Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 683 |
| ensemblid | ENSG00000109743.11 |
| hgncid | 1118 |
| symbol | BST1 |
| name | bone marrow stromal cell antigen 1 |
| refseq_nuc | NM_004334.3 |
| refseq_prot | NP_004325.2 |
| ensembl_nuc | ENST00000265016.9 |
| ensembl_prot | ENSP00000265016.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 15703065 |
| end | 15732787 |
| strand | + |
| ver | v1.2 |
| region | chr4:15703065-15732787 |
| region5000 | chr4:15698065-15737787 |
| regionname0 | BST1_chr4_15703065_15732787 |
| regionname5000 | BST1_chr4_15698065_15737787 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 318 | 286 | 68 | 55 | 115 | 9 | 38 | 90 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0002 | 0/0 | 318 | 58 | 6 | 1 | 47 | 0 | 4 | 36 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0003 | 0/0 | 318 | 44 | 1 | 5 | 36 | 0 | 2 | 26 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0004 | 0/1 | 318 | 25 | 0 | 8 | 11 | 5 | 0 | 11 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0005 | 0/0 | 318 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0006 | 0/0 | 318 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0007 | 0/0 | 318 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0008 | 0/0 | 318 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0009 | 0/0 | 318 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0010 | 0/0 | 318 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0011 | 0/0 | 318 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| a0012 | 0/0 | 318 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | MAAQG others(313): Show |
chr4 | 15698065 | 15737787 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 954 | 243 | 56 | 53 | 86 | 9 | 38 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0001c0004 | 0/0 | 954 | 34 | 3 | 2 | 29 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0001c0010 | 0/0 | 954 | 4 | 4 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0001c0013 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0001c0015 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0001c0022 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0001c0025 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0002c0002 | 0/0 | 954 | 47 | 5 | 1 | 37 | 0 | 4 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0002c0007 | 0/0 | 954 | 9 | 1 | 0 | 8 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0002c0019 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0002c0020 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0003c0003 | 0/0 | 954 | 40 | 1 | 4 | 33 | 0 | 2 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0003c0009 | 0/0 | 954 | 4 | 0 | 1 | 3 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0004c0005 | 0/1 | 954 | 24 | 0 | 8 | 10 | 5 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0004c0017 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0005c0006 | 0/0 | 954 | 10 | 9 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0006c0008 | 0/0 | 954 | 7 | 7 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0006c0011 | 0/0 | 954 | 3 | 3 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0007c0014 | 0/0 | 954 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0007c0024 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0008c0012 | 0/0 | 954 | 2 | 0 | 0 | 1 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0009c0023 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0010c0021 | 0/0 | 954 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0011c0018 | 0/0 | 954 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 | ||
| a0012c0016 | 0/0 | 954 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATGGC others(949): Show |
chr4 | 15698065 | 15737787 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1979 | 238 | 54 | 50 | 86 | 9 | 38 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0001t0004 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0001t0005 | 0/0 | 1979 | 2 | 0 | 2 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0001t0006 | 0/0 | 1979 | 2 | 1 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0004t0001 | 0/0 | 1979 | 17 | 1 | 2 | 14 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0004t0002 | 0/0 | 1979 | 16 | 2 | 0 | 14 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0004t0007 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0010t0001 | 0/0 | 1979 | 4 | 4 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0013t0001 | 0/0 | 1979 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0015t0001 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0022t0001 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0001c0025t0008 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0002t0001 | 0/0 | 1979 | 44 | 5 | 1 | 34 | 0 | 4 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0002t0007 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0002t0009 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0002t0011 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0007t0001 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0007t0002 | 0/0 | 1979 | 8 | 0 | 0 | 8 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0019t0001 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0002c0020t0001 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0003c0003t0002 | 0/0 | 1979 | 40 | 1 | 4 | 33 | 0 | 2 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0003c0009t0001 | 0/0 | 1979 | 4 | 0 | 1 | 3 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0004c0005t0001 | 0/1 | 1979 | 21 | 0 | 7 | 10 | 3 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0004c0005t0003 | 0/0 | 1979 | 3 | 0 | 1 | 0 | 2 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0004c0017t0002 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0005c0006t0001 | 0/0 | 1979 | 10 | 9 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0006c0008t0001 | 0/0 | 1979 | 6 | 6 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0006c0008t0010 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0006c0011t0001 | 0/0 | 1979 | 3 | 3 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0007c0014t0001 | 0/0 | 1979 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0007c0024t0001 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0008c0012t0001 | 0/0 | 1979 | 2 | 0 | 0 | 1 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0009c0023t0001 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0010c0021t0004 | 0/0 | 1979 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0011c0018t0001 | 0/0 | 1979 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| a0012c0016t0001 | 0/0 | 1979 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | ATCAG others(1974): Show |
chr4 | 15698065 | 15737787 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 1 | 6 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0023 | 1/0 | 3 | 0 | 0 | 0 | 2 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0055 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0005g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0001t0006g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0065 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0004t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0010t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0010t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0013t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0013t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0015t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0022t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0001c0025t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0009g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0002t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0007t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0007t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0007t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0007t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0007t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0007t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0019t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0002c0020t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0003t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0009t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0009t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0009t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0003c0009t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0005t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0004c0017t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0005c0006t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0008t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0008t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0008t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0008t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0008t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0011t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0011t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0006c0011t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0007c0014t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0007c0014t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0007c0024t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0008c0012t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0008c0012t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0009c0023t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0010c0021t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0011c0018t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| a0012c0016t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | GBR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00099 | hp2 | a0004 | c0005 | t0001 | g0090 | EUR | GBR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | FIN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00423 | hp2 | a0003 | c0003 | t0002 | g0079 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0026 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00544 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00558 | hp2 | a0003 | c0003 | t0002 | g0030 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00597 | hp1 | a0003 | c0003 | t0002 | g0108 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00609 | hp1 | a0003 | c0003 | t0002 | g0082 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00621 | hp1 | a0002 | c0020 | t0001 | g0173 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0065 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00673 | hp1 | a0001 | c0004 | t0002 | g0153 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00733 | hp2 | a0001 | c0001 | t0005 | g0314 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00735 | hp2 | a0004 | c0005 | t0003 | g0091 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0315 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01081 | hp2 | a0004 | c0005 | t0001 | g0096 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01099 | hp2 | a0004 | c0005 | t0001 | g0006 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01109 | hp1 | a0004 | c0005 | t0001 | g0006 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0034 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01167 | hp2 | a0003 | c0003 | t0002 | g0030 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01192 | hp1 | a0003 | c0003 | t0002 | g0013 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01192 | hp2 | a0004 | c0005 | t0001 | g0095 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01243 | hp1 | a0005 | c0006 | t0001 | g0265 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01261 | hp1 | a0004 | c0005 | t0001 | g0006 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01515 | hp1 | a0004 | c0005 | t0003 | g0029 | EUR | IBS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | IBS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01516 | hp1 | a0004 | c0005 | t0001 | g0028 | EUR | IBS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01517 | hp1 | a0004 | c0005 | t0003 | g0029 | EUR | IBS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01517 | hp2 | a0004 | c0005 | t0001 | g0028 | EUR | IBS | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01884 | hp1 | a0001 | c0004 | t0002 | g0116 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01884 | hp2 | a0005 | c0006 | t0001 | g0193 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01891 | hp2 | a0005 | c0006 | t0001 | g0196 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01928 | hp1 | a0001 | c0004 | t0001 | g0044 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01943 | hp2 | a0003 | c0003 | t0002 | g0102 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01952 | hp1 | a0004 | c0005 | t0001 | g0006 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01952 | hp2 | a0003 | c0009 | t0001 | g0103 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01978 | hp2 | a0003 | c0003 | t0002 | g0106 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0024 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0074 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02055 | hp2 | a0001 | c0004 | t0002 | g0219 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02071 | hp1 | a0008 | c0012 | t0001 | g0132 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02074 | hp1 | a0009 | c0023 | t0001 | g0186 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0081 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02145 | hp1 | a0001 | c0013 | t0001 | g0248 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02148 | hp1 | a0001 | c0004 | t0001 | g0044 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02155 | hp1 | a0003 | c0003 | t0002 | g0024 | EAS | CDX | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | CDX | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | CDX | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02257 | hp1 | a0001 | c0010 | t0001 | g0032 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02258 | hp1 | a0006 | c0011 | t0001 | g0252 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02258 | hp2 | a0001 | c0010 | t0001 | g0031 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02293 | hp1 | a0004 | c0005 | t0001 | g0006 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02451 | hp1 | a0001 | c0010 | t0001 | g0031 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0057 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02615 | hp2 | a0006 | c0011 | t0001 | g0318 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02622 | hp1 | a0006 | c0008 | t0001 | g0020 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02630 | hp1 | a0001 | c0010 | t0001 | g0032 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02647 | hp2 | a0010 | c0021 | t0004 | g0125 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02717 | hp1 | a0005 | c0006 | t0001 | g0268 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02717 | hp2 | a0001 | c0025 | t0008 | g0066 