Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 150350 |
| ensemblid | ENSG00000176177.10 |
| hgncid | 26352 |
| symbol | ENTHD1 |
| name | ENTH domain containing 1 |
| refseq_nuc | NM_152512.4 |
| refseq_prot | NP_689725.2 |
| ensembl_nuc | ENST00000325157.7 |
| ensembl_prot | ENSP00000317431.6 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 39743044 |
| end | 39893760 |
| strand | - |
| ver | v1.2 |
| region | chr22:39743044-39893760 |
| region5000 | chr22:39738044-39898760 |
| regionname0 | ENTHD1_chr22_39743044_39893760 |
| regionname5000 | ENTHD1_chr22_39738044_39898760 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 607 | 206 | 55 | 41 | 81 | 6 | 21 | 63 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | MAFRR others(602): Show |
chr22 | 39738044 | 39898760 |
| a0002 | 0/0 | 607 | 8 | 0 | 7 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | MAFRR others(602): Show |
chr22 | 39738044 | 39898760 |
| a0003 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | MAFRR others(602): Show |
chr22 | 39738044 | 39898760 |
| a0004 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | MAFRR others(602): Show |
chr22 | 39738044 | 39898760 |
| a0005 | 0/0 | 607 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | MAFRR others(602): Show |
chr22 | 39738044 | 39898760 |
| a0006 | 0/0 | 607 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | MAFRR others(602): Show |
chr22 | 39738044 | 39898760 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1821 | 200 | 50 | 41 | 80 | 6 | 21 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0001c0003 | 0/0 | 1821 | 3 | 3 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0001c0004 | 0/0 | 1821 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0001c0008 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0002c0002 | 0/0 | 1821 | 8 | 0 | 7 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0003c0005 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0004c0006 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0005c0009 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 | ||
| a0006c0007 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | ATGGC others(1816): Show |
chr22 | 39738044 | 39898760 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2680 | 167 | 46 | 30 | 69 | 5 | 16 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0001t0002 | 0/0 | 2680 | 27 | 0 | 11 | 11 | 1 | 4 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0001t0003 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0001t0004 | 0/0 | 2680 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0001t0005 | 0/1 | 2680 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0001t0006 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0001t0007 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0001t0008 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0003t0001 | 0/0 | 2680 | 3 | 3 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0004t0001 | 0/0 | 2680 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0001c0008t0001 | 0/0 | 2680 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0002c0002t0001 | 0/0 | 2680 | 8 | 0 | 7 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0003c0005t0001 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0004c0006t0001 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0005c0009t0001 | 0/0 | 2680 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| a0006c0007t0001 | 0/0 | 2680 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | GGAGT others(2675): Show |
chr22 | 39738044 | 39898760 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0004g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0005g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0003t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0003t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0001c0008t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0003c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0004c0006t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0005c0009t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| a0006c0007t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | FIN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01891 | hp1 | a0003 | c0005 | t0001 | g0019 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0195 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0192 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0095 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0094 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0008 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02717 | hp1 | a0004 | c0006 | t0001 | g0198 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0214 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02922 | hp1 | a0005 | c0009 | t0001 | g0154 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | BEB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | STU | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18983 | hp2 | a0001 | c0008 | t0001 | g0141 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19000 | hp1 | a0006 | c0007 | t0001 | g0126 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | GIH | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | GIH | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0015 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | USA | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0114 | REF | REF | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0059 | REF | REF | ENTHD1_chr22_39738044_39898760 | ENTHD1 | chr22 | 39738044 | 39898760 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39743860 | A | G | 1 | a0005 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1643T>C | p.Ile548Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1864/2680 | 1643/1824 | 548/607 | chr22 | 39743860 | |||
| chr22:39744176 | C | T | 1 | a0006 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.1327G>A | p.Gly443Arg | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1548/2680 | 1327/1824 | 443/607 | chr22 | 39744176 | |||
| chr22:39765300 | A | G | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1142T>C | p.Val381Ala | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/7 | 1363/2680 | 1142/1824 | 381/607 | chr22 | 39765300 | |||
| chr22:39765434 | C | G | 1 | a0003 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1008G>C | p.Trp336Cys | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/7 | 1229/2680 | 1008/1824 | 336/607 | chr22 | 39765434 | |||
| chr22:39765567 | C | G | 1 | a0003 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.875G>C | p.Arg292Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/7 | 1096/2680 | 875/1824 | 292/607 | chr22 | 39765567 | |||
| chr22:39861778 | C | G | 1 | a0003 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.579G>C | p.Arg193Ser | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/7 | 800/2680 | 579/1824 | 193/607 | chr22 | 39861778 | |||
| chr22:39887423 | A | G | 1 | a0002 | 8 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(5): Show |
missense_variant | MODERATE | c.326T>C | p.Ile109Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/7 | 547/2680 | 326/1824 | 109/607 | chr22 | 39887423 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39744132 | G | T | 1 | a0001c0008 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.1371C>A | p.Thr457Thr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1592/2680 | 1371/1824 | 457/607 | chr22 | 39744132 | |||
| chr22:39744158 | G | A | 1 | a0003c0005 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1345C>T | p.Leu449Leu | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 1566/2680 | 1345/1824 | 449/607 | chr22 | 39744158 | |||
| chr22:39862000 | A | G | 1 | a0001c0004 | 2 | HG02258.hp1 HG02572.hp2 |
synonymous_variant | LOW | c.357T>C | p.Tyr119Tyr | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/7 | 578/2680 | 357/1824 | 119/607 | chr22 | 39862000 | |||
| chr22:39887557 | A | G | 1 | a0001c0003 | 3 | HG02622.hp2 HG02723.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.192T>C | p.His64His | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/7 | 413/2680 | 192/1824 | 64/607 | chr22 | 39887557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39743145 | T | C | 1 | a0001c0001t0007 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*534A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 534 | chr22 | 39743145 | ||||||
| chr22:39743243 | G | A | 1 | a0001c0001t0008 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 436 | chr22 | 39743243 | ||||||
| chr22:39743251 | C | G | 1 | a0001c0001t0006 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 428 | chr22 | 39743251 | ||||||
| chr22:39743434 | A | G | 2 | a0001c0001t0002 a0001c0001t0004 |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*245T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 7/7 | 245 | chr22 | 39743434 | ||||||
| chr22:39893708 | C | T | 1 | a0001c0001t0004 | 1 | HG03927.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/7 | 5960 | chr22 | 39893708 | ||||||
| chr22:39893722 | C | T | 1 | a0001c0001t0003 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-183G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/7 | 5974 | chr22 | 39893722 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:39744294 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1220-11A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744294 | |||||||
| chr22:39744439 | A | C | 30 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(27): Show |
30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1220-156T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744439 | |||||||
| chr22:39744469 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0029 others(1): Show |
4 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220-186G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744469 | |||||||
| chr22:39744527 | TTCATCTT others(3): Show |
T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1220-254_1220-245d others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744527 | |||||||
| chr22:39744734 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1220-451G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744734 | |||||||
| chr22:39744963 | T | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-680A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39744963 | |||||||
| chr22:39745045 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1220-762A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745045 | |||||||
| chr22:39745284 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0006g0214 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1220-1001G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745284 | |||||||
| chr22:39745539 | T | G | 3 | a0001c0001t0001g0023 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-1256A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745539 | |||||||
| chr22:39745658 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1220-1375G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745658 | |||||||
| chr22:39745768 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0098 a0001c0001t0001g0106 others(2): Show |
5 | HG00438.hp2 NA18984.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220-1485C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745768 | |||||||
| chr22:39745794 | G | A | 27 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1220-1511C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745794 | |||||||
| chr22:39745894 | G | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1220-1611C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745894 | |||||||
| chr22:39745917 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-1634G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39745917 | |||||||
| chr22:39746210 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-1927T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746210 | |||||||
| chr22:39746244 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1220-1961T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746244 | |||||||
| chr22:39746526 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-2243G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746526 | |||||||
| chr22:39746567 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1220-2284C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746567 | |||||||
| chr22:39746901 | T | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-2618A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39746901 | |||||||
| chr22:39747286 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0142 |
2 | NA18988.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1220-3003G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747286 | |||||||
| chr22:39747324 | A | T | 5 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0036 others(2): Show |
5 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220-3041T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747324 | |||||||
| chr22:39747346 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1220-3063C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747346 | |||||||
| chr22:39747572 | A | G | 27 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1220-3289T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747572 | |||||||
| chr22:39747977 | G | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(17): Show |
21 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1220-3694C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39747977 | |||||||
| chr22:39748024 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1220-3741C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748024 | |||||||
| chr22:39748030 | C | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1220-3747G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748030 | |||||||
| chr22:39748041 | G | A | 1 | a0005c0009t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1220-3758C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748041 | |||||||
| chr22:39748047 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1220-3764C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748047 | |||||||
| chr22:39748249 | C | CA | 11 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0089 others(8): Show |
11 | HG00738.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1220-3967dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748249 | |||||||
| chr22:39748379 | C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-4096G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748379 | |||||||
| chr22:39748385 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1220-4102G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748385 | |||||||
| chr22:39748386 | G | A | 1 | a0005c0009t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1220-4103C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748386 | |||||||
| chr22:39748427 | CT | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1220-4145delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748427 | |||||||
| chr22:39748432 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1220-4149A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748432 | |||||||
| chr22:39748507 | T | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-4224A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748507 | |||||||
| chr22:39748512 | C | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0098 a0001c0001t0001g0106 others(2): Show |
5 | HG00438.hp2 NA18984.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1220-4229G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748512 | |||||||
| chr22:39748557 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1220-4274T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748557 | |||||||
| chr22:39748569 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1220-4286G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748569 | |||||||
| chr22:39748586 | AT | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1220-4304delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748586 | |||||||
| chr22:39748595 | T | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0057 others(1): Show |
4 | HG02135.hp2 NA18979.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1220-4312A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748595 | |||||||
| chr22:39748599 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-4316C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748599 | |||||||
| chr22:39748669 | T | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-4386A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39748669 | |||||||
| chr22:39749031 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1220-4748G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749031 | |||||||
| chr22:39749354 | T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-5071A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749354 | |||||||
| chr22:39749454 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-5171C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749454 | |||||||
| chr22:39749612 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1220-5329A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749612 | |||||||
| chr22:39749698 | T | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0002g0155 others(30): Show |
33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1220-5415A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749698 | |||||||
| chr22:39749836 | A | G | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1220-5553T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749836 | |||||||
| chr22:39749857 | G | A | 2 | a0001c0001t0001g0023 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-5574C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749857 | |||||||
| chr22:39749989 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0122 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1220-5706G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39749989 | |||||||
| chr22:39750280 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0131 |
2 | NA18968.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1220-5997C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750280 | |||||||
| chr22:39750526 | G | T | 2 | a0001c0001t0001g0023 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-6243C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750526 | |||||||
| chr22:39750743 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-6460T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750743 | |||||||
| chr22:39750754 | T | A | 2 | a0001c0001t0001g0023 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1220-6471A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39750754 | |||||||
| chr22:39751146 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-6863C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751146 | |||||||
| chr22:39751505 | T | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0199 |
3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1220-7222A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751505 | |||||||
| chr22:39751759 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1220-7476A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751759 | |||||||
| chr22:39751985 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0003g0004 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1220-7702C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39751985 | |||||||
| chr22:39752114 | G | GATATACT others(19): Show |
1 | a0001c0001t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1220-7857_1220-783 others(30): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39752114 | |||||||
| chr22:39752114 | G | T | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1220-7831C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39752114 | |||||||
| chr22:39753022 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1220-8739C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753022 | |||||||
| chr22:39753037 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-8754T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753037 | |||||||
| chr22:39753213 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1220-8930A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753213 | |||||||
| chr22:39753389 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1220-9106T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753389 | |||||||
| chr22:39753696 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0191 |
3 | HG01884.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1220-9413C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753696 | |||||||
| chr22:39753725 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1220-9442A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753725 | |||||||
| chr22:39753739 | C | T | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1220-9456G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753739 | |||||||
| chr22:39753913 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-9630C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39753913 | |||||||
| chr22:39754048 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-9765G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754048 | |||||||
| chr22:39754066 | G | A | 2 | a0001c0001t0006g0214 a0003c0005t0001g0019 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1220-9783C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754066 | |||||||
| chr22:39754280 | T | C | 4 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0001g0102 others(1): Show |
4 | HG00597.hp1 HG00673.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1220-9997A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754280 | |||||||
| chr22:39754281 | A | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1220-9998T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754281 | |||||||
| chr22:39754741 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1220-10458G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754741 | |||||||
| chr22:39754977 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1219+10246G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39754977 | |||||||
| chr22:39755172 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+10051G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755172 | |||||||
| chr22:39755229 | T | C | 2 | a0001c0001t0001g0023 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1219+9994A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755229 | |||||||
| chr22:39755338 | G | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+9885C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755338 | |||||||
| chr22:39755438 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219+9785G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755438 | |||||||
| chr22:39755515 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1219+9708G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755515 | |||||||
| chr22:39755560 | G | C | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1219+9663C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755560 | |||||||
| chr22:39755874 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1219+9349T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39755874 | |||||||
| chr22:39756281 | G | GTC | 2 | a0001c0001t0001g0117 a0001c0001t0001g0191 |
2 | HG01884.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1219+8940_1219+894 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756281 | |||||||
| chr22:39756287 | G | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0191 |
3 | HG01884.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1219+8936C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | |||||||
| chr22:39756287 | G | GTC | 36 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(33): Show |
36 | HG00735.hp1 HG01257.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.1219+8934_1219+893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | |||||||
| chr22:39756287 | G | GTCTC | 11 | a0001c0001t0001g0049 a0001c0001t0001g0130 a0001c0001t0001g0132 others(8): Show |
11 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219+8932_1219+893 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | |||||||
| chr22:39756287 | GTC | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0030 others(31): Show |
35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1219+8934_1219+893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | |||||||
| chr22:39756287 | GTCTCTC | G | 2 | a0001c0001t0001g0177 a0001c0001t0002g0155 |
2 | NA18522.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1219+8930_1219+893 others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756287 | |||||||
| chr22:39756308 | TCTCTCTC others(3): Show |
T | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1219+8905_1219+891 others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756308 | |||||||
| chr22:39756314 | T | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0081 |
2 | HG00621.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1219+8909A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756314 | |||||||
| chr22:39756314 | T | TCA | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(2): Show |
5 | HG02083.hp1 NA18944.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219+8908_1219+890 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756314 | |||||||
| chr22:39756316 | T | A | 70 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0030 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1219+8907A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756316 | |||||||
| chr22:39756316 | T | TCA | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(30): Show |
35 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1219+8905_1219+890 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756316 | |||||||
