Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9025 |
| ensemblid | ENSG00000112130.17 |
| hgncid | 10071 |
| symbol | RNF8 |
| name | ring finger protein 8 |
| refseq_nuc | NM_003958.4 |
| refseq_prot | NP_003949.1 |
| ensembl_nuc | ENST00000373479.9 |
| ensembl_prot | ENSP00000362578.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 37353983 |
| end | 37394734 |
| strand | + |
| ver | v1.2 |
| region | chr6:37353983-37394734 |
| region5000 | chr6:37348983-37399734 |
| regionname0 | RNF8_chr6_37353983_37394734 |
| regionname5000 | RNF8_chr6_37348983_37399734 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1455 | 206 | 58 | 30 | 98 | 5 | 14 | RNF8_chr6_37348983_37399734 | RNF8 | ATGGG others(1450): Show |
chr6 | 37348983 | 37399734 | ||
| a0001c0002 | 1/0 | 1455 | 113 | 38 | 25 | 32 | 3 | 14 | RNF8_chr6_37348983_37399734 | RNF8 | ATGGG others(1450): Show |
chr6 | 37348983 | 37399734 | ||
| a0001c0003 | 0/0 | 1455 | 3 | 0 | 3 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | ATGGG others(1450): Show |
chr6 | 37348983 | 37399734 | ||
| a0001c0004 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | ATGGG others(1450): Show |
chr6 | 37348983 | 37399734 | ||
| a0001c0005 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | ATGGG others(1450): Show |
chr6 | 37348983 | 37399734 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5616 | 95 | 3 | 17 | 60 | 3 | 11 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0002 | 0/0 | 5616 | 8 | 4 | 1 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0003 | 0/0 | 5616 | 28 | 9 | 0 | 19 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0004 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0005 | 0/0 | 5616 | 16 | 15 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0006 | 0/0 | 5616 | 12 | 1 | 7 | 2 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0007 | 0/0 | 5616 | 11 | 3 | 3 | 5 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0008 | 0/0 | 5616 | 10 | 9 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0009 | 0/0 | 5616 | 5 | 5 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0010 | 0/0 | 5616 | 4 | 0 | 0 | 2 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0011 | 0/0 | 5616 | 3 | 0 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0014 | 0/0 | 5616 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0015 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0016 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0017 | 0/0 | 5616 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0018 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0019 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0020 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0021 | 0/0 | 5616 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0022 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0001t0024 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0002t0001 | 1/0 | 5616 | 45 | 5 | 16 | 9 | 3 | 11 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0002t0002 | 0/0 | 5616 | 41 | 9 | 7 | 22 | 0 | 3 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0002t0004 | 0/0 | 5616 | 20 | 18 | 2 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0002t0012 | 0/0 | 5616 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0002t0013 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0002t0015 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0002t0023 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0003t0001 | 0/0 | 5616 | 3 | 0 | 3 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0004t0004 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| a0001c0005t0004 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | GTAGT others(5611): Show |
chr6 | 37348983 | 37399734 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 7 | 6 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0007 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0028 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0010g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0011g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0014g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0014g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0015g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0016g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0016g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0017g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0017g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0018g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0019g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0020g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0021g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0022g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0001t0024g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0003 | 1/0 | 4 | 1 | 0 | 1 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0005 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0008 | 0/0 | 4 | 1 | 0 | 2 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0012g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0012g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0013g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0013g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0015g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0002t0023g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0003t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0003t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0004t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| a0001c0005t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0006 | g0065 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0023 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00323 | hp1 | a0001 | c0001 | t0010 | g0110 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0122 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0097 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0177 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01099 | hp2 | a0001 | c0003 | t0001 | g0043 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0020 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0020 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0003 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0181 | AMR | PUR | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0096 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0228 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0148 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0009 | EUR | IBS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0174 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01884 | hp2 | a0001 | c0002 | t0012 | g0026 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0223 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0156 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02055 | hp2 | a0001 | c0001 | t0016 | g0165 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02074 | hp1 | a0001 | c0002 | t0023 | g0195 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02080 | hp2 | a0001 | c0001 | t0010 | g0125 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02145 | hp1 | a0001 | c0002 | t0004 | g0206 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CDX | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02257 | hp2 | a0001 | c0001 | t0015 | g0150 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02258 | hp1 | a0001 | c0001 | t0019 | g0160 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0218 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0197 | AMR | PEL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | KHV | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0187 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0146 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0224 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0190 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0044 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02723 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0023 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0158 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02818 | hp2 | a0001 | c0001 | t0024 | g0176 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0161 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0250 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0185 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0186 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0159 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0008 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0030 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03041 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0178 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03195 | hp1 | a0001 | c0005 | t0004 | g0182 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0180 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03225 | hp1 | a0001 | c0002 | t0004 | g0203 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03225 | hp2 | a0001 | c0001 | t0018 | g0163 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0230 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0199 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03486 | hp2 | a0001 | c0002 | t0012 | g0220 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | ESN | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03579 | hp1 | a0001 | c0002 | t0004 | g0183 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0012 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03688 | hp1 | a0001 | c0001 | t0010 | g0094 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0216 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03942 | hp1 | a0001 | c0001 | t0021 | g0072 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0095 | SAS | BEB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | STU | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18522 | hp1 | a0001 | c0002 | t0012 | g0026 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0154 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18943 | hp2 | a0001 | c0001 | t0017 | g0235 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18947 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18948 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18956 | hp2 | a0001 | c0002 | t0002 | g0215 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18961 | hp1 | a0001 | c0001 | t0014 | g0112 