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02723 | hp1 | a0006 | c0008 | t0001 | g0020 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0184 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02818 | hp1 | a0003 | c0003 | t0002 | g0198 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02818 | hp2 | a0006 | c0011 | t0001 | g0200 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02886 | hp2 | a0005 | c0006 | t0001 | g0061 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02922 | hp2 | a0007 | c0014 | t0001 | g0246 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02965 | hp1 | a0006 | c0008 | t0010 | g0202 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02970 | hp2 | a0006 | c0008 | t0001 | g0309 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02976 | hp1 | a0001 | c0022 | t0001 | g0111 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03041 | hp2 | a0005 | c0006 | t0001 | g0061 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03130 | hp1 | a0001 | c0013 | t0001 | g0247 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03130 | hp2 | a0005 | c0006 | t0001 | g0195 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03209 | hp1 | a0007 | c0014 | t0001 | g0050 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03225 | hp2 | a0007 | c0024 | t0001 | g0050 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03453 | hp1 | a0005 | c0006 | t0001 | g0284 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03516 | hp2 | a0005 | c0006 | t0001 | g0194 | AFR | ESN | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0212 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03579 | hp2 | a0006 | c0008 | t0001 | g0020 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03669 | hp2 | a0008 | c0012 | t0001 | g0142 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03710 | hp2 | a0003 | c0003 | t0002 | g0073 | SAS | PJL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0181 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03942 | hp1 | a0003 | c0003 | t0002 | g0089 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04115 | hp2 | a0011 | c0018 | t0001 | g0119 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | BEB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | STU | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | YRI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18612 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | CHB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18747 | hp2 | a0001 | c0004 | t0002 | g0149 | EAS | CHB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | YRI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18939 | hp1 | a0001 | c0004 | t0001 | g0057 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18939 | hp2 | a0004 | c0005 | t0001 | g0097 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18944 | hp1 | a0001 | c0004 | t0001 | g0065 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18944 | hp2 | a0004 | c0005 | t0001 | g0014 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18945 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18952 | hp1 | a0002 | c0019 | t0001 | g0175 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18953 | hp1 | a0001 | c0004 | t0001 | g0286 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18959 | hp1 | a0001 | c0004 | t0007 | g0225 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18959 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18960 | hp1 | a0001 | c0004 | t0001 | g0021 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18960 | hp2 | a0003 | c0003 | t0002 | g0072 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18961 | hp2 | a0002 | c0007 | t0002 | g0015 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18964 | hp2 | a0003 | c0003 | t0002 | g0026 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18965 | hp2 | a0002 | c0002 | t0007 | g0167 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18966 | hp1 | a0003 | c0009 | t0001 | g0077 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18966 | hp2 | a0003 | c0003 | t0002 | g0105 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18967 | hp2 | a0002 | c0007 | t0002 | g0133 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18968 | hp1 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18969 | hp2 | a0002 | c0007 | t0002 | g0035 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18970 | hp2 | a0002 | c0007 | t0002 | g0134 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18972 | hp1 | a0004 | c0017 | t0002 | g0092 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18974 | hp2 | a0004 | c0005 | t0001 | g0094 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18978 | hp2 | a0003 | c0003 | t0002 | g0087 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18979 | hp2 | a0001 | c0004 | t0001 | g0287 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18980 | hp2 | a0001 | c0004 | t0002 | g0235 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18981 | hp1 | a0004 | c0005 | t0001 | g0101 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18982 | hp1 | a0003 | c0003 | t0002 | g0086 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18983 | hp1 | a0002 | c0007 | t0002 | g0015 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18984 | hp1 | a0003 | c0003 | t0002 | g0076 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18985 | hp2 | a0002 | c0007 | t0002 | g0015 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18988 | hp2 | a0003 | c0003 | t0002 | g0107 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0078 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0027 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18991 | hp2 | a0003 | c0003 | t0002 | g0104 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18995 | hp1 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18998 | hp2 | a0003 | c0003 | t0002 | g0027 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18999 | hp2 | a0001 | c0004 | t0001 | g0064 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0262 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19000 | hp2 | a0001 | c0004 | t0001 | g0271 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19001 | hp1 | a0003 | c0003 | t0002 | g0071 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19001 | hp2 | a0004 | c0005 | t0001 | g0093 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19003 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19004 | hp1 | a0003 | c0009 | t0001 | g0070 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19006 | hp1 | a0003 | c0003 | t0002 | g0083 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19010 | hp1 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19054 | hp2 | a0001 | c0004 | t0002 | g0237 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0025 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19057 | hp1 | a0004 | c0005 | t0001 | g0014 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19057 | hp2 | a0001 | c0004 | t0002 | g0004 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19066 | hp2 | a0002 | c0007 | t0002 | g0135 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19067 | hp1 | a0004 | c0005 | t0001 | g0100 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19068 | hp1 | a0001 | c0004 | t0002 | g0151 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19068 | hp2 | a0004 | c0005 | t0001 | g0098 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0075 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19074 | hp2 | a0012 | c0016 | t0001 | g0109 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19076 | hp1 | a0003 | c0003 | t0002 | g0084 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19076 | hp2 | a0002 | c0002 | t0009 | g0168 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19078 | hp1 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19080 | hp1 | a0003 | c0003 | t0002 | g0025 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19081 | hp1 | a0002 | c0007 | t0002 | g0035 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19081 | hp2 | a0004 | c0005 | t0001 | g0099 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19083 | hp1 | a0001 | c0004 | t0001 | g0269 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19083 | hp2 | a0004 | c0005 | t0001 | g0014 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0080 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19085 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19086 | hp1 | a0001 | c0004 | t0002 | g0190 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19088 | hp2 | a0003 | c0009 | t0001 | g0068 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19090 | hp1 | a0001 | c0004 | t0002 | g0155 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19090 | hp2 | a0001 | c0004 | t0001 | g0064 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19091 | hp1 | a0002 | c0002 | t0011 | g0176 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA19240 | hp2 | a0002 | c0007 | t0001 | g0192 | AFR | YRI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | ASW | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ASW | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | GIH | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | GIH | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG02559 | hp2 | a0006 | c0008 | t0001 | g0199 | AFR | ACB | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03471 | hp1 | a0001 | c0015 | t0001 | g0063 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG03471 | hp2 | a0006 | c0008 | t0001 | g0197 | AFR | MSL | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | USA | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18955 | hp1 | a0001 | c0004 | t0002 | g0303 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | USA | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | USA | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA21309 | hp1 | a0005 | c0006 | t0001 | g0264 | AFR | LWK | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| homoSapiens | chm13v2 | a0004 | c0005 | t0001 | g0110 | REF | REF | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0023 | REF | REF | BST1_chr4_15698065_15737787 | BST1 | chr4 | 15698065 | 15737787 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15703251 | G | C | 2 | a0003 a0012 |
45 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(42): Show |
missense_variant | MODERATE | c.107G>C | p.Gly36Ala | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/9 | 187/1979 | 107/957 | 36/318 | chr4 | 15703251 | |||
| chr4:15705585 | C | T | 1 | a0007 | 3 | HG02922.hp2 HG03209.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.259C>T | p.Pro87Ser | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/9 | 339/1979 | 259/957 | 87/318 | chr4 | 15705585 | |||
| chr4:15705627 | A | G | 1 | a0005 | 10 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
missense_variant | MODERATE | c.301A>G | p.Ile101Val | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/9 | 381/1979 | 301/957 | 101/318 | chr4 | 15705627 | |||
| chr4:15707565 | C | T | 1 | a0009 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.370C>T | p.Arg124Cys | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/9 | 450/1979 | 370/957 | 124/318 | chr4 | 15707565 | |||
| chr4:15707569 | G | A | 1 | a0004 | 24 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(21): Show |
missense_variant | MODERATE | c.374G>A | p.Arg125His | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/9 | 454/1979 | 374/957 | 125/318 | chr4 | 15707569 | |||
| chr4:15707572 | T | A | 1 | a0011 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.377T>A | p.Phe126Tyr | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/9 | 457/1979 | 377/957 | 126/318 | chr4 | 15707572 | |||
| chr4:15707629 | G | A | 3 | a0002 a0009 a0012 |
60 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(57): Show |
missense_variant | MODERATE | c.434G>A | p.Arg145Gln | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/9 | 514/1979 | 434/957 | 145/318 | chr4 | 15707629 | |||
| chr4:15718917 | G | A | 1 | a0006 | 10 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
missense_variant | MODERATE | c.715G>A | p.Gly239Arg | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/9 | 795/1979 | 715/957 | 239/318 | chr4 | 15718917 | |||
| chr4:15722897 | G | A | 1 | a0008 | 2 | HG02071.hp1 HG03669.hp2 |
missense_variant | MODERATE | c.814G>A | p.Val272Met | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/9 | 894/1979 | 814/957 | 272/318 | chr4 | 15722897 | |||
| chr4:15722901 | A | T | 1 | a0010 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.818A>T | p.Asp273Val | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/9 | 898/1979 | 818/957 | 273/318 | chr4 | 15722901 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15703165 | G | C | 1 | a0001c0015 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.21G>C | p.Ala7Ala | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/9 | 101/1979 | 21/957 | 7/318 | chr4 | 15703165 | |||
| chr4:15705578 | C | T | 1 | a0001c0025 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.252C>T | p.Ser84Ser | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/9 | 332/1979 | 252/957 | 84/318 | chr4 | 15705578 | |||
| chr4:15707630 | A | G | 1 | a0001c0013 | 2 | HG02145.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.435A>G | p.Arg145Arg | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/9 | 515/1979 | 435/957 | 145/318 | chr4 | 15707630 | |||
| chr4:15711823 | C | T | 7 | a0001c0010 a0001c0022 a0001c0025 others(4): Show |
56 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(53): Show |
synonymous_variant | LOW | c.468C>T | p.Ser156Ser | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/9 | 548/1979 | 468/957 | 156/318 | chr4 | 15711823 | |||
| chr4:15715740 | G | A | 1 | a0007c0024 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.645G>A | p.Gln215Gln | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/9 | 725/1979 | 645/957 | 215/318 | chr4 | 15715740 | |||
| chr4:15731831 | A | C | 9 | a0001c0004 a0001c0022 a0002c0002 others(6): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
synonymous_variant | LOW | c.943A>C | p.Arg315Arg | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 1023/1979 | 943/957 | 315/318 | chr4 | 15731831 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15703075 | G | C | 1 | a0001c0025t0008 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/9 | 70 | chr4 | 15703075 | ||||||
| chr4:15731959 | G | A | 1 | a0002c0002t0009 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 114 | chr4 | 15731959 | ||||||
| chr4:15732187 | A | G | 1 | a0001c0025t0008 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 342 | chr4 | 15732187 | ||||||
| chr4:15732202 | C | T | 2 | a0001c0004t0007 a0002c0002t0007 |
2 | NA18959.hp1 NA18965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*357C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 357 | chr4 | 15732202 | ||||||