| chr22:39756316 | T | TCTCTCTC others(19): Show |
1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+8906_1219+890 others(30): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756316 | |||||||
| chr22:39756318 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1219+8905T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756318 | |||||||
| chr22:39756327 | C | G | 27 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1219+8896G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756327 | |||||||
| chr22:39756340 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219+8883C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756340 | |||||||
| chr22:39756342 | A | ACG | 2 | a0001c0001t0001g0093 a0001c0001t0001g0116 |
2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1219+8880_1219+888 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756342 | |||||||
| chr22:39756342 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0191 a0001c0001t0006g0214 |
3 | HG01884.hp2 HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1219+8881T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756342 | |||||||
| chr22:39756622 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+8601T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756622 | |||||||
| chr22:39756628 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+8595G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756628 | |||||||
| chr22:39756659 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1219+8564T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39756659 | |||||||
| chr22:39757014 | C | CA | 8 | a0001c0001t0001g0043 a0001c0001t0001g0182 a0001c0001t0001g0188 others(5): Show |
8 | HG01891.hp1 HG02145.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1219+8208dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757014 | |||||||
| chr22:39757014 | CA | C | 34 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0045 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.1219+8208delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757014 | |||||||
| chr22:39757311 | T | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+7912A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757311 | |||||||
| chr22:39757441 | T | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+7782A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757441 | |||||||
| chr22:39757508 | C | G | 1 | a0001c0001t0002g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1219+7715G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757508 | |||||||
| chr22:39757520 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1219+7703A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757520 | |||||||
| chr22:39757576 | C | CTGAGGCA others(11): Show |
1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1219+7629_1219+764 others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757576 | |||||||
| chr22:39757690 | T | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02886.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1219+7533A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757690 | |||||||
| chr22:39757783 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1219+7440G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39757783 | |||||||
| chr22:39758031 | A | G | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1219+7192T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758031 | |||||||
| chr22:39758038 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1219+7185G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758038 | |||||||
| chr22:39758205 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1219+7018A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758205 | |||||||
| chr22:39758450 | T | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+6773A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758450 | |||||||
| chr22:39758583 | C | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+6640G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758583 | |||||||
| chr22:39758811 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+6412T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758811 | |||||||
| chr22:39758871 | A | T | 21 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0055 others(18): Show |
21 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.1219+6352T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758871 | |||||||
| chr22:39758947 | G | A | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1219+6276C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39758947 | |||||||
| chr22:39759172 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1219+6051C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759172 | |||||||
| chr22:39759281 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0131 |
2 | NA18968.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1219+5942T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759281 | |||||||
| chr22:39759551 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1219+5672G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759551 | |||||||
| chr22:39759632 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
17 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.1219+5591A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759632 | |||||||
| chr22:39759693 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1219+5530G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759693 | |||||||
| chr22:39759926 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1219+5297C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759926 | |||||||
| chr22:39759928 | G | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+5295C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39759928 | |||||||
| chr22:39760076 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1219+5147C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760076 | |||||||
| chr22:39760203 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1219+5020T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760203 | |||||||
| chr22:39760268 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1219+4955G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760268 | |||||||
| chr22:39760980 | C | T | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1219+4243G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39760980 | |||||||
| chr22:39761111 | T | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+4112A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761111 | |||||||
| chr22:39761246 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1219+3977T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761246 | |||||||
| chr22:39761249 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1219+3974C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761249 | |||||||
| chr22:39761499 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+3724C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761499 | |||||||
| chr22:39761580 | GAC | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1219+3641_1219+364 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39761580 | |||||||
| chr22:39762196 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0006c0007t0001g0126 |
3 | NA18977.hp1 NA19000.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1219+3027G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762196 | |||||||
| chr22:39762212 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1219+3011G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762212 | |||||||
| chr22:39762223 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1219+3000A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762223 | |||||||
| chr22:39762438 | ATCTCACT others(13): Show |
A | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1219+2765_1219+278 others(24): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762438 | |||||||
| chr22:39762526 | C | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+2697G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762526 | |||||||
| chr22:39762622 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+2601C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762622 | |||||||
| chr22:39762928 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1219+2295A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39762928 | |||||||
| chr22:39763248 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1219+1975A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39763248 | |||||||
| chr22:39763407 | T | C | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1219+1816A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39763407 | |||||||
| chr22:39763438 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1219+1785G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39763438 | |||||||
| chr22:39764094 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1219+1129A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764094 | |||||||
| chr22:39764198 | A | G | 5 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0006g0214 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1219+1025T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764198 | |||||||
| chr22:39764299 | C | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+924G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764299 | |||||||
| chr22:39764503 | A | G | 9 | a0001c0001t0001g0051 a0001c0001t0001g0072 a0001c0001t0001g0078 others(6): Show |
9 | HG00738.hp2 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1219+720T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764503 | |||||||
| chr22:39764524 | TATGTAAG others(40): Show |
T | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1219+652_1219+698d others(49): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764524 | |||||||
| chr22:39764542 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1219+681T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764542 | |||||||
| chr22:39764786 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1219+437T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764786 | |||||||
| chr22:39764860 | A | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+363T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764860 | |||||||
| chr22:39764861 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+362G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764861 | |||||||
| chr22:39764935 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+288T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764935 | |||||||
| chr22:39764976 | T | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1219+247A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39764976 | |||||||
| chr22:39765176 | T | TTG | 23 | a0001c0001t0001g0049 a0001c0001t0001g0055 a0001c0001t0001g0062 others(20): Show |
23 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1219+45_1219+46dup others(2): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | |||||||
| chr22:39765176 | T | TTGTGTG | 3 | a0001c0001t0001g0153 a0001c0001t0001g0203 a0001c0001t0008g0015 |
3 | HG00639.hp2 HG02559.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1219+41_1219+46dup others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | |||||||
| chr22:39765176 | T | TTGTGTGT others(1): Show |
24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1219+39_1219+46dup others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | |||||||
| chr22:39765176 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1219+37_1219+46dup others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | |||||||
| chr22:39765176 | TTG | T | 29 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0044 others(26): Show |
29 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.1219+45_1219+46del others(2): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | |||||||
| chr22:39765176 | TTGTG | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0188 |
2 | HG02258.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1219+43_1219+46del others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 6/6 | chr22 | 39765176 | |||||||
| chr22:39765678 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.833-69A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39765678 | |||||||
| chr22:39765826 | C | G | 3 | a0001c0001t0001g0200 a0001c0003t0001g0006 a0004c0006t0001g0198 |
3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.833-217G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39765826 | |||||||
| chr22:39766019 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0207 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.833-420_833-411dup others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(4): Show |
8 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 others(5): Show |
8 | HG00323.hp1 HG01070.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.833-421_833-411dup others(11): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(5): Show |
7 | a0001c0001t0002g0155 a0001c0001t0002g0157 a0001c0001t0002g0159 others(4): Show |
7 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.833-422_833-411dup others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0206 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.833-423_833-411dup others(13): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0002g0158 a0001c0001t0002g0210 |
2 | HG00642.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.833-424_833-411dup others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0004g0005 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.833-425_833-411dup others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.833-426_833-411dup others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0002g0164 a0001c0001t0002g0171 |
2 | NA19002.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.833-427_833-411dup others(17): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0002g0156 a0001c0001t0002g0168 a0001c0001t0002g0173 |
3 | NA19010.hp2 NA19077.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.833-428_833-411dup others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0002g0163 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.833-429_833-411dup others(19): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0170 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.833-430_833-411dup others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | CA | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(106): Show |
111 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.833-411delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | CAA | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00673.hp1 HG00735.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.833-412_833-411del others(2): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0172 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.833-422_833-411del others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | CAAAAAAA others(6): Show |
C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-423_833-411del others(13): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766019 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02886.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.833-424_833-411del others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766019 | |||||||
| chr22:39766107 | T | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-498A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766107 | |||||||
| chr22:39766593 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.833-984G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766593 | |||||||
| chr22:39766594 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-985C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766594 | |||||||
| chr22:39766613 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-1004C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766613 | |||||||
| chr22:39766642 | A | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.833-1033T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766642 | |||||||
| chr22:39766656 | T | A | 1 | a0001c0001t0002g0155 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.833-1047A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766656 | |||||||
| chr22:39766802 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0185 |
2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.833-1193T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39766802 | |||||||
| chr22:39767042 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0122 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.833-1433A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767042 | |||||||
| chr22:39767462 | A | C | 1 | a0001c0001t0001g0152 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.833-1853T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767462 | |||||||
| chr22:39767462 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-1863_833-1854d others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767462 | |||||||
| chr22:39767492 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-1883T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767492 | |||||||
| chr22:39767617 | T | C | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-2008A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767617 | |||||||
| chr22:39767630 | T | C | 1 | a0005c0009t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.833-2021A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767630 | |||||||
| chr22:39767752 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.833-2143T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767752 | |||||||
| chr22:39767888 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.833-2279G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39767888 | |||||||
| chr22:39768155 | C | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(14): Show |
18 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-2546G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768155 | |||||||
| chr22:39768286 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-2677C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768286 | |||||||
| chr22:39768434 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.833-2825T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768434 | |||||||
| chr22:39768441 | A | C | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-2832T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768441 | |||||||
| chr22:39768623 | C | T | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.833-3014G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768623 | |||||||
| chr22:39768682 | A | G | 1 | a0001c0001t0001g0012 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.833-3073T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768682 | |||||||
| chr22:39768867 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.833-3258C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768867 | |||||||
| chr22:39768946 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-3337T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768946 | |||||||
| chr22:39768987 | C | CACACACT others(23): Show |
1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-3408_833-3379d others(32): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768987 | |||||||
| chr22:39768987 | CACACACT others(23): Show |
C | 1 | a0001c0001t0001g0092 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.833-3408_833-3379d others(32): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39768987 | |||||||
| chr22:39769079 | T | TACACACA others(57): Show |
1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-3471_833-3470i others(66): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769079 | |||||||
| chr22:39769088 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-3479T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769088 | |||||||
| chr22:39769154 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(82): Show |
87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.833-3545C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769154 | |||||||
| chr22:39769227 | T | C | 7 | a0001c0001t0002g0156 a0001c0001t0002g0163 a0001c0001t0002g0164 others(4): Show |
7 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.833-3618A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769227 | |||||||
| chr22:39769331 | G | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-3722C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769331 | |||||||
| chr22:39769568 | G | C | 30 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(27): Show |
30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.833-3959C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769568 | |||||||
| chr22:39769569 | G | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-3960C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769569 | |||||||
| chr22:39769659 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.833-4050T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769659 | |||||||
| chr22:39769687 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.833-4078T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769687 | |||||||
| chr22:39769850 | T | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(16): Show |
20 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.833-4241A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769850 | |||||||
| chr22:39769934 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-4325G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769934 | |||||||
| chr22:39769941 | G | GATTGTGA others(18): Show |
1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-4333_833-4332i others(27): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769941 | |||||||
| chr22:39769942 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-4333A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39769942 | |||||||
| chr22:39770352 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.833-4743G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770352 | |||||||
| chr22:39770462 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-4853G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770462 | |||||||
| chr22:39770469 | A | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-4860T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770469 | |||||||
| chr22:39770605 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(152): Show |
158 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.833-4996C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770605 | |||||||
| chr22:39770652 | T | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-5043A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770652 | |||||||
| chr22:39770762 | A | ACTTGGAT others(29): Show |
1 | a0001c0001t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.833-5189_833-5154d others(38): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770762 | |||||||
| chr22:39770982 | T | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-5373A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39770982 | |||||||
| chr22:39771077 | G | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0018 others(66): Show |
70 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.833-5468C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771077 | |||||||
| chr22:39771085 | C | CT | 4 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0032 others(1): Show |
5 | HG01891.hp1 HG02055.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-5477dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771085 | |||||||
| chr22:39771125 | TG | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0061 |
2 | NA18942.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.833-5517delC | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771125 | |||||||
| chr22:39771138 | G | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.833-5529C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771138 | |||||||
| chr22:39771185 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-5576C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771185 | |||||||
| chr22:39771988 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.833-6379G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39771988 | |||||||
| chr22:39772433 | G | T | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.833-6824C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39772433 | |||||||
| chr22:39772605 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.833-6996T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39772605 | |||||||
| chr22:39773117 | C | CA | 18 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0063 others(15): Show |
18 | HG00621.hp2 HG01081.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.833-7509dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | |||||||
| chr22:39773117 | C | CAAAAAAA others(5): Show |
1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-7520_833-7509d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | |||||||
| chr22:39773117 | CA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(61): Show |
66 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.833-7509delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | |||||||
| chr22:39773117 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0038 |
3 | HG02055.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.833-7520_833-7509d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | |||||||
| chr22:39773117 | CAAAAAAA others(6): Show |
C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(17): Show |
21 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.833-7521_833-7509d others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773117 | |||||||
| chr22:39773921 | T | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(84): Show |
