Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55140 |
| ensemblid | ENSG00000134014.18 |
| hgncid | 20696 |
| symbol | ELP3 |
| name | elongator acetyltransferase complex subunit 3 |
| refseq_nuc | NM_018091.6 |
| refseq_prot | NP_060561.3 |
| ensembl_nuc | ENST00000256398.13 |
| ensembl_prot | ENSP00000256398.8 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 28093139 |
| end | 28191153 |
| strand | + |
| ver | v1.2 |
| region | chr8:28093139-28191153 |
| region5000 | chr8:28088139-28196153 |
| regionname0 | ELP3_chr8_28093139_28191153 |
| regionname5000 | ELP3_chr8_28088139_28196153 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 547 | 397 | 94 | 76 | 172 | 17 | 36 | 136 | ELP3_chr8_28088139_28196153 | ELP3 | MRQKR others(542): Show |
chr8 | 28088139 | 28196153 |
| a0002 | 0/0 | 547 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | MRQKR others(542): Show |
chr8 | 28088139 | 28196153 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1641 | 382 | 86 | 75 | 166 | 17 | 36 | ELP3_chr8_28088139_28196153 | ELP3 | ATGAG others(1636): Show |
chr8 | 28088139 | 28196153 | ||
| a0001c0002 | 0/0 | 1641 | 8 | 7 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | ATGAG others(1636): Show |
chr8 | 28088139 | 28196153 | ||
| a0001c0003 | 0/0 | 1641 | 6 | 0 | 0 | 6 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | ATGAG others(1636): Show |
chr8 | 28088139 | 28196153 | ||
| a0001c0004 | 0/0 | 1641 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | ATGAG others(1636): Show |
chr8 | 28088139 | 28196153 | ||
| a0002c0005 | 0/0 | 1641 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | ATGAG others(1636): Show |
chr8 | 28088139 | 28196153 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3148 | 111 | 40 | 5 | 54 | 2 | 9 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0002 | 0/0 | 3148 | 103 | 11 | 26 | 46 | 7 | 13 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0003 | 0/1 | 3149 | 75 | 18 | 28 | 9 | 7 | 12 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0004 | 0/0 | 3150 | 59 | 3 | 11 | 44 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3145): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0005 | 0/0 | 3154 | 9 | 0 | 5 | 4 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3149): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0006 | 0/0 | 3150 | 7 | 7 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3145): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0007 | 0/0 | 3150 | 6 | 6 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3145): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0010 | 0/0 | 3149 | 3 | 0 | 0 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0012 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0013 | 0/0 | 3149 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0014 | 0/0 | 3148 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0015 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0016 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0017 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0018 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0019 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3145): Show |
chr8 | 28088139 | 28196153 |
| a0001c0001t0020 | 0/0 | 3149 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3144): Show |
chr8 | 28088139 | 28196153 |
| a0001c0002t0001 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| a0001c0002t0009 | 0/0 | 3148 | 5 | 4 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| a0001c0002t0011 | 0/0 | 3148 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| a0001c0003t0008 | 0/0 | 3150 | 6 | 0 | 0 | 6 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3145): Show |
chr8 | 28088139 | 28196153 |
| a0001c0004t0001 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| a0002c0005t0002 | 0/0 | 3148 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | GGCTG others(3143): Show |
chr8 | 28088139 | 28196153 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0322 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 2 | 1 | 1 | 2 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0005 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0307 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0003 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0010g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0010g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0010g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0012g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0013g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0014g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0015g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0016g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0017g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0018g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0019g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0001t0020g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0009g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0002t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0003t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| a0002c0005t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0310 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | GBR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0038 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0038 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00323 | hp2 | a0002 | c0005 | t0002 | g0021 | EUR | FIN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00597 | hp1 | a0001 | c0003 | t0008 | g0111 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0334 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0328 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0320 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0326 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0315 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0269 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0335 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01243 | hp1 | a0001 | c0002 | t0009 | g0144 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0256 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0333 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0271 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0316 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0037 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0037 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0149 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0276 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0243 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01975 | hp1 | a0001 | c0001 | t0004 | g0254 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0237 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0252 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02015 | hp2 | a0001 | c0001 | t0020 | g0137 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02155 | hp2 | a0001 | c0001 | t0010 | g0331 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02257 | hp1 | a0001 | c0002 | t0011 | g0141 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0277 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0220 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0323 | AMR | PEL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0332 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0304 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0148 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0324 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0282 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02895 | hp1 | a0001 | c0002 | t0009 | g0142 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02965 | hp2 | a0001 | c0002 | t0009 | g0023 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0295 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0150 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0190 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03669 | hp2 | a0001 | c0001 | t0013 | g0329 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0312 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0336 | SAS | PJL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0292 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0321 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | BEB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0305 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | STU | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0140 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CHB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18612 | hp2 | a0001 | c0001 | t0010 | g0330 | EAS | CHB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18948 | hp2 | a0001 | c0001 | t0018 | g0030 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18951 | hp1 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18952 | hp1 | a0001 | c0001 | t0010 | g0165 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18965 | hp1 | a0001 | c0003 | t0008 | g0112 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18966 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18968 | hp1 | a0001 | c0003 | t0008 | g0110 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18974 | hp2 | a0001 | c0001 | t0016 | g0009 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18977 | hp1 | a0001 | c0001 | t0015 | g0309 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18987 | hp2 | a0001 | c0003 | t0008 | g0114 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18993 | hp2 | a0001 | c0001 | t0019 | g0266 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19000 | hp2 | a0001 | c0003 | t0008 | g0113 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19030 | hp2 | a0001 | c0002 | t0011 | g0146 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19076 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19085 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0041 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0221 | AFR | YRI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ASW | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ASW | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0325 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0005 | EUR | TSI | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18955 | hp1 | a0001 | c0003 | t0008 | g0109 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA20300 | hp2 | a0001 | c0002 | t0009 | g0023 | AFR | USA | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | LWK | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0307 | REF | REF | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0322 | REF | REF | ELP3_chr8_28088139_28196153 | ELP3 | chr8 | 28088139 | 28196153 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28106776 | A | T | 1 | a0002 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.322A>T | p.Ile108Leu | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/15 | 398/3148 | 322/1644 | 108/547 | chr8 | 28106776 | |||
| chr8:28191151 | A | C | 1 | a0001 | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
splice_region_variant | LOW | c.*1426A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | chr8 | 28191151 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28097289 | C | T | 1 | a0001c0003 | 6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
synonymous_variant | LOW | c.90C>T | p.His30His | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/15 | 166/3148 | 90/1644 | 30/547 | chr8 | 28097289 | |||
| chr8:28099858 | C | A | 2 | a0001c0002 a0001c0004 |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
synonymous_variant | LOW | c.150C>A | p.Gly50Gly | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/15 | 226/3148 | 150/1644 | 50/547 | chr8 | 28099858 | |||
| chr8:28160288 | C | T | 1 | a0001c0002 | 8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
synonymous_variant | LOW | c.1317C>T | p.Tyr439Tyr | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/15 | 1393/3148 | 1317/1644 | 439/547 | chr8 | 28160288 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28093153 | C | T | 3 | a0001c0001t0002 a0001c0001t0020 a0002c0005t0002 |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/15 | 62 | chr8 | 28093153 | ||||||
| chr8:28189774 | G | A | 1 | a0001c0001t0007 | 6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*49G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 49 | chr8 | 28189774 | ||||||
| chr8:28189905 | C | G | 7 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(4): Show |
79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*180C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 180 | chr8 | 28189905 | ||||||
| chr8:28189912 | C | T | 1 | a0001c0001t0019 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 187 | chr8 | 28189912 | ||||||
| chr8:28189930 | C | T | 1 | a0001c0001t0015 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*205C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 205 | chr8 | 28189930 | ||||||
| chr8:28190024 | G | A | 1 | a0001c0001t0012 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*299G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 299 | chr8 | 28190024 | ||||||
| chr8:28190087 | C | G | 1 | a0001c0001t0014 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 362 | chr8 | 28190087 | ||||||
| chr8:28190096 | A | AACTT | 1 | a0001c0001t0005 | 9 | HG01257.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*373_*376dupCTTA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 377 | INFO_REALIGN_3_PRIME | chr8 | 28190096 | |||||
| chr8:28190519 | T | C | 1 | a0001c0002t0011 | 2 | HG02257.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*794T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 794 | chr8 | 28190519 | ||||||
| chr8:28190573 | A | AT | 9 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0012 others(6): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*862dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 863 | INFO_REALIGN_3_PRIME | chr8 | 28190573 | |||||
| chr8:28190573 | A | ATT | 6 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(3): Show |
88 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*861_*862dupTT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 863 | INFO_REALIGN_3_PRIME | chr8 | 28190573 | |||||
| chr8:28190650 | C | T | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(2): Show |
77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*925C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 925 | chr8 | 28190650 | ||||||
| chr8:28190651 | G | C | 1 | a0001c0001t0016 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*926G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 926 | chr8 | 28190651 | ||||||
| chr8:28190839 | A | G | 1 | a0001c0001t0013 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 1114 | chr8 | 28190839 | ||||||
| chr8:28190849 | G | A | 2 | a0001c0002t0009 a0001c0002t0011 |
7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 1124 | chr8 | 28190849 | ||||||
| chr8:28191016 | T | C | 1 | a0001c0001t0006 | 7 | HG02055.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1291T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 15/15 | 1291 | chr8 | 28191016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:28093508 | G | A | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(111): Show |
133 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.19+275G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093508 | |||||||
| chr8:28093541 | C | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+308C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093541 | |||||||
| chr8:28093568 | G | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0039 others(4): Show |
7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+335G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093568 | |||||||
| chr8:28093644 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(83): Show |
101 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.19+411T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093644 | |||||||
| chr8:28093692 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0215 |
3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.19+459T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093692 | |||||||
| chr8:28093914 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.19+681A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28093914 | |||||||
| chr8:28094039 | C | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.19+806C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094039 | |||||||
| chr8:28094184 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(83): Show |
101 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.19+951C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094184 | |||||||
| chr8:28094199 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.19+966T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094199 | |||||||
| chr8:28094249 | A | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.19+1016A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094249 | |||||||
| chr8:28094303 | C | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.19+1070C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094303 | |||||||
| chr8:28094350 | T | C | 1 | a0001c0001t0020g0137 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.19+1117T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094350 | |||||||
| chr8:28094618 | G | GGAGGCT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.19+1403_19+1408dup others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 28094618 | ||||||
| chr8:28094641 | C | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+1408C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094641 | |||||||
| chr8:28094681 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.19+1448G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094681 | |||||||
| chr8:28094741 | C | CA | 3 | a0001c0001t0001g0216 a0001c0001t0002g0046 a0001c0001t0002g0047 |
3 | NA18978.hp2 NA19057.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.19+1513dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 28094741 | ||||||
| chr8:28094747 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.19+1514G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094747 | |||||||
| chr8:28094931 | A | G | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.19+1698A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094931 | |||||||
| chr8:28094976 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.19+1743A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28094976 | |||||||
| chr8:28095062 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.19+1829C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095062 | |||||||
| chr8:28095073 | CCTGTTAG others(4): Show |
C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.19+1844_19+1854del others(11): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr8 | 28095073 | ||||||
| chr8:28095358 | A | G | 24 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0020 others(21): Show |
28 | HG00323.hp2 HG01358.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.20-1861A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095358 | |||||||
| chr8:28095392 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20-1827G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095392 | |||||||
| chr8:28095504 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(3): Show |
11 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1715G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095504 | |||||||
| chr8:28095540 | G | T | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.20-1679G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095540 | |||||||
| chr8:28095579 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.20-1640T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095579 | |||||||
| chr8:28095758 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.20-1461G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095758 | |||||||
| chr8:28095762 | A | G | 1 | a0001c0001t0003g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.20-1457A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095762 | |||||||
| chr8:28095777 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(3): Show |
11 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.20-1442C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095777 | |||||||
| chr8:28095797 | A | C | 1 | a0001c0001t0003g0335 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-1422A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28095797 | |||||||
| chr8:28096039 | C | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-1180C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096039 | |||||||
| chr8:28096359 | G | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(104): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.20-860G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096359 | |||||||
| chr8:28096452 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.20-767C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096452 | |||||||
| chr8:28096589 | G | A | 1 | a0001c0001t0005g0220 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.20-630G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096589 | |||||||
| chr8:28096948 | C | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(104): Show |
126 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.20-271C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28096948 | |||||||
| chr8:28097108 | A | G | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-111A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28097108 | |||||||
| chr8:28097134 | C | T | 8 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(5): Show |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-85C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 1/14 | chr8 | 28097134 | |||||||
| chr8:28097398 | T | G | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.119+80T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097398 | |||||||
| chr8:28097405 | C | G | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.119+87C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097405 | |||||||
| chr8:28097449 | G | A | 1 | a0001c0001t0006g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.119+131G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097449 | |||||||
| chr8:28097460 | C | CT | 4 | a0001c0001t0001g0007 a0001c0001t0001g0108 a0001c0001t0002g0105 others(1): Show |
6 | HG02109.hp1 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+155dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28097460 | ||||||
| chr8:28097460 | CT | C | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(89): Show |
107 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.119+155delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28097460 | ||||||
| chr8:28097492 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.119+174G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097492 | |||||||
| chr8:28097495 | A | C | 1 | a0001c0001t0001g0213 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.119+177A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097495 | |||||||
| chr8:28097587 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0001t0001g0222 others(2): Show |
6 | HG03139.hp2 HG03195.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.119+269G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097587 | |||||||
| chr8:28097611 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.119+293C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097611 | |||||||
| chr8:28097685 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.119+367C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097685 | |||||||
| chr8:28097811 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.119+493C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097811 | |||||||
| chr8:28097887 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.119+569G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097887 | |||||||
| chr8:28097978 | T | G | 4 | a0001c0001t0001g0034 a0001c0001t0003g0284 a0001c0001t0003g0285 others(1): Show |
5 | HG02056.hp2 NA18954.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.119+660T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097978 | |||||||
| chr8:28097990 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.119+672G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28097990 | |||||||
| chr8:28098060 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.119+742C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098060 | |||||||
| chr8:28098091 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.119+773C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098091 | |||||||
| chr8:28098203 | AT | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.119+895delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28098203 | ||||||
| chr8:28098284 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0018g0030 |
2 | NA18948.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.119+966G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098284 | |||||||
| chr8:28098367 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.119+1049T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098367 | |||||||
| chr8:28098458 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.119+1140C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098458 | |||||||
| chr8:28098588 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0154 a0001c0001t0001g0155 others(7): Show |
16 | HG00558.hp1 HG02015.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.120-1240T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098588 | |||||||
| chr8:28098760 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.120-1068T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098760 | |||||||
| chr8:28098929 | ATG | A | 5 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0042 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.120-889_120-888del others(2): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr8 | 28098929 | ||||||
| chr8:28098934 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120-894T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28098934 | |||||||
| chr8:28099084 | C | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.120-744C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099084 | |||||||
| chr8:28099302 | C | G | 16 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0007g0147 others(13): Show |
17 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.120-526C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099302 | |||||||
| chr8:28099422 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.120-406A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099422 | |||||||
| chr8:28099515 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.120-313G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099515 | |||||||
| chr8:28099570 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.120-258T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099570 | |||||||
| chr8:28099593 | C | T | 1 | a0001c0001t0004g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.120-235C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099593 | |||||||
| chr8:28099655 | G | A | 1 | a0001c0001t0002g0018 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.120-173G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099655 | |||||||
| chr8:28099747 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120-81G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099747 | |||||||
| chr8:28099796 | A | G | 98 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0052 others(95): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.120-32A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 2/14 | chr8 | 28099796 | |||||||
