0071 |
3 | HG00642.hp2 HG01496.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.311+44C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 3/9 | chr14 | 93956722 | |||||||
chr14:93956878 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG01943.hp1 | splice_region_variant&intron_variant | LOW | c.207-8C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93956878 | |||||||
chr14:93956925 | C | G | 4 | a0001c0001t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0062 others(1): Show |
4 | NA18948.hp1 NA18967.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.207-55G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93956925 | |||||||
chr14:93956948 | T | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(124): Show |
135 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.207-78A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93956948 | |||||||
chr14:93956981 | T | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
5 | HG00741.hp1 HG01361.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.207-111A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93956981 | |||||||
chr14:93956981 | T | TGACA | 112 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(109): Show |
119 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.207-115_207-112dup others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93956981 | |||||||
chr14:93957054 | G | A | 1 | a0001c0001t0002g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.207-184C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957054 | |||||||
chr14:93957332 | A | G | 2 | a0001c0008t0002g0156 a0010c0012t0002g0155 |
2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207-462T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957332 | |||||||
chr14:93957336 | C | A | 2 | a0001c0008t0002g0156 a0010c0012t0002g0155 |
2 | HG01255.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.207-466G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957336 | |||||||
chr14:93957363 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0188 |
3 | HG02965.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.207-493T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957363 | |||||||
chr14:93957381 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(117): Show |
127 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.207-511C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957381 | |||||||
chr14:93957402 | A | G | 4 | a0001c0001t0001g0036 a0001c0002t0002g0015 a0001c0003t0001g0224 others(1): Show |
5 | HG02717.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.207-532T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957402 | |||||||
chr14:93957410 | C | A | 6 | a0001c0001t0001g0030 a0001c0002t0001g0004 a0001c0002t0002g0028 others(3): Show |
7 | HG02723.hp1 HG02809.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.207-540G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957410 | |||||||
chr14:93957553 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
14 | HG00741.hp1 HG01081.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.207-683G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957553 | |||||||
chr14:93957576 | G | T | 246 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0020 others(243): Show |
259 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.207-706C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957576 | |||||||
chr14:93957597 | C | T | 1 | a0001c0002t0004g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.207-727G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957597 | |||||||
chr14:93957651 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
14 | HG00741.hp1 HG01081.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.207-781C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957651 | |||||||
chr14:93957690 | T | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(267): Show |
285 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(282): Show |
intron_variant | MODIFIER | c.207-820A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957690 | |||||||
chr14:93957907 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(10): Show |
14 | HG00741.hp1 HG01081.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.207-1037A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957907 | |||||||
chr14:93957919 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.207-1049A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957919 | |||||||
chr14:93957943 | A | C | 105 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(102): Show |
111 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.207-1073T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957943 | |||||||
chr14:93957959 | G | A | 1 | a0001c0002t0002g0329 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207-1089C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93957959 | |||||||
chr14:93958112 | T | C | 109 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(106): Show |
115 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.207-1242A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958112 | |||||||
chr14:93958176 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.207-1306G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958176 | |||||||
chr14:93958195 | T | G | 104 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(101): Show |
109 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.207-1325A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958195 | |||||||
chr14:93958249 | T | C | 1 | a0001c0018t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207-1379A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958249 | |||||||
chr14:93958277 | G | A | 1 | a0001c0003t0001g0078 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.207-1407C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958277 | |||||||
chr14:93958309 | G | C | 304 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(301): Show |
322 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.207-1439C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958309 | |||||||
chr14:93958310 | G | A | 11 | a0001c0002t0002g0047 a0001c0003t0001g0046 a0001c0003t0001g0048 others(8): Show |
11 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.207-1440C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958310 | |||||||
chr14:93958349 | T | G | 104 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(101): Show |
109 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.207-1479A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958349 | |||||||
chr14:93958354 | A | G | 104 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(101): Show |
109 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.207-1484T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958354 | |||||||
chr14:93958390 | G | C | 1 | a0001c0003t0001g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.207-1520C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958390 | |||||||
chr14:93958394 | G | A | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.207-1524C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958394 | |||||||
chr14:93958741 | G | T | 5 | a0001c0001t0001g0144 a0001c0002t0002g0141 a0001c0003t0001g0142 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.207-1871C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958741 | |||||||
chr14:93958769 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.207-1899C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958769 | |||||||