| chr4:15732287 | C | T | 1 | a0002c0002t0011 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 442 | chr4 | 15732287 | ||||||
| chr4:15732299 | A | G | 1 | a0001c0001t0006 | 2 | HG01109.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*454A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 454 | chr4 | 15732299 | ||||||
| chr4:15732445 | G | A | 1 | a0004c0005t0003 | 3 | HG00735.hp2 HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*600G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 600 | chr4 | 15732445 | ||||||
| chr4:15732577 | C | G | 1 | a0006c0008t0010 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 732 | chr4 | 15732577 | ||||||
| chr4:15732597 | C | T | 4 | a0001c0004t0002 a0002c0007t0002 a0003c0003t0002 others(1): Show |
65 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*752C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 752 | chr4 | 15732597 | ||||||
| chr4:15732756 | T | A | 2 | a0001c0001t0004 a0010c0021t0004 |
2 | HG02647.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*911T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 911 | chr4 | 15732756 | ||||||
| chr4:15732758 | A | C | 1 | a0001c0001t0005 | 2 | HG00733.hp2 HG01069.hp2 |
3_prime_UTR_variant | MODIFIER | c.*913A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 9/9 | 913 | chr4 | 15732758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15703416 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(161): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.188+84T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703416 | |||||||
| chr4:15703539 | C | T | 1 | a0003c0003t0002g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.188+207C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703539 | |||||||
| chr4:15703631 | G | GGT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(100): Show |
152 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.188+300_188+301ins others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15703631 | ||||||
| chr4:15703633 | G | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(101): Show |
153 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.188+301G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703633 | |||||||
| chr4:15703645 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
160 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.188+313C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703645 | |||||||
| chr4:15703647 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
160 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.188+315C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703647 | |||||||
| chr4:15703715 | G | GGT | 2 | a0001c0010t0001g0031 a0001c0010t0001g0032 |
4 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+384_188+385ins others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15703715 | ||||||
| chr4:15703717 | G | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(103): Show |
157 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.188+385G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703717 | |||||||
| chr4:15703719 | T | G | 1 | a0001c0004t0001g0044 | 2 | HG01928.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.188+387T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703719 | |||||||
| chr4:15703900 | G | A | 1 | a0006c0008t0001g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.188+568G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703900 | |||||||
| chr4:15703905 | CTCTAGAG others(17): Show |
C | 1 | a0001c0001t0001g0316 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.188+596_188+619del others(24): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15703905 | ||||||
| chr4:15703989 | GAT | G | 5 | a0005c0006t0001g0193 a0005c0006t0001g0194 a0005c0006t0001g0195 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+658_188+659del others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15703989 | |||||||
| chr4:15703990 | ATG | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0136 |
4 | HG02698.hp2 HG03492.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+672_188+673del others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15703990 | ||||||
| chr4:15704041 | G | T | 2 | a0001c0001t0005g0314 a0001c0001t0005g0315 |
2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.188+709G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704041 | |||||||
| chr4:15704074 | T | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0201 a0001c0010t0001g0031 others(5): Show |
10 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+742T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704074 | |||||||
| chr4:15704119 | TAGGTGAG others(19): Show |
T | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.188+823_188+848del others(26): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15704119 | ||||||
| chr4:15704188 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.188+856T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704188 | |||||||
| chr4:15704230 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.188+898G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704230 | |||||||
| chr4:15704283 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.188+951T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704283 | |||||||
| chr4:15704289 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.188+957T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704289 | |||||||
| chr4:15704356 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.188+1024G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704356 | |||||||
| chr4:15704399 | GAT | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0201 a0001c0010t0001g0031 others(5): Show |
10 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+1068_188+1069d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704399 | |||||||
| chr4:15704399 | GATGT | G | 2 | a0002c0002t0001g0016 a0002c0007t0001g0192 |
4 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+1068_188+1071d others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704399 | |||||||
| chr4:15704400 | ATG | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(217): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.188+1084_188+1085d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15704400 | ||||||
| chr4:15704400 | ATGTG | A | 3 | a0001c0001t0001g0245 a0004c0005t0001g0099 a0004c0005t0001g0101 |
3 | HG02109.hp1 NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.188+1082_188+1085d others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15704400 | ||||||
| chr4:15704404 | GTGTGTGT others(19): Show |
G | 1 | a0001c0001t0001g0191 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.188+1084_189-1074d others(28): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15704404 | ||||||
| chr4:15704453 | G | A | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.189-1062G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704453 | |||||||
| chr4:15704496 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.189-1019A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704496 | |||||||
| chr4:15704570 | G | A | 134 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(131): Show |
173 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.189-945G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704570 | |||||||
| chr4:15704609 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.189-906G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704609 | |||||||
| chr4:15704735 | T | C | 2 | a0005c0006t0001g0193 a0005c0006t0001g0194 |
2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.189-780T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704735 | |||||||
| chr4:15704750 | C | G | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.189-765C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704750 | |||||||
| chr4:15704804 | G | A | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG03486.hp1 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.189-711G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704804 | |||||||
| chr4:15704811 | C | T | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.189-704C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704811 | |||||||
| chr4:15704843 | T | C | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
100 | HG00099.hp1 HG00423.hp1 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.189-672T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704843 | |||||||
| chr4:15704857 | C | A | 2 | a0001c0001t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189-658C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15704857 | |||||||
| chr4:15704879 | G | GTC | 153 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(150): Show |
197 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.189-634_189-633dup others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 15704879 | ||||||
| chr4:15705165 | A | T | 1 | a0001c0004t0002g0190 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.189-350A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705165 | |||||||
| chr4:15705167 | T | A | 145 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(142): Show |
186 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.189-348T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705167 | |||||||
| chr4:15705245 | G | A | 1 | a0003c0003t0002g0067 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.189-270G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705245 | |||||||
| chr4:15705267 | G | A | 44 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0004t0002g0116 others(41): Show |
53 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.189-248G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705267 | |||||||
| chr4:15705297 | C | T | 16 | a0004c0005t0001g0006 a0004c0005t0001g0014 a0004c0005t0001g0028 others(13): Show |
24 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.189-218C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705297 | |||||||
| chr4:15705315 | G | T | 1 | a0001c0001t0001g0321 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.189-200G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705315 | |||||||
| chr4:15705361 | C | T | 5 | a0001c0001t0001g0259 a0001c0001t0001g0308 a0001c0001t0001g0310 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-154C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705361 | |||||||
| chr4:15705378 | C | A | 2 | a0004c0005t0001g0028 a0004c0005t0001g0090 |
3 | HG00099.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.189-137C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705378 | |||||||
| chr4:15705478 | C | T | 1 | a0003c0003t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.189-37C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 1/8 | chr4 | 15705478 | |||||||
| chr4:15705911 | C | G | 1 | a0001c0001t0001g0307 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.315+270C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15705911 | |||||||
| chr4:15706191 | C | G | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
18 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.315+550C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15706191 | |||||||
| chr4:15706203 | G | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(318): Show |
437 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(434): Show |
intron_variant | MODIFIER | c.315+562G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15706203 | |||||||
| chr4:15706213 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.315+572C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15706213 | |||||||
| chr4:15706916 | A | G | 2 | a0001c0013t0001g0247 a0001c0013t0001g0248 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.316-595A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15706916 | |||||||
| chr4:15707092 | C | CAG | 4 | a0002c0007t0002g0035 a0002c0007t0002g0133 a0002c0007t0002g0134 others(1): Show |
5 | NA18967.hp2 NA18969.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-418_316-417dup others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 15707092 | ||||||
| chr4:15707144 | A | T | 57 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0115 others(54): Show |
70 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.316-367A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15707144 | |||||||
| chr4:15707264 | G | A | 4 | a0001c0001t0001g0112 a0001c0010t0001g0031 a0001c0010t0001g0032 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.316-247G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15707264 | |||||||
| chr4:15707336 | T | A | 2 | a0001c0001t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-175T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 2/8 | chr4 | 15707336 | |||||||
| chr4:15707673 | G | T | 8 | a0003c0003t0002g0030 a0003c0003t0002g0102 a0003c0003t0002g0104 others(5): Show |
9 | HG00558.hp2 HG00597.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+27G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707673 | |||||||
| chr4:15707834 | A | ACT | 16 | a0001c0001t0001g0055 a0003c0003t0002g0013 a0003c0003t0002g0067 others(13): Show |
19 | HG00544.hp2 HG00597.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.451+209_451+210dup others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707834 | ||||||
| chr4:15707834 | A | ACTCT | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
162 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.451+207_451+210dup others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707834 | ||||||
| chr4:15707834 | A | ACTCTCT | 30 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(27): Show |
42 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.451+205_451+210dup others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707834 | ||||||
| chr4:15707834 | A | ACTCTCTC others(1): Show |
29 | a0001c0001t0001g0054 a0001c0001t0001g0228 a0001c0001t0001g0253 others(26): Show |
44 | HG00408.hp2 HG00438.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.451+203_451+210dup others(8): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707834 | ||||||
| chr4:15707834 | A | ACTCTCTC others(3): Show |
14 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0236 others(11): Show |
21 | HG01169.hp1 HG01516.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.451+201_451+210dup others(10): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707834 | ||||||
| chr4:15707834 | A | ACTCTCTC others(5): Show |
6 | a0001c0001t0001g0201 a0001c0001t0001g0242 a0001c0001t0001g0243 others(3): Show |
6 | HG02040.hp1 HG02109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.451+199_451+210dup others(12): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707834 | ||||||
| chr4:15707834 | A | ACTCTCTC others(8518): Show |
1 | a0001c0001t0001g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.451+210_451+211ins others(8525): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707834 | ||||||
| chr4:15707855 | C | A | 3 | a0001c0001t0001g0211 a0001c0001t0001g0255 a0001c0004t0001g0212 |
