Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 127544 |
| ensemblid | ENSG00000116514.17 |
| hgncid | 26886 |
| symbol | RNF19B |
| name | ring finger protein 19B |
| refseq_nuc | NM_001300826.2 |
| refseq_prot | NP_001287755.1 |
| ensembl_nuc | ENST00000235150.5 |
| ensembl_prot | ENSP00000235150.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 32936449 |
| end | 32964809 |
| strand | - |
| ver | v1.2 |
| region | chr1:32936449-32964809 |
| region5000 | chr1:32931449-32969809 |
| regionname0 | RNF19B_chr1_32936449_32964809 |
| regionname5000 | RNF19B_chr1_32931449_32969809 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 731 | 312 | 87 | 60 | 120 | 8 | 36 | 91 | RNF19B_chr1_32931449_32969809 | RNF19B | MGSEK others(726): Show |
chr1 | 32931449 | 32969809 |
| a0002 | 0/0 | 731 | 13 | 0 | 0 | 12 | 0 | 1 | 9 | RNF19B_chr1_32931449_32969809 | RNF19B | MGSEK others(726): Show |
chr1 | 32931449 | 32969809 |
| a0003 | 0/0 | 733 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | MGSEK others(728): Show |
chr1 | 32931449 | 32969809 |
| a0004 | 0/0 | 731 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | MGSEK others(726): Show |
chr1 | 32931449 | 32969809 |
| a0005 | 0/1 | 731 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | MGSEK others(726): Show |
chr1 | 32931449 | 32969809 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2193 | 226 | 82 | 42 | 72 | 5 | 24 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 | ||
| a0001c0002 | 0/0 | 2193 | 70 | 2 | 10 | 48 | 3 | 7 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 | ||
| a0001c0003 | 0/0 | 2193 | 14 | 2 | 7 | 0 | 0 | 5 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 | ||
| a0001c0007 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 | ||
| a0001c0009 | 0/0 | 2193 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 | ||
| a0002c0004 | 0/0 | 2193 | 13 | 0 | 0 | 12 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 | ||
| a0003c0005 | 0/0 | 2199 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2194): Show |
chr1 | 32931449 | 32969809 | ||
| a0004c0006 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 | ||
| a0005c0008 | 0/1 | 2193 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATGGG others(2188): Show |
chr1 | 32931449 | 32969809 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2677 | 186 | 53 | 37 | 66 | 5 | 24 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| a0001c0001t0003 | 0/0 | 2678 | 30 | 25 | 3 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2673): Show |
chr1 | 32931449 | 32969809 |
| a0001c0001t0004 | 0/0 | 2676 | 8 | 4 | 2 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2671): Show |
chr1 | 32931449 | 32969809 |
| a0001c0001t0006 | 0/0 | 2677 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| a0001c0001t0007 | 0/0 | 2677 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| a0001c0002t0002 | 0/0 | 2677 | 66 | 2 | 10 | 45 | 2 | 7 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| a0001c0002t0005 | 0/0 | 2676 | 4 | 0 | 0 | 3 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2671): Show |
chr1 | 32931449 | 32969809 |
| a0001c0003t0001 | 0/0 | 2677 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| a0001c0003t0003 | 0/0 | 2678 | 13 | 2 | 7 | 0 | 0 | 4 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2673): Show |
chr1 | 32931449 | 32969809 |
| a0001c0007t0001 | 0/0 | 2677 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| a0001c0009t0003 | 0/0 | 2678 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2673): Show |
chr1 | 32931449 | 32969809 |
| a0002c0004t0004 | 0/0 | 2676 | 13 | 0 | 0 | 12 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2671): Show |
chr1 | 32931449 | 32969809 |
| a0003c0005t0003 | 0/0 | 2684 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2679): Show |
chr1 | 32931449 | 32969809 |
| a0004c0006t0001 | 0/0 | 2677 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| a0005c0008t0001 | 0/1 | 2677 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | ATCGC others(2672): Show |
chr1 | 32931449 | 32969809 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 16 | 0 | 5 | 7 | 2 | 2 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0003 | 1/0 | 9 | 2 | 1 | 5 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 0 | 3 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0007 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0001t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0001 | 0/0 | 20 | 0 | 2 | 14 | 1 | 3 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0002t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0006 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0003t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0007t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0001c0009t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0002c0004t0004g0004 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0002c0004t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0002c0004t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0002c0004t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0002c0004t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0003c0005t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0003c0005t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0003c0005t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0004c0006t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| a0005c0008t0001g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00621 | hp2 | a0002 | c0004 | t0004 | g0239 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0152 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00673 | hp1 | a0002 | c0004 | t0004 | g0004 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00741 | hp1 | a0001 | c0003 | t0003 | g0045 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0014 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01361 | hp1 | a0001 | c0003 | t0003 | g0006 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01433 | hp2 | a0001 | c0003 | t0003 | g0014 | AMR | CLM | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01515 | hp2 | a0001 | c0002 | t0005 | g0054 | EUR | IBS | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01891 | hp2 | a0001 | c0007 | t0001 | g0100 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01934 | hp2 | a0001 | c0009 | t0003 | g0242 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0042 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02015 | hp2 | a0001 | c0002 | t0005 | g0052 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02040 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02080 | hp2 | a0001 | c0002 | t0005 | g0058 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CDX | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0040 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02293 | hp1 | a0001 | c0003 | t0003 | g0046 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02300 | hp2 | a0001 | c0003 | t0003 | g0006 | AMR | PEL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02523 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | KHV | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02698 | hp1 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02896 | hp2 | a0003 | c0005 | t0003 | g0033 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02897 | hp1 | a0003 | c0005 | t0003 | g0034 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0041 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03490 | hp2 | a0001 | c0003 | t0001 | g0047 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0070 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ESN | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0006 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03669 | hp1 | a0001 | c0003 | t0003 | g0044 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0015 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0063 | SAS | PJL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03927 | hp1 | a0001 | c0003 | t0003 | g0043 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04115 | hp2 | a0004 | c0006 | t0001 | g0031 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04184 | hp1 | a0002 | c0004 | t0004 | g0004 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | BEB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | STU | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18946 | hp1 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18954 | hp1 | a0002 | c0004 | t0004 | g0240 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0207 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18961 | hp2 | a0001 | c0002 | t0005 | g0223 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18978 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18979 | hp1 | a0002 | c0004 | t0004 | g0238 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18980 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18981 | hp1 | a0002 | c0004 | t0004 | g0237 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19064 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19067 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19086 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0147 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | YRI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0015 | EUR | TSI | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG06807 | hp1 | a0003 | c0005 | t0003 | g0032 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | USA | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | LWK | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| homoSapiens | chm13v2 | a0005 | c0008 | t0001 | g0241 | REF | REF | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0003 | REF | REF | RNF19B_chr1_32931449_32969809 | RNF19B | chr1 | 32931449 | 32969809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32964396 | G | A | 1 | a0002 | 13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