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18961 | hp2 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18968 | hp2 | a0001 | c0001 | t0014 | g0162 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18978 | hp1 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18999 | hp2 | a0001 | c0001 | t0011 | g0234 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0196 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19043 | hp2 | a0001 | c0002 | t0015 | g0256 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0191 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19064 | hp2 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19074 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19078 | hp1 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19078 | hp2 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19090 | hp1 | a0001 | c0001 | t0017 | g0236 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19240 | hp1 | a0001 | c0001 | t0016 | g0164 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | YRI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0147 | AFR | ASW | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | ASW | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0064 | EUR | TSI | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0157 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0188 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02559 | hp1 | a0001 | c0002 | t0013 | g0168 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0012 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG06807 | hp1 | a0001 | c0002 | t0013 | g0169 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0167 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0093 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA20300 | hp2 | a0001 | c0001 | t0022 | g0170 | AFR | USA | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| NA21309 | hp2 | a0001 | c0004 | t0004 | g0171 | AFR | LWK | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0127 | REF | REF | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0003 | REF | REF | RNF8_chr6_37348983_37399734 | RNF8 | chr6 | 37348983 | 37399734 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:37369050 | C | T | 1 | a0001c0005 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.807C>T | p.Ala269Ala | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/8 | 989/5616 | 807/1458 | 269/485 | chr6 | 37369050 | |||
| chr6:37371547 | G | A | 1 | a0001c0004 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1011G>A | p.Lys337Lys | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/8 | 1193/5616 | 1011/1458 | 337/485 | chr6 | 37371547 | |||
| chr6:37381257 | G | A | 2 | a0001c0001 a0001c0004 |
206 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
synonymous_variant | LOW | c.1344G>A | p.Thr448Thr | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/8 | 1526/5616 | 1344/1458 | 448/485 | chr6 | 37381257 | |||
| chr6:37381290 | G | A | 1 | a0001c0003 | 3 | HG01099.hp2 HG01106.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1377G>A | p.Lys459Lys | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/8 | 1559/5616 | 1377/1458 | 459/485 | chr6 | 37381290 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:37354015 | G | T | 2 | a0001c0001t0006 a0001c0001t0010 |
16 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-150G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/8 | 150 | chr6 | 37354015 | ||||||
| chr6:37354031 | C | G | 13 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(10): Show |
126 | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(123): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-134C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/8 | chr6 | 37354031 | |||||||
| chr6:37354076 | G | T | 1 | a0001c0001t0016 | 2 | HG02055.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-89G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/8 | 89 | chr6 | 37354076 | ||||||
| chr6:37391130 | C | T | 4 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0022 others(1): Show |
9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*372C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 372 | chr6 | 37391130 | ||||||
| chr6:37391348 | A | T | 1 | a0001c0002t0012 | 3 | HG01884.hp2 HG03486.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*590A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 590 | chr6 | 37391348 | ||||||
| chr6:37391421 | C | T | 1 | a0001c0001t0011 | 3 | NA18961.hp2 NA18999.hp2 NA19064.hp2 |
3_prime_UTR_variant | MODIFIER | c.*663C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 663 | chr6 | 37391421 | ||||||
| chr6:37391433 | G | A | 1 | a0001c0002t0013 | 2 | HG02559.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*675G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 675 | chr6 | 37391433 | ||||||
| chr6:37391539 | C | T | 4 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0022 others(1): Show |
9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*781C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 781 | chr6 | 37391539 | ||||||
| chr6:37391771 | A | G | 1 | a0001c0001t0021 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1013A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1013 | chr6 | 37391771 | ||||||
| chr6:37392170 | A | G | 7 | a0001c0001t0004 a0001c0001t0015 a0001c0002t0004 others(4): Show |
27 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1412A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1412 | chr6 | 37392170 | ||||||
| chr6:37392292 | G | A | 1 | a0001c0001t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1534G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1534 | chr6 | 37392292 | ||||||
| chr6:37392296 | A | G | 1 | a0001c0001t0014 | 2 | NA18961.hp1 NA18968.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1538A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1538 | chr6 | 37392296 | ||||||
| chr6:37392443 | C | G | 1 | a0001c0001t0017 | 2 | NA18943.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1685C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1685 | chr6 | 37392443 | ||||||
| chr6:37392674 | G | A | 4 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0019 others(1): Show |
28 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1916G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 1916 | chr6 | 37392674 | ||||||
| chr6:37392778 | A | G | 1 | a0001c0001t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2020 | chr6 | 37392778 | ||||||
| chr6:37392781 | T | C | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(17): Show |
118 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2023T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2023 | chr6 | 37392781 | ||||||
| chr6:37393208 | C | T | 1 | a0001c0001t0020 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2450C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2450 | chr6 | 37393208 | ||||||
| chr6:37393660 | G | A | 1 | a0001c0002t0023 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2902G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2902 | chr6 | 37393660 | ||||||
| chr6:37393733 | C | T | 3 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0020 |
27 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2975C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 2975 | chr6 | 37393733 | ||||||
| chr6:37393762 | A | C | 4 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0022 others(1): Show |
9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3004A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 3004 | chr6 | 37393762 | ||||||
| chr6:37394145 | A | G | 1 | a0001c0002t0013 | 2 | HG02559.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3387A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 3387 | chr6 | 37394145 | ||||||
| chr6:37394454 | G | A | 1 | a0001c0001t0022 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3696G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 8/8 | 3696 | chr6 | 37394454 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:37354383 | C | G | 2 | a0001c0002t0001g0257 a0001c0002t0015g0256 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111+108C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354383 | |||||||
| chr6:37354416 | G | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(4): Show |
7 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.111+141G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354416 | |||||||
| chr6:37354419 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.111+144G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354419 | |||||||
| chr6:37354513 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG02040.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.111+238G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354513 | |||||||
| chr6:37354569 | A | T | 99 | a0001c0001t0002g0172 a0001c0001t0002g0200 a0001c0001t0002g0209 others(96): Show |
127 | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(124): Show |
intron_variant | MODIFIER | c.111+294A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354569 | |||||||
| chr6:37354595 | G | A | 1 | a0001c0001t0022g0170 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.111+320G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354595 | |||||||
| chr6:37354774 | G | GC | 130 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(127): Show |
158 | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(155): Show |
intron_variant | MODIFIER | c.111+501dupC | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37354774 | ||||||
| chr6:37354896 | G | A | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.111+621G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37354896 | |||||||
| chr6:37355219 | C | G | 1 | a0001c0002t0002g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.111+944C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355219 | |||||||
| chr6:37355263 | A | G | 27 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(24): Show |
37 | HG02056.hp1 HG02109.hp2 HG02559.hp2 others(34): Show |
intron_variant | MODIFIER | c.111+988A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355263 | |||||||
| chr6:37355269 | T | C | 5 | a0001c0001t0002g0237 a0001c0001t0011g0027 a0001c0001t0011g0234 others(2): Show |
6 | NA18943.hp2 NA18961.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.111+994T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355269 | |||||||
