Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11319 |
| ensemblid | ENSG00000122882.11 |
| hgncid | 17029 |
| symbol | ECD |
| name | ecdysoneless cell cycle regulator |
| refseq_nuc | NM_007265.3 |
| refseq_prot | NP_009196.1 |
| ensembl_nuc | ENST00000372979.9 |
| ensembl_prot | ENSP00000362070.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 73133668 |
| end | 73168008 |
| strand | - |
| ver | v1.2 |
| region | chr10:73133668-73168008 |
| region5000 | chr10:73128668-73173008 |
| regionname0 | ECD_chr10_73133668_73168008 |
| regionname5000 | ECD_chr10_73128668_73173008 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 644 | 162 | 49 | 20 | 73 | 0 | 18 | 54 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0002 | 0/0 | 644 | 82 | 14 | 8 | 51 | 0 | 9 | 36 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0003 | 0/0 | 644 | 21 | 19 | 2 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0004 | 0/0 | 644 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0005 | 0/0 | 644 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0006 | 0/0 | 644 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | MEESM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0007 | 0/0 | 644 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0008 | 0/0 | 644 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| a0009 | 0/0 | 644 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ECD_chr10_73128668_73173008 | ECD | MEETM others(639): Show |
chr10 | 73128668 | 73173008 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1932 | 154 | 42 | 20 | 72 | 0 | 18 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0001c0006 | 0/0 | 1932 | 6 | 6 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0001c0011 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0001c0012 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0002c0002 | 0/0 | 1932 | 51 | 14 | 7 | 21 | 0 | 9 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0002c0003 | 0/0 | 1932 | 30 | 0 | 1 | 29 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0002c0008 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0003c0004 | 0/0 | 1932 | 14 | 14 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0003c0005 | 0/0 | 1932 | 7 | 5 | 2 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0004c0007 | 0/0 | 1932 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0005c0009 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0006c0015 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0007c0010 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0008c0013 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 | ||
| a0009c0014 | 0/0 | 1932 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | ATGGA others(1927): Show |
chr10 | 73128668 | 73173008 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3006 | 148 | 36 | 20 | 72 | 0 | 18 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0001c0001t0005 | 0/0 | 3006 | 6 | 6 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0001c0006t0001 | 0/0 | 3006 | 6 | 6 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0001c0011t0001 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0001c0012t0001 | 0/0 | 3006 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0002c0002t0002 | 0/0 | 3006 | 38 | 4 | 4 | 21 | 0 | 9 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0002c0002t0003 | 0/0 | 3006 | 13 | 10 | 3 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0002c0003t0002 | 0/0 | 3006 | 24 | 0 | 1 | 23 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0002c0003t0004 | 0/0 | 3006 | 6 | 0 | 0 | 6 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0002c0008t0002 | 0/0 | 3006 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0003c0004t0003 | 0/0 | 3006 | 14 | 14 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0003c0005t0003 | 0/0 | 3006 | 7 | 5 | 2 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0004c0007t0001 | 0/0 | 3006 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0005c0009t0002 | 0/0 | 3006 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0006c0015t0002 | 0/0 | 3006 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0007c0010t0003 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0008c0013t0001 | 0/0 | 3006 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| a0009c0014t0001 | 0/0 | 3006 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | GGCTT others(3001): Show |
chr10 | 73128668 | 73173008 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 2 | 1 | 3 | 0 | 4 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0004 | 0/0 | 6 | 3 | 1 | 1 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0005g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0005g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0006t0001g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0006t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0011t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0001c0012t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0009 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0002c0008t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0004t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0005t0003g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0005t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0005t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0005t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0003c0005t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0004c0007t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0004c0007t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0005c0009t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0006c0015t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0007c0010t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0008c0013t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| a0009c0014t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00408 | hp2 | a0002 | c0003 | t0002 | g0072 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00423 | hp2 | a0002 | c0003 | t0002 | g0073 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00438 | hp1 | a0005 | c0009 | t0002 | g0068 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00558 | hp1 | a0002 | c0003 | t0002 | g0008 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00621 | hp1 | a0002 | c0003 | t0002 | g0016 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0047 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00673 | hp2 | a0002 | c0003 | t0002 | g0060 | EAS | CHS | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0071 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG00735 | hp2 | a0003 | c0005 | t0003 | g0096 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0041 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01243 | hp2 | a0003 | c0005 | t0003 | g0020 | AMR | PUR | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01346 | hp2 | a0002 | c0002 | t0003 | g0044 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01884 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01891 | hp2 | a0003 | c0004 | t0003 | g0101 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01978 | hp1 | a0002 | c0003 | t0002 | g0052 | AMR | PEL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02015 | hp2 | a0001 | c0012 | t0001 | g0127 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02040 | hp2 | a0006 | c0015 | t0002 | g0088 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0051 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02080 | hp2 | a0002 | c0003 | t0002 | g0016 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02083 | hp2 | a0002 | c0003 | t0002 | g0078 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02145 | hp1 | a0003 | c0004 | t0003 | g0095 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | CDX | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02165 | hp1 | a0002 | c0003 | t0002 | g0008 | EAS | CDX | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | CDX | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0045 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02280 | hp1 | a0001 | c0006 | t0001 | g0005 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02280 | hp2 | a0003 | c0005 | t0003 | g0021 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | KHV | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02615 | hp1 | a0001 | c0011 | t0001 | g0122 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02615 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02622 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02647 | hp2 | a0003 | c0004 | t0003 | g0102 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0043 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02818 | hp2 | a0003 | c0004 | t0003 | g0106 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02896 | hp2 | a0003 | c0004 | t0003 | g0105 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02897 | hp1 | a0001 | c0006 | t0001 | g0164 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02897 | hp2 | a0003 | c0004 | t0003 | g0104 | AFR | GWD | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02922 | hp1 | a0003 | c0004 | t0003 | g0022 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0092 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02970 | hp2 | a0003 | c0004 | t0003 | g0094 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03098 | hp2 | a0003 | c0004 | t0003 | g0108 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03130 | hp1 | a0003 | c0004 | t0003 | g0099 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03130 | hp2 | a0003 | c0005 | t0003 | g0021 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0048 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03453 | hp1 | a0003 | c0004 | t0003 | g0098 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03453 | hp2 | a0007 | c0010 | t0003 | g0091 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03486 | hp1 | a0003 | c0004 | t0003 | g0022 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0087 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0070 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03516 | hp1 | a0003 | c0004 | t0003 | g0100 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | STU | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0037 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03710 | hp1 | a0009 | c0014 | t0001 | g0167 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0081 | SAS | BEB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | STU | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18522 | hp1 | a0003 | c0005 | t0003 | g0097 | AFR | YRI | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18747 | hp2 | a0002 | c0003 | t0002 | g0018 | EAS | CHB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | YRI | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18941 | hp2 | a0002 | c0003 | t0002 | g0059 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18949 | hp2 | a0002 | c0003 | t0002 | g0057 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18952 | hp2 | a0002 | c0003 | t0004 | g0012 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18953 | hp2 | a0002 | c0003 | t0002 | g0008 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18963 | hp2 | a0002 | c0008 | t0002 | g0069 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18965 | hp1 | a0004 | c0007 | t0001 | g0201 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18966 | hp1 | a0002 | c0003 | t0002 | g0058 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18970 | hp1 | a0002 | c0003 | t0004 | g0035 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18971 | hp1 | a0002 | c0003 | t0002 | g0065 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18980 | hp2 | a0002 | c0003 | t0004 | g0012 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0089 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18986 | hp1 | a0002 | c0003 | t0002 | g0018 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0090 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18998 | hp1 | a0002 | c0003 | t0002 | g0063 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19005 | hp2 | a0002 | c0003 | t0004 | g0034 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19006 | hp2 | a0002 | c0003 | t0002 | g0083 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19009 | hp1 | a0002 | c0003 | t0002 | g0086 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0046 | AFR | LWK | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19057 | hp1 | a0002 | c0003 | t0004 | g0036 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19074 | hp2 | a0004 | c0007 | t0001 | g0200 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19077 | hp1 | a0002 | c0003 | t0002 | g0066 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19078 | hp1 | a0002 | c0003 | t0002 | g0075 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19082 | hp2 | a0002 | c0003 | t0002 | g0064 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19083 | hp2 | a0002 | c0003 | t0004 | g0033 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0042 | AFR | ASW | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0009 | AFR | ASW | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | GIH | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | GIH | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02486 | hp1 | a0001 | c0006 | t0001 | g0005 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02486 | hp2 | a0003 | c0005 | t0003 | g0093 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02559 | hp1 | a0003 | c0005 | t0003 | g0020 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03471 | hp1 | a0008 | c0013 | t0001 | g0124 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG03471 | hp2 | a0001 | c0006 | t0001 | g0005 | AFR | MSL | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG06807 | hp1 | a0003 | c0004 | t0003 | g0103 | AFR | USA | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | USA | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | USA | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0125 | REF | REF | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0199 | REF | REF | ECD_chr10_73128668_73173008 | ECD | chr10 | 73128668 | 73173008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73134617 | T | C | 4 | a0002 a0005 a0006 others(1): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
missense_variant | MODERATE | c.1901A>G | p.Asp634Gly | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 14/14 | 2057/3006 | 1901/1935 | 634/644 | chr10 | 73134617 | |||
| chr10:73134708 | T | A | 1 | a0008 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.1810A>T | p.Ile604Leu | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 14/14 | 1966/3006 | 1810/1935 | 604/644 | chr10 | 73134708 | |||
| chr10:73136906 | T | C | 4 | a0002 a0005 a0006 others(1): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
missense_variant | MODERATE | c.1502A>G | p.Asn501Ser | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/14 | 1658/3006 | 1502/1935 | 501/644 | chr10 | 73136906 | |||
| chr10:73138026 | A | C | 1 | a0005 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.1466T>G | p.Leu489Arg | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/14 | 1622/3006 | 1466/1935 | 489/644 | chr10 | 73138026 | |||
| chr10:73139376 | C | G | 5 | a0002 a0003 a0005 others(2): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
missense_variant | MODERATE | c.1354G>C | p.Glu452Gln | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/14 | 1510/3006 | 1354/1935 | 452/644 | chr10 | 73139376 | |||
| chr10:73139400 | T | C | 1 | a0007 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1330A>G | p.Lys444Glu | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/14 | 1486/3006 | 1330/1935 | 444/644 | chr10 | 73139400 | |||
| chr10:73139710 | T | A | 1 | a0004 | 2 | NA18965.hp1 NA19074.hp2 |
missense_variant | MODERATE | c.1155A>T | p.Glu385Asp | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 10/14 | 1311/3006 | 1155/1935 | 385/644 | chr10 | 73139710 | |||
| chr10:73156440 | T | C | 1 | a0009 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.425A>G | p.His142Arg | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/14 | 581/3006 | 425/1935 | 142/644 | chr10 | 73156440 | |||
| chr10:73163804 | C | T | 5 | a0002 a0003 a0005 others(2): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
missense_variant | MODERATE | c.134G>A | p.Arg45Gln | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/14 | 290/3006 | 134/1935 | 45/644 | chr10 | 73163804 | |||
| chr10:73163927 | G | C | 1 | a0006 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.11C>G | p.Thr4Ser | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/14 | 167/3006 | 11/1935 | 4/644 | chr10 | 73163927 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73138058 | C | T | 7 | a0002c0002 a0002c0003 a0003c0004 others(4): Show |
105 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
synonymous_variant | LOW | c.1434G>A | p.Glu478Glu | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/14 | 1590/3006 | 1434/1935 | 478/644 | chr10 | 73138058 | |||
| chr10:73139353 | A | G | 2 | a0002c0003 a0002c0008 |
31 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(28): Show |
synonymous_variant | LOW | c.1377T>C | p.Ala459Ala | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/14 | 1533/3006 | 1377/1935 | 459/644 | chr10 | 73139353 | |||
| chr10:73139410 | G | A | 1 | a0003c0005 | 7 | HG00735.hp2 HG01243.hp2 HG02280.hp2 others(4): Show |
synonymous_variant | LOW | c.1320C>T | p.Ser440Ser | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/14 | 1476/3006 | 1320/1935 | 440/644 | chr10 | 73139410 | |||
| chr10:73139413 | A | G | 1 | a0001c0012 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1317T>C | p.Val439Val | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/14 | 1473/3006 | 1317/1935 | 439/644 | chr10 | 73139413 | |||
| chr10:73154304 | A | C | 1 | a0001c0006 | 6 | HG02280.hp1 HG02486.hp1 HG02615.hp2 others(3): Show |
synonymous_variant | LOW | c.735T>G | p.Ala245Ala | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/14 | 891/3006 | 735/1935 | 245/644 | chr10 | 73154304 | |||
| chr10:73154367 | G | T | 1 | a0001c0011 | 1 | HG02615.hp1 | synonymous_variant | LOW | c.672C>A | p.Arg224Arg | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/14 | 828/3006 | 672/1935 | 224/644 | chr10 | 73154367 | |||
| chr10:73156415 | T | A | 6 | a0002c0002 a0002c0003 a0002c0008 others(3): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
synonymous_variant | LOW | c.450A>T | p.Ala150Ala | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/14 | 606/3006 | 450/1935 | 150/644 | chr10 | 73156415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73133689 | G | A | 1 | a0001c0001t0005 | 6 | HG01891.hp1 HG02572.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*894C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 14/14 | 894 | chr10 | 73133689 | ||||||
| chr10:73133775 | A | T | 10 | a0002c0002t0002 a0002c0002t0003 a0002c0003t0002 others(7): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*808T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 14/14 | 808 | chr10 | 73133775 | ||||||
| chr10:73134174 | A | G | 6 | a0002c0002t0002 a0002c0003t0002 a0002c0003t0004 others(3): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*409T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 14/14 | 409 | chr10 | 73134174 | ||||||
| chr10:73134205 | G | C | 10 | a0002c0002t0002 a0002c0002t0003 a0002c0003t0002 others(7): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*378C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 14/14 | 378 | chr10 | 73134205 | ||||||
| chr10:73134500 | T | C | 10 | a0002c0002t0002 a0002c0002t0003 a0002c0003t0002 others(7): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*83A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 14/14 | 83 | chr10 | 73134500 | ||||||
| chr10:73167887 | C | T | 1 | a0002c0003t0004 | 6 | NA18952.hp2 NA18970.hp1 NA18980.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/14 | 3950 | chr10 | 73167887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:73135038 | A | G | 60 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1705-225T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135038 | |||||||
| chr10:73135206 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1705-393C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135206 | |||||||
| chr10:73135487 | G | C | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1705-674C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135487 | |||||||
| chr10:73135537 | A | G | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1705-724T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135537 | |||||||
| chr10:73135540 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1705-727C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135540 | |||||||
| chr10:73135668 | C | T | 60 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1705-855G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135668 | |||||||
| chr10:73135727 | A | AAAT | 8 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0041 others(5): Show |
9 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1705-917_1705-915d others(5): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135727 | |||||||