chr14:93958815 | C | T | 1 | a0001c0003t0001g0101 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.207-1945G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958815 | |||||||
chr14:93958858 | G | A | 10 | a0001c0001t0001g0258 a0001c0001t0002g0014 a0001c0001t0002g0254 others(7): Show |
11 | HG00280.hp2 HG00438.hp2 HG04228.hp1 others(8): Show |
intron_variant | MODIFIER | c.207-1988C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958858 | |||||||
chr14:93958898 | G | C | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.207-2028C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93958898 | |||||||
chr14:93959048 | A | T | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
21 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.207-2178T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959048 | |||||||
chr14:93959056 | C | T | 3 | a0001c0002t0002g0015 a0001c0003t0001g0224 a0011c0017t0003g0291 |
4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-2186G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959056 | |||||||
chr14:93959242 | C | G | 103 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(100): Show |
109 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.207-2372G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959242 | |||||||
chr14:93959254 | G | A | 21 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
21 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.207-2384C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959254 | |||||||
chr14:93959308 | C | T | 2 | a0001c0001t0001g0278 a0001c0003t0001g0280 |
2 | HG01517.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.207-2438G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959308 | |||||||
chr14:93959331 | G | T | 1 | a0001c0002t0002g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.207-2461C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959331 | |||||||
chr14:93959357 | A | G | 242 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0020 others(239): Show |
256 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.207-2487T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959357 | |||||||
chr14:93959375 | G | C | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207-2505C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959375 | |||||||
chr14:93959377 | G | A | 134 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0065 others(131): Show |
141 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.207-2507C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959377 | |||||||
chr14:93959394 | G | A | 3 | a0001c0002t0002g0015 a0001c0003t0001g0224 a0011c0017t0003g0291 |
4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-2524C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959394 | |||||||
chr14:93959465 | C | T | 3 | a0001c0002t0002g0015 a0001c0003t0001g0224 a0011c0017t0003g0291 |
4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.207-2595G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959465 | |||||||
chr14:93959607 | C | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.207-2737G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959607 | |||||||
chr14:93959658 | T | C | 1 | a0001c0001t0002g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.207-2788A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959658 | |||||||
chr14:93959664 | G | A | 11 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(8): Show |
11 | HG01884.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.207-2794C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959664 | |||||||
chr14:93959757 | C | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
6 | HG01081.hp1 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.207-2887G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959757 | |||||||
chr14:93959764 | G | A | 3 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0290 |
3 | HG02922.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.207-2894C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959764 | |||||||
chr14:93959780 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.207-2910C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959780 | |||||||
chr14:93959788 | A | C | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.207-2918T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959788 | |||||||
chr14:93959908 | A | G | 155 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0065 others(152): Show |
162 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.207-3038T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959908 | |||||||
chr14:93959970 | GTGCCATG others(22): Show |
G | 41 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0035 others(38): Show |
43 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.207-3129_207-3101d others(31): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959970 | |||||||
chr14:93959976 | T | C | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.207-3106A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93959976 | |||||||
chr14:93960023 | A | G | 36 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
38 | HG00735.hp1 HG00741.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.207-3153T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960023 | |||||||
chr14:93960185 | G | A | 1 | a0004c0006t0003g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.207-3315C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960185 | |||||||
chr14:93960224 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0247 |
2 | HG00621.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.207-3354A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960224 | |||||||
chr14:93960326 | T | A | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.207-3456A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960326 | |||||||
chr14:93960582 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0352 |
3 | NA18939.hp1 NA18975.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.207-3712G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960582 | |||||||
chr14:93960602 | T | G | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+3732A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960602 | |||||||
chr14:93960716 | G | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(289): Show |
308 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.206+3618C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960716 | |||||||
chr14:93960753 | T | C | 293 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(290): Show |
309 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.206+3581A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960753 | |||||||
chr14:93960882 | G | A | 2 | a0001c0001t0002g0248 a0001c0001t0002g0271 |
2 | NA18955.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.206+3452C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960882 | |||||||
chr14:93960883 | G | T | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+3451C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960883 | |||||||
chr14:93960918 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.206+3416T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960918 | |||||||
chr14:93960950 | G | GATAA | 65 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0033 others(62): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.206+3380_206+3383d others(6): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960950 | |||||||
chr14:93960950 | G | GATAAATA others(1): Show |