| chr8:28100003 | G | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+37G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100003 | |||||||
| chr8:28100012 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.258+46C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100012 | |||||||
| chr8:28100039 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(203): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.258+73G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100039 | |||||||
| chr8:28100040 | C | G | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 |
3 | HG02056.hp2 NA18954.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.258+74C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100040 | |||||||
| chr8:28100404 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.258+438A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100404 | |||||||
| chr8:28100442 | A | C | 1 | a0001c0001t0003g0334 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258+476A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100442 | |||||||
| chr8:28100536 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.258+570C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100536 | |||||||
| chr8:28100543 | G | C | 1 | a0001c0001t0003g0287 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.258+577G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100543 | |||||||
| chr8:28100832 | A | G | 1 | a0001c0001t0004g0280 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.258+866A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28100832 | |||||||
| chr8:28101010 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0103 |
3 | HG01257.hp2 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.258+1044C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101010 | |||||||
| chr8:28101026 | A | C | 1 | a0001c0002t0011g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258+1060A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101026 | |||||||
| chr8:28101101 | TTTTG | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.258+1145_258+1148d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28101101 | ||||||
| chr8:28101132 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+1166T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101132 | |||||||
| chr8:28101166 | C | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+1200C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101166 | |||||||
| chr8:28101183 | C | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+1217C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101183 | |||||||
| chr8:28101207 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.258+1241G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101207 | |||||||
| chr8:28101219 | C | G | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.258+1253C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101219 | |||||||
| chr8:28101231 | G | A | 5 | a0001c0001t0004g0031 a0001c0001t0004g0225 a0001c0001t0004g0226 others(2): Show |
6 | HG02523.hp1 NA18941.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+1265G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101231 | |||||||
| chr8:28101314 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.258+1348A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101314 | |||||||
| chr8:28101345 | G | C | 2 | a0001c0001t0003g0288 a0001c0001t0003g0289 |
2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.258+1379G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101345 | |||||||
| chr8:28101549 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.258+1583A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101549 | |||||||
| chr8:28101590 | C | CT | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(244): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.258+1639dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28101590 | ||||||
| chr8:28101590 | C | CTT | 10 | a0001c0001t0001g0108 a0001c0001t0001g0162 a0001c0001t0001g0210 others(7): Show |
10 | HG01243.hp1 HG01952.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.258+1638_258+1639d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28101590 | ||||||
| chr8:28101608 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.258+1642C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101608 | |||||||
| chr8:28101643 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.258+1677A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101643 | |||||||
| chr8:28101823 | G | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.258+1857G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101823 | |||||||
| chr8:28101869 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+1903C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101869 | |||||||
| chr8:28101933 | A | G | 1 | a0001c0001t0003g0043 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258+1967A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28101933 | |||||||
| chr8:28102096 | G | A | 29 | a0001c0001t0001g0034 a0001c0001t0001g0293 a0001c0001t0003g0035 others(26): Show |
32 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.258+2130G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102096 | |||||||
| chr8:28102150 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.258+2184G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102150 | |||||||
| chr8:28102302 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.258+2336C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102302 | |||||||
| chr8:28102324 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.258+2358C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102324 | |||||||
| chr8:28102333 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258+2367A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102333 | |||||||
| chr8:28102472 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.258+2506A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102472 | |||||||
| chr8:28102647 | A | G | 1 | a0001c0001t0004g0279 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.258+2681A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102647 | |||||||
| chr8:28102768 | C | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.258+2802C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102768 | |||||||
| chr8:28102972 | C | G | 3 | a0001c0003t0008g0112 a0001c0003t0008g0113 a0001c0003t0008g0114 |
3 | NA18965.hp1 NA18987.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.258+3006C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28102972 | |||||||
| chr8:28103023 | A | T | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.258+3057A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103023 | |||||||
| chr8:28103043 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.258+3077G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103043 | |||||||
| chr8:28103118 | C | T | 1 | a0001c0001t0004g0278 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.258+3152C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103118 | |||||||
| chr8:28103167 | C | G | 1 | a0001c0001t0004g0277 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.258+3201C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103167 | |||||||
| chr8:28103169 | CAAAA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.258+3207_258+3210d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28103169 | ||||||
| chr8:28103173 | AAAAC | A | 6 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0224 others(3): Show |
7 | HG02055.hp2 HG02572.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+3231_258+3234d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28103173 | ||||||
| chr8:28103309 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.258+3343C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103309 | |||||||
| chr8:28103363 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-3350A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103363 | |||||||
| chr8:28103427 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.259-3286G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103427 | |||||||
| chr8:28103437 | C | T | 1 | a0001c0001t0005g0276 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.259-3276C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103437 | |||||||
| chr8:28103633 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.259-3080A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103633 | |||||||
| chr8:28103649 | G | C | 2 | a0001c0001t0003g0310 a0001c0001t0003g0311 |
2 | HG00099.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.259-3064G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103649 | |||||||
| chr8:28103713 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.259-3000C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103713 | |||||||
| chr8:28103935 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-2778C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28103935 | |||||||
| chr8:28104059 | T | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.259-2654T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104059 | |||||||
| chr8:28104160 | G | A | 14 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(11): Show |
15 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.259-2553G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104160 | |||||||
| chr8:28104362 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.259-2351C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104362 | |||||||
| chr8:28104600 | A | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.259-2113A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104600 | |||||||
| chr8:28104670 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.259-2043G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104670 | |||||||
| chr8:28104696 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.259-2017A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104696 | |||||||
| chr8:28104743 | G | T | 1 | a0001c0001t0002g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.259-1970G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104743 | |||||||
| chr8:28104990 | G | A | 68 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.259-1723G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28104990 | |||||||
| chr8:28105052 | T | G | 8 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(5): Show |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.259-1661T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105052 | |||||||
| chr8:28105219 | T | TA | 6 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0001t0001g0138 others(3): Show |
6 | HG02109.hp2 HG03098.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-1482dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28105219 | ||||||
| chr8:28105227 | A | AG | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.259-1486_259-1485i others(3): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105227 | |||||||
| chr8:28105314 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.259-1399C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105314 | |||||||
| chr8:28105347 | G | A | 1 | a0001c0001t0004g0231 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.259-1366G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105347 | |||||||
| chr8:28105370 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.259-1343A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105370 | |||||||
| chr8:28105384 | C | T | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-1329C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105384 | |||||||
| chr8:28105411 | T | A | 1 | a0001c0001t0003g0312 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.259-1302T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105411 | |||||||
| chr8:28105438 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.259-1275T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105438 | |||||||
| chr8:28105638 | C | T | 4 | a0001c0001t0001g0272 a0001c0001t0004g0273 a0001c0001t0004g0274 others(1): Show |
4 | NA18949.hp1 NA18953.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-1075C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105638 | |||||||
| chr8:28105687 | A | C | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.259-1026A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105687 | |||||||
| chr8:28105695 | C | T | 90 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(87): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.259-1018C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105695 | |||||||
| chr8:28105710 | C | T | 1 | a0001c0002t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.259-1003C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105710 | |||||||
| chr8:28105726 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-987T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105726 | |||||||
| chr8:28105825 | T | A | 1 | a0001c0001t0010g0165 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.259-888T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28105825 | |||||||
| chr8:28106040 | A | G | 1 | a0001c0001t0005g0271 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.259-673A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106040 | |||||||
| chr8:28106283 | G | A | 1 | a0001c0001t0007g0147 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.259-430G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106283 | |||||||
| chr8:28106307 | G | A | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-406G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106307 | |||||||
| chr8:28106356 | C | T | 1 | a0001c0001t0004g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.259-357C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106356 | |||||||
| chr8:28106368 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.259-345G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106368 | |||||||
| chr8:28106397 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.259-316G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106397 | |||||||
| chr8:28106409 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.259-304G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106409 | |||||||
| chr8:28106465 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.259-248G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106465 | |||||||
| chr8:28106472 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.259-241G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106472 | |||||||
| chr8:28106517 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.259-196G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106517 | |||||||
| chr8:28106539 | C | CA | 21 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0003g0011 others(18): Show |
25 | HG00423.hp1 HG00597.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.259-146dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | ||||||
| chr8:28106539 | CAAAAAA | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0052 a0001c0001t0001g0216 others(2): Show |
6 | HG02723.hp1 HG02818.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-151_259-146del others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | ||||||
| chr8:28106539 | CAAAAAAA | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.259-152_259-146del others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | ||||||
| chr8:28106539 | CAAAAAAA others(1): Show |
C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0217 others(6): Show |
9 | HG02451.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.259-153_259-146del others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | ||||||
| chr8:28106539 | CAAAAAAA others(7): Show |
C | 1 | a0001c0002t0011g0141 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.259-159_259-146del others(14): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | ||||||
| chr8:28106539 | CAAAAAAA others(8): Show |
C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(242): Show |
284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.259-160_259-146del others(15): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | ||||||
| chr8:28106539 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0004g0269 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.259-161_259-146del others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr8 | 28106539 | ||||||
| chr8:28106628 | C | G | 1 | a0001c0001t0004g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.259-85C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 3/14 | chr8 | 28106628 | |||||||
| chr8:28107163 | G | A | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.329+380G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107163 | |||||||
| chr8:28107197 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.329+414G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107197 | |||||||
| chr8:28107321 | A | G | 1 | a0001c0001t0015g0309 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.329+538A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107321 | |||||||
| chr8:28107339 | G | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(245): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.329+556G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107339 | |||||||
| chr8:28107470 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.330-443A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107470 | |||||||
| chr8:28107483 | G | C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0217 others(6): Show |
9 | HG02451.hp1 HG02572.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.330-430G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107483 | |||||||
| chr8:28107583 | G | A | 6 | a0001c0001t0006g0221 a0001c0001t0006g0232 a0001c0001t0006g0233 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-330G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107583 | |||||||
| chr8:28107607 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.330-306G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107607 | |||||||
| chr8:28107822 | T | C | 2 | a0001c0002t0009g0023 a0001c0002t0009g0140 |
3 | HG02965.hp2 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.330-91T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 4/14 | chr8 | 28107822 | |||||||
| chr8:28108194 | A | C | 76 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0016 others(73): Show |
83 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.393+218A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108194 | |||||||
| chr8:28108332 | A | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.393+356A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108332 | |||||||
| chr8:28108457 | C | CT | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(252): Show |
294 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.393+499dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 28108457 | ||||||
| chr8:28108457 | C | CTT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0002g0065 others(6): Show |
9 | HG01981.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+498_393+499dup others(2): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 28108457 | ||||||
| chr8:28108457 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0118 |
3 | HG02080.hp2 NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.393+489_393+499del others(11): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr8 | 28108457 | ||||||
| chr8:28108464 | T | C | 1 | a0001c0001t0003g0294 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.393+488T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108464 | |||||||
| chr8:28108508 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.393+532A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108508 | |||||||
| chr8:28108528 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.393+552T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108528 | |||||||
| chr8:28108552 | G | A | 1 | a0001c0001t0003g0312 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.393+576G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108552 | |||||||
| chr8:28108584 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.393+608G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108584 | |||||||
| chr8:28108614 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.393+638G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108614 | |||||||
| chr8:28108700 | G | A | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+724G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108700 | |||||||
| chr8:28108723 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.393+747T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108723 | |||||||
| chr8:28108774 | T | A | 70 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(67): Show |
80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.393+798T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108774 | |||||||
| chr8:28108874 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+898G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28108874 | |||||||
| chr8:28109118 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+1142G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109118 | |||||||
| chr8:28109257 | G | A | 1 | a0001c0001t0004g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.394-1113G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109257 | |||||||
| chr8:28109392 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0001t0001g0283 others(1): Show |
4 | HG02109.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-978C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109392 | |||||||
| chr8:28109440 | T | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.394-930T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109440 | |||||||
| chr8:28109506 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.394-864A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109506 | |||||||
| chr8:28109518 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.394-852G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109518 | |||||||
| chr8:28109526 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-844A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109526 | |||||||
| chr8:28109722 | C | T | 3 | a0001c0001t0004g0264 a0001c0001t0004g0265 a0001c0001t0004g0278 |
3 | HG00438.hp2 NA18970.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.394-648C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109722 | |||||||
| chr8:28109724 | T | A | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.394-646T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109724 | |||||||
| chr8:28109848 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.394-522G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28109848 | |||||||
| chr8:28110178 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0169 a0001c0001t0001g0216 |
4 | NA18947.hp1 NA18978.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-192G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28110178 | |||||||
| chr8:28110339 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.394-31A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 5/14 | chr8 | 28110339 | |||||||
| chr8:28110628 | T | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+190T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110628 | |||||||
| chr8:28110718 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.462+280A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110718 | |||||||
| chr8:28110742 | A | G | 1 | a0001c0001t0003g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.462+304A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110742 | |||||||
| chr8:28110746 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.462+308G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28110746 | |||||||
| chr8:28111037 | C | G | 2 | a0001c0001t0002g0130 a0001c0001t0002g0134 |
2 | HG01952.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.462+599C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111037 | |||||||
| chr8:28111481 | G | A | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+1043G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111481 | |||||||
| chr8:28111556 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02572.hp1 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.462+1118C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111556 | |||||||
| chr8:28111824 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.463-1195G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111824 | |||||||
| chr8:28111891 | A | C | 8 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0003t0008g0109 others(5): Show |
8 | HG00597.hp1 HG03098.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.463-1128A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111891 | |||||||
| chr8:28111903 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.463-1116A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28111903 | |||||||
| chr8:28112037 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0039 others(4): Show |
7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.463-982T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112037 | |||||||
| chr8:28112149 | A | T | 1 | a0001c0001t0004g0263 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.463-870A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112149 | |||||||
| chr8:28112152 | T | A | 129 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(126): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.463-867T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112152 | |||||||
| chr8:28112155 | T | A | 11 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0067 others(8): Show |
11 | HG00438.hp1 HG00597.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.463-864T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112155 | |||||||
| chr8:28112226 | C | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0215 |
3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.463-793C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112226 | |||||||
| chr8:28112231 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.463-788G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112231 | |||||||
| chr8:28112246 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.463-773C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112246 | |||||||
| chr8:28112288 | A | G | 97 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0002g0002 others(94): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.463-731A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112288 | |||||||
| chr8:28112421 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.463-598C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112421 | |||||||
| chr8:28112694 | G | C | 1 | a0001c0001t0003g0011 | 3 | HG01069.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.463-325G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112694 | |||||||
| chr8:28112878 | A | G | 1 | a0001c0001t0002g0097 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463-141A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 6/14 | chr8 | 28112878 | |||||||
| chr8:28113274 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.617+101A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113274 | |||||||
| chr8:28113333 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.617+160C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113333 | |||||||
| chr8:28113416 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.617+243T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113416 | |||||||
| chr8:28113443 | G | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.617+270G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113443 | |||||||
| chr8:28113465 | C | CTTTTCAG others(47): Show |
277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(274): Show |
322 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.617+301_617+302ins others(54): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28113465 | ||||||
| chr8:28113471 | A | AGCCTTAG others(47): Show |
