Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51105 |
| ensemblid | ENSG00000129292.21 |
| hgncid | 24280 |
| symbol | PHF20L1 |
| name | PHD finger protein 20 like 1 |
| refseq_nuc | NM_016018.5 |
| refseq_prot | NP_057102.4 |
| ensembl_nuc | ENST00000395386.7 |
| ensembl_prot | ENSP00000378784.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 132775388 |
| end | 132848807 |
| strand | + |
| ver | v1.2 |
| region | chr8:132775388-132848807 |
| region5000 | chr8:132770388-132853807 |
| regionname0 | PHF20L1_chr8_132775388_132848807 |
| regionname5000 | PHF20L1_chr8_132770388_132853807 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1017 | 391 | 86 | 69 | 184 | 14 | 36 | 148 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | MSKKP others(1012): Show |
chr8 | 132770388 | 132853807 |
| a0002 | 0/0 | 1017 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | MSKKP others(1012): Show |
chr8 | 132770388 | 132853807 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3051 | 225 | 43 | 38 | 113 | 7 | 22 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0002 | 0/0 | 3051 | 123 | 39 | 27 | 37 | 7 | 13 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0003 | 0/0 | 3051 | 23 | 0 | 0 | 23 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0004 | 0/0 | 3051 | 8 | 0 | 3 | 4 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0005 | 0/0 | 3051 | 4 | 0 | 0 | 4 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0006 | 0/0 | 3051 | 3 | 0 | 0 | 3 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0007 | 0/0 | 3051 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0009 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0010 | 0/0 | 3051 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0001c0011 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 | ||
| a0002c0008 | 0/0 | 3051 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | ATGAG others(3046): Show |
chr8 | 132770388 | 132853807 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6233 | 115 | 29 | 13 | 64 | 1 | 8 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0003 | 0/1 | 6233 | 59 | 12 | 6 | 33 | 3 | 4 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0004 | 1/0 | 6233 | 40 | 1 | 15 | 14 | 1 | 8 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0009 | 0/0 | 6233 | 5 | 0 | 3 | 0 | 2 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0011 | 0/0 | 6221 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6216): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0014 | 0/0 | 6233 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0015 | 0/0 | 6233 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0016 | 0/0 | 6233 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0001t0017 | 0/0 | 6233 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0002 | 0/0 | 6228 | 62 | 1 | 18 | 27 | 6 | 10 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6223): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0005 | 0/0 | 6232 | 40 | 29 | 9 | 0 | 1 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6227): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0007 | 0/0 | 6234 | 8 | 8 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6229): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0008 | 0/0 | 6225 | 6 | 0 | 0 | 6 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6220): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0010 | 0/0 | 6228 | 3 | 0 | 0 | 3 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6223): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0012 | 0/0 | 6228 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6223): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0013 | 0/0 | 6228 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6223): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0019 | 0/0 | 6228 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6223): Show |
chr8 | 132770388 | 132853807 |
| a0001c0002t0020 | 0/0 | 6228 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6223): Show |
chr8 | 132770388 | 132853807 |
| a0001c0003t0006 | 0/0 | 6231 | 23 | 0 | 0 | 23 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6226): Show |
chr8 | 132770388 | 132853807 |
| a0001c0004t0002 | 0/0 | 6228 | 8 | 0 | 3 | 4 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6223): Show |
chr8 | 132770388 | 132853807 |
| a0001c0005t0001 | 0/0 | 6233 | 4 | 0 | 0 | 4 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0006t0003 | 0/0 | 6233 | 3 | 0 | 0 | 3 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0007t0001 | 0/0 | 6233 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0009t0018 | 0/0 | 6233 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0010t0004 | 0/0 | 6233 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| a0001c0011t0005 | 0/0 | 6232 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6227): Show |
chr8 | 132770388 | 132853807 |
| a0002c0008t0004 | 0/0 | 6233 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | AGGGC others(6228): Show |
chr8 | 132770388 | 132853807 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 0 | 4 | 10 | 0 | 2 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0011 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0134 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0156 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0009g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0009g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0009g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0009g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0011g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0011g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0014g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0016g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0001t0017g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0002 | 0/0 | 13 | 0 | 3 | 6 | 1 | 3 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0007g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0008g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0010g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0010g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0013g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0019g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0002t0020g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0003t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0004t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0004t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0004t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0004t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0005t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0006t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0006t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0006t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0007t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0009t0018g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0010t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0001c0011t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| a0002c0008t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0009 | g0062 | EUR | GBR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | GBR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0031 | EUR | GBR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0022 | EUR | GBR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00280 | hp1 | a0001 | c0001 | t0009 | g0064 | EUR | FIN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0166 | EUR | FIN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | FIN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0006 | EUR | FIN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00408 | hp2 | a0001 | c0003 | t0006 | g0043 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00544 | hp2 | a0001 | c0003 | t0006 | g0201 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00597 | hp1 | a0001 | c0003 | t0006 | g0042 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00639 | hp1 | a0001 | c0004 | t0002 | g0112 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0235 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0224 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00738 | hp1 | a0001 | c0002 | t0005 | g0219 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0065 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0155 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01070 | hp1 | a0001 | c0001 | t0009 | g0061 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0098 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0097 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01081 | hp2 | a0001 | c0002 | t0005 | g0225 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0072 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01099 | hp2 | a0001 | c0002 | t0005 | g0217 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01167 | hp1 | a0001 | c0002 | t0005 | g0236 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0125 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0126 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01243 | hp1 | a0001 | c0001 | t0017 | g0050 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0132 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0016 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01258 | hp1 | a0001 | c0002 | t0005 | g0016 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0115 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01358 | hp2 | a0001 | c0004 | t0002 | g0028 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0094 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0096 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0068 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01496 | hp1 | a0001 | c0004 | t0002 | g0028 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0129 | EUR | IBS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0071 | EUR | IBS | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0231 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01934 | hp1 | a0002 | c0008 | t0004 | g0076 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01943 | hp2 | a0001 | c0011 | t0005 | g0223 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0107 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0085 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0077 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02027 | hp1 | a0001 | c0004 | t0002 | g0030 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02027 | hp2 | a0001 | c0005 | t0001 | g0267 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02040 | hp2 | a0001 | c0003 | t0006 | g0014 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0018 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02056 | hp1 | a0001 | c0003 | t0006 | g0203 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02074 | hp1 | a0001 | c0003 | t0006 | g0042 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02083 | hp1 | a0001 | c0003 | t0006 | g0014 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | KHV | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0087 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CDX | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | CDX | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02258 | hp2 | a0001 | c0002 | t0005 | g0237 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02451 | hp1 | a0001 | c0002 | t0005 | g0232 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0228 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0017 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0183 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02615 | hp1 | a0001 | c0002 | t0005 | g0220 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02615 | hp2 | a0001 | c0002 | t0005 | g0045 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0013 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0045 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02647 | hp2 | a0001 | c0002 | t0005 | g0226 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02683 | hp1 | a0001 | c0002 | t0019 | g0131 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0044 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0189 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02818 | hp1 | a0001 | c0002 | t0007 | g0187 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02818 | hp2 | a0001 | c0010 | t0004 | g0182 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02886 | hp1 | a0001 | c0002 | t0005 | g0019 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02886 | hp2 | a0001 | c0007 | t0001 | g0059 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0019 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02895 | hp2 | a0001 | c0002 | t0007 | g0055 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02896 | hp2 | a0001 | c0009 | t0018 | g0247 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02897 | hp2 | a0001 | c0002 | t0007 | g0186 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02965 | hp1 | a0001 | c0002 | t0005 | g0216 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0214 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03017 | hp2 | a0001 | c0002 | t0020 | g0095 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03041 | hp1 | a0001 | c0007 | t0001 | g0060 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0227 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03139 | hp1 | a0001 | c0002 | t0005 | g0238 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0230 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03195 | hp1 | a0001 | c0002 | t0005 | g0044 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0136 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0013 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0019 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03492 | hp1 | a0001 | c0004 | t0002 | g0104 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0025 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0215 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0088 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03669 | hp1 | a0001 | c0002 | t0005 | g0221 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0103 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0110 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0058 | SAS | BEB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03927 | hp1 | a0001 | c0001 | t0015 | g0063 | SAS | BEB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0121 | SAS | BEB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0086 | SAS | BEB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0128 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0213 | SAS | STU | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | YRI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | YRI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18612 | hp2 | a0001 | c0001 | t0011 | g0159 | EAS | CHB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CHB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18951 | hp1 | a0001 | c0002 | t0010 | g0117 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18954 | hp1 | a0001 | c0005 | t0001 | g0245 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18954 | hp2 | a0001 | c0003 | t0006 | g0200 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18965 | hp2 | a0001 | c0003 | t0006 | g0014 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18969 | hp1 | a0001 | c0002 | t0010 | g0029 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18975 | hp1 | a0001 | c0002 | t0008 | g0057 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18978 | hp2 | a0001 | c0003 | t0006 | g0212 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18979 | hp1 | a0001 | c0004 | t0002 | g0030 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18982 | hp2 | a0001 | c0004 | t0002 | g0127 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18984 | hp1 | a0001 | c0005 | t0001 | g0251 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18985 | hp2 | a0001 | c0003 | t0006 | g0210 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18988 | hp1 | a0001 | c0003 | t0006 | g0015 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18988 | hp2 | a0001 | c0006 | t0003 | g0147 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18990 | hp1 | a0001 | c0001 | t0011 | g0160 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18991 | hp2 | a0001 | c0005 | t0001 | g0253 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18993 | hp2 | a0001 | c0006 | t0003 | g0146 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18994 | hp1 | a0001 | c0003 | t0006 | g0206 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18999 | hp1 | a0001 | c0002 | t0008 | g0124 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19002 | hp2 | a0001 | c0003 | t0006 | g0209 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19005 | hp2 | a0001 | c0002 | t0008 | g0027 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19007 | hp1 | a0001 | c0003 | t0006 | g0015 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19009 | hp1 | a0001 | c0003 | t0006 | g0202 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19010 | hp1 | a0001 | c0002 | t0010 | g0029 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19012 | hp1 | a0001 | c0002 | t0008 | g0027 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19043 | hp2 | a0001 | c0002 | t0007 | g0040 | AFR | LWK | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19057 | hp2 | a0001 | c0002 | t0013 | g0007 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19065 | hp1 | a0001 | c0003 | t0006 | g0015 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19068 | hp2 | a0001 | c0003 | t0006 | g0207 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19074 | hp2 | a0001 | c0003 | t0006 | g0208 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19077 | hp1 | a0001 | c0003 | t0006 | g0204 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19079 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19087 | hp1 | a0001 | c0004 | t0002 | g0122 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19087 | hp2 | a0001 | c0003 | t0006 | g0211 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19088 | hp2 | a0001 | c0002 | t0008 | g0105 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19089 | hp1 | a0001 | c0003 | t0006 | g0205 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19089 | hp2 | a0001 | c0002 | t0008 | g0002 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19090 | hp2 | a0001 | c0006 | t0003 | g0003 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19091 | hp2 | a0001 | c0003 | t0006 | g0043 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0233 | AFR | YRI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0234 | AFR | ASW | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0116 | EUR | TSI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0056 | EUR | TSI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0093 | EUR | TSI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20805 | hp2 | a0001 | c0002 | t0005 | g0016 | EUR | TSI | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01123 | hp1 | a0001 | c0002 | t0005 | g0218 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0017 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02486 | hp2 | a0001 | c0002 | t0005 | g0018 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02559 | hp1 | a0001 | c0002 | t0012 | g0184 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0222 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | USA | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| HG06807 | hp2 | a0001 | c0002 | t0005 | g0229 | AFR | USA | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0017 | AFR | USA | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | USA | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA21309 | hp1 | a0001 | c0002 | t0007 | g0040 | AFR | LWK | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0018 | AFR | LWK | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0134 | REF | REF | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0156 | REF | REF | PHF20L1_chr8_132770388_132853807 | PHF20L1 | chr8 | 132770388 | 132853807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132839503 | T | G | 1 | a0002 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.2308T>G | p.Ser770Ala | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/21 | 2603/6233 | 2308/3054 | 770/1017 | chr8 | 132839503 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132799148 | G | A | 1 | a0001c0004 | 8 | HG00639.hp1 HG01358.hp2 HG01496.hp1 others(5): Show |
synonymous_variant | LOW | c.483G>A | p.Ser161Ser | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/21 | 778/6233 | 483/3054 | 161/1017 | chr8 | 132799148 | |||
| chr8:132804667 | A | G | 1 | a0001c0011 | 1 | HG01943.hp2 | synonymous_variant | LOW | c.774A>G | p.Thr258Thr | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/21 | 1069/6233 | 774/3054 | 258/1017 | chr8 | 132804667 | |||
| chr8:132832263 | C | T | 3 | a0001c0002 a0001c0004 a0001c0011 |
132 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(129): Show |
synonymous_variant | LOW | c.1773C>T | p.Leu591Leu | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/21 | 2068/6233 | 1773/3054 | 591/1017 | chr8 | 132832263 | |||
| chr8:132832353 | C | T | 1 | a0001c0005 | 4 | HG02027.hp2 NA18954.hp1 NA18984.hp1 others(1): Show |
synonymous_variant | LOW | c.1863C>T | p.Thr621Thr | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/21 | 2158/6233 | 1863/3054 | 621/1017 | chr8 | 132832353 | |||
| chr8:132842554 | C | T | 1 | a0001c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.2427C>T | p.Ser809Ser | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/21 | 2722/6233 | 2427/3054 | 809/1017 | chr8 | 132842554 | |||
| chr8:132842560 | G | A | 1 | a0001c0007 | 2 | HG02886.hp2 HG03041.hp1 |
synonymous_variant | LOW | c.2433G>A | p.Lys811Lys | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/21 | 2728/6233 | 2433/3054 | 811/1017 | chr8 | 132842560 | |||
| chr8:132842725 | A | G | 1 | a0001c0003 | 23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
synonymous_variant | LOW | c.2598A>G | p.Pro866Pro | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/21 | 2893/6233 | 2598/3054 | 866/1017 | chr8 | 132842725 | |||
| chr8:132844191 | T | C | 1 | a0001c0009 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.2784T>C | p.Asn928Asn | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 20/21 | 3079/6233 | 2784/3054 | 928/1017 | chr8 | 132844191 | |||
| chr8:132844206 | C | T | 1 | a0001c0006 | 3 | NA18988.hp2 NA18993.hp2 NA19090.hp2 |
synonymous_variant | LOW | c.2799C>T | p.Thr933Thr | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 20/21 | 3094/6233 | 2799/3054 | 933/1017 | chr8 | 132844206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132775406 | AGGCGGCG others(5): Show |
A | 1 | a0001c0001t0011 | 2 | NA18612.hp2 NA18990.hp1 |
5_prime_UTR_variant | MODIFIER | c.-269_-258delGCGGCG others(6): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/21 | 2404 | INFO_REALIGN_3_PRIME | chr8 | 132775406 | |||||
| chr8:132846238 | CAA | C | 1 | a0001c0003t0006 | 23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*316_*317delAA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 316 | chr8 | 132846238 | ||||||
| chr8:132846409 | G | T | 1 | a0001c0002t0020 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 486 | chr8 | 132846409 | ||||||
| chr8:132846463 | G | T | 1 | a0001c0002t0019 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 540 | chr8 | 132846463 | ||||||
| chr8:132846467 | G | A | 8 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0010 others(5): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*544G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 544 | chr8 | 132846467 | ||||||
| chr8:132846663 | G | A | 1 | a0001c0001t0014 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*740G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 740 | chr8 | 132846663 | ||||||
| chr8:132846830 | G | GA | 1 | a0001c0002t0007 | 8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*918dupA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 919 | INFO_REALIGN_3_PRIME | chr8 | 132846830 | |||||
| chr8:132846830 | GA | G | 10 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0008 others(7): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*918delA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 918 | INFO_REALIGN_3_PRIME | chr8 | 132846830 | |||||
| chr8:132846875 | T | G | 1 | a0001c0001t0009 | 5 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*952T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 952 | chr8 | 132846875 | ||||||
| chr8:132847294 | A | T | 1 | a0001c0002t0013 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1371A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 1371 | chr8 | 132847294 | ||||||
| chr8:132847352 | TAAG | T | 1 | a0001c0002t0008 | 6 | NA18975.hp1 NA18999.hp1 NA19005.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1431_*1433delAGA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 1431 | INFO_REALIGN_3_PRIME | chr8 | 132847352 | |||||
| chr8:132847626 | T | A | 6 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(3): Show |
70 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1703T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 1703 | chr8 | 132847626 | ||||||
| chr8:132847632 | G | T | 7 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0010 others(4): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1709G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 1709 | chr8 | 132847632 | ||||||
| chr8:132847720 | A | G | 1 | a0001c0002t0010 | 3 | NA18951.hp1 NA18969.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1797A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 1797 | chr8 | 132847720 | ||||||
| chr8:132848172 | A | G | 2 | a0001c0001t0015 a0001c0001t0016 |
2 | HG02602.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2249A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2249 | chr8 | 132848172 | ||||||
| chr8:132848208 | A | G | 2 | a0001c0002t0005 a0001c0011t0005 |
41 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2285A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2285 | chr8 | 132848208 | ||||||
| chr8:132848238 | A | T | 1 | a0001c0009t0018 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2315A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2315 | chr8 | 132848238 | ||||||
| chr8:132848336 | C | G | 1 | a0001c0001t0016 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2413C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2413 | chr8 | 132848336 | ||||||
| chr8:132848400 | G | A | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(21): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*2477G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2477 | chr8 | 132848400 | ||||||
| chr8:132848665 | G | C | 10 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0008 others(7): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*2742G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2742 | chr8 | 132848665 | ||||||
| chr8:132848684 | G | T | 1 | a0001c0001t0017 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2761 | chr8 | 132848684 | ||||||
| chr8:132848745 | ATATT | A | 8 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0010 others(5): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2824_*2827delATTT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2824 | INFO_REALIGN_3_PRIME | chr8 | 132848745 | |||||
| chr8:132848751 | C | G | 8 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0010 others(5): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*2828C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 21/21 | 2828 | chr8 | 132848751 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:132775679 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-38+34C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132775679 | |||||||
| chr8:132775696 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-38+51C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132775696 | |||||||
| chr8:132775726 | C | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
88 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.-38+81C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132775726 | |||||||
| chr8:132775737 | G | A | 1 | a0001c0001t0003g0052 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-38+92G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132775737 | |||||||
| chr8:132775748 | G | GC | 4 | a0001c0001t0001g0241 a0001c0001t0003g0054 a0001c0002t0002g0053 others(1): Show |
4 | HG01496.hp2 HG01934.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+105dupC | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr8 | 132775748 | ||||||
| chr8:132775836 | G | A | 2 | a0001c0001t0003g0022 a0001c0001t0003g0056 |
3 | HG00140.hp2 HG02293.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-38+191G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132775836 | |||||||
| chr8:132775861 | T | C | 1 | a0001c0002t0008g0057 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-38+216T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132775861 | |||||||
| chr8:132775896 | C | T | 1 | a0001c0002t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-38+251C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132775896 | |||||||
| chr8:132776120 | T | C | 1 | a0001c0002t0002g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-38+475T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776120 | |||||||
| chr8:132776278 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0239 |
3 | HG02976.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-38+633C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776278 | |||||||
| chr8:132776291 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-38+646A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776291 | |||||||
| chr8:132776311 | A | G | 33 | a0001c0001t0001g0046 a0001c0001t0001g0239 a0001c0002t0005g0016 others(30): Show |
44 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-38+666A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776311 | |||||||
| chr8:132776348 | C | G | 1 | a0001c0001t0003g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38+703C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776348 | |||||||
| chr8:132776355 | C | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-38+710C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776355 | |||||||
| chr8:132776446 | A | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG02258.hp1 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-38+801A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776446 | |||||||
| chr8:132776542 | G | C | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-38+897G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776542 | |||||||
| chr8:132776550 | A | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+905A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776550 | |||||||
| chr8:132776674 | T | A | 3 | a0001c0002t0005g0214 a0001c0002t0005g0215 a0001c0002t0005g0216 |
3 | HG02965.hp1 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-38+1029T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776674 | |||||||
| chr8:132776845 | A | G | 1 | a0001c0001t0004g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-37-947A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776845 | |||||||
| chr8:132776868 | A | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.-37-924A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776868 | |||||||
| chr8:132776885 | T | A | 2 | a0001c0001t0009g0061 a0001c0001t0009g0062 |
2 | HG00099.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.-37-907T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776885 | |||||||
| chr8:132776995 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-37-797C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776995 | |||||||
| chr8:132776996 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-37-796T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132776996 | |||||||
| chr8:132777191 | A | C | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-37-601A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132777191 | |||||||
| chr8:132777269 | C | G | 1 | a0001c0001t0001g0285 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-37-523C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132777269 | |||||||
| chr8:132777409 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-37-383A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132777409 | |||||||
| chr8:132777459 | C | G | 1 | a0001c0002t0012g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-37-333C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132777459 | |||||||
| chr8:132777549 | C | G | 1 | a0001c0001t0001g0284 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-37-243C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132777549 | |||||||
| chr8:132777649 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-143A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 1/20 | chr8 | 132777649 | |||||||
| chr8:132777990 | A | C | 1 | a0001c0001t0016g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.83+79A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132777990 | |||||||
| chr8:132778180 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.83+269A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132778180 | |||||||
| chr8:132778245 | G | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0242 |
3 | NA18973.hp1 NA18978.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.83+334G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132778245 | |||||||
| chr8:132778439 | G | C | 1 | a0001c0001t0015g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.83+528G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132778439 | |||||||
| chr8:132778591 | G | T | 1 | a0001c0010t0004g0182 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.83+680G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132778591 | |||||||
