Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 140460 |
| ensemblid | ENSG00000183475.13 |
| hgncid | 17182 |
| symbol | ASB7 |
| name | ankyrin repeat and SOCS box containing 7 |
| refseq_nuc | NM_198243.3 |
| refseq_prot | NP_937886.1 |
| ensembl_nuc | ENST00000332783.12 |
| ensembl_prot | ENSP00000328327.8 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 100602589 |
| end | 100651701 |
| strand | + |
| ver | v1.2 |
| region | chr15:100602589-100651701 |
| region5000 | chr15:100597589-100656701 |
| regionname0 | ASB7_chr15_100602589_100651701 |
| regionname5000 | ASB7_chr15_100597589_100656701 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 954 | 350 | 81 | 64 | 146 | 17 | 40 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 | ||
| a0001c0002 | 0/0 | 954 | 5 | 5 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 | ||
| a0001c0003 | 0/0 | 954 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 | ||
| a0001c0004 | 0/0 | 954 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 | ||
| a0001c0005 | 0/0 | 954 | 3 | 0 | 3 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 | ||
| a0001c0006 | 0/0 | 954 | 2 | 1 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 | ||
| a0001c0007 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 | ||
| a0001c0008 | 0/0 | 954 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | ATGTT others(949): Show |
chr15 | 100597589 | 100656701 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4926 | 190 | 13 | 38 | 109 | 8 | 21 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0002 | 1/0 | 4926 | 70 | 31 | 9 | 18 | 3 | 8 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0003 | 0/0 | 4925 | 26 | 2 | 5 | 14 | 0 | 5 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0004 | 0/0 | 4925 | 15 | 13 | 2 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0005 | 0/0 | 4926 | 8 | 0 | 3 | 0 | 5 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0006 | 0/0 | 4926 | 5 | 4 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0007 | 0/0 | 4926 | 5 | 3 | 2 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0008 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0009 | 0/0 | 4926 | 4 | 0 | 0 | 4 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0010 | 0/0 | 4926 | 4 | 1 | 1 | 0 | 0 | 2 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0011 | 0/0 | 4924 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4919): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0012 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0013 | 0/0 | 4926 | 2 | 2 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0014 | 0/0 | 4926 | 2 | 2 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0015 | 0/0 | 4925 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0016 | 0/0 | 4925 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0017 | 0/0 | 4926 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0018 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0019 | 0/0 | 4926 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0020 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0021 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0022 | 0/0 | 4925 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0023 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0024 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0025 | 0/0 | 4925 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0001t0026 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0002t0002 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0002t0004 | 0/0 | 4925 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0002t0008 | 0/0 | 4926 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0003t0002 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0004t0008 | 0/0 | 4926 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0005t0003 | 0/0 | 4925 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0005t0005 | 0/0 | 4926 | 2 | 0 | 2 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0006t0002 | 0/0 | 4926 | 2 | 1 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| a0001c0007t0004 | 0/0 | 4925 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4920): Show |
chr15 | 100597589 | 100656701 |
| a0001c0008t0002 | 0/0 | 4926 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | AGTGA others(4921): Show |
chr15 | 100597589 | 100656701 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0005g0001 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0008g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0009g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0009g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0010g0011 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0012g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0016g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0017g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0018g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0019g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0020g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0022g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0023g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0024g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0025g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0001t0026g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0002t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0003t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0004t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0004t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0005t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0005t0005g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0006t0002g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0007t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| a0001c0008t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0283 | EUR | GBR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0279 | EUR | GBR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | FIN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | FIN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | FIN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00642 | hp1 | a0001 | c0001 | t0017 | g0313 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00733 | hp2 | a0001 | c0006 | t0002 | g0019 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG00738 | hp2 | a0001 | c0005 | t0003 | g0193 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01074 | hp1 | a0001 | c0001 | t0019 | g0213 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01074 | hp2 | a0001 | c0001 | t0025 | g0152 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0068 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0067 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01346 | hp1 | a0001 | c0001 | t0007 | g0130 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0001 | EUR | IBS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01515 | hp2 | a0001 | c0001 | t0016 | g0055 | EUR | IBS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | IBS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0181 | EUR | IBS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | IBS | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0165 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01884 | hp2 | a0001 | c0001 | t0011 | g0134 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01952 | hp1 | a0001 | c0005 | t0005 | g0026 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01981 | hp2 | a0001 | c0005 | t0005 | g0026 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02055 | hp2 | a0001 | c0004 | t0008 | g0023 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02145 | hp2 | a0001 | c0003 | t0002 | g0150 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CDX | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0059 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02300 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02451 | hp2 | a0001 | c0001 | t0012 | g0153 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02615 | hp2 | a0001 | c0006 | t0002 | g0019 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02622 | hp2 | a0001 | c0001 | t0007 | g0058 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0264 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02698 | hp1 | a0001 | c0001 | t0018 | g0066 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0053 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02735 | hp1 | a0001 | c0001 | t0026 | g0029 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02809 | hp2 | a0001 | c0001 | t0010 | g0011 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0148 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02886 | hp2 | a0001 | c0001 | t0021 | g0184 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02896 | hp1 | a0001 | c0001 | t0014 | g0202 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0052 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0203 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02970 | hp1 | a0001 | c0004 | t0008 | g0166 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0206 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0275 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03209 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0164 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03239 | hp1 | a0001 | c0001 | t0023 | g0198 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03486 | hp2 | a0001 | c0002 | t0008 | g0036 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03490 | hp2 | a0001 | c0001 | t0010 | g0011 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0286 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03540 | hp2 | a0001 | c0007 | t0004 | g0253 | AFR | GWD | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03688 | hp2 | a0001 | c0001 | t0010 | g0151 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | BEB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03942 | hp1 | a0001 | c0001 | t0020 | g0034 | SAS | BEB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0159 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0262 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | STU | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18522 | hp1 | a0001 | c0004 | t0008 | g0023 | AFR | YRI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | YRI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | YRI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18940 | hp1 | a0001 | c0001 | t0009 | g0276 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18965 | hp1 | a0001 | c0001 | t0022 | g0123 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18965 | hp2 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19002 | hp1 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | LWK | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19030 | hp2 | a0001 | c0001 | t0024 | g0008 | AFR | LWK | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19043 | hp1 | a0001 | c0001 | t0011 | g0147 | AFR | LWK | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0180 | AFR | LWK | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19060 | hp2 | a0001 | c0001 | t0009 | g0089 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | YRI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | ASW | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0093 | EUR | TSI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20752 | hp2 | a0001 | c0008 | t0002 | g0303 | EUR | TSI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0304 | EUR | TSI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | GIH | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0057 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | USA | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | USA | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | USA | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | USA | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | LWK | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0291 | REF | REF | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0251 | REF | REF | ASB7_chr15_100597589_100656701 | ASB7 | chr15 | 100597589 | 100656701 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:100612336 | G | T | 1 | a0001c0008 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.120G>T | p.Pro40Pro | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/6 | 850/4926 | 120/957 | 40/318 | chr15 | 100612336 | |||
| chr15:100629438 | T | C | 1 | a0001c0006 | 2 | HG00733.hp2 HG02615.hp2 |
splice_region_variant&synonymous_variant | LOW | c.213T>C | p.Ala71Ala | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/6 | 943/4926 | 213/957 | 71/318 | chr15 | 100629438 | |||
| chr15:100629489 | A | G | 1 | a0001c0005 | 3 | HG00738.hp2 HG01952.hp1 HG01981.hp2 |
synonymous_variant | LOW | c.264A>G | p.Ala88Ala | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/6 | 994/4926 | 264/957 | 88/318 | chr15 | 100629489 | |||
| chr15:100629573 | C | T | 1 | a0001c0007 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.348C>T | p.Asp116Asp | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/6 | 1078/4926 | 348/957 | 116/318 | chr15 | 100629573 | |||
| chr15:100629606 | C | T | 1 | a0001c0004 | 3 | HG02055.hp2 HG02970.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.381C>T | p.Tyr127Tyr | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/6 | 1111/4926 | 381/957 | 127/318 | chr15 | 100629606 | |||
| chr15:100629924 | A | G | 1 | a0001c0002 | 5 | HG02451.hp1 HG03195.hp2 HG03486.hp2 others(2): Show |
synonymous_variant | LOW | c.699A>G | p.Leu233Leu | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/6 | 1429/4926 | 699/957 | 233/318 | chr15 | 100629924 | |||
| chr15:100648396 | A | G | 1 | a0001c0003 | 3 | HG02145.hp2 HG02896.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.891A>G | p.Leu297Leu | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1621/4926 | 891/957 | 297/318 | chr15 | 100648396 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:100602651 | G | A | 4 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0015 others(1): Show |
12 | HG01106.hp1 HG01167.hp1 HG01346.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-668G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/6 | 9566 | chr15 | 100602651 | ||||||
| chr15:100602817 | G | C | 1 | a0001c0001t0017 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-502G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/6 | 9400 | chr15 | 100602817 | ||||||
| chr15:100602847 | C | A | 1 | a0001c0001t0018 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-472C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/6 | 9370 | chr15 | 100602847 | ||||||
| chr15:100603292 | C | T | 1 | a0001c0001t0026 | 1 | HG02735.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-195C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/6 | chr15 | 100603292 | |||||||
| chr15:100609756 | C | T | 2 | a0001c0001t0010 a0001c0001t0025 |
5 | HG01074.hp2 HG02300.hp1 HG02809.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-124C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/6 | 2461 | chr15 | 100609756 | ||||||
| chr15:100648699 | GT | G | 1 | a0001c0001t0011 | 3 | HG01884.hp1 HG01884.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*240delT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 240 | INFO_REALIGN_3_PRIME | chr15 | 100648699 | |||||
| chr15:100648775 | A | G | 3 | a0001c0001t0008 a0001c0002t0008 a0001c0004t0008 |
5 | HG02055.hp2 HG02970.hp1 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*313A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 313 | chr15 | 100648775 | ||||||
| chr15:100648967 | G | A | 1 | a0001c0001t0012 | 3 | HG02451.hp2 HG02630.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*505G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 505 | chr15 | 100648967 | ||||||
| chr15:100649068 | T | C | 1 | a0001c0001t0013 | 2 | HG02818.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*606T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 606 | chr15 | 100649068 | ||||||
| chr15:100649357 | C | T | 1 | a0001c0001t0014 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*895C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 895 | chr15 | 100649357 | ||||||
| chr15:100649430 | T | C | 1 | a0001c0001t0019 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 968 | chr15 | 100649430 | ||||||
| chr15:100649691 | C | T | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(13): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
3_prime_UTR_variant | MODIFIER | c.*1229C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1229 | chr15 | 100649691 | ||||||