| chr6:37355392 | T | C | 3 | a0001c0001t0008g0146 a0001c0001t0008g0147 a0001c0001t0008g0148 |
3 | HG01361.hp1 HG02615.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.111+1117T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355392 | |||||||
| chr6:37355482 | G | A | 2 | a0001c0002t0001g0257 a0001c0002t0015g0256 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.111+1207G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355482 | |||||||
| chr6:37355733 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.111+1458G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37355733 | |||||||
| chr6:37356106 | A | C | 2 | a0001c0002t0013g0168 a0001c0002t0013g0169 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.111+1831A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356106 | |||||||
| chr6:37356144 | A | G | 2 | a0001c0001t0007g0166 a0001c0001t0007g0167 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.111+1869A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356144 | |||||||
| chr6:37356234 | T | C | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.111+1959T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356234 | |||||||
| chr6:37356336 | ATGG | A | 21 | a0001c0001t0004g0184 a0001c0001t0024g0176 a0001c0002t0002g0175 others(18): Show |
25 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.111+2063_111+2065d others(5): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37356336 | ||||||
| chr6:37356740 | G | A | 2 | a0001c0001t0007g0166 a0001c0001t0007g0167 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.111+2465G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356740 | |||||||
| chr6:37356892 | C | T | 3 | a0001c0001t0016g0164 a0001c0001t0016g0165 a0001c0001t0018g0163 |
3 | HG02055.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.111+2617C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37356892 | |||||||
| chr6:37357081 | G | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(106): Show |
139 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.111+2806G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357081 | |||||||
| chr6:37357117 | C | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(112): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.111+2842C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357117 | |||||||
| chr6:37357170 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.111+2895A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357170 | |||||||
| chr6:37357200 | G | A | 1 | a0001c0001t0006g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.111+2925G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357200 | |||||||
| chr6:37357418 | T | C | 2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.112-3028T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357418 | |||||||
| chr6:37357556 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.112-2890G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357556 | |||||||
| chr6:37357639 | T | G | 1 | a0001c0001t0006g0065 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.112-2807T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357639 | |||||||
| chr6:37357916 | A | C | 30 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(27): Show |
40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-2530A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357916 | |||||||
| chr6:37357936 | C | T | 1 | a0001c0001t0007g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.112-2510C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37357936 | |||||||
| chr6:37358104 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.112-2342T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358104 | |||||||
| chr6:37358253 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | NA18979.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.112-2193A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358253 | |||||||
| chr6:37358441 | T | A | 30 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(27): Show |
40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-2005T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358441 | |||||||
| chr6:37358468 | A | G | 1 | a0001c0002t0001g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.112-1978A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358468 | |||||||
| chr6:37358819 | G | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | NA18979.hp1 NA18982.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.112-1627G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358819 | |||||||
| chr6:37358823 | G | A | 30 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(27): Show |
40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-1623G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358823 | |||||||
| chr6:37358913 | A | G | 1 | a0001c0001t0003g0029 | 2 | NA18949.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.112-1533A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358913 | |||||||
| chr6:37358996 | T | C | 1 | a0001c0001t0008g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.112-1450T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37358996 | |||||||
| chr6:37359022 | G | A | 12 | a0001c0001t0022g0170 a0001c0002t0001g0149 a0001c0002t0002g0004 others(9): Show |
16 | HG01943.hp1 HG02004.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.112-1424G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359022 | |||||||
| chr6:37359089 | C | CTG | 30 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(27): Show |
40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-1356_112-1355i others(4): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37359089 | ||||||
| chr6:37359570 | A | G | 1 | a0001c0002t0001g0141 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.112-876A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359570 | |||||||
| chr6:37359618 | A | G | 30 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(27): Show |
40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-828A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359618 | |||||||
| chr6:37359863 | C | G | 5 | a0001c0001t0007g0166 a0001c0001t0007g0167 a0001c0002t0013g0168 others(2): Show |
5 | HG02559.hp1 HG03098.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-583C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359863 | |||||||
| chr6:37359885 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.112-561G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37359885 | |||||||
| chr6:37360036 | A | G | 1 | a0001c0002t0002g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.112-410A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360036 | |||||||
| chr6:37360223 | C | T | 51 | a0001c0001t0002g0172 a0001c0001t0003g0230 a0001c0001t0004g0184 others(48): Show |
58 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(55): Show |
intron_variant | MODIFIER | c.112-223C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360223 | |||||||
| chr6:37360388 | G | A | 30 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(27): Show |
40 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-58G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360388 | |||||||
| chr6:37360402 | G | A | 3 | a0001c0001t0005g0013 a0001c0001t0005g0218 a0001c0001t0005g0219 |
5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-44G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | chr6 | 37360402 | |||||||
| chr6:37360439 | C | CT | 86 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(83): Show |
103 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(100): Show |
splice_region_variant&intron_variant | LOW | c.112-6dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | 37360439 | ||||||
| chr6:37360623 | C | CT | 27 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(24): Show |
37 | HG02056.hp1 HG02109.hp2 HG02559.hp2 others(34): Show |
intron_variant | MODIFIER | c.240+63dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37360623 | ||||||
| chr6:37360623 | CT | C | 54 | a0001c0001t0001g0014 a0001c0001t0001g0067 a0001c0001t0001g0068 others(51): Show |
62 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.240+63delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37360623 | ||||||
| chr6:37360777 | A | G | 35 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(32): Show |
45 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(42): Show |
intron_variant | MODIFIER | c.240+203A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37360777 | |||||||
| chr6:37360788 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.240+214A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37360788 | |||||||
| chr6:37361225 | A | G | 84 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(81): Show |
101 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(98): Show |
intron_variant | MODIFIER | c.240+651A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361225 | |||||||
| chr6:37361505 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.240+931C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361505 | |||||||
| chr6:37361552 | C | T | 1 | a0001c0001t0006g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.240+978C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361552 | |||||||
| chr6:37361772 | G | A | 49 | a0001c0001t0002g0172 a0001c0001t0003g0230 a0001c0001t0004g0184 others(46): Show |
56 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.240+1198G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361772 | |||||||
| chr6:37361796 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.240+1222C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361796 | |||||||
| chr6:37361984 | C | G | 4 | a0001c0001t0003g0029 a0001c0001t0003g0217 a0001c0001t0003g0253 others(1): Show |
5 | NA18949.hp2 NA18962.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.240+1410C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37361984 | |||||||
| chr6:37362024 | A | G | 11 | a0001c0002t0001g0054 a0001c0002t0001g0055 a0001c0002t0001g0056 others(8): Show |
11 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.240+1450A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362024 | |||||||
| chr6:37362102 | C | T | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+1528C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362102 | |||||||
| chr6:37362117 | C | T | 1 | a0001c0002t0002g0216 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.240+1543C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362117 | |||||||
