Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25926 |
| ensemblid | ENSG00000130935.10 |
| hgncid | 24557 |
| symbol | NOL11 |
| name | nucleolar protein 11 |
| refseq_nuc | NM_015462.5 |
| refseq_prot | NP_056277.2 |
| ensembl_nuc | ENST00000253247.9 |
| ensembl_prot | ENSP00000253247.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 67717936 |
| end | 67744531 |
| strand | + |
| ver | v1.2 |
| region | chr17:67717936-67744531 |
| region5000 | chr17:67712936-67749531 |
| regionname0 | NOL11_chr17_67717936_67744531 |
| regionname5000 | NOL11_chr17_67712936_67749531 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 719 | 317 | 79 | 64 | 125 | 10 | 37 | 96 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0002 | 0/0 | 719 | 55 | 0 | 2 | 52 | 0 | 1 | 42 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0003 | 0/0 | 719 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0004 | 0/0 | 719 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0005 | 0/0 | 719 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0006 | 0/0 | 719 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0007 | 0/0 | 719 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0008 | 0/0 | 719 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0009 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| a0010 | 0/0 | 360 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(355): Show |
chr17 | 67712936 | 67749531 |
| a0011 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | MAALE others(714): Show |
chr17 | 67712936 | 67749531 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2157 | 156 | 28 | 34 | 76 | 4 | 14 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0001c0002 | 1/0 | 2157 | 115 | 45 | 22 | 21 | 4 | 22 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0001c0004 | 0/1 | 2157 | 40 | 5 | 6 | 26 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0001c0009 | 0/0 | 2157 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0001c0013 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0001c0014 | 0/0 | 2157 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0001c0016 | 0/0 | 2157 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0001c0018 | 0/0 | 2157 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0002c0003 | 0/0 | 2157 | 55 | 0 | 2 | 52 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0003c0005 | 0/0 | 2157 | 10 | 9 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0004c0006 | 0/0 | 2157 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0004c0012 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0005c0008 | 0/0 | 2157 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0006c0007 | 0/0 | 2157 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0007c0011 | 0/0 | 2157 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0008c0019 | 0/0 | 2157 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0009c0017 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 | ||
| a0010c0015 | 0/0 | 2239 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2234): Show |
chr17 | 67712936 | 67749531 | ||
| a0011c0010 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | ATGGC others(2152): Show |
chr17 | 67712936 | 67749531 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2844 | 152 | 28 | 34 | 72 | 4 | 14 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0001t0006 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0001t0007 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0002t0001 | 0/0 | 2844 | 60 | 14 | 8 | 18 | 4 | 16 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0002t0002 | 1/0 | 2844 | 48 | 24 | 14 | 3 | 0 | 6 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0002t0003 | 0/0 | 2844 | 5 | 5 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0002t0008 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0002t0010 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0004t0001 | 0/1 | 2844 | 34 | 5 | 6 | 20 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0004t0004 | 0/0 | 2844 | 6 | 0 | 0 | 6 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0009t0001 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0013t0002 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0014t0001 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0016t0001 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0001c0018t0001 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0002c0003t0001 | 0/0 | 2844 | 54 | 0 | 2 | 51 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0002c0003t0009 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0003c0005t0003 | 0/0 | 2844 | 10 | 9 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0004c0006t0005 | 0/0 | 2844 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0004c0012t0005 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0005c0008t0001 | 0/0 | 2844 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0006c0007t0001 | 0/0 | 2844 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0007c0011t0001 | 0/0 | 2844 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0008c0019t0001 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0009c0017t0001 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| a0010c0015t0001 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2921): Show |
chr17 | 67712936 | 67749531 |
| a0011c0010t0001 | 0/0 | 2844 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | GGTTT others(2839): Show |
chr17 | 67712936 | 67749531 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 1 | 4 | 14 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0003 | 0/0 | 14 | 1 | 2 | 11 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0004 | 0/0 | 9 | 3 | 3 | 2 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0005 | 0/0 | 10 | 1 | 2 | 1 | 2 | 4 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0007 | 0/0 | 6 | 2 | 1 | 2 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0009 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0017 | 1/0 | 4 | 0 | 3 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0002t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0008 | 0/0 | 6 | 2 | 0 | 3 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0030 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0050 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0004t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0009t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0013t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0014t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0016t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0001c0018t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0002 | 0/0 | 18 | 0 | 2 | 16 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0002c0003t0009g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0003c0005t0003g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0003c0005t0003g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0003c0005t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0003c0005t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0003c0005t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0004c0006t0005g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0004c0012t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0005c0008t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0005c0008t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0006c0007t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0007c0011t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0008c0019t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0009c0017t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0010c0015t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| a0011c0010t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00099 | hp2 | a0001 | c0004 | t0001 | g0008 | EUR | GBR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00280 | hp1 | a0001 | c0004 | t0001 | g0030 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00408 | hp1 | a0001 | c0004 | t0001 | g0216 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00408 | hp2 | a0001 | c0004 | t0001 | g0213 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00423 | hp2 | a0002 | c0003 | t0001 | g0028 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0176 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00544 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0046 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0169 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00621 | hp2 | a0001 | c0004 | t0001 | g0050 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0028 | EAS | CHS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0220 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01109 | hp1 | a0003 | c0005 | t0003 | g0029 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0198 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0050 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0223 | AMR | PUR | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0030 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0206 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01358 | hp1 | a0001 | c0018 | t0001 | g0035 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01496 | hp1 | a0001 | c0014 | t0001 | g0125 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0016 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0043 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0043 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01884 | hp2 | a0004 | c0006 | t0005 | g0022 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0008 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01934 | hp2 | a0007 | c0011 | t0001 | g0012 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0002 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02015 | hp2 | a0002 | c0003 | t0001 | g0168 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02040 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0046 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0221 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02080 | hp1 | a0001 | c0004 | t0001 | g0051 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02148 | hp2 | a0001 | c0004 | t0001 | g0051 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02155 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02165 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | CDX | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02257 | hp2 | a0003 | c0005 | t0003 | g0191 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0147 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0197 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0008 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0063 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0062 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0074 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0047 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02723 | hp2 | a0005 | c0008 | t0001 | g0122 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02886 | hp1 | a0003 | c0005 | t0003 | g0015 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0209 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0208 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02922 | hp2 | a0005 | c0008 | t0001 | g0121 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02965 | hp1 | a0004 | c0006 | t0005 | g0022 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02970 | hp2 | a0008 | c0019 | t0001 | g0067 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02976 | hp2 | a0003 | c0005 | t0003 | g0029 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03098 | hp1 | a0001 | c0013 | t0002 | g0010 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03130 | hp2 | a0004 | c0012 | t0005 | g0022 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0066 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03139 | hp2 | a0001 | c0004 | t0001 | g0204 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0194 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03209 | hp1 | a0003 | c0005 | t0003 | g0190 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0189 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03486 | hp2 | a0001 | c0002 | t0010 | g0048 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0042 