| chr15:100649827 | G | A | 3 | a0001c0001t0005 a0001c0001t0019 a0001c0005t0005 |
11 | HG00140.hp2 HG01074.hp1 HG01081.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1365G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1365 | chr15 | 100649827 | ||||||
| chr15:100649895 | C | T | 1 | a0001c0001t0009 | 4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1433C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1433 | chr15 | 100649895 | ||||||
| chr15:100649910 | G | A | 1 | a0001c0001t0022 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1448G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1448 | chr15 | 100649910 | ||||||
| chr15:100649940 | G | A | 1 | a0001c0001t0023 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1478G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1478 | chr15 | 100649940 | ||||||
| chr15:100650129 | T | C | 1 | a0001c0001t0020 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1667 | chr15 | 100650129 | ||||||
| chr15:100650163 | C | T | 1 | a0001c0001t0024 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1701C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 1701 | chr15 | 100650163 | ||||||
| chr15:100650638 | A | C | 1 | a0001c0001t0021 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2176A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 2176 | chr15 | 100650638 | ||||||
| chr15:100650803 | A | C | 1 | a0001c0001t0012 | 3 | HG02451.hp2 HG02630.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2341A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 2341 | chr15 | 100650803 | ||||||
| chr15:100651197 | GT | G | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0011 others(7): Show |
51 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2748delT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 6/6 | 2748 | INFO_REALIGN_3_PRIME | chr15 | 100651197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:100603074 | A | C | 46 | a0001c0001t0001g0015 a0001c0001t0001g0277 a0001c0001t0001g0282 others(43): Show |
54 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-273+28A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/5 | chr15 | 100603074 | |||||||
| chr15:100603130 | C | A | 1 | a0001c0001t0004g0035 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-273+84C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/5 | chr15 | 100603130 | |||||||
| chr15:100603145 | GCCCCTTT others(8): Show |
G | 3 | a0001c0001t0002g0016 a0001c0001t0004g0017 a0001c0001t0004g0035 |
5 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.-272-65_-272-51del others(15): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr15 | 100603145 | ||||||
| chr15:100603166 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0029 others(26): Show |
35 | HG00558.hp1 HG00597.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-272-49C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/5 | chr15 | 100603166 | |||||||
| chr15:100603175 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(296): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.-272-40T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 1/5 | chr15 | 100603175 | |||||||
| chr15:100603326 | C | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(100): Show |
118 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.-174+13C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603326 | |||||||
| chr15:100603420 | C | G | 31 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0022 others(28): Show |
37 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.-174+107C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603420 | |||||||
| chr15:100603438 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0009g0032 |
3 | NA18965.hp2 NA18994.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-174+125A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603438 | |||||||
| chr15:100603484 | A | G | 3 | a0001c0001t0002g0212 a0001c0001t0002g0214 a0001c0001t0019g0213 |
3 | HG01074.hp1 HG01175.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-174+171A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603484 | |||||||
| chr15:100603634 | C | G | 8 | a0001c0001t0001g0207 a0001c0001t0002g0204 a0001c0001t0002g0208 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-174+321C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603634 | |||||||
| chr15:100603751 | C | T | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-174+438C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603751 | |||||||
| chr15:100603776 | T | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-174+463T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603776 | |||||||
| chr15:100603790 | C | G | 13 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0192 others(10): Show |
17 | HG00323.hp2 HG00639.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.-174+477C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603790 | |||||||
| chr15:100603862 | T | C | 6 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(3): Show |
6 | HG02027.hp2 NA18943.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-174+549T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603862 | |||||||
| chr15:100603876 | C | A | 5 | a0001c0001t0002g0016 a0001c0001t0004g0017 a0001c0001t0004g0035 others(2): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-174+563C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603876 | |||||||
| chr15:100603900 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.-174+587G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100603900 | |||||||
| chr15:100604040 | G | A | 310 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(307): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-174+727G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100604040 | |||||||
| chr15:100604197 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-174+884A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100604197 | |||||||
| chr15:100604412 | T | C | 2 | a0001c0001t0003g0154 a0001c0001t0012g0153 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-174+1099T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100604412 | |||||||
| chr15:100604708 | T | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(190): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-174+1395T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100604708 | |||||||
| chr15:100604980 | C | T | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-174+1667C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100604980 | |||||||
| chr15:100605157 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-174+1844A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605157 | |||||||
| chr15:100605548 | G | A | 1 | a0001c0001t0011g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-174+2235G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605548 | |||||||
| chr15:100605606 | G | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-174+2293G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605606 | |||||||
| chr15:100605625 | G | A | 313 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(310): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-174+2312G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605625 | |||||||
| chr15:100605649 | A | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(190): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-174+2336A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605649 | |||||||
| chr15:100605703 | A | C | 1 | a0001c0001t0011g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-174+2390A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605703 | |||||||
| chr15:100605703 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0163 |
2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-174+2390A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605703 | |||||||
| chr15:100605879 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-174+2566T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100605879 | |||||||
| chr15:100606001 | C | A | 5 | a0001c0001t0002g0016 a0001c0001t0004g0017 a0001c0001t0004g0035 others(2): Show |
7 | HG01167.hp2 HG01169.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-174+2688C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606001 | |||||||
| chr15:100606017 | G | A | 31 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(28): Show |
36 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.-174+2704G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606017 | |||||||
| chr15:100606192 | G | GC | 6 | a0001c0001t0001g0038 a0001c0002t0002g0018 a0001c0002t0002g0037 others(3): Show |
6 | HG01099.hp1 HG02451.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-174+2879_-174+288 others(5): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606192 | |||||||
| chr15:100606192 | G | GT | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(118): Show |
141 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.-174+2889dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 100606192 | ||||||
| chr15:100606369 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-174+3056A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606369 | |||||||
| chr15:100606382 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-174+3069T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606382 | |||||||
| chr15:100606419 | A | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-174+3106A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606419 | |||||||
| chr15:100606482 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-174+3169A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606482 | |||||||
| chr15:100606551 | G | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-173-3156G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606551 | |||||||
| chr15:100606611 | A | G | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-173-3096A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606611 | |||||||
| chr15:100606656 | T | G | 31 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(28): Show |
36 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.-173-3051T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606656 | |||||||
| chr15:100606756 | T | C | 6 | a0001c0001t0001g0038 a0001c0002t0002g0018 a0001c0002t0002g0037 others(3): Show |
6 | HG01099.hp1 HG02451.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-173-2951T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606756 | |||||||
| chr15:100606886 | G | T | 1 | a0001c0001t0015g0053 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-173-2821G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606886 | |||||||
| chr15:100606918 | G | A | 1 | a0001c0001t0003g0169 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-173-2789G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606918 | |||||||
| chr15:100606950 | C | T | 2 | a0001c0001t0003g0154 a0001c0001t0012g0153 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-173-2757C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606950 | |||||||
| chr15:100606972 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0191 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-173-2735G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100606972 | |||||||
| chr15:100607008 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-173-2699C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607008 | |||||||
| chr15:100607024 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0004g0009 |
4 | HG01496.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-173-2683G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607024 | |||||||
| chr15:100607083 | G | A | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-173-2624G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607083 | |||||||
| chr15:100607151 | C | CA | 43 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(40): Show |
50 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.-173-2542dupA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr15 | 100607151 | ||||||
| chr15:100607282 | C | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-173-2425C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607282 | |||||||
| chr15:100607294 | T | C | 11 | a0001c0001t0001g0160 a0001c0001t0001g0207 a0001c0001t0002g0051 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-173-2413T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607294 | |||||||
| chr15:100607444 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-173-2263T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607444 | |||||||
| chr15:100607464 | A | G | 11 | a0001c0001t0001g0160 a0001c0001t0001g0207 a0001c0001t0002g0051 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-173-2243A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607464 | |||||||
| chr15:100607467 | A | G | 46 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(43): Show |
54 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.-173-2240A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607467 | |||||||
| chr15:100607492 | G | T | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-173-2215G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607492 | |||||||
| chr15:100607521 | G | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(132): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-173-2186G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607521 | |||||||
| chr15:100607596 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-173-2111G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607596 | |||||||
| chr15:100607716 | T | C | 9 | a0001c0001t0001g0063 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
10 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-173-1991T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607716 | |||||||
| chr15:100607717 | A | G | 31 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(28): Show |
36 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.-173-1990A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607717 | |||||||
| chr15:100607843 | T | G | 314 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.-173-1864T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100607843 | |||||||
| chr15:100608028 | T | C | 56 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(53): Show |
62 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.-173-1679T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608028 | |||||||
| chr15:100608035 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-173-1672A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608035 | |||||||
| chr15:100608130 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(183): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-173-1577T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608130 | |||||||
| chr15:100608137 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-173-1570C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608137 | |||||||
| chr15:100608186 | C | T | 301 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(298): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.-173-1521C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608186 | |||||||
| chr15:100608194 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0163 |
2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-173-1513A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608194 | |||||||
| chr15:100608237 | G | A | 5 | a0001c0001t0002g0012 a0001c0001t0004g0161 a0001c0001t0006g0057 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-173-1470G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608237 | |||||||
| chr15:100608251 | A | G | 1 | a0001c0001t0019g0213 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-173-1456A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608251 | |||||||
| chr15:100608302 | C | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(197): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.-173-1405C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608302 | |||||||
| chr15:100608349 | C | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.-173-1358C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608349 | |||||||
| chr15:100608400 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-173-1307A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608400 | |||||||
| chr15:100608416 | A | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG01496.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-173-1291A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608416 | |||||||