| chr8:132778816 | G | A | 1 | a0001c0001t0009g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.83+905G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132778816 | |||||||
| chr8:132778865 | T | C | 153 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(150): Show |
205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.83+954T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132778865 | |||||||
| chr8:132778929 | C | G | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.83+1018C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132778929 | |||||||
| chr8:132779165 | A | T | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG02258.hp1 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.83+1254A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132779165 | |||||||
| chr8:132779511 | A | T | 60 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(57): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.83+1600A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132779511 | |||||||
| chr8:132779893 | G | A | 1 | a0001c0001t0009g0065 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.83+1982G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132779893 | |||||||
| chr8:132779947 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.83+2036G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132779947 | |||||||
| chr8:132779985 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.83+2074C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132779985 | |||||||
| chr8:132780061 | ACT | A | 6 | a0001c0002t0005g0018 a0001c0002t0005g0019 a0001c0002t0005g0235 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+2153_83+2154del others(2): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132780061 | ||||||
| chr8:132780083 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.83+2172A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132780083 | |||||||
| chr8:132780292 | T | C | 153 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(150): Show |
205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.83+2381T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132780292 | |||||||
| chr8:132780300 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+2389G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132780300 | |||||||
| chr8:132780400 | T | G | 1 | a0001c0001t0001g0243 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.83+2489T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132780400 | |||||||
| chr8:132780494 | A | T | 63 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0023 others(60): Show |
82 | HG00621.hp1 HG00639.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.83+2583A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132780494 | |||||||
| chr8:132780844 | C | CT | 7 | a0001c0001t0001g0239 a0001c0001t0003g0054 a0001c0001t0003g0181 others(4): Show |
7 | HG03017.hp1 HG03654.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.83+2951dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132780844 | ||||||
| chr8:132780858 | T | C | 1 | a0001c0001t0015g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.83+2947T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132780858 | |||||||
| chr8:132780867 | CAG | C | 7 | a0001c0002t0005g0017 a0001c0002t0005g0044 a0001c0002t0005g0045 others(4): Show |
11 | HG01884.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.83+2959_83+2960del others(2): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132780867 | ||||||
| chr8:132780932 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.83+3021C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132780932 | |||||||
| chr8:132781023 | A | T | 1 | a0001c0002t0002g0133 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.83+3112A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781023 | |||||||
| chr8:132781024 | T | A | 7 | a0001c0001t0004g0004 a0001c0001t0004g0066 a0001c0001t0004g0067 others(4): Show |
10 | HG00735.hp2 HG00741.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.83+3113T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781024 | |||||||
| chr8:132781514 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0239 a0001c0001t0001g0288 |
4 | HG02004.hp1 HG02976.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.83+3603C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781514 | |||||||
| chr8:132781515 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+3604G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781515 | |||||||
| chr8:132781533 | A | G | 136 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(133): Show |
182 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.83+3622A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781533 | |||||||
| chr8:132781658 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.83+3747C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781658 | |||||||
| chr8:132781950 | T | G | 2 | a0001c0001t0001g0188 a0001c0002t0002g0133 |
2 | HG03486.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.83+4039T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781950 | |||||||
| chr8:132781975 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0174 a0001c0001t0001g0175 others(14): Show |
20 | HG00323.hp1 HG00597.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.83+4064A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781975 | |||||||
| chr8:132781975 | A | T | 2 | a0001c0002t0005g0233 a0001c0002t0005g0234 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83+4064A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132781975 | |||||||
| chr8:132782255 | CTG | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.83+4346_83+4347del others(2): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132782255 | ||||||
| chr8:132782332 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.83+4421C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782332 | |||||||
| chr8:132782407 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.83+4496A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782407 | |||||||
| chr8:132782590 | C | CT | 59 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.83+4689dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132782590 | ||||||
| chr8:132782641 | C | T | 16 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0043 others(13): Show |
21 | HG00408.hp2 HG00544.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.83+4730C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782641 | |||||||
| chr8:132782680 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 |
5 | HG01123.hp2 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.83+4769C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782680 | |||||||
| chr8:132782693 | A | G | 1 | a0001c0002t0002g0053 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.83+4782A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782693 | |||||||
| chr8:132782771 | T | C | 1 | a0001c0002t0002g0133 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.83+4860T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782771 | |||||||
| chr8:132782772 | C | CT | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.83+4874dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132782772 | ||||||
| chr8:132782772 | C | T | 1 | a0001c0002t0002g0133 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.83+4861C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782772 | |||||||
| chr8:132782797 | C | T | 5 | a0001c0002t0005g0226 a0001c0002t0005g0227 a0001c0002t0005g0228 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.83+4886C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782797 | |||||||
| chr8:132782909 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.83+4998C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132782909 | |||||||
| chr8:132783080 | C | G | 1 | a0001c0002t0019g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.83+5169C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132783080 | |||||||
| chr8:132783607 | A | G | 3 | a0001c0002t0005g0017 a0001c0002t0005g0045 a0001c0002t0005g0232 |
6 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.83+5696A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132783607 | |||||||
| chr8:132783626 | T | C | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.83+5715T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132783626 | |||||||
| chr8:132783662 | C | A | 1 | a0001c0001t0003g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.83+5751C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132783662 | |||||||
| chr8:132783759 | A | G | 1 | a0001c0002t0005g0225 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.83+5848A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132783759 | |||||||
| chr8:132783775 | T | C | 153 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(150): Show |
205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.83+5864T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132783775 | |||||||
| chr8:132783849 | C | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.83+5938C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132783849 | |||||||
| chr8:132784020 | C | T | 32 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0023 others(29): Show |
41 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.83+6109C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132784020 | |||||||
| chr8:132784222 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
98 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.83+6311G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132784222 | |||||||
| chr8:132784339 | G | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(66): Show |
98 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.83+6428G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132784339 | |||||||
| chr8:132784685 | C | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.83+6774C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132784685 | |||||||
| chr8:132784986 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.83+7075A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132784986 | |||||||
| chr8:132785150 | G | T | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0173 others(1): Show |
6 | HG02040.hp1 HG02132.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.83+7239G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132785150 | |||||||
| chr8:132785430 | T | A | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | HG01358.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.83+7519T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132785430 | |||||||
| chr8:132785514 | A | G | 1 | a0001c0002t0005g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.83+7603A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132785514 | |||||||
| chr8:132785624 | C | T | 1 | a0001c0002t0019g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.83+7713C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132785624 | |||||||
| chr8:132785743 | A | G | 2 | a0001c0002t0002g0129 a0001c0002t0002g0130 |
2 | HG01106.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.83+7832A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132785743 | |||||||
| chr8:132785786 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.83+7875T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132785786 | |||||||
| chr8:132785821 | A | T | 1 | a0001c0002t0012g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.83+7910A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132785821 | |||||||
| chr8:132786269 | A | T | 1 | a0001c0001t0001g0281 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.84-8141A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132786269 | |||||||
| chr8:132786362 | T | C | 12 | a0001c0002t0005g0017 a0001c0002t0005g0044 a0001c0002t0005g0045 others(9): Show |
16 | HG00733.hp2 HG01099.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.84-8048T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132786362 | |||||||
| chr8:132786367 | G | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-8043G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132786367 | |||||||
| chr8:132786556 | G | A | 3 | a0001c0002t0002g0090 a0001c0002t0002g0091 a0001c0002t0002g0092 |
3 | NA18940.hp2 NA18956.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.84-7854G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132786556 | |||||||
| chr8:132786673 | C | T | 60 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(57): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.84-7737C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132786673 | |||||||
| chr8:132786849 | T | C | 1 | a0001c0002t0002g0093 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.84-7561T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132786849 | |||||||
| chr8:132787034 | C | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-7376C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787034 | |||||||
| chr8:132787053 | G | GA | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.84-7351dupA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132787053 | ||||||
| chr8:132787211 | G | A | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.84-7199G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787211 | |||||||
| chr8:132787462 | G | A | 1 | a0001c0002t0002g0094 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.84-6948G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787462 | |||||||
| chr8:132787493 | G | C | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.84-6917G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787493 | |||||||
| chr8:132787523 | T | C | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.84-6887T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787523 | |||||||
| chr8:132787554 | G | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-6856G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787554 | |||||||
| chr8:132787587 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.84-6823T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787587 | |||||||
| chr8:132787721 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.84-6689C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787721 | |||||||
| chr8:132787779 | T | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG02258.hp1 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.84-6631T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787779 | |||||||
| chr8:132787915 | G | A | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.84-6495G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132787915 | |||||||
| chr8:132788600 | CT | C | 102 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(99): Show |
139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.84-5799delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132788600 | ||||||
| chr8:132788806 | TA | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.84-5602delA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132788806 | ||||||
| chr8:132788867 | G | A | 1 | a0001c0002t0020g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.84-5543G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132788867 | |||||||
| chr8:132788913 | A | G | 3 | a0001c0002t0005g0017 a0001c0002t0005g0045 a0001c0002t0005g0232 |
6 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-5497A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132788913 | |||||||
| chr8:132789235 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
5 | HG01884.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.84-5175C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132789235 | |||||||
| chr8:132789593 | G | A | 1 | a0001c0002t0002g0096 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.84-4817G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132789593 | |||||||
| chr8:132789626 | T | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-4784T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132789626 | |||||||
| chr8:132789852 | G | T | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.84-4558G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132789852 | |||||||
| chr8:132790299 | A | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-4111A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790299 | |||||||
| chr8:132790397 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0280 |
2 | HG03486.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.84-4013C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790397 | |||||||
| chr8:132790416 | G | A | 1 | a0001c0003t0006g0200 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.84-3994G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790416 | |||||||
| chr8:132790481 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.84-3929T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790481 | |||||||
| chr8:132790513 | C | G | 1 | a0001c0002t0005g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.84-3897C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790513 | |||||||
| chr8:132790592 | T | C | 1 | a0001c0002t0002g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.84-3818T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790592 | |||||||