| chr6:37362263 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.240+1689T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362263 | |||||||
| chr6:37362458 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.240+1884T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362458 | |||||||
| chr6:37362515 | A | G | 5 | a0001c0002t0002g0211 a0001c0002t0002g0212 a0001c0002t0002g0213 others(2): Show |
5 | NA18955.hp1 NA18956.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+1941A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362515 | |||||||
| chr6:37362516 | TTTAA | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(153): Show |
192 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.240+1945_240+1948d others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37362516 | ||||||
| chr6:37362543 | G | A | 1 | a0001c0002t0012g0220 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.240+1969G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362543 | |||||||
| chr6:37362679 | A | G | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+2105A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362679 | |||||||
| chr6:37362838 | T | C | 2 | a0001c0001t0008g0030 a0001c0001t0008g0031 |
2 | HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.240+2264T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362838 | |||||||
| chr6:37362975 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(80): Show |
108 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.240+2401C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37362975 | |||||||
| chr6:37363240 | C | G | 1 | a0001c0002t0001g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.240+2666C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363240 | |||||||
| chr6:37363273 | C | G | 16 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0066 others(13): Show |
18 | HG00323.hp2 HG02015.hp1 HG03669.hp2 others(15): Show |
intron_variant | MODIFIER | c.240+2699C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363273 | |||||||
| chr6:37363499 | A | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG00609.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.240+2925A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363499 | |||||||
| chr6:37363564 | T | C | 1 | a0001c0001t0005g0218 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.240+2990T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363564 | |||||||
| chr6:37363578 | C | T | 1 | a0001c0002t0004g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.240+3004C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363578 | |||||||
| chr6:37363680 | A | ATTAC | 31 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(28): Show |
41 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.240+3108_240+3109i others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37363680 | ||||||
| chr6:37363698 | C | T | 1 | a0001c0002t0001g0063 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.240+3124C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363698 | |||||||
| chr6:37363720 | T | C | 3 | a0001c0001t0007g0166 a0001c0001t0007g0167 a0001c0004t0004g0171 |
3 | HG03098.hp2 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.240+3146T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363720 | |||||||
| chr6:37363876 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.240+3302C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363876 | |||||||
| chr6:37363986 | T | C | 1 | a0001c0001t0021g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.240+3412T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37363986 | |||||||
| chr6:37364023 | T | C | 29 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(26): Show |
39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.240+3449T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364023 | |||||||
| chr6:37364039 | C | T | 1 | a0001c0001t0008g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.240+3465C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364039 | |||||||
| chr6:37364178 | C | CA | 128 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(125): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.240+3625dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | ||||||
| chr6:37364178 | C | CAA | 25 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0052 others(22): Show |
27 | HG00741.hp1 HG01109.hp1 HG02135.hp2 others(24): Show |
intron_variant | MODIFIER | c.240+3624_240+3625d others(4): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | ||||||
| chr6:37364178 | C | CAAAAAA | 23 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(20): Show |
32 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.240+3620_240+3625d others(8): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | ||||||
| chr6:37364178 | C | CAAAAAAA | 5 | a0001c0001t0003g0028 a0001c0001t0003g0238 a0001c0001t0003g0253 others(2): Show |
6 | HG03209.hp2 HG03471.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+3619_240+3625d others(9): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364178 | ||||||
| chr6:37364261 | T | TAAAACCA others(274): Show |
1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(283): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | ||||||
| chr6:37364261 | T | TAAAACCA others(274): Show |
4 | a0001c0001t0009g0152 a0001c0001t0009g0153 a0001c0001t0009g0154 others(1): Show |
4 | HG02647.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+3697_240+3698i others(283): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | ||||||
| chr6:37364261 | T | TAAAACCA others(275): Show |
1 | a0001c0001t0009g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.240+3697_240+3698i others(284): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | ||||||
| chr6:37364261 | T | TAAAACCA others(276): Show |
1 | a0001c0001t0015g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(285): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | ||||||
| chr6:37364261 | T | TAAAACCA others(274): Show |
1 | a0001c0001t0007g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(283): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | ||||||
| chr6:37364261 | T | TAAAACCA others(275): Show |
1 | a0001c0001t0007g0166 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.240+3697_240+3698i others(284): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37364261 | ||||||
| chr6:37364437 | A | G | 1 | a0001c0001t0003g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.240+3863A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364437 | |||||||
| chr6:37364440 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.240+3866G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364440 | |||||||
| chr6:37364489 | T | A | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.240+3915T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364489 | |||||||
| chr6:37364781 | A | G | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.241-3703A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364781 | |||||||
| chr6:37364801 | G | A | 29 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(26): Show |
39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-3683G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37364801 | |||||||
| chr6:37365255 | T | C | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.241-3229T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365255 | |||||||
| chr6:37365329 | C | T | 3 | a0001c0001t0016g0164 a0001c0001t0016g0165 a0001c0001t0018g0163 |
3 | HG02055.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-3155C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365329 | |||||||
| chr6:37365394 | G | T | 29 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(26): Show |
39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-3090G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365394 | |||||||
| chr6:37365508 | A | G | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-2976A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365508 | |||||||
| chr6:37365542 | G | A | 64 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(61): Show |
78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.241-2942G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365542 | |||||||
| chr6:37365674 | A | G | 29 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(26): Show |
39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-2810A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365674 | |||||||
| chr6:37365801 | A | AG | 33 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(30): Show |
37 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.241-2682dupG | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37365801 | ||||||
| chr6:37365811 | T | C | 1 | a0001c0002t0001g0039 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.241-2673T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365811 | |||||||
| chr6:37365831 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.241-2653A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365831 | |||||||
| chr6:37365908 | C | A | 1 | a0001c0001t0007g0106 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.241-2576C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37365908 | |||||||
| chr6:37366020 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(180): Show |
229 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.241-2464C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366020 | |||||||
| chr6:37366091 | C | G | 29 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(26): Show |
39 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(36): Show |
intron_variant | MODIFIER | c.241-2393C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366091 | |||||||
| chr6:37366394 | T | C | 64 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(61): Show |
78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.241-2090T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366394 | |||||||
| chr6:37366658 | C | T | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.241-1826C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366658 | |||||||
| chr6:37366683 | T | TCCCTCAT others(10): Show |
2 | a0001c0002t0001g0105 a0001c0002t0001g0130 |
2 | HG00639.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.241-1800_241-1784d others(19): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr6 | 37366683 | ||||||
| chr6:37366953 | C | T | 1 | a0001c0002t0004g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.241-1531C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366953 | |||||||
