Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 682 |
| ensemblid | ENSG00000172270.22 |
| hgncid | 1116 |
| symbol | BSG |
| name | basigin (Ok blood group) |
| refseq_nuc | NM_001728.4 |
| refseq_prot | NP_001719.2 |
| ensembl_nuc | ENST00000333511.9 |
| ensembl_prot | ENSP00000333769.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 572596 |
| end | 583493 |
| strand | + |
| ver | v1.2 |
| region | chr19:572596-583493 |
| region5000 | chr19:567596-588493 |
| regionname0 | BSG_chr19_572596_583493 |
| regionname5000 | BSG_chr19_567596_588493 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 385 | 294 | 71 | 70 | 99 | 16 | 36 | 66 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| a0002 | 0/0 | 385 | 3 | 0 | 1 | 2 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| a0003 | 0/0 | 385 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| a0004 | 0/0 | 385 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| a0005 | 0/0 | 385 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| a0006 | 0/0 | 385 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| a0007 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| a0008 | 0/0 | 385 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | MAAAL others(380): Show |
chr19 | 567596 | 588493 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1155 | 139 | 37 | 42 | 37 | 10 | 11 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0002 | 0/0 | 1155 | 88 | 16 | 16 | 41 | 1 | 14 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0003 | 0/0 | 1155 | 54 | 12 | 10 | 20 | 3 | 9 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0004 | 0/0 | 1155 | 3 | 3 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0006 | 0/0 | 1155 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0008 | 0/0 | 1155 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0010 | 0/0 | 1155 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0013 | 0/0 | 1155 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0015 | 0/0 | 1155 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0016 | 0/0 | 1155 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0001c0018 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0002c0007 | 0/0 | 1155 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0002c0014 | 0/0 | 1155 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0003c0005 | 0/0 | 1155 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0004c0009 | 0/0 | 1155 | 2 | 0 | 0 | 1 | 0 | 1 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0005c0011 | 0/0 | 1155 | 2 | 1 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0006c0019 | 0/0 | 1155 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0007c0017 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 | ||
| a0008c0012 | 0/0 | 1155 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | ATGGC others(1150): Show |
chr19 | 567596 | 588493 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1946 | 3 | 3 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0002 | 1/1 | 1946 | 69 | 3 | 23 | 25 | 9 | 7 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0003 | 0/0 | 1946 | 36 | 22 | 5 | 9 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0005 | 0/0 | 1946 | 15 | 1 | 11 | 2 | 0 | 1 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0007 | 0/0 | 1946 | 8 | 2 | 3 | 0 | 0 | 3 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0011 | 0/0 | 1946 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0015 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0017 | 0/0 | 1945 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1940): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0020 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0021 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0023 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0001t0024 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | GGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0002t0001 | 0/0 | 1946 | 83 | 14 | 15 | 40 | 1 | 13 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0002t0002 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0002t0012 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0002t0016 | 0/0 | 1945 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1940): Show |
chr19 | 567596 | 588493 |
| a0001c0002t0018 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0002t0019 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0003t0001 | 0/0 | 1946 | 3 | 0 | 1 | 0 | 1 | 1 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0003t0004 | 0/0 | 1946 | 35 | 6 | 6 | 13 | 2 | 8 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0003t0006 | 0/0 | 1946 | 8 | 6 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0003t0008 | 0/0 | 1946 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0003t0009 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0003t0010 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0003t0014 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0004t0003 | 0/0 | 1946 | 3 | 3 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0006t0002 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0006t0013 | 0/0 | 1945 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1940): Show |
chr19 | 567596 | 588493 |
| a0001c0008t0002 | 0/0 | 1946 | 2 | 0 | 1 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0010t0001 | 0/0 | 1946 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0013t0001 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0015t0004 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0016t0005 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0001c0018t0001 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0002c0007t0001 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0002c0014t0001 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0003c0005t0001 | 0/0 | 1946 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0004c0009t0003 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0004c0009t0022 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0005c0011t0002 | 0/0 | 1946 | 2 | 1 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0006c0019t0005 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0007c0017t0002 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| a0008c0012t0001 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | AGCGG others(1941): Show |
chr19 | 567596 | 588493 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0002 | 1/1 | 23 | 1 | 5 | 12 | 1 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0004 | 0/0 | 8 | 1 | 2 | 1 | 2 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0007g0009 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0007g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0015g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0017g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0020g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0021g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0023g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0001t0024g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0001 | 0/0 | 23 | 1 | 3 | 16 | 0 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0006 | 0/0 | 6 | 0 | 2 | 1 | 0 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0018g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0002t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0003 | 0/0 | 9 | 0 | 4 | 1 | 1 | 3 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0006g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0008g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0009g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0009g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0003t0014g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0004t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0004t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0006t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0006t0013g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0008t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0008t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0010t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0010t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0013t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0015t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0016t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0001c0018t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0002c0007t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0002c0014t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0003c0005t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0003c0005t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0004c0009t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0004c0009t0022g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0005c0011t0002g0004 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0006c0019t0005g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0007c0017t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| a0008c0012t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0066 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00140 | hp1 | a0001 | c0001 | t0015 | g0004 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0124 | EUR | GBR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0037 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0154 | EUR | FIN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00408 | hp1 | a0001 | c0003 | t0004 | g0157 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00423 | hp1 | a0001 | c0018 | t0001 | g0131 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00544 | hp2 | a0001 | c0003 | t0008 | g0003 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00621 | hp2 | a0001 | c0003 | t0014 | g0054 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00639 | hp1 | a0006 | c0019 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00642 | hp2 | a0001 | c0003 | t0004 | g0003 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00673 | hp2 | a0001 | c0003 | t0009 | g0003 | EAS | CHS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0110 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01074 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01099 | hp1 | a0001 | c0003 | t0004 | g0003 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0082 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01106 | hp2 | a0001 | c0003 | t0004 | g0062 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01109 | hp2 | a0001 | c0003 | t0006 | g0039 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01167 | hp2 | a0001 | c0008 | t0002 | g0007 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01168 | hp2 | a0001 | c0006 | t0013 | g0146 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0107 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01243 | hp2 | a0001 | c0003 | t0006 | g0003 | AMR | PUR | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0029 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01256 | hp1 | a0001 | c0003 | t0004 | g0003 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01361 | hp2 | a0001 | c0003 | t0004 | g0003 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01516 | hp2 | a0001 | c0003 | t0004 | g0003 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0150 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01517 | hp2 | a0001 | c0003 | t0004 | g0019 | EUR | IBS | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01884 | hp2 | a0001 | c0001 | t0020 | g0024 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01891 | hp1 | a0001 | c0004 | t0003 | g0022 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0077 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01943 | hp1 | a0001 | c0001 | t0007 | g0114 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01943 | hp2 | a0003 | c0005 | t0001 | g0116 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01952 | hp1 | a0003 | c0005 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01975 | hp2 | a0001 | c0003 | t0004 | g0020 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0167 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01981 | hp2 | a0002 | c0014 | t0001 | g0118 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02004 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02015 | hp2 | a0001 | c0003 | t0004 | g0019 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02027 | hp2 | a0001 | c0003 | t0009 | g0038 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02040 | hp1 | a0002 | c0007 | t0001 | g0010 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02056 | hp1 | a0001 | c0001 | t0017 | g0023 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02074 | hp1 | a0001 | c0003 | t0004 | g0035 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02129 | hp1 | a0001 | c0003 | t0004 | g0035 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02129 | hp2 | a0001 | c0003 | t0004 | g0003 | EAS | KHV | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02145 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CDX | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02155 | hp2 | a0001 | c0001 | t0005 | g0080 | EAS | CDX | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0073 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0079 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02300 | hp2 | a0001 | c0003 | t0008 | g0003 | AMR | PEL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02451 | hp1 | a0001 | c0003 | t0006 | g0059 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02451 | hp2 | a0001 | c0010 | t0001 | g0070 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02572 | hp2 | a0001 | c0003 | t0006 | g0061 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02602 | hp2 | a0001 | c0003 | t0004 | g0003 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0100 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02647 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02698 | hp2 | a0001 | c0003 | t0004 | g0071 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0113 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0009 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02896 | hp1 | a0001 | c0002 | t0019 | g0090 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0067 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02922 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02970 | hp1 | a0001 | c0001 | t0024 | g0072 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03017 | hp1 | a0001 | c0016 | t0005 | g0075 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0148 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0053 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03209 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03239 | hp1 | a0004 | c0009 | t0003 | g0094 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0076 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03516 | hp2 | a0001 | c0004 | t0003 | g0022 | AFR | ESN | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03540 | hp2 | a0001 | c0010 | t0001 | g0084 | AFR | GWD | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03579 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03579 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03654 | hp1 | a0001 | c0002 | t0018 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03704 | hp2 | a0005 | c0011 | t0002 | g0004 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0033 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03831 | hp2 | a0001 | c0003 | t0004 | g0040 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03834 | hp1 | a0001 | c0015 | t0004 | g0064 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03942 | hp2 | a0001 | c0003 | t0004 | g0058 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04184 | hp1 | a0001 | c0003 | t0004 | g0003 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04184 | hp2 | a0001 | c0003 | t0004 | g0020 | SAS | BEB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0033 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04199 | hp2 | a0001 | c0003 | t0004 | g0056 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0103 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG04228 | hp2 | a0001 | c0003 | t0004 | g0003 | SAS | STU | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18522 | hp1 | a0001 | c0004 | t0003 | g0092 | AFR | YRI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18939 | hp1 | a0001 | c0003 | t0008 | g0063 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18952 | hp2 | a0001 | c0003 | t0004 | g0018 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18964 | hp1 | a0001 | c0003 | t0004 | g0156 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18970 | hp2 | a0001 | c0003 | t0004 | g0057 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18979 | hp1 | a0001 | c0003 | t0004 | g0162 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18982 | hp1 | a0001 | c0002 | t0016 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18995 | hp2 | a0001 | c0003 | t0004 | g0018 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA18998 | hp2 | a0001 | c0003 | t0004 | g0060 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19007 | hp1 | a0001 | c0003 | t0010 | g0003 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19043 | hp2 | a0001 | c0002 | t0012 | g0001 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19060 | hp2 | a0007 | c0017 | t0002 | g0007 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19066 | hp2 | a0001 | c0003 | t0004 | g0052 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19074 | hp1 | a0001 | c0003 | t0010 | g0055 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19082 | hp2 | a0004 | c0009 | t0022 | g0093 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19085 | hp2 | a0008 | c0012 | t0001 | g0145 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19088 | hp2 | a0002 | c0007 | t0001 | g0010 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19091 | hp1 | a0001 | c0003 | t0004 | g0018 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ASW | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ASW | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20752 | hp1 | a0001 | c0006 | t0002 | g0105 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20805 | hp2 | a0001 | c0008 | t0002 | g0011 | EUR | TSI | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0108 | SAS | GIH | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0065 | SAS | GIH | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02109 | hp1 | a0001 | c0013 | t0001 | g0001 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02486 | hp1 | a0001 | c0001 | t0021 | g0074 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | MSL | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG06807 | hp1 | a0005 | c0011 | t0002 | g0004 | AFR | USA | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| HG06807 | hp2 | a0001 | c0001 | t0023 | g0068 | AFR | USA | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | LWK | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0002 | REF | REF | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | BSG_chr19_567596_588493 | BSG | chr19 | 567596 | 588493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:572663 | G | A | 1 | a0003 | 2 | HG01943.hp2 HG01952.hp1 |
missense_variant | MODERATE | c.29G>A | p.Gly10Glu | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 68/1946 | 29/1158 | 10/385 | chr19 | 572663 | |||
| chr19:572680 | A | G | 1 | a0005 | 2 | HG03704.hp2 HG06807.hp1 |
missense_variant | MODERATE | c.46A>G | p.Thr16Ala | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 85/1946 | 46/1158 | 16/385 | chr19 | 572680 | |||
| chr19:577776 | G | A | 1 | a0008 | 1 | NA19085.hp2 | missense_variant&splice_region_variant | MODERATE | c.70G>A | p.Gly24Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 109/1946 | 70/1158 | 24/385 | chr19 | 577776 | |||
| chr19:577782 | G | T | 1 | a0006 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.76G>T | p.Val26Phe | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 115/1946 | 76/1158 | 26/385 | chr19 | 577782 | |||
| chr19:577963 | A | G | 1 | a0007 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.257A>G | p.His86Arg | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 296/1946 | 257/1158 | 86/385 | chr19 | 577963 | |||
| chr19:580389 | G | A | 1 | a0002 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.583G>A | p.Asp195Asn | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/9 | 622/1946 | 583/1158 | 195/385 | chr19 | 580389 | |||
| chr19:580389 | G | C | 1 | a0002 | 2 | HG02040.hp1 NA19088.hp2 |
missense_variant | MODERATE | c.583G>C | p.Asp195His | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/9 | 622/1946 | 583/1158 | 195/385 | chr19 | 580389 | |||
| chr19:582310 | C | G | 1 | a0004 | 2 | HG03239.hp1 NA19082.hp2 |
missense_variant | MODERATE | c.1074C>G | p.Asp358Glu | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/9 | 1113/1946 | 1074/1158 | 358/385 | chr19 | 582310 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:577793 | G | A | 1 | a0001c0006 | 2 | HG01168.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.87G>A | p.Pro29Pro | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 126/1946 | 87/1158 | 29/385 | chr19 | 577793 | |||
| chr19:577952 | C | T | 1 | a0001c0018 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.246C>T | p.His82His | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 285/1946 | 246/1158 | 82/385 | chr19 | 577952 | |||
| chr19:578105 | C | T | 1 | a0001c0010 | 2 | HG02451.hp2 HG03540.hp2 |
synonymous_variant | LOW | c.399C>T | p.Val133Val | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/9 | 438/1946 | 399/1158 | 133/385 | chr19 | 578105 | |||
| chr19:579519 | C | T | 1 | a0001c0016 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.435C>T | p.Thr145Thr | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/9 | 474/1946 | 435/1158 | 145/385 | chr19 | 579519 | |||
| chr19:579627 | C | T | 2 | a0001c0003 a0001c0015 |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