1 | a0001c0003t0008g0111 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.617+301_617+302ins others(54): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28113471 | ||||||
| chr8:28113529 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.617+356G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113529 | |||||||
| chr8:28113753 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.617+580G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113753 | |||||||
| chr8:28113771 | C | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.617+598C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113771 | |||||||
| chr8:28113929 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+756A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28113929 | |||||||
| chr8:28114091 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617+918C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114091 | |||||||
| chr8:28114199 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(3): Show |
11 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.617+1026G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114199 | |||||||
| chr8:28114266 | C | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02559.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.617+1093C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114266 | |||||||
| chr8:28114271 | G | A | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+1098G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114271 | |||||||
| chr8:28114493 | A | C | 68 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.617+1320A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114493 | |||||||
| chr8:28114495 | A | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.617+1322A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114495 | |||||||
| chr8:28114498 | A | T | 8 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(5): Show |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+1325A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114498 | |||||||
| chr8:28114522 | CTT | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.617+1352_617+1353d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28114522 | ||||||
| chr8:28114542 | C | G | 3 | a0001c0001t0003g0314 a0001c0001t0010g0330 a0001c0001t0010g0331 |
3 | HG02155.hp2 HG02280.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.617+1369C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114542 | |||||||
| chr8:28114587 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.617+1414G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114587 | |||||||
| chr8:28114755 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.617+1582G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114755 | |||||||
| chr8:28114828 | A | T | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | NA19056.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.617+1655A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114828 | |||||||
| chr8:28114845 | A | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+1672A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114845 | |||||||
| chr8:28114865 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.617+1692G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114865 | |||||||
| chr8:28114875 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+1702C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28114875 | |||||||
| chr8:28115046 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+1873T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115046 | |||||||
| chr8:28115103 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.617+1930T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115103 | |||||||
| chr8:28115221 | A | G | 2 | a0001c0001t0002g0094 a0001c0001t0002g0106 |
2 | NA18995.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.617+2048A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115221 | |||||||
| chr8:28115243 | C | G | 5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02818.hp2 HG03139.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.617+2070C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115243 | |||||||
| chr8:28115243 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.617+2070C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115243 | |||||||
| chr8:28115287 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.617+2114T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115287 | |||||||
| chr8:28115545 | G | C | 1 | a0001c0001t0001g0293 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.617+2372G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115545 | |||||||
| chr8:28115631 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617+2458G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115631 | |||||||
| chr8:28115632 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+2459G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115632 | |||||||
| chr8:28115698 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+2525A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115698 | |||||||
| chr8:28115841 | C | G | 1 | a0001c0001t0001g0203 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.617+2668C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115841 | |||||||
| chr8:28115918 | T | C | 1 | a0001c0001t0006g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.617+2745T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115918 | |||||||
| chr8:28115940 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.617+2767C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115940 | |||||||
| chr8:28115957 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.617+2784T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115957 | |||||||
| chr8:28115973 | G | A | 1 | a0001c0001t0004g0263 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.617+2800G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28115973 | |||||||
| chr8:28116006 | T | C | 1 | a0001c0001t0005g0237 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.617+2833T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116006 | |||||||
| chr8:28116016 | G | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.617+2843G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116016 | |||||||
| chr8:28116164 | C | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.617+2991C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116164 | |||||||
| chr8:28116261 | C | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.617+3088C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116261 | |||||||
| chr8:28116281 | G | A | 1 | a0001c0001t0003g0295 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.617+3108G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116281 | |||||||
| chr8:28116369 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(157): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.617+3196T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116369 | |||||||
| chr8:28116403 | A | C | 68 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.617+3230A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116403 | |||||||
| chr8:28116417 | T | C | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+3244T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116417 | |||||||
| chr8:28116440 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.617+3267G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116440 | |||||||
| chr8:28116519 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.617+3346A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116519 | |||||||
| chr8:28116763 | A | C | 1 | a0001c0001t0013g0329 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.617+3590A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116763 | |||||||
| chr8:28116926 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.617+3753G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116926 | |||||||
| chr8:28116932 | G | T | 1 | a0001c0001t0003g0289 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.617+3759G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28116932 | |||||||
| chr8:28117074 | A | G | 1 | a0001c0001t0001g0029 | 2 | NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.617+3901A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117074 | |||||||
| chr8:28117189 | A | G | 1 | a0001c0001t0002g0013 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.617+4016A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117189 | |||||||
| chr8:28117208 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.617+4035A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117208 | |||||||
| chr8:28117726 | C | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(21): Show |
30 | HG00597.hp1 HG00733.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.617+4553C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117726 | |||||||
| chr8:28117907 | A | G | 1 | a0001c0001t0007g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.617+4734A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117907 | |||||||
| chr8:28117954 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.617+4781T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28117954 | |||||||
| chr8:28118203 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.617+5030T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118203 | |||||||
| chr8:28118508 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(158): Show |
189 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.617+5335A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118508 | |||||||
| chr8:28118550 | T | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0001t0001g0283 others(1): Show |
4 | HG02109.hp2 HG02818.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.617+5377T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118550 | |||||||
| chr8:28118596 | G | A | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.617+5423G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118596 | |||||||
| chr8:28118636 | G | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+5463G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118636 | |||||||
| chr8:28118716 | T | C | 1 | a0001c0001t0001g0007 | 3 | HG02109.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.617+5543T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118716 | |||||||
| chr8:28118775 | T | C | 1 | a0001c0001t0003g0320 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.617+5602T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118775 | |||||||
| chr8:28118892 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+5719C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118892 | |||||||
| chr8:28118900 | T | G | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.617+5727T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28118900 | |||||||
| chr8:28119324 | C | G | 1 | a0001c0001t0007g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.617+6151C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119324 | |||||||
| chr8:28119373 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.617+6200G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119373 | |||||||
| chr8:28119380 | C | T | 5 | a0001c0001t0003g0039 a0001c0001t0003g0040 a0001c0001t0003g0042 others(2): Show |
5 | HG02451.hp1 HG02976.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.617+6207C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119380 | |||||||
| chr8:28119416 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.617+6243G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119416 | |||||||
| chr8:28119418 | G | A | 1 | a0001c0001t0006g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.617+6245G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119418 | |||||||
| chr8:28119425 | T | G | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.617+6252T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119425 | |||||||
| chr8:28119548 | C | A | 1 | a0001c0001t0002g0069 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.617+6375C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119548 | |||||||
| chr8:28119549 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.617+6376A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119549 | |||||||
| chr8:28119569 | GTTTTATA others(4): Show |
G | 1 | a0001c0001t0002g0103 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.617+6398_617+6408d others(13): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119569 | ||||||
| chr8:28119572 | TTA | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0002g0018 others(3): Show |
7 | HG01515.hp2 HG01517.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.617+6455_617+6456d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATA | T | 19 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0155 others(16): Show |
19 | HG00597.hp2 HG00642.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.617+6453_617+6456d others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATA | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0024 others(35): Show |
39 | HG00099.hp2 HG00140.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.617+6451_617+6456d others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(1): Show |
T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(36): Show |
42 | HG00323.hp1 HG00408.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.617+6449_617+6456d others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(3): Show |
T | 45 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0025 others(42): Show |
47 | HG00280.hp2 HG00544.hp2 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.617+6447_617+6456d others(12): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(5): Show |
T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0025 others(39): Show |
47 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.617+6445_617+6456d others(14): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(7): Show |
T | 43 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0177 others(40): Show |
46 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.617+6443_617+6456d others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(9): Show |
T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0050 others(21): Show |
28 | HG00733.hp1 HG01074.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.617+6441_617+6456d others(18): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(11): Show |
T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0052 a0001c0001t0001g0164 others(4): Show |
7 | HG02257.hp2 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.617+6439_617+6456d others(20): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(13): Show |
T | 4 | a0001c0001t0001g0216 a0001c0001t0002g0002 a0001c0001t0002g0076 others(1): Show |
4 | HG01069.hp1 HG01081.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+6437_617+6456d others(22): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(15): Show |
T | 7 | a0001c0001t0001g0163 a0001c0001t0002g0092 a0001c0001t0003g0035 others(4): Show |
8 | HG00733.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.617+6435_617+6456d others(24): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(17): Show |
T | 1 | a0001c0001t0004g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.617+6433_617+6456d others(26): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(19): Show |
T | 4 | a0001c0001t0003g0288 a0001c0001t0003g0289 a0001c0001t0004g0227 others(1): Show |
4 | HG01891.hp2 HG03540.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+6431_617+6456d others(28): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(21): Show |
T | 6 | a0001c0001t0003g0043 a0001c0001t0004g0003 a0001c0001t0004g0010 others(3): Show |
6 | HG01167.hp1 HG02155.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+6429_617+6456d others(30): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(23): Show |
T | 65 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(62): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.617+6427_617+6456d others(32): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(27): Show |
T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | HG02572.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.617+6423_617+6456d others(36): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(29): Show |
T | 1 | a0001c0001t0002g0093 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.617+6421_617+6456d others(38): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(31): Show |
T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.617+6419_617+6456d others(40): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119572 | TTATATAT others(35): Show |
T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.617+6415_617+6456d others(44): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28119572 | ||||||
| chr8:28119674 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617+6501C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119674 | |||||||
| chr8:28119680 | C | G | 1 | a0001c0001t0003g0202 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.617+6507C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119680 | |||||||
| chr8:28119722 | A | G | 1 | a0001c0001t0003g0328 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.617+6549A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119722 | |||||||
| chr8:28119818 | G | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.617+6645G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119818 | |||||||
| chr8:28119821 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(244): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.617+6648T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28119821 | |||||||
| chr8:28120066 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.617+6893G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120066 | |||||||
| chr8:28120112 | A | C | 9 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0001t0004g0262 others(6): Show |
10 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.617+6939A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120112 | |||||||
| chr8:28120465 | A | G | 67 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(64): Show |
77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.617+7292A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120465 | |||||||
| chr8:28120524 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0039 others(4): Show |
7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.617+7351C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120524 | |||||||
| chr8:28120548 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.617+7375G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120548 | |||||||
| chr8:28120622 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.617+7449C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120622 | |||||||
| chr8:28120828 | C | G | 1 | a0001c0001t0003g0042 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.617+7655C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120828 | |||||||
| chr8:28120870 | C | A | 1 | a0001c0001t0002g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.617+7697C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120870 | |||||||
| chr8:28120945 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.617+7772G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120945 | |||||||
| chr8:28120951 | T | C | 1 | a0001c0001t0003g0296 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.617+7778T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120951 | |||||||
| chr8:28120986 | T | A | 8 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(5): Show |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.617+7813T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28120986 | |||||||
| chr8:28121054 | G | A | 2 | a0001c0001t0003g0288 a0001c0001t0003g0289 |
2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.617+7881G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121054 | |||||||
| chr8:28121187 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.617+8014A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121187 | |||||||
| chr8:28121301 | T | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0010g0330 |
3 | HG02572.hp1 HG02922.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.617+8128T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121301 | |||||||
| chr8:28121318 | A | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0201 |
3 | NA18940.hp1 NA18991.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.617+8145A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121318 | |||||||
| chr8:28121321 | A | AT | 3 | a0001c0001t0001g0108 a0001c0001t0001g0283 a0001c0001t0006g0282 |
3 | HG02818.hp2 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.617+8150dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28121321 | ||||||
| chr8:28121321 | A | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(71): Show |
89 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.617+8148A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121321 | |||||||
| chr8:28121324 | A | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(287): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.617+8151A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121324 | |||||||
| chr8:28121327 | T | A | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0138 others(1): Show |
4 | HG01106.hp1 HG03139.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.617+8154T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121327 | |||||||
| chr8:28121380 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.618-8122C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121380 | |||||||
| chr8:28121381 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.618-8121G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121381 | |||||||
| chr8:28121413 | G | C | 3 | a0001c0001t0004g0229 a0001c0001t0004g0230 a0001c0001t0004g0238 |
3 | NA18943.hp2 NA18977.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.618-8089G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121413 | |||||||
| chr8:28121439 | C | T | 83 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(80): Show |
94 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.618-8063C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121439 | |||||||
| chr8:28121528 | C | T | 1 | a0001c0001t0003g0037 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.618-7974C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121528 | |||||||
| chr8:28121562 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-7940C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121562 | |||||||
| chr8:28121571 | C | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-7931C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121571 | |||||||
| chr8:28121599 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.618-7903T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121599 | |||||||
| chr8:28121720 | T | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0001t0004g0262 |
4 | NA18978.hp2 NA18979.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-7782T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121720 | |||||||
| chr8:28121926 | G | T | 1 | a0001c0001t0004g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.618-7576G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121926 | |||||||
| chr8:28121928 | A | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-7574A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28121928 | |||||||
| chr8:28122098 | T | A | 1 | a0001c0001t0003g0294 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.618-7404T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122098 | |||||||
| chr8:28122153 | A | G | 10 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0052 others(7): Show |
10 | HG02451.hp1 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.618-7349A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122153 | |||||||
| chr8:28122281 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-7221G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122281 | |||||||
| chr8:28122339 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-7163C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122339 | |||||||
| chr8:28122434 | T | C | 1 | a0001c0001t0002g0013 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.618-7068T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122434 | |||||||
| chr8:28122474 | A | C | 1 | a0001c0001t0002g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.618-7028A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122474 | |||||||
| chr8:28122688 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-6814G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122688 | |||||||
| chr8:28122799 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.618-6703A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122799 | |||||||
| chr8:28122899 | G | A | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-6603G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122899 | |||||||
| chr8:28122966 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.618-6536A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28122966 | |||||||
| chr8:28123136 | A | G | 67 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(64): Show |
77 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.618-6366A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123136 | |||||||
| chr8:28123202 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618-6300T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123202 | |||||||
| chr8:28123209 | G | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.618-6293G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123209 | |||||||
| chr8:28123243 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.618-6259T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123243 | |||||||
| chr8:28123260 | A | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.618-6242A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123260 | |||||||
| chr8:28123344 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-6158T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123344 | |||||||
| chr8:28123598 | T | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-5904T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123598 | |||||||
| chr8:28123669 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-5833G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123669 | |||||||
| chr8:28123671 | A | T | 1 | a0001c0001t0005g0260 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.618-5831A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123671 | |||||||
| chr8:28123787 | C | T | 1 | a0001c0001t0003g0295 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.618-5715C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123787 | |||||||
| chr8:28123828 | G | GTCACAGC others(1): Show |
274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.618-5671_618-5670i others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28123828 | ||||||
| chr8:28123910 | A | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-5592A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28123910 | |||||||
| chr8:28123943 | CT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(9): Show |
18 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.618-5548delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28123943 | ||||||
| chr8:28124021 | G | A | 2 | a0001c0001t0004g0239 a0001c0001t0019g0266 |
2 | NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.618-5481G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124021 | |||||||
| chr8:28124206 | A | T | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.618-5296A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124206 | |||||||
| chr8:28124288 | G | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-5214G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124288 | |||||||