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | ESN | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03540 | hp2 | a0003 | c0005 | t0003 | g0015 | AFR | GWD | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0196 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0166 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03942 | hp1 | a0001 | c0016 | t0001 | g0004 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0167 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0199 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0146 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04228 | hp1 | a0002 | c0003 | t0001 | g0182 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0192 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18612 | hp1 | a0009 | c0017 | t0001 | g0103 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0203 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18906 | hp2 | a0003 | c0005 | t0003 | g0015 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18940 | hp1 | a0001 | c0009 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18941 | hp1 | a0001 | c0004 | t0001 | g0214 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18941 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18943 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18944 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0052 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18945 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18946 | hp1 | a0002 | c0003 | t0009 | g0024 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18947 | hp2 | a0001 | c0004 | t0004 | g0229 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18948 | hp1 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18950 | hp2 | a0001 | c0004 | t0004 | g0230 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18953 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18954 | hp2 | a0010 | c0015 | t0001 | g0082 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18956 | hp2 | a0001 | c0004 | t0001 | g0222 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18957 | hp2 | a0001 | c0004 | t0004 | g0226 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18959 | hp2 | a0001 | c0004 | t0004 | g0231 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18964 | hp1 | a0006 | c0007 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18966 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18969 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0177 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18971 | hp1 | a0002 | c0003 | t0001 | g0174 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0179 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18977 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18978 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18979 | hp1 | a0001 | c0004 | t0001 | g0225 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18981 | hp1 | a0001 | c0004 | t0001 | g0210 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18981 | hp2 | a0011 | c0010 | t0001 | g0178 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18985 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18987 | hp2 | a0001 | c0004 | t0001 | g0224 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18997 | hp1 | a0001 | c0004 | t0001 | g0212 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA18999 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19000 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19001 | hp2 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0173 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19005 | hp2 | a0001 | c0004 | t0001 | g0218 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19009 | hp2 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19011 | hp1 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0061 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19030 | hp2 | a0003 | c0005 | t0003 | g0029 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19043 | hp2 | a0003 | c0005 | t0003 | g0015 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19055 | hp1 | a0002 | c0003 | t0001 | g0170 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0024 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19070 | hp2 | a0001 | c0004 | t0004 | g0228 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19072 | hp1 | a0002 | c0003 | t0001 | g0172 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19075 | hp2 | a0002 | c0003 | t0001 | g0171 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0028 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19078 | hp2 | a0002 | c0003 | t0001 | g0180 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19082 | hp2 | a0001 | c0004 | t0001 | g0049 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19084 | hp1 | a0006 | c0007 | t0001 | g0003 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19086 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19086 | hp2 | a0001 | c0009 | t0001 | g0021 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19087 | hp1 | a0001 | c0004 | t0004 | g0227 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19087 | hp2 | a0002 | c0003 | t0001 | g0175 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19088 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19089 | hp1 | a0002 | c0003 | t0001 | g0184 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | YRI | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA20129 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | ASW | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0018 | SAS | GIH | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | GIH | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0017 | AMR | CLM | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02109 | hp1 | a0003 | c0005 | t0003 | g0193 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0048 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | ACB | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0047 | AFR | MSL | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0060 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | USA | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0001 | g0215 | REF | REF | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0017 | REF | REF | NOL11_chr17_67712936_67749531 | NOL11 | chr17 | 67712936 | 67749531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:67717979 | C | T | 1 | a0008 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.32C>T | p.Ser11Phe | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/18 | 44/2844 | 32/2160 | 11/719 | chr17 | 67717979 | |||
| chr17:67721409 | T | C | 2 | a0002 a0011 |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
missense_variant | MODERATE | c.344T>C | p.Val115Ala | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/18 | 356/2844 | 344/2160 | 115/719 | chr17 | 67721409 | |||
| chr17:67721493 | T | C | 1 | a0007 | 1 | HG01934.hp2 | missense_variant | MODERATE | c.428T>C | p.Ile143Thr | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/18 | 440/2844 | 428/2160 | 143/719 | chr17 | 67721493 | |||
| chr17:67722626 | A | C | 1 | a0005 | 2 | HG02723.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.508A>C | p.Ile170Leu | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/18 | 520/2844 | 508/2160 | 170/719 | chr17 | 67722626 | |||
| chr17:67724164 | A | G | 1 | a0009 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.635A>G | p.Asp212Gly | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/18 | 647/2844 | 635/2160 | 212/719 | chr17 | 67724164 | |||
| chr17:67726574 | G | A | 1 | a0004 | 3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
missense_variant | MODERATE | c.779G>A | p.Arg260Gln | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/18 | 791/2844 | 779/2160 | 260/719 | chr17 | 67726574 | |||
| chr17:67726588 | C | G | 1 | a0003 | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
missense_variant | MODERATE | c.793C>G | p.Leu265Val | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/18 | 805/2844 | 793/2160 | 265/719 | chr17 | 67726588 | |||
| chr17:67738142 | A | C | 1 | a0011 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1550A>C | p.Gln517Pro | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/18 | 1562/2844 | 1550/2160 | 517/719 | chr17 | 67738142 | |||
| chr17:67738162 | G | C | 1 | a0006 | 2 | NA18964.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.1570G>C | p.Glu524Gln | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/18 | 1582/2844 | 1570/2160 | 524/719 | chr17 | 67738162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:67718013 | C | T | 1 | a0001c0009 | 2 | NA18940.hp1 NA19086.hp2 |
synonymous_variant | LOW | c.66C>T | p.Leu22Leu | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/18 | 78/2844 | 66/2160 | 22/719 | chr17 | 67718013 | |||
| chr17:67722634 | A | G | 1 | a0003c0005 | 10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
synonymous_variant | LOW | c.516A>G | p.Glu172Glu | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/18 | 528/2844 | 516/2160 | 172/719 | chr17 | 67722634 | |||
| chr17:67724108 | A | G | 1 | a0001c0018 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.579A>G | p.Thr193Thr | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/18 | 591/2844 | 579/2160 | 193/719 | chr17 | 67724108 | |||
| chr17:67735977 | A | G | 1 | a0001c0004 | 39 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
synonymous_variant | LOW | c.1008A>G | p.Ser336Ser | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/18 | 1020/2844 | 1008/2160 | 336/719 | chr17 | 67735977 | |||
| chr17:67735980 | A | T | 1 | a0001c0016 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.1011A>T | p.Ser337Ser | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/18 | 1023/2844 | 1011/2160 | 337/719 | chr17 | 67735980 | |||
| chr17:67738233 | A | G | 1 | a0001c0014 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1641A>G | p.Gln547Gln | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/18 | 1653/2844 | 1641/2160 | 547/719 | chr17 | 67738233 | |||
| chr17:67738938 | A | G | 1 | a0004c0012 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1770A>G | p.Ala590Ala | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/18 | 1782/2844 | 1770/2160 | 590/719 | chr17 | 67738938 | |||
| chr17:67738959 | C | T | 1 | a0001c0013 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1791C>T | p.Ser597Ser | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/18 | 1803/2844 | 1791/2160 | 597/719 | chr17 | 67738959 | |||
| chr17:67743511 | A | G | 10 | a0001c0001 a0001c0009 a0001c0014 others(7): Show |
168 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(165): Show |
synonymous_variant | LOW | c.1968A>G | p.Ala656Ala | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/18 | 1980/2844 | 1968/2160 | 656/719 | chr17 | 67743511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:67743911 | C | T | 2 | a0004c0006t0005 a0004c0012t0005 |
3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*52C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 52 | chr17 | 67743911 | ||||||
| chr17:67744009 | C | T | 1 | a0001c0004t0004 | 6 | NA18947.hp2 NA18950.hp2 NA18957.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*150C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 150 | chr17 | 67744009 | ||||||
| chr17:67744138 | A | C | 1 | a0001c0002t0010 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*279A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 279 | chr17 | 67744138 | ||||||
| chr17:67744246 | T | C | 3 | a0001c0002t0003 a0001c0002t0010 a0003c0005t0003 |
16 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*387T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 387 | chr17 | 67744246 | ||||||
| chr17:67744375 | A | G | 1 | a0002c0003t0009 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 516 | chr17 | 67744375 | ||||||
| chr17:67744403 | G | T | 1 | a0001c0002t0008 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 544 | chr17 | 67744403 | ||||||
| chr17:67744470 | G | A | 1 | a0001c0001t0006 | 2 | NA18945.hp1 NA18977.hp1 |
3_prime_UTR_variant | MODIFIER | c.*611G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 611 | chr17 | 67744470 | ||||||