| chr6:37366983 | C | T | 64 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(61): Show |
78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.241-1501C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37366983 | |||||||
| chr6:37367064 | G | A | 31 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0002g0237 others(28): Show |
41 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.241-1420G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367064 | |||||||
| chr6:37367071 | T | C | 1 | a0001c0001t0003g0239 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.241-1413T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367071 | |||||||
| chr6:37367142 | G | A | 2 | a0001c0001t0016g0164 a0001c0001t0016g0165 |
2 | HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-1342G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367142 | |||||||
| chr6:37367175 | G | A | 1 | a0001c0001t0005g0224 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.241-1309G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367175 | |||||||
| chr6:37367360 | C | G | 1 | a0001c0002t0001g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.241-1124C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367360 | |||||||
| chr6:37367369 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.241-1115A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367369 | |||||||
| chr6:37367387 | T | C | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.241-1097T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367387 | |||||||
| chr6:37367553 | A | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.241-931A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367553 | |||||||
| chr6:37367565 | G | A | 3 | a0001c0001t0016g0164 a0001c0001t0016g0165 a0001c0001t0018g0163 |
3 | HG02055.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-919G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367565 | |||||||
| chr6:37367588 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.241-896G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367588 | |||||||
| chr6:37367683 | T | C | 5 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0016g0164 others(2): Show |
5 | HG02055.hp2 HG02451.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-801T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367683 | |||||||
| chr6:37367684 | G | C | 1 | a0001c0001t0005g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.241-800G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367684 | |||||||
| chr6:37367722 | A | G | 26 | a0001c0001t0002g0237 a0001c0001t0002g0245 a0001c0001t0003g0006 others(23): Show |
36 | HG02056.hp1 HG02109.hp2 HG02559.hp2 others(33): Show |
intron_variant | MODIFIER | c.241-762A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367722 | |||||||
| chr6:37367845 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.241-639G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37367845 | |||||||
| chr6:37368057 | C | T | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.241-427C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37368057 | |||||||
| chr6:37368440 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0128 |
3 | NA18948.hp2 NA18979.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.241-44C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 2/7 | chr6 | 37368440 | |||||||
| chr6:37369375 | A | C | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.975+157A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37369375 | |||||||
| chr6:37369583 | T | C | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.975+365T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37369583 | |||||||
| chr6:37370258 | G | A | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.975+1040G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370258 | |||||||
| chr6:37370529 | T | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-983T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370529 | |||||||
| chr6:37370566 | G | A | 2 | a0001c0002t0001g0051 a0001c0002t0002g0201 |
2 | HG01346.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.976-946G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370566 | |||||||
| chr6:37370573 | A | T | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(60): Show |
77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.976-939A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370573 | |||||||
| chr6:37370638 | C | G | 3 | a0001c0002t0002g0175 a0001c0002t0002g0189 a0001c0002t0004g0174 |
3 | HG01884.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.976-874C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370638 | |||||||
| chr6:37370701 | C | CT | 211 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(208): Show |
269 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.976-796dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 37370701 | ||||||
| chr6:37370701 | C | CTT | 7 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(4): Show |
7 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.976-797_976-796dup others(2): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr6 | 37370701 | ||||||
| chr6:37370925 | A | C | 1 | a0001c0002t0001g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.976-587A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37370925 | |||||||
| chr6:37371193 | G | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(93): Show |
126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.976-319G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371193 | |||||||
| chr6:37371241 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(93): Show |
126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.976-271A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371241 | |||||||
| chr6:37371298 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.976-214C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371298 | |||||||
| chr6:37371343 | T | C | 28 | a0001c0001t0002g0245 a0001c0001t0003g0006 a0001c0001t0003g0007 others(25): Show |
38 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(35): Show |
intron_variant | MODIFIER | c.976-169T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371343 | |||||||
| chr6:37371454 | G | A | 3 | a0001c0002t0002g0175 a0001c0002t0002g0189 a0001c0002t0004g0174 |
3 | HG01884.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.976-58G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 3/7 | chr6 | 37371454 | |||||||
| chr6:37371591 | A | G | 1 | a0001c0001t0007g0020 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1038+17A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371591 | |||||||
| chr6:37371743 | C | A | 1 | a0001c0002t0004g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1038+169C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371743 | |||||||
| chr6:37371794 | A | G | 1 | a0001c0001t0002g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1038+220A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371794 | |||||||
| chr6:37371805 | T | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0134 |
3 | HG00323.hp2 NA18975.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1038+231T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371805 | |||||||
| chr6:37371846 | T | C | 4 | a0001c0001t0005g0221 a0001c0001t0005g0226 a0001c0001t0005g0250 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+272T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371846 | |||||||
| chr6:37371975 | T | C | 34 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(31): Show |
38 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.1038+401T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37371975 | |||||||
| chr6:37372545 | G | A | 2 | a0001c0001t0007g0166 a0001c0001t0007g0167 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1038+971G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372545 | |||||||
| chr6:37372604 | C | T | 1 | a0001c0001t0003g0252 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1038+1030C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372604 | |||||||
| chr6:37372691 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1038+1117C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372691 | |||||||
| chr6:37372697 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1038+1123C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372697 | |||||||
| chr6:37372698 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1038+1124G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372698 | |||||||
| chr6:37372786 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1038+1212A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372786 | |||||||
| chr6:37372796 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0091 |
3 | NA18940.hp1 NA18960.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1038+1222C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372796 | |||||||
| chr6:37372838 | G | A | 23 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0218 others(20): Show |
25 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+1264G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372838 | |||||||
| chr6:37372841 | T | C | 19 | a0001c0001t0002g0172 a0001c0001t0003g0230 a0001c0001t0004g0184 others(16): Show |
23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1038+1267T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372841 | |||||||
| chr6:37372996 | A | G | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1038+1422A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37372996 | |||||||
| chr6:37373025 | C | G | 19 | a0001c0001t0002g0172 a0001c0001t0003g0230 a0001c0001t0004g0184 others(16): Show |
23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1038+1451C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373025 | |||||||
| chr6:37373249 | C | CCTT | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(60): Show |
77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.1039-1369_1039-136 others(7): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr6 | 37373249 | ||||||
| chr6:37373458 | G | A | 9 | a0001c0001t0008g0146 a0001c0001t0008g0147 a0001c0001t0008g0148 others(6): Show |
9 | HG01361.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039-1162G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373458 | |||||||
| chr6:37373516 | C | A | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1039-1104C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373516 | |||||||