missense_variant | MODERATE | c.290C>T | p.Ala97Val | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 414/2677 | 290/2196 | 97/731 | chr1 | 32964396 | |||
| chr1:32964416 | C | CGCCTCG | 1 | a0003 | 3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
disruptive_inframe_insertion | MODERATE | c.264_269dupCGAGGC | p.Ala90_Glu91insGluA others(2): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 393/2677 | 269/2196 | 90/731 | chr1 | 32964416 | |||
| chr1:32964520 | G | T | 1 | a0004 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.166C>A | p.Pro56Thr | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 290/2677 | 166/2196 | 56/731 | chr1 | 32964520 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32936914 | C | T | 1 | a0001c0003 | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
synonymous_variant | LOW | c.2088G>A | p.Ser696Ser | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 2212/2677 | 2088/2196 | 696/731 | chr1 | 32936914 | |||
| chr1:32936941 | G | C | 1 | a0001c0003 | 14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
synonymous_variant | LOW | c.2061C>G | p.Pro687Pro | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 2185/2677 | 2061/2196 | 687/731 | chr1 | 32936941 | |||
| chr1:32944092 | G | A | 1 | a0001c0002 | 70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
synonymous_variant | LOW | c.1329C>T | p.Gly443Gly | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/9 | 1453/2677 | 1329/2196 | 443/731 | chr1 | 32944092 | |||
| chr1:32948338 | G | A | 1 | a0001c0007 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.867C>T | p.Cys289Cys | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/9 | 991/2677 | 867/2196 | 289/731 | chr1 | 32948338 | |||
| chr1:32964569 | G | A | 1 | a0001c0009 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.117C>T | p.Phe39Phe | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/9 | 241/2677 | 117/2196 | 39/731 | chr1 | 32964569 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32936571 | C | T | 2 | a0001c0002t0002 a0001c0002t0005 |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*235G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 235 | chr1 | 32936571 | ||||||
| chr1:32936722 | T | C | 1 | a0001c0001t0006 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*84A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 84 | chr1 | 32936722 | ||||||
| chr1:32936733 | G | GA | 4 | a0001c0001t0003 a0001c0003t0003 a0001c0009t0003 others(1): Show |
47 | HG00423.hp2 HG00639.hp1 HG00741.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*72dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 72 | chr1 | 32936733 | ||||||
| chr1:32936733 | GA | G | 3 | a0001c0001t0004 a0001c0002t0005 a0002c0004t0004 |
25 | HG00621.hp2 HG00639.hp2 HG00673.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*72delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 72 | chr1 | 32936733 | ||||||
| chr1:32936805 | T | G | 1 | a0001c0001t0007 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 9/9 | 1 | chr1 | 32936805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:32937603 | G | C | 4 | a0001c0001t0003g0007 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1743-344C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32937603 | |||||||
| chr1:32937880 | T | C | 46 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1742+517A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32937880 | |||||||
| chr1:32938140 | C | CA | 41 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0097 others(38): Show |
43 | HG00609.hp1 HG00639.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.1742+256dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938140 | |||||||
| chr1:32938140 | C | CAA | 20 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0003g0019 others(17): Show |
33 | HG00621.hp2 HG00673.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1742+255_1742+256d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938140 | |||||||
| chr1:32938140 | CA | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0112 others(3): Show |
7 | NA18941.hp2 NA18960.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1742+256delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938140 | |||||||
| chr1:32938141 | A | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0183 |
2 | HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1742+256T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938141 | |||||||
| chr1:32938295 | G | A | 1 | a0001c0001t0004g0196 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1742+102C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938295 | |||||||
| chr1:32938362 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0183 |
2 | HG01109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1742+35A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 8/8 | chr1 | 32938362 | |||||||
| chr1:32938540 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1611-12C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938540 | |||||||
| chr1:32938600 | A | G | 1 | a0001c0001t0003g0225 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1611-72T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938600 | |||||||
| chr1:32938619 | T | C | 1 | a0001c0002t0002g0062 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1611-91A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938619 | |||||||
| chr1:32938766 | C | T | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1611-238G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938766 | |||||||
| chr1:32938931 | G | C | 1 | a0004c0006t0001g0031 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1611-403C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938931 | |||||||
| chr1:32938970 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0166 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1611-442C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32938970 | |||||||
| chr1:32939290 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1611-762G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939290 | |||||||
| chr1:32939442 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1611-914T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939442 | |||||||
| chr1:32939480 | CTTA | C | 3 | a0001c0001t0001g0088 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1611-955_1611-953d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939480 | |||||||
| chr1:32939717 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0029 others(5): Show |
12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1611-1189T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939717 | |||||||
| chr1:32939864 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0153 |
2 | HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1611-1336G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939864 | |||||||
| chr1:32939934 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1611-1406C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32939934 | |||||||
| chr1:32940264 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1611-1736C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940264 | |||||||
| chr1:32940371 | A | C | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1611-1843T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940371 | |||||||
| chr1:32940372 | T | C | 1 | a0001c0001t0006g0207 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1611-1844A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940372 | |||||||
| chr1:32940395 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1610+1857A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940395 | |||||||