111 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0021 others(108): Show |
119 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.206+3376_206+3383d others(10): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960950 | |||||||
chr14:93960950 | G | GATAAATA others(5): Show |
28 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0152 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.206+3372_206+3383d others(14): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960950 | |||||||
chr14:93960950 | G | GATAAATA others(9): Show |
2 | a0001c0002t0002g0196 a0001c0002t0002g0273 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.206+3368_206+3383d others(18): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960950 | |||||||
chr14:93960950 | GATAAATA others(1): Show |
G | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.206+3376_206+3383d others(10): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960950 | |||||||
chr14:93960979 | A | T | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+3355T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960979 | |||||||
chr14:93960984 | T | TAAACAAA others(5): Show |
2 | a0001c0002t0002g0015 a0011c0017t0003g0291 |
3 | HG02895.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.206+3349_206+3350i others(14): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960984 | |||||||
chr14:93960984 | T | TAAATAAA others(5): Show |
1 | a0001c0001t0001g0279 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.206+3349_206+3350i others(14): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960984 | |||||||
chr14:93960984 | T | TAAATAAA others(5): Show |
2 | a0001c0016t0001g0032 a0012c0019t0001g0034 |
2 | HG02280.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.206+3349_206+3350i others(14): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960984 | |||||||
chr14:93960984 | T | TAAATAAA others(9): Show |
1 | a0001c0003t0001g0280 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.206+3349_206+3350i others(18): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960984 | |||||||
chr14:93960984 | TAAAC | T | 5 | a0003c0010t0004g0347 a0003c0010t0004g0351 a0003c0011t0001g0348 others(2): Show |
5 | HG00735.hp1 HG00741.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+3346_206+3349d others(6): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960984 | |||||||
chr14:93960988 | C | T | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
12 | HG00741.hp1 HG01099.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.206+3346G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93960988 | |||||||
chr14:93961098 | C | G | 5 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0002t0002g0154 others(2): Show |
5 | HG02280.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.206+3236G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961098 | |||||||
chr14:93961171 | A | T | 3 | a0001c0002t0002g0015 a0001c0003t0001g0224 a0011c0017t0003g0291 |
4 | HG02895.hp2 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+3163T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961171 | |||||||
chr14:93961195 | T | C | 292 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(289): Show |
308 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.206+3139A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961195 | |||||||
chr14:93961303 | G | A | 7 | a0001c0001t0001g0095 a0001c0001t0002g0092 a0001c0001t0002g0093 others(4): Show |
7 | NA18955.hp1 NA18968.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.206+3031C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961303 | |||||||
chr14:93961394 | A | G | 17 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
17 | HG00741.hp1 HG01099.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.206+2940T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961394 | |||||||
chr14:93961397 | C | T | 1 | a0001c0003t0001g0317 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.206+2937G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961397 | |||||||
chr14:93961455 | C | T | 3 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0002t0002g0309 |
3 | HG01109.hp1 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.206+2879G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961455 | |||||||
chr14:93961505 | T | C | 143 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0030 others(140): Show |
151 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.206+2829A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961505 | |||||||
chr14:93961506 | G | C | 146 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0030 others(143): Show |
154 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.206+2828C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961506 | |||||||
chr14:93961539 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.206+2795A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961539 | |||||||
chr14:93961634 | T | C | 6 | a0003c0010t0004g0347 a0003c0010t0004g0351 a0003c0011t0001g0348 others(3): Show |
6 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.206+2700A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961634 | |||||||
chr14:93961639 | T | C | 2 | a0001c0001t0001g0272 a0001c0002t0002g0273 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.206+2695A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961639 | |||||||
chr14:93961641 | T | C | 1 | a0001c0018t0001g0267 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.206+2693A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961641 | |||||||
chr14:93961657 | A | C | 288 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(285): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.206+2677T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961657 | |||||||
chr14:93961685 | T | A | 291 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(288): Show |
307 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.206+2649A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961685 | |||||||
chr14:93961751 | G | C | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.206+2583C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961751 | |||||||
chr14:93961825 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.206+2509G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961825 | |||||||
chr14:93961878 | G | T | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+2456C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961878 | |||||||
chr14:93961978 | G | A | 1 | a0001c0003t0001g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.206+2356C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93961978 | |||||||
chr14:93962080 | G | T | 5 | a0001c0002t0001g0123 a0001c0002t0002g0122 a0001c0002t0002g0124 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+2254C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962080 | |||||||
chr14:93962107 | C | CT | 23 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(20): Show |
24 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.206+2226dupA | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962107 | C | CTT | 15 | a0001c0001t0001g0023 a0001c0001t0001g0258 a0001c0001t0001g0298 others(12): Show |
15 | HG02145.hp2 HG02257.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.206+2225_206+2226d others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962107 | C | CTTT | 77 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(74): Show |