| chr10:73135767 | A | T | 60 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1704+937T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135767 | |||||||
| chr10:73135842 | T | C | 1 | a0003c0004t0003g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1704+862A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73135842 | |||||||
| chr10:73136032 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1704+672A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73136032 | |||||||
| chr10:73136472 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1704+232A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73136472 | |||||||
| chr10:73136503 | G | A | 1 | a0002c0003t0002g0063 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1704+201C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73136503 | |||||||
| chr10:73136571 | G | C | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1704+133C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 13/13 | chr10 | 73136571 | |||||||
| chr10:73136954 | AATT | A | 60 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1490-39_1490-37del others(3): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73136954 | |||||||
| chr10:73136954 | AATTATT | A | 30 | a0002c0002t0003g0014 a0002c0002t0003g0039 a0002c0002t0003g0040 others(27): Show |
34 | HG00642.hp2 HG00735.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1490-42_1490-37del others(6): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73136954 | |||||||
| chr10:73136954 | AATTATTA others(2): Show |
A | 1 | a0001c0001t0001g0026 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1490-45_1490-37del others(9): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73136954 | |||||||
| chr10:73136982 | A | T | 1 | a0002c0008t0002g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1490-64T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73136982 | |||||||
| chr10:73136985 | A | ATTT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0119 others(9): Show |
21 | HG00733.hp2 HG01074.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1490-70_1490-68dup others(3): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73136985 | |||||||
| chr10:73136985 | A | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(150): Show |
197 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.1490-67T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73136985 | |||||||
| chr10:73137091 | T | C | 3 | a0002c0002t0003g0042 a0002c0002t0003g0043 a0007c0010t0003g0091 |
3 | HG02809.hp1 HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1490-173A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137091 | |||||||
| chr10:73137154 | T | TA | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1490-237dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137154 | |||||||
| chr10:73137513 | C | T | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1489+490G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137513 | |||||||
| chr10:73137707 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1489+296G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137707 | |||||||
| chr10:73137770 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1489+233A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137770 | |||||||
| chr10:73137775 | C | CA | 74 | a0001c0001t0001g0128 a0001c0001t0001g0169 a0001c0001t0001g0178 others(71): Show |
86 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1489+227dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137775 | |||||||
| chr10:73137775 | C | CAA | 19 | a0002c0002t0002g0076 a0002c0003t0002g0057 a0003c0004t0003g0022 others(16): Show |
22 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1489+226_1489+227d others(4): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137775 | |||||||
| chr10:73137792 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0170 |
2 | HG01074.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1489+211T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137792 | |||||||
| chr10:73137895 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1489+108C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137895 | |||||||
| chr10:73137933 | A | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1489+70T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 12/13 | chr10 | 73137933 | |||||||
| chr10:73138498 | T | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1422-428A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138498 | |||||||
| chr10:73138520 | C | T | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1422-450G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138520 | |||||||
| chr10:73138574 | G | GT | 8 | a0001c0001t0001g0024 a0001c0001t0001g0139 a0001c0001t0001g0161 others(5): Show |
10 | HG00438.hp2 HG01243.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1422-505dupA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138574 | |||||||
| chr10:73138590 | G | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1422-520C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138590 | |||||||
| chr10:73138707 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1421+602A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138707 | |||||||
| chr10:73138720 | C | A | 8 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0041 others(5): Show |
9 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1421+589G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138720 | |||||||
| chr10:73138721 | C | T | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1421+588G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138721 | |||||||
| chr10:73138724 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1421+585T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138724 | |||||||
| chr10:73138953 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1421+356A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138953 | |||||||
| chr10:73138956 | T | TTTGAG | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1421+352_1421+353i others(7): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138956 | |||||||
| chr10:73138967 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0138 a0001c0001t0001g0153 others(4): Show |
8 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1421+342G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73138967 | |||||||
| chr10:73139216 | CA | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0130 others(16): Show |
25 | HG00408.hp1 HG01978.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1421+92delT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73139216 | |||||||
| chr10:73139216 | CAA | C | 90 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(87): Show |
105 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1421+91_1421+92del others(2): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73139216 | |||||||
| chr10:73139229 | A | G | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1421+80T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 11/13 | chr10 | 73139229 | |||||||
| chr10:73139847 | G | GT | 68 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(65): Show |
79 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1128-111dupA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73139847 | |||||||
| chr10:73139849 | G | GT | 19 | a0001c0001t0001g0160 a0001c0001t0001g0177 a0003c0004t0003g0022 others(16): Show |
22 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1128-113dupA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73139849 | |||||||
| chr10:73139849 | G | T | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1128-112C>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73139849 | |||||||
| chr10:73139854 | T | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0149 |
2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1128-117A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73139854 | |||||||
| chr10:73139887 | T | G | 1 | a0002c0008t0002g0069 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1128-150A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73139887 | |||||||
| chr10:73139982 | C | T | 8 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0041 others(5): Show |
9 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1128-245G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73139982 | |||||||
| chr10:73140087 | A | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1128-350T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140087 | |||||||
| chr10:73140272 | C | T | 3 | a0002c0002t0002g0067 a0002c0002t0002g0077 a0002c0002t0002g0082 |
3 | NA18999.hp2 NA19054.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1128-535G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140272 | |||||||
| chr10:73140281 | C | G | 18 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(15): Show |
21 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1128-544G>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140281 | |||||||
| chr10:73140363 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
216 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.1128-626G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140363 | |||||||
| chr10:73140523 | A | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0137 a0001c0001t0001g0165 |
4 | HG01081.hp1 HG01256.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128-786T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140523 | |||||||
| chr10:73140589 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1128-852C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140589 | |||||||
| chr10:73140612 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1128-875C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140612 | |||||||
| chr10:73140739 | GCCTT | G | 3 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0046 |
4 | HG01884.hp2 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-1006_1128-100 others(8): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140739 | |||||||
| chr10:73140799 | G | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1128-1062C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140799 | |||||||
| chr10:73140842 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1128-1105G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140842 | |||||||
| chr10:73140877 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1128-1140T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140877 | |||||||
| chr10:73140953 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1128-1216G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73140953 | |||||||