synonymous_variant | LOW | c.543C>T | p.Asp181Asp | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/9 | 582/1946 | 543/1158 | 181/385 | chr19 | 579627 | |||
| chr19:579630 | G | A | 1 | a0001c0013 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.546G>A | p.Ala182Ala | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/9 | 585/1946 | 546/1158 | 182/385 | chr19 | 579630 | |||
| chr19:580388 | C | G | 2 | a0001c0003 a0001c0015 |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
synonymous_variant | LOW | c.582C>G | p.Ser194Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/9 | 621/1946 | 582/1158 | 194/385 | chr19 | 580388 | |||
| chr19:580665 | T | C | 8 | a0001c0002 a0001c0010 a0001c0013 others(5): Show |
98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
synonymous_variant | LOW | c.675T>C | p.Ala225Ala | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/9 | 714/1946 | 675/1158 | 225/385 | chr19 | 580665 | |||
| chr19:580710 | G | A | 1 | a0001c0008 | 2 | HG01167.hp2 NA20805.hp2 |
synonymous_variant | LOW | c.720G>A | p.Leu240Leu | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/9 | 759/1946 | 720/1158 | 240/385 | chr19 | 580710 | |||
| chr19:581332 | C | G | 1 | a0001c0015 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.810C>G | p.Ser270Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/9 | 849/1946 | 810/1158 | 270/385 | chr19 | 581332 | |||
| chr19:581371 | A | G | 1 | a0001c0004 | 3 | HG01891.hp1 HG03516.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.849A>G | p.Ser283Ser | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/9 | 888/1946 | 849/1158 | 283/385 | chr19 | 581371 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:572596 | A | G | 1 | a0001c0001t0024 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 39 | chr19 | 572596 | ||||||
| chr19:572602 | T | A | 1 | a0001c0002t0012 | 1 | NA19043.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 33 | chr19 | 572602 | ||||||
| chr19:572610 | G | T | 1 | a0001c0001t0023 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | 25 | chr19 | 572610 | ||||||
| chr19:572628 | A | G | 1 | a0001c0003t0008 | 3 | HG00544.hp2 HG02300.hp2 NA18939.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/9 | chr19 | 572628 | |||||||
| chr19:582775 | A | G | 34 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(31): Show |
227 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*31A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 198 | chr19 | 582775 | ||||||
| chr19:582878 | CT | C | 3 | a0001c0001t0017 a0001c0002t0016 a0001c0006t0013 |
3 | HG01168.hp2 HG02056.hp1 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*140delT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 307 | INFO_REALIGN_3_PRIME | chr19 | 582878 | |||||
| chr19:582927 | T | A | 21 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0012 others(18): Show |
155 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*183T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 350 | chr19 | 582927 | ||||||
| chr19:582982 | C | T | 1 | a0001c0003t0006 | 8 | HG01109.hp2 HG01243.hp2 HG02451.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 405 | chr19 | 582982 | ||||||
| chr19:583224 | T | G | 1 | a0001c0001t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 647 | chr19 | 583224 | ||||||
| chr19:583255 | C | T | 1 | a0004c0009t0022 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*511C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 678 | chr19 | 583255 | ||||||
| chr19:583256 | G | A | 1 | a0001c0002t0018 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 679 | chr19 | 583256 | ||||||
| chr19:583268 | G | A | 3 | a0001c0001t0005 a0001c0016t0005 a0006c0019t0005 |
17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*524G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 691 | chr19 | 583268 | ||||||
| chr19:583314 | C | T | 1 | a0001c0001t0021 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*570C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 737 | chr19 | 583314 | ||||||
| chr19:583361 | G | A | 1 | a0001c0002t0019 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 784 | chr19 | 583361 | ||||||
| chr19:583418 | T | C | 7 | a0001c0003t0004 a0001c0003t0006 a0001c0003t0008 others(4): Show |
52 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*674T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 841 | chr19 | 583418 | ||||||
| chr19:583435 | C | T | 1 | a0001c0003t0010 | 2 | NA19007.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*691C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 858 | chr19 | 583435 | ||||||
| chr19:583443 | C | G | 1 | a0001c0001t0011 | 2 | HG02717.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 866 | chr19 | 583443 | ||||||
| chr19:583450 | C | T | 1 | a0001c0001t0007 | 8 | HG01167.hp1 HG01169.hp2 HG01943.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*706C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 873 | chr19 | 583450 | ||||||
| chr19:583460 | G | A | 6 | a0001c0003t0004 a0001c0003t0006 a0001c0003t0008 others(3): Show |
50 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*716G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 883 | chr19 | 583460 | ||||||
| chr19:583490 | C | T | 1 | a0001c0001t0015 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*746C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 9/9 | 913 | chr19 | 583490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:572721 | C | CG | 13 | a0001c0001t0002g0013 a0001c0001t0002g0047 a0001c0001t0002g0049 others(10): Show |
15 | HG00408.hp2 HG00735.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.67+25dupG | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 572721 | ||||||
| chr19:572721 | C | G | 2 | a0001c0001t0005g0167 a0001c0002t0001g0168 |
2 | HG01978.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.67+20C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572721 | |||||||
| chr19:572764 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.67+63C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572764 | |||||||
| chr19:572811 | G | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0049 |
3 | HG00099.hp1 HG00323.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.67+110G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572811 | |||||||
| chr19:572860 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.67+159G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572860 | |||||||
| chr19:572878 | T | C | 32 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 others(29): Show |
50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+177T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572878 | |||||||
| chr19:572884 | G | C | 1 | a0001c0001t0003g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.67+183G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572884 | |||||||
| chr19:572934 | TCCGGCCT others(5): Show |
T | 32 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 others(29): Show |
50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+242_67+253delGA others(10): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 572934 | ||||||
| chr19:572988 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0073 a0001c0001t0021g0074 others(1): Show |
5 | HG02257.hp2 HG02486.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+287G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572988 | |||||||
| chr19:572998 | G | C | 11 | a0001c0001t0005g0005 a0001c0001t0005g0041 a0001c0001t0005g0076 others(8): Show |
17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+297G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 572998 | |||||||
| chr19:573068 | T | TTTCCCGG others(11): Show |
32 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 others(29): Show |
50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+367_67+368insTT others(16): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573068 | |||||||
| chr19:573070 | A | ATCTCG | 32 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 others(29): Show |
50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+369_67+370insTC others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573070 | |||||||
| chr19:573132 | T | C | 1 | a0001c0016t0005g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.67+431T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573132 | |||||||
| chr19:573145 | G | T | 2 | a0001c0001t0002g0036 a0001c0001t0002g0165 |
3 | HG02155.hp1 NA18983.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.67+444G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573145 | |||||||
| chr19:573188 | C | G | 1 | a0001c0001t0005g0081 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.67+487C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573188 | |||||||
| chr19:573205 | T | C | 32 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 others(29): Show |
50 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.67+504T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573205 | |||||||
| chr19:573522 | C | T | 2 | a0001c0002t0001g0163 a0001c0002t0001g0164 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.67+821C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573522 | |||||||
| chr19:573623 | A | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.67+922A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573623 | |||||||
| chr19:573698 | C | G | 7 | a0001c0001t0003g0021 a0001c0001t0003g0073 a0001c0001t0003g0091 others(4): Show |
9 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+997C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573698 | |||||||
| chr19:573712 | AG | A | 31 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 others(28): Show |
49 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.67+1016delG | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 573712 | ||||||
| chr19:573777 | C | G | 3 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 |
3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67+1076C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573777 | |||||||
| chr19:573869 | G | A | 1 | a0001c0001t0005g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.67+1168G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573869 | |||||||
| chr19:573967 | T | C | 1 | a0001c0003t0004g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.67+1266T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 573967 | |||||||
| chr19:574025 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.67+1324C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574025 | |||||||
| chr19:574199 | G | A | 8 | a0001c0002t0001g0083 a0001c0002t0001g0085 a0001c0002t0001g0086 others(5): Show |
8 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+1498G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574199 | |||||||
| chr19:574253 | T | TA | 19 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(16): Show |
24 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.67+1568dupA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574253 | ||||||