3 | HG02976.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.451+209C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707855 | |||||||
| chr4:15707855 | C | CTATA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0001g0206 others(6): Show |
9 | HG01243.hp1 HG01891.hp2 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+226_451+229dup others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTA | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0051 others(27): Show |
42 | HG00639.hp1 HG01070.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.451+210_451+211ins others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTATA | 10 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(7): Show |
10 | HG00099.hp1 HG00408.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+210_451+211ins others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTA | 17 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0220 others(14): Show |
22 | HG00639.hp2 HG00673.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.451+210_451+211ins others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTAT others(1): Show |
4 | a0001c0001t0001g0052 a0001c0004t0002g0155 a0004c0005t0001g0006 others(1): Show |
10 | HG01099.hp2 HG01109.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.451+210_451+211ins others(8): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTAT others(5): Show |
1 | a0001c0001t0001g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.451+210_451+211ins others(12): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTCT others(1): Show |
13 | a0001c0001t0001g0053 a0001c0001t0001g0227 a0001c0001t0001g0251 others(10): Show |
16 | HG00099.hp2 HG01081.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+210_451+211ins others(8): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTCT others(3): Show |
1 | a0006c0011t0001g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.451+210_451+211ins others(10): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTCT others(5): Show |
1 | a0006c0008t0001g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.451+210_451+211ins others(12): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTCT others(3): Show |
8 | a0001c0001t0001g0019 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
10 | HG00642.hp1 HG00733.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+210_451+211ins others(10): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0208 a0001c0001t0001g0317 |
2 | NA18906.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.451+210_451+211ins others(12): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTCT others(5): Show |
1 | a0001c0001t0001g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.451+210_451+211ins others(12): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707855 | C | CTCTCTCT others(7): Show |
1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.451+210_451+211ins others(14): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707855 | ||||||
| chr4:15707857 | A | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(60): Show |
91 | HG00280.hp1 HG00438.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.451+211A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707857 | |||||||
| chr4:15707859 | A | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0189 others(5): Show |
8 | HG00438.hp2 HG02074.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.451+213A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707859 | |||||||
| chr4:15707861 | A | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0189 a0001c0001t0001g0245 |
3 | HG00438.hp2 HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.451+215A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707861 | |||||||
| chr4:15707863 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.451+217A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707863 | |||||||
| chr4:15707874 | T | C | 70 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0128 others(67): Show |
92 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.451+228T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707874 | |||||||
| chr4:15707874 | T | TATAC | 6 | a0001c0001t0001g0115 a0001c0004t0002g0116 a0003c0003t0002g0024 others(3): Show |
8 | HG00558.hp2 HG01167.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.451+229_451+230ins others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707874 | ||||||
| chr4:15707878 | C | CAT | 111 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(108): Show |
149 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.451+240_451+241dup others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 15707878 | ||||||
| chr4:15707878 | C | T | 75 | a0001c0001t0001g0033 a0001c0001t0001g0115 a0001c0001t0001g0126 others(72): Show |
99 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.451+232C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707878 | |||||||
| chr4:15707917 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.451+271A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15707917 | |||||||
| chr4:15708040 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0006g0034 |
4 | HG01109.hp2 HG02809.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+394G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708040 | |||||||
| chr4:15708067 | G | A | 4 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG02145.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+421G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708067 | |||||||
| chr4:15708099 | A | G | 1 | a0009c0023t0001g0186 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.451+453A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708099 | |||||||
| chr4:15708473 | C | A | 1 | a0006c0008t0001g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.451+827C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708473 | |||||||
| chr4:15708616 | C | T | 1 | a0002c0002t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.451+970C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708616 | |||||||
| chr4:15708677 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.451+1031G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708677 | |||||||
| chr4:15708707 | A | C | 185 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(182): Show |
247 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.451+1061A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708707 | |||||||
| chr4:15708752 | A | G | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.451+1106A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15708752 | |||||||
| chr4:15709099 | T | A | 1 | a0006c0008t0010g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.451+1453T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15709099 | |||||||
| chr4:15709204 | C | T | 6 | a0004c0005t0001g0014 a0004c0005t0001g0097 a0004c0005t0001g0098 others(3): Show |
8 | NA18939.hp2 NA18944.hp2 NA18981.hp1 others(5): Show |
intron_variant | MODIFIER | c.451+1558C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15709204 | |||||||
| chr4:15709314 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.451+1668G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15709314 | |||||||
| chr4:15709461 | T | A | 45 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0004t0002g0116 others(42): Show |
54 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.451+1815T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15709461 | |||||||
| chr4:15709714 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.451+2068A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15709714 | |||||||
| chr4:15709941 | T | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0307 |
2 | HG02071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.452-1866T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15709941 | |||||||
| chr4:15709978 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.452-1829A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15709978 | |||||||
| chr4:15710015 | C | T | 5 | a0001c0001t0001g0259 a0001c0001t0001g0308 a0001c0001t0001g0310 others(2): Show |
5 | HG02145.hp2 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-1792C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710015 | |||||||
| chr4:15710039 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.452-1768C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710039 | |||||||
| chr4:15710120 | C | T | 2 | a0001c0013t0001g0247 a0001c0013t0001g0248 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.452-1687C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710120 | |||||||
| chr4:15710310 | T | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(246): Show |
343 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.452-1497T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710310 | |||||||
| chr4:15710342 | A | G | 4 | a0001c0010t0001g0031 a0001c0010t0001g0032 a0001c0022t0001g0111 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.452-1465A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710342 | |||||||
| chr4:15710402 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.452-1405C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710402 | |||||||
| chr4:15710566 | C | T | 2 | a0001c0001t0004g0127 a0010c0021t0004g0125 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.452-1241C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710566 | |||||||
| chr4:15710580 | C | G | 46 | a0001c0001t0001g0115 a0001c0004t0002g0116 a0001c0004t0002g0190 others(43): Show |
56 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.452-1227C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710580 | |||||||
| chr4:15710678 | C | T | 1 | a0001c0004t0001g0262 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.452-1129C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710678 | |||||||
| chr4:15710710 | A | C | 1 | a0001c0001t0001g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.452-1097A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710710 | |||||||
| chr4:15710779 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(287): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(392): Show |
intron_variant | MODIFIER | c.452-1028C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710779 | |||||||
| chr4:15710781 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.452-1026T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710781 | |||||||
| chr4:15710852 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0296 |
2 | NA18982.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.452-955C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710852 | |||||||
| chr4:15710927 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(126): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.452-880C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710927 | |||||||
| chr4:15710943 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.452-864C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15710943 | |||||||
| chr4:15711164 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(132): Show |
187 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.452-643T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711164 | |||||||
| chr4:15711231 | G | A | 15 | a0004c0005t0001g0006 a0004c0005t0001g0014 a0004c0005t0001g0028 others(12): Show |
23 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.452-576G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711231 | |||||||
| chr4:15711321 | T | G | 1 | a0006c0008t0010g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.452-486T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711321 | |||||||
| chr4:15711380 | G | T | 110 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0115 others(107): Show |
152 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.452-427G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711380 | |||||||
| chr4:15711490 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.452-317A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711490 | |||||||
| chr4:15711518 | C | G | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.452-289C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711518 | |||||||
| chr4:15711594 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.452-213C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711594 | |||||||
| chr4:15711635 | C | G | 1 | a0003c0003t0002g0082 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.452-172C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 3/8 | chr4 | 15711635 | |||||||
| chr4:15711958 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.534+69A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15711958 | |||||||
| chr4:15711969 | C | T | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
18 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+80C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15711969 | |||||||
| chr4:15711985 | A | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0275 a0001c0001t0001g0295 |
3 | HG00741.hp1 HG03017.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.534+96A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15711985 | |||||||
| chr4:15711995 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0255 |
3 | HG01433.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.534+106G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15711995 | |||||||
| chr4:15712094 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.534+205G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712094 | |||||||
| chr4:15712180 | T | C | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
18 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.534+291T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712180 | |||||||
| chr4:15712382 | A | G | 4 | a0001c0010t0001g0031 a0001c0010t0001g0032 a0001c0022t0001g0111 others(1): Show |
6 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+493A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712382 | |||||||
| chr4:15712491 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.534+602G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712491 | |||||||
| chr4:15712566 | C | A | 54 | a0001c0010t0001g0031 a0001c0010t0001g0032 a0001c0022t0001g0111 others(51): Show |
84 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.534+677C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712566 | |||||||
| chr4:15712588 | C | T | 2 | a0002c0002t0001g0183 a0002c0002t0001g0188 |
2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.534+699C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712588 | |||||||
| chr4:15712632 | C | T | 1 | a0004c0005t0003g0029 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.534+743C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712632 | |||||||
| chr4:15712938 | A | G | 1 | a0002c0002t0001g0182 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.534+1049A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15712938 | |||||||
| chr4:15713018 | A | G | 15 | a0004c0005t0001g0006 a0004c0005t0001g0014 a0004c0005t0001g0028 others(12): Show |