| chr10:73141017 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0165 |
3 | HG01081.hp1 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1128-1280A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141017 | |||||||
| chr10:73141025 | C | T | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1128-1288G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141025 | |||||||
| chr10:73141177 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1128-1440A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141177 | |||||||
| chr10:73141241 | C | T | 1 | a0002c0002t0002g0070 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1128-1504G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141241 | |||||||
| chr10:73141274 | C | T | 1 | a0003c0004t0003g0099 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1128-1537G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141274 | |||||||
| chr10:73141339 | T | TA | 9 | a0001c0001t0001g0030 a0001c0001t0001g0119 a0001c0001t0001g0133 others(6): Show |
10 | HG00673.hp1 HG01891.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.1128-1603dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141339 | |||||||
| chr10:73141339 | T | TAA | 30 | a0001c0001t0001g0175 a0002c0002t0002g0061 a0002c0002t0003g0014 others(27): Show |
34 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1128-1604_1128-160 others(6): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141339 | |||||||
| chr10:73141339 | T | TAAA | 56 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(53): Show |
67 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1128-1605_1128-160 others(7): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141339 | |||||||
| chr10:73141380 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1128-1643A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141380 | |||||||
| chr10:73141429 | G | A | 18 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(15): Show |
21 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1128-1692C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141429 | |||||||
| chr10:73141507 | G | T | 60 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1128-1770C>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141507 | |||||||
| chr10:73141738 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1128-2001T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141738 | |||||||
| chr10:73141743 | C | T | 1 | a0002c0002t0002g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1128-2006G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141743 | |||||||
| chr10:73141812 | A | G | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1128-2075T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141812 | |||||||
| chr10:73141813 | T | C | 6 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0145 others(3): Show |
9 | HG00642.hp1 HG01433.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1128-2076A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73141813 | |||||||
| chr10:73142151 | G | A | 2 | a0003c0004t0003g0104 a0003c0004t0003g0105 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1128-2414C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142151 | |||||||
| chr10:73142169 | G | A | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1128-2432C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142169 | |||||||
| chr10:73142270 | A | T | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1128-2533T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142270 | |||||||
| chr10:73142373 | G | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1128-2636C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142373 | |||||||
| chr10:73142508 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1128-2771G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142508 | |||||||
| chr10:73142596 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1128-2859A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142596 | |||||||
| chr10:73142632 | C | CA | 10 | a0001c0001t0001g0113 a0001c0001t0001g0121 a0001c0001t0001g0129 others(7): Show |
10 | HG01433.hp1 HG01433.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1128-2896dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142632 | |||||||
| chr10:73142632 | CA | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0135 a0001c0001t0001g0174 others(7): Show |
13 | HG02258.hp2 HG02559.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1128-2896delT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142632 | |||||||
| chr10:73142632 | CAAAAAA | C | 84 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(81): Show |
99 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1128-2901_1128-289 others(10): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142632 | |||||||
| chr10:73142632 | CAAAAAAA | C | 7 | a0002c0002t0002g0049 a0002c0002t0003g0039 a0002c0002t0003g0047 others(4): Show |
7 | HG00642.hp2 HG02965.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128-2902_1128-289 others(11): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142632 | |||||||
| chr10:73142661 | G | A | 18 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(15): Show |
21 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1128-2924C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73142661 | |||||||
| chr10:73143092 | C | A | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1127+3184G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143092 | |||||||
| chr10:73143128 | A | G | 3 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0046 |
4 | HG01884.hp2 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+3148T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143128 | |||||||
| chr10:73143234 | T | C | 1 | a0002c0002t0003g0047 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1127+3042A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143234 | |||||||
| chr10:73143294 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1127+2982C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143294 | |||||||
| chr10:73143390 | A | G | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1127+2886T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143390 | |||||||
| chr10:73143449 | A | G | 1 | a0002c0002t0003g0043 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1127+2827T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143449 | |||||||
| chr10:73143497 | T | C | 1 | a0002c0003t0002g0066 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1127+2779A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143497 | |||||||
| chr10:73143651 | T | A | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1127+2625A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143651 | |||||||
| chr10:73143752 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1127+2524T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143752 | |||||||
| chr10:73143785 | AT | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(179): Show |
245 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.1127+2490delA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143785 | |||||||
| chr10:73143832 | C | CTT | 8 | a0002c0002t0002g0061 a0002c0002t0002g0109 a0002c0002t0002g0110 others(5): Show |
9 | HG01081.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1127+2442_1127+244 others(6): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143832 | |||||||
| chr10:73143832 | C | CTTT | 63 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(60): Show |
74 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1127+2441_1127+244 others(7): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143832 | |||||||
| chr10:73143832 | C | CTTTT | 18 | a0002c0002t0002g0038 a0002c0002t0002g0079 a0003c0004t0003g0022 others(15): Show |
21 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1127+2440_1127+244 others(8): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73143832 | |||||||
| chr10:73144123 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1127+2153T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73144123 | |||||||
| chr10:73144255 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1127+2021G>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73144255 | |||||||
| chr10:73144283 | T | A | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1127+1993A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73144283 | |||||||
| chr10:73144336 | A | C | 3 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0099 |
4 | HG02922.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+1940T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73144336 | |||||||
| chr10:73144733 | C | A | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1127+1543G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73144733 | |||||||
| chr10:73145101 | C | T | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1127+1175G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145101 | |||||||
| chr10:73145303 | T | C | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1127+973A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145303 | |||||||
| chr10:73145650 | T | C | 1 | a0002c0002t0002g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1127+626A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145650 | |||||||
| chr10:73145657 | C | CT | 5 | a0001c0001t0001g0023 a0001c0001t0001g0130 a0001c0001t0001g0165 others(2): Show |
7 | HG01081.hp1 HG02055.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+618dupA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145657 | |||||||
| chr10:73145657 | C | CTT | 64 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(61): Show |
75 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.1127+617_1127+618d others(4): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145657 | |||||||
| chr10:73145657 | C | CTTT | 8 | a0002c0002t0002g0038 a0002c0002t0002g0050 a0002c0002t0002g0051 others(5): Show |
8 | HG02055.hp1 HG03688.hp2 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.1127+616_1127+618d others(5): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145657 | |||||||
| chr10:73145657 | CT | C | 18 | a0001c0001t0001g0150 a0001c0001t0005g0151 a0003c0004t0003g0022 others(15): Show |
21 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1127+618delA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145657 | |||||||
| chr10:73145708 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0132 |
6 | HG02056.hp1 NA18947.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1127+568T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145708 | |||||||