| chr17:67744503 | G | T | 25 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(22): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*644G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 644 | chr17 | 67744503 | ||||||
| chr17:67744512 | A | C | 1 | a0001c0001t0007 | 2 | NA18969.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*653A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 18/18 | 653 | chr17 | 67744512 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:67718116 | C | G | 36 | a0001c0001t0001g0219 a0001c0002t0001g0018 a0001c0002t0001g0207 others(33): Show |
50 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.141+28C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718116 | |||||||
| chr17:67718243 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(227): Show |
366 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.141+155G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718243 | |||||||
| chr17:67718389 | C | T | 1 | a0002c0003t0001g0195 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.141+301C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718389 | |||||||
| chr17:67718453 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0006g0052 a0001c0001t0006g0053 |
3 | HG00741.hp2 NA18945.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.141+365G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718453 | |||||||
| chr17:67718467 | C | G | 1 | a0001c0002t0002g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.141+379C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718467 | |||||||
| chr17:67718474 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.141+386G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718474 | |||||||
| chr17:67718524 | G | A | 36 | a0001c0001t0001g0219 a0001c0002t0001g0018 a0001c0002t0001g0207 others(33): Show |
50 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.141+436G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718524 | |||||||
| chr17:67718562 | G | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0188 a0001c0002t0001g0189 others(6): Show |
17 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.141+474G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718562 | |||||||
| chr17:67718616 | G | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.141+528G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718616 | |||||||
| chr17:67718622 | A | G | 1 | a0001c0002t0001g0185 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.141+534A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718622 | |||||||
| chr17:67718810 | G | C | 1 | a0001c0004t0001g0204 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+722G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67718810 | |||||||
| chr17:67719031 | A | G | 28 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(25): Show |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-643A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719031 | |||||||
| chr17:67719048 | A | C | 4 | a0001c0002t0001g0023 a0001c0002t0001g0165 a0001c0002t0001g0166 others(1): Show |
6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-626A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719048 | |||||||
| chr17:67719057 | C | T | 2 | a0004c0006t0005g0022 a0004c0012t0005g0022 |
3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.142-617C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719057 | |||||||
| chr17:67719063 | T | C | 1 | a0001c0002t0002g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.142-611T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719063 | |||||||
| chr17:67719071 | T | C | 1 | a0001c0004t0001g0205 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.142-603T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719071 | |||||||
| chr17:67719112 | G | A | 2 | a0001c0004t0001g0030 a0001c0004t0001g0206 |
4 | HG00280.hp1 HG01255.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-562G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719112 | |||||||
| chr17:67719165 | C | T | 7 | a0001c0002t0001g0189 a0001c0002t0008g0192 a0003c0005t0003g0015 others(4): Show |
12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-509C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719165 | |||||||
| chr17:67719266 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0188 |
5 | HG02647.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-408A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719266 | |||||||
| chr17:67719325 | A | G | 28 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(25): Show |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-349A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719325 | |||||||
| chr17:67719333 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(172): Show |
271 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.142-341C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719333 | |||||||
| chr17:67719407 | C | A | 3 | a0001c0001t0001g0054 a0001c0001t0006g0052 a0001c0001t0006g0053 |
3 | HG00741.hp2 NA18945.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.142-267C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 1/17 | chr17 | 67719407 | |||||||
| chr17:67720107 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.312+145A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720107 | |||||||
| chr17:67720157 | A | G | 1 | a0003c0005t0003g0193 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.312+195A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720157 | |||||||
| chr17:67720161 | G | C | 50 | a0001c0002t0001g0018 a0001c0002t0001g0189 a0001c0002t0001g0207 others(47): Show |
88 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.312+199G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720161 | |||||||
| chr17:67720184 | T | C | 1 | a0001c0002t0002g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312+222T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720184 | |||||||
| chr17:67720300 | C | CT | 29 | a0001c0001t0001g0161 a0001c0002t0001g0162 a0002c0003t0001g0002 others(26): Show |
57 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.312+356dupT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 67720300 | ||||||
| chr17:67720300 | CT | C | 18 | a0001c0001t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0073 others(15): Show |
21 | HG01069.hp1 HG01346.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.312+356delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr17 | 67720300 | ||||||
| chr17:67720387 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.312+425C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720387 | |||||||
| chr17:67720415 | C | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
171 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.312+453C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720415 | |||||||
| chr17:67720432 | G | A | 22 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(19): Show |
38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.312+470G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720432 | |||||||
| chr17:67720581 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.312+619A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720581 | |||||||
| chr17:67720652 | A | G | 2 | a0001c0002t0001g0189 a0001c0002t0008g0192 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312+690A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720652 | |||||||
| chr17:67720709 | T | G | 1 | a0001c0002t0002g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.313-669T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720709 | |||||||
| chr17:67720760 | A | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.313-618A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720760 | |||||||
| chr17:67720974 | T | C | 29 | a0001c0001t0001g0219 a0001c0004t0001g0008 a0001c0004t0001g0030 others(26): Show |
39 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.313-404T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67720974 | |||||||
| chr17:67721016 | G | A | 7 | a0001c0002t0001g0189 a0001c0002t0008g0192 a0003c0005t0003g0015 others(4): Show |
12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.313-362G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67721016 | |||||||
| chr17:67721067 | G | A | 1 | a0001c0004t0001g0210 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.313-311G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67721067 | |||||||
| chr17:67721345 | G | A | 2 | a0004c0006t0005g0022 a0004c0012t0005g0022 |
3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.313-33G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 3/17 | chr17 | 67721345 | |||||||
| chr17:67721557 | C | T | 1 | a0001c0002t0002g0202 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.461+31C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721557 | |||||||
| chr17:67721709 | A | G | 7 | a0001c0002t0001g0073 a0001c0002t0001g0156 a0001c0002t0001g0157 others(4): Show |
7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.461+183A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721709 | |||||||
| chr17:67721753 | A | G | 2 | a0001c0002t0001g0040 a0001c0002t0001g0072 |
3 | HG03041.hp1 HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.461+227A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721753 | |||||||
| chr17:67721758 | G | A | 1 | a0001c0002t0001g0156 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.461+232G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721758 | |||||||
| chr17:67721888 | C | G | 52 | a0001c0002t0001g0018 a0001c0002t0001g0189 a0001c0002t0001g0207 others(49): Show |
90 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.461+362C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721888 | |||||||
| chr17:67721940 | G | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01192.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.461+414G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67721940 | |||||||
| chr17:67722002 | T | TA | 9 | a0001c0002t0001g0189 a0001c0002t0003g0048 a0001c0002t0008g0192 others(6): Show |
14 | HG01109.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.461+477dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr17 | 67722002 | ||||||
| chr17:67722026 | G | C | 1 | a0002c0003t0001g0170 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.461+500G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722026 | |||||||
| chr17:67722075 | G | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.462-505G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722075 | |||||||
| chr17:67722094 | A | G | 1 | a0002c0003t0001g0184 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.462-486A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722094 | |||||||
| chr17:67722177 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.462-403T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722177 | |||||||
| chr17:67722186 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.462-394A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722186 | |||||||
| chr17:67722264 | G | A | 2 | a0001c0002t0003g0048 a0001c0002t0010g0048 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.462-316G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722264 | |||||||
| chr17:67722376 | A | G | 6 | a0001c0004t0004g0226 a0001c0004t0004g0227 a0001c0004t0004g0228 others(3): Show |
6 | NA18947.hp2 NA18950.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.462-204A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722376 | |||||||
| chr17:67722431 | A | G | 2 | a0001c0002t0002g0065 a0001c0002t0002g0066 |
2 | HG01346.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.462-149A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722431 | |||||||
| chr17:67722442 | C | T | 7 | a0001c0002t0001g0073 a0001c0002t0001g0156 a0001c0002t0001g0157 others(4): Show |
7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.462-138C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 4/17 | chr17 | 67722442 | |||||||
| chr17:67722682 | TA | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.519+57delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67722682 | ||||||
| chr17:67722694 | A | T | 1 | a0001c0002t0001g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.519+57A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722694 | |||||||