| chr8:132790695 | A | G | 1 | a0001c0003t0006g0211 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.84-3715A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790695 | |||||||
| chr8:132790757 | A | G | 31 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(28): Show |
41 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.84-3653A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790757 | |||||||
| chr8:132790857 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.84-3553A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790857 | |||||||
| chr8:132790872 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.84-3538A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790872 | |||||||
| chr8:132790917 | CA | C | 6 | a0001c0002t0005g0226 a0001c0002t0005g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01943.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.84-3492delA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132790917 | |||||||
| chr8:132791167 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.84-3243C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132791167 | |||||||
| chr8:132791168 | G | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.84-3242G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132791168 | |||||||
| chr8:132791254 | C | CT | 21 | a0001c0001t0001g0172 a0001c0001t0001g0268 a0001c0001t0001g0281 others(18): Show |
23 | HG00140.hp1 HG01167.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.84-3133dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132791254 | ||||||
| chr8:132791254 | CT | C | 42 | a0001c0001t0001g0174 a0001c0001t0001g0275 a0001c0001t0001g0276 others(39): Show |
55 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.84-3133delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132791254 | ||||||
| chr8:132791254 | CTTT | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG00544.hp2 HG01106.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.84-3135_84-3133del others(3): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132791254 | ||||||
| chr8:132791504 | C | T | 3 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0167 |
3 | HG00280.hp2 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.84-2906C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132791504 | |||||||
| chr8:132791556 | T | A | 1 | a0001c0003t0006g0202 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.84-2854T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132791556 | |||||||
| chr8:132791561 | T | C | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 |
3 | NA18966.hp2 NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.84-2849T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132791561 | |||||||
| chr8:132791584 | A | G | 1 | a0001c0002t0002g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.84-2826A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132791584 | |||||||
| chr8:132791971 | A | C | 1 | a0001c0001t0001g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.84-2439A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132791971 | |||||||
| chr8:132792066 | T | C | 1 | a0001c0002t0002g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.84-2344T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792066 | |||||||
| chr8:132792380 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.84-2030C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792380 | |||||||
| chr8:132792414 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.84-1996C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792414 | |||||||
| chr8:132792499 | C | G | 1 | a0001c0002t0002g0118 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.84-1911C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792499 | |||||||
| chr8:132792517 | A | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.84-1893A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792517 | |||||||
| chr8:132792527 | A | G | 1 | a0001c0004t0002g0127 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.84-1883A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792527 | |||||||
| chr8:132792964 | C | CT | 69 | a0001c0001t0001g0041 a0001c0001t0001g0191 a0001c0001t0001g0192 others(66): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.84-1428dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132792964 | ||||||
| chr8:132792964 | C | CTT | 56 | a0001c0001t0001g0193 a0001c0001t0004g0004 a0001c0001t0004g0005 others(53): Show |
75 | HG00621.hp1 HG00733.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.84-1429_84-1428dup others(2): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132792964 | ||||||
| chr8:132792964 | CT | C | 8 | a0001c0001t0001g0170 a0001c0001t0001g0180 a0001c0001t0001g0246 others(5): Show |
8 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.84-1428delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132792964 | ||||||
| chr8:132792964 | CTT | C | 17 | a0001c0001t0001g0169 a0001c0003t0006g0014 a0001c0003t0006g0015 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.84-1429_84-1428del others(2): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr8 | 132792964 | ||||||
| chr8:132792967 | T | TC | 3 | a0001c0002t0007g0040 a0001c0002t0007g0055 a0001c0002t0007g0186 |
4 | HG02895.hp2 HG02897.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.84-1443_84-1442ins others(1): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792967 | |||||||
| chr8:132792968 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0239 a0001c0001t0003g0142 |
4 | HG02976.hp2 HG03579.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.84-1442T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132792968 | |||||||
| chr8:132793199 | C | T | 1 | a0001c0001t0004g0025 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.84-1211C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793199 | |||||||
| chr8:132793217 | T | G | 123 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0023 others(120): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.84-1193T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793217 | |||||||
| chr8:132793240 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.84-1170C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793240 | |||||||
| chr8:132793398 | A | T | 1 | a0001c0001t0003g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.84-1012A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793398 | |||||||
| chr8:132793402 | G | A | 1 | a0001c0009t0018g0247 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.84-1008G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793402 | |||||||
| chr8:132793470 | A | G | 1 | a0001c0001t0003g0056 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.84-940A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793470 | |||||||
| chr8:132793519 | A | G | 153 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(150): Show |
205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.84-891A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793519 | |||||||
| chr8:132793643 | T | G | 123 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0023 others(120): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.84-767T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793643 | |||||||
| chr8:132793670 | A | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.84-740A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793670 | |||||||
| chr8:132793709 | C | G | 1 | a0001c0002t0005g0229 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.84-701C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793709 | |||||||
| chr8:132793869 | C | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.84-541C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793869 | |||||||
| chr8:132793892 | T | C | 63 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0023 others(60): Show |
82 | HG00621.hp1 HG00639.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.84-518T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132793892 | |||||||
| chr8:132794234 | C | T | 2 | a0001c0002t0010g0029 a0001c0002t0010g0117 |
3 | NA18951.hp1 NA18969.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.84-176C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132794234 | |||||||
| chr8:132794261 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0268 |
3 | HG02015.hp2 NA18940.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.84-149A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132794261 | |||||||
| chr8:132794289 | C | T | 1 | a0001c0002t0005g0019 | 3 | HG02886.hp1 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.84-121C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 2/20 | chr8 | 132794289 | |||||||
| chr8:132794659 | T | C | 1 | a0001c0001t0004g0072 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.256-74T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 3/20 | chr8 | 132794659 | |||||||
| chr8:132794938 | GTATT | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+122_340+125del others(4): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132794938 | |||||||
| chr8:132795348 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.340+531T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132795348 | |||||||
| chr8:132796169 | A | G | 156 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(153): Show |
208 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.340+1352A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132796169 | |||||||
| chr8:132796608 | C | T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0162 |
2 | HG02074.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.340+1791C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132796608 | |||||||
| chr8:132796638 | G | T | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.340+1821G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132796638 | |||||||
| chr8:132796895 | A | G | 6 | a0001c0002t0005g0226 a0001c0002t0005g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01943.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.341-1877A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132796895 | |||||||
| chr8:132797022 | A | C | 1 | a0001c0001t0003g0056 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.341-1750A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132797022 | |||||||
| chr8:132797269 | G | A | 3 | a0001c0001t0003g0032 a0001c0001t0003g0142 a0001c0001t0003g0143 |
4 | HG02965.hp2 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-1503G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132797269 | |||||||
| chr8:132797657 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
7 | NA18945.hp2 NA18980.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-1115A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132797657 | |||||||
| chr8:132797729 | T | G | 123 | a0001c0001t0004g0004 a0001c0001t0004g0005 a0001c0001t0004g0023 others(120): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.341-1043T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132797729 | |||||||
| chr8:132798361 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.341-411A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132798361 | |||||||
| chr8:132798630 | T | C | 5 | a0001c0001t0004g0005 a0001c0001t0004g0023 a0001c0001t0004g0070 others(2): Show |
9 | NA18955.hp2 NA18963.hp1 NA18992.hp1 others(6): Show |
intron_variant | MODIFIER | c.341-142T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | chr8 | 132798630 | |||||||
| chr8:132798665 | TGCATTCC others(4): Show |
T | 1 | a0001c0001t0011g0160 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.341-101_341-91delC others(10): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr8 | 132798665 | ||||||
| chr8:132798872 | C | T | 1 | a0001c0002t0012g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.429+12C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 5/20 | chr8 | 132798872 | |||||||
| chr8:132799189 | T | A | 100 | a0001c0001t0003g0033 a0001c0001t0003g0144 a0001c0001t0003g0163 others(97): Show |
137 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.507+17T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132799189 | |||||||
| chr8:132799325 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.507+153C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132799325 | |||||||
| chr8:132799481 | G | T | 1 | a0001c0003t0006g0207 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.507+309G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132799481 | |||||||
| chr8:132799748 | A | G | 3 | a0001c0002t0002g0120 a0001c0002t0002g0125 a0001c0002t0002g0126 |
3 | HG01167.hp2 HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.507+576A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132799748 | |||||||
| chr8:132800041 | A | AT | 7 | a0001c0001t0001g0192 a0001c0001t0001g0269 a0001c0001t0004g0086 others(4): Show |
7 | HG01106.hp2 HG01109.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+886dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr8 | 132800041 | ||||||
| chr8:132800216 | T | C | 1 | a0001c0001t0003g0145 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.507+1044T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800216 | |||||||
| chr8:132800221 | G | A | 8 | a0001c0001t0003g0003 a0001c0001t0003g0038 a0001c0001t0003g0039 others(5): Show |
13 | HG02040.hp1 HG02132.hp2 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.507+1049G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800221 | |||||||
| chr8:132800275 | T | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+1103T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800275 | |||||||
| chr8:132800424 | A | T | 1 | a0001c0006t0003g0147 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.507+1252A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800424 | |||||||
| chr8:132800506 | A | AG | 60 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(57): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.507+1340dupG | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr8 | 132800506 | ||||||
| chr8:132800521 | G | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+1349G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800521 | |||||||
| chr8:132800613 | T | A | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.507+1441T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800613 | |||||||
| chr8:132800617 | C | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
109 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.507+1445C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800617 | |||||||
| chr8:132800686 | C | T | 1 | a0001c0002t0005g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.507+1514C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132800686 | |||||||
| chr8:132801069 | C | A | 1 | a0001c0001t0003g0142 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507+1897C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801069 | |||||||
| chr8:132801229 | C | A | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.507+2057C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801229 | |||||||
| chr8:132801391 | G | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.507+2219G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801391 | |||||||
| chr8:132801441 | G | A | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.507+2269G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801441 | |||||||
| chr8:132801571 | C | G | 1 | a0001c0002t0008g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.508-2248C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801571 | |||||||
| chr8:132801639 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.508-2180G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801639 | |||||||
| chr8:132801641 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.508-2178T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801641 | |||||||
| chr8:132801744 | G | A | 1 | a0001c0003t0006g0203 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.508-2075G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801744 | |||||||
| chr8:132801772 | CATAAAA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.508-2040_508-2035d others(8): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr8 | 132801772 | ||||||
| chr8:132801830 | T | C | 2 | a0001c0002t0005g0218 a0001c0002t0005g0219 |
2 | HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.508-1989T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801830 | |||||||
| chr8:132801843 | A | T | 1 | a0001c0002t0008g0124 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.508-1976A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132801843 | |||||||
| chr8:132802048 | G | A | 2 | a0001c0002t0002g0100 a0001c0002t0002g0103 |
2 | HG03491.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.508-1771G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802048 | |||||||
| chr8:132802144 | CT | C | 120 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0172 others(117): Show |
163 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.508-1662delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr8 | 132802144 | ||||||