89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.833-8312A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773921 | |||||||
| chr22:39773959 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-8350C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39773959 | |||||||
| chr22:39774067 | C | T | 9 | a0001c0001t0001g0051 a0001c0001t0001g0072 a0001c0001t0001g0078 others(6): Show |
9 | HG00738.hp2 HG01106.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-8458G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774067 | |||||||
| chr22:39774413 | T | C | 3 | a0001c0001t0001g0200 a0001c0003t0001g0006 a0004c0006t0001g0198 |
3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.833-8804A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774413 | |||||||
| chr22:39774462 | A | C | 1 | a0001c0001t0001g0090 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.833-8853T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774462 | |||||||
| chr22:39774578 | C | A | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.833-8969G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774578 | |||||||
| chr22:39774629 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.833-9020A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774629 | |||||||
| chr22:39774772 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.833-9163G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774772 | |||||||
| chr22:39774885 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.833-9276G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39774885 | |||||||
| chr22:39775245 | T | G | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.833-9636A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775245 | |||||||
| chr22:39775269 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.833-9660G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775269 | |||||||
| chr22:39775383 | A | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0132 |
2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.833-9774T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775383 | |||||||
| chr22:39775706 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.833-10097G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775706 | |||||||
| chr22:39775828 | T | A | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0147 others(2): Show |
5 | HG02735.hp1 NA18977.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.833-10219A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39775828 | |||||||
| chr22:39776037 | GC | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0082 others(1): Show |
4 | HG02258.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-10429delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776037 | |||||||
| chr22:39776083 | G | A | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-10474C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776083 | |||||||
| chr22:39776130 | T | G | 2 | a0001c0001t0001g0190 a0001c0001t0003g0004 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-10521A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776130 | |||||||
| chr22:39776193 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-10584T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776193 | |||||||
| chr22:39776712 | A | C | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-11103T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39776712 | |||||||
| chr22:39777267 | T | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.833-11658A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777267 | |||||||
| chr22:39777555 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.833-11946T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777555 | |||||||
| chr22:39777893 | C | T | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-12284G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777893 | |||||||
| chr22:39777915 | G | T | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.833-12306C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777915 | |||||||
| chr22:39777916 | C | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-12307G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39777916 | |||||||
| chr22:39778165 | G | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0104 a0001c0001t0001g0110 others(1): Show |
4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-12556C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778165 | |||||||
| chr22:39778367 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0185 |
2 | HG02523.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.833-12758T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778367 | |||||||
| chr22:39778457 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-12848G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778457 | |||||||
| chr22:39778599 | T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-12990A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778599 | |||||||
| chr22:39778680 | A | G | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.833-13071T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778680 | |||||||
| chr22:39778865 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-13256A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778865 | |||||||
| chr22:39778887 | A | C | 2 | a0001c0001t0001g0190 a0001c0001t0003g0004 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-13278T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778887 | |||||||
| chr22:39778890 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-13281G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39778890 | |||||||
| chr22:39779249 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.833-13640T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779249 | |||||||
| chr22:39779336 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.833-13727C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779336 | |||||||
| chr22:39779402 | C | T | 4 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(1): Show |
4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-13793G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779402 | |||||||
| chr22:39779434 | A | G | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.833-13825T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779434 | |||||||
| chr22:39779556 | GA | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(22): Show |
26 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.833-13948delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39779556 | |||||||
| chr22:39780098 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-14489C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780098 | |||||||
| chr22:39780140 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.833-14531T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780140 | |||||||
| chr22:39780166 | G | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-14557C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780166 | |||||||
| chr22:39780240 | C | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(16): Show |
20 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.833-14631G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780240 | |||||||
| chr22:39780249 | C | T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-14640G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780249 | |||||||
| chr22:39780280 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.833-14671C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780280 | |||||||
| chr22:39780312 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.833-14703C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780312 | |||||||
| chr22:39780375 | C | CA | 15 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0056 others(12): Show |
15 | HG00735.hp1 HG00735.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.833-14767dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780375 | |||||||
| chr22:39780375 | C | CAA | 37 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0050 others(34): Show |
37 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.833-14768_833-1476 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780375 | |||||||
| chr22:39780375 | CA | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0026 others(20): Show |
23 | HG00639.hp2 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.833-14767delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780375 | |||||||
| chr22:39780568 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(16): Show |
20 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.833-14959T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780568 | |||||||
| chr22:39780569 | GTTATAC | G | 2 | a0001c0001t0001g0190 a0001c0001t0003g0004 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-14966_833-1496 others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780569 | |||||||
| chr22:39780644 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.833-15035A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780644 | |||||||
| chr22:39780766 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833-15157C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780766 | |||||||
| chr22:39780799 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.833-15190G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780799 | |||||||
| chr22:39780870 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.833-15261C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780870 | |||||||
| chr22:39780998 | C | CA | 27 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.833-15390dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780998 | |||||||
| chr22:39780998 | C | CAAAAAAA others(3): Show |
20 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(17): Show |
21 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.833-15399_833-1539 others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780998 | |||||||
| chr22:39780998 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0028 a0001c0001t0001g0034 |
2 | HG02257.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.833-15400_833-1539 others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39780998 | |||||||
| chr22:39781225 | A | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.833-15616T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781225 | |||||||
| chr22:39781280 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.833-15671A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781280 | |||||||
| chr22:39781987 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-16378T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781987 | |||||||
| chr22:39781991 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.833-16382A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39781991 | |||||||
| chr22:39782032 | A | G | 1 | a0001c0001t0002g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.833-16423T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782032 | |||||||
| chr22:39782038 | G | T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-16429C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782038 | |||||||
| chr22:39782060 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-16451C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782060 | |||||||
| chr22:39782220 | A | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-16611T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782220 | |||||||
| chr22:39782231 | G | T | 10 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0052 others(7): Show |
10 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.833-16622C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782231 | |||||||
| chr22:39782614 | T | C | 3 | a0001c0001t0001g0200 a0001c0003t0001g0006 a0004c0006t0001g0198 |
3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.833-17005A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782614 | |||||||
| chr22:39782629 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-17020T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782629 | |||||||
| chr22:39782983 | G | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(67): Show |
71 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.833-17374C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39782983 | |||||||
| chr22:39783521 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.833-17912G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39783521 | |||||||
| chr22:39783635 | G | GA | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-18027dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39783635 | |||||||
| chr22:39783823 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0003g0004 |
2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.833-18214T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39783823 | |||||||
| chr22:39784325 | G | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.833-18716C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784325 | |||||||
| chr22:39784543 | T | TAC | 18 | a0001c0001t0001g0045 a0001c0001t0001g0121 a0001c0001t0001g0144 others(15): Show |
18 | HG01496.hp2 HG02145.hp1 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-18936_833-1893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACAC | 9 | a0001c0001t0001g0020 a0001c0001t0001g0093 a0001c0001t0001g0190 others(6): Show |
9 | HG01070.hp2 HG01192.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.833-18938_833-1893 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACAC | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0082 others(6): Show |
9 | HG00323.hp1 HG00642.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.833-18940_833-1893 others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACACA others(1): Show |
6 | a0001c0001t0002g0156 a0001c0001t0002g0162 a0001c0001t0002g0163 others(3): Show |
6 | NA18998.hp2 NA19010.hp2 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-18942_833-1893 others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0083 a0001c0001t0002g0155 a0001c0001t0002g0165 others(1): Show |
4 | HG02258.hp2 NA18988.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-18944_833-1893 others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACACA others(5): Show |
2 | a0001c0001t0002g0158 a0001c0001t0002g0164 |
2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.833-18946_833-1893 others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACACA others(7): Show |
5 | a0001c0001t0001g0014 a0001c0001t0002g0157 a0001c0001t0002g0161 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-18948_833-1893 others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACACA others(9): Show |
3 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0166 |
3 | HG01081.hp2 HG01257.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.833-18950_833-1893 others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACACA others(11): Show |
1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-18952_833-1893 others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | T | TACACACA others(15): Show |
1 | a0001c0001t0002g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.833-18956_833-1893 others(26): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | TAC | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(62): Show |
66 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.833-18936_833-1893 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | TACAC | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0052 a0001c0001t0001g0066 others(9): Show |
12 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.833-18938_833-1893 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784543 | TACACACA others(5): Show |
T | 1 | a0001c0001t0001g0197 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.833-18946_833-1893 others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784543 | |||||||
| chr22:39784582 | A | ACT | 13 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0027 others(10): Show |
13 | HG01496.hp1 HG02486.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.833-18975_833-1897 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784582 | |||||||
| chr22:39784582 | A | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0024 others(7): Show |
11 | HG00323.hp2 HG01069.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.833-18973T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784582 | |||||||
| chr22:39784586 | G | A | 30 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(27): Show |
30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.833-18977C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784586 | |||||||
| chr22:39784812 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.833-19203C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784812 | |||||||
| chr22:39784880 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.833-19271A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39784880 | |||||||
| chr22:39785132 | A | AAGAT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
63 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.833-19527_833-1952 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785132 | |||||||
| chr22:39785155 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.833-19546T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785155 | |||||||
| chr22:39785169 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.833-19560G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785169 | |||||||
| chr22:39785193 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-19584C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785193 | |||||||
| chr22:39785311 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.833-19702C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785311 | |||||||
| chr22:39785327 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.833-19718C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785327 | |||||||
| chr22:39785583 | T | C | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-19974A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785583 | |||||||
| chr22:39785827 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.833-20218T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39785827 | |||||||
| chr22:39786268 | T | G | 3 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0161 |
3 | HG01081.hp2 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.833-20659A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786268 | |||||||
| chr22:39786424 | AT | A | 5 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 others(2): Show |
5 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-20816delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786424 | |||||||
| chr22:39786438 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.833-20829C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786438 | |||||||
| chr22:39786526 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG00597.hp1 HG00673.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.833-20917G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786526 | |||||||
| chr22:39786671 | AC | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0122 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.833-21063delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786671 | |||||||
| chr22:39786676 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.833-21067A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786676 | |||||||
| chr22:39786694 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0107 |
2 | NA18982.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.833-21085T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786694 | |||||||
| chr22:39786704 | C | G | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-21095G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786704 | |||||||
| chr22:39786781 | A | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-21172T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786781 | |||||||
| chr22:39786841 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.833-21232A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786841 | |||||||
| chr22:39786876 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.833-21267T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786876 | |||||||
| chr22:39786896 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-21287G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786896 | |||||||
| chr22:39786917 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.833-21308G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39786917 | |||||||
| chr22:39787053 | C | CTG | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(85): Show |
90 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.833-21446_833-2144 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787053 | |||||||
| chr22:39787362 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.833-21753T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787362 | |||||||
| chr22:39787413 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.833-21804G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787413 | |||||||
| chr22:39787594 | G | A | 1 | a0001c0001t0002g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.833-21985C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39787594 | |||||||
| chr22:39788003 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-22394T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39788003 | |||||||
| chr22:39788466 | C | T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-22857G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39788466 | |||||||
| chr22:39788915 | A | G | 62 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
63 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.833-23306T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39788915 | |||||||
| chr22:39789150 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-23541T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39789150 | |||||||
| chr22:39789279 | G | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.833-23670C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39789279 | |||||||
| chr22:39789876 | G | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-24267C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39789876 | |||||||
| chr22:39790175 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.833-24566G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790175 | |||||||
| chr22:39790181 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-24572G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790181 | |||||||
| chr22:39790261 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.833-24652T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790261 | |||||||
| chr22:39790461 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.833-24852T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790461 | |||||||
| chr22:39790541 | C | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0029 others(1): Show |
4 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.833-24932G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790541 | |||||||
| chr22:39790811 | G | A | 4 | a0001c0001t0001g0063 a0001c0001t0001g0104 a0001c0001t0001g0110 others(1): Show |
4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.833-25202C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39790811 | |||||||
| chr22:39791520 | G | A | 1 | a0001c0004t0001g0095 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.833-25911C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39791520 | |||||||
| chr22:39791842 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.833-26233A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39791842 | |||||||
| chr22:39792305 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.833-26696G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792305 | |||||||
| chr22:39792392 | C | T | 1 | a0001c0008t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.833-26783G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792392 | |||||||
| chr22:39792421 | C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.833-26812G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792421 | |||||||
| chr22:39792509 | C | CTTAT | 2 | a0001c0001t0001g0071 a0001c0001t0001g0115 |
2 | HG01069.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.833-26904_833-2690 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792509 | |||||||
| chr22:39792723 | C | G | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-27114G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792723 | |||||||
| chr22:39792795 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-27186A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792795 | |||||||
| chr22:39792817 | C | CT | 22 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(19): Show |
23 | HG00621.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-27209dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792817 | |||||||
| chr22:39792921 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.833-27312A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792921 | |||||||
| chr22:39792985 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.833-27376A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39792985 | |||||||
| chr22:39793005 | C | T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.833-27396G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793005 | |||||||
| chr22:39793032 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.833-27423A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793032 | |||||||
| chr22:39793337 | A | AGTT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+27653_832+2765 others(7): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793337 | |||||||
| chr22:39793341 | G | GT | 6 | a0001c0001t0001g0023 a0001c0001t0001g0082 a0001c0001t0001g0190 others(3): Show |