| chr19:574253 | T | TAA | 7 | a0001c0001t0003g0021 a0001c0001t0003g0073 a0001c0001t0003g0091 others(4): Show |
9 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+1567_67+1568dup others(2): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574253 | ||||||
| chr19:574253 | TA | T | 53 | a0001c0001t0002g0007 a0001c0001t0002g0151 a0001c0001t0002g0152 others(50): Show |
79 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.67+1568delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574253 | ||||||
| chr19:574254 | A | T | 1 | a0001c0001t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67+1553A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574254 | |||||||
| chr19:574255 | A | T | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+1554A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574255 | |||||||
| chr19:574301 | C | T | 31 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(28): Show |
42 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.67+1600C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574301 | |||||||
| chr19:574429 | T | A | 11 | a0001c0001t0005g0005 a0001c0001t0005g0041 a0001c0001t0005g0076 others(8): Show |
17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.67+1728T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574429 | |||||||
| chr19:574448 | G | A | 1 | a0001c0003t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67+1747G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574448 | |||||||
| chr19:574449 | A | G | 1 | a0001c0003t0004g0071 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67+1748A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574449 | |||||||
| chr19:574477 | A | C | 1 | a0001c0002t0001g0140 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.67+1776A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574477 | |||||||
| chr19:574484 | C | T | 1 | a0001c0003t0004g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.67+1783C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574484 | |||||||
| chr19:574489 | C | G | 1 | a0001c0002t0001g0096 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.67+1788C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574489 | |||||||
| chr19:574532 | G | A | 3 | a0001c0001t0003g0021 a0001c0001t0003g0073 a0001c0001t0024g0072 |
4 | HG02257.hp2 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+1831G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574532 | |||||||
| chr19:574545 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+1844C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574545 | |||||||
| chr19:574547 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+1846C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574547 | |||||||
| chr19:574552 | C | CA | 35 | a0001c0001t0003g0091 a0001c0002t0001g0103 a0001c0003t0001g0065 others(32): Show |
56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.67+1860dupA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574552 | ||||||
| chr19:574562 | C | A | 1 | a0001c0003t0004g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.67+1861C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574562 | |||||||
| chr19:574568 | AAAAATTT others(20): Show |
A | 1 | a0001c0001t0005g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.67+1870_67+1896del others(27): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574568 | ||||||
| chr19:574573 | T | A | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+1872T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574573 | |||||||
| chr19:574636 | C | G | 1 | a0001c0003t0004g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.67+1935C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574636 | |||||||
| chr19:574641 | G | A | 3 | a0001c0001t0003g0043 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.67+1940G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574641 | |||||||
| chr19:574824 | G | A | 1 | a0008c0012t0001g0145 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.67+2123G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574824 | |||||||
| chr19:574852 | CAGAT | C | 1 | a0001c0003t0004g0008 | 4 | HG02145.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+2154_67+2157del others(4): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 574852 | ||||||
| chr19:574861 | G | A | 1 | a0001c0002t0001g0083 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67+2160G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574861 | |||||||
| chr19:574882 | G | A | 2 | a0004c0009t0003g0094 a0004c0009t0022g0093 |
2 | HG03239.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.67+2181G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574882 | |||||||
| chr19:574893 | C | T | 1 | a0001c0002t0001g0139 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.67+2192C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574893 | |||||||
| chr19:574927 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+2226C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574927 | |||||||
| chr19:574951 | G | A | 1 | a0001c0001t0005g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.67+2250G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574951 | |||||||
| chr19:574973 | T | G | 1 | a0001c0002t0001g0104 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.67+2272T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 574973 | |||||||
| chr19:575083 | G | C | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+2382G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575083 | |||||||
| chr19:575159 | G | A | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.67+2458G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575159 | |||||||
| chr19:575255 | G | A | 17 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(14): Show |
22 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.68-2519G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575255 | |||||||
| chr19:575353 | G | T | 3 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 |
3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-2421G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575353 | |||||||
| chr19:575406 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.68-2368C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575406 | |||||||
| chr19:575445 | C | T | 11 | a0001c0001t0005g0005 a0001c0001t0005g0041 a0001c0001t0005g0076 others(8): Show |
17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-2329C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575445 | |||||||
| chr19:575605 | TGGGTGGG others(9): Show |
T | 1 | a0001c0001t0002g0138 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.68-2160_68-2145del others(16): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 575605 | ||||||
| chr19:575647 | G | C | 2 | a0001c0006t0002g0105 a0001c0006t0013g0146 |
2 | HG01168.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.68-2127G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575647 | |||||||
| chr19:575675 | C | A | 1 | a0001c0002t0001g0106 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.68-2099C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575675 | |||||||
| chr19:575697 | TG | T | 35 | a0001c0001t0007g0107 a0001c0003t0001g0065 a0001c0003t0001g0066 others(32): Show |
56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.68-2074delG | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 575697 | ||||||
| chr19:575754 | T | C | 10 | a0001c0002t0001g0017 a0001c0002t0001g0044 a0001c0002t0001g0108 others(7): Show |
12 | HG00735.hp1 HG00738.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-2020T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575754 | |||||||
| chr19:575780 | T | A | 1 | a0001c0001t0003g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.68-1994T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575780 | |||||||
| chr19:575782 | C | T | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.68-1992C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575782 | |||||||
| chr19:575805 | G | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-1969G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575805 | |||||||
| chr19:575818 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0155 |
4 | HG00423.hp2 HG01070.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-1956C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575818 | |||||||
| chr19:575886 | G | A | 1 | a0001c0001t0024g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.68-1888G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575886 | |||||||
| chr19:575910 | G | A | 1 | a0001c0003t0004g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.68-1864G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575910 | |||||||
| chr19:575921 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0102 a0001c0001t0003g0142 |
5 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-1853A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575921 | |||||||
| chr19:575942 | C | T | 20 | a0001c0002t0001g0012 a0001c0002t0001g0017 a0001c0002t0001g0044 others(17): Show |
25 | HG00735.hp1 HG00738.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-1832C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575942 | |||||||
| chr19:575943 | G | GC | 17 | a0001c0001t0002g0011 a0001c0001t0002g0050 a0001c0001t0002g0135 others(14): Show |
25 | HG00408.hp1 HG01175.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.68-1824dupC | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 575943 | ||||||
| chr19:575964 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-1810C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575964 | |||||||
| chr19:575997 | C | T | 3 | a0001c0001t0003g0043 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.68-1777C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 575997 | |||||||
| chr19:576010 | G | A | 1 | a0001c0002t0001g0147 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.68-1764G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576010 | |||||||
| chr19:576157 | C | G | 1 | a0001c0018t0001g0131 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.68-1617C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576157 | |||||||
| chr19:576377 | G | T | 11 | a0001c0001t0005g0005 a0001c0001t0005g0041 a0001c0001t0005g0076 others(8): Show |
17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-1397G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576377 | |||||||
| chr19:576466 | A | C | 11 | a0001c0001t0005g0005 a0001c0001t0005g0041 a0001c0001t0005g0076 others(8): Show |
17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-1308A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576466 | |||||||
| chr19:576487 | C | G | 2 | a0001c0010t0001g0070 a0001c0010t0001g0084 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.68-1287C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576487 | |||||||
| chr19:576499 | C | T | 1 | a0001c0001t0003g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.68-1275C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576499 | |||||||