| chr15:100608522 | G | A | 2 | a0001c0001t0002g0212 a0001c0001t0019g0213 |
2 | HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-173-1185G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608522 | |||||||
| chr15:100608554 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-173-1153C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608554 | |||||||
| chr15:100608555 | G | A | 6 | a0001c0001t0002g0149 a0001c0001t0004g0009 a0001c0001t0004g0010 others(3): Show |
10 | HG01496.hp2 HG02145.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-173-1152G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608555 | |||||||
| chr15:100608782 | T | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(195): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-173-925T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608782 | |||||||
| chr15:100608977 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-173-730A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100608977 | |||||||
| chr15:100609157 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(187): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.-173-550C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100609157 | |||||||
| chr15:100609305 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-173-402G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100609305 | |||||||
| chr15:100609419 | C | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-173-288C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100609419 | |||||||
| chr15:100609499 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-173-208G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100609499 | |||||||
| chr15:100609562 | A | T | 30 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(27): Show |
35 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.-173-145A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 2/5 | chr15 | 100609562 | |||||||
| chr15:100609846 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-52+18C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100609846 | |||||||
| chr15:100610223 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(296): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-52+395A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610223 | |||||||
| chr15:100610230 | C | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(130): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-52+402C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610230 | |||||||
| chr15:100610309 | A | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(105): Show |
125 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-52+481A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610309 | |||||||
| chr15:100610322 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-52+494G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610322 | |||||||
| chr15:100610351 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG02027.hp2 NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-52+523C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610351 | |||||||
| chr15:100610356 | G | A | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0239 |
3 | NA18946.hp1 NA19004.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-52+528G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610356 | |||||||
| chr15:100610423 | A | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(124): Show |
147 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-52+595A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610423 | |||||||
| chr15:100610465 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-52+637A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610465 | |||||||
| chr15:100610494 | C | CAA | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(113): Show |
136 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-52+677_-52+678dup others(2): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100610494 | ||||||
| chr15:100610494 | C | CAAA | 11 | a0001c0001t0001g0207 a0001c0001t0002g0204 a0001c0001t0002g0208 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-52+676_-52+678dup others(3): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100610494 | ||||||
| chr15:100610708 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-52+880C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610708 | |||||||
| chr15:100610841 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-52+1013G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610841 | |||||||
| chr15:100610870 | A | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-52+1042A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610870 | |||||||
| chr15:100610871 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-52+1043T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100610871 | |||||||
| chr15:100611012 | G | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-51-1154G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611012 | |||||||
| chr15:100611038 | A | G | 9 | a0001c0001t0002g0012 a0001c0001t0002g0222 a0001c0001t0004g0161 others(6): Show |
13 | HG01074.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51-1128A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611038 | |||||||
| chr15:100611077 | C | T | 127 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(124): Show |
147 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.-51-1089C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611077 | |||||||
| chr15:100611150 | T | C | 5 | a0001c0001t0002g0012 a0001c0001t0004g0161 a0001c0001t0006g0057 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51-1016T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611150 | |||||||
| chr15:100611163 | A | G | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-1003A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611163 | |||||||
| chr15:100611461 | T | C | 1 | a0001c0001t0002g0171 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-51-705T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611461 | |||||||
| chr15:100611484 | C | CTTT | 27 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0050 others(24): Show |
31 | HG00323.hp2 HG00597.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.-51-671_-51-669dup others(3): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(3): Show |
20 | a0001c0001t0001g0056 a0001c0001t0001g0156 a0001c0001t0001g0290 others(17): Show |
20 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.-51-678_-51-669dup others(10): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(4): Show |
17 | a0001c0001t0001g0207 a0001c0001t0001g0300 a0001c0001t0001g0301 others(14): Show |
21 | HG00140.hp2 HG00738.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51-679_-51-669dup others(11): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-51-680_-51-669dup others(12): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(9): Show |
10 | a0001c0001t0001g0063 a0001c0001t0001g0237 a0001c0001t0001g0247 others(7): Show |
10 | HG00735.hp1 HG01074.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(16): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(10): Show |
61 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0038 others(58): Show |
71 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(17): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(11): Show |
45 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(42): Show |
51 | HG00099.hp2 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(18): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(12): Show |
28 | a0001c0001t0001g0024 a0001c0001t0001g0135 a0001c0001t0001g0136 others(25): Show |
29 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(19): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(13): Show |
33 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(30): Show |
38 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(20): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(14): Show |
22 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0082 others(19): Show |
25 | HG00544.hp2 HG00639.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(21): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(15): Show |
20 | a0001c0001t0001g0013 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
26 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(22): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02071.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(23): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0001g0218 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-51-669_-51-668ins others(24): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(18): Show |
2 | a0001c0001t0009g0032 a0001c0001t0009g0276 |
3 | NA18940.hp1 NA18965.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-51-669_-51-668ins others(25): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-51-669_-51-668ins others(26): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611484 | CT | C | 7 | a0001c0001t0002g0149 a0001c0001t0004g0009 a0001c0001t0004g0010 others(4): Show |
11 | HG01496.hp2 HG02145.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51-669delT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611484 | ||||||
| chr15:100611516 | C | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(113): Show |
136 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-51-650C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611516 | |||||||
| chr15:100611555 | A | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(296): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-51-611A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611555 | |||||||
| chr15:100611679 | T | C | 306 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(303): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.-51-487T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611679 | |||||||
| chr15:100611694 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0003g0169 |
3 | NA18979.hp1 NA18990.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-51-472G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611694 | |||||||
| chr15:100611819 | C | CT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0309 others(7): Show |
12 | HG00140.hp1 HG00280.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51-329dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611819 | ||||||
| chr15:100611819 | CT | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
236 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.-51-329delT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr15 | 100611819 | ||||||
| chr15:100611854 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51-312C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611854 | |||||||
| chr15:100611899 | C | A | 311 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.-51-267C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100611899 | |||||||
| chr15:100612022 | C | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(110): Show |
132 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.-51-144C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100612022 | |||||||
| chr15:100612084 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-51-82G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 3/5 | chr15 | 100612084 | |||||||
| chr15:100612540 | A | C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.211+113A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100612540 | |||||||
| chr15:100612580 | C | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0191 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.211+153C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100612580 | |||||||
| chr15:100612837 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.211+410A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100612837 | |||||||
| chr15:100613114 | G | A | 1 | a0001c0003t0002g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.211+687G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100613114 | |||||||
| chr15:100613125 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.211+698A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100613125 | |||||||
| chr15:100613670 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0073 |
2 | NA18947.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.211+1243G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100613670 | |||||||
| chr15:100613714 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+1287C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100613714 | |||||||
| chr15:100613752 | C | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(110): Show |
132 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.211+1325C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100613752 | |||||||
| chr15:100613782 | T | C | 1 | a0001c0003t0002g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.211+1355T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100613782 | |||||||
| chr15:100613918 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.211+1491G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100613918 | |||||||
| chr15:100614080 | T | G | 11 | a0001c0001t0001g0207 a0001c0001t0002g0204 a0001c0001t0002g0208 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.211+1653T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614080 | |||||||
| chr15:100614207 | G | A | 82 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0028 others(79): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.211+1780G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614207 | |||||||
| chr15:100614209 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.211+1782G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614209 | |||||||
| chr15:100614272 | C | CA | 6 | a0001c0001t0001g0277 a0001c0001t0003g0154 a0001c0001t0004g0275 others(3): Show |
7 | HG02451.hp2 HG02723.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+1861dupA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100614272 | ||||||
| chr15:100614272 | CA | C | 32 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(29): Show |
37 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.211+1861delA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100614272 | ||||||
| chr15:100614457 | T | G | 1 | a0001c0001t0003g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.211+2030T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614457 | |||||||
| chr15:100614513 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2086A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614513 | |||||||
| chr15:100614649 | C | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(152): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.211+2222C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614649 | |||||||
| chr15:100614679 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(172): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.211+2252C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614679 | |||||||
| chr15:100614727 | A | G | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2300A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614727 | |||||||
| chr15:100614731 | C | T | 5 | a0001c0001t0002g0012 a0001c0001t0004g0161 a0001c0001t0006g0057 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+2304C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614731 | |||||||
| chr15:100614742 | C | CA | 29 | a0001c0001t0001g0008 a0001c0001t0001g0047 a0001c0001t0001g0072 others(26): Show |
30 | HG00438.hp1 HG00544.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.211+2334dupA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100614742 | ||||||
| chr15:100614742 | C | CAA | 16 | a0001c0001t0001g0207 a0001c0001t0002g0012 a0001c0001t0002g0201 others(13): Show |
18 | HG01109.hp1 HG01243.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.211+2333_211+2334d others(4): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100614742 | ||||||
| chr15:100614742 | CA | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0234 a0001c0001t0001g0277 others(4): Show |
8 | HG00639.hp1 HG06807.hp1 NA18940.hp1 others(5): Show |
intron_variant | MODIFIER | c.211+2334delA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100614742 | ||||||
| chr15:100614793 | T | C | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.211+2366T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614793 | |||||||
| chr15:100614921 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+2494C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100614921 | |||||||
| chr15:100615361 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.211+2934A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615361 | |||||||