6 | HG02717.hp1 HG03139.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.832+27651dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793341 | |||||||
| chr22:39793344 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.832+27649A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793344 | |||||||
| chr22:39793780 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.832+27213A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793780 | |||||||
| chr22:39793912 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+27081A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39793912 | |||||||
| chr22:39794182 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+26811C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794182 | |||||||
| chr22:39794352 | T | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+26641A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794352 | |||||||
| chr22:39794613 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+26380A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794613 | |||||||
| chr22:39794629 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.832+26364G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794629 | |||||||
| chr22:39794631 | T | C | 3 | a0001c0001t0001g0200 a0001c0003t0001g0006 a0004c0006t0001g0198 |
3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.832+26362A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794631 | |||||||
| chr22:39794803 | C | CA | 5 | a0001c0001t0001g0037 a0001c0001t0001g0045 a0001c0001t0001g0082 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+26189dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794803 | |||||||
| chr22:39794803 | CA | C | 9 | a0001c0001t0001g0177 a0001c0001t0002g0156 a0001c0001t0002g0163 others(6): Show |
9 | HG02886.hp1 NA18522.hp2 NA18988.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+26189delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794803 | |||||||
| chr22:39794996 | C | T | 2 | a0001c0001t0006g0214 a0003c0005t0001g0019 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.832+25997G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39794996 | |||||||
| chr22:39795054 | T | C | 8 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(5): Show |
8 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.832+25939A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795054 | |||||||
| chr22:39795194 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+25799C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795194 | |||||||
| chr22:39795259 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+25734C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795259 | |||||||
| chr22:39795318 | T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25675A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795318 | |||||||
| chr22:39795328 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25665T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795328 | |||||||
| chr22:39795445 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25548C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795445 | |||||||
| chr22:39795515 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.832+25478G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795515 | |||||||
| chr22:39795586 | C | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
12 | HG00621.hp1 HG01993.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.832+25407G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795586 | |||||||
| chr22:39795594 | AT | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
71 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.832+25398delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795594 | |||||||
| chr22:39795605 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.832+25388A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795605 | |||||||
| chr22:39795772 | T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25221A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795772 | |||||||
| chr22:39795826 | C | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+25167G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39795826 | |||||||
| chr22:39796018 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+24975T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796018 | |||||||
| chr22:39796227 | G | C | 2 | a0001c0001t0001g0099 a0002c0002t0001g0186 |
2 | HG00642.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.832+24766C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796227 | |||||||
| chr22:39796261 | C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+24732G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796261 | |||||||
| chr22:39796333 | T | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+24660A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796333 | |||||||
| chr22:39796340 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+24653C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796340 | |||||||
| chr22:39796457 | G | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0199 |
3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+24536C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796457 | |||||||
| chr22:39796487 | C | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(3): Show |
6 | HG00639.hp1 HG01081.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.832+24506G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796487 | |||||||
| chr22:39796872 | C | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0001g0112 |
3 | HG00621.hp2 HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.832+24121G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796872 | |||||||
| chr22:39796874 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+24119C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796874 | |||||||
| chr22:39796897 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+24096C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796897 | |||||||
| chr22:39796922 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+24071A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39796922 | |||||||
| chr22:39797099 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.832+23894G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797099 | |||||||
| chr22:39797266 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+23727G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797266 | |||||||
| chr22:39797498 | C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+23495G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797498 | |||||||
| chr22:39797577 | A | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+23416T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797577 | |||||||
| chr22:39797634 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+23359A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797634 | |||||||
| chr22:39797923 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.832+23070C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39797923 | |||||||
| chr22:39798376 | G | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+22617C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798376 | |||||||
| chr22:39798575 | C | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+22418G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798575 | |||||||
| chr22:39798593 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+22400C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798593 | |||||||
| chr22:39798637 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.832+22356T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798637 | |||||||
| chr22:39798645 | G | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+22348C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798645 | |||||||
| chr22:39798752 | C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+22241G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39798752 | |||||||
| chr22:39799012 | C | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(2): Show |
5 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+21981G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799012 | |||||||
| chr22:39799204 | G | A | 1 | a0005c0009t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.832+21789C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799204 | |||||||
| chr22:39799220 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.832+21773G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799220 | |||||||
| chr22:39799230 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+21763C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799230 | |||||||
| chr22:39799377 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+21616C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799377 | |||||||
| chr22:39799388 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+21605G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799388 | |||||||
| chr22:39799460 | G | A | 1 | a0002c0002t0001g0174 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.832+21533C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799460 | |||||||
| chr22:39799666 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+21327G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39799666 | |||||||
| chr22:39800059 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+20934A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800059 | |||||||
| chr22:39800748 | C | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+20245G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800748 | |||||||
| chr22:39800749 | G | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+20244C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800749 | |||||||
| chr22:39800946 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(21): Show |
25 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.832+20047T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39800946 | |||||||
| chr22:39801371 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.832+19622A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801371 | |||||||
| chr22:39801387 | CAA | C | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.832+19604_832+1960 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801387 | |||||||
| chr22:39801525 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+19468C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801525 | |||||||
| chr22:39801630 | G | A | 38 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+19363C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801630 | |||||||
| chr22:39801678 | G | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0201 others(2): Show |
5 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+19315C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801678 | |||||||
| chr22:39801721 | A | G | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+19272T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801721 | |||||||
| chr22:39801808 | T | C | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.832+19185A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801808 | |||||||
| chr22:39801925 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.832+19068C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39801925 | |||||||
| chr22:39802435 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.832+18558A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39802435 | |||||||
| chr22:39802514 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.832+18479G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39802514 | |||||||
| chr22:39802949 | G | A | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+18044C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39802949 | |||||||
| chr22:39803073 | A | G | 1 | a0001c0001t0002g0162 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.832+17920T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803073 | |||||||
| chr22:39803107 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.832+17886G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803107 | |||||||
| chr22:39803211 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.832+17782C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803211 | |||||||
| chr22:39803286 | C | T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+17707G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803286 | |||||||
| chr22:39803287 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.832+17706C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803287 | |||||||
| chr22:39803334 | C | T | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+17659G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803334 | |||||||
| chr22:39803535 | A | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+17458T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803535 | |||||||
| chr22:39803780 | T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+17213A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803780 | |||||||
| chr22:39803887 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+17106A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39803887 | |||||||
| chr22:39804452 | C | CA | 21 | a0001c0001t0001g0051 a0001c0001t0001g0062 a0001c0001t0001g0067 others(18): Show |
21 | HG00621.hp2 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.832+16540dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804452 | |||||||
| chr22:39804452 | CA | C | 12 | a0001c0001t0001g0022 a0001c0001t0001g0065 a0001c0001t0001g0111 others(9): Show |
12 | HG01070.hp2 HG01167.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.832+16540delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804452 | |||||||
| chr22:39804502 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0190 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.832+16491G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804502 | |||||||
| chr22:39804525 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832+16468C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39804525 | |||||||
| chr22:39805034 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+15959G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805034 | |||||||
| chr22:39805073 | C | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02027.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.832+15920G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805073 | |||||||
| chr22:39805145 | T | A | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+15848A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805145 | |||||||
| chr22:39805315 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.832+15678C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805315 | |||||||
| chr22:39805379 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+15614A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805379 | |||||||
| chr22:39805386 | G | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0006g0214 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+15607C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805386 | |||||||
| chr22:39805629 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+15364G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805629 | |||||||
| chr22:39805698 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0136 a0001c0001t0001g0152 others(1): Show |
4 | HG01257.hp2 HG01261.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+15295C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39805698 | |||||||
| chr22:39806196 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+14797G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39806196 | |||||||
| chr22:39806404 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.832+14589G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39806404 | |||||||
| chr22:39806967 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832+14026G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39806967 | |||||||
| chr22:39807241 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0004g0005 |
2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.832+13752G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807241 | |||||||
| chr22:39807720 | G | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+13273C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807720 | |||||||
| chr22:39807888 | C | CGT | 11 | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0069 others(8): Show |
11 | HG00140.hp2 HG00639.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.832+13103_832+1310 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807888 | |||||||
| chr22:39807888 | CGT | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 |
3 | HG00639.hp1 HG01081.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.832+13103_832+1310 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807888 | |||||||
| chr22:39807911 | G | A | 2 | a0003c0005t0001g0019 a0005c0009t0001g0154 |
2 | HG01891.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+13082C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807911 | |||||||
| chr22:39807913 | G | A | 36 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0045 others(33): Show |
36 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.832+13080C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807913 | |||||||
| chr22:39807913 | G | GTA | 3 | a0001c0001t0001g0009 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02055.hp1 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+13078_832+1307 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807913 | |||||||
| chr22:39807915 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0047 others(1): Show |
4 | HG02257.hp2 HG02896.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+13078T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807915 | |||||||
| chr22:39807917 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+13076T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39807917 | |||||||
| chr22:39808087 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+12906C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808087 | |||||||
| chr22:39808196 | AC | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+12796delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808196 | |||||||
| chr22:39808278 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.832+12715G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808278 | |||||||
| chr22:39808324 | G | A | 5 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 others(2): Show |
5 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+12669C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808324 | |||||||
| chr22:39808339 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+12654C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808339 | |||||||
| chr22:39808426 | A | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+12567T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808426 | |||||||
| chr22:39808437 | T | C | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.832+12556A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39808437 | |||||||
| chr22:39809493 | G | A | 32 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(29): Show |
32 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.832+11500C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39809493 | |||||||
| chr22:39809728 | C | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(27): Show |
30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.832+11265G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39809728 | |||||||
| chr22:39810038 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.832+10955C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810038 | |||||||
| chr22:39810088 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02015.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.832+10905T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810088 | |||||||
| chr22:39810332 | T | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.832+10661A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810332 | |||||||
| chr22:39810430 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.832+10563T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810430 | |||||||
| chr22:39810536 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+10457A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810536 | |||||||
| chr22:39810582 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0004g0005 |
2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.832+10411G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810582 | |||||||
| chr22:39810643 | T | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+10350A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810643 | |||||||
| chr22:39810644 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.832+10349C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810644 | |||||||
| chr22:39810806 | C | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(69): Show |
73 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.832+10187G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39810806 | |||||||
| chr22:39811296 | CA | C | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+9696delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811296 | |||||||
| chr22:39811348 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.832+9645G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811348 | |||||||
| chr22:39811367 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.832+9626G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811367 | |||||||
| chr22:39811396 | C | G | 1 | a0001c0001t0002g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.832+9597G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811396 | |||||||
| chr22:39811851 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+9142G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811851 | |||||||
| chr22:39811873 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.832+9120C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811873 | |||||||
| chr22:39811879 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+9114A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811879 | |||||||
| chr22:39811885 | A | G | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.832+9108T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811885 | |||||||
| chr22:39811957 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.832+9036G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39811957 | |||||||
| chr22:39812011 | C | CA | 4 | a0001c0001t0001g0092 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+8981dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812011 | |||||||
| chr22:39812015 | C | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+8978G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812015 | |||||||
| chr22:39812015 | C | CA | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
141 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.832+8977dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812015 | |||||||
| chr22:39812015 | C | CAA | 5 | a0001c0001t0001g0033 a0001c0001t0001g0077 a0001c0001t0001g0146 others(2): Show |
5 | HG00597.hp2 HG02647.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+8976_832+8977d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812015 | |||||||
| chr22:39812018 | A | AC | 3 | a0001c0001t0001g0052 a0001c0001t0001g0122 a0001c0001t0002g0210 |
3 | HG00642.hp1 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.832+8974_832+8975i others(3): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812018 | |||||||
| chr22:39812025 | A | AC | 49 | a0001c0001t0001g0023 a0001c0001t0001g0046 a0001c0001t0001g0049 others(46): Show |
49 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.832+8967dupG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812025 | |||||||
| chr22:39812220 | T | C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0104 a0001c0001t0001g0110 others(1): Show |
4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.832+8773A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812220 | |||||||
| chr22:39812269 | A | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.832+8724T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812269 | |||||||
| chr22:39812449 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.832+8544T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812449 | |||||||
| chr22:39812843 | C | T | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+8150G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812843 | |||||||
| chr22:39812970 | G | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+8023C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39812970 | |||||||
| chr22:39813026 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.832+7967C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813026 | |||||||
| chr22:39813069 | C | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+7924G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813069 | |||||||
| chr22:39813072 | T | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+7921A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813072 | |||||||
| chr22:39813113 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(25): Show |
29 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.832+7880A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813113 | |||||||
| chr22:39813170 | A | G | 34 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.832+7823T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813170 | |||||||
| chr22:39813282 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.832+7711T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813282 | |||||||
| chr22:39813925 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.832+7068G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813925 | |||||||
| chr22:39813992 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.832+7001C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39813992 | |||||||