23 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.534+1129A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713018 | |||||||
| chr4:15713053 | C | G | 2 | a0001c0001t0005g0314 a0001c0001t0005g0315 |
2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.534+1164C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713053 | |||||||
| chr4:15713128 | A | C | 1 | a0002c0002t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.534+1239A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713128 | |||||||
| chr4:15713139 | G | A | 54 | a0001c0010t0001g0031 a0001c0010t0001g0032 a0001c0022t0001g0111 others(51): Show |
84 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.534+1250G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713139 | |||||||
| chr4:15713206 | C | CT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.534+1338dupT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 15713206 | ||||||
| chr4:15713206 | CT | C | 35 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0112 others(32): Show |
53 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.534+1338delT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 15713206 | ||||||
| chr4:15713206 | CTTTTTTT | C | 43 | a0001c0001t0001g0115 a0001c0004t0002g0116 a0001c0004t0002g0190 others(40): Show |
53 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.534+1332_534+1338d others(9): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 15713206 | ||||||
| chr4:15713207 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0130 a0001c0001t0006g0034 |
4 | HG01109.hp2 HG02809.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.534+1318T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713207 | |||||||
| chr4:15713213 | T | C | 1 | a0003c0003t0002g0069 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.534+1324T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713213 | |||||||
| chr4:15713221 | T | TC | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0282 |
3 | NA18949.hp2 NA18989.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.534+1332_534+1333i others(3): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713221 | |||||||
| chr4:15713233 | G | A | 15 | a0004c0005t0001g0006 a0004c0005t0001g0014 a0004c0005t0001g0028 others(12): Show |
23 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.534+1344G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713233 | |||||||
| chr4:15713533 | C | T | 1 | a0002c0002t0001g0174 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.534+1644C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713533 | |||||||
| chr4:15713794 | C | T | 3 | a0007c0014t0001g0050 a0007c0014t0001g0246 a0007c0024t0001g0050 |
3 | HG02922.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.535-1491C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713794 | |||||||
| chr4:15713829 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.535-1456G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713829 | |||||||
| chr4:15713851 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.535-1434G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15713851 | |||||||
| chr4:15714217 | A | G | 1 | a0001c0001t0001g0294 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.535-1068A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15714217 | |||||||
| chr4:15714254 | A | T | 32 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0012 others(29): Show |
50 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.535-1031A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15714254 | |||||||
| chr4:15714269 | C | T | 1 | a0002c0002t0001g0181 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.535-1016C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15714269 | |||||||
| chr4:15714466 | A | C | 58 | a0001c0001t0001g0241 a0001c0010t0001g0031 a0001c0010t0001g0032 others(55): Show |
88 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.535-819A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15714466 | |||||||
| chr4:15714482 | C | A | 42 | a0001c0010t0001g0031 a0001c0010t0001g0032 a0001c0022t0001g0111 others(39): Show |
64 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.535-803C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15714482 | |||||||
| chr4:15714552 | C | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0122 others(3): Show |
8 | NA18942.hp1 NA18945.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.535-733C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15714552 | |||||||
| chr4:15714737 | C | T | 2 | a0001c0001t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.535-548C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15714737 | |||||||
| chr4:15715028 | T | A | 2 | a0001c0001t0001g0211 a0001c0004t0001g0212 |
2 | HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.535-257T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15715028 | |||||||
| chr4:15715231 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0283 |
3 | NA18981.hp2 NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.535-54T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 4/8 | chr4 | 15715231 | |||||||
| chr4:15715603 | T | C | 59 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(56): Show |
72 | HG00099.hp1 HG00423.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.612-104T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 5/8 | chr4 | 15715603 | |||||||
| chr4:15715698 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(120): Show |
175 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.612-9G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 5/8 | chr4 | 15715698 | |||||||
| chr4:15715706 | G | A | 1 | a0011c0018t0001g0119 | 1 | HG04115.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.612-1G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 5/8 | chr4 | 15715706 | |||||||
| chr4:15715939 | A | T | 2 | a0004c0005t0001g0099 a0004c0005t0001g0101 |
2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.704+140A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15715939 | |||||||
| chr4:15716117 | G | A | 1 | a0001c0004t0002g0237 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.704+318G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716117 | |||||||
| chr4:15716369 | G | T | 1 | a0006c0008t0001g0197 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704+570G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716369 | |||||||
| chr4:15716395 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704+596A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716395 | |||||||
| chr4:15716427 | A | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(288): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(393): Show |
intron_variant | MODIFIER | c.704+628A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716427 | |||||||
| chr4:15716615 | C | G | 15 | a0004c0005t0001g0006 a0004c0005t0001g0014 a0004c0005t0001g0028 others(12): Show |
23 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.704+816C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716615 | |||||||
| chr4:15716623 | C | G | 1 | a0003c0003t0002g0067 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.704+824C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716623 | |||||||
| chr4:15716781 | T | C | 2 | a0006c0008t0001g0197 a0006c0008t0010g0202 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.704+982T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716781 | |||||||
| chr4:15716851 | C | T | 1 | a0006c0008t0001g0199 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.704+1052C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716851 | |||||||
| chr4:15716869 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.704+1070G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716869 | |||||||
| chr4:15716918 | G | C | 1 | a0006c0011t0001g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704+1119G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716918 | |||||||
| chr4:15716932 | C | T | 1 | a0001c0022t0001g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.704+1133C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15716932 | |||||||
| chr4:15717077 | T | G | 73 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0128 others(70): Show |
105 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.704+1278T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717077 | |||||||
| chr4:15717183 | C | A | 1 | a0001c0001t0001g0302 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.704+1384C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717183 | |||||||
| chr4:15717187 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.704+1388G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717187 | |||||||
| chr4:15717203 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704+1404C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717203 | |||||||
| chr4:15717402 | C | T | 42 | a0001c0004t0002g0116 a0001c0004t0002g0149 a0001c0004t0002g0190 others(39): Show |
52 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.705-1505C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717402 | |||||||
| chr4:15717515 | C | T | 1 | a0011c0018t0001g0119 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.705-1392C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717515 | |||||||
| chr4:15717782 | T | G | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.705-1125T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717782 | |||||||
| chr4:15717816 | G | A | 52 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0128 others(49): Show |
74 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.705-1091G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15717816 | |||||||
| chr4:15718176 | C | T | 1 | a0004c0005t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.705-731C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15718176 | |||||||
| chr4:15718244 | A | AGT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(164): Show |
232 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.705-638_705-637dup others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 15718244 | ||||||
| chr4:15718244 | A | AGTGT | 42 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0261 others(39): Show |
62 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.705-640_705-637dup others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 15718244 | ||||||
| chr4:15718244 | A | AGTGTGT | 4 | a0001c0001t0001g0300 a0002c0002t0001g0183 a0002c0002t0001g0187 others(1): Show |
4 | HG03139.hp2 HG03491.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-642_705-637dup others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 15718244 | ||||||
| chr4:15718244 | AGT | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0144 a0001c0001t0001g0211 others(1): Show |
4 | HG03195.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-638_705-637del others(2): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 15718244 | ||||||
| chr4:15718244 | AGTGT | A | 43 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0045 others(40): Show |
54 | HG00099.hp1 HG00423.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.705-640_705-637del others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 15718244 | ||||||
| chr4:15718244 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0245 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.705-646_705-637del others(10): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 15718244 | ||||||
| chr4:15718347 | T | G | 117 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(114): Show |
160 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.705-560T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15718347 | |||||||
| chr4:15718427 | T | C | 2 | a0004c0005t0001g0093 a0004c0005t0001g0094 |
2 | NA18974.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.705-480T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15718427 | |||||||
| chr4:15718455 | T | A | 1 | a0001c0001t0001g0205 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.705-452T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15718455 | |||||||
| chr4:15718542 | T | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.705-365T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15718542 | |||||||
| chr4:15718756 | G | T | 1 | a0001c0004t0002g0116 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.705-151G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 6/8 | chr4 | 15718756 | |||||||
| chr4:15719045 | G | C | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.791+52G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719045 | |||||||
| chr4:15719061 | G | A | 13 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0128 others(10): Show |
15 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.791+68G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719061 | |||||||
| chr4:15719077 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG00738.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.791+84C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719077 | |||||||
| chr4:15719428 | C | A | 3 | a0001c0010t0001g0031 a0001c0010t0001g0032 a0001c0022t0001g0111 |
5 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.791+435C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719428 | |||||||
| chr4:15719515 | T | A | 169 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(166): Show |
222 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.791+522T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719515 | |||||||
| chr4:15719516 | T | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(286): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(391): Show |
intron_variant | MODIFIER | c.791+523T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719516 | |||||||
| chr4:15719521 | A | T | 1 | a0001c0022t0001g0111 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.791+528A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719521 | |||||||
| chr4:15719569 | C | T | 3 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0004t0007g0225 |
3 | NA18959.hp1 NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.791+576C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719569 | |||||||
| chr4:15719700 | G | T | 7 | a0001c0001t0001g0126 a0001c0001t0001g0129 a0001c0001t0001g0131 others(4): Show |
7 | HG02809.hp2 HG02922.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.791+707G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719700 | |||||||
| chr4:15719831 | C | T | 1 | a0006c0008t0001g0309 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.791+838C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719831 | |||||||
| chr4:15719996 | T | C | 58 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(55): Show |
71 | HG00099.hp1 HG00423.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.791+1003T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15719996 | |||||||