83 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.206+2224_206+2226d others(5): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962107 | C | CTTTT | 121 | a0001c0001t0001g0020 a0001c0001t0001g0065 a0001c0001t0001g0066 others(118): Show |
129 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.206+2223_206+2226d others(6): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962107 | C | CTTTTT | 19 | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0150 others(16): Show |
19 | HG00558.hp1 HG00673.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.206+2222_206+2226d others(7): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962107 | CT | C | 6 | a0001c0001t0001g0272 a0001c0001t0002g0266 a0001c0002t0002g0273 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.206+2226delA | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962107 | CTT | C | 18 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(15): Show |
18 | HG01517.hp1 HG01884.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.206+2225_206+2226d others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962107 | CTTTTTTT others(7): Show |
C | 1 | a0001c0003t0001g0336 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.206+2213_206+2226d others(16): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962107 | |||||||
chr14:93962137 | T | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(269): Show |
287 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.206+2197A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962137 | |||||||
chr14:93962154 | G | A | 2 | a0006c0009t0003g0337 a0006c0009t0003g0338 |
2 | NA18977.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.206+2180C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962154 | |||||||
chr14:93962167 | T | G | 1 | a0001c0002t0002g0345 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.206+2167A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962167 | |||||||
chr14:93962171 | G | A | 4 | a0001c0001t0001g0030 a0001c0002t0001g0004 a0001c0002t0002g0028 others(1): Show |
5 | HG02723.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+2163C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962171 | |||||||
chr14:93962175 | C | T | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.206+2159G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962175 | |||||||
chr14:93962205 | C | T | 5 | a0001c0002t0001g0123 a0001c0002t0002g0122 a0001c0002t0002g0124 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+2129G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962205 | |||||||
chr14:93962207 | CG | C | 238 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(235): Show |
253 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.206+2126delC | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962207 | |||||||
chr14:93962216 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(249): Show |
267 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.206+2118T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962216 | |||||||
chr14:93962223 | T | C | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(17): Show |
20 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.206+2111A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962223 | |||||||
chr14:93962235 | T | C | 3 | a0001c0001t0001g0103 a0001c0002t0002g0345 a0001c0003t0001g0202 |
3 | HG00323.hp2 HG01099.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.206+2099A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962235 | |||||||
chr14:93962260 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+2074C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962260 | |||||||
chr14:93962272 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG01884.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.206+2062C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962272 | |||||||
chr14:93962307 | G | T | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.206+2027C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962307 | |||||||
chr14:93962390 | C | G | 1 | a0001c0001t0002g0225 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.206+1944G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962390 | |||||||
chr14:93962402 | A | G | 2 | a0001c0001t0001g0272 a0001c0002t0002g0273 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.206+1932T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962402 | |||||||
chr14:93962537 | C | T | 297 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(294): Show |
313 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.206+1797G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962537 | |||||||
chr14:93962727 | T | A | 1 | a0003c0010t0004g0351 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.206+1607A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962727 | |||||||
chr14:93962858 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.206+1476C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962858 | |||||||
chr14:93962865 | C | T | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
13 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.206+1469G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962865 | |||||||
chr14:93962866 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.206+1468C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962866 | |||||||
chr14:93962914 | C | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(226): Show |
243 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.206+1420G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93962914 | |||||||
chr14:93963003 | TCTTTCC | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.206+1325_206+1330d others(8): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963003 | |||||||
chr14:93963198 | TTTG | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.206+1133_206+1135d others(5): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963198 | |||||||
chr14:93963236 | T | C | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.206+1098A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963236 | |||||||
chr14:93963405 | A | G | 304 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(301): Show |
322 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(319): Show |
intron_variant | MODIFIER | c.206+929T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963405 | |||||||
chr14:93963580 | C | T | 9 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.206+754G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963580 | |||||||
chr14:93963646 | G | A | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.206+688C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963646 | |||||||
chr14:93963743 | A | G | 1 | a0001c0001t0006g0353 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.206+591T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963743 | |||||||
chr14:93963836 | T | C | 1 | a0001c0003t0001g0204 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.206+498A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963836 | |||||||
chr14:93963841 | A | G | 1 | a0001c0005t0004g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.206+493T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963841 | |||||||
chr14:93963977 | G | A | 301 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(298): Show |
317 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.206+357C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93963977 | |||||||
chr14:93964235 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0002g0207 a0001c0003t0001g0206 |