| chr22:39814052 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+6941A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814052 | |||||||
| chr22:39814135 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.832+6858A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814135 | |||||||
| chr22:39814295 | C | CAAAAAAA others(6): Show |
1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+6685_832+6697d others(15): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | |||||||
| chr22:39814295 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0093 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG01891.hp2 HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.832+6684_832+6697d others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | |||||||
| chr22:39814295 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0002g0163 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.832+6683_832+6697d others(17): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | |||||||
| chr22:39814295 | C | CAAAAAAA others(9): Show |
22 | a0001c0001t0001g0045 a0001c0001t0002g0155 a0001c0001t0002g0156 others(19): Show |
22 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.832+6682_832+6697d others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | |||||||
| chr22:39814295 | C | CAAAAAAA others(10): Show |
5 | a0001c0001t0002g0167 a0001c0001t0002g0170 a0001c0001t0002g0171 others(2): Show |
5 | HG01106.hp2 HG02922.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+6697_832+6698i others(19): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | |||||||
| chr22:39814295 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+6697_832+6698i others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | |||||||
| chr22:39814295 | CA | C | 5 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+6697delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814295 | |||||||
| chr22:39814312 | T | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+6681A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814312 | |||||||
| chr22:39814364 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.832+6629C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814364 | |||||||
| chr22:39814428 | C | G | 46 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0050 others(43): Show |
46 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.832+6565G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814428 | |||||||
| chr22:39814438 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.832+6555G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814438 | |||||||
| chr22:39814536 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+6457T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814536 | |||||||
| chr22:39814540 | CTATT | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+6449_832+6452d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39814540 | |||||||
| chr22:39815015 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0130 others(9): Show |
13 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.832+5978C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815015 | |||||||
| chr22:39815304 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+5689C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815304 | |||||||
| chr22:39815420 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.832+5573C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815420 | |||||||
| chr22:39815554 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0145 |
2 | NA19082.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.832+5439A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815554 | |||||||
| chr22:39815602 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832+5391G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815602 | |||||||
| chr22:39815638 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.832+5355G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815638 | |||||||
| chr22:39815733 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+5260C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815733 | |||||||
| chr22:39815804 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.832+5189C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39815804 | |||||||
| chr22:39816009 | G | A | 30 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(27): Show |
30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.832+4984C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816009 | |||||||
| chr22:39816041 | G | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+4952C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816041 | |||||||
| chr22:39816354 | C | T | 31 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(28): Show |
31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.832+4639G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816354 | |||||||
| chr22:39816666 | C | T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.832+4327G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816666 | |||||||
| chr22:39816678 | A | T | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.832+4315T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816678 | |||||||
| chr22:39816762 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.832+4231T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39816762 | |||||||
| chr22:39817238 | A | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.832+3755T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817238 | |||||||
| chr22:39817275 | A | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(16): Show |
20 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.832+3718T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817275 | |||||||
| chr22:39817590 | C | T | 8 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0066 others(5): Show |
8 | HG00438.hp2 HG02083.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.832+3403G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817590 | |||||||
| chr22:39817617 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.832+3376G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817617 | |||||||
| chr22:39817795 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
17 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.832+3198G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817795 | |||||||
| chr22:39817832 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+3161A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817832 | |||||||
| chr22:39817919 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.832+3074A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39817919 | |||||||
| chr22:39818084 | C | T | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+2909G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818084 | |||||||
| chr22:39818189 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.832+2804T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818189 | |||||||
| chr22:39818261 | C | T | 9 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0084 others(6): Show |
9 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+2732G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818261 | |||||||
| chr22:39818419 | G | A | 9 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0084 others(6): Show |
9 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.832+2574C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818419 | |||||||
| chr22:39818561 | G | A | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.832+2432C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818561 | |||||||
| chr22:39818588 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.832+2405C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818588 | |||||||
| chr22:39818634 | T | C | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0199 |
3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+2359A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39818634 | |||||||
| chr22:39819233 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+1760G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819233 | |||||||
| chr22:39819309 | G | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0199 |
3 | HG02630.hp1 HG02896.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.832+1684C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819309 | |||||||
| chr22:39819380 | AC | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(30): Show |
33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.832+1612delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819380 | |||||||
| chr22:39819381 | C | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0006g0214 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.832+1612G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819381 | |||||||
| chr22:39819723 | A | G | 33 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(30): Show |
33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.832+1270T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819723 | |||||||
| chr22:39819760 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0007g0025 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.832+1233C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819760 | |||||||
| chr22:39819923 | A | G | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.832+1070T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819923 | |||||||
| chr22:39819991 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(81): Show |
86 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.832+1002A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39819991 | |||||||
| chr22:39820313 | T | C | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.832+680A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820313 | |||||||
| chr22:39820388 | T | A | 1 | a0001c0001t0001g0177 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.832+605A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820388 | |||||||
| chr22:39820547 | T | C | 3 | a0001c0001t0001g0200 a0001c0003t0001g0006 a0004c0006t0001g0198 |
3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.832+446A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820547 | |||||||
| chr22:39820604 | C | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.832+389G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 5/6 | chr22 | 39820604 | |||||||
| chr22:39821310 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.712-197G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39821310 | |||||||
| chr22:39821931 | C | T | 31 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(28): Show |
31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.712-818G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39821931 | |||||||
| chr22:39821958 | C | G | 1 | a0001c0001t0002g0162 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.712-845G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39821958 | |||||||
| chr22:39822011 | C | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(27): Show |
30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.712-898G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822011 | |||||||
| chr22:39822104 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.712-991T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822104 | |||||||
| chr22:39822108 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.712-995G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822108 | |||||||
| chr22:39822192 | TC | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0021 others(33): Show |
37 | HG00597.hp2 HG00673.hp1 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.712-1080delG | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822192 | |||||||
| chr22:39822631 | C | T | 31 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(28): Show |
31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.712-1518G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39822631 | |||||||
| chr22:39823378 | T | G | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.712-2265A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823378 | |||||||
| chr22:39823405 | C | T | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.712-2292G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823405 | |||||||
| chr22:39823450 | T | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.712-2337A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823450 | |||||||
| chr22:39823788 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.712-2675A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823788 | |||||||
| chr22:39823798 | A | C | 1 | a0001c0001t0001g0053 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.712-2685T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823798 | |||||||
| chr22:39823882 | A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.712-2769T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823882 | |||||||
| chr22:39823923 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.712-2810G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39823923 | |||||||
| chr22:39824128 | G | A | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-3015C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824128 | |||||||
| chr22:39824201 | C | CT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(137): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.712-3089dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824201 | |||||||
| chr22:39824201 | C | CTT | 29 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0038 others(26): Show |
29 | HG00438.hp1 HG00621.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.712-3090_712-3089d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824201 | |||||||
| chr22:39824201 | CT | C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0001g0042 others(2): Show |
5 | HG01943.hp2 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-3089delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824201 | |||||||
| chr22:39824279 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.712-3166C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824279 | |||||||
| chr22:39824354 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0061 |
3 | NA18942.hp1 NA18955.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.712-3241G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824354 | |||||||
| chr22:39824357 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.712-3244T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824357 | |||||||
| chr22:39824456 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.712-3343C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824456 | |||||||
| chr22:39824739 | T | C | 33 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(30): Show |
33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.712-3626A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824739 | |||||||
| chr22:39824935 | T | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-3822A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824935 | |||||||
| chr22:39824994 | GAAT | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0130 |
2 | NA18984.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.712-3884_712-3882d others(5): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39824994 | |||||||
| chr22:39825112 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.712-3999G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825112 | |||||||
| chr22:39825366 | T | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.712-4253A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825366 | |||||||
| chr22:39825475 | C | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.712-4362G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825475 | |||||||
| chr22:39825708 | T | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.712-4595A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825708 | |||||||
| chr22:39825995 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.712-4882G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39825995 | |||||||
| chr22:39826126 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0004t0001g0094 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-5013C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826126 | |||||||
| chr22:39826196 | T | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712-5083A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826196 | |||||||
| chr22:39826244 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.712-5131G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826244 | |||||||
| chr22:39826307 | G | T | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-5194C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826307 | |||||||
| chr22:39826308 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0036 others(2): Show |
5 | HG02572.hp1 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-5195C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826308 | |||||||
| chr22:39826500 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.712-5387C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826500 | |||||||
| chr22:39826905 | CTCTG | C | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-5796_712-5793d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39826905 | |||||||
| chr22:39827014 | A | AT | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0122 others(3): Show |
6 | HG02135.hp1 HG02148.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-5902dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827014 | |||||||
| chr22:39827084 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0178 |
2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.712-5971G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827084 | |||||||
| chr22:39827117 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.712-6004C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827117 | |||||||
| chr22:39827205 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0006g0214 |
2 | HG02886.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.712-6092G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827205 | |||||||
| chr22:39827250 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0001g0066 a0001c0001t0001g0105 |
3 | HG02083.hp2 NA18947.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.712-6137G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827250 | |||||||
| chr22:39827262 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712-6149C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39827262 | |||||||
| chr22:39828021 | G | A | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-6908C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828021 | |||||||
| chr22:39828162 | A | G | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.712-7049T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828162 | |||||||
| chr22:39828743 | T | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0139 a0001c0001t0001g0146 |
3 | HG00597.hp2 HG00673.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.711+7097A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828743 | |||||||
| chr22:39828839 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.711+7001T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828839 | |||||||
| chr22:39828919 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.711+6921C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828919 | |||||||
| chr22:39828998 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.711+6842C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39828998 | |||||||
| chr22:39829010 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.711+6830C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829010 | |||||||
| chr22:39829082 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG00597.hp1 HG00673.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.711+6758T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829082 | |||||||
| chr22:39829142 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0104 a0001c0001t0001g0110 others(1): Show |
4 | HG00621.hp2 HG02027.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+6698G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829142 | |||||||
| chr22:39829267 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.711+6573C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829267 | |||||||
| chr22:39829379 | C | CA | 9 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01891.hp2 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+6460dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829379 | |||||||
| chr22:39829379 | CA | C | 53 | a0001c0001t0001g0014 a0001c0001t0001g0046 a0001c0001t0001g0051 others(50): Show |
53 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.711+6460delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829379 | |||||||
| chr22:39829648 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.711+6192C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829648 | |||||||
| chr22:39829790 | C | CAATA | 60 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(57): Show |
62 | HG00140.hp1 HG00323.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.711+6046_711+6049d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | |||||||
| chr22:39829790 | C | CAATAAAT others(1): Show |
9 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.711+6042_711+6049d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | |||||||
| chr22:39829790 | C | CAATAAAT others(5): Show |
3 | a0001c0001t0002g0171 a0001c0004t0001g0094 a0005c0009t0001g0154 |
3 | HG02572.hp2 HG02922.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.711+6038_711+6049d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | |||||||
| chr22:39829790 | C | CAATAAAT others(9): Show |
23 | a0001c0001t0001g0009 a0001c0001t0002g0155 a0001c0001t0002g0156 others(20): Show |
23 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.711+6034_711+6049d others(18): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | |||||||
| chr22:39829790 | C | CAATAAAT others(13): Show |
4 | a0001c0001t0002g0166 a0001c0001t0002g0170 a0001c0001t0002g0172 others(1): Show |
4 | HG04115.hp2 NA18988.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+6030_711+6049d others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | |||||||
| chr22:39829790 | C | CAATAAAT others(17): Show |
3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0001c0001t0002g0168 |
3 | NA18998.hp2 NA19002.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.711+6026_711+6049d others(26): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829790 | |||||||
| chr22:39829973 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.711+5867A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39829973 | |||||||
| chr22:39830170 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.711+5670C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830170 | |||||||
| chr22:39830236 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0004t0001g0094 others(1): Show |
4 | HG02258.hp1 HG02572.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+5604G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830236 | |||||||
| chr22:39830357 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.711+5483C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830357 | |||||||
| chr22:39830661 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.711+5179T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830661 | |||||||
| chr22:39830677 | A | T | 1 | a0001c0001t0002g0163 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.711+5163T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830677 | |||||||
| chr22:39830697 | T | C | 38 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.711+5143A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830697 | |||||||
| chr22:39830786 | C | T | 31 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(28): Show |
31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.711+5054G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39830786 | |||||||
| chr22:39831199 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.711+4641T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831199 | |||||||
| chr22:39831216 | A | G | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.711+4624T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831216 | |||||||
| chr22:39831261 | C | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.711+4579G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831261 | |||||||
| chr22:39831271 | A | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+4569T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831271 | |||||||
| chr22:39831467 | A | G | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.711+4373T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831467 | |||||||
| chr22:39831537 | T | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.711+4303A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831537 | |||||||
| chr22:39831553 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.711+4287C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831553 | |||||||
| chr22:39831699 | G | A | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.711+4141C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831699 | |||||||
| chr22:39831855 | T | C | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.711+3985A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39831855 | |||||||
| chr22:39832226 | G | A | 1 | a0001c0008t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.711+3614C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832226 | |||||||
| chr22:39832360 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.711+3480C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832360 | |||||||
| chr22:39832369 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.711+3471G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832369 | |||||||