| chr10:73145894 | C | T | 1 | a0003c0004t0003g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1127+382G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73145894 | |||||||
| chr10:73146162 | A | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1127+114T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73146162 | |||||||
| chr10:73146172 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
7 | HG02258.hp2 HG02559.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1127+104G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 9/13 | chr10 | 73146172 | |||||||
| chr10:73146546 | C | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1042-185G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73146546 | |||||||
| chr10:73146546 | C | T | 1 | a0002c0002t0003g0044 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1042-185G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73146546 | |||||||
| chr10:73146706 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1042-345T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73146706 | |||||||
| chr10:73146711 | C | T | 2 | a0002c0002t0003g0042 a0002c0002t0003g0043 |
2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1042-350G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73146711 | |||||||
| chr10:73146789 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1042-428T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73146789 | |||||||
| chr10:73147003 | A | C | 1 | a0002c0003t0002g0063 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1042-642T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73147003 | |||||||
| chr10:73147122 | C | CTA | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1042-763_1042-762d others(4): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73147122 | |||||||
| chr10:73147247 | CAAT | C | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1042-889_1042-887d others(5): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73147247 | |||||||
| chr10:73147276 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1042-915C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73147276 | |||||||
| chr10:73147483 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1041+793C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73147483 | |||||||
| chr10:73147632 | T | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1041+644A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73147632 | |||||||
| chr10:73147671 | A | T | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1041+605T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73147671 | |||||||
| chr10:73148224 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1041+52G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73148224 | |||||||
| chr10:73148263 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0153 a0001c0001t0001g0162 others(1): Show |
5 | HG02451.hp1 HG02717.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041+13A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 8/13 | chr10 | 73148263 | |||||||
| chr10:73148594 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.913-190A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73148594 | |||||||
| chr10:73148782 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.913-378T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73148782 | |||||||
| chr10:73149020 | C | G | 1 | a0009c0014t0001g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.913-616G>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149020 | |||||||
| chr10:73149107 | G | A | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.913-703C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149107 | |||||||
| chr10:73149339 | C | CA | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.913-936dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149339 | |||||||
| chr10:73149352 | T | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
10 | HG02258.hp2 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.913-948A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149352 | |||||||
| chr10:73149397 | C | T | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.913-993G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149397 | |||||||
| chr10:73149430 | A | G | 60 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.913-1026T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149430 | |||||||
| chr10:73149555 | A | G | 1 | a0001c0011t0001g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913-1151T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149555 | |||||||
| chr10:73149794 | A | G | 1 | a0002c0002t0003g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.913-1390T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149794 | |||||||
| chr10:73149824 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.913-1420T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149824 | |||||||
| chr10:73149835 | T | C | 2 | a0002c0003t0004g0012 a0002c0003t0004g0036 |
3 | NA18952.hp2 NA18980.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.913-1431A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149835 | |||||||
| chr10:73149911 | G | GAGGAAGA others(41): Show |
1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.913-1508_913-1507i others(50): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149911 | |||||||
| chr10:73149930 | A | G | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.913-1526T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149930 | |||||||
| chr10:73149942 | T | A | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.913-1538A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73149942 | |||||||
| chr10:73150038 | A | G | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.913-1634T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150038 | |||||||
| chr10:73150043 | A | C | 92 | a0001c0011t0001g0122 a0002c0002t0002g0009 a0002c0002t0002g0013 others(89): Show |
107 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.913-1639T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150043 | |||||||
| chr10:73150055 | T | C | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.913-1651A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150055 | |||||||
| chr10:73150056 | G | A | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.913-1652C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150056 | |||||||
| chr10:73150060 | T | C | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.913-1656A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150060 | |||||||
| chr10:73150265 | A | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.913-1861T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150265 | |||||||
| chr10:73150276 | C | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.913-1872G>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150276 | |||||||
| chr10:73150421 | C | A | 1 | a0009c0014t0001g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.912+1872G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150421 | |||||||
| chr10:73150600 | G | C | 1 | a0002c0003t0002g0072 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.912+1693C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150600 | |||||||
| chr10:73150694 | C | T | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.912+1599G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150694 | |||||||
| chr10:73150706 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.912+1587A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150706 | |||||||
| chr10:73150711 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.912+1582T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150711 | |||||||
| chr10:73150790 | G | A | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.912+1503C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73150790 | |||||||
| chr10:73151025 | G | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.912+1268C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151025 | |||||||
| chr10:73151077 | G | A | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.912+1216C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151077 | |||||||
| chr10:73151319 | T | C | 2 | a0002c0002t0003g0047 a0002c0002t0003g0048 |
2 | HG00642.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.912+974A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151319 | |||||||
| chr10:73151337 | C | T | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.912+956G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151337 | |||||||
| chr10:73151389 | A | G | 1 | a0002c0002t0002g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.912+904T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151389 | |||||||
| chr10:73151419 | C | A | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.912+874G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151419 | |||||||
| chr10:73151473 | G | A | 1 | a0002c0003t0002g0073 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.912+820C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151473 | |||||||
| chr10:73151529 | TA | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0123 others(112): Show |
143 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.912+763delT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151529 | |||||||
| chr10:73151757 | T | C | 1 | a0003c0004t0003g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.912+536A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73151757 | |||||||
| chr10:73152050 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.912+243G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73152050 | |||||||
| chr10:73152246 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.912+47A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 7/13 | chr10 | 73152246 | |||||||
| chr10:73152676 | C | T | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.784-255G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152676 | |||||||
| chr10:73152785 | G | A | 6 | a0002c0002t0002g0019 a0002c0002t0002g0055 a0002c0002t0002g0056 others(3): Show |
7 | HG02040.hp2 HG02071.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.784-364C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152785 | |||||||
| chr10:73152794 | C | A | 5 | a0002c0002t0003g0039 a0002c0002t0003g0047 a0002c0002t0003g0048 others(2): Show |
5 | HG00642.hp2 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-373G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152794 | |||||||
| chr10:73152818 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.784-397T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152818 | |||||||