3 | HG00558.hp2 NA19000.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.206+99C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 2/9 | chr14 | 93964235 | |||||||
chr14:93964768 | T | TATCC | 301 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(298): Show |
317 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.-73-160_-73-157dup others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93964768 | |||||||
chr14:93964863 | C | T | 1 | a0001c0002t0002g0005 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-73-251G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93964863 | |||||||
chr14:93965048 | G | A | 7 | a0001c0001t0001g0272 a0001c0002t0001g0123 a0001c0002t0002g0122 others(4): Show |
7 | HG02145.hp1 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-73-436C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93965048 | |||||||
chr14:93965096 | G | C | 2 | a0001c0001t0005g0019 a0001c0002t0002g0209 |
2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-73-484C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93965096 | |||||||
chr14:93965205 | T | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-73-593A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93965205 | |||||||
chr14:93965536 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-73-924A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93965536 | |||||||
chr14:93965892 | C | G | 6 | a0003c0010t0004g0347 a0003c0010t0004g0351 a0003c0011t0001g0348 others(3): Show |
6 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-1280G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93965892 | |||||||
chr14:93966002 | C | A | 1 | a0001c0002t0002g0212 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-73-1390G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966002 | |||||||
chr14:93966054 | G | T | 5 | a0001c0001t0001g0030 a0001c0002t0001g0004 a0001c0002t0002g0028 others(2): Show |
6 | HG02723.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73-1442C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966054 | |||||||
chr14:93966114 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-73-1502G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966114 | |||||||
chr14:93966132 | A | G | 90 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(87): Show |
96 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-73-1520T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966132 | |||||||
chr14:93966177 | T | A | 16 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(13): Show |
17 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-73-1565A>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966177 | |||||||
chr14:93966290 | G | A | 90 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(87): Show |
96 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-73-1678C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966290 | |||||||
chr14:93966354 | G | A | 1 | a0001c0003t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-73-1742C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966354 | |||||||
chr14:93966437 | T | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(253): Show |
270 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.-73-1825A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966437 | |||||||
chr14:93966478 | C | G | 1 | a0001c0002t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-73-1866G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966478 | |||||||
chr14:93966727 | A | G | 302 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(299): Show |
318 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.-73-2115T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966727 | |||||||
chr14:93966733 | T | C | 5 | a0001c0002t0001g0123 a0001c0002t0002g0122 a0001c0002t0002g0124 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-2121A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966733 | |||||||
chr14:93966785 | T | C | 302 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(299): Show |
318 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.-73-2173A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966785 | |||||||
chr14:93966983 | T | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
27 | HG01081.hp1 HG01099.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.-73-2371A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93966983 | |||||||
chr14:93967094 | C | T | 5 | a0001c0001t0001g0144 a0001c0002t0002g0141 a0001c0003t0001g0142 others(2): Show |
5 | HG02451.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-2482G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967094 | |||||||
chr14:93967241 | T | C | 302 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(299): Show |
318 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.-73-2629A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967241 | |||||||
chr14:93967328 | G | A | 1 | a0001c0003t0001g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-73-2716C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967328 | |||||||
chr14:93967331 | A | G | 2 | a0001c0001t0001g0272 a0001c0002t0002g0273 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-73-2719T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967331 | |||||||
chr14:93967338 | C | CCTCCT | 140 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0065 others(137): Show |
147 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.-73-2727_-73-2726i others(7): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967338 | |||||||
chr14:93967358 | GTC | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(21): Show |
25 | HG01081.hp1 HG01517.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-73-2748_-73-2747d others(4): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967358 | |||||||
chr14:93967361 | T | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(21): Show |
25 | HG01081.hp1 HG01517.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.-73-2749A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967361 | |||||||
chr14:93967380 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(5): Show |
9 | HG01081.hp1 HG02486.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-73-2768C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967380 | |||||||
chr14:93967553 | G | T | 139 | a0001c0001t0001g0020 a0001c0001t0001g0064 a0001c0001t0001g0065 others(136): Show |
146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.-73-2941C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967553 | |||||||
chr14:93967558 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(48): Show |
53 | HG00735.hp1 HG00741.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.-73-2946C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967558 | |||||||
chr14:93967631 | G | A | 5 | a0001c0002t0002g0047 a0001c0003t0001g0046 a0001c0003t0001g0048 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-73-3019C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967631 | |||||||
chr14:93967664 | A | C | 1 | a0001c0001t0002g0140 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-73-3052T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967664 | |||||||
chr14:93967693 | C | T | 1 | a0001c0003t0001g0308 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-73-3081G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967693 | |||||||
chr14:93967717 | A | G | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73-3105T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967717 | |||||||