| chr22:39832846 | G | A | 27 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.711+2994C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832846 | |||||||
| chr22:39832889 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.711+2951T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39832889 | |||||||
| chr22:39833230 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.711+2610G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833230 | |||||||
| chr22:39833275 | C | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0082 others(1): Show |
4 | HG02258.hp2 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+2565G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833275 | |||||||
| chr22:39833430 | G | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
17 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(14): Show |
intron_variant | MODIFIER | c.711+2410C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833430 | |||||||
| chr22:39833589 | A | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(51): Show |
55 | HG00597.hp2 HG00642.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.711+2251T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833589 | |||||||
| chr22:39833670 | A | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.711+2170T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833670 | |||||||
| chr22:39833745 | A | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.711+2095T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833745 | |||||||
| chr22:39833769 | A | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.711+2071T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833769 | |||||||
| chr22:39833941 | C | CA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0016 others(96): Show |
100 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.711+1898dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | |||||||
| chr22:39833941 | C | CAA | 8 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0082 others(5): Show |
8 | HG00735.hp2 HG00738.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+1897_711+1898d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | |||||||
| chr22:39833941 | CAAAA | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0132 others(6): Show |
10 | HG00597.hp2 HG00673.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+1895_711+1898d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | |||||||
| chr22:39833941 | CAAAAA | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0055 a0001c0001t0001g0058 others(2): Show |
5 | HG00639.hp1 HG00639.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+1894_711+1898d others(7): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | |||||||
| chr22:39833941 | CAAAAAA | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(60): Show |
64 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.711+1893_711+1898d others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39833941 | |||||||
| chr22:39834151 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.711+1689A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39834151 | |||||||
| chr22:39834902 | T | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.711+938A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39834902 | |||||||
| chr22:39835057 | A | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.711+783T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835057 | |||||||
| chr22:39835645 | A | T | 1 | a0001c0001t0004g0005 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.711+195T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835645 | |||||||
| chr22:39835653 | C | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.711+187G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835653 | |||||||
| chr22:39835834 | A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | splice_region_variant&intron_variant | LOW | c.711+6T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 4/6 | chr22 | 39835834 | |||||||
| chr22:39836413 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-455A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39836413 | |||||||
| chr22:39836668 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.593-710T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39836668 | |||||||
| chr22:39836711 | G | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-753C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39836711 | |||||||
| chr22:39837306 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.593-1348C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39837306 | |||||||
| chr22:39837589 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.593-1631C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39837589 | |||||||
| chr22:39838000 | A | G | 5 | a0001c0001t0001g0056 a0001c0001t0001g0068 a0001c0001t0001g0069 others(2): Show |
5 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-2042T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838000 | |||||||
| chr22:39838091 | T | C | 34 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-2133A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838091 | |||||||
| chr22:39838199 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-2241A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838199 | |||||||
| chr22:39838219 | G | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-2261C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39838219 | |||||||
| chr22:39839279 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0178 |
2 | HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.593-3321T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839279 | |||||||
| chr22:39839408 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.593-3450A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839408 | |||||||
| chr22:39839434 | C | T | 1 | a0005c0009t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.593-3476G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839434 | |||||||
| chr22:39839682 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.593-3724G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839682 | |||||||
| chr22:39839831 | T | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.593-3873A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39839831 | |||||||
| chr22:39840030 | T | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-4072A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840030 | |||||||
| chr22:39840593 | AACAG | A | 9 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(6): Show |
9 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-4639_593-4636d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840593 | |||||||
| chr22:39840759 | CT | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.593-4802delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840759 | |||||||
| chr22:39840777 | C | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(27): Show |
30 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.593-4819G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840777 | |||||||
| chr22:39840877 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.593-4919G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840877 | |||||||
| chr22:39840961 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.593-5003G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39840961 | |||||||
| chr22:39841030 | G | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-5072C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841030 | |||||||
| chr22:39841134 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.593-5176A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841134 | |||||||
| chr22:39841193 | A | G | 34 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-5235T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841193 | |||||||
| chr22:39841566 | T | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-5608A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841566 | |||||||
| chr22:39841605 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.593-5647G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841605 | |||||||
| chr22:39841624 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.593-5666C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841624 | |||||||
| chr22:39841778 | G | T | 4 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(1): Show |
4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-5820C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841778 | |||||||
| chr22:39841782 | C | A | 4 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0210 others(1): Show |
4 | HG00642.hp1 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-5824G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841782 | |||||||
| chr22:39841832 | C | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-5874G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841832 | |||||||
| chr22:39841907 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0107 |
2 | NA18982.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.593-5949G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39841907 | |||||||
| chr22:39842197 | A | T | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-6239T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842197 | |||||||
| chr22:39842394 | C | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.593-6436G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842394 | |||||||
| chr22:39842397 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.593-6439A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842397 | |||||||
| chr22:39842524 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-6566G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842524 | |||||||
| chr22:39842536 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-6578C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842536 | |||||||
| chr22:39842799 | G | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-6841C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39842799 | |||||||
| chr22:39843053 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0122 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.593-7095T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843053 | |||||||
| chr22:39843100 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-7142G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843100 | |||||||
| chr22:39843174 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.593-7216C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843174 | |||||||
| chr22:39843354 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0062 |
2 | NA18984.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.593-7396C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843354 | |||||||
| chr22:39843362 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-7404T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843362 | |||||||
| chr22:39843402 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-7444A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843402 | |||||||
| chr22:39843466 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.593-7508C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843466 | |||||||
| chr22:39843478 | T | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-7520A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843478 | |||||||
| chr22:39843567 | A | G | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-7609T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843567 | |||||||
| chr22:39843606 | A | G | 52 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0050 others(49): Show |
52 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.593-7648T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39843606 | |||||||
| chr22:39844025 | G | GTGTACAA others(43): Show |
1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.593-8117_593-8068d others(52): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844025 | |||||||
| chr22:39844025 | GTGTACAA others(43): Show |
G | 1 | a0001c0001t0001g0134 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.593-8117_593-8068d others(52): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844025 | |||||||
| chr22:39844196 | G | C | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.593-8238C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844196 | |||||||
| chr22:39844494 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.593-8536T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844494 | |||||||
| chr22:39844521 | A | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.593-8563T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844521 | |||||||
| chr22:39844528 | T | C | 34 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-8570A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844528 | |||||||
| chr22:39844569 | T | C | 1 | a0001c0001t0001g0050 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.593-8611A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844569 | |||||||
| chr22:39844572 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.593-8614A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844572 | |||||||
| chr22:39844700 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-8742A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844700 | |||||||
| chr22:39844712 | G | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.593-8754C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844712 | |||||||
| chr22:39844798 | G | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(33): Show |
36 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.593-8840C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844798 | |||||||
| chr22:39844911 | C | G | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.593-8953G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39844911 | |||||||
| chr22:39845039 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG00597.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.593-9081A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845039 | |||||||
| chr22:39845074 | T | TA | 6 | a0001c0001t0002g0166 a0001c0001t0008g0015 a0001c0004t0001g0094 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.593-9117dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845074 | |||||||
| chr22:39845180 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.593-9222T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845180 | |||||||
| chr22:39845208 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.593-9250A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845208 | |||||||
| chr22:39845283 | C | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.593-9325G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845283 | |||||||
| chr22:39845473 | C | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-9515G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845473 | |||||||
| chr22:39845622 | T | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-9664A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845622 | |||||||
| chr22:39845657 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(82): Show |
87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.593-9699C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845657 | |||||||
| chr22:39845907 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.593-9949A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39845907 | |||||||
| chr22:39846005 | C | A | 1 | a0001c0001t0002g0207 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.593-10047G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846005 | |||||||
| chr22:39846063 | C | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0110 a0001c0001t0001g0112 |
3 | HG00621.hp2 HG02027.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.593-10105G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846063 | |||||||
| chr22:39846378 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.593-10420A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846378 | |||||||
| chr22:39846507 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.593-10549C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846507 | |||||||
| chr22:39846546 | T | C | 35 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(32): Show |
35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.593-10588A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846546 | |||||||
| chr22:39846860 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.593-10902C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39846860 | |||||||
| chr22:39847084 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.593-11126C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847084 | |||||||
| chr22:39847140 | A | G | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.593-11182T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847140 | |||||||
| chr22:39847143 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.593-11185C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847143 | |||||||
| chr22:39847382 | A | AG | 7 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0048 others(4): Show |
7 | HG01192.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-11425dupC | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847382 | |||||||
| chr22:39847466 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.593-11508G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847466 | |||||||
| chr22:39847708 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0122 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.593-11750C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847708 | |||||||
| chr22:39847890 | G | C | 34 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.593-11932C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847890 | |||||||
| chr22:39847965 | G | A | 3 | a0001c0001t0001g0200 a0001c0003t0001g0006 a0004c0006t0001g0198 |
3 | HG02145.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.593-12007C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39847965 | |||||||
| chr22:39848008 | C | A | 1 | a0002c0002t0001g0192 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.593-12050G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848008 | |||||||
| chr22:39848277 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.593-12319G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848277 | |||||||
| chr22:39848278 | G | A | 1 | a0001c0004t0001g0095 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.593-12320C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848278 | |||||||
| chr22:39848300 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.593-12342G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848300 | |||||||
| chr22:39848572 | C | T | 1 | a0002c0002t0001g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.593-12614G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848572 | |||||||
| chr22:39848634 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.593-12676A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848634 | |||||||
| chr22:39848879 | C | T | 5 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 others(2): Show |
5 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+12886G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848879 | |||||||
| chr22:39848998 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0182 |
3 | HG02886.hp2 HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.592+12767G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39848998 | |||||||
| chr22:39849418 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.592+12347A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849418 | |||||||
| chr22:39849706 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.592+12059A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849706 | |||||||
| chr22:39849820 | G | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+11945C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849820 | |||||||
| chr22:39849919 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0008g0015 |
2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.592+11846G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39849919 | |||||||
| chr22:39850103 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+11662T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850103 | |||||||
| chr22:39850257 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+11508A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850257 | |||||||
| chr22:39850310 | A | G | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+11455T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850310 | |||||||
| chr22:39850381 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18977.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.592+11384A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850381 | |||||||
| chr22:39850434 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.592+11331A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850434 | |||||||
| chr22:39850674 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.592+11091G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850674 | |||||||
| chr22:39850833 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.592+10932C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850833 | |||||||
| chr22:39850906 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+10859G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39850906 | |||||||
| chr22:39851111 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+10654A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39851111 | |||||||
| chr22:39851895 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+9870C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39851895 | |||||||
| chr22:39852170 | C | CA | 5 | a0001c0001t0001g0131 a0001c0001t0001g0200 a0001c0001t0004g0005 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+9594dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852170 | |||||||
| chr22:39852250 | G | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+9515C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852250 | |||||||
| chr22:39852337 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+9428T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852337 | |||||||
| chr22:39852622 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.592+9143G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852622 | |||||||
| chr22:39852678 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.592+9087A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852678 | |||||||
| chr22:39852980 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.592+8785A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39852980 | |||||||
| chr22:39853368 | T | TA | 13 | a0001c0001t0001g0002 a0001c0001t0001g0074 a0001c0001t0001g0075 others(10): Show |
14 | HG00621.hp1 HG01993.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.592+8396dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853368 | |||||||
| chr22:39853576 | C | A | 3 | a0001c0001t0001g0014 a0001c0001t0006g0214 a0001c0001t0008g0015 |
3 | HG02559.hp1 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.592+8189G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853576 | |||||||
| chr22:39853576 | CTTATTA | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+8183_592+8188d others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853576 | |||||||
| chr22:39853579 | A | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0056 others(1): Show |
4 | HG03490.hp2 HG03492.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+8186T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853579 | |||||||
| chr22:39853635 | G | A | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.592+8130C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853635 | |||||||
| chr22:39853850 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.592+7915G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853850 | |||||||
| chr22:39853978 | G | A | 1 | a0001c0004t0001g0095 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.592+7787C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39853978 | |||||||
| chr22:39854142 | G | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+7623C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854142 | |||||||
| chr22:39854218 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.592+7547T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854218 | |||||||
| chr22:39854320 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.592+7445A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854320 | |||||||
| chr22:39854819 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.592+6946G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854819 | |||||||
| chr22:39854865 | C | G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(32): Show |
35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.592+6900G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39854865 | |||||||
| chr22:39855023 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+6742T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855023 | |||||||
| chr22:39855247 | A | T | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+6518T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855247 | |||||||
| chr22:39855270 | A | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+6495T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855270 | |||||||
| chr22:39855487 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+6278G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855487 | |||||||
| chr22:39855589 | TA | T | 31 | a0001c0001t0001g0009 a0001c0001t0002g0155 a0001c0001t0002g0156 others(28): Show |
31 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.592+6175delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855589 | |||||||