| chr10:73152859 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.784-438C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152859 | |||||||
| chr10:73152908 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.784-487G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152908 | |||||||
| chr10:73152914 | C | CAAAAAAA others(4): Show |
28 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0003g0014 others(25): Show |
32 | HG00642.hp2 HG00735.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.784-494_784-493ins others(11): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152914 | |||||||
| chr10:73152914 | C | CAAAAAAA others(5): Show |
54 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(51): Show |
65 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.784-494_784-493ins others(12): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152914 | |||||||
| chr10:73152914 | C | CAAAAAAA others(6): Show |
9 | a0002c0002t0002g0051 a0002c0002t0002g0076 a0002c0002t0002g0077 others(6): Show |
9 | HG01261.hp2 HG01978.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-494_784-493ins others(13): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152914 | |||||||
| chr10:73152930 | C | T | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.784-509G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73152930 | |||||||
| chr10:73153190 | G | A | 1 | a0004c0007t0001g0201 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.784-769C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153190 | |||||||
| chr10:73153279 | C | T | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.784-858G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153279 | |||||||
| chr10:73153324 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.784-903A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153324 | |||||||
| chr10:73153422 | T | C | 2 | a0003c0004t0003g0100 a0003c0004t0003g0101 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.783+834A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153422 | |||||||
| chr10:73153534 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.783+722G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153534 | |||||||
| chr10:73153558 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.783+698C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153558 | |||||||
| chr10:73153701 | G | C | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.783+555C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153701 | |||||||
| chr10:73153723 | C | G | 1 | a0001c0011t0001g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.783+533G>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153723 | |||||||
| chr10:73153725 | C | CA | 17 | a0001c0001t0001g0032 a0001c0001t0001g0156 a0001c0001t0001g0157 others(14): Show |
18 | HG00621.hp2 HG00735.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.783+530dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153725 | |||||||
| chr10:73153725 | CA | C | 6 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0011t0001g0122 others(3): Show |
6 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+530delT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153725 | |||||||
| chr10:73153725 | CAA | C | 15 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0098 others(12): Show |
18 | HG00735.hp2 HG01243.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.783+529_783+530del others(2): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153725 | |||||||
| chr10:73153725 | CAAAAAAA | C | 70 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(67): Show |
82 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.783+524_783+530del others(7): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153725 | |||||||
| chr10:73153725 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0189 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.783+518_783+530del others(13): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153725 | |||||||
| chr10:73153866 | C | T | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.783+390G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153866 | |||||||
| chr10:73153935 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.783+321C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153935 | |||||||
| chr10:73153944 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.783+312G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 6/13 | chr10 | 73153944 | |||||||
| chr10:73154498 | T | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.591-50A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73154498 | |||||||
| chr10:73154544 | A | T | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.591-96T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73154544 | |||||||
| chr10:73154641 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.591-193A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73154641 | |||||||
| chr10:73154716 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0012t0001g0127 |
3 | HG02015.hp2 HG02071.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.591-268G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73154716 | |||||||
| chr10:73154720 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.591-272C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73154720 | |||||||
| chr10:73154835 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.591-387C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73154835 | |||||||
| chr10:73154891 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.591-443C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73154891 | |||||||
| chr10:73155177 | T | G | 2 | a0002c0002t0002g0053 a0002c0002t0002g0080 |
2 | NA18940.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.591-729A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155177 | |||||||
| chr10:73155180 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.591-732C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155180 | |||||||
| chr10:73155346 | G | A | 1 | a0002c0002t0002g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.591-898C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155346 | |||||||
| chr10:73155370 | A | C | 1 | a0002c0003t0002g0060 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.590+905T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155370 | |||||||
| chr10:73155414 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590+861A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155414 | |||||||
| chr10:73155441 | G | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.590+834C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155441 | |||||||
| chr10:73155450 | A | G | 5 | a0002c0003t0002g0057 a0002c0003t0002g0058 a0002c0003t0002g0059 others(2): Show |
5 | NA18941.hp2 NA18949.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.590+825T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155450 | |||||||
| chr10:73155594 | C | CT | 8 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0195 others(5): Show |
9 | HG01884.hp2 HG02451.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.590+680dupA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155594 | |||||||
| chr10:73155594 | CT | C | 8 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0194 others(5): Show |
8 | HG01081.hp1 HG02145.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.590+680delA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155594 | |||||||
| chr10:73155594 | CTT | C | 15 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0098 others(12): Show |
18 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.590+679_590+680del others(2): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155594 | |||||||
| chr10:73155634 | T | C | 1 | a0002c0002t0002g0053 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.590+641A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155634 | |||||||
| chr10:73155638 | G | A | 5 | a0002c0002t0003g0039 a0002c0002t0003g0047 a0002c0002t0003g0048 others(2): Show |
5 | HG00642.hp2 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.590+637C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155638 | |||||||
| chr10:73155692 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.590+583C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155692 | |||||||
| chr10:73155730 | G | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.590+545C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155730 | |||||||
| chr10:73155893 | C | T | 2 | a0002c0002t0002g0013 a0002c0002t0002g0038 |
3 | HG02698.hp2 HG03688.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.590+382G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155893 | |||||||
| chr10:73155897 | C | T | 1 | a0003c0004t0003g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.590+378G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73155897 | |||||||
| chr10:73156169 | C | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | NA18747.hp1 NA18942.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.590+106G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73156169 | |||||||
| chr10:73156175 | C | T | 1 | a0002c0002t0003g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.590+100G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73156175 | |||||||
| chr10:73156244 | T | G | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.590+31A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 5/13 | chr10 | 73156244 | |||||||
| chr10:73157068 | G | A | 1 | a0002c0002t0003g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.324-413C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157068 | |||||||
| chr10:73157199 | G | A | 5 | a0002c0002t0003g0039 a0002c0002t0003g0047 a0002c0002t0003g0048 others(2): Show |
5 | HG00642.hp2 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.324-544C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157199 | |||||||
| chr10:73157203 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.324-548A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157203 | |||||||
| chr10:73157246 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
10 | HG02258.hp2 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.324-591G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157246 | |||||||
| chr10:73157413 | A | T | 23 | a0002c0002t0003g0039 a0002c0002t0003g0047 a0002c0002t0003g0048 others(20): Show |
26 | HG00642.hp2 HG00735.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.324-758T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157413 | |||||||