| chr8:132802144 | CTT | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-1663_508-1662d others(4): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr8 | 132802144 | ||||||
| chr8:132802160 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.508-1659T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802160 | |||||||
| chr8:132802173 | C | T | 1 | a0001c0001t0004g0089 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.508-1646C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802173 | |||||||
| chr8:132802212 | T | G | 1 | a0001c0001t0015g0063 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.508-1607T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802212 | |||||||
| chr8:132802257 | A | G | 3 | a0001c0002t0005g0214 a0001c0002t0005g0215 a0001c0002t0005g0216 |
3 | HG02965.hp1 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.508-1562A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802257 | |||||||
| chr8:132802264 | T | G | 1 | a0001c0002t0002g0133 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.508-1555T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802264 | |||||||
| chr8:132802369 | C | T | 4 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0173 others(1): Show |
6 | HG02040.hp1 HG02132.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.508-1450C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802369 | |||||||
| chr8:132802397 | A | G | 5 | a0001c0001t0004g0154 a0001c0001t0009g0061 a0001c0001t0009g0062 others(2): Show |
5 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.508-1422A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802397 | |||||||
| chr8:132802492 | A | C | 1 | a0001c0001t0001g0279 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.508-1327A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802492 | |||||||
| chr8:132802545 | C | T | 1 | a0001c0009t0018g0247 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.508-1274C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802545 | |||||||
| chr8:132802568 | C | T | 1 | a0001c0001t0003g0164 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.508-1251C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802568 | |||||||
| chr8:132802822 | C | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-997C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132802822 | |||||||
| chr8:132803228 | C | T | 1 | a0001c0001t0003g0037 | 2 | HG00558.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.508-591C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132803228 | |||||||
| chr8:132803233 | G | A | 1 | a0001c0001t0016g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.508-586G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132803233 | |||||||
| chr8:132803331 | A | G | 113 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(110): Show |
155 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.508-488A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132803331 | |||||||
| chr8:132803426 | T | C | 31 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(28): Show |
41 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.508-393T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132803426 | |||||||
| chr8:132803481 | G | A | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.508-338G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132803481 | |||||||
| chr8:132803529 | T | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.508-290T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132803529 | |||||||
| chr8:132803626 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
107 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.508-193A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 6/20 | chr8 | 132803626 | |||||||
| chr8:132804276 | A | C | 1 | a0001c0002t0002g0116 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.721+244A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 7/20 | chr8 | 132804276 | |||||||
| chr8:132804330 | G | GT | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.722-279dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr8 | 132804330 | ||||||
| chr8:132804488 | G | T | 7 | a0001c0001t0001g0050 a0001c0001t0001g0241 a0001c0001t0001g0263 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.722-127G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 7/20 | chr8 | 132804488 | |||||||
| chr8:132805025 | T | C | 1 | a0001c0001t0003g0139 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.847+285T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132805025 | |||||||
| chr8:132805172 | C | T | 1 | a0001c0002t0002g0115 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.847+432C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132805172 | |||||||
| chr8:132805387 | G | T | 1 | a0001c0002t0002g0132 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.847+647G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132805387 | |||||||
| chr8:132805762 | T | C | 1 | a0001c0001t0011g0160 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.847+1022T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132805762 | |||||||
| chr8:132805868 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.847+1128C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132805868 | |||||||
| chr8:132805976 | T | C | 1 | a0001c0001t0003g0052 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.847+1236T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132805976 | |||||||
| chr8:132806007 | T | C | 1 | a0001c0002t0010g0117 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.847+1267T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806007 | |||||||
| chr8:132806119 | C | T | 1 | a0001c0002t0020g0095 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.847+1379C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806119 | |||||||
| chr8:132806280 | C | G | 1 | a0001c0001t0003g0153 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.847+1540C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806280 | |||||||
| chr8:132806371 | C | T | 10 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG00558.hp2 HG00673.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.847+1631C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806371 | |||||||
| chr8:132806415 | C | T | 11 | a0001c0001t0001g0261 a0001c0001t0003g0032 a0001c0001t0003g0142 others(8): Show |
12 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.847+1675C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806415 | |||||||
| chr8:132806614 | A | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.847+1874A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806614 | |||||||
| chr8:132806822 | C | T | 1 | a0001c0002t0005g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.847+2082C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806822 | |||||||
| chr8:132806830 | A | T | 96 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(93): Show |
132 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.847+2090A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806830 | |||||||
| chr8:132806865 | A | G | 1 | a0001c0002t0002g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.847+2125A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806865 | |||||||
| chr8:132806901 | C | T | 1 | a0001c0001t0004g0085 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.847+2161C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132806901 | |||||||
| chr8:132807010 | T | A | 1 | a0001c0001t0011g0159 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.847+2270T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807010 | |||||||
| chr8:132807191 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.847+2451T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807191 | |||||||
| chr8:132807215 | C | T | 1 | a0001c0002t0005g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.847+2475C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807215 | |||||||
| chr8:132807284 | A | G | 60 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(57): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.847+2544A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807284 | |||||||
| chr8:132807293 | G | A | 1 | a0001c0002t0002g0026 | 2 | NA18943.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.847+2553G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807293 | |||||||
| chr8:132807389 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+2649A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807389 | |||||||
| chr8:132807509 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.847+2769A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807509 | |||||||
| chr8:132807563 | T | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.847+2823T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807563 | |||||||
| chr8:132807943 | C | G | 1 | a0001c0002t0002g0128 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.848-3103C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132807943 | |||||||
| chr8:132808035 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
8 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-3011C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808035 | |||||||
| chr8:132808077 | A | G | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.848-2969A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808077 | |||||||
| chr8:132808081 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.848-2965A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808081 | |||||||
| chr8:132808271 | A | G | 1 | a0001c0002t0002g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.848-2775A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808271 | |||||||
| chr8:132808361 | G | A | 7 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | NA18951.hp2 NA18992.hp2 NA19006.hp1 others(4): Show |
intron_variant | MODIFIER | c.848-2685G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808361 | |||||||
| chr8:132808422 | T | A | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-2624T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808422 | |||||||
| chr8:132808526 | T | C | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-2520T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808526 | |||||||
| chr8:132808816 | CT | C | 122 | a0001c0001t0001g0041 a0001c0001t0001g0171 a0001c0001t0001g0190 others(119): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.848-2214delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr8 | 132808816 | ||||||
| chr8:132808832 | T | A | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.848-2214T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808832 | |||||||
| chr8:132808844 | T | C | 1 | a0001c0002t0002g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.848-2202T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808844 | |||||||
| chr8:132808954 | A | C | 31 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(28): Show |
41 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.848-2092A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808954 | |||||||
| chr8:132808962 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.848-2084C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132808962 | |||||||
| chr8:132809130 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.848-1916A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132809130 | |||||||
| chr8:132809154 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
107 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.848-1892T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132809154 | |||||||
| chr8:132809731 | AT | A | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.848-1314delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132809731 | |||||||
| chr8:132809789 | A | G | 1 | a0001c0001t0004g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.848-1257A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132809789 | |||||||
| chr8:132809871 | G | A | 2 | a0001c0003t0006g0207 a0001c0003t0006g0212 |
2 | NA18978.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.848-1175G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132809871 | |||||||
| chr8:132810049 | C | CT | 60 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(57): Show |
91 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.848-984dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr8 | 132810049 | ||||||
| chr8:132810086 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.848-960C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132810086 | |||||||
| chr8:132810211 | T | C | 1 | a0001c0001t0004g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.848-835T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132810211 | |||||||
| chr8:132810290 | C | G | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.848-756C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132810290 | |||||||
| chr8:132810334 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.848-712G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132810334 | |||||||
| chr8:132810673 | T | C | 1 | a0001c0004t0002g0104 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.848-373T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 8/20 | chr8 | 132810673 | |||||||
| chr8:132811959 | A | G | 1 | a0001c0002t0002g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.930+831A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132811959 | |||||||
| chr8:132812132 | C | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.930+1004C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132812132 | |||||||
| chr8:132812230 | A | G | 3 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0167 |
3 | HG00280.hp2 HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.930+1102A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132812230 | |||||||
| chr8:132812477 | T | C | 1 | a0001c0002t0005g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.930+1349T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132812477 | |||||||
| chr8:132812759 | A | G | 1 | a0001c0002t0002g0113 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.930+1631A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132812759 | |||||||
| chr8:132813251 | A | G | 31 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(28): Show |
41 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.931-1386A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132813251 | |||||||
| chr8:132813279 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.931-1358A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132813279 | |||||||
| chr8:132813494 | A | G | 1 | a0001c0002t0005g0219 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.931-1143A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132813494 | |||||||
| chr8:132813701 | A | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.931-936A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132813701 | |||||||
| chr8:132813980 | G | GT | 12 | a0001c0001t0004g0005 a0001c0001t0004g0023 a0001c0001t0004g0024 others(9): Show |
18 | HG00621.hp1 HG02602.hp2 HG03471.hp1 others(15): Show |
intron_variant | MODIFIER | c.931-647dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr8 | 132813980 | ||||||
| chr8:132814163 | A | G | 1 | a0001c0002t0002g0102 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.931-474A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132814163 | |||||||
| chr8:132814176 | A | T | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.931-461A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132814176 | |||||||
| chr8:132814305 | G | A | 1 | a0001c0001t0004g0189 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.931-332G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132814305 | |||||||
| chr8:132814396 | A | G | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.931-241A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 9/20 | chr8 | 132814396 | |||||||
| chr8:132815045 | A | G | 2 | a0001c0001t0015g0063 a0001c0001t0016g0183 |
2 | HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1183+156A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132815045 | |||||||
| chr8:132815340 | GA | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0270 a0001c0001t0001g0284 others(1): Show |
6 | HG02004.hp1 NA18953.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183+460delA | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr8 | 132815340 | ||||||
| chr8:132815345 | A | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0270 a0001c0001t0001g0284 others(1): Show |
6 | HG02004.hp1 NA18953.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183+456A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132815345 | |||||||
| chr8:132815347 | A | G | 6 | a0001c0002t0005g0226 a0001c0002t0005g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01943.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183+458A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132815347 | |||||||
| chr8:132815817 | A | G | 59 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1183+928A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132815817 | |||||||