| chr1:32940498 | A | C | 5 | a0002c0004t0004g0004 a0002c0004t0004g0237 a0002c0004t0004g0238 others(2): Show |
13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1610+1754T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940498 | |||||||
| chr1:32940542 | A | G | 1 | a0001c0001t0003g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1610+1710T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940542 | |||||||
| chr1:32940642 | T | G | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1610+1610A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940642 | |||||||
| chr1:32940860 | T | C | 2 | a0001c0001t0004g0150 a0001c0001t0004g0152 |
2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1610+1392A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32940860 | |||||||
| chr1:32941101 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0111 |
2 | NA18942.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1610+1151A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941101 | |||||||
| chr1:32941154 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1610+1098A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941154 | |||||||
| chr1:32941206 | C | G | 93 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(90): Show |
139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.1610+1046G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941206 | |||||||
| chr1:32941315 | C | T | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1610+937G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941315 | |||||||
| chr1:32941483 | C | T | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610+769G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941483 | |||||||
| chr1:32941542 | A | AAAAAT | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1610+705_1610+709d others(7): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941542 | |||||||
| chr1:32941553 | AAAAT | A | 3 | a0003c0005t0003g0032 a0003c0005t0003g0033 a0003c0005t0003g0034 |
3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1610+695_1610+698d others(6): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941553 | |||||||
| chr1:32941846 | C | A | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610+406G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941846 | |||||||
| chr1:32941994 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0166 a0001c0001t0001g0199 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1610+258C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32941994 | |||||||
| chr1:32942011 | C | T | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1610+241G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942011 | |||||||
| chr1:32942053 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1610+199G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942053 | |||||||
| chr1:32942092 | G | A | 46 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.1610+160C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942092 | |||||||
| chr1:32942159 | G | T | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1610+93C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 7/8 | chr1 | 32942159 | |||||||
| chr1:32942537 | T | G | 35 | a0001c0001t0001g0020 a0001c0001t0001g0088 a0001c0001t0001g0097 others(32): Show |
41 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1403-78A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942537 | |||||||
| chr1:32942554 | T | C | 1 | a0001c0001t0003g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1403-95A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942554 | |||||||
| chr1:32942721 | C | T | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1403-262G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942721 | |||||||
| chr1:32942799 | A | C | 4 | a0001c0001t0001g0167 a0001c0001t0001g0176 a0001c0001t0001g0186 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1403-340T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942799 | |||||||
| chr1:32942859 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1403-400C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942859 | |||||||
| chr1:32942868 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1403-409G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32942868 | |||||||
| chr1:32943034 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1403-575C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943034 | |||||||
| chr1:32943140 | CA | C | 88 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(85): Show |
130 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.1403-682delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943140 | |||||||
| chr1:32943192 | T | TCTACGTT others(9): Show |
2 | a0003c0005t0003g0033 a0003c0005t0003g0034 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1403-749_1403-734d others(18): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943192 | |||||||
| chr1:32943212 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1403-753G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943212 | |||||||
| chr1:32943325 | A | G | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1402+694T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943325 | |||||||
| chr1:32943408 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1402+611C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943408 | |||||||
| chr1:32943578 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1402+441G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943578 | |||||||
| chr1:32943628 | A | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0029 others(5): Show |
12 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1402+391T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943628 | |||||||
| chr1:32943654 | T | C | 1 | a0001c0002t0002g0073 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1402+365A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943654 | |||||||
| chr1:32943831 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0169 |
2 | NA18956.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1402+188G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943831 | |||||||
| chr1:32943950 | C | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(90): Show |
139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.1402+69G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943950 | |||||||
| chr1:32943999 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1402+20T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 6/8 | chr1 | 32943999 | |||||||
| chr1:32944199 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1262-40A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944199 | |||||||
| chr1:32944217 | C | T | 3 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG00639.hp1 HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1262-58G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944217 | |||||||
| chr1:32944439 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1262-280T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944439 | |||||||
| chr1:32944632 | G | A | 1 | a0001c0002t0002g0060 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1262-473C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944632 | |||||||
| chr1:32944835 | C | A | 1 | a0001c0001t0003g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1262-676G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944835 | |||||||
| chr1:32944836 | C | T | 1 | a0002c0004t0004g0238 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1262-677G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944836 | |||||||
| chr1:32944849 | C | T | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1261+665G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944849 | |||||||
| chr1:32944890 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1261+624C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944890 | |||||||
| chr1:32944967 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1261+547G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944967 | |||||||
| chr1:32944968 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1261+546C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32944968 | |||||||
| chr1:32945078 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1261+436G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945078 | |||||||
| chr1:32945146 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1261+368G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945146 | |||||||
| chr1:32945297 | G | C | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1261+217C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945297 | |||||||
| chr1:32945377 | T | G | 1 | a0001c0003t0003g0044 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1261+137A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945377 | |||||||
| chr1:32945414 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0216 |