| chr19:576500 | G | A | 3 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0158 |
3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-1274G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576500 | |||||||
| chr19:576552 | G | C | 3 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 |
3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-1222G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576552 | |||||||
| chr19:576589 | G | A | 1 | a0001c0002t0001g0028 | 2 | HG00609.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.68-1185G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576589 | |||||||
| chr19:576628 | G | A | 1 | a0001c0003t0004g0052 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.68-1146G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576628 | |||||||
| chr19:576675 | T | C | 146 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(143): Show |
223 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.68-1099T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576675 | |||||||
| chr19:576686 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.68-1088G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576686 | |||||||
| chr19:576716 | A | G | 139 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(136): Show |
212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.68-1058A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576716 | |||||||
| chr19:576748 | CA | C | 62 | a0001c0001t0002g0037 a0001c0001t0002g0049 a0001c0001t0002g0130 others(59): Show |
101 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.68-1012delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576748 | ||||||
| chr19:576760 | A | AAAG | 36 | a0001c0001t0003g0014 a0001c0001t0003g0023 a0001c0001t0003g0024 others(33): Show |
46 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-1006_68-1004dup others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576760 | ||||||
| chr19:576768 | AGAG | A | 30 | a0001c0003t0001g0065 a0001c0003t0001g0082 a0001c0003t0004g0003 others(27): Show |
50 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.68-1002_68-1000del others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576768 | ||||||
| chr19:576771 | G | A | 4 | a0001c0003t0001g0066 a0001c0003t0004g0020 a0001c0003t0004g0071 others(1): Show |
5 | HG00099.hp2 HG01975.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-1003G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576771 | |||||||
| chr19:576777 | A | G | 2 | a0001c0001t0003g0051 a0001c0001t0003g0069 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68-997A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576777 | |||||||
| chr19:576919 | A | G | 1 | a0001c0001t0003g0100 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.68-855A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576919 | |||||||
| chr19:576932 | T | C | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-842T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576932 | |||||||
| chr19:576936 | TTG | T | 3 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 |
3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.68-830_68-829delGT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576936 | ||||||
| chr19:576961 | C | CGTGTGTG others(1): Show |
28 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(25): Show |
47 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.68-813_68-812insGT others(6): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576961 | |||||||
| chr19:576961 | C | CGTGTGTG others(3): Show |
4 | a0001c0003t0004g0019 a0001c0003t0004g0058 a0001c0003t0004g0071 others(1): Show |
5 | HG01517.hp2 HG02015.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.68-813_68-812insGT others(8): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576961 | |||||||
| chr19:576961 | C | CGTGTGTG others(5): Show |
1 | a0001c0003t0004g0035 | 2 | HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.68-813_68-812insGT others(10): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576961 | |||||||
| chr19:576962 | T | G | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-812T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 576962 | |||||||
| chr19:576962 | TTG | T | 76 | a0001c0001t0003g0021 a0001c0001t0003g0043 a0001c0001t0003g0051 others(73): Show |
117 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.68-796_68-795delGT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 576962 | ||||||
| chr19:577157 | G | C | 12 | a0001c0001t0003g0021 a0001c0001t0003g0051 a0001c0001t0003g0069 others(9): Show |
14 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-617G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577157 | |||||||
| chr19:577157 | G | T | 11 | a0001c0001t0005g0005 a0001c0001t0005g0041 a0001c0001t0005g0076 others(8): Show |
17 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68-617G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577157 | |||||||
| chr19:577246 | G | A | 31 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(28): Show |
42 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.68-528G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577246 | |||||||
| chr19:577247 | CCT | C | 59 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(56): Show |
98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-520_68-519delCT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 577247 | ||||||
| chr19:577261 | G | A | 1 | a0001c0003t0006g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-513G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577261 | |||||||
| chr19:577321 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-453C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577321 | |||||||
| chr19:577347 | C | T | 59 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(56): Show |
98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.68-427C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577347 | |||||||
| chr19:577426 | T | G | 148 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(145): Show |
225 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.68-348T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577426 | |||||||
| chr19:577435 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.68-339G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577435 | |||||||
| chr19:577436 | G | C | 148 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(145): Show |
225 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.68-338G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577436 | |||||||
| chr19:577489 | C | T | 1 | a0001c0002t0001g0121 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.68-285C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577489 | |||||||
| chr19:577596 | C | G | 2 | a0001c0002t0001g0163 a0001c0002t0001g0164 |
2 | HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.68-178C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577596 | |||||||
| chr19:577622 | T | G | 1 | a0001c0001t0011g0148 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.68-152T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577622 | |||||||
| chr19:577664 | G | C | 3 | a0001c0001t0003g0043 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.68-110G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577664 | |||||||
| chr19:577665 | G | A | 3 | a0001c0001t0003g0043 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.68-109G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577665 | |||||||
| chr19:577707 | T | C | 1 | a0001c0001t0005g0078 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.68-67T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577707 | |||||||
| chr19:577760 | T | C | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.68-14T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 1/8 | chr19 | 577760 | |||||||
| chr19:578157 | G | C | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.415+36G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578157 | |||||||
| chr19:578208 | C | T | 34 | a0001c0002t0001g0031 a0001c0003t0001g0065 a0001c0003t0001g0066 others(31): Show |
56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.415+87C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578208 | |||||||
| chr19:578236 | C | G | 1 | a0001c0001t0007g0107 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.415+115C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578236 | |||||||
| chr19:578239 | C | T | 107 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(104): Show |
161 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.415+118C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578239 | |||||||
| chr19:578268 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.415+147C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578268 | |||||||
| chr19:578316 | G | T | 6 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0003g0143 others(3): Show |
6 | HG02723.hp2 HG03195.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.415+195G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578316 | |||||||
| chr19:578345 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.415+224C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578345 | |||||||
| chr19:578394 | C | G | 1 | a0001c0003t0001g0065 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.415+273C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578394 | |||||||
| chr19:578417 | G | A | 3 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0158 |
3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.415+296G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578417 | |||||||
| chr19:578549 | A | G | 1 | a0001c0002t0001g0139 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.415+428A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578549 | |||||||
| chr19:578556 | G | C | 1 | a0001c0001t0002g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.415+435G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578556 | |||||||
| chr19:578661 | C | T | 1 | a0008c0012t0001g0145 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.415+540C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578661 | |||||||
| chr19:578668 | G | T | 1 | a0001c0003t0004g0008 | 4 | HG02145.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+547G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578668 | |||||||
| chr19:578718 | C | CA | 139 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(136): Show |
212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.415+597_415+598ins others(1): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578718 | |||||||
| chr19:578734 | AT | A | 49 | a0001c0001t0002g0125 a0001c0001t0003g0014 a0001c0001t0003g0023 others(46): Show |
73 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.415+627delT | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 578734 | ||||||
| chr19:578759 | G | T | 1 | a0001c0002t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.415+638G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578759 | |||||||