| chr10:73157420 | T | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG00423.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.324-765A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157420 | |||||||
| chr10:73157616 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.324-961C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157616 | |||||||
| chr10:73157651 | G | A | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.324-996C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157651 | |||||||
| chr10:73157722 | C | CA | 91 | a0001c0001t0001g0204 a0002c0002t0002g0009 a0002c0002t0002g0013 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.324-1068dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157722 | |||||||
| chr10:73157855 | A | G | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.324-1200T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157855 | |||||||
| chr10:73157920 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.324-1265G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157920 | |||||||
| chr10:73157946 | ATTATT | A | 89 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(86): Show |
104 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.324-1296_324-1292d others(7): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157946 | |||||||
| chr10:73157946 | ATTATTTT others(3): Show |
A | 2 | a0002c0002t0002g0054 a0003c0004t0003g0108 |
2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.324-1301_324-1292d others(12): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73157946 | |||||||
| chr10:73158271 | T | G | 1 | a0007c0010t0003g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.324-1616A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158271 | |||||||
| chr10:73158352 | G | A | 1 | a0002c0002t0002g0055 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.324-1697C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158352 | |||||||
| chr10:73158438 | A | C | 18 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(15): Show |
21 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.324-1783T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158438 | |||||||
| chr10:73158510 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.324-1855A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158510 | |||||||
| chr10:73158643 | A | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.323+1791T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158643 | |||||||
| chr10:73158651 | G | T | 1 | a0002c0002t0002g0081 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.323+1783C>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158651 | |||||||
| chr10:73158728 | C | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.323+1706G>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158728 | |||||||
| chr10:73158792 | G | A | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.323+1642C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158792 | |||||||
| chr10:73158840 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.323+1594G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158840 | |||||||
| chr10:73158865 | C | T | 1 | a0002c0002t0002g0037 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.323+1569G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158865 | |||||||
| chr10:73158866 | C | T | 7 | a0003c0004t0003g0095 a0003c0004t0003g0108 a0003c0005t0003g0020 others(4): Show |
9 | HG00735.hp2 HG01243.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.323+1568G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158866 | |||||||
| chr10:73158872 | T | C | 8 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0041 others(5): Show |
9 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.323+1562A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158872 | |||||||
| chr10:73158948 | A | G | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.323+1486T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73158948 | |||||||
| chr10:73159229 | G | A | 18 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(15): Show |
21 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.323+1205C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159229 | |||||||
| chr10:73159541 | A | G | 1 | a0002c0002t0002g0056 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.323+893T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159541 | |||||||
| chr10:73159603 | T | C | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.323+831A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159603 | |||||||
| chr10:73159642 | A | ATTTTTT | 13 | a0002c0002t0002g0081 a0002c0002t0002g0082 a0002c0002t0002g0084 others(10): Show |
14 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.323+786_323+791dup others(6): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159642 | |||||||
| chr10:73159642 | A | ATTTTTTT | 46 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(43): Show |
55 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.323+785_323+791dup others(7): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159642 | |||||||
| chr10:73159642 | A | ATTTTTTT others(1): Show |
24 | a0002c0002t0002g0017 a0002c0002t0002g0050 a0002c0002t0002g0051 others(21): Show |
29 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.323+784_323+791dup others(8): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159642 | |||||||
| chr10:73159642 | A | ATTTTTTT others(2): Show |
5 | a0002c0002t0003g0039 a0002c0002t0003g0048 a0002c0002t0003g0092 others(2): Show |
5 | HG02486.hp2 HG02965.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.323+783_323+791dup others(9): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159642 | |||||||
| chr10:73159642 | A | ATTTTTTT others(3): Show |
1 | a0007c0010t0003g0091 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.323+782_323+791dup others(10): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159642 | |||||||
| chr10:73159642 | A | ATTTTTTT others(5): Show |
1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.323+780_323+791dup others(12): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159642 | |||||||
| chr10:73159667 | C | CAG | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.323+765_323+766dup others(2): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159667 | |||||||
| chr10:73159891 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.323+543G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159891 | |||||||
| chr10:73159932 | G | A | 16 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(13): Show |
19 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.323+502C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73159932 | |||||||
| chr10:73160035 | A | G | 2 | a0002c0002t0002g0015 a0002c0002t0002g0049 |
3 | NA18942.hp2 NA18980.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.323+399T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73160035 | |||||||
| chr10:73160047 | G | C | 1 | a0003c0004t0003g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.323+387C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73160047 | |||||||
| chr10:73160096 | A | G | 112 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0117 others(109): Show |
136 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.323+338T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73160096 | |||||||
| chr10:73160104 | T | G | 2 | a0002c0002t0003g0042 a0002c0002t0003g0043 |
2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.323+330A>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73160104 | |||||||
| chr10:73160283 | CA | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.323+150delT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73160283 | |||||||
| chr10:73160291 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.323+143T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73160291 | |||||||
| chr10:73160428 | C | T | 1 | a0001c0011t0001g0122 | 1 | HG02615.hp1 | splice_region_variant&intron_variant | LOW | c.323+6G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 3/13 | chr10 | 73160428 | |||||||
| chr10:73160569 | G | A | 1 | a0002c0003t0002g0086 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.206-18C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73160569 | |||||||
| chr10:73160639 | C | A | 1 | a0003c0004t0003g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.206-88G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73160639 | |||||||
| chr10:73160678 | C | T | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.206-127G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73160678 | |||||||
| chr10:73160807 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.206-256T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73160807 | |||||||
| chr10:73160856 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.206-305C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73160856 | |||||||
| chr10:73161164 | CA | C | 89 | a0001c0001t0001g0120 a0001c0001t0001g0173 a0002c0002t0002g0009 others(86): Show |
104 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.206-614delT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161164 | |||||||
| chr10:73161240 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.206-689A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161240 | |||||||
| chr10:73161293 | A | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | NA18961.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.206-742T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161293 | |||||||
| chr10:73161306 | A | G | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.206-755T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161306 | |||||||
| chr10:73161324 | C | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.206-773G>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161324 | |||||||
| chr10:73161359 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.206-808C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161359 | |||||||
| chr10:73161388 | T | C | 1 | a0002c0002t0003g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.206-837A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161388 | |||||||
| chr10:73161800 | T | A | 13 | a0002c0002t0003g0014 a0002c0002t0003g0039 a0002c0002t0003g0040 others(10): Show |
14 | HG00642.hp2 HG01074.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.206-1249A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161800 | |||||||
| chr10:73161940 | T | C | 3 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0046 |
4 | HG01884.hp2 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.206-1389A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73161940 | |||||||