3 | HG01081.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1261+100G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 5/8 | chr1 | 32945414 | |||||||
| chr1:32945724 | C | T | 2 | a0001c0002t0002g0057 a0001c0002t0002g0065 |
2 | HG01256.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1147-96G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945724 | |||||||
| chr1:32945726 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1147-98T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945726 | |||||||
| chr1:32945841 | C | G | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1147-213G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945841 | |||||||
| chr1:32945880 | A | ATT | 39 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(36): Show |
68 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1147-254_1147-253d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945880 | |||||||
| chr1:32945925 | C | A | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.1147-297G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32945925 | |||||||
| chr1:32946032 | T | A | 1 | a0001c0001t0003g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1146+370A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946032 | |||||||
| chr1:32946089 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1146+313G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946089 | |||||||
| chr1:32946125 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0003g0225 a0001c0001t0003g0226 others(1): Show |
4 | HG00639.hp1 HG01243.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+277G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946125 | |||||||
| chr1:32946174 | G | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0094 a0001c0001t0003g0104 |
4 | HG01891.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1146+228C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946174 | |||||||
| chr1:32946201 | A | T | 1 | a0001c0001t0003g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1146+201T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946201 | |||||||
| chr1:32946242 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1146+160C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946242 | |||||||
| chr1:32946271 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1146+131T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 4/8 | chr1 | 32946271 | |||||||
| chr1:32946784 | G | C | 1 | a0001c0001t0003g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.984-220C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32946784 | |||||||
| chr1:32946843 | A | G | 1 | a0001c0002t0002g0065 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.984-279T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32946843 | |||||||
| chr1:32946995 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.984-431G>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32946995 | |||||||
| chr1:32947297 | TTTTG | T | 3 | a0003c0005t0003g0032 a0003c0005t0003g0033 a0003c0005t0003g0034 |
3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.984-737_984-734del others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947297 | |||||||
| chr1:32947435 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18939.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.983+787C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947435 | |||||||
| chr1:32947495 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.983+727G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947495 | |||||||
| chr1:32947589 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.983+633C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947589 | |||||||
| chr1:32947658 | T | TA | 10 | a0001c0001t0001g0088 a0001c0001t0001g0174 a0001c0001t0001g0180 others(7): Show |
10 | HG01106.hp2 HG01934.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.983+563dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947658 | |||||||
| chr1:32947711 | A | C | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.983+511T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947711 | |||||||
| chr1:32947801 | A | C | 1 | a0001c0002t0002g0051 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.983+421T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32947801 | |||||||
| chr1:32948093 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG00609.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.983+129A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 3/8 | chr1 | 32948093 | |||||||
| chr1:32948439 | G | A | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0216 |
3 | HG01081.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.842-76C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948439 | |||||||
| chr1:32948515 | G | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0098 others(7): Show |
11 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.842-152C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948515 | |||||||
| chr1:32948516 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.842-153C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948516 | |||||||
| chr1:32948647 | A | C | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.842-284T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948647 | |||||||
| chr1:32948973 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.841+596C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32948973 | |||||||
| chr1:32949031 | A | G | 1 | a0001c0001t0003g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.841+538T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949031 | |||||||
| chr1:32949062 | T | C | 45 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(42): Show |
54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.841+507A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949062 | |||||||
| chr1:32949266 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+303A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949266 | |||||||
| chr1:32949329 | A | C | 1 | a0001c0001t0001g0117 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.841+240T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949329 | |||||||
| chr1:32949412 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.841+157A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 2/8 | chr1 | 32949412 | |||||||
| chr1:32949799 | A | G | 3 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG00639.hp1 HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.636-25T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949799 | |||||||
| chr1:32949808 | G | GT | 45 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(42): Show |
54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.636-35dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949808 | |||||||
| chr1:32949850 | AAC | A | 4 | a0001c0001t0003g0007 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.636-78_636-77delGT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949850 | |||||||
| chr1:32949865 | T | C | 45 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(42): Show |
54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.636-91A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949865 | |||||||
| chr1:32949958 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.636-184C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949958 | |||||||
| chr1:32949971 | CT | C | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.636-198delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32949971 | |||||||
| chr1:32950022 | T | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(90): Show |
139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.636-248A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950022 | |||||||
| chr1:32950220 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.636-446C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950220 | |||||||
| chr1:32950335 | T | C | 3 | a0001c0001t0003g0019 a0001c0001t0003g0094 a0001c0001t0003g0104 |
4 | HG01891.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-561A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950335 | |||||||
| chr1:32950424 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.636-650G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950424 | |||||||
| chr1:32950457 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.636-683G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950457 | |||||||
| chr1:32950488 | C | T | 3 | a0003c0005t0003g0032 a0003c0005t0003g0033 a0003c0005t0003g0034 |
3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.636-714G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950488 | |||||||
| chr1:32950570 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.636-796C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950570 | |||||||