| chr22:39855830 | A | T | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.592+5935T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855830 | |||||||
| chr22:39855914 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | NA18967.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.592+5851T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855914 | |||||||
| chr22:39855990 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.592+5775C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855990 | |||||||
| chr22:39855999 | C | T | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.592+5766G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39855999 | |||||||
| chr22:39856000 | G | A | 2 | a0001c0001t0002g0166 a0001c0001t0004g0005 |
2 | HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.592+5765C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856000 | |||||||
| chr22:39856012 | C | T | 2 | a0001c0001t0001g0056 a0003c0005t0001g0019 |
2 | HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.592+5753G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856012 | |||||||
| chr22:39856215 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0199 others(6): Show |
9 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.592+5550C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856215 | |||||||
| chr22:39856274 | C | CA | 35 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0200 others(32): Show |
35 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.592+5490dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856274 | |||||||
| chr22:39856274 | CA | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0093 others(3): Show |
6 | HG00673.hp2 HG01069.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+5490delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856274 | |||||||
| chr22:39856413 | C | T | 1 | a0001c0001t0002g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.592+5352G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856413 | |||||||
| chr22:39856536 | T | C | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.592+5229A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856536 | |||||||
| chr22:39856560 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.592+5205A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856560 | |||||||
| chr22:39856813 | A | C | 1 | a0001c0001t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.592+4952T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856813 | |||||||
| chr22:39856852 | CA | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0028 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+4912delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856852 | |||||||
| chr22:39856865 | A | G | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+4900T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856865 | |||||||
| chr22:39856867 | AAG | A | 29 | a0001c0001t0001g0045 a0001c0001t0002g0155 a0001c0001t0002g0156 others(26): Show |
29 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.592+4896_592+4897d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856867 | |||||||
| chr22:39856869 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(2): Show |
5 | HG02055.hp1 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+4896C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856869 | |||||||
| chr22:39856873 | G | A | 34 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0155 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.592+4892C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39856873 | |||||||
| chr22:39857150 | G | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.592+4615C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857150 | |||||||
| chr22:39857360 | C | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.592+4405G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857360 | |||||||
| chr22:39857412 | C | T | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0003t0001g0006 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+4353G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857412 | |||||||
| chr22:39857443 | CA | C | 25 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(22): Show |
26 | HG01496.hp1 HG02015.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.592+4321delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857443 | |||||||
| chr22:39857443 | CAA | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0029 others(19): Show |
23 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.592+4320_592+4321d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857443 | |||||||
| chr22:39857471 | A | AAAAT | 5 | a0001c0001t0002g0164 a0001c0001t0002g0171 a0001c0001t0002g0172 others(2): Show |
5 | HG01106.hp2 HG02293.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+4293_592+4294i others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | |||||||
| chr22:39857471 | A | AAAT | 24 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(21): Show |
24 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.592+4293_592+4294i others(5): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | |||||||
| chr22:39857471 | A | AT | 16 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0083 others(13): Show |
17 | HG00642.hp2 HG01106.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.592+4293_592+4294i others(3): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | |||||||
| chr22:39857471 | A | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(118): Show |
123 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.592+4294T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857471 | |||||||
| chr22:39857712 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592+4053T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857712 | |||||||
| chr22:39857911 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.592+3854C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39857911 | |||||||
| chr22:39858034 | T | G | 1 | a0005c0009t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.592+3731A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39858034 | |||||||
| chr22:39859087 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+2678C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859087 | |||||||
| chr22:39859242 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+2523A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859242 | |||||||
| chr22:39859270 | A | G | 1 | a0001c0001t0002g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.592+2495T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859270 | |||||||
| chr22:39859804 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0061 |
2 | NA18942.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.592+1961C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39859804 | |||||||
| chr22:39860144 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.592+1621A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860144 | |||||||
| chr22:39860158 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.592+1607A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860158 | |||||||
| chr22:39860480 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.592+1285G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860480 | |||||||
| chr22:39860481 | G | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(64): Show |
68 | HG00597.hp2 HG00639.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.592+1284C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860481 | |||||||
| chr22:39860660 | C | A | 3 | a0002c0002t0001g0176 a0002c0002t0001g0192 a0002c0002t0001g0195 |
3 | HG00735.hp2 HG01943.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.592+1105G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39860660 | |||||||
| chr22:39861018 | G | T | 1 | a0001c0001t0001g0049 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.592+747C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861018 | |||||||
| chr22:39861054 | T | C | 1 | a0002c0002t0001g0186 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.592+711A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861054 | |||||||
| chr22:39861430 | C | T | 2 | a0002c0002t0001g0180 a0002c0002t0001g0186 |
2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.592+335G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861430 | |||||||
| chr22:39861455 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.592+310C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861455 | |||||||
| chr22:39861535 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.592+230C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861535 | |||||||
| chr22:39861620 | G | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0123 |
3 | HG01168.hp2 HG01169.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.592+145C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 3/6 | chr22 | 39861620 | |||||||
| chr22:39862081 | A | T | 11 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0084 others(8): Show |
11 | HG00738.hp2 HG01106.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-74T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862081 | |||||||
| chr22:39862100 | T | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-93A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862100 | |||||||
| chr22:39862150 | T | C | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.350-143A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862150 | |||||||
| chr22:39862373 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-366G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862373 | |||||||
| chr22:39862411 | G | C | 2 | a0001c0001t0001g0009 a0005c0009t0001g0154 |
2 | HG02055.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.350-404C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862411 | |||||||
| chr22:39862532 | G | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-525C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862532 | |||||||
| chr22:39862546 | C | CA | 17 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(14): Show |
17 | HG02258.hp1 HG02258.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.350-540dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862546 | |||||||
| chr22:39862560 | AAAAG | A | 5 | a0001c0001t0001g0106 a0001c0001t0001g0199 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-557_350-554del others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862560 | |||||||
| chr22:39862563 | AG | A | 26 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0002g0156 others(23): Show |
26 | HG00642.hp1 HG00738.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.350-557delC | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862563 | |||||||
| chr22:39862564 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0002g0155 others(6): Show |
9 | HG01891.hp1 HG02258.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.350-557C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862564 | |||||||
| chr22:39862661 | C | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-654G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862661 | |||||||
| chr22:39862722 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-715A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862722 | |||||||
| chr22:39862770 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.350-763T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862770 | |||||||
| chr22:39862986 | G | A | 1 | a0001c0003t0001g0007 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.350-979C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39862986 | |||||||
| chr22:39863075 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.350-1068T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863075 | |||||||
| chr22:39863316 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-1309T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863316 | |||||||
| chr22:39863531 | A | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0122 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.350-1524T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863531 | |||||||
| chr22:39863798 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0034 |
2 | NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.350-1791C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863798 | |||||||
| chr22:39863856 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0045 others(30): Show |
33 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.350-1849G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863856 | |||||||
| chr22:39863906 | G | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350-1899C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39863906 | |||||||
| chr22:39864017 | T | TA | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0191 |
3 | HG01884.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.350-2011dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864017 | |||||||
| chr22:39864457 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-2450A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864457 | |||||||
| chr22:39864591 | A | G | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-2584T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864591 | |||||||
| chr22:39864627 | T | C | 3 | a0001c0001t0001g0014 a0001c0004t0001g0094 a0001c0004t0001g0095 |
3 | HG02258.hp1 HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.350-2620A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39864627 | |||||||
| chr22:39865271 | C | T | 4 | a0001c0001t0002g0157 a0001c0001t0002g0159 a0001c0001t0002g0160 others(1): Show |
4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-3264G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865271 | |||||||
| chr22:39865414 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.350-3407T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865414 | |||||||
| chr22:39865450 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-3443T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865450 | |||||||
| chr22:39865551 | C | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-3544G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865551 | |||||||
| chr22:39865631 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.350-3624G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39865631 | |||||||
| chr22:39866380 | G | A | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.350-4373C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866380 | |||||||
| chr22:39866477 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(82): Show |
87 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.350-4470T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866477 | |||||||
| chr22:39866502 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.350-4495C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866502 | |||||||
| chr22:39866795 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-4788A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866795 | |||||||
| chr22:39866975 | C | T | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-4968G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39866975 | |||||||
| chr22:39867063 | C | T | 1 | a0001c0003t0001g0008 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.350-5056G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867063 | |||||||
| chr22:39867115 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(17): Show |
21 | HG00438.hp1 HG00621.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.350-5108C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867115 | |||||||
| chr22:39867280 | T | C | 1 | a0005c0009t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.350-5273A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867280 | |||||||
| chr22:39867355 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-5348A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867355 | |||||||
| chr22:39867499 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.350-5492C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867499 | |||||||
| chr22:39867525 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-5518G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867525 | |||||||
| chr22:39867642 | C | T | 8 | a0001c0001t0002g0156 a0001c0001t0002g0163 a0001c0001t0002g0164 others(5): Show |
8 | NA18988.hp2 NA18998.hp2 NA19002.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-5635G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867642 | |||||||
| chr22:39867993 | C | T | 19 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0054 others(16): Show |
19 | HG00438.hp2 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.350-5986G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39867993 | |||||||
| chr22:39868281 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.350-6274A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868281 | |||||||
| chr22:39868329 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.350-6322G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868329 | |||||||
| chr22:39868350 | T | TA | 5 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0151 others(2): Show |
5 | HG00642.hp2 HG01168.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-6344dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868350 | |||||||
| chr22:39868350 | T | TAA | 31 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(28): Show |
31 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.350-6345_350-6344d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868350 | |||||||
| chr22:39868350 | TA | T | 13 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0043 others(10): Show |
13 | HG02055.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-6344delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868350 | |||||||
| chr22:39868547 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
89 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.350-6540G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868547 | |||||||
| chr22:39868580 | G | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.350-6573C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39868580 | |||||||
| chr22:39869098 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.350-7091C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869098 | |||||||
| chr22:39869121 | T | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0061 |
3 | NA18942.hp1 NA18955.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.350-7114A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869121 | |||||||
| chr22:39869246 | G | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-7239C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869246 | |||||||
| chr22:39869586 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-7579C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869586 | |||||||
| chr22:39869637 | TA | T | 9 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0052 others(6): Show |
9 | HG01943.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-7631delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869637 | |||||||
| chr22:39869650 | A | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350-7643T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869650 | |||||||
| chr22:39869910 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.350-7903T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869910 | |||||||
| chr22:39869983 | C | CTTTA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.350-7980_350-7977d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | |||||||
| chr22:39869983 | C | CTTTATTT others(1): Show |
19 | a0001c0001t0001g0033 a0001c0001t0001g0036 a0001c0001t0001g0038 others(16): Show |
19 | HG00738.hp2 HG01106.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.350-7984_350-7977d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | |||||||
| chr22:39869983 | C | CTTTATTT others(5): Show |
8 | a0001c0001t0001g0026 a0001c0001t0001g0073 a0001c0001t0001g0078 others(5): Show |
8 | HG00735.hp1 HG01081.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-7988_350-7977d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | |||||||
| chr22:39869983 | CTTTA | C | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-7980_350-7977d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869983 | |||||||
| chr22:39869998 | T | TATTTATT others(1): Show |
15 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.350-7992_350-7991i others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39869998 | |||||||
| chr22:39870121 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350-8114T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870121 | |||||||
| chr22:39870268 | CAA | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0031 others(1): Show |
5 | HG02055.hp2 HG03139.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-8263_350-8262d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870268 | |||||||
| chr22:39870368 | A | G | 2 | a0002c0002t0001g0193 a0002c0002t0001g0194 |
2 | HG00738.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.350-8361T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870368 | |||||||
| chr22:39870457 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.350-8450T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870457 | |||||||
| chr22:39870639 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.350-8632A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39870639 | |||||||
| chr22:39871172 | A | AAAAT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(44): Show |
49 | HG00621.hp1 HG00642.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.350-9169_350-9166d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | |||||||
| chr22:39871172 | A | AAAATAAA others(1): Show |
18 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0036 others(15): Show |
19 | HG01257.hp1 HG01993.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.350-9173_350-9166d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | |||||||
| chr22:39871172 | A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02027.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.350-9177_350-9166d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | |||||||
| chr22:39871172 | AAAAT | A | 38 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0049 others(35): Show |
38 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.350-9169_350-9166d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | |||||||
| chr22:39871172 | AAAATAAA others(1): Show |
A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0063 others(5): Show |
8 | HG00438.hp2 HG01891.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-9173_350-9166d others(10): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | |||||||
| chr22:39871172 | AAAATAAA others(5): Show |
A | 4 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0003t0001g0006 others(1): Show |
4 | HG02145.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-9177_350-9166d others(14): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | |||||||
| chr22:39871172 | AAAATAAA others(13): Show |
A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-9185_350-9166d others(22): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871172 | |||||||
| chr22:39871337 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.350-9330G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871337 | |||||||
| chr22:39871471 | G | A | 1 | a0001c0001t0001g0003 | 2 | NA18979.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.350-9464C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871471 | |||||||
| chr22:39871839 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
2 | HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.350-9832T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39871839 | |||||||
| chr22:39872283 | T | C | 2 | a0001c0003t0001g0007 a0001c0003t0001g0008 |
2 | HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.350-10276A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872283 | |||||||
| chr22:39872813 | A | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0020 others(38): Show |
41 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.350-10806T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872813 | |||||||
| chr22:39872850 | C | CT | 5 | a0001c0001t0001g0049 a0001c0001t0001g0082 a0001c0001t0001g0132 others(2): Show |
5 | HG04199.hp2 NA18947.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-10844dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872850 | |||||||
| chr22:39872852 | T | A | 1 | a0001c0001t0001g0083 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.350-10845A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872852 | |||||||
| chr22:39872994 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.350-10987A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39872994 | |||||||
| chr22:39873434 | G | T | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-11427C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39873434 | |||||||
| chr22:39874005 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.350-11998G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874005 | |||||||
| chr22:39874023 | A | G | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-12016T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874023 | |||||||
| chr22:39874429 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.350-12422G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874429 | |||||||
| chr22:39874463 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.350-12456G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874463 | |||||||
| chr22:39874609 | CTATAA | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.350-12607_350-1260 others(9): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874609 | |||||||
| chr22:39874724 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+12676A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874724 | |||||||