| chr8:28124300 | A | G | 2 | a0001c0001t0004g0239 a0001c0001t0019g0266 |
2 | NA18993.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.618-5202A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124300 | |||||||
| chr8:28124355 | C | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-5147C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124355 | |||||||
| chr8:28124635 | A | G | 96 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0002g0002 others(93): Show |
110 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.618-4867A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124635 | |||||||
| chr8:28124651 | G | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-4851G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124651 | |||||||
| chr8:28124677 | C | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-4825C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124677 | |||||||
| chr8:28124750 | C | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-4752C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124750 | |||||||
| chr8:28124799 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(244): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.618-4703C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124799 | |||||||
| chr8:28124876 | T | C | 1 | a0001c0001t0017g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.618-4626T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124876 | |||||||
| chr8:28124903 | G | A | 1 | a0001c0001t0003g0321 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.618-4599G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28124903 | |||||||
| chr8:28125095 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.618-4407G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125095 | |||||||
| chr8:28125148 | C | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.618-4354C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125148 | |||||||
| chr8:28125327 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0039 others(4): Show |
7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-4175G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125327 | |||||||
| chr8:28125353 | G | A | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
318 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.618-4149G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125353 | |||||||
| chr8:28125437 | A | G | 99 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0222 others(96): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.618-4065A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125437 | |||||||
| chr8:28125469 | G | A | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-4033G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125469 | |||||||
| chr8:28125594 | G | T | 1 | a0001c0001t0002g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.618-3908G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125594 | |||||||
| chr8:28125672 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.618-3830C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125672 | |||||||
| chr8:28125750 | G | A | 2 | a0001c0001t0003g0297 a0001c0001t0020g0137 |
2 | HG02015.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.618-3752G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28125750 | |||||||
| chr8:28125759 | C | CT | 6 | a0001c0001t0001g0200 a0001c0001t0003g0038 a0001c0001t0003g0292 others(3): Show |
7 | HG00280.hp2 HG00323.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-3720dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | ||||||
| chr8:28125759 | CT | C | 32 | a0001c0001t0001g0029 a0001c0001t0001g0108 a0001c0001t0001g0197 others(29): Show |
34 | HG00597.hp1 HG01168.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.618-3720delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | ||||||
| chr8:28125759 | CTT | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(157): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.618-3721_618-3720d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | ||||||
| chr8:28125759 | CTTT | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(82): Show |
100 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.618-3722_618-3720d others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28125759 | ||||||
| chr8:28126027 | A | AT | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-3475_618-3474i others(3): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126027 | |||||||
| chr8:28126028 | C | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-3474C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126028 | |||||||
| chr8:28126152 | G | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.618-3350G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126152 | |||||||
| chr8:28126437 | C | T | 1 | a0001c0001t0004g0255 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.618-3065C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126437 | |||||||
| chr8:28126542 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | NA19056.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.618-2960G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126542 | |||||||
| chr8:28126792 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.618-2710A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126792 | |||||||
| chr8:28126798 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.618-2704A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126798 | |||||||
| chr8:28126816 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0153 a0001c0001t0001g0174 others(3): Show |
7 | HG01884.hp2 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.618-2686T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126816 | |||||||
| chr8:28126842 | T | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.618-2660T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126842 | |||||||
| chr8:28126960 | C | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.618-2542C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28126960 | |||||||
| chr8:28127016 | A | G | 1 | a0001c0001t0003g0038 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.618-2486A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127016 | |||||||
| chr8:28127086 | G | A | 1 | a0001c0001t0003g0321 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.618-2416G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127086 | |||||||
| chr8:28127157 | A | G | 1 | a0001c0001t0003g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.618-2345A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127157 | |||||||
| chr8:28127213 | T | C | 1 | a0001c0002t0009g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.618-2289T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127213 | |||||||
| chr8:28127412 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(68): Show |
85 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.618-2090A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127412 | |||||||
| chr8:28127477 | G | A | 14 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(11): Show |
15 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.618-2025G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127477 | |||||||
| chr8:28127636 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.618-1866G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127636 | |||||||
| chr8:28127648 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.618-1854C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127648 | |||||||
| chr8:28127661 | A | G | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.618-1841A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127661 | |||||||
| chr8:28127741 | CTG | C | 75 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0016 others(72): Show |
82 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.618-1760_618-1759d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127741 | |||||||
| chr8:28127981 | T | C | 89 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0014 others(86): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.618-1521T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28127981 | |||||||
| chr8:28128124 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.618-1378C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128124 | |||||||
| chr8:28128200 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.618-1302G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128200 | |||||||
| chr8:28128239 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(261): Show |
308 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.618-1263C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128239 | |||||||
| chr8:28128272 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.618-1230G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128272 | |||||||
| chr8:28128347 | G | A | 14 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0017 others(11): Show |
21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.618-1155G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128347 | |||||||
| chr8:28128349 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.618-1153A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128349 | |||||||
| chr8:28128518 | G | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.618-984G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128518 | |||||||
| chr8:28128776 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.618-726G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128776 | |||||||
| chr8:28128873 | A | C | 4 | a0001c0001t0001g0171 a0001c0001t0001g0194 a0001c0001t0001g0195 others(1): Show |
4 | HG01261.hp1 HG01928.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.618-629A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28128873 | |||||||
| chr8:28129047 | TTTTTC | T | 8 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(5): Show |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.618-451_618-447del others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr8 | 28129047 | ||||||
| chr8:28129268 | A | G | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.618-234A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129268 | |||||||
| chr8:28129348 | G | A | 1 | a0001c0001t0002g0074 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.618-154G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129348 | |||||||
| chr8:28129475 | G | A | 1 | a0001c0001t0003g0321 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.618-27G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129475 | |||||||
| chr8:28129489 | A | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0327 |
5 | HG00642.hp2 HG01975.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.618-13A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 7/14 | chr8 | 28129489 | |||||||
| chr8:28129876 | C | T | 1 | a0001c0001t0010g0331 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.779+213C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28129876 | |||||||
| chr8:28130201 | C | T | 4 | a0001c0001t0005g0257 a0001c0001t0005g0258 a0001c0001t0005g0259 others(1): Show |
4 | NA18951.hp1 NA18967.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.779+538C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130201 | |||||||
| chr8:28130299 | G | T | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.779+636G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130299 | |||||||
| chr8:28130356 | C | T | 70 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(67): Show |
80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.779+693C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130356 | |||||||
| chr8:28130437 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG00733.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.779+774C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130437 | |||||||
| chr8:28130686 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.779+1023G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130686 | |||||||
| chr8:28130778 | G | C | 1 | a0001c0001t0003g0176 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.779+1115G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130778 | |||||||
| chr8:28130795 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.779+1132A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130795 | |||||||
| chr8:28130969 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.779+1306C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28130969 | |||||||
| chr8:28131019 | A | G | 1 | a0001c0001t0004g0280 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.780-1259A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131019 | |||||||
| chr8:28131021 | C | T | 8 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(5): Show |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.780-1257C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131021 | |||||||
| chr8:28131124 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.780-1154A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131124 | |||||||
| chr8:28131387 | C | T | 5 | a0001c0001t0004g0252 a0001c0001t0004g0253 a0001c0001t0004g0254 others(2): Show |
5 | HG01106.hp2 HG01168.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.780-891C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131387 | |||||||
| chr8:28131572 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.780-706G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131572 | |||||||
| chr8:28131773 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.780-505A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28131773 | |||||||
| chr8:28132044 | C | T | 1 | a0001c0001t0003g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.780-234C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28132044 | |||||||
| chr8:28132129 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.780-149A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28132129 | |||||||
| chr8:28132223 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.780-55C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 8/14 | chr8 | 28132223 | |||||||
| chr8:28132540 | A | T | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.906+136A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132540 | |||||||
| chr8:28132615 | T | A | 1 | a0001c0001t0002g0134 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.906+211T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132615 | |||||||
| chr8:28132664 | A | G | 1 | a0001c0001t0002g0088 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.906+260A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132664 | |||||||
| chr8:28132825 | C | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(9): Show |
17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.906+421C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132825 | |||||||
| chr8:28132870 | A | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+466A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132870 | |||||||
| chr8:28132883 | G | A | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.906+479G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132883 | |||||||
| chr8:28132999 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.906+595T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28132999 | |||||||
| chr8:28133030 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.906+626A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133030 | |||||||
| chr8:28133114 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(64): Show |
81 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.906+710C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133114 | |||||||
| chr8:28133161 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(9): Show |
17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.906+757C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133161 | |||||||
| chr8:28133272 | A | C | 1 | a0001c0001t0004g0265 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.906+868A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133272 | |||||||
| chr8:28133273 | T | G | 70 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(67): Show |
80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.906+869T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133273 | |||||||
| chr8:28133378 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.906+974C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133378 | |||||||
| chr8:28133426 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.906+1022T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133426 | |||||||
| chr8:28133428 | C | CT | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(256): Show |
299 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.906+1038dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133428 | ||||||
| chr8:28133428 | C | CTT | 16 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(13): Show |
21 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.906+1037_906+1038d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133428 | ||||||
| chr8:28133428 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.906+1024C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133428 | |||||||
| chr8:28133453 | C | T | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(251): Show |
293 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.906+1049C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133453 | |||||||
| chr8:28133564 | A | G | 1 | a0001c0001t0004g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.906+1160A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133564 | |||||||
| chr8:28133829 | C | T | 8 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(5): Show |
9 | HG01243.hp1 HG02257.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.906+1425C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133829 | |||||||
| chr8:28133830 | G | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0108 others(2): Show |
5 | HG02109.hp2 HG02572.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+1426G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133830 | |||||||
| chr8:28133840 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.906+1436C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133840 | |||||||
| chr8:28133879 | C | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(66): Show |
83 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.906+1475C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133879 | |||||||
| chr8:28133886 | T | TA | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(167): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.906+1484dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133886 | ||||||
| chr8:28133905 | C | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.906+1501C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28133905 | |||||||
| chr8:28133952 | G | GATT | 5 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0001t0001g0217 others(2): Show |
5 | HG00597.hp1 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+1566_906+1568d others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28133952 | ||||||
| chr8:28134036 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.906+1632C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134036 | |||||||
| chr8:28134173 | G | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.906+1769G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134173 | |||||||
| chr8:28134194 | G | T | 68 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.906+1790G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134194 | |||||||
| chr8:28134277 | C | A | 68 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.906+1873C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134277 | |||||||
| chr8:28134408 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.906+2004T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134408 | |||||||
| chr8:28134476 | C | G | 2 | a0001c0001t0003g0011 a0001c0001t0003g0037 |
5 | HG01069.hp2 HG01071.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+2072C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134476 | |||||||
| chr8:28134631 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.906+2227A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134631 | |||||||
| chr8:28134684 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.906+2280C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134684 | |||||||
| chr8:28134717 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.906+2313T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134717 | |||||||
| chr8:28134722 | C | G | 84 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(81): Show |
95 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.906+2318C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134722 | |||||||
| chr8:28134746 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02165.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.906+2342T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134746 | |||||||
| chr8:28134915 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.906+2511C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134915 | |||||||
| chr8:28134929 | C | CT | 10 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0016 others(7): Show |
13 | HG00438.hp1 HG01346.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+2538dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28134929 | ||||||
| chr8:28134932 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0006g0282 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.906+2528T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28134932 | |||||||
| chr8:28135010 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.906+2606C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135010 | |||||||
| chr8:28135017 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.906+2613C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135017 | |||||||
| chr8:28135078 | A | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-2620A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135078 | |||||||
| chr8:28135142 | C | G | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(9): Show |
17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.907-2556C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135142 | |||||||
| chr8:28135171 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.907-2527G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135171 | |||||||
| chr8:28135171 | G | T | 1 | a0001c0001t0002g0086 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.907-2527G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135171 | |||||||
| chr8:28135219 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(9): Show |
17 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.907-2479C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135219 | |||||||
| chr8:28135340 | G | A | 1 | a0001c0001t0004g0032 | 2 | HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.907-2358G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135340 | |||||||
| chr8:28135360 | C | T | 1 | a0001c0001t0003g0294 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.907-2338C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135360 | |||||||
| chr8:28135368 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.907-2330T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135368 | |||||||
| chr8:28135502 | T | C | 2 | a0001c0001t0005g0257 a0001c0001t0005g0258 |
2 | NA18973.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.907-2196T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135502 | |||||||
| chr8:28135513 | A | C | 10 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0001t0001g0138 others(7): Show |
10 | HG00597.hp1 HG02109.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.907-2185A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135513 | |||||||
| chr8:28135751 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.907-1947G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135751 | |||||||
| chr8:28135852 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(67): Show |
84 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.907-1846G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135852 | |||||||
| chr8:28135918 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.907-1780G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135918 | |||||||
| chr8:28135960 | C | CT | 10 | a0001c0001t0001g0216 a0001c0001t0001g0283 a0001c0001t0002g0051 others(7): Show |
10 | HG00597.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.907-1722dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr8 | 28135960 | ||||||
| chr8:28135976 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.907-1722T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28135976 | |||||||
| chr8:28136107 | G | A | 1 | a0001c0001t0002g0013 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.907-1591G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136107 | |||||||
| chr8:28136179 | C | T | 2 | a0001c0001t0004g0250 a0001c0001t0004g0277 |
2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.907-1519C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136179 | |||||||
| chr8:28136371 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.907-1327G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136371 | |||||||
| chr8:28136378 | C | G | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.907-1320C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136378 | |||||||
| chr8:28136541 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(244): Show |
286 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.907-1157T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136541 | |||||||
| chr8:28136546 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-1152C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136546 | |||||||
| chr8:28136600 | G | T | 1 | a0001c0001t0006g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.907-1098G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136600 | |||||||
| chr8:28136637 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.907-1061A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136637 | |||||||
| chr8:28136647 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.907-1051G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136647 | |||||||
| chr8:28136657 | A | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.907-1041A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136657 | |||||||
| chr8:28136724 | T | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-974T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136724 | |||||||
| chr8:28136779 | G | C | 1 | a0001c0001t0002g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.907-919G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136779 | |||||||
| chr8:28136984 | C | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(275): Show |
323 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.907-714C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28136984 | |||||||
| chr8:28137585 | G | A | 1 | a0001c0001t0002g0018 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.907-113G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28137585 | |||||||
| chr8:28137596 | G | C | 1 | a0001c0001t0002g0076 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.907-102G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 9/14 | chr8 | 28137596 | |||||||
| chr8:28138030 | A | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+139A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138030 | |||||||
| chr8:28138072 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1100+181A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138072 | |||||||
| chr8:28138077 | G | A | 9 | a0001c0001t0004g0240 a0001c0001t0004g0250 a0001c0001t0004g0277 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1100+186G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138077 | |||||||