| chr15:100615521 | T | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(158): Show |
188 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.211+3094T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615521 | |||||||
| chr15:100615647 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.211+3220C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615647 | |||||||
| chr15:100615658 | G | C | 1 | a0001c0001t0003g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.211+3231G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615658 | |||||||
| chr15:100615727 | T | C | 5 | a0001c0001t0002g0012 a0001c0001t0004g0161 a0001c0001t0006g0057 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+3300T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615727 | |||||||
| chr15:100615807 | C | A | 314 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.211+3380C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615807 | |||||||
| chr15:100615820 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.211+3393T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615820 | |||||||
| chr15:100615956 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.211+3529A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100615956 | |||||||
| chr15:100616041 | C | T | 1 | a0001c0001t0001g0299 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.211+3614C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616041 | |||||||
| chr15:100616108 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.211+3681T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616108 | |||||||
| chr15:100616156 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.211+3729A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616156 | |||||||
| chr15:100616286 | A | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(140): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.211+3859A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616286 | |||||||
| chr15:100616307 | G | GT | 50 | a0001c0001t0001g0031 a0001c0001t0001g0056 a0001c0001t0001g0156 others(47): Show |
59 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.211+3886dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100616307 | ||||||
| chr15:100616389 | G | A | 1 | a0001c0001t0013g0091 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.211+3962G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616389 | |||||||
| chr15:100616418 | G | A | 113 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(110): Show |
132 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.211+3991G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616418 | |||||||
| chr15:100616428 | G | A | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+4001G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616428 | |||||||
| chr15:100616545 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.211+4118A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616545 | |||||||
| chr15:100616546 | T | C | 3 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0003g0289 |
3 | HG00609.hp1 HG00673.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.211+4119T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616546 | |||||||
| chr15:100616569 | T | C | 2 | a0001c0004t0008g0023 a0001c0004t0008g0166 |
3 | HG02055.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.211+4142T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616569 | |||||||
| chr15:100616714 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.211+4287C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616714 | |||||||
| chr15:100616852 | A | G | 6 | a0001c0001t0002g0149 a0001c0001t0004g0009 a0001c0001t0004g0010 others(3): Show |
10 | HG01496.hp2 HG02145.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+4425A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100616852 | |||||||
| chr15:100617044 | T | A | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+4617T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617044 | |||||||
| chr15:100617240 | C | T | 2 | a0001c0001t0002g0214 a0001c0001t0005g0093 |
2 | HG03927.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.211+4813C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617240 | |||||||
| chr15:100617461 | C | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+5034C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617461 | |||||||
| chr15:100617714 | A | G | 9 | a0001c0001t0002g0012 a0001c0001t0002g0222 a0001c0001t0004g0161 others(6): Show |
13 | HG01074.hp2 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+5287A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617714 | |||||||
| chr15:100617747 | T | A | 1 | a0001c0001t0011g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.211+5320T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617747 | |||||||
| chr15:100617880 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.211+5453A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617880 | |||||||
| chr15:100617921 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0298 |
2 | HG03927.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.211+5494C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617921 | |||||||
| chr15:100617961 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0003g0286 |
2 | HG03491.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.211+5534C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100617961 | |||||||
| chr15:100618032 | A | G | 2 | a0001c0001t0008g0164 a0001c0001t0011g0147 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211+5605A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618032 | |||||||
| chr15:100618099 | A | G | 2 | a0001c0001t0003g0154 a0001c0001t0012g0153 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.211+5672A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618099 | |||||||
| chr15:100618129 | T | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0140 |
2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.211+5702T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618129 | |||||||
| chr15:100618192 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.211+5765C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618192 | |||||||
| chr15:100618203 | G | A | 2 | a0001c0001t0008g0164 a0001c0001t0011g0147 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211+5776G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618203 | |||||||
| chr15:100618241 | C | T | 6 | a0001c0001t0001g0297 a0001c0001t0002g0012 a0001c0001t0004g0161 others(3): Show |
8 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+5814C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618241 | |||||||
| chr15:100618283 | A | AT | 9 | a0001c0001t0001g0050 a0001c0001t0001g0142 a0001c0001t0001g0143 others(6): Show |
9 | HG00423.hp2 HG00597.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+5867dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100618283 | ||||||
| chr15:100618428 | A | G | 2 | a0001c0001t0008g0164 a0001c0001t0011g0147 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211+6001A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618428 | |||||||
| chr15:100618579 | C | A | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+6152C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618579 | |||||||
| chr15:100618618 | G | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(71): Show |
87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.211+6191G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618618 | |||||||
| chr15:100618622 | G | GGT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(74): Show |
94 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.211+6217_211+6218d others(4): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100618622 | ||||||
| chr15:100618622 | G | GGTGT | 79 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(76): Show |
91 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.211+6215_211+6218d others(6): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100618622 | ||||||
| chr15:100618622 | G | GGTGTGT | 9 | a0001c0001t0001g0115 a0001c0001t0001g0307 a0001c0001t0002g0106 others(6): Show |
9 | HG00733.hp1 HG02698.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.211+6213_211+6218d others(8): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100618622 | ||||||
| chr15:100618652 | C | A | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+6225C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618652 | |||||||
| chr15:100618652 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+6225C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618652 | |||||||
| chr15:100618711 | A | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(137): Show |
161 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.211+6284A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618711 | |||||||
| chr15:100618964 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0163 a0001c0001t0002g0200 |
3 | HG02109.hp2 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+6537C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100618964 | |||||||
| chr15:100619016 | C | G | 1 | a0001c0001t0001g0301 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.211+6589C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619016 | |||||||
| chr15:100619073 | G | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(306): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.211+6646G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619073 | |||||||
| chr15:100619093 | T | G | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+6666T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619093 | |||||||
| chr15:100619216 | T | C | 27 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0088 others(24): Show |
29 | HG00423.hp2 HG00597.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.211+6789T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619216 | |||||||
| chr15:100619281 | A | C | 2 | a0001c0001t0008g0164 a0001c0001t0011g0147 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211+6854A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619281 | |||||||
| chr15:100619380 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.211+6953C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619380 | |||||||
| chr15:100619420 | T | C | 2 | a0001c0001t0008g0164 a0001c0001t0011g0147 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211+6993T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619420 | |||||||
| chr15:100619567 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.211+7140G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619567 | |||||||
| chr15:100619612 | A | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0188 |
2 | HG00621.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.211+7185A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619612 | |||||||
| chr15:100619718 | C | A | 19 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0167 others(16): Show |
20 | HG00735.hp1 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.211+7291C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619718 | |||||||
| chr15:100619865 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0021g0184 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.211+7438G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619865 | |||||||
| chr15:100619876 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(62): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.211+7449G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619876 | |||||||
| chr15:100619907 | G | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.211+7480G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619907 | |||||||
| chr15:100619937 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.211+7510C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619937 | |||||||
| chr15:100619954 | A | G | 2 | a0001c0001t0008g0164 a0001c0001t0011g0147 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.211+7527A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100619954 | |||||||
| chr15:100620046 | T | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(144): Show |
170 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.211+7619T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100620046 | |||||||
| chr15:100620286 | T | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(65): Show |
80 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(77): Show |
intron_variant | MODIFIER | c.211+7859T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100620286 | |||||||
| chr15:100620361 | A | G | 4 | a0001c0001t0001g0269 a0001c0001t0002g0125 a0001c0001t0002g0146 others(1): Show |
4 | HG02976.hp2 NA18967.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+7934A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100620361 | |||||||
| chr15:100620446 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.211+8019C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100620446 | |||||||
| chr15:100620512 | AATGGGAT others(85): Show |
A | 71 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(68): Show |
83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.211+8107_211+8198d others(94): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100620512 | ||||||
| chr15:100620534 | ATCTGTAC others(39): Show |
A | 4 | a0001c0001t0001g0277 a0001c0001t0008g0164 a0001c0001t0009g0032 others(1): Show |
5 | HG03225.hp1 NA18940.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.211+8173_211+8218d others(48): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100620534 | ||||||
| chr15:100620989 | TA | T | 15 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0247 others(12): Show |
16 | HG00735.hp1 HG01099.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.212-8447delA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100620989 | |||||||
| chr15:100620996 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-8441G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100620996 | |||||||
| chr15:100621140 | A | G | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-8297A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621140 | |||||||
| chr15:100621159 | A | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0077 others(4): Show |
9 | HG00438.hp2 HG00642.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-8278A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621159 | |||||||
| chr15:100621312 | C | T | 1 | a0001c0001t0012g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.212-8125C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621312 | |||||||
| chr15:100621445 | T | C | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-7992T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621445 | |||||||
| chr15:100621538 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.212-7899A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621538 | |||||||
| chr15:100621543 | G | A | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-7894G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621543 | |||||||
| chr15:100621634 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-7803A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621634 | |||||||
| chr15:100621668 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.212-7769T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621668 | |||||||
| chr15:100621713 | G | A | 16 | a0001c0001t0001g0028 a0001c0001t0001g0040 a0001c0001t0001g0048 others(13): Show |
17 | HG00558.hp2 HG00621.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.212-7724G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621713 | |||||||
| chr15:100621738 | C | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(64): Show |
79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.212-7699C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621738 | |||||||
| chr15:100621817 | C | A | 5 | a0001c0002t0002g0018 a0001c0002t0002g0037 a0001c0002t0002g0039 others(2): Show |
5 | HG02451.hp1 HG03195.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-7620C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621817 | |||||||
| chr15:100621835 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-7602A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621835 | |||||||
| chr15:100621853 | T | C | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-7584T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621853 | |||||||
| chr15:100621861 | T | TG | 27 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0088 others(24): Show |
29 | HG00423.hp2 HG00597.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-7575dupG | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100621861 | ||||||