| chr19:578763 | C | G | 1 | a0001c0003t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.415+642C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578763 | |||||||
| chr19:578785 | T | C | 106 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(103): Show |
158 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.415+664T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578785 | |||||||
| chr19:578794 | A | G | 148 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(145): Show |
225 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.415+673A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578794 | |||||||
| chr19:578812 | C | A | 1 | a0001c0001t0007g0107 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.416-688C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578812 | |||||||
| chr19:578813 | T | C | 1 | a0001c0001t0007g0107 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.416-687T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578813 | |||||||
| chr19:578815 | C | T | 1 | a0001c0001t0007g0107 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.416-685C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578815 | |||||||
| chr19:578907 | T | C | 2 | a0001c0002t0001g0115 a0001c0002t0001g0133 |
2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.416-593T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578907 | |||||||
| chr19:578924 | G | T | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-576G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578924 | |||||||
| chr19:578976 | C | T | 1 | a0001c0001t0005g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.416-524C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 578976 | |||||||
| chr19:579010 | G | A | 139 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(136): Show |
212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.416-490G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579010 | |||||||
| chr19:579022 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.416-478G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579022 | |||||||
| chr19:579035 | C | T | 58 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(55): Show |
97 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.416-465C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579035 | |||||||
| chr19:579084 | G | C | 1 | a0001c0002t0001g0089 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.416-416G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579084 | |||||||
| chr19:579100 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-400C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579100 | |||||||
| chr19:579157 | T | C | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-343T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579157 | |||||||
| chr19:579175 | T | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-325T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579175 | |||||||
| chr19:579186 | G | C | 3 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 |
3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.416-314G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579186 | |||||||
| chr19:579192 | C | T | 2 | a0001c0001t0003g0144 a0001c0001t0003g0158 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.416-308C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579192 | |||||||
| chr19:579222 | C | T | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-278C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579222 | |||||||
| chr19:579224 | T | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-276T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579224 | |||||||
| chr19:579250 | G | A | 1 | a0001c0003t0004g0067 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.416-250G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579250 | |||||||
| chr19:579252 | AGGGTGCC others(10): Show |
A | 34 | a0001c0001t0002g0125 a0001c0003t0001g0065 a0001c0003t0001g0066 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-228_416-212del others(17): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 579252 | ||||||
| chr19:579254 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.416-246G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579254 | |||||||
| chr19:579267 | AGGGGGTG others(11): Show |
A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-229_416-212del others(18): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr19 | 579267 | ||||||
| chr19:579282 | G | A | 1 | a0001c0001t0003g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.416-218G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579282 | |||||||
| chr19:579354 | C | G | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-146C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579354 | |||||||
| chr19:579356 | G | T | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-144G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579356 | |||||||
| chr19:579357 | T | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-143T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579357 | |||||||
| chr19:579383 | A | T | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-117A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579383 | |||||||
| chr19:579384 | T | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.416-116T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579384 | |||||||
| chr19:579432 | G | C | 15 | a0001c0001t0003g0014 a0001c0001t0003g0023 a0001c0001t0003g0024 others(12): Show |
19 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.416-68G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579432 | |||||||
| chr19:579448 | G | T | 1 | a0001c0002t0001g0112 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.416-52G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579448 | |||||||
| chr19:579450 | G | A | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.416-50G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 2/8 | chr19 | 579450 | |||||||
| chr19:579687 | T | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+31T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579687 | |||||||
| chr19:579699 | C | T | 35 | a0001c0001t0003g0025 a0001c0003t0001g0065 a0001c0003t0001g0066 others(32): Show |
57 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.572+43C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579699 | |||||||
| chr19:579700 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.572+44G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579700 | |||||||
| chr19:579701 | G | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+45G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579701 | |||||||
| chr19:579707 | T | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+51T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579707 | |||||||
| chr19:579713 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.572+57C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579713 | |||||||
| chr19:579768 | G | A | 2 | a0001c0002t0001g0115 a0001c0002t0001g0133 |
2 | HG02056.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.572+112G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579768 | |||||||
| chr19:579773 | T | G | 1 | a0001c0003t0004g0060 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.572+117T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579773 | |||||||
| chr19:579809 | C | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+153C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579809 | |||||||
| chr19:579825 | G | C | 1 | a0003c0005t0001g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.572+169G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579825 | |||||||
| chr19:579907 | G | A | 2 | a0001c0002t0001g0134 a0001c0002t0001g0150 |
2 | HG01517.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.572+251G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579907 | |||||||
| chr19:579913 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.572+257G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579913 | |||||||
| chr19:579915 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.572+259G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579915 | |||||||
| chr19:579944 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.572+288C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 579944 | |||||||
| chr19:580012 | C | A | 33 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(30): Show |
54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.572+356C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580012 | |||||||
| chr19:580012 | C | G | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+356C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580012 | |||||||
| chr19:580014 | G | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.572+358G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580014 | |||||||
| chr19:580100 | A | G | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.573-279A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580100 | |||||||
| chr19:580101 | G | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.573-278G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580101 | |||||||
| chr19:580115 | GTGGGGT | G | 4 | a0001c0002t0001g0010 a0001c0002t0001g0031 a0001c0002t0001g0149 others(1): Show |
7 | HG00558.hp2 HG02040.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.573-263_573-258del others(6): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580115 | |||||||
| chr19:580124 | A | AC | 4 | a0001c0002t0001g0010 a0001c0002t0001g0031 a0001c0002t0001g0149 others(1): Show |
7 | HG00558.hp2 HG02040.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.573-255_573-254ins others(1): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580124 | |||||||
| chr19:580154 | A | G | 139 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(136): Show |
212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.573-225A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580154 | |||||||
| chr19:580163 | GA | G | 143 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(140): Show |
220 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.573-214delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 580163 | ||||||
| chr19:580206 | C | A | 1 | a0001c0001t0007g0107 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.573-173C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580206 | |||||||
| chr19:580230 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.573-149G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580230 | |||||||
| chr19:580268 | G | C | 59 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(56): Show |
98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.573-111G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580268 | |||||||
| chr19:580299 | T | C | 1 | a0001c0001t0002g0032 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.573-80T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580299 | |||||||