| chr17:67722723 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.519+86C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722723 | |||||||
| chr17:67722751 | G | A | 22 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(19): Show |
38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.519+114G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722751 | |||||||
| chr17:67722758 | C | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.519+121C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722758 | |||||||
| chr17:67722818 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.519+181C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722818 | |||||||
| chr17:67722892 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.519+255A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67722892 | |||||||
| chr17:67723005 | C | CT | 11 | a0001c0002t0002g0019 a0001c0002t0002g0056 a0001c0002t0002g0058 others(8): Show |
13 | HG01346.hp1 HG02258.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+392dupT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723005 | ||||||
| chr17:67723005 | CT | C | 31 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0068 others(28): Show |
62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.519+392delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723005 | ||||||
| chr17:67723005 | CTTTTTTT | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.519+386_519+392del others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723005 | ||||||
| chr17:67723076 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.519+439G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723076 | |||||||
| chr17:67723103 | C | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.519+466C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723103 | |||||||
| chr17:67723114 | G | A | 2 | a0001c0002t0001g0018 a0001c0002t0001g0207 |
5 | NA18963.hp2 NA18990.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.519+477G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723114 | |||||||
| chr17:67723127 | C | T | 1 | a0001c0004t0001g0138 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.519+490C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723127 | |||||||
| chr17:67723138 | G | A | 49 | a0001c0002t0001g0018 a0001c0002t0001g0189 a0001c0002t0001g0207 others(46): Show |
87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.519+501G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723138 | |||||||
| chr17:67723156 | G | A | 3 | a0001c0002t0002g0058 a0001c0002t0002g0065 a0001c0002t0002g0066 |
3 | HG01346.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.519+519G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723156 | |||||||
| chr17:67723238 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.519+601C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723238 | |||||||
| chr17:67723287 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.519+650C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723287 | |||||||
| chr17:67723307 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.519+670T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723307 | |||||||
| chr17:67723310 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.519+673C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723310 | |||||||
| chr17:67723347 | G | A | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
357 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.520-702G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723347 | |||||||
| chr17:67723370 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0002g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.520-652_520-642dup others(11): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | AT | A | 8 | a0001c0002t0002g0009 a0001c0002t0002g0060 a0001c0002t0002g0061 others(5): Show |
12 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-642delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATT | A | 3 | a0001c0002t0002g0016 a0001c0002t0002g0057 a0001c0002t0002g0059 |
6 | HG00735.hp2 HG01255.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-643_520-642del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTT | A | 13 | a0001c0001t0001g0219 a0001c0002t0001g0165 a0001c0002t0001g0166 others(10): Show |
15 | HG00609.hp2 HG00621.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.520-646_520-642del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTT | A | 16 | a0001c0002t0001g0156 a0001c0002t0001g0159 a0001c0004t0001g0008 others(13): Show |
23 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.520-647_520-642del others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT | A | 8 | a0001c0001t0001g0136 a0001c0002t0001g0153 a0001c0002t0001g0154 others(5): Show |
8 | HG01358.hp2 HG02451.hp2 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-648_520-642del others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(1): Show |
A | 32 | a0001c0001t0001g0021 a0001c0001t0001g0039 a0001c0001t0001g0076 others(29): Show |
51 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.520-649_520-642del others(8): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(2): Show |
A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(83): Show |
145 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.520-650_520-642del others(9): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(3): Show |
A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0031 a0001c0001t0001g0032 others(7): Show |
15 | HG01071.hp1 HG01517.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-651_520-642del others(10): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(5): Show |
A | 2 | a0001c0002t0002g0198 a0003c0005t0003g0191 |
2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.520-653_520-642del others(12): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(6): Show |
A | 8 | a0002c0003t0001g0046 a0002c0003t0001g0170 a0002c0003t0001g0183 others(5): Show |
14 | HG00597.hp2 HG01109.hp1 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-654_520-642del others(13): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(7): Show |
A | 20 | a0002c0003t0001g0002 a0002c0003t0001g0025 a0002c0003t0001g0026 others(17): Show |
46 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.520-655_520-642del others(14): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(8): Show |
A | 6 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0002c0003t0001g0024 others(3): Show |
10 | NA18946.hp1 NA18962.hp2 NA18963.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-656_520-642del others(15): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(9): Show |
A | 1 | a0001c0002t0003g0047 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.520-657_520-642del others(16): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(10): Show |
A | 4 | a0001c0002t0003g0048 a0001c0002t0003g0208 a0001c0002t0003g0209 others(1): Show |
4 | HG02109.hp2 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-658_520-642del others(17): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(12): Show |
A | 3 | a0001c0002t0001g0073 a0001c0002t0001g0157 a0001c0002t0001g0162 |
3 | HG02486.hp2 HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.520-660_520-642del others(19): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723370 | ATTTTTTT others(13): Show |
A | 1 | a0001c0002t0001g0160 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.520-661_520-642del others(20): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723370 | ||||||
| chr17:67723413 | G | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.520-636G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723413 | |||||||
| chr17:67723435 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.520-614T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723435 | |||||||
| chr17:67723544 | A | G | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-505A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723544 | |||||||
| chr17:67723608 | C | T | 1 | a0001c0004t0001g0223 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.520-441C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723608 | |||||||
| chr17:67723632 | C | T | 2 | a0001c0002t0001g0189 a0001c0002t0008g0192 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.520-417C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723632 | |||||||
| chr17:67723662 | C | T | 3 | a0001c0004t0001g0210 a0001c0004t0001g0224 a0001c0004t0001g0225 |
3 | NA18979.hp1 NA18981.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.520-387C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723662 | |||||||
| chr17:67723740 | C | G | 2 | a0001c0002t0001g0189 a0001c0002t0008g0192 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.520-309C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723740 | |||||||
| chr17:67723744 | T | TA | 33 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(30): Show |
51 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.520-292dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723744 | ||||||
| chr17:67723744 | TA | T | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-292delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67723744 | ||||||
| chr17:67723847 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0126 |
3 | NA18948.hp2 NA18953.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.520-202A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723847 | |||||||
| chr17:67723848 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.520-201A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723848 | |||||||
| chr17:67723892 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.520-157C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723892 | |||||||
| chr17:67723915 | A | C | 1 | a0001c0002t0003g0047 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.520-134A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723915 | |||||||
| chr17:67723932 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.520-117A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723932 | |||||||
| chr17:67723982 | T | C | 2 | a0001c0002t0001g0073 a0001c0002t0001g0157 |
2 | HG02809.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.520-67T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | chr17 | 67723982 | |||||||
| chr17:67724034 | C | CT | 13 | a0001c0001t0001g0078 a0001c0001t0001g0124 a0001c0001t0001g0163 others(10): Show |
14 | HG01099.hp1 HG01496.hp1 HG02258.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.520-5dupT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67724034 | ||||||
| chr17:67724034 | CT | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.520-5delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr17 | 67724034 | ||||||
| chr17:67724224 | T | A | 1 | a0003c0005t0003g0190 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.664+31T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724224 | |||||||
| chr17:67724230 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
164 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.664+37A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724230 | |||||||
| chr17:67724244 | T | C | 1 | a0008c0019t0001g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.664+51T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724244 | |||||||
| chr17:67724328 | T | C | 1 | a0002c0003t0001g0173 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.664+135T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724328 | |||||||
| chr17:67724332 | CT | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
293 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.664+158delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr17 | 67724332 | ||||||
| chr17:67724332 | CTT | C | 14 | a0001c0001t0001g0089 a0001c0002t0001g0018 a0001c0002t0001g0073 others(11): Show |
23 | HG01109.hp1 HG01168.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.664+157_664+158del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr17 | 67724332 | ||||||
| chr17:67724364 | C | T | 2 | a0001c0002t0001g0018 a0001c0002t0001g0207 |
5 | NA18963.hp2 NA18990.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.664+171C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724364 | |||||||