| chr15:100621862 | G | GA | 4 | a0001c0001t0001g0178 a0001c0001t0001g0189 a0001c0001t0002g0146 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-7568dupA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100621862 | ||||||
| chr15:100621870 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(306): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.212-7567G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621870 | |||||||
| chr15:100621953 | C | G | 5 | a0001c0001t0002g0012 a0001c0001t0004g0161 a0001c0001t0006g0057 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-7484C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100621953 | |||||||
| chr15:100622112 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.212-7325A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622112 | |||||||
| chr15:100622179 | G | C | 4 | a0001c0001t0001g0277 a0001c0001t0008g0164 a0001c0001t0009g0032 others(1): Show |
5 | HG03225.hp1 NA18940.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-7258G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622179 | |||||||
| chr15:100622200 | C | CAAAAAGA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(82): Show |
99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.212-7224_212-7218d others(9): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100622200 | ||||||
| chr15:100622200 | C | CAAAAAGA others(7): Show |
224 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(221): Show |
258 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.212-7231_212-7218d others(16): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100622200 | ||||||
| chr15:100622302 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.212-7135C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622302 | |||||||
| chr15:100622440 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0266 |
3 | NA18947.hp1 NA18951.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.212-6997A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622440 | |||||||
| chr15:100622500 | G | C | 1 | a0001c0001t0002g0199 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.212-6937G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622500 | |||||||
| chr15:100622639 | C | G | 1 | a0001c0001t0003g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.212-6798C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622639 | |||||||
| chr15:100622896 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.212-6541C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622896 | |||||||
| chr15:100622966 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.212-6471G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622966 | |||||||
| chr15:100622976 | CAATT | C | 4 | a0001c0001t0001g0194 a0001c0001t0001g0263 a0001c0001t0003g0260 others(1): Show |
4 | HG01255.hp1 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-6457_212-6454d others(6): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100622976 | ||||||
| chr15:100622998 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(306): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.212-6439G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100622998 | |||||||
| chr15:100623325 | C | T | 87 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(84): Show |
99 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.212-6112C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623325 | |||||||
| chr15:100623545 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.212-5892C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623545 | |||||||
| chr15:100623705 | A | G | 3 | a0001c0001t0002g0062 a0001c0001t0002g0163 a0001c0001t0002g0200 |
3 | HG02109.hp2 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.212-5732A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623705 | |||||||
| chr15:100623761 | A | C | 1 | a0001c0001t0002g0208 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.212-5676A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623761 | |||||||
| chr15:100623848 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-5589C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623848 | |||||||
| chr15:100623851 | A | G | 86 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(83): Show |
98 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.212-5586A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623851 | |||||||
| chr15:100623858 | A | G | 5 | a0001c0001t0001g0088 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG02132.hp1 NA18979.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-5579A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623858 | |||||||
| chr15:100623954 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0192 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-5483G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623954 | |||||||
| chr15:100623955 | G | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0141 a0001c0001t0001g0192 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-5482G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100623955 | |||||||
| chr15:100624002 | C | A | 1 | a0001c0001t0003g0174 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.212-5435C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624002 | |||||||
| chr15:100624137 | A | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-5300A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624137 | |||||||
| chr15:100624145 | G | A | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-5292G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624145 | |||||||
| chr15:100624300 | G | T | 1 | a0001c0001t0012g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.212-5137G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624300 | |||||||
| chr15:100624336 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-5101G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624336 | |||||||
| chr15:100624356 | A | T | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-5081A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624356 | |||||||
| chr15:100624357 | C | T | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-5080C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624357 | |||||||
| chr15:100624358 | G | A | 8 | a0001c0001t0002g0199 a0001c0001t0002g0236 a0001c0001t0002g0252 others(5): Show |
9 | HG01891.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-5079G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624358 | |||||||
| chr15:100624367 | C | T | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-5070C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624367 | |||||||
| chr15:100624396 | G | A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(83): Show |
98 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.212-5041G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624396 | |||||||
| chr15:100624475 | A | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-4962A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624475 | |||||||
| chr15:100624543 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-4894A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624543 | |||||||
| chr15:100624663 | A | G | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-4774A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624663 | |||||||
| chr15:100624771 | T | C | 9 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0236 others(6): Show |
10 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-4666T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624771 | |||||||
| chr15:100624807 | C | T | 5 | a0001c0001t0002g0012 a0001c0001t0004g0161 a0001c0001t0006g0057 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-4630C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624807 | |||||||
| chr15:100624828 | A | G | 4 | a0001c0001t0001g0178 a0001c0001t0002g0171 a0001c0001t0002g0185 others(1): Show |
4 | HG02280.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-4609A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624828 | |||||||
| chr15:100624836 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0002g0157 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.212-4601A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624836 | |||||||
| chr15:100624841 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.212-4596T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624841 | |||||||
| chr15:100624858 | C | A | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.212-4579C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624858 | |||||||
| chr15:100624900 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.212-4537G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624900 | |||||||
| chr15:100624903 | T | TA | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.212-4525dupA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100624903 | ||||||
| chr15:100624937 | C | T | 4 | a0001c0001t0002g0070 a0001c0001t0003g0071 a0001c0001t0006g0067 others(1): Show |
4 | HG01106.hp1 HG01167.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-4500C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624937 | |||||||
| chr15:100624993 | C | T | 3 | a0001c0001t0001g0167 a0001c0001t0002g0168 a0001c0001t0013g0091 |
3 | HG02486.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.212-4444C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100624993 | |||||||
| chr15:100625057 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.212-4380A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625057 | |||||||
| chr15:100625130 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.212-4307C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625130 | |||||||
| chr15:100625131 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.212-4306G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625131 | |||||||
| chr15:100625155 | C | A | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-4282C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625155 | |||||||
| chr15:100625261 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(65): Show |
81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.212-4176G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625261 | |||||||
| chr15:100625279 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.212-4158A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625279 | |||||||
| chr15:100625300 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0083 |
2 | NA18995.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.212-4137G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625300 | |||||||
| chr15:100625443 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.212-3994A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625443 | |||||||
| chr15:100625464 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.212-3973A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100625464 | |||||||
| chr15:100626086 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.212-3351G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626086 | |||||||
| chr15:100626273 | G | A | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.212-3164G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626273 | |||||||
| chr15:100626301 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.212-3136A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626301 | |||||||
| chr15:100626331 | A | G | 1 | a0001c0001t0012g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.212-3106A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626331 | |||||||
| chr15:100626355 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0234 |
2 | NA18967.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.212-3082G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626355 | |||||||
| chr15:100626520 | A | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-2917A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626520 | |||||||
| chr15:100626637 | CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.212-2790_212-2777d others(16): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100626637 | ||||||
| chr15:100626863 | A | G | 5 | a0001c0001t0002g0070 a0001c0001t0003g0071 a0001c0001t0006g0067 others(2): Show |
5 | HG01074.hp1 HG01106.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-2574A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626863 | |||||||
| chr15:100626878 | T | C | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-2559T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626878 | |||||||
| chr15:100626886 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-2551C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626886 | |||||||
| chr15:100626976 | A | G | 1 | a0001c0001t0011g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.212-2461A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626976 | |||||||
| chr15:100626988 | A | G | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.212-2449A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100626988 | |||||||
| chr15:100627089 | GA | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0271 a0001c0001t0001g0277 others(3): Show |
9 | HG02257.hp1 NA18940.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.212-2337delA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100627089 | ||||||
| chr15:100627385 | A | C | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-2052A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627385 | |||||||
| chr15:100627413 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.212-2024T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627413 | |||||||
| chr15:100627418 | G | A | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-2019G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627418 | |||||||
| chr15:100627450 | T | C | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-1987T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627450 | |||||||
| chr15:100627547 | T | C | 3 | a0001c0001t0010g0011 a0001c0001t0010g0151 a0001c0001t0025g0152 |
5 | HG01074.hp2 HG02300.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-1890T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627547 | |||||||
| chr15:100627564 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.212-1873T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627564 | |||||||
| chr15:100627647 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-1790G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627647 | |||||||
| chr15:100627656 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-1781A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627656 | |||||||
| chr15:100627726 | G | A | 5 | a0001c0002t0002g0018 a0001c0002t0002g0037 a0001c0002t0002g0039 others(2): Show |
5 | HG02451.hp1 HG03195.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-1711G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627726 | |||||||
| chr15:100627761 | T | G | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.212-1676T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627761 | |||||||
| chr15:100627779 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0266 |
3 | NA18947.hp1 NA18951.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.212-1658G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627779 | |||||||
| chr15:100627859 | A | G | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-1578A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627859 | |||||||
| chr15:100627864 | GTAGATTT others(6): Show |
G | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-1571_212-1559d others(15): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr15 | 100627864 | ||||||
| chr15:100627939 | C | G | 2 | a0001c0001t0001g0269 a0001c0001t0002g0267 |
2 | NA18967.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.212-1498C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100627939 | |||||||
| chr15:100628178 | A | G | 5 | a0001c0002t0002g0018 a0001c0002t0002g0037 a0001c0002t0002g0039 others(2): Show |
5 | HG02451.hp1 HG03195.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-1259A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628178 | |||||||
| chr15:100628295 | T | C | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-1142T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628295 | |||||||
| chr15:100628578 | G | C | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-859G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628578 | |||||||
| chr15:100628580 | C | T | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-857C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628580 | |||||||