| chr1:32950684 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.636-910C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950684 | |||||||
| chr1:32950755 | G | C | 1 | a0001c0001t0003g0102 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.636-981C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950755 | |||||||
| chr1:32950764 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0003g0102 a0003c0005t0003g0032 others(2): Show |
5 | HG02630.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-990G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950764 | |||||||
| chr1:32950774 | C | G | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG02109.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.636-1000G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950774 | |||||||
| chr1:32950843 | C | CT | 9 | a0001c0001t0001g0108 a0001c0001t0001g0155 a0001c0001t0001g0224 others(6): Show |
17 | HG00621.hp2 HG00673.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.636-1070dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950843 | |||||||
| chr1:32950843 | CT | C | 52 | a0001c0001t0001g0231 a0001c0001t0003g0019 a0001c0001t0003g0089 others(49): Show |
82 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.636-1070delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950843 | |||||||
| chr1:32950932 | C | T | 45 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(42): Show |
54 | HG00639.hp1 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.636-1158G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32950932 | |||||||
| chr1:32951027 | T | C | 93 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(90): Show |
139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.636-1253A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951027 | |||||||
| chr1:32951080 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-1306C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951080 | |||||||
| chr1:32951234 | A | T | 1 | a0001c0002t0002g0015 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.636-1460T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951234 | |||||||
| chr1:32951306 | G | A | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.636-1532C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951306 | |||||||
| chr1:32951484 | A | T | 5 | a0002c0004t0004g0004 a0002c0004t0004g0237 a0002c0004t0004g0238 others(2): Show |
13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.636-1710T>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951484 | |||||||
| chr1:32951510 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.636-1736G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951510 | |||||||
| chr1:32951547 | T | C | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-1773A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951547 | |||||||
| chr1:32951649 | G | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0166 |
2 | HG02622.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.636-1875C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951649 | |||||||
| chr1:32951857 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0003g0225 a0001c0001t0003g0226 others(1): Show |
4 | HG00639.hp1 HG01243.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-2083C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951857 | |||||||
| chr1:32951957 | GC | G | 3 | a0003c0005t0003g0032 a0003c0005t0003g0033 a0003c0005t0003g0034 |
3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.636-2184delG | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951957 | |||||||
| chr1:32951958 | C | CT | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(24): Show |
29 | HG00673.hp2 HG01106.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.636-2185dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951958 | |||||||
| chr1:32951958 | CT | C | 67 | a0001c0001t0001g0117 a0001c0001t0001g0179 a0001c0001t0003g0007 others(64): Show |
102 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.636-2185delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32951958 | |||||||
| chr1:32952184 | A | G | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.636-2410T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952184 | |||||||
| chr1:32952212 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.636-2438A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952212 | |||||||
| chr1:32952429 | T | TA | 45 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0023 others(42): Show |
54 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.636-2656dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | T | TAA | 21 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0119 others(18): Show |
23 | HG00639.hp2 HG01070.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-2657_636-2656d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | T | TAAA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0084 a0001c0001t0001g0137 others(4): Show |
9 | HG01243.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.636-2658_636-2656d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | TA | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0109 a0001c0001t0001g0111 others(5): Show |
8 | HG01074.hp2 HG02083.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.636-2656delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | TAA | T | 6 | a0001c0001t0001g0154 a0001c0001t0003g0087 a0001c0001t0003g0095 others(3): Show |
7 | HG00741.hp1 HG01109.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.636-2657_636-2656d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | TAAA | T | 17 | a0001c0001t0001g0088 a0001c0001t0003g0019 a0001c0001t0003g0086 others(14): Show |
21 | HG01361.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.636-2658_636-2656d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | TAAAA | T | 22 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0097 others(19): Show |
23 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.636-2659_636-2656d others(6): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | TAAAAA | T | 40 | a0001c0001t0003g0007 a0001c0001t0003g0102 a0001c0002t0002g0001 others(37): Show |
72 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.636-2660_636-2656d others(7): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | TAAAAAA | T | 7 | a0001c0001t0003g0081 a0001c0002t0005g0223 a0002c0004t0004g0004 others(4): Show |
15 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.636-2661_636-2656d others(8): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952429 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0116 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.636-2668_636-2656d others(15): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952429 | |||||||
| chr1:32952449 | A | C | 43 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(40): Show |
79 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.636-2675T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952449 | |||||||
| chr1:32952452 | A | C | 1 | a0001c0001t0003g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.636-2678T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952452 | |||||||
| chr1:32952478 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.636-2704G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952478 | |||||||
| chr1:32952552 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0029 others(9): Show |
16 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.636-2778G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952552 | |||||||
| chr1:32952599 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(52): Show |
72 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.636-2825C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952599 | |||||||
| chr1:32952611 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.636-2837C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952611 | |||||||
| chr1:32952650 | G | A | 35 | a0001c0001t0001g0020 a0001c0001t0001g0088 a0001c0001t0001g0097 others(32): Show |
41 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.636-2876C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952650 | |||||||
| chr1:32952748 | C | CA | 15 | a0001c0001t0001g0027 a0001c0001t0001g0122 a0001c0001t0001g0132 others(12): Show |
16 | HG01109.hp1 HG01346.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.636-2975dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952748 | |||||||
| chr1:32952748 | CA | C | 8 | a0001c0001t0001g0133 a0001c0001t0001g0184 a0001c0001t0003g0007 others(5): Show |
11 | HG01069.hp1 HG01258.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.636-2975delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952748 | |||||||
| chr1:32952748 | CAA | C | 87 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(84): Show |