| chr17:67724436 | C | T | 1 | a0008c0019t0001g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.664+243C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724436 | |||||||
| chr17:67724438 | A | G | 1 | a0001c0002t0001g0023 | 3 | NA18944.hp2 NA18947.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.664+245A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724438 | |||||||
| chr17:67724468 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.664+275G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724468 | |||||||
| chr17:67724480 | C | T | 1 | a0003c0005t0003g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.664+287C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724480 | |||||||
| chr17:67724596 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.664+403C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724596 | |||||||
| chr17:67724627 | C | G | 2 | a0005c0008t0001g0121 a0005c0008t0001g0122 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.664+434C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724627 | |||||||
| chr17:67724628 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.664+435G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724628 | |||||||
| chr17:67724664 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
171 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.664+471G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724664 | |||||||
| chr17:67724718 | A | C | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+525A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724718 | |||||||
| chr17:67724788 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.664+595A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724788 | |||||||
| chr17:67724834 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.664+641A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724834 | |||||||
| chr17:67724873 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.664+680A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724873 | |||||||
| chr17:67724927 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.664+734G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724927 | |||||||
| chr17:67724990 | G | A | 12 | a0001c0002t0002g0019 a0001c0002t0002g0056 a0001c0002t0002g0057 others(9): Show |
14 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.664+797G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67724990 | |||||||
| chr17:67725013 | G | A | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.664+820G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725013 | |||||||
| chr17:67725052 | G | A | 1 | a0001c0002t0001g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.664+859G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725052 | |||||||
| chr17:67725059 | G | A | 1 | a0001c0002t0001g0041 | 2 | HG00642.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.664+866G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725059 | |||||||
| chr17:67725068 | A | G | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+875A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725068 | |||||||
| chr17:67725090 | A | G | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.664+897A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725090 | |||||||
| chr17:67725137 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.664+944T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725137 | |||||||
| chr17:67725174 | T | C | 3 | a0002c0003t0001g0025 a0002c0003t0001g0172 a0002c0003t0001g0183 |
5 | NA18943.hp2 NA18961.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+981T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725174 | |||||||
| chr17:67725193 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.664+1000T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725193 | |||||||
| chr17:67725331 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.665-1129A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725331 | |||||||
| chr17:67725449 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.665-1011C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725449 | |||||||
| chr17:67725779 | G | A | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.665-681G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725779 | |||||||
| chr17:67725780 | G | A | 1 | a0001c0002t0003g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.665-680G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725780 | |||||||
| chr17:67725830 | G | A | 3 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0008c0019t0001g0067 |
6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-630G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725830 | |||||||
| chr17:67725845 | C | G | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-615C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725845 | |||||||
| chr17:67725881 | A | C | 3 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0008c0019t0001g0067 |
6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-579A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67725881 | |||||||
| chr17:67726187 | G | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.665-273G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67726187 | |||||||
| chr17:67726258 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.665-202T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67726258 | |||||||
| chr17:67726281 | C | T | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-179C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 6/17 | chr17 | 67726281 | |||||||
| chr17:67726696 | C | T | 2 | a0004c0006t0005g0022 a0004c0012t0005g0022 |
3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.853+48C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726696 | |||||||
| chr17:67726733 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.853+85G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726733 | |||||||
| chr17:67726775 | A | G | 1 | a0001c0001t0001g0014 | 4 | HG02647.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+127A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726775 | |||||||
| chr17:67726865 | A | G | 3 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0008c0019t0001g0067 |
6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+217A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726865 | |||||||
| chr17:67726900 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.853+252C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67726900 | |||||||
| chr17:67727137 | A | G | 1 | a0002c0003t0001g0181 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.853+489A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727137 | |||||||
| chr17:67727310 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.853+662A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727310 | |||||||
| chr17:67727595 | C | T | 2 | a0001c0002t0001g0044 a0001c0002t0002g0069 |
3 | HG01361.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.853+947C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727595 | |||||||
| chr17:67727604 | C | T | 47 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0019 others(44): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+956C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727604 | |||||||
| chr17:67727644 | C | T | 2 | a0001c0002t0001g0143 a0001c0002t0001g0150 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.853+996C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727644 | |||||||
| chr17:67727645 | G | A | 3 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0008c0019t0001g0067 |
6 | HG02970.hp2 NA18963.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+997G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727645 | |||||||
| chr17:67727653 | G | A | 4 | a0001c0002t0002g0059 a0001c0002t0002g0060 a0001c0002t0002g0062 others(1): Show |
4 | HG02258.hp1 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+1005G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727653 | |||||||
| chr17:67727657 | C | CA | 5 | a0001c0002t0002g0065 a0001c0002t0002g0066 a0002c0003t0001g0170 others(2): Show |
6 | HG01346.hp1 HG01884.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.853+1021dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727657 | ||||||
| chr17:67727657 | CA | C | 7 | a0001c0001t0001g0118 a0002c0003t0001g0180 a0003c0005t0003g0015 others(4): Show |
12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+1021delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727657 | ||||||
| chr17:67727759 | T | G | 47 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0019 others(44): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1111T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727759 | |||||||
| chr17:67727761 | C | T | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.853+1113C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727761 | |||||||
| chr17:67727793 | A | G | 47 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0019 others(44): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1145A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727793 | |||||||
| chr17:67727842 | A | G | 47 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0019 others(44): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1194A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727842 | |||||||
| chr17:67727918 | CA | C | 17 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0002t0002g0010 others(14): Show |
31 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.853+1295delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | ||||||
| chr17:67727918 | CAAA | C | 8 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(5): Show |
12 | HG00544.hp1 HG00621.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+1293_853+1295d others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | ||||||
| chr17:67727918 | CAAAA | C | 42 | a0001c0002t0001g0144 a0001c0002t0001g0156 a0001c0002t0001g0157 others(39): Show |
69 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.853+1292_853+1295d others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | ||||||
| chr17:67727918 | CAAAAA | C | 37 | a0001c0001t0001g0092 a0001c0001t0001g0127 a0001c0001t0001g0135 others(34): Show |
61 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.853+1291_853+1295d others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | ||||||
| chr17:67727918 | CAAAAAA | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(56): Show |
106 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.853+1290_853+1295d others(8): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | ||||||
| chr17:67727918 | CAAAAAAA | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.853+1289_853+1295d others(9): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | ||||||
| chr17:67727918 | CAAAAAAA others(7): Show |
C | 6 | a0001c0002t0001g0023 a0001c0002t0001g0165 a0001c0002t0001g0166 others(3): Show |
9 | HG00609.hp2 HG01884.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+1282_853+1295d others(16): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67727918 | ||||||
| chr17:67727937 | A | C | 27 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(24): Show |
55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.853+1289A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727937 | |||||||
| chr17:67727982 | C | T | 6 | a0001c0002t0001g0013 a0001c0002t0001g0148 a0001c0002t0001g0149 others(3): Show |
9 | NA18943.hp1 NA18949.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+1334C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67727982 | |||||||
| chr17:67728043 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.853+1395A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728043 | |||||||
| chr17:67728076 | T | C | 50 | a0001c0001t0001g0093 a0001c0002t0001g0018 a0001c0002t0001g0040 others(47): Show |
89 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.853+1428T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728076 | |||||||
| chr17:67728093 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(222): Show |
361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.853+1445C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728093 | |||||||
| chr17:67728175 | G | A | 3 | a0002c0003t0001g0027 a0002c0003t0001g0171 a0002c0003t0001g0174 |