| chr8:28138129 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1100+238G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138129 | |||||||
| chr8:28138153 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1100+262C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138153 | |||||||
| chr8:28138163 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1100+272A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138163 | |||||||
| chr8:28138205 | T | G | 92 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0002 others(89): Show |
106 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1100+314T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138205 | |||||||
| chr8:28138236 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1100+345T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138236 | |||||||
| chr8:28138267 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(4): Show |
12 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1100+376C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138267 | |||||||
| chr8:28138404 | TCTCATTT others(21): Show |
T | 1 | a0001c0001t0001g0216 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1100+516_1100+543d others(30): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28138404 | ||||||
| chr8:28138520 | C | G | 1 | a0001c0001t0002g0074 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1100+629C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138520 | |||||||
| chr8:28138532 | C | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(8): Show |
16 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1100+641C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138532 | |||||||
| chr8:28138609 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0068 |
2 | NA18944.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1100+718A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138609 | |||||||
| chr8:28138617 | A | G | 1 | a0001c0001t0003g0319 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1100+726A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138617 | |||||||
| chr8:28138714 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
5 | HG03098.hp2 HG03471.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1100+823C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138714 | |||||||
| chr8:28138787 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0212 |
2 | HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1100+896A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138787 | |||||||
| chr8:28138849 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(276): Show |
324 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1100+958G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138849 | |||||||
| chr8:28138863 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1100+972G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138863 | |||||||
| chr8:28138923 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(76): Show |
98 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1100+1032G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138923 | |||||||
| chr8:28138932 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1100+1041G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138932 | |||||||
| chr8:28138990 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+1099C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28138990 | |||||||
| chr8:28139002 | C | T | 31 | a0001c0001t0001g0034 a0001c0001t0001g0293 a0001c0001t0002g0064 others(28): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1100+1111C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139002 | |||||||
| chr8:28139003 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(67): Show |
89 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1100+1112G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139003 | |||||||
| chr8:28139051 | A | G | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+1160A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139051 | |||||||
| chr8:28139144 | C | G | 1 | a0001c0001t0001g0034 | 2 | NA18999.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1100+1253C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139144 | |||||||
| chr8:28139298 | G | GT | 61 | a0001c0001t0001g0034 a0001c0001t0002g0014 a0001c0001t0002g0017 others(58): Show |
73 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1100+1415dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28139298 | ||||||
| chr8:28139515 | GA | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(131): Show |
158 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1100+1628delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28139515 | ||||||
| chr8:28139528 | A | G | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1100+1637A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139528 | |||||||
| chr8:28139631 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+1740A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139631 | |||||||
| chr8:28139720 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+1829G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139720 | |||||||
| chr8:28139742 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1100+1851C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139742 | |||||||
| chr8:28139916 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(246): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1100+2025A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139916 | |||||||
| chr8:28139996 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1100+2105G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28139996 | |||||||
| chr8:28140035 | T | C | 1 | a0001c0001t0003g0319 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1100+2144T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140035 | |||||||
| chr8:28140114 | T | TTG | 49 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0283 others(46): Show |
54 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1100+2263_1100+226 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | T | TTGTG | 4 | a0001c0001t0002g0002 a0001c0001t0003g0036 a0001c0001t0003g0037 others(1): Show |
8 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1100+2261_1100+226 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | T | TTGTGTG | 3 | a0001c0001t0003g0005 a0001c0001t0003g0324 a0001c0001t0003g0327 |
5 | HG01975.hp2 HG02809.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100+2259_1100+226 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | T | TTGTGTGT others(5): Show |
3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1100+2253_1100+226 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | TTG | T | 7 | a0001c0001t0001g0049 a0001c0001t0001g0139 a0001c0001t0001g0178 others(4): Show |
7 | HG01943.hp1 HG03098.hp2 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1100+2263_1100+226 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | TTGTG | T | 30 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0153 others(27): Show |
35 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1100+2261_1100+226 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | TTGTGTG | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
211 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1100+2259_1100+226 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | TTGTGTGT others(1): Show |
T | 16 | a0001c0001t0001g0108 a0001c0001t0001g0138 a0001c0001t0001g0217 others(13): Show |
16 | HG00597.hp1 HG01261.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.1100+2257_1100+226 others(12): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | TTGTGTGT others(3): Show |
T | 4 | a0001c0001t0001g0034 a0001c0001t0003g0284 a0001c0001t0003g0285 others(1): Show |
5 | HG02056.hp2 NA18954.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1100+2255_1100+226 others(14): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140114 | TTGTGTGT others(5): Show |
T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+2253_1100+226 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28140114 | ||||||
| chr8:28140150 | G | C | 1 | a0001c0001t0003g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1100+2259G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140150 | |||||||
| chr8:28140196 | T | A | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1100+2305T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140196 | |||||||
| chr8:28140205 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1100+2314G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140205 | |||||||
| chr8:28140270 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1100+2379T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140270 | |||||||
| chr8:28140346 | T | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(262): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.1100+2455T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140346 | |||||||
| chr8:28140513 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1100+2622C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140513 | |||||||
| chr8:28140581 | T | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0039 others(4): Show |
7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1100+2690T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140581 | |||||||
| chr8:28140645 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1100+2754C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140645 | |||||||
| chr8:28140728 | G | A | 69 | a0001c0001t0001g0052 a0001c0001t0001g0272 a0001c0001t0004g0003 others(66): Show |
79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1100+2837G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140728 | |||||||
| chr8:28140758 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1100+2867T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140758 | |||||||
| chr8:28140857 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1100+2966C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140857 | |||||||
| chr8:28140858 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(277): Show |
325 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.1100+2967A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140858 | |||||||
| chr8:28140974 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1100+3083C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28140974 | |||||||
| chr8:28141019 | T | C | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+3128T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141019 | |||||||
| chr8:28141024 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+3133A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141024 | |||||||
| chr8:28141046 | G | A | 1 | a0001c0001t0003g0300 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1100+3155G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141046 | |||||||
| chr8:28141250 | T | A | 1 | a0001c0001t0003g0294 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1100+3359T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141250 | |||||||
| chr8:28141331 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1100+3440G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141331 | |||||||
| chr8:28141555 | C | A | 1 | a0001c0001t0003g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1100+3664C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141555 | |||||||
| chr8:28141613 | T | A | 1 | a0001c0001t0001g0024 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1100+3722T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141613 | |||||||
| chr8:28141760 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1100+3869G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141760 | |||||||
| chr8:28141848 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0139 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1100+3957A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141848 | |||||||
| chr8:28141977 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1100+4086C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141977 | |||||||
| chr8:28141984 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0158 a0001c0001t0001g0216 |
4 | NA18950.hp2 NA18978.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1100+4093G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28141984 | |||||||
| chr8:28142217 | C | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1100+4326C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142217 | |||||||
| chr8:28142310 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1100+4419T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142310 | |||||||
| chr8:28142329 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1100+4438C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142329 | |||||||
| chr8:28142379 | C | T | 3 | a0001c0001t0007g0147 a0001c0001t0007g0149 a0001c0001t0007g0150 |
3 | HG01891.hp1 HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1100+4488C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142379 | |||||||
| chr8:28142464 | A | G | 2 | a0001c0001t0003g0315 a0001c0001t0003g0326 |
2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1100+4573A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142464 | |||||||
| chr8:28142492 | A | T | 68 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1100+4601A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142492 | |||||||
| chr8:28142536 | G | C | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+4645G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142536 | |||||||
| chr8:28142578 | C | A | 10 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0222 others(7): Show |
10 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1100+4687C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142578 | |||||||
| chr8:28142767 | T | G | 1 | a0001c0001t0006g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1100+4876T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142767 | |||||||
| chr8:28142815 | G | A | 1 | a0001c0001t0006g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1100+4924G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142815 | |||||||
| chr8:28142845 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1100+4954C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142845 | |||||||
| chr8:28142848 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1100+4957G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142848 | |||||||
| chr8:28142864 | AT | A | 8 | a0001c0001t0003g0314 a0001c0001t0005g0260 a0001c0003t0008g0109 others(5): Show |
8 | HG00597.hp1 HG02280.hp1 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.1100+4983delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28142864 | ||||||
| chr8:28142868 | T | C | 2 | a0001c0001t0003g0315 a0001c0001t0003g0326 |
2 | HG01074.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1100+4977T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142868 | |||||||
| chr8:28142884 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1100+4993T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28142884 | |||||||
| chr8:28143009 | G | A | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1100+5118G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143009 | |||||||
| chr8:28143163 | A | G | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(274): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1100+5272A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143163 | |||||||
| chr8:28143244 | TC | T | 24 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(21): Show |
30 | HG00597.hp1 HG00733.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1100+5356delC | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28143244 | ||||||
| chr8:28143289 | TC | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0167 others(6): Show |
12 | HG00408.hp1 HG02165.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1100+5405delC | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28143289 | ||||||
| chr8:28143310 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+5419A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143310 | |||||||
| chr8:28143389 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1100+5498T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143389 | |||||||
| chr8:28143445 | A | G | 1 | a0001c0001t0006g0282 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1100+5554A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143445 | |||||||
| chr8:28143491 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(258): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1100+5600G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143491 | |||||||
| chr8:28143605 | C | A | 10 | a0001c0001t0002g0018 a0001c0001t0002g0020 a0001c0001t0002g0021 others(7): Show |
12 | HG00323.hp2 HG01358.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1100+5714C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143605 | |||||||
| chr8:28143684 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1100+5793T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143684 | |||||||
| chr8:28143704 | A | G | 82 | a0001c0001t0001g0138 a0001c0001t0001g0178 a0001c0001t0001g0179 others(79): Show |
89 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1100+5813A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28143704 | |||||||
| chr8:28144163 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1100+6272A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144163 | |||||||
| chr8:28144191 | C | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+6300C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144191 | |||||||
| chr8:28144407 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+6516C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144407 | |||||||
| chr8:28144435 | C | A | 10 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0222 others(7): Show |
10 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1100+6544C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144435 | |||||||
| chr8:28144743 | A | G | 1 | a0001c0001t0003g0326 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1100+6852A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144743 | |||||||
| chr8:28144764 | C | T | 91 | a0001c0001t0001g0029 a0001c0001t0001g0108 a0001c0001t0001g0138 others(88): Show |
99 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1100+6873C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144764 | |||||||
| chr8:28144996 | C | T | 1 | a0001c0001t0005g0259 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1100+7105C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28144996 | |||||||
| chr8:28145265 | A | T | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1100+7374A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145265 | |||||||
| chr8:28145330 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1100+7439C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145330 | |||||||
| chr8:28145432 | A | G | 1 | a0001c0001t0002g0129 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1100+7541A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145432 | |||||||
| chr8:28145472 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1100+7581A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145472 | |||||||
| chr8:28145505 | T | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1100+7614T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145505 | |||||||
| chr8:28145627 | T | TG | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1100+7736_1100+773 others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145627 | |||||||
| chr8:28145648 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+7757A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145648 | |||||||
| chr8:28145725 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1100+7834G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145725 | |||||||
| chr8:28145843 | C | T | 1 | a0001c0001t0001g0007 | 3 | HG02109.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1100+7952C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145843 | |||||||
| chr8:28145885 | A | G | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0224 others(5): Show |
8 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1100+7994A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145885 | |||||||
| chr8:28145930 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1100+8039A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28145930 | |||||||
| chr8:28146257 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1100+8366T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146257 | |||||||
| chr8:28146300 | T | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(64): Show |
81 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1100+8409T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146300 | |||||||
| chr8:28146345 | A | G | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1100+8454A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146345 | |||||||
| chr8:28146389 | C | CA | 8 | a0001c0001t0002g0022 a0001c0001t0002g0117 a0001c0001t0002g0123 others(5): Show |
9 | HG02040.hp1 NA18942.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1100+8505dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28146389 | ||||||
| chr8:28146554 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1100+8663A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146554 | |||||||
| chr8:28146565 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0139 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1100+8674A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146565 | |||||||
| chr8:28146587 | A | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1100+8696A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146587 | |||||||
| chr8:28146925 | C | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1101-9017C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146925 | |||||||
| chr8:28146933 | A | G | 9 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1101-9009A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28146933 | |||||||
| chr8:28147014 | A | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(247): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.1101-8928A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147014 | |||||||
| chr8:28147039 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-8903C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147039 | |||||||
| chr8:28147059 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1101-8883T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147059 | |||||||
| chr8:28147202 | T | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-8740T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147202 | |||||||
| chr8:28147456 | A | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-8486A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147456 | |||||||
| chr8:28147635 | C | G | 1 | a0001c0001t0003g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1101-8307C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147635 | |||||||
| chr8:28147793 | T | A | 246 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(243): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1101-8149T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147793 | |||||||
| chr8:28147824 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1101-8118C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147824 | |||||||
| chr8:28147849 | T | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(274): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.1101-8093T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147849 | |||||||
| chr8:28147942 | A | C | 1 | a0001c0001t0019g0266 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1101-8000A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28147942 | |||||||
| chr8:28148032 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1101-7910T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148032 | |||||||
| chr8:28148064 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-7878T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148064 | |||||||
| chr8:28148066 | A | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-7876A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148066 | |||||||
| chr8:28148355 | T | C | 1 | a0001c0001t0004g0240 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1101-7587T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148355 | |||||||
| chr8:28148364 | T | G | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-7578T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148364 | |||||||
| chr8:28148375 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1101-7567C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148375 | |||||||
| chr8:28148457 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1101-7485T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148457 | |||||||
| chr8:28148528 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1101-7414G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148528 | |||||||
| chr8:28148564 | C | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1101-7378C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148564 | |||||||
| chr8:28148842 | T | C | 1 | a0001c0001t0003g0296 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1101-7100T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148842 | |||||||
| chr8:28148902 | A | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1101-7040A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28148902 | |||||||
| chr8:28149068 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1101-6874C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149068 | |||||||
| chr8:28149284 | C | T | 1 | a0001c0001t0003g0321 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1101-6658C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149284 | |||||||
| chr8:28149298 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0124 |
2 | NA18947.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1101-6644T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149298 | |||||||
| chr8:28149443 | G | C | 2 | a0001c0001t0004g0030 a0001c0001t0018g0030 |
2 | NA18948.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1101-6499G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149443 | |||||||
| chr8:28149466 | AGTT | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1101-6472_1101-647 others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28149466 | ||||||
| chr8:28149514 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1101-6428G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149514 | |||||||
| chr8:28149530 | T | C | 1 | a0001c0002t0011g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1101-6412T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149530 | |||||||
| chr8:28149547 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(243): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1101-6395A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149547 | |||||||
| chr8:28149649 | C | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1101-6293C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149649 | |||||||
| chr8:28149735 | G | C | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-6207G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149735 | |||||||
| chr8:28149971 | G | A | 4 | a0001c0001t0004g0003 a0001c0001t0004g0243 a0001c0001t0004g0244 others(1): Show |
8 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-5971G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149971 | |||||||
| chr8:28149975 | G | C | 1 | a0001c0001t0003g0039 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1101-5967G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28149975 | |||||||
| chr8:28150105 | T | C | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(264): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1101-5837T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150105 | |||||||