| chr15:100628601 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.212-836G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628601 | |||||||
| chr15:100628643 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.212-794C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628643 | |||||||
| chr15:100628708 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.212-729C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628708 | |||||||
| chr15:100628862 | T | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.212-575T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100628862 | |||||||
| chr15:100629003 | G | C | 1 | a0001c0002t0008g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.212-434G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100629003 | |||||||
| chr15:100629008 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.212-429G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100629008 | |||||||
| chr15:100629009 | C | A | 86 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(83): Show |
98 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.212-428C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100629009 | |||||||
| chr15:100629041 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0004g0120 |
2 | HG01243.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.212-396C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100629041 | |||||||
| chr15:100629181 | G | A | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.212-256G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100629181 | |||||||
| chr15:100629194 | A | G | 78 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(75): Show |
89 | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.212-243A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 4/5 | chr15 | 100629194 | |||||||
| chr15:100630100 | G | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0247 a0001c0001t0001g0248 others(3): Show |
7 | HG00735.hp1 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.817+58G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630100 | |||||||
| chr15:100630104 | A | G | 1 | a0001c0001t0002g0259 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.817+62A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630104 | |||||||
| chr15:100630233 | A | G | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.817+191A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630233 | |||||||
| chr15:100630413 | G | A | 227 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(224): Show |
260 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.817+371G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630413 | |||||||
| chr15:100630472 | C | T | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.817+430C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630472 | |||||||
| chr15:100630522 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.817+480A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630522 | |||||||
| chr15:100630560 | A | G | 311 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.817+518A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630560 | |||||||
| chr15:100630713 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.817+671T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630713 | |||||||
| chr15:100630716 | G | A | 227 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(224): Show |
260 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.817+674G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630716 | |||||||
| chr15:100630726 | G | A | 10 | a0001c0001t0001g0167 a0001c0001t0002g0168 a0001c0001t0002g0191 others(7): Show |
10 | HG02451.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.817+684G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630726 | |||||||
| chr15:100630802 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0156 |
3 | HG00544.hp1 HG02071.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.817+760G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630802 | |||||||
| chr15:100630906 | CCT | C | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+866_817+867del others(2): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100630906 | ||||||
| chr15:100630940 | C | T | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.817+898C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100630940 | |||||||
| chr15:100631022 | C | A | 1 | a0001c0001t0012g0180 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.817+980C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631022 | |||||||
| chr15:100631101 | A | G | 10 | a0001c0001t0001g0167 a0001c0001t0002g0168 a0001c0001t0002g0191 others(7): Show |
10 | HG02451.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.817+1059A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631101 | |||||||
| chr15:100631214 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.817+1172T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631214 | |||||||
| chr15:100631383 | C | G | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.817+1341C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631383 | |||||||
| chr15:100631497 | C | T | 4 | a0001c0001t0001g0081 a0001c0001t0001g0188 a0001c0001t0001g0294 others(1): Show |
4 | HG00621.hp2 NA18983.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+1455C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631497 | |||||||
| chr15:100631521 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.817+1479C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631521 | |||||||
| chr15:100631523 | A | G | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.817+1481A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631523 | |||||||
| chr15:100631560 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0002g0033 a0001c0001t0002g0278 |
4 | HG02559.hp2 HG03516.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+1518C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631560 | |||||||
| chr15:100631683 | T | G | 1 | a0001c0001t0001g0299 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.817+1641T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631683 | |||||||
| chr15:100631845 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.817+1803C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631845 | |||||||
| chr15:100631849 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(306): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.817+1807G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100631849 | |||||||
| chr15:100632003 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0163 a0001c0001t0002g0200 |
3 | HG02109.hp2 HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.817+1961C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632003 | |||||||
| chr15:100632009 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817+1967C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632009 | |||||||
| chr15:100632043 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(63): Show |
78 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.817+2001C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632043 | |||||||
| chr15:100632053 | G | A | 232 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(229): Show |
265 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(262): Show |
intron_variant | MODIFIER | c.817+2011G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632053 | |||||||
| chr15:100632079 | C | G | 4 | a0001c0001t0001g0269 a0001c0001t0002g0125 a0001c0001t0002g0146 others(1): Show |
4 | HG02976.hp2 NA18967.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+2037C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632079 | |||||||
| chr15:100632125 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.817+2083T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632125 | |||||||
| chr15:100632386 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.817+2344C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632386 | |||||||
| chr15:100632520 | G | A | 227 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(224): Show |
260 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.817+2478G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632520 | |||||||
| chr15:100632577 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.817+2535A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632577 | |||||||
| chr15:100632597 | G | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0263 a0001c0001t0003g0260 others(1): Show |
4 | HG01255.hp1 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+2555G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632597 | |||||||
| chr15:100632616 | C | T | 4 | a0001c0001t0002g0016 a0001c0001t0004g0017 a0001c0001t0013g0148 others(1): Show |
6 | HG01167.hp2 HG01169.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.817+2574C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632616 | |||||||
| chr15:100632622 | C | A | 4 | a0001c0001t0001g0269 a0001c0001t0002g0125 a0001c0001t0002g0146 others(1): Show |
4 | HG02976.hp2 NA18967.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+2580C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632622 | |||||||
| chr15:100632655 | A | G | 27 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0056 others(24): Show |
33 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.817+2613A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632655 | |||||||
| chr15:100632832 | G | A | 1 | a0001c0001t0007g0130 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.817+2790G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632832 | |||||||
| chr15:100632856 | C | CA | 5 | a0001c0001t0001g0248 a0001c0001t0001g0277 a0001c0001t0002g0199 others(2): Show |
6 | HG02145.hp1 HG02572.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+2830dupA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100632856 | ||||||
| chr15:100632856 | C | CAA | 6 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(3): Show |
6 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.817+2829_817+2830d others(4): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100632856 | ||||||
| chr15:100632860 | A | AAC | 8 | a0001c0001t0001g0269 a0001c0001t0001g0284 a0001c0001t0001g0299 others(5): Show |
8 | HG02976.hp2 HG03927.hp2 HG03942.hp1 others(5): Show |
intron_variant | MODIFIER | c.817+2819_817+2820i others(4): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100632860 | ||||||
| chr15:100632861 | A | AC | 218 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(215): Show |
251 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.817+2819_817+2820i others(3): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632861 | |||||||
| chr15:100632973 | A | G | 8 | a0001c0001t0002g0149 a0001c0001t0002g0209 a0001c0001t0004g0009 others(5): Show |
12 | HG01496.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.817+2931A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100632973 | |||||||
| chr15:100633034 | C | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.817+2992C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633034 | |||||||
| chr15:100633046 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.817+3004C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633046 | |||||||
| chr15:100633093 | C | T | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+3051C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633093 | |||||||
| chr15:100633111 | C | T | 1 | a0001c0006t0002g0019 | 2 | HG00733.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.817+3069C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633111 | |||||||
| chr15:100633209 | C | CA | 13 | a0001c0001t0001g0045 a0001c0001t0001g0186 a0001c0001t0001g0190 others(10): Show |
15 | HG01981.hp1 HG02257.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.817+3183dupA | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100633209 | ||||||
| chr15:100633269 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.817+3227C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633269 | |||||||
| chr15:100633285 | T | C | 1 | a0001c0001t0002g0280 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.817+3243T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633285 | |||||||
| chr15:100633342 | T | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(67): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.817+3300T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633342 | |||||||
| chr15:100633347 | C | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0008 others(220): Show |
256 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.817+3305C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633347 | |||||||
| chr15:100633411 | T | C | 1 | a0001c0001t0003g0169 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.817+3369T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633411 | |||||||
| chr15:100633583 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0223 a0001c0001t0001g0232 |
3 | NA18942.hp2 NA18957.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.817+3541A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633583 | |||||||
| chr15:100633616 | GGAAA | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0247 others(4): Show |
8 | HG00735.hp1 HG01099.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.817+3580_817+3583d others(6): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100633616 | ||||||
| chr15:100633645 | AGAAGGAA others(8): Show |
A | 6 | a0001c0001t0001g0006 a0001c0001t0002g0201 a0001c0001t0006g0060 others(3): Show |
6 | HG01069.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+3631_817+3645d others(17): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100633645 | ||||||
| chr15:100633674 | AGGAAGGA others(6): Show |
A | 1 | a0001c0001t0003g0254 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.817+3646_817+3658d others(15): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100633674 | ||||||
| chr15:100633687 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0189 |
2 | NA18950.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.817+3645G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633687 | |||||||
| chr15:100633916 | C | G | 1 | a0001c0001t0002g0051 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.817+3874C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100633916 | |||||||
| chr15:100634071 | C | G | 1 | a0001c0001t0001g0268 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.817+4029C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100634071 | |||||||
| chr15:100634319 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0002g0125 a0001c0001t0002g0146 others(1): Show |
4 | HG02976.hp2 NA18967.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+4277G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100634319 | |||||||
| chr15:100634396 | T | C | 3 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0001t0003g0289 |
3 | HG00609.hp1 HG00673.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.817+4354T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100634396 | |||||||
| chr15:100634473 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.817+4431C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100634473 | |||||||
| chr15:100634621 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.817+4579T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100634621 | |||||||
| chr15:100634632 | C | T | 4 | a0001c0001t0001g0269 a0001c0001t0002g0125 a0001c0001t0002g0146 others(1): Show |
4 | HG02976.hp2 NA18967.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+4590C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100634632 | |||||||
| chr15:100634866 | G | T | 3 | a0001c0001t0002g0185 a0001c0001t0021g0184 a0001c0006t0002g0019 |
4 | HG00733.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+4824G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100634866 | |||||||
| chr15:100635058 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.817+5016G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635058 | |||||||
| chr15:100635128 | G | A | 111 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0028 others(108): Show |
128 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.817+5086G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635128 | |||||||
| chr15:100635173 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.817+5131A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635173 | |||||||
| chr15:100635204 | A | G | 1 | a0001c0001t0008g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.817+5162A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635204 | |||||||
| chr15:100635266 | A | T | 1 | a0001c0001t0011g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.817+5224A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635266 | |||||||