| chr6:37373553 | C | T | 19 | a0001c0001t0002g0172 a0001c0001t0003g0230 a0001c0001t0004g0184 others(16): Show |
23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-1067C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373553 | |||||||
| chr6:37373615 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1039-1005C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373615 | |||||||
| chr6:37373646 | C | G | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(60): Show |
77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.1039-974C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373646 | |||||||
| chr6:37373850 | A | G | 24 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0218 others(21): Show |
26 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1039-770A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373850 | |||||||
| chr6:37373920 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1039-700A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37373920 | |||||||
| chr6:37374006 | A | G | 1 | a0001c0001t0005g0173 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1039-614A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374006 | |||||||
| chr6:37374082 | T | C | 9 | a0001c0001t0008g0146 a0001c0001t0008g0147 a0001c0001t0008g0148 others(6): Show |
9 | HG01361.hp1 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1039-538T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374082 | |||||||
| chr6:37374144 | A | G | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(60): Show |
77 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(74): Show |
intron_variant | MODIFIER | c.1039-476A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374144 | |||||||
| chr6:37374359 | T | G | 1 | a0001c0001t0009g0152 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1039-261T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374359 | |||||||
| chr6:37374373 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1039-247A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374373 | |||||||
| chr6:37374414 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1039-206G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 4/7 | chr6 | 37374414 | |||||||
| chr6:37375083 | T | C | 1 | a0001c0002t0001g0139 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1128+374T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375083 | |||||||
| chr6:37375301 | G | T | 1 | a0001c0002t0002g0215 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1128+592G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375301 | |||||||
| chr6:37375392 | A | G | 3 | a0001c0001t0007g0166 a0001c0001t0007g0167 a0001c0004t0004g0171 |
3 | HG03098.hp2 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1128+683A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375392 | |||||||
| chr6:37375535 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1128+826C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375535 | |||||||
| chr6:37375648 | T | G | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1128+939T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375648 | |||||||
| chr6:37375688 | G | A | 1 | a0001c0001t0008g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1128+979G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375688 | |||||||
| chr6:37375694 | A | G | 1 | a0001c0001t0020g0159 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1128+985A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375694 | |||||||
| chr6:37375924 | C | T | 3 | a0001c0001t0007g0166 a0001c0001t0007g0167 a0001c0004t0004g0171 |
3 | HG03098.hp2 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1129-1002C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375924 | |||||||
| chr6:37375928 | G | C | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129-998G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375928 | |||||||
| chr6:37375982 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1129-944G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375982 | |||||||
| chr6:37375983 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1129-943G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37375983 | |||||||
| chr6:37376070 | T | C | 19 | a0001c0001t0002g0172 a0001c0001t0003g0230 a0001c0001t0004g0184 others(16): Show |
23 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1129-856T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376070 | |||||||
| chr6:37376399 | A | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-527A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376399 | |||||||
| chr6:37376546 | G | C | 12 | a0001c0001t0001g0098 a0001c0001t0006g0002 a0001c0001t0006g0065 others(9): Show |
17 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.1129-380G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376546 | |||||||
| chr6:37376560 | C | T | 1 | a0001c0001t0008g0148 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1129-366C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376560 | |||||||
| chr6:37376613 | C | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-313C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 5/7 | chr6 | 37376613 | |||||||
| chr6:37377061 | C | CT | 60 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0049 others(57): Show |
65 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.1236+56dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | ||||||
| chr6:37377061 | C | CTT | 8 | a0001c0001t0001g0052 a0001c0001t0006g0065 a0001c0001t0008g0031 others(5): Show |
10 | HG00280.hp1 HG00735.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1236+55_1236+56dup others(2): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | ||||||
| chr6:37377061 | CT | C | 10 | a0001c0001t0001g0053 a0001c0001t0001g0142 a0001c0001t0005g0222 others(7): Show |
10 | HG02257.hp1 HG02258.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1236+56delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | ||||||
| chr6:37377061 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+49_1236+56del others(8): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | ||||||
| chr6:37377061 | CTTTTTTT others(3): Show |
C | 26 | a0001c0001t0002g0245 a0001c0001t0003g0006 a0001c0001t0003g0007 others(23): Show |
36 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1236+47_1236+56del others(10): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37377061 | ||||||
| chr6:37377367 | A | G | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1236+334A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377367 | |||||||
| chr6:37377674 | G | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1236+641G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377674 | |||||||
| chr6:37377775 | A | G | 1 | a0001c0002t0001g0050 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1236+742A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377775 | |||||||
| chr6:37377787 | A | C | 1 | a0001c0001t0003g0247 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1236+754A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377787 | |||||||
| chr6:37377928 | T | C | 64 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(61): Show |
78 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(75): Show |
intron_variant | MODIFIER | c.1236+895T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37377928 | |||||||
| chr6:37378225 | C | T | 30 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(27): Show |
34 | HG00741.hp1 HG01243.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1236+1192C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378225 | |||||||
| chr6:37378336 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(2): Show |
5 | HG02717.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+1303C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378336 | |||||||
| chr6:37378375 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1236+1342C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378375 | |||||||
| chr6:37378588 | G | A | 4 | a0001c0002t0002g0187 a0001c0002t0002g0188 a0001c0002t0002g0232 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+1555G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378588 | |||||||
| chr6:37378600 | C | CA | 58 | a0001c0001t0001g0033 a0001c0001t0001g0078 a0001c0001t0001g0088 others(55): Show |
72 | HG00609.hp1 HG00741.hp1 HG01243.hp2 others(69): Show |
intron_variant | MODIFIER | c.1236+1590dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37378600 | ||||||
| chr6:37378600 | C | CAA | 6 | a0001c0001t0001g0107 a0001c0001t0002g0237 a0001c0001t0003g0241 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+1589_1236+159 others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37378600 | ||||||
| chr6:37378600 | CAAAAAAA others(6): Show |
C | 6 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+1578_1236+159 others(17): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37378600 | ||||||
| chr6:37378831 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1236+1798T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37378831 | |||||||
| chr6:37379079 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1236+2046C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379079 | |||||||
| chr6:37379102 | C | T | 8 | a0001c0001t0002g0209 a0001c0001t0002g0210 a0001c0001t0009g0151 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-2048C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379102 | |||||||
| chr6:37379457 | G | A | 2 | a0001c0002t0001g0055 a0001c0002t0001g0056 |
2 | HG00642.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1237-1693G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379457 | |||||||
| chr6:37379527 | A | G | 3 | a0001c0001t0005g0013 a0001c0001t0005g0218 a0001c0001t0005g0219 |
5 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237-1623A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379527 | |||||||
| chr6:37379659 | G | A | 1 | a0001c0002t0001g0041 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1237-1491G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379659 | |||||||
| chr6:37379668 | G | T | 1 | a0001c0002t0002g0213 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1237-1482G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379668 | |||||||
| chr6:37379763 | G | A | 63 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(60): Show |
77 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(74): Show |