| chr8:28150305 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0224 others(5): Show |
8 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-5637T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150305 | |||||||
| chr8:28150378 | C | A | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-5564C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150378 | |||||||
| chr8:28150431 | C | A | 2 | a0001c0001t0003g0299 a0001c0001t0003g0335 |
2 | HG01192.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1101-5511C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150431 | |||||||
| chr8:28150807 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1101-5135A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150807 | |||||||
| chr8:28150808 | T | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | NA18974.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1101-5134T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150808 | |||||||
| chr8:28150831 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1101-5111G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150831 | |||||||
| chr8:28150898 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(264): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1101-5044A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28150898 | |||||||
| chr8:28151056 | T | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(11): Show |
19 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1101-4886T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151056 | |||||||
| chr8:28151215 | C | G | 1 | a0001c0001t0002g0083 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1101-4727C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151215 | |||||||
| chr8:28151260 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1101-4682G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151260 | |||||||
| chr8:28151304 | A | AT | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(264): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1101-4635dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr8 | 28151304 | ||||||
| chr8:28151330 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1101-4612C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151330 | |||||||
| chr8:28151556 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1101-4386T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151556 | |||||||
| chr8:28151662 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(11): Show |
19 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1101-4280G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151662 | |||||||
| chr8:28151663 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1101-4279G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151663 | |||||||
| chr8:28151818 | A | C | 1 | a0001c0001t0002g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1101-4124A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151818 | |||||||
| chr8:28151879 | T | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0189 |
2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1101-4063T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151879 | |||||||
| chr8:28151901 | T | C | 1 | a0001c0001t0003g0323 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1101-4041T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151901 | |||||||
| chr8:28151940 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0139 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1101-4002C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28151940 | |||||||
| chr8:28152050 | C | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-3892C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152050 | |||||||
| chr8:28152222 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1101-3720T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152222 | |||||||
| chr8:28152378 | G | T | 2 | a0001c0001t0003g0287 a0001c0001t0003g0300 |
2 | HG00741.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1101-3564G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152378 | |||||||
| chr8:28152662 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-3280C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152662 | |||||||
| chr8:28152666 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(162): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1101-3276T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152666 | |||||||
| chr8:28152737 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0004g0263 |
2 | NA18951.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1101-3205C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152737 | |||||||
| chr8:28152781 | G | A | 12 | a0001c0001t0004g0264 a0001c0001t0004g0265 a0001c0001t0004g0278 others(9): Show |
12 | HG00438.hp2 HG01257.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.1101-3161G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152781 | |||||||
| chr8:28152857 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(162): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1101-3085A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28152857 | |||||||
| chr8:28153037 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(183): Show |
223 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1101-2905C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153037 | |||||||
| chr8:28153040 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(61): Show |
78 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1101-2902C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153040 | |||||||
| chr8:28153402 | A | C | 2 | a0001c0002t0011g0141 a0001c0002t0011g0146 |
2 | HG02257.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1101-2540A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153402 | |||||||
| chr8:28153428 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1101-2514A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153428 | |||||||
| chr8:28153565 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1101-2377A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153565 | |||||||
| chr8:28153831 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1101-2111G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153831 | |||||||
| chr8:28153855 | C | T | 1 | a0001c0001t0010g0330 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1101-2087C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153855 | |||||||
| chr8:28153876 | A | G | 4 | a0001c0001t0003g0287 a0001c0001t0003g0300 a0001c0001t0003g0304 others(1): Show |
4 | HG00741.hp1 HG01934.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1101-2066A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28153876 | |||||||
| chr8:28154050 | A | G | 1 | a0001c0001t0003g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1101-1892A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154050 | |||||||
| chr8:28154274 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1101-1668C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154274 | |||||||
| chr8:28154275 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(142): Show |
166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1101-1667A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154275 | |||||||
| chr8:28154344 | G | A | 2 | a0001c0001t0003g0298 a0001c0001t0003g0306 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1101-1598G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154344 | |||||||
| chr8:28154362 | A | C | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-1580A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154362 | |||||||
| chr8:28154394 | C | T | 1 | a0001c0001t0004g0249 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1101-1548C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154394 | |||||||
| chr8:28154401 | A | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(141): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1101-1541A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154401 | |||||||
| chr8:28154496 | T | C | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1101-1446T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154496 | |||||||
| chr8:28154639 | A | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1101-1303A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154639 | |||||||
| chr8:28154704 | G | A | 2 | a0001c0001t0004g0030 a0001c0001t0018g0030 |
2 | NA18948.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1101-1238G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154704 | |||||||
| chr8:28154858 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1101-1084C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154858 | |||||||
| chr8:28154936 | A | G | 1 | a0001c0001t0003g0311 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1101-1006A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154936 | |||||||
| chr8:28154949 | C | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1101-993C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28154949 | |||||||
| chr8:28155547 | A | C | 1 | a0001c0001t0003g0317 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1101-395A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28155547 | |||||||
| chr8:28155921 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1101-21A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 10/14 | chr8 | 28155921 | |||||||
| chr8:28156062 | A | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(250): Show |
292 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1191+30A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156062 | |||||||
| chr8:28156226 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1191+194A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156226 | |||||||
| chr8:28156347 | G | A | 4 | a0001c0001t0003g0035 a0001c0001t0003g0296 a0001c0001t0003g0301 others(1): Show |
5 | HG01256.hp1 HG01258.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1191+315G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156347 | |||||||
| chr8:28156421 | A | G | 2 | a0001c0001t0003g0036 a0001c0001t0003g0290 |
3 | HG00642.hp1 HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1191+389A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156421 | |||||||
| chr8:28156742 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1191+710A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156742 | |||||||
| chr8:28156859 | G | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(271): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.1191+827G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156859 | |||||||
| chr8:28156908 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1191+876T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28156908 | |||||||
| chr8:28157044 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(242): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1191+1012G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157044 | |||||||
| chr8:28157054 | G | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1191+1022G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157054 | |||||||
| chr8:28157289 | C | CA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(158): Show |
188 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1192-1263dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | ||||||
| chr8:28157289 | C | CAA | 80 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0054 others(77): Show |
91 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1192-1264_1192-126 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | ||||||
| chr8:28157289 | C | CAAA | 6 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0004g0250 others(3): Show |
6 | HG00544.hp1 HG03139.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-1265_1192-126 others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | ||||||
| chr8:28157289 | CA | C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0139 a0001c0001t0001g0217 others(3): Show |
6 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-1263delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | ||||||
| chr8:28157289 | CAA | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192-1264_1192-126 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28157289 | ||||||
| chr8:28157302 | A | AC | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1192-1266_1192-126 others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157302 | |||||||
| chr8:28157509 | T | A | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1192-1059T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157509 | |||||||
| chr8:28157522 | G | A | 1 | a0001c0001t0004g0243 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1192-1046G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157522 | |||||||
| chr8:28157796 | C | T | 1 | a0001c0001t0004g0248 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1192-772C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157796 | |||||||
| chr8:28157893 | A | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192-675A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28157893 | |||||||
| chr8:28158050 | CA | C | 94 | a0001c0001t0001g0044 a0001c0001t0001g0053 a0001c0001t0001g0178 others(91): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1192-498delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158050 | ||||||
| chr8:28158050 | CAA | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(36): Show |
46 | HG00597.hp1 HG00733.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.1192-499_1192-498d others(4): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158050 | ||||||
| chr8:28158050 | CAAA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(134): Show |
167 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1192-500_1192-498d others(5): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158050 | ||||||
| chr8:28158307 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192-261C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158307 | |||||||
| chr8:28158348 | A | G | 1 | a0001c0001t0002g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1192-220A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158348 | |||||||
| chr8:28158390 | G | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(26): Show |
35 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1192-178G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158390 | |||||||
| chr8:28158417 | T | G | 1 | a0001c0001t0003g0289 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1192-151T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158417 | |||||||
| chr8:28158485 | AAATAAAG | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(153): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1192-81_1192-75del others(7): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158485 | ||||||
| chr8:28158543 | C | T | 1 | a0001c0002t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1192-25C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158543 | |||||||
| chr8:28158549 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1192-19C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | chr8 | 28158549 | |||||||
| chr8:28158553 | A | AT | 9 | a0001c0001t0003g0039 a0001c0001t0004g0010 a0001c0001t0004g0033 others(6): Show |
12 | HG00544.hp1 HG00558.hp2 HG03471.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1192-6dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr8 | 28158553 | ||||||
| chr8:28158756 | C | T | 3 | a0001c0003t0008g0112 a0001c0003t0008g0113 a0001c0003t0008g0114 |
3 | NA18965.hp1 NA18987.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1257+123C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28158756 | |||||||
| chr8:28158771 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1257+138G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28158771 | |||||||
| chr8:28158840 | T | C | 2 | a0001c0001t0002g0017 a0001c0001t0002g0103 |
3 | HG01257.hp2 HG01258.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1257+207T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28158840 | |||||||
| chr8:28159023 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(60): Show |
77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1257+390G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159023 | |||||||
| chr8:28159169 | A | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02559.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1257+536A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159169 | |||||||
| chr8:28159409 | A | G | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1257+776A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159409 | |||||||
| chr8:28159578 | A | G | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258-651A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159578 | |||||||
| chr8:28159646 | C | G | 1 | a0001c0001t0002g0125 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1258-583C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159646 | |||||||
| chr8:28159747 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1258-482C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159747 | |||||||
| chr8:28159788 | A | G | 14 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0017 others(11): Show |
21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1258-441A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159788 | |||||||
| chr8:28159825 | T | G | 1 | a0001c0001t0002g0092 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1258-404T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159825 | |||||||
| chr8:28159834 | AACCATTG others(3): Show |
A | 9 | a0001c0001t0005g0220 a0001c0001t0005g0237 a0001c0001t0005g0256 others(6): Show |
9 | HG01257.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258-391_1258-382d others(12): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr8 | 28159834 | ||||||
| chr8:28159944 | A | T | 1 | a0001c0003t0008g0112 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1258-285A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159944 | |||||||
| chr8:28159995 | G | A | 2 | a0001c0001t0004g0252 a0001c0001t0004g0253 |
2 | HG01934.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1258-234G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28159995 | |||||||
| chr8:28160005 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1258-224T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 12/14 | chr8 | 28160005 | |||||||
| chr8:28160700 | A | T | 81 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0108 others(78): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1485+244A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28160700 | |||||||
| chr8:28160704 | G | GT | 5 | a0001c0001t0001g0164 a0001c0001t0001g0203 a0001c0001t0003g0292 others(2): Show |
5 | HG01934.hp1 HG03831.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+256dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28160704 | ||||||
| chr8:28160790 | GTTCAAGT others(2): Show |
G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1485+338_1485+346d others(11): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28160790 | ||||||
| chr8:28160802 | C | G | 1 | a0001c0001t0006g0235 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1485+346C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28160802 | |||||||
| chr8:28160821 | A | G | 12 | a0001c0001t0003g0011 a0001c0001t0003g0037 a0001c0001t0003g0038 others(9): Show |
16 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1485+365A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28160821 | |||||||
| chr8:28161024 | C | T | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1485+568C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161024 | |||||||
| chr8:28161059 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1485+603T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161059 | |||||||
| chr8:28161217 | G | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(18): Show |
27 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1485+761G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161217 | |||||||
| chr8:28161220 | T | C | 2 | a0001c0001t0003g0005 a0001c0001t0003g0327 |
5 | HG00642.hp2 HG01975.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1485+764T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161220 | |||||||
| chr8:28161224 | A | T | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1485+768A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161224 | |||||||
| chr8:28161393 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1486-604G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161393 | |||||||
| chr8:28161435 | G | A | 1 | a0001c0001t0003g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1486-562G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161435 | |||||||
| chr8:28161495 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1486-502G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161495 | |||||||
| chr8:28161506 | G | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1486-491G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161506 | |||||||
| chr8:28161545 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1486-452G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161545 | |||||||
| chr8:28161600 | C | T | 71 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(68): Show |
81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1486-397C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161600 | |||||||
| chr8:28161601 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1486-396G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161601 | |||||||
| chr8:28161610 | GA | G | 13 | a0001c0001t0003g0173 a0001c0001t0003g0176 a0001c0001t0003g0190 others(10): Show |
14 | HG00738.hp2 HG01243.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1486-368delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28161610 | ||||||
| chr8:28161651 | T | TA | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1486-343dupA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr8 | 28161651 | ||||||
| chr8:28161944 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1486-53T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 13/14 | chr8 | 28161944 | |||||||
| chr8:28162094 | C | T | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1567+16C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162094 | |||||||
| chr8:28162265 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(11): Show |
19 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1567+187G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162265 | |||||||
| chr8:28162484 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1567+406C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162484 | |||||||
| chr8:28162494 | A | G | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1567+416A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162494 | |||||||
| chr8:28162524 | T | A | 1 | a0001c0001t0002g0014 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1567+446T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162524 | |||||||
| chr8:28162539 | A | G | 2 | a0001c0001t0003g0028 a0001c0001t0003g0215 |
3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1567+461A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162539 | |||||||
| chr8:28162546 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1567+468G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162546 | |||||||
| chr8:28162554 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+476T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162554 | |||||||
| chr8:28162570 | G | A | 4 | a0001c0001t0003g0173 a0001c0001t0003g0176 a0001c0001t0003g0190 others(1): Show |
4 | HG00738.hp2 HG02258.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+492G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162570 | |||||||
| chr8:28162649 | A | G | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1567+571A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162649 | |||||||
| chr8:28162935 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1567+857G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28162935 | |||||||
| chr8:28163120 | G | T | 8 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0003t0008g0109 others(5): Show |
8 | HG00597.hp1 HG02109.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567+1042G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163120 | |||||||
| chr8:28163187 | C | G | 1 | a0001c0001t0003g0335 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1567+1109C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163187 | |||||||
| chr8:28163376 | A | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0017 others(11): Show |
21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567+1298A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163376 | |||||||
| chr8:28163503 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+1425T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163503 | |||||||
| chr8:28163524 | CT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0029 others(17): Show |
24 | HG00408.hp1 HG00597.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1567+1461delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28163524 | ||||||
| chr8:28163524 | CTT | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.1567+1460_1567+146 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28163524 | ||||||
| chr8:28163588 | G | T | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+1510G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163588 | |||||||
| chr8:28163708 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1567+1630G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163708 | |||||||
| chr8:28163744 | T | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+1666T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163744 | |||||||
| chr8:28163794 | G | A | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+1716G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163794 | |||||||
| chr8:28163827 | C | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG01884.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567+1749C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28163827 | |||||||
| chr8:28164043 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1567+1965A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164043 | |||||||
| chr8:28164169 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1567+2091T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164169 | |||||||
| chr8:28164252 | G | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0017 others(11): Show |
21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567+2174G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164252 | |||||||
| chr8:28164272 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+2194G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164272 | |||||||
| chr8:28164278 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1567+2200C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164278 | |||||||
| chr8:28164548 | G | A | 24 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(21): Show |
30 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1567+2470G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164548 | |||||||
| chr8:28164611 | C | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1567+2533C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164611 | |||||||
| chr8:28164657 | A | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0054 a0001c0001t0001g0108 others(7): Show |
11 | HG00597.hp1 HG02109.hp2 HG03195.hp2 others(8): Show |
intron_variant | MODIFIER | c.1567+2579A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164657 | |||||||
| chr8:28164721 | A | T | 1 | a0001c0001t0002g0086 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1567+2643A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164721 | |||||||