| chr10:73162234 | T | C | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.205+1499A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162234 | |||||||
| chr10:73162235 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.205+1498C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162235 | |||||||
| chr10:73162245 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.205+1488A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162245 | |||||||
| chr10:73162365 | T | C | 1 | a0001c0001t0005g0010 | 3 | HG01891.hp1 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205+1368A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162365 | |||||||
| chr10:73162515 | A | G | 2 | a0002c0002t0003g0042 a0002c0002t0003g0043 |
2 | HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.205+1218T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162515 | |||||||
| chr10:73162642 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0117 others(15): Show |
27 | HG00408.hp1 HG02257.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.205+1091C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162642 | |||||||
| chr10:73162850 | C | A | 1 | a0003c0004t0003g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.205+883G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162850 | |||||||
| chr10:73162869 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.205+864T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162869 | |||||||
| chr10:73162990 | T | A | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.205+743A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73162990 | |||||||
| chr10:73163098 | C | T | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.205+635G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163098 | |||||||
| chr10:73163125 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.205+608G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163125 | |||||||
| chr10:73163337 | A | G | 2 | a0002c0002t0003g0047 a0002c0002t0003g0048 |
2 | HG00642.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.205+396T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163337 | |||||||
| chr10:73163374 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.205+359T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163374 | |||||||
| chr10:73163415 | G | A | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.205+318C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163415 | |||||||
| chr10:73163460 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.205+273A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163460 | |||||||
| chr10:73163460 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
7 | HG02258.hp2 HG02559.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.205+273A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163460 | |||||||
| chr10:73163554 | G | T | 1 | a0002c0002t0003g0041 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.205+179C>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 2/13 | chr10 | 73163554 | |||||||
| chr10:73163951 | CTA | C | 8 | a0002c0002t0003g0014 a0002c0002t0003g0040 a0002c0002t0003g0041 others(5): Show |
9 | HG01074.hp1 HG01346.hp2 HG01884.hp2 others(6): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.-13-3_-13-2delTA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73163951 | |||||||
| chr10:73164033 | C | T | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-13-83G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164033 | |||||||
| chr10:73164102 | G | A | 2 | a0002c0003t0002g0089 a0002c0003t0002g0090 |
2 | NA18984.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-13-152C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164102 | |||||||
| chr10:73164296 | G | A | 60 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(57): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-13-346C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164296 | |||||||
| chr10:73164358 | A | T | 4 | a0001c0001t0001g0117 a0002c0002t0003g0014 a0002c0002t0003g0040 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13-408T>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164358 | |||||||
| chr10:73164361 | AT | A | 5 | a0002c0003t0004g0012 a0002c0003t0004g0033 a0002c0003t0004g0034 others(2): Show |
6 | NA18952.hp2 NA18970.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13-412delA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164361 | |||||||
| chr10:73164362 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
7 | HG02258.hp2 HG02559.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13-412A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164362 | |||||||
| chr10:73164491 | G | A | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-13-541C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164491 | |||||||
| chr10:73164555 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-13-605G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164555 | |||||||
| chr10:73164605 | C | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
8 | HG01346.hp1 HG01978.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-655G>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164605 | |||||||
| chr10:73164981 | T | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
8 | HG01346.hp1 HG01978.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-1031A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164981 | |||||||
| chr10:73164985 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | NA18747.hp1 NA18942.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13-1035C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73164985 | |||||||
| chr10:73165088 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-13-1138A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73165088 | |||||||
| chr10:73165228 | C | T | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-13-1278G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73165228 | |||||||
| chr10:73165574 | ACTCCTGA others(1): Show |
A | 3 | a0002c0002t0003g0039 a0002c0002t0003g0092 a0007c0010t0003g0091 |
3 | HG02965.hp2 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-13-1632_-13-1625d others(10): Show |
ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73165574 | |||||||
| chr10:73165618 | G | GT | 91 | a0001c0001t0001g0114 a0002c0002t0002g0009 a0002c0002t0002g0013 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-13-1669dupA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73165618 | |||||||
| chr10:73165801 | T | TA | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-13-1852dupT | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73165801 | |||||||
| chr10:73165809 | T | A | 2 | a0002c0002t0002g0109 a0002c0002t0002g0110 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-13-1859A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73165809 | |||||||
| chr10:73165844 | G | A | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-13-1894C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73165844 | |||||||
| chr10:73166070 | G | A | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-14+1796C>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166070 | |||||||
| chr10:73166134 | C | T | 1 | a0002c0002t0003g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-14+1732G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166134 | |||||||
| chr10:73166160 | AT | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14+1705delA | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166160 | |||||||
| chr10:73166225 | T | A | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14+1641A>T | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166225 | |||||||
| chr10:73166229 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-14+1637A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166229 | |||||||
| chr10:73166266 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00642.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-14+1600T>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166266 | |||||||
| chr10:73166324 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-14+1542G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166324 | |||||||
| chr10:73166379 | T | C | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14+1487A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166379 | |||||||
| chr10:73166462 | C | T | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-14+1404G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166462 | |||||||
| chr10:73166548 | A | G | 73 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(70): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-14+1318T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166548 | |||||||
| chr10:73166634 | G | T | 3 | a0002c0002t0002g0013 a0002c0002t0002g0037 a0002c0002t0002g0038 |
4 | HG02698.hp2 HG03688.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14+1232C>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166634 | |||||||
| chr10:73166769 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(192): Show |
258 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.-14+1097G>A | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166769 | |||||||
| chr10:73166778 | T | C | 17 | a0003c0004t0003g0022 a0003c0004t0003g0094 a0003c0004t0003g0095 others(14): Show |
20 | HG00735.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14+1088A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166778 | |||||||
| chr10:73166781 | T | C | 1 | a0002c0002t0002g0107 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-14+1085A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166781 | |||||||
| chr10:73166902 | G | C | 1 | a0001c0001t0001g0206 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-14+964C>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166902 | |||||||
| chr10:73166992 | T | C | 1 | a0003c0004t0003g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-14+874A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73166992 | |||||||
| chr10:73167253 | T | C | 2 | a0002c0002t0002g0109 a0002c0002t0002g0110 |
2 | HG01081.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-14+613A>G | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73167253 | |||||||
| chr10:73167311 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-14+555T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73167311 | |||||||
| chr10:73167726 | A | G | 91 | a0002c0002t0002g0009 a0002c0002t0002g0013 a0002c0002t0002g0015 others(88): Show |
106 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-14+140T>C | ECD | ENSG00000122882.11 | transcript | ENST00000372979.9 | protein_coding | 1/13 | chr10 | 73167726 |