chr14:93967756 | G | A | 302 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(299): Show |
318 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.-73-3144C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967756 | |||||||
chr14:93967771 | G | A | 1 | a0001c0003t0001g0216 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-73-3159C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967771 | |||||||
chr14:93967839 | G | C | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
10 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-73-3227C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93967839 | |||||||
chr14:93968225 | C | A | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73-3613G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968225 | |||||||
chr14:93968287 | C | A | 1 | a0001c0005t0001g0040 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-73-3675G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968287 | |||||||
chr14:93968294 | C | T | 16 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0035 others(13): Show |
17 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-73-3682G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968294 | |||||||
chr14:93968364 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-73-3752A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968364 | |||||||
chr14:93968370 | G | T | 301 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(298): Show |
317 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.-73-3758C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968370 | |||||||
chr14:93968376 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-73-3764C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968376 | |||||||
chr14:93968420 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-73-3808C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968420 | |||||||
chr14:93968500 | C | T | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-73-3888G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968500 | |||||||
chr14:93968683 | GGGA | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0002t0001g0137 |
3 | HG02622.hp2 HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-73-4074_-73-4072d others(5): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968683 | |||||||
chr14:93968690 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-73-4078C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968690 | |||||||
chr14:93968750 | C | T | 12 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(9): Show |
13 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-73-4138G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968750 | |||||||
chr14:93968804 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-73-4192C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968804 | |||||||
chr14:93968843 | G | C | 1 | a0001c0002t0001g0132 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-73-4231C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968843 | |||||||
chr14:93968867 | A | T | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-73-4255T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968867 | |||||||
chr14:93968869 | G | GTGAA | 273 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0020 others(270): Show |
288 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-73-4261_-73-4258d others(6): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968869 | |||||||
chr14:93968957 | G | T | 11 | a0001c0002t0001g0123 a0001c0002t0002g0122 a0001c0002t0002g0124 others(8): Show |
11 | HG00735.hp1 HG00741.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-73-4345C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93968957 | |||||||
chr14:93969188 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-73-4576G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969188 | |||||||
chr14:93969269 | C | T | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-73-4657G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969269 | |||||||
chr14:93969273 | G | A | 1 | a0001c0002t0004g0344 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-73-4661C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969273 | |||||||
chr14:93969315 | G | T | 1 | a0001c0003t0001g0075 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-73-4703C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969315 | |||||||
chr14:93969317 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-73-4705C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969317 | |||||||
chr14:93969320 | A | G | 4 | a0001c0002t0001g0025 a0001c0002t0001g0027 a0001c0002t0001g0132 others(1): Show |
4 | HG02486.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-4708T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969320 | |||||||
chr14:93969325 | T | G | 5 | a0001c0001t0001g0272 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG01517.hp1 HG02071.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-4713A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969325 | |||||||
chr14:93969333 | C | T | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-73-4721G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969333 | |||||||
chr14:93969334 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-73-4722C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969334 | |||||||
chr14:93969469 | C | T | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-73-4857G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969469 | |||||||
chr14:93969509 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-73-4897A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969509 | |||||||
chr14:93969667 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-73-5055G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969667 | |||||||
chr14:93969762 | G | T | 1 | a0001c0002t0002g0307 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-73-5150C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969762 | |||||||
chr14:93969895 | C | G | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73-5283G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969895 | |||||||
chr14:93969912 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-73-5300T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969912 | |||||||
chr14:93969937 | G | A | 1 | a0003c0022t0003g0219 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-73-5325C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969937 | |||||||
chr14:93969948 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-73-5336T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969948 | |||||||
chr14:93969966 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
6 | HG01081.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-5354G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969966 | |||||||
chr14:93969998 | C | A | 2 | a0001c0003t0001g0304 a0001c0003t0001g0305 |
2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-73-5386G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93969998 | |||||||
chr14:93970016 | A | G | 2 | a0001c0001t0001g0272 a0001c0002t0002g0273 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-73-5404T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970016 | |||||||
chr14:93970065 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0002g0133 a0001c0002t0002g0135 |
3 | NA18941.hp1 NA18975.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-73-5453G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970065 | |||||||