| chr8:28164900 | G | T | 1 | a0001c0001t0003g0305 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1567+2822G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28164900 | |||||||
| chr8:28165155 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0167 others(6): Show |
12 | HG00408.hp1 HG02165.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1567+3077G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165155 | |||||||
| chr8:28165190 | G | C | 1 | a0001c0002t0009g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1567+3112G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165190 | |||||||
| chr8:28165267 | G | A | 30 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(27): Show |
36 | HG00733.hp1 HG01243.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1567+3189G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165267 | |||||||
| chr8:28165274 | G | A | 9 | a0001c0001t0001g0052 a0001c0001t0001g0139 a0001c0002t0001g0145 others(6): Show |
10 | HG01243.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567+3196G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165274 | |||||||
| chr8:28165409 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(141): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1567+3331C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165409 | |||||||
| chr8:28165439 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(235): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1567+3361T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165439 | |||||||
| chr8:28165539 | G | A | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+3461G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165539 | |||||||
| chr8:28165633 | T | C | 1 | a0001c0001t0002g0015 | 2 | NA18983.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1567+3555T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165633 | |||||||
| chr8:28165720 | G | A | 272 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(269): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.1567+3642G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165720 | |||||||
| chr8:28165864 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0002g0063 |
2 | HG00639.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1567+3786A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165864 | |||||||
| chr8:28165891 | A | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+3813A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28165891 | |||||||
| chr8:28166142 | G | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
302 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1567+4064G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166142 | |||||||
| chr8:28166191 | C | T | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(267): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1567+4113C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166191 | |||||||
| chr8:28166207 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+4129T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166207 | |||||||
| chr8:28166297 | A | G | 1 | a0001c0001t0005g0220 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1567+4219A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166297 | |||||||
| chr8:28166384 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1567+4306T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166384 | |||||||
| chr8:28166581 | C | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1567+4503C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166581 | |||||||
| chr8:28166803 | C | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(60): Show |
77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1567+4725C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166803 | |||||||
| chr8:28166826 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+4748C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166826 | |||||||
| chr8:28166910 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(141): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1567+4832C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166910 | |||||||
| chr8:28166935 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1567+4857T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166935 | |||||||
| chr8:28166951 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1567+4873A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166951 | |||||||
| chr8:28166995 | G | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1567+4917G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28166995 | |||||||
| chr8:28167029 | G | A | 1 | a0001c0001t0003g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1567+4951G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167029 | |||||||
| chr8:28167270 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1567+5192G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167270 | |||||||
| chr8:28167272 | C | G | 1 | a0001c0001t0002g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1567+5194C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167272 | |||||||
| chr8:28167326 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1567+5248G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167326 | |||||||
| chr8:28167327 | A | C | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+5249A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167327 | |||||||
| chr8:28167332 | C | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+5254C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167332 | |||||||
| chr8:28167384 | A | T | 1 | a0001c0001t0001g0212 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1567+5306A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167384 | |||||||
| chr8:28167418 | G | A | 8 | a0001c0001t0001g0054 a0001c0001t0001g0108 a0001c0003t0008g0109 others(5): Show |
8 | HG00597.hp1 HG02109.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.1567+5340G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167418 | |||||||
| chr8:28167424 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(60): Show |
77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1567+5346C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167424 | |||||||
| chr8:28167425 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(234): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1567+5347A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167425 | |||||||
| chr8:28167622 | C | A | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+5544C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167622 | |||||||
| chr8:28167642 | T | A | 2 | a0001c0001t0003g0304 a0001c0001t0003g0305 |
2 | HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1567+5564T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167642 | |||||||
| chr8:28167682 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+5604A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167682 | |||||||
| chr8:28167804 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1567+5726A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167804 | |||||||
| chr8:28167893 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1567+5815A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167893 | |||||||
| chr8:28167900 | A | G | 1 | a0001c0001t0003g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1567+5822A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167900 | |||||||
| chr8:28167960 | G | T | 1 | a0001c0001t0004g0265 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1567+5882G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28167960 | |||||||
| chr8:28168008 | T | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(200): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1567+5930T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168008 | |||||||
| chr8:28168333 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1567+6255T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168333 | |||||||
| chr8:28168410 | G | A | 71 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(68): Show |
81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1567+6332G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168410 | |||||||
| chr8:28168414 | T | C | 9 | a0001c0001t0001g0052 a0001c0001t0001g0139 a0001c0002t0001g0145 others(6): Show |
10 | HG01243.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567+6336T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168414 | |||||||
| chr8:28168649 | T | C | 1 | a0001c0001t0003g0285 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1567+6571T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168649 | |||||||
| chr8:28168669 | T | G | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1567+6591T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168669 | |||||||
| chr8:28168683 | C | A | 1 | a0001c0001t0003g0305 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1567+6605C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168683 | |||||||
| chr8:28168750 | G | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1567+6672G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168750 | |||||||
| chr8:28168776 | C | T | 1 | a0001c0001t0004g0227 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1567+6698C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168776 | |||||||
| chr8:28168824 | T | C | 1 | a0001c0001t0004g0225 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1567+6746T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168824 | |||||||
| chr8:28168868 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+6790G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168868 | |||||||
| chr8:28168928 | A | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1567+6850A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28168928 | |||||||
| chr8:28169226 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1567+7148G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169226 | |||||||
| chr8:28169325 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+7247C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169325 | |||||||
| chr8:28169347 | G | A | 1 | a0001c0001t0004g0255 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1567+7269G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169347 | |||||||
| chr8:28169386 | C | A | 2 | a0001c0001t0001g0337 a0001c0001t0001g0338 |
2 | HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1567+7308C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169386 | |||||||
| chr8:28169441 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+7363T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169441 | |||||||
| chr8:28169476 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+7398A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169476 | |||||||
| chr8:28169489 | A | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(235): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1567+7411A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169489 | |||||||
| chr8:28169634 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1567+7556T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169634 | |||||||
| chr8:28169677 | T | G | 1 | a0001c0001t0003g0291 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1567+7599T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169677 | |||||||
| chr8:28169755 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+7677G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169755 | |||||||
| chr8:28169841 | T | C | 14 | a0001c0001t0002g0002 a0001c0001t0002g0014 a0001c0001t0002g0017 others(11): Show |
21 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1567+7763T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169841 | |||||||
| chr8:28169892 | C | G | 1 | a0001c0001t0003g0299 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1567+7814C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169892 | |||||||
| chr8:28169912 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+7834C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169912 | |||||||
| chr8:28169982 | C | G | 1 | a0001c0001t0004g0262 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1567+7904C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28169982 | |||||||
| chr8:28170001 | A | G | 77 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(74): Show |
87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1567+7923A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170001 | |||||||
| chr8:28170232 | C | G | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1567+8154C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170232 | |||||||
| chr8:28170367 | A | G | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1567+8289A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170367 | |||||||
| chr8:28170493 | G | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(140): Show |
164 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.1567+8415G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170493 | |||||||
| chr8:28170611 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1567+8533A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170611 | |||||||
| chr8:28170632 | G | T | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+8554G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170632 | |||||||
| chr8:28170637 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0139 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1567+8559T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170637 | |||||||
| chr8:28170674 | C | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+8596C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170674 | |||||||
| chr8:28170703 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+8625A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28170703 | |||||||
| chr8:28170907 | A | AT | 1 | a0001c0001t0003g0011 | 3 | HG01069.hp2 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1567+8833dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28170907 | ||||||
| chr8:28171020 | T | C | 1 | a0001c0001t0002g0105 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1567+8942T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171020 | |||||||
| chr8:28171113 | C | G | 1 | a0001c0001t0002g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1567+9035C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171113 | |||||||
| chr8:28171165 | G | C | 77 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(74): Show |
87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1567+9087G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171165 | |||||||
| chr8:28171268 | C | T | 2 | a0001c0001t0001g0053 a0001c0004t0001g0143 |
2 | HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1567+9190C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171268 | |||||||
| chr8:28171279 | C | CT | 5 | a0001c0001t0002g0051 a0001c0001t0002g0083 a0001c0001t0002g0085 others(2): Show |
5 | HG01261.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1567+9202dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28171279 | ||||||
| chr8:28171352 | CT | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(266): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1567+9287delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28171352 | ||||||
| chr8:28171362 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(235): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1567+9284T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171362 | |||||||
| chr8:28171492 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+9414T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171492 | |||||||
| chr8:28171501 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(266): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1567+9423C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171501 | |||||||
| chr8:28171667 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1567+9589G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171667 | |||||||
| chr8:28171810 | G | A | 1 | a0001c0001t0004g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1567+9732G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171810 | |||||||
| chr8:28171856 | A | G | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+9778A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171856 | |||||||
| chr8:28171926 | A | G | 1 | a0001c0001t0006g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1567+9848A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28171926 | |||||||
| chr8:28172142 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG02559.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567+10064A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172142 | |||||||
| chr8:28172227 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1567+10149T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172227 | |||||||
| chr8:28172243 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+10165A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172243 | |||||||
| chr8:28172280 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0108 |
2 | HG02109.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1567+10202A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172280 | |||||||
| chr8:28172384 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1567+10306C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172384 | |||||||
| chr8:28172498 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0212 |
3 | HG03688.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1567+10420T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172498 | |||||||
| chr8:28172864 | T | C | 9 | a0001c0001t0005g0220 a0001c0001t0005g0237 a0001c0001t0005g0256 others(6): Show |
9 | HG01257.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1567+10786T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28172864 | |||||||
| chr8:28173470 | G | A | 1 | a0001c0001t0004g0231 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1567+11392G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28173470 | |||||||
| chr8:28173553 | A | AT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(160): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1567+11486dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28173553 | ||||||
| chr8:28173684 | T | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(242): Show |
283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.1567+11606T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28173684 | |||||||
| chr8:28173767 | G | A | 1 | a0001c0001t0003g0335 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1567+11689G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28173767 | |||||||
| chr8:28173872 | T | TAAGAATG others(325): Show |
1 | a0001c0001t0003g0198 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1567+11810_1567+11 others(338): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28173872 | ||||||
| chr8:28174028 | G | A | 1 | a0001c0001t0003g0332 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1567+11950G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174028 | |||||||
| chr8:28174051 | T | C | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1567+11973T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174051 | |||||||
| chr8:28174139 | C | T | 1 | a0001c0001t0003g0334 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1567+12061C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174139 | |||||||
| chr8:28174257 | T | A | 68 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1567+12179T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174257 | |||||||
| chr8:28174290 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1567+12212A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174290 | |||||||
| chr8:28174409 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1567+12331C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174409 | |||||||
| chr8:28174547 | G | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(142): Show |
166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.1567+12469G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174547 | |||||||
| chr8:28174708 | T | C | 330 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(327): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1567+12630T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174708 | |||||||
| chr8:28174805 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1567+12727G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174805 | |||||||
| chr8:28174925 | G | A | 81 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0293 others(78): Show |
88 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1567+12847G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28174925 | |||||||
| chr8:28175119 | C | G | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+13041C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175119 | |||||||
| chr8:28175129 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(234): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.1567+13051C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175129 | |||||||
| chr8:28175187 | A | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+13109A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175187 | |||||||
| chr8:28175287 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1567+13209A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175287 | |||||||
| chr8:28175320 | T | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(320): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.1567+13242T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175320 | |||||||
| chr8:28175370 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1567+13292G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175370 | |||||||
| chr8:28175386 | T | C | 1 | a0001c0001t0013g0329 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1567+13308T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175386 | |||||||
| chr8:28175500 | C | A | 68 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1567+13422C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175500 | |||||||
| chr8:28175662 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(6): Show |
14 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1567+13584C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175662 | |||||||
| chr8:28175810 | C | CT | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(276): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1567+13753dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | ||||||
| chr8:28175810 | C | CTT | 34 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0156 others(31): Show |
35 | HG00621.hp1 HG00741.hp2 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.1567+13752_1567+13 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | ||||||
| chr8:28175810 | CT | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1567+13753delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | ||||||
| chr8:28175810 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1567+13744_1567+13 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28175810 | ||||||
| chr8:28175831 | T | G | 1 | a0001c0001t0001g0029 | 2 | NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1567+13753T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175831 | |||||||
| chr8:28175883 | C | T | 2 | a0001c0001t0003g0036 a0001c0001t0003g0290 |
3 | HG00642.hp1 HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1568-13766C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175883 | |||||||
| chr8:28175885 | G | T | 81 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0293 others(78): Show |
88 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1568-13764G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175885 | |||||||
| chr8:28175906 | G | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-13743G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175906 | |||||||
| chr8:28175918 | T | A | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1568-13731T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28175918 | |||||||
| chr8:28176005 | C | T | 1 | a0001c0001t0002g0128 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1568-13644C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176005 | |||||||
| chr8:28176027 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0139 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1568-13622A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176027 | |||||||
| chr8:28176055 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1568-13594G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176055 | |||||||
| chr8:28176167 | T | G | 4 | a0001c0001t0001g0034 a0001c0001t0003g0284 a0001c0001t0003g0285 others(1): Show |
5 | HG02056.hp2 NA18954.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1568-13482T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176167 | |||||||
| chr8:28176206 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1568-13443T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176206 | |||||||
| chr8:28176302 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(141): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1568-13347C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176302 | |||||||
| chr8:28176303 | G | A | 1 | a0001c0001t0006g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1568-13346G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176303 | |||||||
| chr8:28176663 | AT | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1568-12985delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176663 | |||||||
| chr8:28176726 | T | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-12923T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176726 | |||||||
| chr8:28176873 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0118 |
3 | HG02080.hp2 NA18963.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1568-12776A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176873 | |||||||
| chr8:28176920 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18985.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1568-12729C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176920 | |||||||
| chr8:28176994 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(240): Show |
281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1568-12655A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28176994 | |||||||
| chr8:28177215 | C | T | 1 | a0001c0001t0012g0325 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1568-12434C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177215 | |||||||
| chr8:28177225 | A | AT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568-12414dupT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28177225 | ||||||
| chr8:28177225 | AT | A | 4 | a0001c0001t0004g0003 a0001c0001t0004g0243 a0001c0001t0004g0244 others(1): Show |
8 | HG00423.hp2 HG00621.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-12414delT | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28177225 | ||||||
| chr8:28177329 | G | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-12320G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177329 | |||||||
| chr8:28177347 | T | C | 135 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0216 others(132): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1568-12302T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177347 | |||||||
| chr8:28177373 | C | T | 1 | a0001c0001t0003g0336 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1568-12276C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177373 | |||||||
| chr8:28177415 | A | G | 1 | a0001c0001t0003g0301 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1568-12234A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177415 | |||||||
| chr8:28177520 | T | A | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-12129T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177520 | |||||||
| chr8:28177711 | CAAGT | C | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-11934_1568-11 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28177711 | ||||||