5 | NA18971.hp1 NA19001.hp1 NA19075.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+1527G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728175 | |||||||
| chr17:67728196 | C | G | 2 | a0001c0002t0002g0056 a0001c0002t0002g0064 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.853+1548C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728196 | |||||||
| chr17:67728328 | A | G | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.853+1680A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728328 | |||||||
| chr17:67728469 | G | A | 47 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0019 others(44): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+1821G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728469 | |||||||
| chr17:67728685 | G | A | 1 | a0005c0008t0001g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.853+2037G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728685 | |||||||
| chr17:67728918 | C | T | 2 | a0001c0002t0003g0048 a0001c0002t0010g0048 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.853+2270C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728918 | |||||||
| chr17:67728950 | G | T | 47 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0019 others(44): Show |
85 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.853+2302G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67728950 | |||||||
| chr17:67729099 | TG | T | 40 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0001c0002t0002g0019 others(37): Show |
73 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.853+2452delG | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729099 | |||||||
| chr17:67729100 | G | T | 7 | a0002c0003t0001g0170 a0002c0003t0001g0180 a0003c0005t0003g0015 others(4): Show |
12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+2452G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729100 | |||||||
| chr17:67729100 | GT | G | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.853+2463delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67729100 | ||||||
| chr17:67729104 | T | G | 7 | a0001c0002t0001g0040 a0001c0002t0001g0072 a0001c0002t0003g0208 others(4): Show |
8 | HG00408.hp1 HG02071.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+2456T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729104 | |||||||
| chr17:67729155 | C | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.853+2507C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729155 | |||||||
| chr17:67729245 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0107 others(2): Show |
10 | HG00642.hp2 HG01069.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.853+2597C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729245 | |||||||
| chr17:67729398 | C | T | 5 | a0001c0004t0001g0138 a0001c0004t0001g0210 a0001c0004t0001g0218 others(2): Show |
5 | NA18979.hp1 NA18981.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+2750C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729398 | |||||||
| chr17:67729584 | CT | C | 7 | a0001c0002t0003g0208 a0001c0002t0003g0209 a0003c0005t0003g0015 others(4): Show |
12 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.853+2948delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67729584 | ||||||
| chr17:67729639 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.853+2991C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729639 | |||||||
| chr17:67729648 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.853+3000G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729648 | |||||||
| chr17:67729671 | C | T | 2 | a0001c0002t0002g0065 a0001c0002t0002g0066 |
2 | HG01346.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.853+3023C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729671 | |||||||
| chr17:67729672 | G | A | 28 | a0001c0002t0001g0144 a0002c0003t0001g0002 a0002c0003t0001g0024 others(25): Show |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.853+3024G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729672 | |||||||
| chr17:67729673 | G | T | 1 | a0001c0001t0001g0106 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.853+3025G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729673 | |||||||
| chr17:67729723 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0119 |
3 | HG01361.hp1 HG01433.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.853+3075C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729723 | |||||||
| chr17:67729831 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0110 others(1): Show |
7 | HG00423.hp1 HG00609.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.853+3183G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729831 | |||||||
| chr17:67729961 | C | G | 2 | a0001c0002t0001g0166 a0001c0002t0001g0167 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.853+3313C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729961 | |||||||
| chr17:67729988 | C | T | 2 | a0001c0002t0001g0166 a0001c0002t0001g0167 |
2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.853+3340C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67729988 | |||||||
| chr17:67730090 | A | G | 1 | a0001c0002t0001g0144 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.853+3442A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730090 | |||||||
| chr17:67730139 | G | A | 22 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(19): Show |
38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.853+3491G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730139 | |||||||
| chr17:67730141 | T | C | 22 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(19): Show |
38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.853+3493T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730141 | |||||||
| chr17:67730205 | A | G | 2 | a0001c0002t0003g0048 a0001c0002t0010g0048 |
2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.853+3557A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730205 | |||||||
| chr17:67730214 | C | A | 27 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(24): Show |
55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.853+3566C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730214 | |||||||
| chr17:67730252 | TTTTG | T | 4 | a0001c0001t0001g0084 a0001c0002t0001g0018 a0001c0002t0001g0207 others(1): Show |
7 | HG02257.hp1 HG02970.hp2 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.853+3620_853+3623d others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67730252 | ||||||
| chr17:67730268 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0188 |
5 | HG02647.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.853+3620G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730268 | |||||||
| chr17:67730353 | C | T | 1 | a0001c0002t0001g0043 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.853+3705C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730353 | |||||||
| chr17:67730552 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.854-3811G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730552 | |||||||
| chr17:67730642 | AT | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.854-3714delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67730642 | ||||||
| chr17:67730734 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.854-3629G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730734 | |||||||
| chr17:67730760 | C | T | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-3603C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730760 | |||||||
| chr17:67730812 | C | T | 27 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(24): Show |
55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.854-3551C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67730812 | |||||||
| chr17:67731084 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.854-3279T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731084 | |||||||
| chr17:67731238 | TTCGTGCA others(269): Show |
T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.854-3107_854-2832d others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731238 | ||||||
| chr17:67731251 | GT | G | 12 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0002t0002g0016 others(9): Show |
17 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.854-3082delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731251 | ||||||
| chr17:67731251 | GTT | G | 6 | a0001c0002t0002g0007 a0001c0002t0002g0009 a0001c0002t0002g0010 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-3083_854-3082d others(4): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731251 | ||||||
| chr17:67731251 | GTTT | G | 7 | a0001c0002t0002g0019 a0001c0002t0002g0057 a0001c0002t0002g0058 others(4): Show |
9 | HG01346.hp1 HG02055.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.854-3084_854-3082d others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67731251 | ||||||
| chr17:67731260 | T | G | 2 | a0001c0002t0002g0065 a0001c0002t0002g0066 |
2 | HG01346.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.854-3103T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731260 | |||||||
| chr17:67731598 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.854-2765C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731598 | |||||||
| chr17:67731633 | C | T | 1 | a0002c0003t0001g0179 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.854-2730C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731633 | |||||||
| chr17:67731751 | G | A | 1 | a0002c0003t0001g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.854-2612G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731751 | |||||||
| chr17:67731826 | A | G | 4 | a0001c0002t0001g0023 a0001c0002t0001g0165 a0001c0002t0001g0166 others(1): Show |
6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-2537A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731826 | |||||||
| chr17:67731916 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.854-2447G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731916 | |||||||
| chr17:67731968 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0105 others(2): Show |
6 | HG01358.hp1 HG01361.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.854-2395A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67731968 | |||||||
| chr17:67732009 | A | G | 1 | a0001c0004t0001g0214 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.854-2354A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732009 | |||||||
| chr17:67732056 | G | A | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-2307G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732056 | |||||||
| chr17:67732146 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.854-2217A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732146 | |||||||
| chr17:67732416 | G | A | 17 | a0001c0002t0002g0019 a0001c0002t0002g0056 a0001c0002t0002g0057 others(14): Show |
24 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-1947G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732416 | |||||||
| chr17:67732432 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.854-1931G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732432 | |||||||
| chr17:67732439 | C | G | 4 | a0001c0002t0001g0023 a0001c0002t0001g0165 a0001c0002t0001g0166 others(1): Show |
6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-1924C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732439 | |||||||
| chr17:67732491 | C | CA | 11 | a0001c0001t0001g0111 a0001c0001t0001g0118 a0001c0001t0001g0132 others(8): Show |
12 | HG00597.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.854-1854dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67732491 | ||||||
| chr17:67732491 | CA | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0080 a0001c0001t0001g0115 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-1854delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67732491 | ||||||
| chr17:67732491 | CAA | C | 17 | a0001c0002t0002g0019 a0001c0002t0002g0056 a0001c0002t0002g0057 others(14): Show |
24 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-1855_854-1854d others(4): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67732491 | ||||||
| chr17:67732573 | A | T | 2 | a0001c0002t0003g0208 a0001c0002t0003g0209 |