| chr19:580333 | G | A | 59 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(56): Show |
98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.573-46G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580333 | |||||||
| chr19:580335 | C | G | 1 | a0001c0001t0002g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.573-44C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580335 | |||||||
| chr19:580349 | A | G | 3 | a0001c0001t0003g0043 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG02922.hp2 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.573-30A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580349 | |||||||
| chr19:580353 | G | A | 2 | a0001c0001t0003g0144 a0001c0001t0003g0158 |
2 | HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.573-26G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 3/8 | chr19 | 580353 | |||||||
| chr19:580486 | G | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655+25G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580486 | |||||||
| chr19:580575 | C | T | 35 | a0001c0001t0002g0153 a0001c0003t0001g0065 a0001c0003t0001g0066 others(32): Show |
56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-71C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580575 | |||||||
| chr19:580602 | G | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.656-44G>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580602 | |||||||
| chr19:580603 | C | T | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.656-43C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580603 | |||||||
| chr19:580613 | G | T | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.656-33G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 4/8 | chr19 | 580613 | |||||||
| chr19:580793 | A | C | 105 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(102): Show |
157 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.792+11A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580793 | |||||||
| chr19:580799 | GCTGGGGG others(39): Show |
G | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.792+28_792+73delTG others(44): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580799 | ||||||
| chr19:580810 | T | C | 145 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(142): Show |
222 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.792+28T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580810 | |||||||
| chr19:580811 | G | A | 59 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(56): Show |
98 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.792+29G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580811 | |||||||
| chr19:580822 | T | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(17): Show |
25 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.792+40T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580822 | |||||||
| chr19:580837 | A | AGGCCTAG others(177): Show |
3 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0089 |
3 | HG01192.hp2 HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.792+104_792+105ins others(184): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580837 | ||||||
| chr19:580837 | A | G | 44 | a0001c0001t0005g0005 a0001c0001t0005g0041 a0001c0001t0005g0076 others(41): Show |
71 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.792+55A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580837 | |||||||
| chr19:580841 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+59C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580841 | |||||||
| chr19:580856 | C | G | 33 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(30): Show |
54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+74C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580856 | |||||||
| chr19:580870 | A | AGGACTGG others(39): Show |
1 | a0001c0002t0001g0085 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.792+104_792+105ins others(46): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | ||||||
| chr19:580870 | A | AGGACTGG others(223): Show |
2 | a0001c0002t0001g0083 a0001c0002t0001g0088 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.792+104_792+105ins others(230): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | ||||||
| chr19:580870 | A | AGGACTGG others(223): Show |
1 | a0001c0002t0001g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.792+104_792+105ins others(230): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | ||||||
| chr19:580870 | A | AGGACTGG others(269): Show |
1 | a0001c0002t0019g0090 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.792+104_792+105ins others(276): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580870 | ||||||
| chr19:580870 | A | C | 33 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(30): Show |
54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+88A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580870 | |||||||
| chr19:580870 | A | T | 1 | a0001c0003t0008g0063 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.792+88A>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580870 | |||||||
| chr19:580883 | G | A | 35 | a0001c0001t0005g0080 a0001c0003t0001g0065 a0001c0003t0001g0066 others(32): Show |
56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.792+101G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580883 | |||||||
| chr19:580884 | G | A | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+102G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580884 | |||||||
| chr19:580887 | C | CAAG | 33 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(30): Show |
54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+105_792+106ins others(3): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580887 | |||||||
| chr19:580887 | C | G | 54 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(51): Show |
93 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.792+105C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580887 | |||||||
| chr19:580888 | T | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+106T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580888 | |||||||
| chr19:580888 | T | G | 33 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(30): Show |
54 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.792+106T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580888 | |||||||
| chr19:580891 | A | G | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+109A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580891 | |||||||
| chr19:580892 | C | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+110C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580892 | |||||||
| chr19:580893 | T | G | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+111T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580893 | |||||||
| chr19:580916 | A | AGGACTGG others(39): Show |
1 | a0001c0001t0002g0126 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.792+226_793-262dup others(46): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580916 | ||||||
| chr19:580916 | A | C | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(90): Show |
153 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.792+134A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580916 | |||||||
| chr19:580927 | A | C | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+145A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580927 | |||||||
| chr19:580928 | G | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+146G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580928 | |||||||
| chr19:580929 | G | A | 32 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(29): Show |
53 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.792+147G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580929 | |||||||
| chr19:580930 | G | A | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+148G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580930 | |||||||
| chr19:580945 | T | G | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+163T>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580945 | |||||||
| chr19:580946 | C | T | 1 | a0001c0003t0004g0162 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.792+164C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580946 | |||||||
| chr19:580962 | C | A | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.792+180C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580962 | |||||||
| chr19:580975 | G | A | 3 | a0001c0001t0003g0051 a0001c0001t0003g0069 a0001c0001t0023g0068 |
3 | HG02723.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.792+193G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580975 | |||||||
| chr19:580979 | C | G | 1 | a0001c0003t0004g0058 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.792+197C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 580979 | |||||||
| chr19:580999 | C | CCAGCCCT others(269): Show |
1 | a0001c0001t0003g0160 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.793-262_793-261ins others(276): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580999 | ||||||
| chr19:580999 | C | CCAGCCCT others(223): Show |
2 | a0001c0001t0003g0043 a0001c0001t0003g0159 |
2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.793-262_793-261ins others(230): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 580999 | ||||||
| chr19:581008 | C | A | 2 | a0001c0002t0001g0085 a0001c0003t0006g0061 |
2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.792+226C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581008 | |||||||
| chr19:581008 | CGGACTGG others(39): Show |
C | 12 | a0001c0001t0003g0021 a0001c0001t0003g0051 a0001c0001t0003g0069 others(9): Show |
14 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.792+233_793-255del others(46): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581008 | ||||||
| chr19:581008 | CGGACTGG others(100): Show |
C | 1 | a0001c0002t0001g0121 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.793-261_793-155del | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581008 | ||||||
| chr19:581009 | GGACTGGG others(54): Show |
G | 1 | a0001c0015t0004g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.793-261_793-201del others(61): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581009 | ||||||
| chr19:581015 | G | T | 1 | a0001c0002t0016g0001 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.792+233G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581015 | |||||||
| chr19:581025 | C | G | 2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | HG01192.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.792+243C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581025 | |||||||
| chr19:581045 | CCAGCCCT others(8): Show |
C | 35 | a0001c0002t0001g0136 a0001c0002t0019g0090 a0001c0003t0001g0065 others(32): Show |
56 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.793-261_793-247del others(15): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581045 | ||||||
| chr19:581054 | T | A | 49 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(46): Show |