| chr8:28177873 | T | C | 1 | a0001c0001t0003g0304 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1568-11776T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177873 | |||||||
| chr8:28177935 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(336): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-11714A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28177935 | |||||||
| chr8:28178070 | A | C | 7 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0039 others(4): Show |
7 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-11579A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178070 | |||||||
| chr8:28178178 | A | G | 6 | a0001c0002t0009g0023 a0001c0002t0009g0140 a0001c0002t0009g0142 others(3): Show |
7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-11471A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178178 | |||||||
| chr8:28178240 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1568-11409A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178240 | |||||||
| chr8:28178244 | G | C | 69 | a0001c0001t0001g0272 a0001c0001t0004g0003 a0001c0001t0004g0009 others(66): Show |
79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1568-11405G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178244 | |||||||
| chr8:28178295 | C | T | 1 | a0001c0001t0003g0321 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1568-11354C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178295 | |||||||
| chr8:28178317 | T | C | 2 | a0001c0001t0003g0005 a0001c0001t0003g0327 |
5 | HG00642.hp2 HG01975.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1568-11332T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178317 | |||||||
| chr8:28178377 | C | CCTAA | 11 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0001t0001g0337 others(8): Show |
12 | HG00597.hp1 HG02615.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.1568-11269_1568-11 others(10): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28178377 | ||||||
| chr8:28178400 | C | T | 3 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0002t0001g0145 |
3 | HG02615.hp1 HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1568-11249C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178400 | |||||||
| chr8:28178401 | G | A | 1 | a0001c0001t0003g0176 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1568-11248G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178401 | |||||||
| chr8:28178461 | T | C | 64 | a0001c0001t0001g0034 a0001c0001t0003g0005 a0001c0001t0003g0011 others(61): Show |
75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1568-11188T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178461 | |||||||
| chr8:28178470 | T | G | 1 | a0001c0001t0001g0049 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1568-11179T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178470 | |||||||
| chr8:28178651 | C | A | 68 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-10998C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178651 | |||||||
| chr8:28178700 | T | C | 1 | a0001c0002t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1568-10949T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178700 | |||||||
| chr8:28178835 | G | A | 1 | a0001c0001t0003g0326 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1568-10814G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178835 | |||||||
| chr8:28178883 | C | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1568-10766C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178883 | |||||||
| chr8:28178925 | G | A | 1 | a0001c0001t0004g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1568-10724G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28178925 | |||||||
| chr8:28179078 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(141): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1568-10571G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179078 | |||||||
| chr8:28179332 | T | G | 1 | a0001c0001t0006g0235 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1568-10317T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179332 | |||||||
| chr8:28179338 | A | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1568-10311A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179338 | |||||||
| chr8:28179345 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1568-10304G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179345 | |||||||
| chr8:28179521 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(5): Show |
13 | HG00733.hp1 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1568-10128G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179521 | |||||||
| chr8:28179739 | G | A | 4 | a0001c0001t0001g0153 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG01884.hp2 HG03041.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-9910G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179739 | |||||||
| chr8:28179763 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1568-9886C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179763 | |||||||
| chr8:28179768 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1568-9881G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179768 | |||||||
| chr8:28179821 | A | C | 71 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(68): Show |
81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1568-9828A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28179821 | |||||||
| chr8:28180047 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1568-9602A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180047 | |||||||
| chr8:28180129 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(60): Show |
77 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1568-9520G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180129 | |||||||
| chr8:28180136 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1568-9513C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180136 | |||||||
| chr8:28180157 | A | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-9492A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180157 | |||||||
| chr8:28180167 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1568-9482T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180167 | |||||||
| chr8:28180202 | A | AACACATG others(5): Show |
4 | a0001c0001t0002g0071 a0001c0001t0002g0099 a0001c0001t0002g0104 others(1): Show |
4 | HG01081.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-9446_1568-943 others(16): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28180202 | ||||||
| chr8:28180309 | T | G | 6 | a0001c0001t0001g0008 a0001c0001t0001g0169 a0001c0001t0001g0184 others(3): Show |
8 | HG00597.hp2 NA18947.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-9340T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180309 | |||||||
| chr8:28180470 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1568-9179A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180470 | |||||||
| chr8:28180489 | T | G | 71 | a0001c0001t0001g0272 a0001c0001t0001g0337 a0001c0001t0001g0338 others(68): Show |
81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1568-9160T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180489 | |||||||
| chr8:28180500 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0283 |
3 | HG02572.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1568-9149A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180500 | |||||||
| chr8:28180503 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1568-9146G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180503 | |||||||
| chr8:28180539 | C | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(254): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1568-9110C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180539 | |||||||
| chr8:28180557 | GTC | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-9088_1568-908 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28180557 | ||||||
| chr8:28180841 | T | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1568-8808T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180841 | |||||||
| chr8:28180877 | C | A | 1 | a0001c0001t0002g0099 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1568-8772C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180877 | |||||||
| chr8:28180910 | C | T | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-8739C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28180910 | |||||||
| chr8:28181259 | A | G | 332 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(329): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.1568-8390A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181259 | |||||||
| chr8:28181272 | C | A | 9 | a0001c0001t0003g0005 a0001c0001t0003g0312 a0001c0001t0003g0315 others(6): Show |
12 | HG00642.hp2 HG00733.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1568-8377C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181272 | |||||||
| chr8:28181314 | C | A | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-8335C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181314 | |||||||
| chr8:28181602 | A | G | 68 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-8047A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181602 | |||||||
| chr8:28181608 | A | G | 6 | a0001c0002t0009g0023 a0001c0002t0009g0140 a0001c0002t0009g0142 others(3): Show |
7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-8041A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181608 | |||||||
| chr8:28181657 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1568-7992G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181657 | |||||||
| chr8:28181713 | C | T | 2 | a0001c0001t0003g0028 a0001c0001t0003g0215 |
3 | HG02055.hp2 HG02970.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1568-7936C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181713 | |||||||
| chr8:28181959 | CTTTG | C | 3 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0006g0232 |
3 | HG02145.hp2 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1568-7674_1568-767 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28181959 | ||||||
| chr8:28181966 | TG | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(78): Show |
98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1568-7682delG | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28181966 | |||||||
| chr8:28182227 | T | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0216 |
3 | NA18978.hp2 NA18995.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1568-7422T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182227 | |||||||
| chr8:28182283 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1568-7366G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182283 | |||||||
| chr8:28182475 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1568-7174C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182475 | |||||||
| chr8:28182517 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1568-7132C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182517 | |||||||
| chr8:28182608 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1568-7041C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182608 | |||||||
| chr8:28182677 | T | G | 1 | a0001c0001t0003g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1568-6972T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182677 | |||||||
| chr8:28182725 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(15): Show |
24 | HG00733.hp1 HG01243.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1568-6924G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182725 | |||||||
| chr8:28182843 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0139 a0001c0001t0001g0167 others(1): Show |
4 | HG02723.hp1 HG03098.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1568-6806C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182843 | |||||||
| chr8:28182854 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1568-6795G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182854 | |||||||
| chr8:28182874 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1568-6775G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182874 | |||||||
| chr8:28182957 | C | G | 5 | a0001c0001t0001g0153 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG01884.hp2 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-6692C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182957 | |||||||
| chr8:28182964 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0216 a0001c0003t0008g0109 others(5): Show |
9 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1568-6685G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28182964 | |||||||
| chr8:28183000 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1568-6649C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183000 | |||||||
| chr8:28183076 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1568-6573C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183076 | |||||||
| chr8:28183158 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1568-6491G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183158 | |||||||
| chr8:28183165 | T | TAAAC | 8 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0224 others(5): Show |
8 | HG02451.hp1 HG02976.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-6482_1568-647 others(8): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28183165 | ||||||
| chr8:28183195 | G | A | 44 | a0001c0001t0002g0013 a0001c0001t0002g0015 a0001c0001t0002g0016 others(41): Show |
48 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.1568-6454G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183195 | |||||||
| chr8:28183531 | C | A | 2 | a0001c0001t0004g0032 a0001c0001t0004g0268 |
3 | HG01074.hp2 HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1568-6118C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183531 | |||||||
| chr8:28183645 | G | T | 68 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-6004G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183645 | |||||||
| chr8:28183651 | C | T | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-5998C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183651 | |||||||
| chr8:28183732 | C | T | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-5917C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183732 | |||||||
| chr8:28183889 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1568-5760G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183889 | |||||||
| chr8:28183916 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1568-5733C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183916 | |||||||
| chr8:28183921 | A | G | 71 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0004g0003 others(68): Show |
81 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1568-5728A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183921 | |||||||
| chr8:28183936 | T | C | 9 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0007g0147 others(6): Show |
9 | HG01891.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1568-5713T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183936 | |||||||
| chr8:28183964 | G | A | 1 | a0001c0001t0012g0325 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1568-5685G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28183964 | |||||||
| chr8:28184045 | T | A | 7 | a0001c0001t0006g0221 a0001c0001t0006g0232 a0001c0001t0006g0233 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-5604T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184045 | |||||||
| chr8:28184128 | A | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(12): Show |
20 | HG00733.hp1 HG01255.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1568-5521A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184128 | |||||||
| chr8:28184154 | G | A | 1 | a0001c0001t0002g0098 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1568-5495G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184154 | |||||||
| chr8:28184392 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0197 |
2 | NA18967.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1568-5257G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184392 | |||||||
| chr8:28184418 | G | T | 4 | a0001c0001t0002g0071 a0001c0001t0002g0099 a0001c0001t0002g0104 others(1): Show |
4 | HG01081.hp1 HG01175.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-5231G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184418 | |||||||
| chr8:28184472 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1568-5177A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184472 | |||||||
| chr8:28184578 | G | A | 14 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0003g0290 others(11): Show |
16 | HG00423.hp1 HG00639.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1568-5071G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184578 | |||||||
| chr8:28184587 | T | C | 7 | a0001c0001t0002g0078 a0001c0001t0002g0090 a0001c0001t0002g0093 others(4): Show |
7 | NA18966.hp2 NA18988.hp2 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.1568-5062T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184587 | |||||||
| chr8:28184593 | T | C | 79 | a0001c0001t0001g0034 a0001c0001t0001g0217 a0001c0001t0001g0218 others(76): Show |
91 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1568-5056T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184593 | |||||||
| chr8:28184605 | G | A | 1 | a0001c0001t0001g0034 | 2 | NA18999.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1568-5044G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184605 | |||||||
| chr8:28184670 | A | G | 149 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0216 others(146): Show |
172 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1568-4979A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184670 | |||||||
| chr8:28184806 | T | TGA | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG03139.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1568-4841_1568-484 others(6): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28184806 | ||||||
| chr8:28184876 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1568-4773T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184876 | |||||||
| chr8:28184961 | T | TC | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(236): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1568-4686dupC | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28184961 | ||||||
| chr8:28184968 | CA | C | 15 | a0001c0001t0001g0185 a0001c0001t0001g0222 a0001c0001t0001g0223 others(12): Show |
15 | HG00597.hp1 HG01168.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1568-4667delA | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28184968 | ||||||
| chr8:28184999 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1568-4650G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28184999 | |||||||
| chr8:28185395 | A | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-4254A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185395 | |||||||
| chr8:28185617 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(149): Show |
175 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.1568-4032A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185617 | |||||||
| chr8:28185772 | A | G | 1 | a0001c0002t0009g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1568-3877A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185772 | |||||||
| chr8:28185857 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0050 others(4): Show |
10 | HG00733.hp1 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1568-3792C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185857 | |||||||
| chr8:28185898 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1568-3751T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185898 | |||||||
| chr8:28185948 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1568-3701C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28185948 | |||||||
| chr8:28186006 | A | G | 7 | a0001c0001t0001g0108 a0001c0001t0007g0147 a0001c0001t0007g0148 others(4): Show |
7 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-3643A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186006 | |||||||
| chr8:28186031 | A | G | 68 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(65): Show |
78 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1568-3618A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186031 | |||||||
| chr8:28186154 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1568-3495A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186154 | |||||||
| chr8:28186156 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(303): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(351): Show |
intron_variant | MODIFIER | c.1568-3493C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186156 | |||||||
| chr8:28186618 | C | T | 1 | a0001c0001t0004g0231 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1568-3031C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186618 | |||||||
| chr8:28186766 | A | T | 1 | a0001c0001t0004g0010 | 3 | NA18944.hp2 NA18955.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1568-2883A>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28186766 | |||||||
| chr8:28187071 | G | A | 6 | a0001c0002t0009g0023 a0001c0002t0009g0140 a0001c0002t0009g0142 others(3): Show |
7 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1568-2578G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187071 | |||||||
| chr8:28187172 | T | C | 1 | a0001c0001t0017g0041 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1568-2477T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187172 | |||||||
| chr8:28187177 | A | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(336): Show |
395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.1568-2472A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187177 | |||||||
| chr8:28187216 | C | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0034 others(71): Show |
88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1568-2433C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187216 | |||||||
| chr8:28187486 | C | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0139 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1568-2163C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187486 | |||||||
| chr8:28187568 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1568-2081G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187568 | |||||||
| chr8:28187572 | G | A | 1 | a0001c0001t0007g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1568-2077G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187572 | |||||||
| chr8:28187697 | G | T | 4 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0002g0080 others(1): Show |
4 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1568-1952G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187697 | |||||||
| chr8:28187848 | T | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0049 others(9): Show |
14 | HG02109.hp1 HG02572.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1568-1801T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187848 | |||||||
| chr8:28187851 | G | A | 1 | a0001c0001t0003g0333 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1568-1798G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28187851 | |||||||
| chr8:28188114 | T | G | 1 | a0001c0001t0002g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1568-1535T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188114 | |||||||
| chr8:28188159 | C | T | 1 | a0001c0003t0008g0111 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1568-1490C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188159 | |||||||
| chr8:28188180 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1568-1469C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188180 | |||||||
| chr8:28188181 | C | T | 1 | a0001c0001t0002g0013 | 2 | HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1568-1468C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188181 | |||||||
| chr8:28188194 | G | A | 7 | a0001c0002t0001g0145 a0001c0002t0009g0023 a0001c0002t0009g0140 others(4): Show |
8 | HG01243.hp1 HG02257.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1568-1455G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188194 | |||||||
| chr8:28188342 | G | C | 1 | a0001c0001t0003g0323 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1568-1307G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188342 | |||||||
| chr8:28188347 | G | T | 77 | a0001c0001t0001g0293 a0001c0001t0002g0013 a0001c0001t0002g0015 others(74): Show |
84 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1568-1302G>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188347 | |||||||
| chr8:28188356 | CAAGGGGC others(12): Show |
C | 70 | a0001c0001t0001g0034 a0001c0001t0003g0005 a0001c0001t0003g0011 others(67): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.1568-1290_1568-127 others(23): Show |
ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr8 | 28188356 | ||||||
| chr8:28188378 | T | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-1271T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188378 | |||||||
| chr8:28188647 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1568-1002C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188647 | |||||||
| chr8:28188679 | T | C | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-970T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188679 | |||||||
| chr8:28188706 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1568-943T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188706 | |||||||
| chr8:28188718 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1568-931G>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188718 | |||||||
| chr8:28188883 | T | C | 69 | a0001c0001t0004g0003 a0001c0001t0004g0009 a0001c0001t0004g0010 others(66): Show |
79 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1568-766T>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188883 | |||||||
| chr8:28188930 | C | T | 5 | a0001c0001t0003g0173 a0001c0001t0003g0176 a0001c0001t0003g0190 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1568-719C>T | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188930 | |||||||
| chr8:28188965 | A | G | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-684A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188965 | |||||||
| chr8:28188974 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1568-675C>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28188974 | |||||||
| chr8:28189137 | A | G | 6 | a0001c0001t0007g0147 a0001c0001t0007g0148 a0001c0001t0007g0149 others(3): Show |
6 | HG01891.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-512A>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189137 | |||||||
| chr8:28189174 | T | G | 6 | a0001c0003t0008g0109 a0001c0003t0008g0110 a0001c0003t0008g0111 others(3): Show |
6 | HG00597.hp1 NA18955.hp1 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1568-475T>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189174 | |||||||
| chr8:28189294 | C | G | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(188): Show |
225 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1568-355C>G | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189294 | |||||||
| chr8:28189348 | A | C | 1 | a0001c0001t0002g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1568-301A>C | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189348 | |||||||
| chr8:28189444 | T | A | 338 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(335): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.1568-205T>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189444 | |||||||
| chr8:28189593 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1568-56G>A | ELP3 | ENSG00000134014.18 | transcript | ENST00000256398.13 | protein_coding | 14/14 | chr8 | 28189593 |