| chr8:132816066 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
99 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184-822A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132816066 | |||||||
| chr8:132816109 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1184-779C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132816109 | |||||||
| chr8:132816136 | A | T | 2 | a0001c0001t0003g0022 a0001c0001t0003g0056 |
3 | HG00140.hp2 HG02293.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1184-752A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132816136 | |||||||
| chr8:132816325 | AT | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184-551delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr8 | 132816325 | ||||||
| chr8:132816376 | G | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0239 |
3 | HG02976.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1184-512G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132816376 | |||||||
| chr8:132816464 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1184-424T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132816464 | |||||||
| chr8:132816521 | A | T | 1 | a0001c0002t0019g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1184-367A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132816521 | |||||||
| chr8:132816574 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1184-314A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 10/20 | chr8 | 132816574 | |||||||
| chr8:132817191 | T | C | 1 | a0001c0002t0002g0090 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1372+115T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 11/20 | chr8 | 132817191 | |||||||
| chr8:132817608 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1579+63T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132817608 | |||||||
| chr8:132817714 | T | G | 96 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(93): Show |
132 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1579+169T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132817714 | |||||||
| chr8:132817732 | A | G | 1 | a0001c0002t0012g0184 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1579+187A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132817732 | |||||||
| chr8:132817779 | A | G | 2 | a0001c0001t0003g0054 a0001c0001t0003g0162 |
2 | HG02074.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1579+234A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132817779 | |||||||
| chr8:132817791 | C | G | 1 | a0001c0003t0006g0206 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1579+246C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132817791 | |||||||
| chr8:132817845 | G | A | 1 | a0001c0001t0004g0075 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1579+300G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132817845 | |||||||
| chr8:132818098 | T | C | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1579+553T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818098 | |||||||
| chr8:132818137 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1579+592T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818137 | |||||||
| chr8:132818237 | A | G | 1 | a0001c0002t0002g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1579+692A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818237 | |||||||
| chr8:132818388 | C | T | 60 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(57): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1579+843C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818388 | |||||||
| chr8:132818459 | T | C | 3 | a0001c0002t0005g0214 a0001c0002t0005g0233 a0001c0002t0005g0234 |
3 | HG02976.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1579+914T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818459 | |||||||
| chr8:132818553 | G | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1579+1008G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818553 | |||||||
| chr8:132818638 | A | G | 3 | a0001c0002t0005g0235 a0001c0002t0005g0236 a0001c0002t0005g0238 |
3 | HG00639.hp2 HG01167.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1579+1093A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818638 | |||||||
| chr8:132818786 | C | T | 1 | a0001c0002t0002g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1579+1241C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818786 | |||||||
| chr8:132818984 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0239 |
3 | HG02976.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1579+1439G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132818984 | |||||||
| chr8:132819053 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1579+1508G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819053 | |||||||
| chr8:132819054 | A | T | 1 | a0001c0002t0019g0131 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1579+1509A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819054 | |||||||
| chr8:132819112 | G | C | 1 | a0001c0001t0016g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1579+1567G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819112 | |||||||
| chr8:132819196 | A | G | 1 | a0001c0002t0005g0227 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1579+1651A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819196 | |||||||
| chr8:132819238 | G | A | 59 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(56): Show |
88 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.1579+1693G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819238 | |||||||
| chr8:132819496 | C | T | 1 | a0001c0001t0003g0151 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1579+1951C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819496 | |||||||
| chr8:132819528 | C | T | 3 | a0001c0002t0005g0227 a0001c0002t0005g0229 a0001c0002t0005g0230 |
3 | HG03130.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1579+1983C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819528 | |||||||
| chr8:132819700 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1579+2155A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132819700 | |||||||
| chr8:132820241 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1579+2696T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820241 | |||||||
| chr8:132820462 | G | A | 2 | a0001c0002t0005g0233 a0001c0002t0005g0234 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1579+2917G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820462 | |||||||
| chr8:132820655 | T | A | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579+3110T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820655 | |||||||
| chr8:132820713 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 |
5 | HG01123.hp2 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1579+3168T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820713 | |||||||
| chr8:132820747 | A | G | 1 | a0001c0001t0009g0155 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1579+3202A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820747 | |||||||
| chr8:132820776 | A | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0174 others(17): Show |
24 | HG00323.hp1 HG00597.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.1580-3228A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820776 | |||||||
| chr8:132820798 | G | A | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1580-3206G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820798 | |||||||
| chr8:132820881 | T | C | 1 | a0001c0002t0002g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1580-3123T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820881 | |||||||
| chr8:132820959 | A | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
22 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1580-3045A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132820959 | |||||||
| chr8:132821017 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1580-2987T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821017 | |||||||
| chr8:132821052 | C | T | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1580-2952C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821052 | |||||||
| chr8:132821078 | G | A | 1 | a0001c0002t0002g0113 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1580-2926G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821078 | |||||||
| chr8:132821082 | C | T | 2 | a0001c0007t0001g0059 a0001c0007t0001g0060 |
2 | HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1580-2922C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821082 | |||||||
| chr8:132821190 | T | G | 12 | a0001c0002t0005g0017 a0001c0002t0005g0044 a0001c0002t0005g0045 others(9): Show |
16 | HG00733.hp2 HG01099.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1580-2814T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821190 | |||||||
| chr8:132821217 | ATTACATA others(5): Show |
A | 1 | a0001c0002t0002g0115 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1580-2773_1580-276 others(16): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr8 | 132821217 | ||||||
| chr8:132821227 | T | A | 1 | a0001c0001t0003g0138 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1580-2777T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821227 | |||||||
| chr8:132821233 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1580-2771C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821233 | |||||||
| chr8:132821616 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1580-2388G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821616 | |||||||
| chr8:132821915 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1580-2089C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132821915 | |||||||
| chr8:132822257 | G | A | 1 | a0001c0001t0004g0025 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1580-1747G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132822257 | |||||||
| chr8:132822636 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1580-1368A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132822636 | |||||||
| chr8:132822696 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1580-1308T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132822696 | |||||||
| chr8:132822710 | A | G | 2 | a0001c0002t0005g0218 a0001c0002t0005g0219 |
2 | HG00738.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1580-1294A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132822710 | |||||||
| chr8:132822903 | CAT | C | 32 | a0001c0001t0003g0143 a0001c0001t0004g0004 a0001c0001t0004g0005 others(29): Show |
41 | HG00621.hp1 HG00735.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.1580-1100_1580-109 others(6): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132822903 | |||||||
| chr8:132822916 | T | C | 1 | a0001c0005t0001g0251 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1580-1088T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132822916 | |||||||
| chr8:132823109 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1580-895A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823109 | |||||||
| chr8:132823153 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1580-851T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823153 | |||||||
| chr8:132823196 | G | A | 1 | a0001c0004t0002g0104 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1580-808G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823196 | |||||||
| chr8:132823304 | G | C | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1580-700G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823304 | |||||||
| chr8:132823590 | A | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1580-414A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823590 | |||||||
| chr8:132823746 | C | T | 1 | a0001c0003t0006g0211 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1580-258C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823746 | |||||||
| chr8:132823812 | A | G | 1 | a0001c0002t0005g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1580-192A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823812 | |||||||
| chr8:132823853 | G | T | 59 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1580-151G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823853 | |||||||
| chr8:132823900 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1580-104A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823900 | |||||||
| chr8:132823961 | A | C | 2 | a0001c0002t0002g0096 a0001c0002t0002g0116 |
2 | HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1580-43A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 12/20 | chr8 | 132823961 | |||||||
| chr8:132824095 | A | G | 1 | a0001c0002t0005g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1636+35A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824095 | |||||||
| chr8:132824187 | C | T | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1636+127C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824187 | |||||||
| chr8:132824422 | A | G | 2 | a0001c0004t0002g0104 a0001c0004t0002g0112 |
2 | HG00639.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1636+362A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824422 | |||||||
| chr8:132824532 | T | C | 1 | a0001c0001t0003g0164 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1636+472T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824532 | |||||||
| chr8:132824660 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1636+600T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824660 | |||||||
| chr8:132824710 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1637-554T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824710 | |||||||
| chr8:132824738 | T | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1637-526T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824738 | |||||||
| chr8:132824864 | G | GT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(164): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1637-388dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr8 | 132824864 | ||||||
| chr8:132824887 | A | G | 12 | a0001c0002t0005g0017 a0001c0002t0005g0044 a0001c0002t0005g0045 others(9): Show |
16 | HG00733.hp2 HG01099.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1637-377A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824887 | |||||||
| chr8:132824970 | C | A | 1 | a0001c0001t0004g0025 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1637-294C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 13/20 | chr8 | 132824970 | |||||||
| chr8:132825397 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1744+26C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825397 | |||||||
| chr8:132825431 | C | T | 1 | a0001c0004t0002g0028 | 2 | HG01358.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1744+60C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825431 | |||||||
| chr8:132825477 | G | C | 1 | a0001c0003t0006g0212 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1744+106G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825477 | |||||||
| chr8:132825557 | A | G | 114 | a0001c0001t0001g0188 a0001c0002t0002g0002 a0001c0002t0002g0006 others(111): Show |
156 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1744+186A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825557 | |||||||
| chr8:132825594 | A | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1744+223A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825594 | |||||||
| chr8:132825810 | A | G | 1 | a0001c0001t0003g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1744+439A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825810 | |||||||
| chr8:132825896 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1744+525C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825896 | |||||||
| chr8:132825973 | T | A | 3 | a0001c0002t0005g0017 a0001c0002t0005g0045 a0001c0002t0005g0232 |
6 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1744+602T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132825973 | |||||||
| chr8:132826057 | C | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(64): Show |
96 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.1744+686C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826057 | |||||||
| chr8:132826120 | T | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1744+749T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826120 | |||||||
| chr8:132826288 | A | G | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1744+917A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826288 | |||||||
| chr8:132826297 | A | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1744+926A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826297 | |||||||
| chr8:132826314 | A | T | 1 | a0001c0002t0002g0092 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1744+943A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826314 | |||||||
| chr8:132826413 | T | C | 1 | a0001c0002t0007g0187 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1744+1042T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826413 | |||||||