intron_variant | MODIFIER | c.1237-1387G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37379763 | |||||||
| chr6:37379912 | G | GTTTGTTT others(6): Show |
1 | a0001c0001t0003g0247 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1237-1234_1237-122 others(17): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37379912 | ||||||
| chr6:37380466 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0210 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1237-684C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380466 | |||||||
| chr6:37380540 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(187): Show |
236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.1237-610A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380540 | |||||||
| chr6:37380543 | C | T | 20 | a0001c0001t0002g0172 a0001c0001t0003g0230 a0001c0001t0024g0176 others(17): Show |
24 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1237-607C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380543 | |||||||
| chr6:37380563 | C | T | 1 | a0001c0001t0019g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1237-587C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380563 | |||||||
| chr6:37380583 | A | C | 2 | a0001c0001t0007g0166 a0001c0001t0007g0167 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1237-567A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380583 | |||||||
| chr6:37380665 | C | T | 1 | a0001c0002t0002g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1237-485C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380665 | |||||||
| chr6:37380670 | C | CA | 32 | a0001c0001t0001g0068 a0001c0001t0001g0091 a0001c0001t0001g0121 others(29): Show |
44 | HG02055.hp2 HG02056.hp1 HG02109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1237-463dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37380670 | ||||||
| chr6:37380670 | CA | C | 25 | a0001c0001t0001g0098 a0001c0001t0001g0120 a0001c0001t0005g0173 others(22): Show |
25 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1237-463delA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr6 | 37380670 | ||||||
| chr6:37380685 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1237-465A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380685 | |||||||
| chr6:37380957 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1237-193A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37380957 | |||||||
| chr6:37381144 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(160): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
splice_region_variant&intron_variant | LOW | c.1237-6C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 6/7 | chr6 | 37381144 | |||||||
| chr6:37381517 | G | A | 1 | a0001c0001t0021g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1441+163G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37381517 | |||||||
| chr6:37381542 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1441+188C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37381542 | |||||||
| chr6:37382031 | A | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0120 others(1): Show |
4 | HG02083.hp1 HG02523.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441+677A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382031 | |||||||
| chr6:37382108 | T | C | 1 | a0001c0002t0001g0042 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1441+754T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382108 | |||||||
| chr6:37382274 | G | T | 15 | a0001c0001t0015g0150 a0001c0002t0004g0012 a0001c0002t0004g0177 others(12): Show |
17 | HG00741.hp1 HG01243.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1441+920G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382274 | |||||||
| chr6:37382280 | G | A | 38 | a0001c0001t0002g0237 a0001c0001t0003g0006 a0001c0001t0003g0007 others(35): Show |
55 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.1441+926G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382280 | |||||||
| chr6:37382959 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0079 |
2 | NA18995.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1441+1605C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37382959 | |||||||
| chr6:37382972 | C | CA | 6 | a0001c0002t0001g0047 a0001c0002t0001g0141 a0001c0002t0002g0205 others(3): Show |
6 | HG00639.hp1 HG02135.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441+1634dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37382972 | ||||||
| chr6:37383037 | A | G | 6 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0001g0087 others(3): Show |
7 | HG00323.hp2 HG02015.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441+1683A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383037 | |||||||
| chr6:37383197 | A | G | 9 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(6): Show |
9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1441+1843A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383197 | |||||||
| chr6:37383300 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1441+1946T>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383300 | |||||||
| chr6:37383438 | C | G | 2 | a0001c0002t0013g0168 a0001c0002t0013g0169 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1441+2084C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383438 | |||||||
| chr6:37383506 | T | C | 1 | a0001c0001t0008g0157 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1441+2152T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383506 | |||||||
| chr6:37383629 | A | G | 1 | a0001c0001t0003g0239 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1441+2275A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383629 | |||||||
| chr6:37383705 | G | A | 4 | a0001c0002t0002g0187 a0001c0002t0002g0188 a0001c0002t0002g0232 others(1): Show |
4 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441+2351G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383705 | |||||||
| chr6:37383726 | G | A | 1 | a0001c0002t0002g0194 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1441+2372G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383726 | |||||||
| chr6:37383830 | A | AT | 26 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0218 others(23): Show |
28 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1441+2482dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37383830 | ||||||
| chr6:37383921 | C | G | 22 | a0001c0001t0015g0150 a0001c0002t0004g0012 a0001c0002t0004g0024 others(19): Show |
26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1441+2567C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383921 | |||||||
| chr6:37383951 | G | A | 3 | a0001c0001t0008g0146 a0001c0001t0008g0148 a0001c0001t0020g0159 |
3 | HG01361.hp1 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1441+2597G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37383951 | |||||||
| chr6:37384131 | A | AT | 31 | a0001c0001t0001g0077 a0001c0001t0001g0082 a0001c0001t0001g0108 others(28): Show |
39 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1441+2796dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37384131 | ||||||
| chr6:37384131 | A | ATT | 41 | a0001c0001t0003g0007 a0001c0001t0003g0028 a0001c0001t0003g0029 others(38): Show |
53 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.1441+2795_1441+279 others(6): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37384131 | ||||||
| chr6:37384131 | AT | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0069 a0001c0001t0001g0075 others(12): Show |
15 | HG01099.hp2 HG01167.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.1441+2796delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37384131 | ||||||
| chr6:37384390 | G | C | 96 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0028 others(93): Show |
118 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.1441+3036G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37384390 | |||||||
| chr6:37384400 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1441+3046C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37384400 | |||||||
| chr6:37384964 | G | A | 1 | a0001c0001t0018g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1441+3610G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37384964 | |||||||
| chr6:37385018 | A | AT | 14 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0066 others(11): Show |
16 | HG00323.hp2 HG02015.hp1 NA18612.hp1 others(13): Show |
intron_variant | MODIFIER | c.1441+3676dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37385018 | ||||||
| chr6:37385035 | T | C | 96 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0028 others(93): Show |
118 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.1441+3681T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385035 | |||||||
| chr6:37385080 | C | G | 1 | a0001c0005t0004g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1441+3726C>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385080 | |||||||
| chr6:37385099 | C | T | 4 | a0001c0001t0005g0221 a0001c0001t0005g0226 a0001c0001t0005g0250 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1441+3745C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385099 | |||||||
| chr6:37385164 | C | T | 22 | a0001c0001t0015g0150 a0001c0002t0004g0012 a0001c0002t0004g0024 others(19): Show |
26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1441+3810C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385164 | |||||||
| chr6:37385174 | C | T | 22 | a0001c0001t0015g0150 a0001c0002t0004g0012 a0001c0002t0004g0024 others(19): Show |
26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1441+3820C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385174 | |||||||
| chr6:37385343 | G | T | 35 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0028 others(32): Show |
51 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1441+3989G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385343 | |||||||
| chr6:37385452 | C | T | 1 | a0001c0002t0001g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1441+4098C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385452 | |||||||
| chr6:37385488 | G | A | 2 | a0001c0001t0006g0092 a0001c0001t0006g0138 |
2 | HG02523.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1441+4134G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385488 | |||||||
| chr6:37385499 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1441+4145C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385499 | |||||||