chr14:93970106 | C | T | 1 | a0011c0017t0003g0291 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-73-5494G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970106 | |||||||
chr14:93970204 | T | C | 5 | a0001c0002t0001g0123 a0001c0002t0002g0122 a0001c0002t0002g0124 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73-5592A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970204 | |||||||
chr14:93970213 | C | T | 4 | a0001c0002t0001g0025 a0001c0002t0001g0027 a0001c0002t0001g0132 others(1): Show |
4 | HG02486.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73-5601G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970213 | |||||||
chr14:93970228 | G | A | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-73-5616C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970228 | |||||||
chr14:93970368 | C | G | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-73-5756G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970368 | |||||||
chr14:93970393 | G | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0130 others(3): Show |
6 | HG00558.hp1 HG01099.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-73-5781C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970393 | |||||||
chr14:93970410 | G | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-73-5798C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970410 | |||||||
chr14:93970636 | G | A | 1 | a0001c0002t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-74+5798C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970636 | |||||||
chr14:93970784 | C | T | 5 | a0001c0002t0001g0123 a0001c0002t0002g0122 a0001c0002t0002g0124 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+5650G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970784 | |||||||
chr14:93970942 | C | T | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-74+5492G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93970942 | |||||||
chr14:93971290 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-74+5144C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93971290 | |||||||
chr14:93971414 | T | C | 3 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0290 |
3 | HG02922.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-74+5020A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93971414 | |||||||
chr14:93971448 | A | G | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-74+4986T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93971448 | |||||||
chr14:93971867 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-74+4567T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93971867 | |||||||
chr14:93972116 | T | C | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-74+4318A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972116 | |||||||
chr14:93972135 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
6 | HG01081.hp1 HG02647.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-74+4299G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972135 | |||||||
chr14:93972136 | G | A | 181 | a0001c0001t0001g0020 a0001c0001t0001g0030 a0001c0001t0001g0033 others(178): Show |
190 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.-74+4298C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972136 | |||||||
chr14:93972196 | A | G | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-74+4238T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972196 | |||||||
chr14:93972208 | GTTCCTTG others(19): Show |
G | 166 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0042 others(163): Show |
174 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.-74+4200_-74+4225d others(28): Show |
ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972208 | |||||||
chr14:93972251 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-74+4183A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972251 | |||||||
chr14:93972306 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-74+4128C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972306 | |||||||
chr14:93972390 | G | A | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-74+4044C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972390 | |||||||
chr14:93972480 | T | G | 1 | a0001c0001t0002g0268 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-74+3954A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972480 | |||||||
chr14:93972533 | G | A | 1 | a0001c0001t0002g0269 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-74+3901C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972533 | |||||||
chr14:93972587 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-74+3847C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972587 | |||||||
chr14:93972590 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-74+3844C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972590 | |||||||
chr14:93972639 | G | C | 94 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0086 others(91): Show |
100 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-74+3795C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972639 | |||||||
chr14:93972683 | C | T | 18 | a0001c0001t0001g0106 a0001c0001t0001g0111 a0001c0001t0001g0112 others(15): Show |
19 | HG01192.hp1 HG02040.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-74+3751G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972683 | |||||||
chr14:93972899 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-74+3535A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972899 | |||||||
chr14:93972925 | C | A | 1 | a0001c0001t0002g0271 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-74+3509G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972925 | |||||||
chr14:93972985 | T | C | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-74+3449A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93972985 | |||||||
chr14:93973022 | G | T | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0003t0001g0280 |
3 | HG01517.hp1 HG02071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-74+3412C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973022 | |||||||
chr14:93973094 | G | C | 2 | a0001c0001t0001g0272 a0001c0002t0002g0273 |
2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-74+3340C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973094 | |||||||
chr14:93973169 | A | G | 1 | a0001c0002t0002g0345 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-74+3265T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973169 | |||||||
chr14:93973290 | C | T | 3 | a0001c0003t0001g0288 a0001c0003t0001g0289 a0001c0003t0001g0290 |
3 | HG02922.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-74+3144G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973290 | |||||||
chr14:93973292 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-74+3142T>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973292 | |||||||
chr14:93973331 | C | T | 4 | a0001c0001t0001g0030 a0001c0002t0001g0004 a0001c0002t0002g0028 others(1): Show |
5 | HG02723.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+3103G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973331 | |||||||
chr14:93973533 | G | A | 7 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0277 others(4): Show |
7 | HG02080.hp2 HG02129.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-74+2901C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973533 | |||||||
chr14:93973641 | G | T | 263 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(260): Show |