| chr8:132826418 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1744+1047C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826418 | |||||||
| chr8:132826446 | G | A | 2 | a0001c0001t0003g0022 a0001c0001t0003g0056 |
3 | HG00140.hp2 HG02293.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1744+1075G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826446 | |||||||
| chr8:132826732 | T | C | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1744+1361T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132826732 | |||||||
| chr8:132827085 | GCT | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+1715_1744+171 others(6): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827085 | |||||||
| chr8:132827088 | T | A | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744+1717T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827088 | |||||||
| chr8:132827089 | T | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1744+1718T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827089 | |||||||
| chr8:132827096 | A | G | 6 | a0001c0001t0004g0071 a0001c0001t0004g0072 a0001c0001t0004g0079 others(3): Show |
6 | HG01074.hp1 HG01099.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1744+1725A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827096 | |||||||
| chr8:132827379 | A | G | 1 | a0001c0001t0004g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1744+2008A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827379 | |||||||
| chr8:132827545 | A | G | 1 | a0001c0001t0001g0265 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1744+2174A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827545 | |||||||
| chr8:132827604 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1744+2233A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827604 | |||||||
| chr8:132827626 | C | T | 1 | a0001c0002t0002g0111 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1744+2255C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827626 | |||||||
| chr8:132827697 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1744+2326C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827697 | |||||||
| chr8:132827737 | C | T | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1744+2366C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132827737 | |||||||
| chr8:132828013 | A | T | 1 | a0001c0001t0003g0167 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1744+2642A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828013 | |||||||
| chr8:132828016 | G | T | 1 | a0001c0003t0006g0205 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1744+2645G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828016 | |||||||
| chr8:132828207 | A | G | 1 | a0001c0002t0002g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1744+2836A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828207 | |||||||
| chr8:132828209 | A | G | 12 | a0001c0002t0005g0017 a0001c0002t0005g0044 a0001c0002t0005g0045 others(9): Show |
16 | HG00733.hp2 HG01099.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1744+2838A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828209 | |||||||
| chr8:132828358 | G | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1744+2987G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828358 | |||||||
| chr8:132828361 | C | G | 20 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0174 others(17): Show |
24 | HG00323.hp1 HG00597.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.1744+2990C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828361 | |||||||
| chr8:132828625 | T | C | 1 | a0001c0002t0008g0105 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1744+3254T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828625 | |||||||
| chr8:132828855 | A | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1745-3380A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828855 | |||||||
| chr8:132828858 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1745-3377A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828858 | |||||||
| chr8:132828987 | T | C | 2 | a0001c0002t0005g0233 a0001c0002t0005g0234 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1745-3248T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132828987 | |||||||
| chr8:132829095 | A | T | 1 | a0001c0002t0002g0109 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1745-3140A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829095 | |||||||
| chr8:132829305 | C | T | 1 | a0001c0001t0003g0141 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1745-2930C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829305 | |||||||
| chr8:132829317 | C | T | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1745-2918C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829317 | |||||||
| chr8:132829338 | G | A | 1 | a0001c0002t0005g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1745-2897G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829338 | |||||||
| chr8:132829391 | T | C | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1745-2844T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829391 | |||||||
| chr8:132829418 | T | C | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1745-2817T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829418 | |||||||
| chr8:132829522 | C | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1745-2713C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829522 | |||||||
| chr8:132829924 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1745-2311C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829924 | |||||||
| chr8:132829945 | C | T | 1 | a0001c0002t0002g0123 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1745-2290C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829945 | |||||||
| chr8:132829970 | A | G | 3 | a0001c0001t0001g0020 a0001c0001t0001g0270 a0001c0001t0001g0284 |
5 | NA18953.hp1 NA19010.hp2 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1745-2265A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829970 | |||||||
| chr8:132829983 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
95 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1745-2252T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132829983 | |||||||
| chr8:132830079 | G | A | 7 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | NA18951.hp2 NA18992.hp2 NA19006.hp1 others(4): Show |
intron_variant | MODIFIER | c.1745-2156G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830079 | |||||||
| chr8:132830219 | T | C | 76 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
107 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1745-2016T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830219 | |||||||
| chr8:132830249 | C | G | 1 | a0001c0001t0001g0276 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1745-1986C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830249 | |||||||
| chr8:132830249 | C | T | 10 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0037 others(7): Show |
13 | HG00558.hp2 HG00673.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.1745-1986C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830249 | |||||||
| chr8:132830396 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1745-1839A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830396 | |||||||
| chr8:132830437 | A | G | 1 | a0001c0002t0002g0098 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1745-1798A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830437 | |||||||
| chr8:132830548 | T | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1745-1687T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830548 | |||||||
| chr8:132830613 | T | G | 22 | a0001c0001t0004g0005 a0001c0001t0004g0023 a0001c0001t0004g0024 others(19): Show |
28 | HG00621.hp1 HG01074.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.1745-1622T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830613 | |||||||
| chr8:132830961 | C | T | 1 | a0001c0001t0004g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1745-1274C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830961 | |||||||
| chr8:132830986 | C | T | 1 | a0001c0001t0009g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1745-1249C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132830986 | |||||||
| chr8:132831068 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1745-1167C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831068 | |||||||
| chr8:132831090 | C | T | 6 | a0001c0002t0005g0226 a0001c0002t0005g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01943.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1745-1145C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831090 | |||||||
| chr8:132831092 | A | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0239 |
3 | HG02976.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1745-1143A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831092 | |||||||
| chr8:132831094 | G | A | 1 | a0001c0002t0005g0215 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1745-1141G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831094 | |||||||
| chr8:132831222 | T | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
279 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.1745-1013T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831222 | |||||||
| chr8:132831282 | C | G | 31 | a0001c0002t0005g0016 a0001c0002t0005g0017 a0001c0002t0005g0018 others(28): Show |
41 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1745-953C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831282 | |||||||
| chr8:132831357 | AC | A | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1745-873delC | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr8 | 132831357 | ||||||
| chr8:132831407 | A | AGG | 3 | a0001c0001t0001g0049 a0001c0001t0001g0246 a0001c0001t0001g0252 |
4 | HG01070.hp2 HG01109.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.1745-827_1745-826i others(4): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr8 | 132831407 | ||||||
| chr8:132831415 | A | G | 1 | a0001c0001t0004g0023 | 2 | NA18963.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1745-820A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831415 | |||||||
| chr8:132831591 | C | T | 2 | a0001c0002t0002g0007 a0001c0002t0013g0007 |
4 | HG00558.hp1 HG00609.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.1745-644C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831591 | |||||||
| chr8:132831628 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1745-607G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831628 | |||||||
| chr8:132831630 | A | G | 1 | a0001c0001t0003g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1745-605A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831630 | |||||||
| chr8:132831729 | A | T | 1 | a0001c0002t0005g0224 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1745-506A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831729 | |||||||
| chr8:132831988 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1745-247A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132831988 | |||||||
| chr8:132832012 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1745-223C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132832012 | |||||||
| chr8:132832039 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1745-196G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132832039 | |||||||
| chr8:132832120 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1745-115C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 14/20 | chr8 | 132832120 | |||||||
| chr8:132832466 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1909+67C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132832466 | |||||||
| chr8:132832612 | A | G | 1 | a0002c0008t0004g0076 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1909+213A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132832612 | |||||||
| chr8:132832686 | G | A | 1 | a0001c0002t0005g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1909+287G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132832686 | |||||||
| chr8:132832716 | C | T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0162 |
2 | HG02074.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1909+317C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132832716 | |||||||
| chr8:132832743 | G | A | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1909+344G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132832743 | |||||||
| chr8:132833102 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1909+703G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833102 | |||||||
| chr8:132833127 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1909+728A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833127 | |||||||
| chr8:132833133 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(67): Show |
100 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1909+734A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833133 | |||||||
| chr8:132833191 | A | G | 47 | a0001c0001t0001g0285 a0001c0001t0003g0054 a0001c0001t0003g0162 others(44): Show |
66 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.1909+792A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833191 | |||||||
| chr8:132833242 | C | T | 3 | a0001c0001t0001g0188 a0001c0007t0001g0059 a0001c0007t0001g0060 |
3 | HG02886.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1909+843C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833242 | |||||||
| chr8:132833316 | T | C | 1 | a0001c0005t0001g0253 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1909+917T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833316 | |||||||
| chr8:132833461 | G | A | 7 | a0001c0003t0006g0043 a0001c0003t0006g0200 a0001c0003t0006g0206 others(4): Show |
8 | HG00408.hp2 NA18954.hp2 NA18978.hp2 others(5): Show |
intron_variant | MODIFIER | c.1909+1062G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833461 | |||||||
| chr8:132833468 | C | T | 1 | a0001c0002t0005g0221 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1909+1069C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833468 | |||||||
| chr8:132833473 | C | G | 1 | a0001c0001t0014g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1909+1074C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833473 | |||||||
| chr8:132833491 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1909+1092A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833491 | |||||||
| chr8:132833582 | A | G | 94 | a0001c0001t0001g0046 a0001c0001t0001g0239 a0001c0002t0002g0002 others(91): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1909+1183A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833582 | |||||||
| chr8:132833845 | C | T | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1909+1446C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132833845 | |||||||
| chr8:132834116 | A | T | 1 | a0001c0002t0005g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1909+1717A>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834116 | |||||||
| chr8:132834156 | C | G | 1 | a0001c0001t0004g0081 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1909+1757C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834156 | |||||||
| chr8:132834192 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1909+1793G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834192 | |||||||
| chr8:132834400 | C | T | 90 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(87): Show |
123 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1909+2001C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834400 | |||||||
| chr8:132834449 | T | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1909+2050T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834449 | |||||||
| chr8:132834450 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1909+2051C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834450 | |||||||
| chr8:132834517 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1910-2023A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834517 | |||||||
| chr8:132834621 | G | A | 1 | a0001c0001t0016g0183 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1910-1919G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834621 | |||||||
| chr8:132834680 | C | T | 1 | a0001c0002t0005g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1910-1860C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834680 | |||||||
| chr8:132834965 | T | C | 1 | a0001c0002t0005g0228 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1910-1575T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132834965 | |||||||
| chr8:132835018 | CAT | C | 2 | a0001c0002t0002g0026 a0001c0002t0002g0108 |
3 | NA18943.hp2 NA19001.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1910-1521_1910-152 others(6): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835018 | |||||||
| chr8:132835113 | C | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
2 | NA19009.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1910-1427C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835113 | |||||||