130 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(127): Show |
intron_variant | MODIFIER | c.636-2976_636-2975d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952748 | |||||||
| chr1:32952791 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.636-3017G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952791 | |||||||
| chr1:32952819 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.636-3045C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952819 | |||||||
| chr1:32952962 | A | AT | 72 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(69): Show |
109 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.636-3189dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952962 | |||||||
| chr1:32952962 | A | ATT | 6 | a0001c0001t0001g0127 a0001c0001t0003g0080 a0001c0001t0003g0089 others(3): Show |
6 | HG01943.hp2 HG02257.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-3190_636-3189d others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952962 | |||||||
| chr1:32952962 | AT | A | 20 | a0001c0001t0001g0028 a0001c0001t0001g0084 a0001c0001t0001g0085 others(17): Show |
21 | HG01070.hp2 HG01081.hp2 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.636-3189delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952962 | |||||||
| chr1:32952986 | A | G | 9 | a0001c0001t0003g0019 a0001c0001t0003g0089 a0001c0001t0003g0090 others(6): Show |
10 | HG01891.hp1 HG02647.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-3212T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32952986 | |||||||
| chr1:32953001 | T | G | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-3227A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953001 | |||||||
| chr1:32953002 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-3228G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953002 | |||||||
| chr1:32953048 | C | T | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-3274G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953048 | |||||||
| chr1:32953074 | C | T | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.636-3300G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953074 | |||||||
| chr1:32953199 | T | C | 46 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.636-3425A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953199 | |||||||
| chr1:32953304 | T | C | 3 | a0001c0002t0002g0009 a0001c0002t0002g0067 a0001c0002t0002g0069 |
5 | NA18747.hp1 NA18942.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-3530A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953304 | |||||||
| chr1:32953374 | T | A | 1 | a0001c0001t0001g0193 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.636-3600A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953374 | |||||||
| chr1:32953383 | G | A | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.636-3609C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953383 | |||||||
| chr1:32953605 | C | T | 88 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(85): Show |
131 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.636-3831G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953605 | |||||||
| chr1:32953641 | T | C | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.636-3867A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953641 | |||||||
| chr1:32953901 | C | CT | 18 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0123 others(15): Show |
27 | HG00673.hp1 HG01106.hp2 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.636-4128dupA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953901 | |||||||
| chr1:32953901 | CT | C | 56 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0029 others(53): Show |
65 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.636-4128delA | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953901 | |||||||
| chr1:32953981 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.636-4207A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953981 | |||||||
| chr1:32953983 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.636-4209T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32953983 | |||||||
| chr1:32954155 | T | G | 46 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.636-4381A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954155 | |||||||
| chr1:32954249 | T | C | 1 | a0001c0002t0002g0067 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.636-4475A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954249 | |||||||
| chr1:32954319 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.636-4545A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954319 | |||||||
| chr1:32954504 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.636-4730G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954504 | |||||||
| chr1:32954520 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.636-4746G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954520 | |||||||
| chr1:32954529 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0198 |
2 | HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.636-4755T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954529 | |||||||
| chr1:32954570 | C | T | 1 | a0001c0002t0002g0050 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.636-4796G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954570 | |||||||
| chr1:32954591 | T | C | 1 | a0001c0003t0003g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.636-4817A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954591 | |||||||
| chr1:32954738 | C | CA | 42 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(39): Show |
67 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.636-4965dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954738 | |||||||
| chr1:32954746 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.636-4972T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954746 | |||||||
| chr1:32954751 | A | C | 1 | a0001c0001t0003g0096 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.636-4977T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954751 | |||||||
| chr1:32954751 | AAAC | A | 4 | a0001c0002t0002g0012 a0001c0002t0002g0068 a0001c0002t0002g0222 others(1): Show |
6 | NA18947.hp2 NA18950.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-4980_636-4978d others(5): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954751 | |||||||
| chr1:32954818 | T | C | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-5044A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954818 | |||||||
| chr1:32954836 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.636-5062T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954836 | |||||||
| chr1:32954884 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
7 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.636-5110C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32954884 | |||||||
| chr1:32955331 | T | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0216 |
3 | HG01081.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.636-5557A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955331 | |||||||
| chr1:32955533 | C | G | 1 | a0001c0001t0003g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.636-5759G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955533 | |||||||
| chr1:32955566 | C | CA | 6 | a0001c0001t0001g0183 a0002c0004t0004g0004 a0002c0004t0004g0237 others(3): Show |
14 | HG00621.hp2 HG00673.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.636-5793dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955566 | |||||||
| chr1:32955579 | T | A | 1 | a0001c0002t0002g0069 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.636-5805A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955579 | |||||||
| chr1:32955653 | G | A | 2 | a0001c0002t0002g0050 a0001c0002t0002g0051 |
2 | NA18612.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.636-5879C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955653 | |||||||
| chr1:32955730 | C | T | 88 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(85): Show |
131 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.636-5956G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955730 | |||||||
| chr1:32955748 | C | CA | 8 | a0001c0001t0001g0030 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
9 | HG02280.hp1 HG02809.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.636-5975dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955748 | |||||||
| chr1:32955748 | CA | C | 68 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0076 others(65): Show |
112 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.636-5975delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955748 | |||||||
| chr1:32955766 | A | G | 1 | a0002c0004t0004g0237 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.636-5992T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955766 | |||||||