| chr4:15720109 | G | A | 6 | a0001c0001t0001g0048 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
7 | HG02602.hp1 HG03654.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.791+1116G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720109 | |||||||
| chr4:15720177 | A | T | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(284): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(389): Show |
intron_variant | MODIFIER | c.791+1184A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720177 | |||||||
| chr4:15720316 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.791+1323T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720316 | |||||||
| chr4:15720319 | A | T | 1 | a0003c0003t0002g0081 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.791+1326A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720319 | |||||||
| chr4:15720361 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.791+1368G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720361 | |||||||
| chr4:15720442 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0191 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.791+1449C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720442 | |||||||
| chr4:15720599 | C | CA | 68 | a0001c0001t0001g0117 a0001c0001t0001g0143 a0001c0001t0001g0206 others(65): Show |
98 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.791+1623dupA | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 15720599 | ||||||
| chr4:15720599 | C | CAA | 8 | a0001c0004t0001g0262 a0001c0010t0001g0031 a0001c0010t0001g0032 others(5): Show |
12 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.791+1622_791+1623d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 15720599 | ||||||
| chr4:15720777 | C | T | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.791+1784C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720777 | |||||||
| chr4:15720821 | G | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0255 |
3 | HG01433.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.791+1828G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720821 | |||||||
| chr4:15720950 | C | T | 58 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(55): Show |
71 | HG00099.hp1 HG00423.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.792-1925C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720950 | |||||||
| chr4:15720992 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.792-1883G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15720992 | |||||||
| chr4:15721166 | G | T | 8 | a0006c0008t0001g0020 a0006c0008t0001g0197 a0006c0008t0001g0199 others(5): Show |
10 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.792-1709G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721166 | |||||||
| chr4:15721219 | A | G | 1 | a0003c0003t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.792-1656A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721219 | |||||||
| chr4:15721528 | C | G | 2 | a0003c0003t0002g0080 a0003c0003t0002g0081 |
2 | HG02132.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.792-1347C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721528 | |||||||
| chr4:15721540 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0191 |
2 | HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.792-1335G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721540 | |||||||
| chr4:15721670 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG01243.hp2 HG01346.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.792-1205G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721670 | |||||||
| chr4:15721711 | C | T | 2 | a0004c0005t0001g0099 a0004c0005t0001g0101 |
2 | NA18981.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.792-1164C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721711 | |||||||
| chr4:15721724 | G | A | 13 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
17 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.792-1151G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721724 | |||||||
| chr4:15721733 | C | A | 13 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
17 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.792-1142C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721733 | |||||||
| chr4:15721771 | G | A | 17 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0004c0005t0001g0006 others(14): Show |
25 | HG00099.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.792-1104G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721771 | |||||||
| chr4:15721877 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.792-998G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721877 | |||||||
| chr4:15721881 | GC | G | 109 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0130 others(106): Show |
148 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.792-992delC | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 15721881 | ||||||
| chr4:15721891 | C | G | 29 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(26): Show |
37 | HG00099.hp1 HG00423.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.792-984C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721891 | |||||||
| chr4:15721903 | G | A | 65 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0130 others(62): Show |
94 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.792-972G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15721903 | |||||||
| chr4:15722038 | G | C | 127 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(124): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.792-837G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722038 | |||||||
| chr4:15722169 | A | T | 108 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(105): Show |
138 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.792-706A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722169 | |||||||
| chr4:15722262 | C | G | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | HG03486.hp1 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.792-613C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722262 | |||||||
| chr4:15722347 | C | A | 51 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(48): Show |
79 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.792-528C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722347 | |||||||
| chr4:15722452 | A | G | 66 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(63): Show |
95 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.792-423A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722452 | |||||||
| chr4:15722527 | C | T | 34 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(31): Show |
44 | HG00099.hp1 HG00423.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.792-348C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722527 | |||||||
| chr4:15722542 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.792-333T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722542 | |||||||
| chr4:15722564 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.792-311T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722564 | |||||||
| chr4:15722583 | A | C | 65 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(62): Show |
94 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.792-292A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722583 | |||||||
| chr4:15722592 | A | AT | 44 | a0001c0001t0001g0040 a0001c0001t0001g0117 a0001c0001t0001g0158 others(41): Show |
48 | HG00597.hp1 HG01123.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.792-262dupT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 15722592 | ||||||
| chr4:15722592 | AT | A | 26 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0045 others(23): Show |
31 | HG00099.hp1 HG00423.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.792-262delT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 15722592 | ||||||
| chr4:15722623 | A | G | 127 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(124): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.792-252A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722623 | |||||||
| chr4:15722624 | G | C | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.792-251G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722624 | |||||||
| chr4:15722630 | G | A | 60 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0130 others(57): Show |
87 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.792-245G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722630 | |||||||
| chr4:15722710 | G | A | 46 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(43): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.792-165G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722710 | |||||||
| chr4:15722711 | G | A | 46 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(43): Show |
70 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.792-164G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722711 | |||||||
| chr4:15722749 | G | A | 2 | a0004c0005t0003g0029 a0004c0005t0003g0091 |
3 | HG00735.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.792-126G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722749 | |||||||
| chr4:15722820 | G | T | 50 | a0001c0001t0001g0059 a0001c0001t0001g0257 a0001c0001t0001g0270 others(47): Show |
75 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.792-55G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722820 | |||||||
| chr4:15722825 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.792-50T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722825 | |||||||
| chr4:15722864 | T | G | 52 | a0001c0001t0001g0059 a0001c0001t0001g0227 a0001c0001t0001g0257 others(49): Show |
77 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.792-11T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 7/8 | chr4 | 15722864 | |||||||
| chr4:15722935 | G | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0282 |
3 | NA18949.hp2 NA18989.hp2 NA19058.hp2 |
splice_donor_variant&intron_variant | HIGH | c.851+1G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15722935 | |||||||
| chr4:15723115 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0131 others(1): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.851+181C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723115 | |||||||
| chr4:15723193 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.851+259T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723193 | |||||||
| chr4:15723239 | A | G | 50 | a0001c0004t0002g0004 a0001c0004t0002g0116 a0001c0004t0002g0149 others(47): Show |
65 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.851+305A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723239 | |||||||
| chr4:15723254 | T | C | 6 | a0005c0006t0001g0196 a0006c0008t0001g0020 a0006c0008t0001g0197 others(3): Show |
8 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.851+320T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723254 | |||||||
| chr4:15723283 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.851+349A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723283 | |||||||
| chr4:15723286 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.851+352G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723286 | |||||||
| chr4:15723305 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.851+371G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723305 | |||||||
| chr4:15723442 | G | T | 64 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(61): Show |
91 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.851+508G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723442 | |||||||
| chr4:15723462 | A | G | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+528A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723462 | |||||||
| chr4:15723479 | G | A | 126 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(123): Show |
172 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.851+545G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723479 | |||||||
| chr4:15723490 | C | T | 1 | a0001c0013t0001g0247 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.851+556C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723490 | |||||||
| chr4:15723530 | A | G | 49 | a0001c0004t0002g0004 a0001c0004t0002g0116 a0001c0004t0002g0149 others(46): Show |
64 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.851+596A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723530 | |||||||
| chr4:15723540 | G | A | 1 | a0001c0001t0001g0056 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.851+606G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723540 | |||||||
| chr4:15723547 | C | T | 10 | a0001c0004t0001g0021 a0001c0004t0001g0269 a0001c0004t0001g0286 others(7): Show |
19 | HG00558.hp1 HG02074.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.851+613C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723547 | |||||||
| chr4:15723813 | G | C | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+879G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723813 | |||||||
| chr4:15723832 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(294): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(403): Show |
intron_variant | MODIFIER | c.851+898A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723832 | |||||||
| chr4:15723849 | G | A | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+915G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723849 | |||||||
| chr4:15723999 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851+1065C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15723999 | |||||||
| chr4:15724056 | C | T | 1 | a0003c0003t0002g0026 | 2 | HG00544.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.851+1122C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724056 | |||||||
| chr4:15724060 | G | C | 1 | a0003c0003t0002g0026 | 2 | HG00544.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.851+1126G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724060 | |||||||
| chr4:15724083 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.851+1149G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724083 | |||||||
| chr4:15724136 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.851+1202A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724136 | |||||||
| chr4:15724143 | T | C | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+1209T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724143 | |||||||
| chr4:15724176 | T | G | 1 | a0002c0002t0001g0187 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.851+1242T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724176 | |||||||
| chr4:15724244 | G | T | 10 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0191 others(7): Show |
10 | HG01891.hp2 HG02258.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+1310G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724244 | |||||||
| chr4:15724245 | C | T | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851+1311C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724245 | |||||||