| chr15:100635284 | T | C | 5 | a0001c0001t0002g0012 a0001c0001t0004g0161 a0001c0001t0006g0057 others(2): Show |
7 | HG02257.hp1 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.817+5242T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635284 | |||||||
| chr15:100635393 | G | T | 2 | a0001c0001t0002g0209 a0001c0001t0004g0035 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.817+5351G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635393 | |||||||
| chr15:100635570 | T | A | 2 | a0001c0001t0001g0167 a0001c0001t0002g0168 |
2 | HG02486.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.817+5528T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635570 | |||||||
| chr15:100635631 | C | T | 3 | a0001c0001t0001g0277 a0001c0001t0009g0032 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+5589C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635631 | |||||||
| chr15:100635652 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.817+5610C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635652 | |||||||
| chr15:100635846 | C | T | 18 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0063 others(15): Show |
21 | HG00735.hp1 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.817+5804C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635846 | |||||||
| chr15:100635891 | T | G | 15 | a0001c0001t0001g0038 a0001c0001t0001g0063 a0001c0001t0001g0247 others(12): Show |
17 | HG00735.hp1 HG01099.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.817+5849T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635891 | |||||||
| chr15:100635990 | C | T | 3 | a0001c0001t0002g0185 a0001c0001t0021g0184 a0001c0006t0002g0019 |
4 | HG00733.hp2 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+5948C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100635990 | |||||||
| chr15:100636130 | T | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0013 others(68): Show |
84 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.817+6088T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636130 | |||||||
| chr15:100636327 | A | G | 5 | a0001c0001t0002g0201 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+6285A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636327 | |||||||
| chr15:100636482 | A | C | 302 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(299): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.817+6440A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636482 | |||||||
| chr15:100636569 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.817+6527G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636569 | |||||||
| chr15:100636784 | C | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(293): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.817+6742C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636784 | |||||||
| chr15:100636897 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0255 |
2 | HG00438.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.817+6855G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636897 | |||||||
| chr15:100636920 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.817+6878A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636920 | |||||||
| chr15:100636953 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0002g0168 a0001c0001t0013g0091 |
3 | HG02486.hp1 HG02615.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.817+6911G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636953 | |||||||
| chr15:100636977 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.817+6935C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636977 | |||||||
| chr15:100636998 | G | A | 1 | a0001c0001t0003g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.817+6956G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100636998 | |||||||
| chr15:100637021 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(76): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.817+6979A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100637021 | |||||||
| chr15:100637122 | G | A | 4 | a0001c0001t0001g0167 a0001c0001t0002g0168 a0001c0001t0002g0191 others(1): Show |
4 | HG02486.hp1 HG02615.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+7080G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100637122 | |||||||
| chr15:100637198 | C | T | 1 | a0001c0001t0005g0304 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.817+7156C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100637198 | |||||||
| chr15:100637309 | G | T | 5 | a0001c0001t0002g0199 a0001c0001t0002g0236 a0001c0001t0002g0252 others(2): Show |
5 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+7267G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100637309 | |||||||
| chr15:100637544 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.817+7502C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100637544 | |||||||
| chr15:100637644 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.817+7602G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100637644 | |||||||
| chr15:100637854 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0271 |
4 | NA18946.hp2 NA18949.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+7812A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100637854 | |||||||
| chr15:100637952 | G | GCTCTTTT others(311): Show |
4 | a0001c0001t0002g0267 a0001c0001t0003g0287 a0001c0001t0003g0288 others(1): Show |
4 | HG00609.hp1 HG00673.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+7926_817+7927i others(320): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100637952 | ||||||
| chr15:100637955 | C | CT | 14 | a0001c0001t0001g0038 a0001c0001t0001g0277 a0001c0001t0002g0033 others(11): Show |
16 | HG01099.hp1 HG01106.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.817+7926dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100637955 | ||||||
| chr15:100637955 | C | CTTTTTTT others(312): Show |
1 | a0001c0001t0002g0146 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.817+7926_817+7927i others(321): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100637955 | ||||||
| chr15:100637955 | C | CTTTTTTT others(313): Show |
1 | a0001c0001t0002g0125 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.817+7926_817+7927i others(322): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100637955 | ||||||
| chr15:100638034 | A | C | 1 | a0001c0001t0001g0167 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.817+7992A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638034 | |||||||
| chr15:100638281 | T | C | 1 | a0001c0001t0006g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.817+8239T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638281 | |||||||
| chr15:100638289 | T | C | 313 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(310): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.817+8247T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638289 | |||||||
| chr15:100638376 | G | A | 5 | a0001c0001t0002g0185 a0001c0001t0006g0060 a0001c0001t0014g0202 others(2): Show |
5 | HG02886.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+8334G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638376 | |||||||
| chr15:100638487 | T | C | 1 | a0001c0001t0001g0043 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.817+8445T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638487 | |||||||
| chr15:100638571 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0002g0103 a0001c0001t0002g0116 others(1): Show |
4 | NA18969.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.817+8529C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638571 | |||||||
| chr15:100638575 | C | T | 1 | a0001c0001t0003g0095 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.817+8533C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638575 | |||||||
| chr15:100638593 | G | A | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+8551G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638593 | |||||||
| chr15:100638595 | G | T | 1 | a0001c0001t0002g0168 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.817+8553G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638595 | |||||||
| chr15:100638636 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.817+8594G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638636 | |||||||
| chr15:100638671 | C | T | 5 | a0001c0001t0004g0017 a0001c0001t0004g0035 a0001c0001t0004g0092 others(2): Show |
6 | HG02055.hp1 HG02647.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.817+8629C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638671 | |||||||
| chr15:100638711 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817+8669A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638711 | |||||||
| chr15:100638768 | C | T | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+8726C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638768 | |||||||
| chr15:100638838 | C | T | 2 | a0001c0001t0009g0032 a0001c0001t0009g0276 |
3 | NA18940.hp1 NA18965.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.817+8796C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638838 | |||||||
| chr15:100638865 | T | C | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+8823T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638865 | |||||||
| chr15:100638889 | T | G | 5 | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0108 others(2): Show |
5 | HG00597.hp2 NA18966.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.817+8847T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638889 | |||||||
| chr15:100638957 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0021g0184 |
2 | HG02886.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.817+8915G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638957 | |||||||
| chr15:100638964 | G | C | 3 | a0001c0001t0002g0033 a0001c0001t0002g0119 a0001c0001t0002g0278 |
4 | HG01243.hp2 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.817+8922G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100638964 | |||||||
| chr15:100639037 | G | T | 2 | a0001c0001t0001g0299 a0001c0001t0003g0117 |
2 | HG02004.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.817+8995G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100639037 | |||||||
| chr15:100639204 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.818-9119G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100639204 | |||||||
| chr15:100639437 | C | CT | 6 | a0001c0001t0002g0016 a0001c0001t0002g0171 a0001c0001t0002g0185 others(3): Show |
7 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.818-8877dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100639437 | ||||||
| chr15:100639615 | C | T | 5 | a0001c0001t0011g0134 a0001c0001t0011g0147 a0001c0001t0011g0165 others(2): Show |
5 | HG01884.hp1 HG01884.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-8708C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100639615 | |||||||
| chr15:100639827 | A | G | 1 | a0001c0004t0008g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.818-8496A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100639827 | |||||||
| chr15:100640410 | G | T | 1 | a0001c0001t0002g0113 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.818-7913G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640410 | |||||||
| chr15:100640426 | G | C | 4 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 others(1): Show |
5 | HG02886.hp2 NA18940.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-7897G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640426 | |||||||
| chr15:100640446 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.818-7877A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640446 | |||||||
| chr15:100640556 | C | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0228 |
3 | HG00558.hp2 NA18953.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.818-7767C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640556 | |||||||
| chr15:100640568 | A | G | 48 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0031 others(45): Show |
56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.818-7755A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640568 | |||||||
| chr15:100640619 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.818-7704C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640619 | |||||||
| chr15:100640728 | C | CAAAT | 4 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 others(1): Show |
5 | HG02886.hp2 NA18940.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-7592_818-7589d others(6): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100640728 | ||||||
| chr15:100640731 | A | G | 2 | a0001c0001t0013g0091 a0001c0001t0013g0148 |
2 | HG02818.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.818-7592A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640731 | |||||||
| chr15:100640811 | C | T | 1 | a0001c0001t0007g0068 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.818-7512C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640811 | |||||||
| chr15:100640926 | C | A | 1 | a0001c0001t0002g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.818-7397C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100640926 | |||||||
| chr15:100641021 | A | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
195 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.818-7302A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641021 | |||||||
| chr15:100641040 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.818-7283C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641040 | |||||||
| chr15:100641083 | T | G | 1 | a0001c0001t0002g0272 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.818-7240T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641083 | |||||||
| chr15:100641086 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.818-7237C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641086 | |||||||
| chr15:100641098 | GAATT | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(305): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.818-7220_818-7217d others(6): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100641098 | ||||||
| chr15:100641128 | G | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0119 a0001c0001t0002g0278 |
4 | HG01243.hp2 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-7195G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641128 | |||||||
| chr15:100641185 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.818-7138T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641185 | |||||||
| chr15:100641248 | T | C | 2 | a0001c0001t0002g0012 a0001c0001t0006g0057 |
4 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-7075T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641248 | |||||||
| chr15:100641428 | C | G | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.818-6895C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641428 | |||||||
| chr15:100641785 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.818-6538T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641785 | |||||||
| chr15:100641835 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0190 |
2 | HG01981.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.818-6488G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641835 | |||||||
| chr15:100641874 | G | A | 4 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 others(1): Show |
5 | HG03209.hp2 NA18940.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-6449G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641874 | |||||||
| chr15:100641897 | T | C | 15 | a0001c0001t0002g0158 a0001c0001t0002g0179 a0001c0001t0002g0181 others(12): Show |
18 | HG01106.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
intron_variant | MODIFIER | c.818-6426T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641897 | |||||||
| chr15:100641925 | C | T | 2 | a0001c0001t0003g0071 a0001c0001t0025g0152 |
2 | HG01074.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.818-6398C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641925 | |||||||
| chr15:100641978 | G | C | 1 | a0001c0002t0002g0039 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.818-6345G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100641978 | |||||||
| chr15:100642015 | A | G | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-6308A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642015 | |||||||
| chr15:100642040 | T | C | 11 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0017 others(8): Show |