2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.854-1790A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732573 | |||||||
| chr17:67732641 | T | G | 17 | a0001c0002t0002g0019 a0001c0002t0002g0056 a0001c0002t0002g0057 others(14): Show |
24 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.854-1722T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732641 | |||||||
| chr17:67732678 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.854-1685G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732678 | |||||||
| chr17:67732781 | C | T | 6 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.854-1582C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67732781 | |||||||
| chr17:67733021 | A | G | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-1342A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733021 | |||||||
| chr17:67733049 | G | A | 2 | a0001c0002t0002g0016 a0001c0002t0002g0200 |
5 | HG00735.hp2 HG00738.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.854-1314G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733049 | |||||||
| chr17:67733070 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.854-1293A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733070 | |||||||
| chr17:67733129 | C | T | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.854-1234C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733129 | |||||||
| chr17:67733320 | G | A | 33 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(30): Show |
66 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.854-1043G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733320 | |||||||
| chr17:67733521 | A | G | 1 | a0002c0003t0001g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.854-842A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733521 | |||||||
| chr17:67733690 | G | T | 7 | a0001c0002t0001g0073 a0001c0002t0001g0156 a0001c0002t0001g0157 others(4): Show |
7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.854-673G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733690 | |||||||
| chr17:67733847 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.854-516T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733847 | |||||||
| chr17:67733935 | A | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(176): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.854-428A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733935 | |||||||
| chr17:67733943 | CTG | C | 2 | a0001c0002t0001g0043 a0001c0002t0001g0141 |
3 | HG01099.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.854-418_854-417del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67733943 | ||||||
| chr17:67733945 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.854-418G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733945 | |||||||
| chr17:67733968 | T | G | 5 | a0001c0002t0001g0042 a0001c0002t0001g0044 a0001c0002t0001g0143 others(2): Show |
7 | HG01168.hp2 HG01169.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.854-395T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67733968 | |||||||
| chr17:67734094 | GAAGCC | G | 24 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0018 others(21): Show |
43 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.854-267_854-263del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr17 | 67734094 | ||||||
| chr17:67734115 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.854-248T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734115 | |||||||
| chr17:67734143 | T | C | 29 | a0001c0004t0001g0008 a0001c0004t0001g0030 a0001c0004t0001g0049 others(26): Show |
39 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.854-220T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734143 | |||||||
| chr17:67734145 | C | G | 1 | a0001c0002t0001g0153 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.854-218C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734145 | |||||||
| chr17:67734145 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.854-218C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734145 | |||||||
| chr17:67734288 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.854-75G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 7/17 | chr17 | 67734288 | |||||||
| chr17:67734542 | T | C | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+103T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734542 | |||||||
| chr17:67734640 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(99): Show |
167 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.930+201A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734640 | |||||||
| chr17:67734731 | A | G | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.930+292A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734731 | |||||||
| chr17:67734755 | A | G | 7 | a0001c0002t0001g0073 a0001c0002t0001g0156 a0001c0002t0001g0157 others(4): Show |
7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.930+316A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734755 | |||||||
| chr17:67734774 | G | A | 1 | a0001c0002t0002g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.930+335G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67734774 | |||||||
| chr17:67735031 | C | G | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.930+592C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735031 | |||||||
| chr17:67735068 | GTGTTAAA | G | 2 | a0002c0003t0001g0027 a0002c0003t0001g0171 |
4 | NA19001.hp1 NA19075.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.930+642_930+648del others(7): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 67735068 | ||||||
| chr17:67735135 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.930+696A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735135 | |||||||
| chr17:67735234 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.931-666T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735234 | |||||||
| chr17:67735332 | TTATAC | T | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.931-566_931-562del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 67735332 | ||||||
| chr17:67735336 | A | C | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.931-564A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735336 | |||||||
| chr17:67735382 | GT | G | 29 | a0001c0004t0001g0008 a0001c0004t0001g0030 a0001c0004t0001g0049 others(26): Show |
39 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.931-517delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735382 | |||||||
| chr17:67735390 | ACT | A | 8 | a0001c0002t0001g0073 a0001c0002t0001g0156 a0001c0002t0001g0157 others(5): Show |
8 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.931-508_931-507del others(2): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr17 | 67735390 | ||||||
| chr17:67735494 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.931-406C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735494 | |||||||
| chr17:67735529 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.931-371T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735529 | |||||||
| chr17:67735677 | A | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.931-223A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735677 | |||||||
| chr17:67735797 | G | A | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.931-103G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735797 | |||||||
| chr17:67735875 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.931-25A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 8/17 | chr17 | 67735875 | |||||||
| chr17:67735958 | C | CATACAAG others(75): Show |
1 | a0010c0015t0001g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.990_1054+17dupATAC others(78): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 67735958 | ||||||
| chr17:67736062 | G | A | 2 | a0001c0001t0001g0079 a0001c0001t0001g0083 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1054+39G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736062 | |||||||
| chr17:67736146 | T | C | 8 | a0001c0002t0001g0023 a0001c0002t0001g0165 a0001c0002t0001g0166 others(5): Show |
11 | HG00609.hp2 HG01884.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.1054+123T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736146 | |||||||
| chr17:67736174 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1054+151G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736174 | |||||||
| chr17:67736236 | G | A | 4 | a0001c0002t0001g0023 a0001c0002t0001g0165 a0001c0002t0001g0166 others(1): Show |
6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054+213G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736236 | |||||||
| chr17:67736292 | G | GA | 13 | a0001c0001t0001g0037 a0001c0001t0001g0084 a0001c0001t0001g0095 others(10): Show |
14 | HG01099.hp1 HG01175.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1054+273dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr17 | 67736292 | ||||||
| chr17:67736296 | AC | A | 3 | a0001c0001t0001g0107 a0001c0002t0001g0189 a0001c0002t0008g0192 |
3 | HG03486.hp1 HG03491.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1054+274delC | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736296 | |||||||
| chr17:67736297 | C | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.1054+274C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736297 | |||||||
| chr17:67736369 | G | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1055-297G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736369 | |||||||
| chr17:67736419 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1055-247A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736419 | |||||||
| chr17:67736458 | A | G | 4 | a0001c0002t0001g0023 a0001c0002t0001g0165 a0001c0002t0001g0166 others(1): Show |
6 | HG00609.hp2 HG03834.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1055-208A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736458 | |||||||
| chr17:67736530 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1055-136G>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 9/17 | chr17 | 67736530 | |||||||
| chr17:67736775 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1143+21T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 10/17 | chr17 | 67736775 | |||||||
| chr17:67736843 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
266 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.1143+89A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 10/17 | chr17 | 67736843 | |||||||
| chr17:67737003 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
160 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1144-68T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 10/17 | chr17 | 67737003 | |||||||
| chr17:67737339 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1219-169T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 11/17 | chr17 | 67737339 | |||||||
| chr17:67737376 | G | A | 2 | a0004c0006t0005g0022 a0004c0012t0005g0022 |
3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1219-132G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 11/17 | chr17 | 67737376 | |||||||
| chr17:67737751 | A | G | 3 | a0001c0004t0001g0216 a0001c0004t0001g0221 a0001c0004t0001g0222 |
3 | HG00408.hp1 HG02071.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1403+59A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 12/17 | chr17 | 67737751 | |||||||
| chr17:67738061 | G | A | 1 | a0001c0002t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1530-61G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 13/17 | chr17 | 67738061 | |||||||
| chr17:67738113 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1530-9C>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 13/17 | chr17 | 67738113 | |||||||
| chr17:67738398 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1763+43A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738398 | |||||||
| chr17:67738473 | T | C | 1 | a0002c0003t0001g0176 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1763+118T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738473 | |||||||
| chr17:67738527 | T | G | 3 | a0001c0002t0002g0058 a0001c0002t0002g0065 a0001c0002t0002g0066 |
3 | HG01346.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1763+172T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738527 | |||||||