| chr4:15724269 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.851+1335C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724269 | |||||||
| chr4:15724280 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0255 |
3 | HG01433.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.851+1346C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724280 | |||||||
| chr4:15724291 | C | T | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+1357C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724291 | |||||||
| chr4:15724308 | T | G | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.851+1374T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724308 | |||||||
| chr4:15724352 | C | A | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+1418C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724352 | |||||||
| chr4:15724369 | T | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0258 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.851+1435T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724369 | |||||||
| chr4:15724462 | G | T | 2 | a0001c0004t0001g0044 a0001c0004t0001g0065 |
4 | HG00621.hp2 HG01928.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1528G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724462 | |||||||
| chr4:15724464 | A | G | 65 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(62): Show |
92 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.851+1530A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724464 | |||||||
| chr4:15724485 | A | G | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+1551A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724485 | |||||||
| chr4:15724704 | A | AAG | 23 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0126 others(20): Show |
26 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.851+1790_851+1791d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15724704 | ||||||
| chr4:15724704 | A | AAGAG | 6 | a0001c0001t0001g0017 a0001c0001t0001g0046 a0001c0001t0001g0221 others(3): Show |
9 | HG00423.hp1 HG02080.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.851+1788_851+1791d others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15724704 | ||||||
| chr4:15724704 | AAG | A | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+1790_851+1791d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15724704 | ||||||
| chr4:15724798 | A | G | 65 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(62): Show |
92 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.851+1864A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724798 | |||||||
| chr4:15724800 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.851+1866A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724800 | |||||||
| chr4:15724941 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0138 others(6): Show |
13 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.851+2007G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724941 | |||||||
| chr4:15724977 | G | A | 1 | a0002c0002t0001g0184 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.851+2043G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15724977 | |||||||
| chr4:15725020 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.851+2086G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725020 | |||||||
| chr4:15725058 | A | G | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+2124A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725058 | |||||||
| chr4:15725124 | A | AC | 112 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(109): Show |
154 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.851+2190_851+2191i others(3): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725124 | |||||||
| chr4:15725125 | T | C | 1 | a0002c0002t0007g0167 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.851+2191T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725125 | |||||||
| chr4:15725139 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0293 |
2 | NA18995.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.851+2205A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725139 | |||||||
| chr4:15725191 | G | A | 27 | a0001c0004t0002g0004 a0001c0004t0002g0155 a0001c0004t0002g0190 others(24): Show |
38 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.851+2257G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725191 | |||||||
| chr4:15725411 | G | A | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851+2477G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725411 | |||||||
| chr4:15725497 | C | G | 3 | a0007c0014t0001g0050 a0007c0014t0001g0246 a0007c0024t0001g0050 |
3 | HG02922.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.851+2563C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725497 | |||||||
| chr4:15725622 | A | G | 1 | a0006c0008t0010g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.851+2688A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725622 | |||||||
| chr4:15725641 | G | T | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+2707G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725641 | |||||||
| chr4:15725708 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.851+2774G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725708 | |||||||
| chr4:15725718 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851+2784C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725718 | |||||||
| chr4:15725719 | G | A | 48 | a0001c0004t0002g0004 a0001c0004t0002g0116 a0001c0004t0002g0149 others(45): Show |
63 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.851+2785G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725719 | |||||||
| chr4:15725766 | T | C | 65 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(62): Show |
92 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.851+2832T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725766 | |||||||
| chr4:15725893 | T | C | 50 | a0001c0004t0002g0004 a0001c0004t0002g0116 a0001c0004t0002g0149 others(47): Show |
65 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.851+2959T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725893 | |||||||
| chr4:15725944 | G | A | 114 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(111): Show |
156 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.851+3010G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725944 | |||||||
| chr4:15725945 | G | T | 114 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(111): Show |
156 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.851+3011G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725945 | |||||||
| chr4:15725947 | C | CT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(124): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.851+3038dupT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15725947 | ||||||
| chr4:15725947 | C | CTT | 18 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0122 others(15): Show |
18 | HG00438.hp2 HG01243.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.851+3037_851+3038d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15725947 | ||||||
| chr4:15725947 | CT | C | 60 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0004g0127 others(57): Show |
75 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.851+3038delT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15725947 | ||||||
| chr4:15725950 | T | A | 1 | a0002c0002t0011g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.851+3016T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725950 | |||||||
| chr4:15725953 | T | C | 1 | a0002c0002t0011g0176 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.851+3019T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15725953 | |||||||
| chr4:15725982 | TCTCTCTC | T | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+3056_851+3062d others(9): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15725982 | ||||||
| chr4:15726063 | G | A | 5 | a0001c0004t0001g0212 a0006c0008t0001g0020 a0006c0008t0001g0197 others(2): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+3129G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726063 | |||||||
| chr4:15726090 | C | T | 185 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0033 others(182): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.851+3156C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726090 | |||||||
| chr4:15726092 | G | T | 13 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
17 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.851+3158G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726092 | |||||||
| chr4:15726119 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.851+3185G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726119 | |||||||
| chr4:15726136 | G | GT | 10 | a0001c0001t0001g0148 a0001c0001t0001g0162 a0001c0001t0001g0165 others(7): Show |
10 | HG00609.hp2 HG02922.hp1 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.851+3221dupT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726136 | ||||||
| chr4:15726136 | G | GTT | 13 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
17 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.851+3220_851+3221d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726136 | ||||||
| chr4:15726136 | G | GTTT | 18 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0130 others(15): Show |
19 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.851+3219_851+3221d others(5): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726136 | ||||||
| chr4:15726136 | G | GTTTT | 82 | a0001c0001t0001g0129 a0001c0004t0001g0021 a0001c0004t0001g0044 others(79): Show |
123 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.851+3218_851+3221d others(6): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726136 | ||||||
| chr4:15726136 | G | GTTTTT | 15 | a0001c0004t0001g0262 a0001c0004t0001g0271 a0001c0004t0001g0287 others(12): Show |
15 | HG00423.hp2 HG02818.hp1 HG03471.hp2 others(12): Show |
intron_variant | MODIFIER | c.851+3217_851+3221d others(7): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726136 | ||||||
| chr4:15726139 | T | TG | 18 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0002c0020t0001g0173 others(15): Show |
26 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.851+3205_851+3206i others(3): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726139 | |||||||
| chr4:15726140 | T | G | 11 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0010t0001g0031 others(8): Show |
15 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.851+3206T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726140 | |||||||
| chr4:15726141 | T | G | 1 | a0005c0006t0001g0284 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.851+3207T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726141 | |||||||
| chr4:15726194 | A | G | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+3260A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726194 | |||||||
| chr4:15726347 | TGAATG | T | 18 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0002c0020t0001g0173 others(15): Show |
26 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.851+3414_851+3418d others(7): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726347 | |||||||
| chr4:15726355 | C | T | 1 | a0002c0007t0001g0192 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.851+3421C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726355 | |||||||
| chr4:15726356 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.851+3422G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726356 | |||||||
| chr4:15726385 | G | A | 113 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(110): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.851+3451G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726385 | |||||||
| chr4:15726404 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.851+3470C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726404 | |||||||
| chr4:15726443 | A | T | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851+3509A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726443 | |||||||
| chr4:15726456 | C | G | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+3522C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726456 | |||||||
| chr4:15726553 | G | A | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+3619G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726553 | |||||||
| chr4:15726598 | C | A | 30 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0236 others(27): Show |
42 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.851+3664C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726598 | |||||||
| chr4:15726614 | T | G | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+3680T>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726614 | |||||||
| chr4:15726671 | C | G | 115 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(112): Show |
157 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.851+3737C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726671 | |||||||
| chr4:15726733 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.851+3799T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726733 | |||||||
| chr4:15726755 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.851+3821C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726755 | |||||||
| chr4:15726758 | C | A | 1 | a0001c0001t0001g0060 | 2 | NA18981.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.851+3824C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726758 | |||||||
| chr4:15726813 | C | A | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.851+3879C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726813 | |||||||
| chr4:15726824 | G | A | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.851+3890G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726824 | |||||||
| chr4:15726832 | A | C | 5 | a0001c0004t0001g0212 a0006c0008t0001g0020 a0006c0008t0001g0197 others(2): Show |
7 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+3898A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726832 | |||||||
| chr4:15726869 | A | AT | 10 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0140 others(7): Show |
10 | HG01123.hp1 HG01361.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.851+3954dupT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726869 | ||||||
| chr4:15726869 | A | ATT | 15 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(12): Show |
16 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.851+3953_851+3954d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726869 | ||||||
| chr4:15726869 | AT | A | 76 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0038 others(73): Show |
111 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.851+3954delT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726869 | ||||||
| chr4:15726869 | ATT | A | 7 | a0001c0001t0001g0319 a0002c0002t0001g0184 a0003c0003t0002g0067 others(4): Show |
7 | HG01978.hp2 HG02735.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.851+3953_851+3954d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726869 | ||||||