| chr6:37385623 | C | T | 2 | a0001c0002t0004g0203 a0001c0002t0004g0206 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1441+4269C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385623 | |||||||
| chr6:37385719 | C | A | 2 | a0001c0001t0010g0122 a0001c0001t0010g0125 |
2 | HG00438.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1441+4365C>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385719 | |||||||
| chr6:37385740 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1441+4386T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37385740 | |||||||
| chr6:37385855 | A | AT | 45 | a0001c0001t0001g0014 a0001c0001t0001g0068 a0001c0001t0001g0069 others(42): Show |
51 | HG00642.hp1 HG01361.hp1 HG01891.hp2 others(48): Show |
intron_variant | MODIFIER | c.1441+4518dupT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37385855 | ||||||
| chr6:37385855 | AT | A | 7 | a0001c0001t0001g0066 a0001c0001t0001g0142 a0001c0001t0003g0241 others(4): Show |
7 | HG02896.hp2 HG03654.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.1441+4518delT | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37385855 | ||||||
| chr6:37386075 | A | G | 3 | a0001c0001t0004g0184 a0001c0001t0007g0166 a0001c0001t0007g0167 |
3 | HG03098.hp2 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1442-4667A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386075 | |||||||
| chr6:37386096 | A | G | 1 | a0001c0001t0003g0238 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1442-4646A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386096 | |||||||
| chr6:37386178 | A | ACCTTATT others(39): Show |
1 | a0001c0002t0001g0023 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1442-4563_1442-456 others(50): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37386178 | ||||||
| chr6:37386180 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0120 |
2 | HG02083.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1442-4562A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386180 | |||||||
| chr6:37386181 | G | C | 1 | a0001c0002t0001g0023 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1442-4561G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386181 | |||||||
| chr6:37386182 | T | C | 1 | a0001c0002t0001g0023 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1442-4560T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386182 | |||||||
| chr6:37386283 | A | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(186): Show |
237 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.1442-4459A>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386283 | |||||||
| chr6:37386422 | C | T | 22 | a0001c0001t0015g0150 a0001c0002t0004g0012 a0001c0002t0004g0024 others(19): Show |
26 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.1442-4320C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386422 | |||||||
| chr6:37386659 | C | T | 95 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0028 others(92): Show |
117 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(114): Show |
intron_variant | MODIFIER | c.1442-4083C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386659 | |||||||
| chr6:37386756 | T | A | 15 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0066 others(12): Show |
17 | HG00323.hp2 HG02015.hp1 NA18612.hp1 others(14): Show |
intron_variant | MODIFIER | c.1442-3986T>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386756 | |||||||
| chr6:37386827 | C | T | 1 | a0001c0001t0018g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1442-3915C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37386827 | |||||||
| chr6:37387012 | T | C | 1 | a0001c0001t0006g0138 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1442-3730T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387012 | |||||||
| chr6:37387437 | G | A | 1 | a0001c0001t0018g0163 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1442-3305G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387437 | |||||||
| chr6:37387482 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1442-3260A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387482 | |||||||
| chr6:37387489 | C | T | 35 | a0001c0001t0003g0006 a0001c0001t0003g0007 a0001c0001t0003g0028 others(32): Show |
51 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1442-3253C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387489 | |||||||
| chr6:37387577 | T | C | 9 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(6): Show |
9 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1442-3165T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387577 | |||||||
| chr6:37387623 | T | C | 1 | a0001c0001t0009g0153 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1442-3119T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37387623 | |||||||
| chr6:37388106 | A | G | 62 | a0001c0001t0002g0237 a0001c0001t0003g0006 a0001c0001t0003g0007 others(59): Show |
80 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1442-2636A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388106 | |||||||
| chr6:37388139 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1442-2603G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388139 | |||||||
| chr6:37388200 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0142 |
2 | NA18982.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1442-2542A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388200 | |||||||
| chr6:37388270 | T | C | 2 | a0001c0002t0004g0196 a0001c0002t0015g0256 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1442-2472T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388270 | |||||||
| chr6:37388522 | G | C | 26 | a0001c0001t0005g0013 a0001c0001t0005g0173 a0001c0001t0005g0218 others(23): Show |
28 | HG01261.hp2 HG01361.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1442-2220G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388522 | |||||||
| chr6:37388642 | G | A | 2 | a0001c0002t0002g0179 a0001c0002t0002g0231 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1442-2100G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388642 | |||||||
| chr6:37388683 | C | T | 1 | a0001c0001t0008g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1442-2059C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388683 | |||||||
| chr6:37388773 | C | CA | 67 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0002g0034 others(64): Show |
85 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.1442-1955dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388773 | ||||||
| chr6:37388913 | A | G | 2 | a0001c0002t0004g0196 a0001c0002t0015g0256 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1442-1829A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37388913 | |||||||
| chr6:37388935 | T | TAAAAAAA others(1): Show |
6 | a0001c0001t0003g0244 a0001c0001t0004g0184 a0001c0001t0005g0250 others(3): Show |
6 | HG01257.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1442-1801_1442-179 others(12): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388935 | ||||||
| chr6:37388935 | T | TAAAAAAA others(2): Show |
87 | a0001c0001t0002g0237 a0001c0001t0003g0006 a0001c0001t0003g0007 others(84): Show |
109 | HG00280.hp1 HG00642.hp1 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.1442-1802_1442-179 others(13): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388935 | ||||||
| chr6:37388935 | T | TAAAAAAA others(3): Show |
4 | a0001c0001t0003g0241 a0001c0001t0006g0093 a0001c0001t0007g0166 others(1): Show |
4 | HG03098.hp2 HG06807.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.1442-1803_1442-179 others(14): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37388935 | ||||||
| chr6:37389024 | A | G | 1 | a0001c0002t0002g0192 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1442-1718A>G | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389024 | |||||||
| chr6:37389140 | G | C | 19 | a0001c0001t0015g0150 a0001c0002t0004g0012 a0001c0002t0004g0024 others(16): Show |
23 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1442-1602G>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389140 | |||||||
| chr6:37389286 | G | A | 1 | a0001c0004t0004g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1442-1456G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389286 | |||||||
| chr6:37389328 | G | A | 17 | a0001c0001t0015g0150 a0001c0002t0004g0012 a0001c0002t0004g0024 others(14): Show |
21 | HG00741.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1442-1414G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389328 | |||||||
| chr6:37389525 | G | A | 2 | a0001c0001t0007g0166 a0001c0001t0007g0167 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1442-1217G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389525 | |||||||
| chr6:37389622 | G | T | 1 | a0001c0001t0004g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1442-1120G>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37389622 | |||||||
| chr6:37390246 | A | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(231): Show |
292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.1442-496A>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390246 | |||||||
| chr6:37390253 | T | C | 1 | a0001c0001t0005g0228 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1442-489T>C | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390253 | |||||||
| chr6:37390283 | GGGTGAT | G | 11 | a0001c0001t0007g0166 a0001c0001t0007g0167 a0001c0001t0009g0151 others(8): Show |
11 | HG02055.hp2 HG02630.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1442-453_1442-448d others(8): Show |
RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37390283 | ||||||
| chr6:37390334 | C | T | 1 | a0001c0002t0001g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1442-408C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390334 | |||||||
| chr6:37390442 | C | CA | 6 | a0001c0001t0001g0115 a0001c0001t0011g0027 a0001c0001t0011g0234 others(3): Show |
7 | NA18957.hp1 NA18961.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1442-298dupA | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr6 | 37390442 | ||||||
| chr6:37390533 | G | A | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG02630.hp1 HG02647.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1442-209G>A | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390533 | |||||||
| chr6:37390665 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1442-77C>T | RNF8 | ENSG00000112130.17 | transcript | ENST00000373479.9 | protein_coding | 7/7 | chr6 | 37390665 |