16 | HG01496.hp2 HG02055.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.818-6283T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642040 | |||||||
| chr15:100642083 | A | G | 1 | a0001c0001t0012g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.818-6240A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642083 | |||||||
| chr15:100642219 | A | ATAACTTG others(9): Show |
1 | a0001c0001t0003g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.818-6101_818-6086d others(18): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100642219 | ||||||
| chr15:100642240 | A | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
188 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.818-6083A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642240 | |||||||
| chr15:100642296 | A | T | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-6027A>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642296 | |||||||
| chr15:100642394 | A | G | 1 | a0001c0001t0004g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.818-5929A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642394 | |||||||
| chr15:100642519 | G | C | 1 | a0001c0001t0001g0027 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.818-5804G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642519 | |||||||
| chr15:100642604 | AG | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
186 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.818-5717delG | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100642604 | ||||||
| chr15:100642622 | C | A | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-5701C>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642622 | |||||||
| chr15:100642647 | A | C | 3 | a0001c0001t0002g0033 a0001c0001t0002g0119 a0001c0001t0002g0278 |
4 | HG01243.hp2 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-5676A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642647 | |||||||
| chr15:100642675 | T | C | 1 | a0001c0001t0006g0067 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.818-5648T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642675 | |||||||
| chr15:100642690 | C | T | 3 | a0001c0001t0002g0033 a0001c0001t0002g0119 a0001c0001t0002g0278 |
4 | HG01243.hp2 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-5633C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642690 | |||||||
| chr15:100642727 | C | T | 4 | a0001c0001t0008g0164 a0001c0002t0008g0036 a0001c0004t0008g0023 others(1): Show |
5 | HG02055.hp2 HG02970.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.818-5596C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642727 | |||||||
| chr15:100642763 | G | A | 1 | a0001c0001t0021g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.818-5560G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642763 | |||||||
| chr15:100642764 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.818-5559C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642764 | |||||||
| chr15:100642802 | C | T | 54 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0031 others(51): Show |
62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.818-5521C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642802 | |||||||
| chr15:100642815 | T | A | 26 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0077 others(23): Show |
26 | HG00408.hp1 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.818-5508T>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642815 | |||||||
| chr15:100642998 | T | C | 2 | a0001c0001t0014g0202 a0001c0001t0014g0203 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.818-5325T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100642998 | |||||||
| chr15:100643084 | G | A | 41 | a0001c0001t0001g0111 a0001c0001t0002g0003 a0001c0001t0002g0012 others(38): Show |
46 | HG00280.hp2 HG00597.hp1 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.818-5239G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643084 | |||||||
| chr15:100643429 | A | G | 1 | a0001c0001t0003g0289 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.818-4894A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643429 | |||||||
| chr15:100643469 | C | G | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-4854C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643469 | |||||||
| chr15:100643474 | C | CT | 5 | a0001c0001t0002g0016 a0001c0001t0002g0171 a0001c0001t0002g0185 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.818-4847dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100643474 | ||||||
| chr15:100643477 | C | CT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0048 others(20): Show |
24 | HG00639.hp2 HG01069.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.818-4820dupT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100643477 | ||||||
| chr15:100643477 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0006g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.818-4829_818-4820d others(12): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100643477 | ||||||
| chr15:100643477 | C | T | 6 | a0001c0001t0002g0016 a0001c0001t0002g0171 a0001c0001t0002g0185 others(3): Show |
7 | HG01167.hp2 HG01169.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.818-4846C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643477 | |||||||
| chr15:100643477 | CT | C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0255 a0001c0001t0001g0299 others(16): Show |
23 | HG01069.hp1 HG01081.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.818-4820delT | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100643477 | ||||||
| chr15:100643477 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-4834_818-4820d others(17): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100643477 | ||||||
| chr15:100643480 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0027 a0001c0001t0001g0196 others(2): Show |
8 | HG00733.hp1 HG01109.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.818-4843T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643480 | |||||||
| chr15:100643524 | C | G | 1 | a0001c0001t0001g0312 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.818-4799C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643524 | |||||||
| chr15:100643559 | G | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0119 a0001c0001t0002g0278 |
4 | HG01243.hp2 HG02559.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-4764G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643559 | |||||||
| chr15:100643695 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.818-4628A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643695 | |||||||
| chr15:100643701 | G | A | 6 | a0001c0001t0002g0051 a0001c0001t0002g0199 a0001c0001t0002g0200 others(3): Show |
7 | HG00733.hp2 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.818-4622G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643701 | |||||||
| chr15:100643735 | C | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0031 others(75): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.818-4588C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643735 | |||||||
| chr15:100643750 | C | T | 1 | a0001c0001t0002g0109 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.818-4573C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643750 | |||||||
| chr15:100643972 | G | A | 1 | a0001c0001t0021g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.818-4351G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643972 | |||||||
| chr15:100643977 | G | A | 4 | a0001c0001t0002g0236 a0001c0001t0002g0252 a0001c0001t0006g0054 others(1): Show |
4 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.818-4346G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100643977 | |||||||
| chr15:100644224 | G | T | 3 | a0001c0001t0001g0063 a0001c0001t0007g0058 a0001c0001t0007g0059 |
3 | HG00735.hp1 HG02257.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.818-4099G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100644224 | |||||||
| chr15:100644414 | AG | A | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-3908delG | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100644414 | |||||||
| chr15:100644418 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0242 a0001c0001t0001g0246 |
4 | NA18943.hp2 NA18951.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.818-3905G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100644418 | |||||||
| chr15:100644496 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0001g0302 |
2 | NA18956.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.818-3827C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100644496 | |||||||
| chr15:100644557 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.818-3766G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100644557 | |||||||
| chr15:100644820 | G | A | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-3503G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100644820 | |||||||
| chr15:100644827 | AGT | A | 130 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0031 others(127): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.818-3485_818-3484d others(4): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100644827 | ||||||
| chr15:100645232 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.818-3091T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645232 | |||||||
| chr15:100645307 | A | C | 2 | a0001c0001t0002g0168 a0001c0001t0002g0274 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.818-3016A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645307 | |||||||
| chr15:100645312 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0002g0191 |
2 | HG03669.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.818-3011T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645312 | |||||||
| chr15:100645415 | T | C | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-2908T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645415 | |||||||
| chr15:100645428 | C | G | 1 | a0001c0001t0023g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.818-2895C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645428 | |||||||
| chr15:100645428 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.818-2895C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645428 | |||||||
| chr15:100645471 | C | G | 1 | a0001c0001t0006g0067 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.818-2852C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645471 | |||||||
| chr15:100645570 | A | G | 3 | a0001c0001t0012g0153 a0001c0001t0012g0180 a0001c0001t0012g0264 |
3 | HG02451.hp2 HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.818-2753A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645570 | |||||||
| chr15:100645793 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.818-2530T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100645793 | |||||||
| chr15:100646080 | A | G | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-2243A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646080 | |||||||
| chr15:100646105 | G | A | 127 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0031 others(124): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.818-2218G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646105 | |||||||
| chr15:100646126 | A | G | 1 | a0001c0001t0001g0007 | 3 | HG00280.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.818-2197A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646126 | |||||||
| chr15:100646334 | C | G | 1 | a0001c0001t0002g0272 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.818-1989C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646334 | |||||||
| chr15:100646428 | G | T | 127 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0031 others(124): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.818-1895G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646428 | |||||||
| chr15:100646435 | T | G | 3 | a0001c0001t0011g0134 a0001c0001t0011g0147 a0001c0001t0011g0165 |
3 | HG01884.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.818-1888T>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646435 | |||||||
| chr15:100646566 | A | C | 1 | a0001c0001t0003g0154 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.818-1757A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646566 | |||||||
| chr15:100646629 | G | T | 41 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0034 others(38): Show |
47 | HG00280.hp2 HG00597.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.818-1694G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646629 | |||||||
| chr15:100646718 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.818-1605G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646718 | |||||||
| chr15:100646814 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.818-1509C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646814 | |||||||
| chr15:100646829 | A | G | 1 | a0001c0001t0021g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.818-1494A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100646829 | |||||||
| chr15:100647018 | C | CATT | 4 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0131 others(1): Show |
4 | HG01192.hp2 HG01261.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-1305_818-1304i others(5): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647018 | |||||||
| chr15:100647019 | G | C | 4 | a0001c0001t0002g0109 a0001c0001t0002g0110 a0001c0001t0002g0131 others(1): Show |
4 | HG01192.hp2 HG01261.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-1304G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647019 | |||||||
| chr15:100647019 | G | GTTC | 300 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(297): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.818-1301_818-1299d others(5): Show |
ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr15 | 100647019 | ||||||
| chr15:100647196 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.818-1127G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647196 | |||||||
| chr15:100647198 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0160 a0001c0001t0002g0101 others(2): Show |
6 | HG01891.hp2 HG02257.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.818-1125T>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647198 | |||||||
| chr15:100647199 | C | T | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-1124C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647199 | |||||||
| chr15:100647201 | C | T | 4 | a0001c0001t0008g0164 a0001c0002t0008g0036 a0001c0004t0008g0023 others(1): Show |
5 | HG02055.hp2 HG02970.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.818-1122C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647201 | |||||||
| chr15:100647235 | A | C | 304 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(301): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.818-1088A>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647235 | |||||||
| chr15:100647327 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.818-996G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647327 | |||||||
| chr15:100647523 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0227 |
3 | NA18942.hp1 NA18960.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.818-800A>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647523 | |||||||
| chr15:100647611 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.818-712G>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100647611 | |||||||
| chr15:100648091 | G | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0016 others(77): Show |
93 | HG00280.hp2 HG00597.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.818-232G>C | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100648091 | |||||||
| chr15:100648124 | C | T | 4 | a0001c0001t0002g0062 a0001c0001t0002g0146 a0001c0001t0002g0163 others(1): Show |
4 | HG02895.hp1 HG02976.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.818-199C>T | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100648124 | |||||||
| chr15:100648135 | C | G | 312 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(309): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.818-188C>G | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100648135 | |||||||
| chr15:100648227 | G | A | 1 | a0001c0001t0005g0279 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.818-96G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100648227 | |||||||
| chr15:100648288 | G | A | 3 | a0001c0001t0009g0032 a0001c0001t0009g0089 a0001c0001t0009g0276 |
4 | NA18940.hp1 NA18965.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-35G>A | ASB7 | ENSG00000183475.13 | transcript | ENST00000332783.12 | protein_coding | 5/5 | chr15 | 100648288 |