| chr1:32955860 | T | C | 46 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.636-6086A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955860 | |||||||
| chr1:32955972 | A | G | 9 | a0001c0001t0003g0019 a0001c0001t0003g0089 a0001c0001t0003g0090 others(6): Show |
10 | HG01891.hp1 HG02647.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.636-6198T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32955972 | |||||||
| chr1:32956087 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.636-6313G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956087 | |||||||
| chr1:32956124 | G | C | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-6350C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956124 | |||||||
| chr1:32956136 | T | C | 4 | a0001c0001t0001g0076 a0003c0005t0003g0032 a0003c0005t0003g0033 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.636-6362A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956136 | |||||||
| chr1:32956177 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.636-6403G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956177 | |||||||
| chr1:32956269 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.636-6495G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956269 | |||||||
| chr1:32956344 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.636-6570A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956344 | |||||||
| chr1:32956420 | C | T | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.636-6646G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956420 | |||||||
| chr1:32956743 | G | GAA | 93 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(90): Show |
139 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.636-6970_636-6969i others(4): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956743 | |||||||
| chr1:32956856 | GC | G | 4 | a0001c0001t0003g0007 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.636-7083delG | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956856 | |||||||
| chr1:32956978 | G | C | 5 | a0002c0004t0004g0004 a0002c0004t0004g0237 a0002c0004t0004g0238 others(2): Show |
13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+7073C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32956978 | |||||||
| chr1:32957074 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.635+6977T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957074 | |||||||
| chr1:32957170 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635+6881A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957170 | |||||||
| chr1:32957253 | C | T | 5 | a0002c0004t0004g0004 a0002c0004t0004g0237 a0002c0004t0004g0238 others(2): Show |
13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+6798G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957253 | |||||||
| chr1:32957381 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.635+6670A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957381 | |||||||
| chr1:32957605 | G | A | 41 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(38): Show |
70 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.635+6446C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957605 | |||||||
| chr1:32957758 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | NA18940.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.635+6293G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957758 | |||||||
| chr1:32957759 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+6292C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957759 | |||||||
| chr1:32957774 | C | T | 3 | a0003c0005t0003g0032 a0003c0005t0003g0033 a0003c0005t0003g0034 |
3 | HG02896.hp2 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.635+6277G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957774 | |||||||
| chr1:32957874 | T | C | 4 | a0001c0001t0003g0007 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.635+6177A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32957874 | |||||||
| chr1:32958005 | C | G | 1 | a0001c0001t0003g0102 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.635+6046G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958005 | |||||||
| chr1:32958045 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.635+6006T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958045 | |||||||
| chr1:32958066 | A | G | 1 | a0001c0003t0001g0047 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.635+5985T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958066 | |||||||
| chr1:32958135 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0110 others(3): Show |
7 | NA18942.hp1 NA18960.hp2 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.635+5916T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958135 | |||||||
| chr1:32958224 | C | T | 5 | a0002c0004t0004g0004 a0002c0004t0004g0237 a0002c0004t0004g0238 others(2): Show |
13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+5827G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958224 | |||||||
| chr1:32958231 | T | C | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+5820A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958231 | |||||||
| chr1:32958245 | T | C | 8 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(5): Show |
12 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.635+5806A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958245 | |||||||
| chr1:32958626 | G | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | NA18983.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.635+5425C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958626 | |||||||
| chr1:32958798 | A | G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG02055.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.635+5253T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958798 | |||||||
| chr1:32958808 | A | C | 1 | a0001c0001t0003g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.635+5243T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958808 | |||||||
| chr1:32958928 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18939.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.635+5123C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958928 | |||||||
| chr1:32958971 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.635+5080T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32958971 | |||||||
| chr1:32959177 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.635+4874T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959177 | |||||||
| chr1:32959360 | G | A | 1 | a0001c0001t0004g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+4691C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959360 | |||||||
| chr1:32959744 | A | G | 1 | a0001c0002t0002g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.635+4307T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959744 | |||||||
| chr1:32959807 | G | A | 1 | a0001c0001t0004g0196 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.635+4244C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959807 | |||||||
| chr1:32959845 | A | G | 92 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(89): Show |
138 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.635+4206T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959845 | |||||||
| chr1:32959881 | C | CA | 9 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0197 others(6): Show |
9 | HG01175.hp2 HG02055.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.635+4169dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959881 | |||||||
| chr1:32959881 | CA | C | 84 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0077 others(81): Show |
129 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.635+4169delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959881 | |||||||
| chr1:32959952 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.635+4099C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32959952 | |||||||
| chr1:32960023 | C | G | 3 | a0001c0001t0001g0088 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | HG02486.hp2 HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635+4028G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960023 | |||||||
| chr1:32960037 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.635+4014G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960037 | |||||||
| chr1:32960060 | A | G | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG00099.hp2 HG01192.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.635+3991T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960060 | |||||||
| chr1:32960072 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.635+3979A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960072 | |||||||
| chr1:32960091 | A | G | 2 | a0001c0003t0003g0040 a0001c0003t0003g0041 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.635+3960T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960091 | |||||||