| chr4:15726869 | ATTT | A | 52 | a0001c0004t0001g0212 a0001c0004t0002g0004 a0001c0004t0002g0116 others(49): Show |
69 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.851+3952_851+3954d others(5): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15726869 | ||||||
| chr4:15726937 | C | G | 1 | a0001c0001t0001g0297 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.851+4003C>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726937 | |||||||
| chr4:15726944 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.851+4010C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726944 | |||||||
| chr4:15726969 | C | T | 50 | a0001c0004t0002g0004 a0001c0004t0002g0116 a0001c0004t0002g0149 others(47): Show |
65 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.851+4035C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726969 | |||||||
| chr4:15726995 | C | T | 1 | a0006c0011t0001g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.851+4061C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15726995 | |||||||
| chr4:15727029 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.851+4095T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727029 | |||||||
| chr4:15727149 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(291): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(400): Show |
intron_variant | MODIFIER | c.851+4215T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727149 | |||||||
| chr4:15727155 | G | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.851+4221G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727155 | |||||||
| chr4:15727168 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.851+4234C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727168 | |||||||
| chr4:15727183 | A | G | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.851+4249A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727183 | |||||||
| chr4:15727273 | G | A | 30 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0236 others(27): Show |
42 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.851+4339G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727273 | |||||||
| chr4:15727335 | A | T | 1 | a0003c0003t0002g0086 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.851+4401A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727335 | |||||||
| chr4:15727550 | A | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-4190A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727550 | |||||||
| chr4:15727690 | T | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-4050T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727690 | |||||||
| chr4:15727894 | G | T | 31 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0059 others(28): Show |
43 | HG00733.hp2 HG01069.hp2 HG01261.hp2 others(40): Show |
intron_variant | MODIFIER | c.852-3846G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727894 | |||||||
| chr4:15727911 | G | A | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-3829G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15727911 | |||||||
| chr4:15728160 | G | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-3580G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728160 | |||||||
| chr4:15728175 | C | T | 50 | a0001c0004t0002g0004 a0001c0004t0002g0116 a0001c0004t0002g0149 others(47): Show |
65 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.852-3565C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728175 | |||||||
| chr4:15728189 | G | A | 1 | a0002c0002t0001g0154 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.852-3551G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728189 | |||||||
| chr4:15728449 | C | CT | 34 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0161 others(31): Show |
46 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.852-3272dupT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15728449 | ||||||
| chr4:15728449 | CT | C | 54 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0160 others(51): Show |
80 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.852-3272delT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15728449 | ||||||
| chr4:15728449 | CTT | C | 49 | a0001c0004t0002g0004 a0001c0004t0002g0116 a0001c0004t0002g0149 others(46): Show |
64 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.852-3273_852-3272d others(4): Show |
BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15728449 | ||||||
| chr4:15728480 | A | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-3260A>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728480 | |||||||
| chr4:15728483 | G | A | 1 | a0005c0006t0001g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.852-3257G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728483 | |||||||
| chr4:15728484 | C | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-3256C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728484 | |||||||
| chr4:15728523 | G | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
152 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.852-3217G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728523 | |||||||
| chr4:15728528 | T | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-3212T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728528 | |||||||
| chr4:15728543 | C | A | 1 | a0001c0001t0006g0034 | 2 | HG01109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.852-3197C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728543 | |||||||
| chr4:15728630 | C | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-3110C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728630 | |||||||
| chr4:15728643 | C | CT | 35 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0039 others(32): Show |
42 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.852-3078dupT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15728643 | ||||||
| chr4:15728643 | CT | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0148 others(16): Show |
24 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.852-3078delT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15728643 | ||||||
| chr4:15728673 | T | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-3067T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728673 | |||||||
| chr4:15728716 | C | T | 1 | a0003c0003t0002g0105 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.852-3024C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728716 | |||||||
| chr4:15728726 | G | C | 30 | a0001c0001t0001g0033 a0001c0001t0001g0112 a0001c0001t0001g0236 others(27): Show |
42 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.852-3014G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728726 | |||||||
| chr4:15728775 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
152 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.852-2965A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728775 | |||||||
| chr4:15728782 | C | A | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-2958C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728782 | |||||||
| chr4:15728832 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.852-2908G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728832 | |||||||
| chr4:15728890 | T | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-2850T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15728890 | |||||||
| chr4:15729126 | A | T | 1 | a0008c0012t0001g0142 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.852-2614A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729126 | |||||||
| chr4:15729199 | C | T | 16 | a0001c0001t0001g0063 a0001c0001t0001g0128 a0001c0001t0001g0129 others(13): Show |
17 | HG01109.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.852-2541C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729199 | |||||||
| chr4:15729238 | A | G | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-2502A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729238 | |||||||
| chr4:15729280 | C | T | 13 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(10): Show |
17 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.852-2460C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729280 | |||||||
| chr4:15729324 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.852-2416T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729324 | |||||||
| chr4:15729413 | T | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-2327T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729413 | |||||||
| chr4:15729486 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.852-2254C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729486 | |||||||
| chr4:15729562 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.852-2178C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729562 | |||||||
| chr4:15729613 | T | C | 8 | a0001c0004t0002g0149 a0003c0003t0002g0024 a0003c0003t0002g0030 others(5): Show |
10 | HG00558.hp2 HG00597.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.852-2127T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729613 | |||||||
| chr4:15729751 | G | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-1989G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729751 | |||||||
| chr4:15729775 | C | T | 1 | a0003c0003t0002g0074 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.852-1965C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729775 | |||||||
| chr4:15729898 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0255 |
3 | HG01433.hp1 HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.852-1842G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729898 | |||||||
| chr4:15729911 | A | G | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-1829A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729911 | |||||||
| chr4:15729937 | G | T | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0046 others(24): Show |
33 | HG00099.hp1 HG00423.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.852-1803G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15729937 | |||||||
| chr4:15730067 | G | A | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0046 others(24): Show |
33 | HG00099.hp1 HG00423.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.852-1673G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730067 | |||||||
| chr4:15730072 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.852-1668T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730072 | |||||||
| chr4:15730570 | C | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-1170C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730570 | |||||||
| chr4:15730680 | G | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-1060G>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730680 | |||||||
| chr4:15730754 | G | A | 2 | a0001c0013t0001g0247 a0001c0013t0001g0248 |
2 | HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.852-986G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730754 | |||||||
| chr4:15730757 | C | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-983C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730757 | |||||||
| chr4:15730833 | T | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-907T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730833 | |||||||
| chr4:15730914 | CT | C | 115 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0046 others(112): Show |
162 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.852-813delT | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr4 | 15730914 | ||||||
| chr4:15730927 | T | A | 1 | a0002c0002t0009g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.852-813T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730927 | |||||||
| chr4:15730928 | A | T | 1 | a0002c0002t0009g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.852-812A>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730928 | |||||||
| chr4:15730929 | T | A | 1 | a0002c0002t0009g0168 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.852-811T>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15730929 | |||||||
| chr4:15731061 | G | A | 1 | a0006c0008t0010g0202 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.852-679G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731061 | |||||||
| chr4:15731168 | C | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-572C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731168 | |||||||
| chr4:15731207 | T | C | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-533T>C | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731207 | |||||||
| chr4:15731226 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.852-514G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731226 | |||||||
| chr4:15731234 | C | T | 1 | a0001c0025t0008g0066 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.852-506C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731234 | |||||||
| chr4:15731317 | C | T | 1 | a0003c0003t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.852-423C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731317 | |||||||
| chr4:15731397 | G | A | 27 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0046 others(24): Show |
33 | HG00099.hp1 HG00423.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.852-343G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731397 | |||||||
| chr4:15731407 | G | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(316): Show |
434 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(431): Show |
intron_variant | MODIFIER | c.852-333G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731407 | |||||||
| chr4:15731445 | G | T | 1 | a0002c0002t0001g0171 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.852-295G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731445 | |||||||
| chr4:15731470 | C | A | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-270C>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731470 | |||||||
| chr4:15731485 | G | T | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-255G>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731485 | |||||||
| chr4:15731536 | A | G | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-204A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731536 | |||||||
| chr4:15731625 | C | T | 43 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(40): Show |
67 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.852-115C>T | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731625 | |||||||
| chr4:15731643 | G | A | 100 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(97): Show |
141 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.852-97G>A | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731643 | |||||||
| chr4:15731674 | A | G | 45 | a0001c0004t0001g0021 a0001c0004t0001g0044 a0001c0004t0001g0057 others(42): Show |
69 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.852-66A>G | BST1 | ENSG00000109743.11 | transcript | ENST00000265016.9 | protein_coding | 8/8 | chr4 | 15731674 |