88 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.793-261T>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581054 | |||||||
| chr19:581054 | T | C | 41 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(38): Show |
52 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.793-261T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581054 | |||||||
| chr19:581055 | GGACTGCA others(8): Show |
G | 3 | a0001c0002t0001g0012 a0001c0002t0001g0106 a0001c0002t0001g0137 |
6 | HG01978.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-254_793-240del others(15): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581055 | ||||||
| chr19:581060 | G | GGGTGAGG others(24): Show |
1 | a0001c0002t0001g0001 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.793-255_793-254ins others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | |||||||
| chr19:581060 | G | GGGTGAGG others(24): Show |
5 | a0001c0002t0001g0083 a0001c0002t0001g0087 a0001c0002t0001g0088 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-255_793-254ins others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | |||||||
| chr19:581060 | G | GGGTGAGG others(70): Show |
2 | a0001c0002t0001g0085 a0001c0002t0001g0086 |
2 | HG01192.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.793-255_793-254ins others(77): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | |||||||
| chr19:581060 | G | GGGTGAGG others(25): Show |
1 | a0001c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.793-255_793-254ins others(32): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | |||||||
| chr19:581060 | G | GGGTGAGG others(24): Show |
45 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(42): Show |
79 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.793-255_793-254ins others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | |||||||
| chr19:581060 | G | GGGTGAGG others(25): Show |
1 | a0001c0002t0001g0006 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.793-255_793-254ins others(32): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581060 | |||||||
| chr19:581069 | C | A | 1 | a0001c0002t0001g0120 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.793-246C>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581069 | |||||||
| chr19:581069 | CA | C | 3 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0158 |
3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.793-245delA | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581069 | |||||||
| chr19:581070 | A | G | 131 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(128): Show |
201 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.793-245A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581070 | |||||||
| chr19:581072 | A | G | 3 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0158 |
3 | HG03195.hp2 HG03209.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.793-243A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581072 | |||||||
| chr19:581086 | C | G | 4 | a0001c0002t0001g0012 a0001c0002t0001g0106 a0001c0002t0001g0120 others(1): Show |
7 | HG01978.hp1 HG02071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-229C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581086 | |||||||
| chr19:581115 | A | C | 92 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(89): Show |
152 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.793-200A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581115 | |||||||
| chr19:581152 | CCAGCCCT others(39): Show |
C | 1 | a0001c0001t0002g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.793-108_793-63delC others(45): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581152 | ||||||
| chr19:581167 | G | A | 14 | a0001c0001t0003g0143 a0001c0001t0003g0144 a0001c0001t0003g0158 others(11): Show |
20 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.793-148G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581167 | |||||||
| chr19:581190 | TCCCGGAC others(7): Show |
T | 47 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(44): Show |
83 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.793-124_793-111del others(14): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581190 | |||||||
| chr19:581198 | T | C | 46 | a0001c0002t0001g0012 a0001c0002t0001g0083 a0001c0002t0001g0085 others(43): Show |
70 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.793-117T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581198 | |||||||
| chr19:581204 | C | CTCCGGAC others(25): Show |
9 | a0001c0002t0001g0083 a0001c0002t0001g0085 a0001c0002t0001g0086 others(6): Show |
9 | HG01192.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-110_793-79dupT others(31): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 581204 | ||||||
| chr19:581236 | TCCCGGAC others(7): Show |
T | 3 | a0001c0002t0001g0012 a0001c0002t0001g0106 a0001c0002t0001g0137 |
6 | HG01978.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-78_793-65delCC others(12): Show |
BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581236 | |||||||
| chr19:581239 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.793-76C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581239 | |||||||
| chr19:581253 | A | C | 37 | a0001c0002t0001g0012 a0001c0002t0001g0106 a0001c0002t0001g0137 others(34): Show |
61 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.793-62A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 5/8 | chr19 | 581253 | |||||||
| chr19:581624 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0098 |
3 | HG02559.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1069+33G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581624 | |||||||
| chr19:581633 | G | A | 44 | a0001c0001t0003g0021 a0001c0001t0003g0073 a0001c0001t0003g0091 others(41): Show |
67 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1069+42G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581633 | |||||||
| chr19:581714 | A | C | 1 | a0001c0001t0011g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1069+123A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581714 | |||||||
| chr19:581729 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1069+138G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581729 | |||||||
| chr19:581783 | A | C | 1 | a0001c0001t0003g0025 | 2 | HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1069+192A>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581783 | |||||||
| chr19:581786 | G | A | 1 | a0001c0002t0001g0030 | 2 | HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1069+195G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581786 | |||||||
| chr19:581806 | C | T | 1 | a0001c0001t0005g0077 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1069+215C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581806 | |||||||
| chr19:581815 | C | T | 78 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0002g0151 others(75): Show |
110 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1069+224C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581815 | |||||||
| chr19:581846 | C | T | 1 | a0001c0002t0001g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1069+255C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581846 | |||||||
| chr19:581915 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1069+324G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581915 | |||||||
| chr19:581920 | C | G | 1 | a0001c0002t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1069+329C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581920 | |||||||
| chr19:581944 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1069+353C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581944 | |||||||
| chr19:581956 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1070-350C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581956 | |||||||
| chr19:581974 | C | T | 34 | a0001c0003t0001g0065 a0001c0003t0001g0066 a0001c0003t0001g0082 others(31): Show |
55 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.1070-332C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 581974 | |||||||
| chr19:582006 | G | A | 2 | a0001c0001t0003g0024 a0001c0001t0020g0024 |
2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1070-300G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582006 | |||||||
| chr19:582077 | A | G | 7 | a0001c0001t0003g0021 a0001c0001t0003g0073 a0001c0001t0003g0091 others(4): Show |
9 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-229A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582077 | |||||||
| chr19:582092 | C | G | 1 | a0001c0001t0002g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1070-214C>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582092 | |||||||
| chr19:582137 | G | A | 1 | a0001c0001t0011g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1070-169G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582137 | |||||||
| chr19:582140 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1070-166C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582140 | |||||||
| chr19:582253 | T | C | 161 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0002g0004 others(158): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1070-53T>C | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582253 | |||||||
| chr19:582292 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1070-14C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 6/8 | chr19 | 582292 | |||||||
| chr19:582352 | C | T | 1 | a0001c0001t0005g0080 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1094+22C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582352 | |||||||
| chr19:582429 | G | T | 1 | a0001c0003t0004g0062 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1095-85G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582429 | |||||||
| chr19:582468 | A | G | 138 | a0001c0001t0001g0027 a0001c0001t0001g0098 a0001c0001t0003g0014 others(135): Show |
211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.1095-46A>G | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582468 | |||||||
| chr19:582481 | G | T | 1 | a0004c0009t0003g0094 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1095-33G>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582481 | |||||||
| chr19:582505 | G | A | 56 | a0001c0001t0003g0021 a0001c0002t0001g0001 a0001c0002t0001g0006 others(53): Show |
96 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1095-9G>A | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 7/8 | chr19 | 582505 | |||||||
| chr19:582586 | C | T | 2 | a0004c0009t0003g0094 a0004c0009t0022g0093 |
2 | HG03239.hp1 NA19082.hp2 |
splice_region_variant&intron_variant | LOW | c.*5+4C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 8/8 | chr19 | 582586 | |||||||
| chr19:582693 | C | T | 57 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0010 others(54): Show |
96 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.*6-57C>T | BSG | ENSG00000172270.22 | transcript | ENST00000333511.9 | protein_coding | 8/8 | chr19 | 582693 |