| chr17:67738539 | A | T | 1 | a0011c0010t0001g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1763+184A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738539 | |||||||
| chr17:67738541 | T | A | 1 | a0011c0010t0001g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1763+186T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738541 | |||||||
| chr17:67738597 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1763+242C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738597 | |||||||
| chr17:67738598 | G | A | 2 | a0001c0002t0002g0057 a0001c0002t0002g0061 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1763+243G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738598 | |||||||
| chr17:67738678 | TA | T | 39 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0001g0110 others(36): Show |
70 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1764-240delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr17 | 67738678 | ||||||
| chr17:67738712 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1764-220A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738712 | |||||||
| chr17:67738722 | T | C | 1 | a0001c0002t0001g0156 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1764-210T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738722 | |||||||
| chr17:67738912 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0113 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1764-20G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 14/17 | chr17 | 67738912 | |||||||
| chr17:67739295 | A | G | 1 | a0001c0002t0001g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1843-221A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739295 | |||||||
| chr17:67739300 | T | A | 1 | a0001c0004t0001g0218 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1843-216T>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739300 | |||||||
| chr17:67739405 | G | A | 8 | a0001c0001t0001g0080 a0001c0001t0001g0098 a0001c0001t0001g0099 others(5): Show |
8 | HG02523.hp2 NA18954.hp1 NA18997.hp2 others(5): Show |
intron_variant | MODIFIER | c.1843-111G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739405 | |||||||
| chr17:67739427 | G | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0130 |
2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1843-89G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739427 | |||||||
| chr17:67739430 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0130 |
2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1843-86C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739430 | |||||||
| chr17:67739431 | A | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0130 |
2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1843-85A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739431 | |||||||
| chr17:67739447 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
171 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1843-69G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 15/17 | chr17 | 67739447 | |||||||
| chr17:67739626 | CTTTGA | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0188 |
5 | HG02647.hp1 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1935+23_1935+27del others(5): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67739626 | ||||||
| chr17:67739681 | C | T | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+73C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67739681 | |||||||
| chr17:67739756 | A | G | 22 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(19): Show |
38 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1935+148A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67739756 | |||||||
| chr17:67739905 | C | T | 12 | a0001c0002t0002g0019 a0001c0002t0002g0056 a0001c0002t0002g0057 others(9): Show |
14 | HG01346.hp1 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1935+297C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67739905 | |||||||
| chr17:67740102 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0120 |
3 | HG02132.hp1 HG02523.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1935+494G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740102 | |||||||
| chr17:67740192 | G | A | 1 | a0002c0003t0001g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1935+584G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740192 | |||||||
| chr17:67740233 | CA | C | 18 | a0001c0002t0001g0040 a0001c0002t0001g0072 a0001c0002t0002g0019 others(15): Show |
26 | HG01109.hp1 HG01346.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1935+636delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740233 | ||||||
| chr17:67740247 | G | A | 2 | a0001c0002t0001g0189 a0001c0002t0008g0192 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1935+639G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740247 | |||||||
| chr17:67740333 | G | C | 28 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(25): Show |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1935+725G>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740333 | |||||||
| chr17:67740443 | C | T | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+835C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740443 | |||||||
| chr17:67740530 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1935+922A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740530 | |||||||
| chr17:67740534 | G | A | 2 | a0004c0006t0005g0022 a0004c0012t0005g0022 |
3 | HG01884.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1935+926G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740534 | |||||||
| chr17:67740609 | C | CA | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1935+1016dupA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740609 | ||||||
| chr17:67740609 | C | CAA | 9 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0081 others(6): Show |
9 | HG01069.hp1 HG01891.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.1935+1015_1935+101 others(6): Show |
NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740609 | ||||||
| chr17:67740609 | CA | C | 28 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(25): Show |
56 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.1935+1016delA | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740609 | ||||||
| chr17:67740696 | C | T | 1 | a0001c0002t0002g0200 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1935+1088C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740696 | |||||||
| chr17:67740796 | A | G | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1935+1188A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740796 | |||||||
| chr17:67740797 | T | C | 29 | a0001c0004t0001g0008 a0001c0004t0001g0030 a0001c0004t0001g0049 others(26): Show |
39 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(36): Show |
intron_variant | MODIFIER | c.1935+1189T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740797 | |||||||
| chr17:67740820 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1935+1212T>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67740820 | |||||||
| chr17:67740900 | CT | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1935+1303delT | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr17 | 67740900 | ||||||
| chr17:67741101 | G | A | 31 | a0001c0002t0001g0018 a0001c0002t0001g0207 a0002c0003t0001g0002 others(28): Show |
62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1935+1493G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741101 | |||||||
| chr17:67741103 | T | C | 5 | a0001c0002t0003g0047 a0001c0002t0003g0048 a0001c0002t0003g0208 others(2): Show |
6 | HG02109.hp2 HG02723.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1935+1495T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741103 | |||||||
| chr17:67741133 | G | A | 2 | a0001c0002t0001g0158 a0001c0002t0001g0159 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1935+1525G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741133 | |||||||
| chr17:67741152 | C | G | 1 | a0003c0005t0003g0029 | 3 | HG01109.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1935+1544C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741152 | |||||||
| chr17:67741156 | G | A | 2 | a0001c0002t0001g0189 a0001c0002t0008g0192 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1935+1548G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741156 | |||||||
| chr17:67741270 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1935+1662G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741270 | |||||||
| chr17:67741282 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1935+1674C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741282 | |||||||
| chr17:67741288 | T | C | 5 | a0003c0005t0003g0015 a0003c0005t0003g0029 a0003c0005t0003g0190 others(2): Show |
10 | HG01109.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1935+1680T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741288 | |||||||
| chr17:67741588 | C | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1936-1891C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741588 | |||||||
| chr17:67741686 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(40): Show |
73 | HG00438.hp1 HG00642.hp2 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.1936-1793C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741686 | |||||||
| chr17:67741753 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1936-1726G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741753 | |||||||
| chr17:67741909 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1936-1570C>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67741909 | |||||||
| chr17:67742216 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(221): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1936-1263T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742216 | |||||||
| chr17:67742444 | C | G | 1 | a0001c0002t0003g0209 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1936-1035C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742444 | |||||||
| chr17:67742657 | G | A | 21 | a0001c0002t0001g0005 a0001c0002t0001g0013 a0001c0002t0001g0041 others(18): Show |
37 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1936-822G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742657 | |||||||
| chr17:67742823 | A | C | 1 | a0001c0002t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1936-656A>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742823 | |||||||
| chr17:67742961 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1936-518T>C | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742961 | |||||||
| chr17:67742968 | G | A | 7 | a0001c0002t0001g0073 a0001c0002t0001g0156 a0001c0002t0001g0157 others(4): Show |
7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1936-511G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67742968 | |||||||
| chr17:67743109 | G | A | 1 | a0001c0002t0003g0047 | 2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1936-370G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743109 | |||||||
| chr17:67743113 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1936-366A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743113 | |||||||
| chr17:67743163 | G | A | 2 | a0002c0003t0001g0026 a0002c0003t0001g0028 |
6 | HG00423.hp2 HG00673.hp2 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-316G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743163 | |||||||
| chr17:67743312 | G | A | 27 | a0002c0003t0001g0002 a0002c0003t0001g0024 a0002c0003t0001g0025 others(24): Show |
55 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.1936-167G>A | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 16/17 | chr17 | 67743312 | |||||||
| chr17:67743673 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.2044-70A>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/17 | chr17 | 67743673 | |||||||
| chr17:67743680 | C | G | 7 | a0001c0002t0001g0073 a0001c0002t0001g0156 a0001c0002t0001g0157 others(4): Show |
7 | HG01099.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044-63C>G | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/17 | chr17 | 67743680 | |||||||
| chr17:67743681 | A | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.2044-62A>T | NOL11 | ENSG00000130935.10 | transcript | ENST00000253247.9 | protein_coding | 17/17 | chr17 | 67743681 |