| chr8:132835125 | C | T | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1910-1415C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835125 | |||||||
| chr8:132835247 | T | C | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1910-1293T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835247 | |||||||
| chr8:132835300 | A | G | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1910-1240A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835300 | |||||||
| chr8:132835445 | C | G | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
124 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1910-1095C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835445 | |||||||
| chr8:132835565 | C | T | 6 | a0001c0002t0005g0226 a0001c0002t0005g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01943.hp2 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1910-975C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835565 | |||||||
| chr8:132835702 | C | T | 113 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(110): Show |
155 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1910-838C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835702 | |||||||
| chr8:132835735 | T | G | 2 | a0001c0002t0007g0055 a0001c0002t0007g0186 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1910-805T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835735 | |||||||
| chr8:132835906 | A | G | 1 | a0001c0002t0002g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1910-634A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132835906 | |||||||
| chr8:132835997 | GT | G | 22 | a0001c0001t0001g0188 a0001c0001t0003g0035 a0001c0001t0003g0037 others(19): Show |
30 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.1910-532delT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr8 | 132835997 | ||||||
| chr8:132836151 | G | A | 113 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(110): Show |
155 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1910-389G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132836151 | |||||||
| chr8:132836440 | G | A | 59 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(56): Show |
82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1910-100G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132836440 | |||||||
| chr8:132836479 | T | C | 1 | a0001c0002t0005g0231 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1910-61T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132836479 | |||||||
| chr8:132836531 | A | G | 2 | a0001c0001t0001g0048 a0001c0001t0001g0282 |
3 | HG00609.hp1 NA19001.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1910-9A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 15/20 | chr8 | 132836531 | |||||||
| chr8:132836758 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2091+37T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132836758 | |||||||
| chr8:132836882 | A | G | 1 | a0001c0001t0004g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2091+161A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132836882 | |||||||
| chr8:132836989 | A | G | 204 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(201): Show |
279 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.2091+268A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132836989 | |||||||
| chr8:132836998 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2091+277C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132836998 | |||||||
| chr8:132837169 | G | T | 4 | a0001c0003t0006g0015 a0001c0003t0006g0204 a0001c0003t0006g0205 others(1): Show |
6 | NA18985.hp2 NA18988.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.2091+448G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132837169 | |||||||
| chr8:132837186 | AG | A | 4 | a0001c0001t0003g0010 a0001c0001t0003g0033 a0001c0001t0003g0163 others(1): Show |
7 | HG01243.hp2 HG02145.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2091+467delG | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr8 | 132837186 | ||||||
| chr8:132837215 | CAGA | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2092-493_2092-491d others(5): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr8 | 132837215 | ||||||
| chr8:132837387 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2092-325C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132837387 | |||||||
| chr8:132837410 | G | C | 1 | a0001c0001t0003g0165 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2092-302G>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132837410 | |||||||
| chr8:132837517 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2092-195C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132837517 | |||||||
| chr8:132837565 | C | T | 1 | a0001c0001t0011g0160 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2092-147C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132837565 | |||||||
| chr8:132837600 | T | C | 1 | a0001c0001t0004g0025 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2092-112T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 16/20 | chr8 | 132837600 | |||||||
| chr8:132837882 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2191+71G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132837882 | |||||||
| chr8:132837897 | A | G | 1 | a0001c0002t0002g0109 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2191+86A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132837897 | |||||||
| chr8:132838034 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2191+223G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838034 | |||||||
| chr8:132838049 | A | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2191+238A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838049 | |||||||
| chr8:132838076 | A | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.2191+265A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838076 | |||||||
| chr8:132838312 | G | A | 1 | a0001c0002t0002g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2191+501G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838312 | |||||||
| chr8:132838385 | G | A | 1 | a0001c0002t0002g0133 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2191+574G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838385 | |||||||
| chr8:132838390 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2191+579G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838390 | |||||||
| chr8:132838492 | CCTT | C | 4 | a0001c0005t0001g0245 a0001c0005t0001g0251 a0001c0005t0001g0253 others(1): Show |
4 | HG02027.hp2 NA18954.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.2191+687_2191+689d others(5): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr8 | 132838492 | ||||||
| chr8:132838524 | A | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.2191+713A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838524 | |||||||
| chr8:132838600 | G | T | 2 | a0001c0001t0003g0054 a0001c0001t0003g0162 |
2 | HG02074.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2192-787G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838600 | |||||||
| chr8:132838624 | A | G | 1 | a0001c0002t0005g0217 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2192-763A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838624 | |||||||
| chr8:132838697 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2192-690A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838697 | |||||||
| chr8:132838877 | T | C | 1 | a0001c0006t0003g0146 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2192-510T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838877 | |||||||
| chr8:132838989 | A | G | 3 | a0001c0001t0003g0039 a0001c0001t0003g0173 a0001c0001t0003g0181 |
4 | HG02132.hp2 NA18949.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.2192-398A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132838989 | |||||||
| chr8:132839168 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2192-219T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 17/20 | chr8 | 132839168 | |||||||
| chr8:132839617 | C | T | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2387+35C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132839617 | |||||||
| chr8:132839633 | T | G | 1 | a0001c0002t0002g0129 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2387+51T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132839633 | |||||||
| chr8:132839750 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2387+168G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132839750 | |||||||
| chr8:132840008 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2387+426C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840008 | |||||||
| chr8:132840341 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2387+759C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840341 | |||||||
| chr8:132840346 | A | C | 3 | a0001c0002t0005g0017 a0001c0002t0005g0045 a0001c0002t0005g0232 |
6 | HG02451.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2387+764A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840346 | |||||||
| chr8:132840439 | A | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.2387+857A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840439 | |||||||
| chr8:132840457 | C | T | 1 | a0001c0002t0008g0027 | 2 | NA19005.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.2387+875C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840457 | |||||||
| chr8:132840559 | A | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.2387+977A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840559 | |||||||
| chr8:132840598 | A | G | 1 | a0001c0001t0004g0074 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2387+1016A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840598 | |||||||
| chr8:132840693 | C | A | 1 | a0001c0005t0001g0251 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2387+1111C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840693 | |||||||
| chr8:132840973 | C | T | 1 | a0001c0002t0005g0236 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2387+1391C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132840973 | |||||||
| chr8:132841055 | AC | A | 4 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0172 others(1): Show |
5 | HG01884.hp2 HG02622.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2388-1458delC | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr8 | 132841055 | ||||||
| chr8:132841197 | G | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2388-1318G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841197 | |||||||
| chr8:132841210 | T | G | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2388-1305T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841210 | |||||||
| chr8:132841222 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2388-1293T>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841222 | |||||||
| chr8:132841389 | T | C | 1 | a0001c0002t0002g0115 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2388-1126T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841389 | |||||||
| chr8:132841568 | A | G | 6 | a0001c0002t0005g0016 a0001c0002t0005g0218 a0001c0002t0005g0219 others(3): Show |
8 | HG00738.hp1 HG01081.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.2388-947A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841568 | |||||||
| chr8:132841919 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2388-596A>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841919 | |||||||
| chr8:132841920 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2388-595G>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841920 | |||||||
| chr8:132841927 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2388-588C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132841927 | |||||||
| chr8:132842158 | G | A | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2388-357G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132842158 | |||||||
| chr8:132842288 | A | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.2388-227A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132842288 | |||||||
| chr8:132842371 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2388-144G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | chr8 | 132842371 | |||||||
| chr8:132842469 | A | AT | 11 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(8): Show |
12 | HG01106.hp2 HG01123.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2388-33dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr8 | 132842469 | ||||||
| chr8:132842981 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2748+106A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132842981 | |||||||
| chr8:132843011 | A | AT | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2748+143dupT | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843011 | ||||||
| chr8:132843026 | C | G | 17 | a0001c0003t0006g0014 a0001c0003t0006g0015 a0001c0003t0006g0042 others(14): Show |
23 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.2748+151C>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843026 | |||||||
| chr8:132843190 | A | G | 1 | a0001c0002t0002g0240 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2748+315A>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843190 | |||||||
| chr8:132843282 | T | G | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2748+407T>G | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843282 | |||||||
| chr8:132843425 | T | C | 1 | a0001c0002t0002g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2748+550T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843425 | |||||||
| chr8:132843479 | C | T | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2748+604C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843479 | |||||||
| chr8:132843605 | T | TTG | 201 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(198): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2749-518_2749-517d others(4): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843605 | T | TTGTG | 22 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0170 others(19): Show |
22 | HG00733.hp2 HG00738.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.2749-520_2749-517d others(6): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843605 | T | TTGTGTG | 16 | a0001c0001t0001g0012 a0001c0001t0001g0157 a0001c0001t0004g0083 others(13): Show |
23 | HG01081.hp2 HG01256.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.2749-522_2749-517d others(8): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843605 | T | TTGTGTGT others(1): Show |
13 | a0001c0002t0005g0018 a0001c0002t0005g0019 a0001c0002t0005g0226 others(10): Show |
17 | HG00639.hp2 HG01167.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.2749-524_2749-517d others(10): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843605 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2749-526_2749-517d others(12): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843605 | TTG | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
7 | HG01884.hp2 HG02622.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2749-518_2749-517d others(4): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843605 | TTGTG | T | 5 | a0001c0002t0007g0013 a0001c0002t0007g0040 a0001c0002t0007g0055 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2749-520_2749-517d others(6): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843605 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0003g0164 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2749-526_2749-517d others(12): Show |
PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr8 | 132843605 | ||||||
| chr8:132843725 | G | A | 1 | a0001c0002t0008g0057 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2749-431G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843725 | |||||||
| chr8:132843830 | T | C | 8 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
9 | HG01106.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2749-326T>C | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843830 | |||||||
| chr8:132843943 | G | A | 1 | a0001c0002t0002g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2749-213G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 19/20 | chr8 | 132843943 | |||||||
| chr8:132844486 | C | T | 1 | a0001c0002t0002g0097 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2911+168C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 20/20 | chr8 | 132844486 | |||||||
| chr8:132844487 | G | A | 1 | a0001c0002t0002g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2911+169G>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 20/20 | chr8 | 132844487 | |||||||
| chr8:132844972 | C | A | 10 | a0001c0001t0003g0032 a0001c0001t0003g0142 a0001c0001t0003g0143 others(7): Show |
11 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.2911+654C>A | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 20/20 | chr8 | 132844972 | |||||||
| chr8:132845764 | C | T | 121 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0191 others(118): Show |
164 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.2912-17C>T | PHF20L1 | ENSG00000129292.21 | transcript | ENST00000395386.7 | protein_coding | 20/20 | chr8 | 132845764 |