| chr1:32960501 | T | A | 6 | a0001c0002t0002g0071 a0001c0002t0002g0072 a0001c0002t0002g0073 others(3): Show |
6 | HG02071.hp1 HG02074.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.635+3550A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960501 | |||||||
| chr1:32960794 | C | T | 2 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.635+3257G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960794 | |||||||
| chr1:32960899 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0006g0207 |
3 | NA18959.hp2 NA18961.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.635+3152C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32960899 | |||||||
| chr1:32961005 | G | A | 88 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(85): Show |
131 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.635+3046C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961005 | |||||||
| chr1:32961008 | G | C | 1 | a0001c0001t0003g0104 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.635+3043C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961008 | |||||||
| chr1:32961015 | CA | C | 92 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(89): Show |
138 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.635+3035delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961015 | |||||||
| chr1:32961069 | T | C | 40 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0088 others(37): Show |
46 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.635+2982A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961069 | |||||||
| chr1:32961106 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.635+2945A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961106 | |||||||
| chr1:32961212 | T | C | 4 | a0001c0001t0003g0007 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.635+2839A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961212 | |||||||
| chr1:32961281 | T | C | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | NA18974.hp1 NA18982.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+2770A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961281 | |||||||
| chr1:32961355 | G | T | 2 | a0001c0002t0002g0053 a0001c0002t0002g0229 |
2 | NA19060.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.635+2696C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961355 | |||||||
| chr1:32961375 | A | C | 1 | a0001c0009t0003g0242 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.635+2676T>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961375 | |||||||
| chr1:32961451 | A | G | 4 | a0001c0001t0003g0007 a0001c0001t0003g0080 a0001c0001t0003g0081 others(1): Show |
7 | HG01069.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.635+2600T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961451 | |||||||
| chr1:32961557 | A | G | 94 | a0001c0001t0001g0020 a0001c0001t0001g0076 a0001c0001t0001g0084 others(91): Show |
140 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(137): Show |
intron_variant | MODIFIER | c.635+2494T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961557 | |||||||
| chr1:32961630 | T | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG03490.hp1 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.635+2421A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961630 | |||||||
| chr1:32961719 | A | G | 46 | a0001c0002t0002g0001 a0001c0002t0002g0008 a0001c0002t0002g0009 others(43): Show |
83 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.635+2332T>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961719 | |||||||
| chr1:32961877 | C | T | 1 | a0001c0002t0005g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.635+2174G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961877 | |||||||
| chr1:32961975 | G | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01074.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.635+2076C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961975 | |||||||
| chr1:32961980 | T | G | 2 | a0001c0001t0001g0216 a0001c0009t0003g0242 |
2 | HG01081.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.635+2071A>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32961980 | |||||||
| chr1:32962000 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.635+2051A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962000 | |||||||
| chr1:32962197 | G | C | 5 | a0002c0004t0004g0004 a0002c0004t0004g0237 a0002c0004t0004g0238 others(2): Show |
13 | HG00621.hp2 HG00673.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+1854C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962197 | |||||||
| chr1:32962248 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.635+1803G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962248 | |||||||
| chr1:32962249 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.635+1802C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962249 | |||||||
| chr1:32962428 | G | T | 4 | a0001c0001t0001g0076 a0003c0005t0003g0032 a0003c0005t0003g0033 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.635+1623C>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962428 | |||||||
| chr1:32962640 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.635+1411A>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962640 | |||||||
| chr1:32962768 | GA | G | 47 | a0001c0001t0001g0231 a0001c0002t0002g0001 a0001c0002t0002g0008 others(44): Show |
84 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.635+1282delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962768 | |||||||
| chr1:32962807 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.635+1244C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32962807 | |||||||
| chr1:32963039 | GA | G | 3 | a0001c0002t0002g0049 a0001c0002t0002g0050 a0001c0002t0002g0051 |
3 | NA18612.hp1 NA18969.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.635+1011delT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963039 | |||||||
| chr1:32963108 | G | C | 3 | a0001c0002t0002g0012 a0001c0002t0002g0222 a0001c0002t0005g0223 |
5 | NA18947.hp2 NA18950.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+943C>G | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963108 | |||||||
| chr1:32963294 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.635+757G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963294 | |||||||
| chr1:32963299 | C | T | 10 | a0001c0003t0001g0047 a0001c0003t0003g0006 a0001c0003t0003g0014 others(7): Show |
14 | HG00741.hp1 HG01109.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.635+752G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963299 | |||||||
| chr1:32963335 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.635+716C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963335 | |||||||
| chr1:32963424 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.635+627A>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963424 | |||||||
| chr1:32963444 | G | A | 3 | a0001c0001t0003g0225 a0001c0001t0003g0226 a0001c0001t0003g0227 |
3 | HG00639.hp1 HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.635+607C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963444 | |||||||
| chr1:32963489 | G | A | 1 | a0001c0001t0003g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.635+562C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963489 | |||||||
| chr1:32963712 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.635+339G>A | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963712 | |||||||
| chr1:32963718 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0038 |
4 | HG02055.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.635+319_635+332del others(14): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963718 | |||||||
| chr1:32963783 | C | CA | 6 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0234 others(3): Show |
6 | HG01981.hp2 HG02071.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.635+267dupT | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963783 | |||||||
| chr1:32963807 | C | G | 1 | a0001c0002t0002g0036 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.635+244G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963807 | |||||||
| chr1:32963938 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.635+113C>T | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32963938 | |||||||
| chr1:32964007 | T | TCGGCTGC others(28): Show |
1 | a0001c0001t0003g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.635+9_635+43dupGGG others(32): Show |
RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32964007 | |||||||
| chr1:32964019 | C | G | 1 | a0001c0002t0002g0035 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.635+32G>C | RNF19B | ENSG00000116514.17 | transcript | ENST00000235150.5 | protein_coding | 1/8 | chr1 | 32964019 |