278 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.-74+2793C>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973641 | |||||||
chr14:93973692 | A | T | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-74+2742T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973692 | |||||||
chr14:93973762 | A | AC | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-74+2671dupG | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973762 | |||||||
chr14:93973791 | C | T | 31 | a0001c0001t0001g0086 a0001c0001t0001g0090 a0001c0001t0001g0095 others(28): Show |
33 | HG00544.hp2 HG00597.hp1 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.-74+2643G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93973791 | |||||||
chr14:93974147 | C | T | 1 | a0001c0016t0001g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-74+2287G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974147 | |||||||
chr14:93974262 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-74+2172T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974262 | |||||||
chr14:93974376 | A | G | 1 | a0001c0002t0002g0345 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-74+2058T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974376 | |||||||
chr14:93974583 | C | T | 4 | a0001c0001t0001g0030 a0001c0002t0001g0004 a0001c0002t0002g0028 others(1): Show |
5 | HG02723.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-74+1851G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974583 | |||||||
chr14:93974667 | G | A | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-74+1767C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974667 | |||||||
chr14:93974673 | T | G | 3 | a0001c0001t0001g0282 a0001c0001t0002g0283 a0001c0001t0002g0284 |
3 | HG02080.hp2 HG02135.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-74+1761A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974673 | |||||||
chr14:93974764 | T | C | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-74+1670A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974764 | |||||||
chr14:93974799 | G | A | 299 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(296): Show |
315 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.-74+1635C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974799 | |||||||
chr14:93974857 | C | T | 1 | a0001c0003t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-74+1577G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974857 | |||||||
chr14:93974885 | C | T | 5 | a0001c0001t0001g0030 a0001c0002t0001g0004 a0001c0002t0002g0028 others(2): Show |
6 | HG02723.hp1 HG02809.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-74+1549G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974885 | |||||||
chr14:93974907 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0002g0072 |
2 | NA18945.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.-74+1527G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974907 | |||||||
chr14:93974917 | G | A | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-74+1517C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974917 | |||||||
chr14:93974926 | A | T | 1 | a0001c0003t0001g0306 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-74+1508T>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93974926 | |||||||
chr14:93975094 | T | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(296): Show |
315 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.-74+1340A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975094 | |||||||
chr14:93975288 | C | A | 1 | a0001c0002t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-74+1146G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975288 | |||||||
chr14:93975392 | G | C | 1 | a0001c0001t0001g0286 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-74+1042C>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975392 | |||||||
chr14:93975460 | C | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(283): Show |
302 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.-74+974G>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975460 | |||||||
chr14:93975533 | C | T | 13 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0298 others(10): Show |
13 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-74+901G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975533 | |||||||
chr14:93975607 | C | G | 8 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(5): Show |
8 | HG01175.hp1 HG01256.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-74+827G>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975607 | |||||||
chr14:93975622 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-74+812G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975622 | |||||||
chr14:93975656 | C | T | 4 | a0001c0001t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0062 others(1): Show |
4 | NA18948.hp1 NA18967.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.-74+778G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975656 | |||||||
chr14:93975810 | T | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(250): Show |
267 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-74+624A>G | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975810 | |||||||
chr14:93975855 | A | G | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-74+579T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975855 | |||||||
chr14:93975866 | G | A | 1 | a0001c0003t0001g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-74+568C>T | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975866 | |||||||
chr14:93975915 | T | G | 15 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
16 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-74+519A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975915 | |||||||
chr14:93975940 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-74+494G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975940 | |||||||
chr14:93975958 | A | G | 3 | a0001c0002t0001g0025 a0001c0002t0001g0027 a0001c0002t0002g0026 |
3 | HG02486.hp2 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-74+476T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93975958 | |||||||
chr14:93976061 | C | T | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
10 | HG00741.hp1 HG01361.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-74+373G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93976061 | |||||||
chr14:93976074 | A | G | 17 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0035 others(14): Show |
18 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.-74+360T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93976074 | |||||||
chr14:93976109 | C | T | 288 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-74+325G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93976109 | |||||||
chr14:93976134 | T | G | 1 | a0001c0001t0001g0352 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-74+300A>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93976134 | |||||||
chr14:93976246 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-74+188G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93976246 | |||||||
chr14:93976267 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
5 | HG01081.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-74+167G>A | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93976267 | |||||||
chr14:93976410 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-74+24T>C | ASB2 | ENSG00000100628.12 | transcript | ENST00000555019.6 | protein_coding | 1/9 | chr14 | 93976410 |