| chr22:39874924 | A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+12476T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39874924 | |||||||
| chr22:39875310 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+12090C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875310 | |||||||
| chr22:39875492 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.349+11908C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875492 | |||||||
| chr22:39875610 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
104 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.349+11790G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875610 | |||||||
| chr22:39875686 | C | T | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.349+11714G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875686 | |||||||
| chr22:39875727 | T | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0130 a0001c0001t0001g0143 |
4 | NA18979.hp2 NA18984.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+11673A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875727 | |||||||
| chr22:39875818 | A | G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(32): Show |
35 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.349+11582T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875818 | |||||||
| chr22:39875836 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.349+11564C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39875836 | |||||||
| chr22:39876138 | C | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG00323.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.349+11262G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876138 | |||||||
| chr22:39876455 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+10945C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876455 | |||||||
| chr22:39876514 | T | TA | 7 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(4): Show |
7 | HG02145.hp2 HG03017.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+10885dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876514 | |||||||
| chr22:39876514 | TA | T | 9 | a0001c0001t0001g0049 a0001c0001t0001g0053 a0001c0001t0001g0127 others(6): Show |
9 | HG00323.hp1 HG01884.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.349+10885delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876514 | |||||||
| chr22:39876530 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0005c0009t0001g0154 |
3 | HG02896.hp2 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.349+10870T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39876530 | |||||||
| chr22:39877025 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.349+10375T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877025 | |||||||
| chr22:39877137 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.349+10263T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877137 | |||||||
| chr22:39877239 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.349+10161T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877239 | |||||||
| chr22:39877366 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.349+10034G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877366 | |||||||
| chr22:39877544 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+9856C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877544 | |||||||
| chr22:39877987 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.349+9413C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39877987 | |||||||
| chr22:39878203 | G | C | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349+9197C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878203 | |||||||
| chr22:39878444 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.349+8956G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878444 | |||||||
| chr22:39878486 | T | TA | 11 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+8913_349+8914i others(3): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878486 | |||||||
| chr22:39878495 | CA | C | 6 | a0001c0001t0001g0055 a0001c0001t0001g0099 a0001c0001t0001g0101 others(3): Show |
6 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+8904delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878495 | |||||||
| chr22:39878799 | A | G | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+8601T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878799 | |||||||
| chr22:39878916 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.349+8484A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39878916 | |||||||
| chr22:39879156 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.349+8244C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879156 | |||||||
| chr22:39879185 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0023 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+8215C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879185 | |||||||
| chr22:39879378 | G | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+8022C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879378 | |||||||
| chr22:39879462 | C | CA | 65 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0023 others(62): Show |
65 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.349+7937dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879462 | |||||||
| chr22:39879462 | C | CAA | 7 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0044 others(4): Show |
7 | HG01257.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+7936_349+7937d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879462 | |||||||
| chr22:39879462 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.349+7924_349+7937d others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879462 | |||||||
| chr22:39879673 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.349+7727C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879673 | |||||||
| chr22:39879687 | T | C | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+7713A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879687 | |||||||
| chr22:39879694 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.349+7706C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879694 | |||||||
| chr22:39879712 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.349+7688A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879712 | |||||||
| chr22:39879713 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.349+7687A>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879713 | |||||||
| chr22:39879869 | C | T | 7 | a0001c0001t0001g0078 a0001c0001t0001g0084 a0001c0001t0001g0085 others(4): Show |
7 | HG01123.hp1 HG01928.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+7531G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879869 | |||||||
| chr22:39879944 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349+7456C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39879944 | |||||||
| chr22:39880504 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.349+6896C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39880504 | |||||||
| chr22:39881096 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.349+6304C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39881096 | |||||||
| chr22:39881230 | T | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0048 others(14): Show |
18 | HG00621.hp1 HG01928.hp2 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+6170A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39881230 | |||||||
| chr22:39881244 | A | C | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.349+6156T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39881244 | |||||||
| chr22:39882002 | G | A | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+5398C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882002 | |||||||
| chr22:39882094 | A | G | 27 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+5306T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882094 | |||||||
| chr22:39882313 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0005c0009t0001g0154 |
3 | HG02055.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.349+5087C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882313 | |||||||
| chr22:39882336 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.349+5064T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882336 | |||||||
| chr22:39882389 | C | T | 41 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(38): Show |
41 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.349+5011G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882389 | |||||||
| chr22:39882828 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0007g0025 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.349+4572G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882828 | |||||||
| chr22:39882945 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.349+4455T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39882945 | |||||||
| chr22:39883003 | C | CA | 8 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0001g0145 others(5): Show |
8 | HG00597.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.349+4396dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883003 | |||||||
| chr22:39883003 | CA | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(40): Show |
44 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.349+4396delT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883003 | |||||||
| chr22:39883088 | A | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+4312T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883088 | |||||||
| chr22:39883526 | T | C | 39 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(36): Show |
39 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.349+3874A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883526 | |||||||
| chr22:39883587 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.349+3813A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883587 | |||||||
| chr22:39883617 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.349+3783C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883617 | |||||||
| chr22:39883790 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.349+3610C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883790 | |||||||
| chr22:39883819 | A | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(1): Show |
4 | HG02083.hp1 NA18944.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+3581T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883819 | |||||||
| chr22:39883855 | C | CA | 37 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(34): Show |
37 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.349+3544dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883855 | |||||||
| chr22:39883855 | C | CAA | 26 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(23): Show |
27 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+3543_349+3544d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39883855 | |||||||
| chr22:39884029 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+3371C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884029 | |||||||
| chr22:39884059 | AAAAG | A | 8 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0199 others(5): Show |
8 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.349+3337_349+3340d others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884059 | |||||||
| chr22:39884087 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.349+3313A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884087 | |||||||
| chr22:39884372 | G | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.349+3028C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884372 | |||||||
| chr22:39884380 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.349+3020T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884380 | |||||||
| chr22:39884381 | T | C | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.349+3019A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884381 | |||||||
| chr22:39884551 | G | GA | 27 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0158 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.349+2848dupT | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39884551 | |||||||
| chr22:39885050 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0034 |
2 | NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.349+2350T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885050 | |||||||
| chr22:39885167 | A | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.349+2233T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885167 | |||||||
| chr22:39885203 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0016 others(59): Show |
64 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.349+2197T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885203 | |||||||
| chr22:39885301 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG01069.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.349+2099T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885301 | |||||||
| chr22:39885363 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.349+2037G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885363 | |||||||
| chr22:39885446 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349+1954A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885446 | |||||||
| chr22:39885671 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+1729A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885671 | |||||||
| chr22:39885691 | C | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(37): Show |
40 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.349+1709G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39885691 | |||||||
| chr22:39886058 | GT | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(37): Show |
40 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.349+1341delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886058 | |||||||
| chr22:39886070 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+1330T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886070 | |||||||
| chr22:39886095 | T | C | 5 | a0001c0001t0001g0190 a0001c0001t0003g0004 a0001c0003t0001g0006 others(2): Show |
5 | HG02622.hp2 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1305A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886095 | |||||||
| chr22:39886292 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.349+1108T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886292 | |||||||
| chr22:39886667 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.349+733A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886667 | |||||||
| chr22:39886680 | AGAGAGGA others(6): Show |
A | 1 | a0001c0001t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.349+707_349+719del others(13): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39886680 | |||||||
| chr22:39887181 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.349+219A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 2/6 | chr22 | 39887181 | |||||||
| chr22:39888194 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-155-291C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888194 | |||||||
| chr22:39888260 | C | CT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
19 | HG00621.hp1 HG01928.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.-155-358dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | |||||||
| chr22:39888260 | CT | C | 76 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(73): Show |
76 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.-155-358delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | |||||||
| chr22:39888260 | CTT | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0052 a0001c0001t0001g0122 others(8): Show |
11 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-155-359_-155-358d others(4): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | |||||||
| chr22:39888260 | CTTTTTTT | C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(2): Show |
5 | HG00735.hp1 HG01069.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-364_-155-358d others(9): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | |||||||
| chr22:39888260 | CTTTTTTT others(3): Show |
C | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-155-367_-155-358d others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888260 | |||||||
| chr22:39888264 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(1): Show |
4 | HG00140.hp1 HG01070.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-361A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888264 | |||||||
| chr22:39888516 | C | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0201 others(2): Show |
5 | HG00639.hp2 HG01496.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-155-613G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888516 | |||||||
| chr22:39888519 | C | A | 1 | a0001c0001t0001g0150 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-155-616G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888519 | |||||||
| chr22:39888535 | A | C | 34 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0052 others(31): Show |
34 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-155-632T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888535 | |||||||
| chr22:39888722 | G | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-155-819C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888722 | |||||||
| chr22:39888865 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-962A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888865 | |||||||
| chr22:39888866 | C | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0095 |
2 | HG02258.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-155-963G>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39888866 | |||||||
| chr22:39889670 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-155-1767T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889670 | |||||||
| chr22:39889734 | T | A | 5 | a0002c0002t0001g0176 a0002c0002t0001g0192 a0002c0002t0001g0193 others(2): Show |
5 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-1831A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889734 | |||||||
| chr22:39889735 | A | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0006c0007t0001g0126 |
3 | NA18977.hp1 NA19000.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-155-1832T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889735 | |||||||
| chr22:39889767 | T | C | 1 | a0001c0001t0003g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-155-1864A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889767 | |||||||
| chr22:39889868 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-155-1965C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39889868 | |||||||
| chr22:39890016 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
171 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.-155-2113C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890016 | |||||||
| chr22:39890099 | A | AAAAT | 9 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0049 others(6): Show |
9 | HG01069.hp1 HG02148.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-155-2200_-155-219 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | |||||||
| chr22:39890099 | AAAAT | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(92): Show |
96 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-155-2200_-155-219 others(8): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | |||||||
| chr22:39890099 | AAAATAAA others(1): Show |
A | 46 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(43): Show |
46 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-155-2204_-155-219 others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | |||||||
| chr22:39890099 | AAAATAAA others(5): Show |
A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0175 |
2 | HG02523.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-155-2208_-155-219 others(16): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | |||||||
| chr22:39890099 | AAAATAAA others(9): Show |
A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0196 |
2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-155-2212_-155-219 others(20): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | |||||||
| chr22:39890099 | AAAATAAA others(21): Show |
A | 1 | a0001c0001t0001g0152 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-155-2224_-155-219 others(32): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890099 | |||||||
| chr22:39890143 | TAAATAAA others(1): Show |
T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | NA18967.hp2 NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-155-2248_-155-224 others(12): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890143 | |||||||
| chr22:39890266 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
36 | HG00438.hp1 HG00597.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.-155-2363C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890266 | |||||||
| chr22:39890363 | GT | G | 8 | a0001c0001t0001g0153 a0001c0001t0001g0197 a0001c0001t0001g0199 others(5): Show |
8 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-155-2461delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890363 | |||||||
| chr22:39890381 | CT | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0005c0009t0001g0154 |
3 | HG02055.hp1 HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-155-2479delA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890381 | |||||||
| chr22:39890751 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(19): Show |
23 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.-155-2848G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39890751 | |||||||
| chr22:39891366 | A | G | 1 | a0002c0002t0001g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-156+2329T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891366 | |||||||
| chr22:39891475 | C | CT | 11 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0043 others(8): Show |
11 | HG01891.hp1 HG02145.hp1 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-156+2219dupA | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891475 | |||||||
| chr22:39891475 | C | CTT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
24 | HG00323.hp2 HG01069.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.-156+2218_-156+221 others(6): Show |
ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891475 | |||||||
| chr22:39891620 | A | T | 1 | a0001c0001t0001g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-156+2075T>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891620 | |||||||
| chr22:39891621 | T | A | 28 | a0001c0001t0002g0155 a0001c0001t0002g0156 a0001c0001t0002g0157 others(25): Show |
28 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-156+2074A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891621 | |||||||
| chr22:39891645 | G | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | NA19059.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-156+2050C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891645 | |||||||
| chr22:39891808 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-156+1887G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891808 | |||||||
| chr22:39891909 | C | G | 1 | a0003c0005t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-156+1786G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891909 | |||||||
| chr22:39891930 | T | A | 3 | a0001c0001t0001g0045 a0002c0002t0001g0180 a0002c0002t0001g0186 |
3 | HG00642.hp2 HG01168.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-156+1765A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891930 | |||||||
| chr22:39891973 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-156+1722T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39891973 | |||||||
| chr22:39892243 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-156+1452T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892243 | |||||||
| chr22:39892381 | T | C | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
45 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.-156+1314A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892381 | |||||||
| chr22:39892614 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-156+1081A>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892614 | |||||||
| chr22:39892648 | C | T | 1 | a0001c0001t0008g0015 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-156+1047G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892648 | |||||||
| chr22:39892668 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1027C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892668 | |||||||
| chr22:39892669 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1026C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892669 | |||||||
| chr22:39892670 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1025C>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892670 | |||||||
| chr22:39892671 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1024T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892671 | |||||||
| chr22:39892675 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1020A>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892675 | |||||||
| chr22:39892676 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-156+1019T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892676 | |||||||
| chr22:39892749 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-156+946C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892749 | |||||||
| chr22:39892826 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 |
3 | HG03017.hp2 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-156+869T>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39892826 | |||||||
| chr22:39893456 | G | A | 1 | a0001c0001t0006g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-156+239C>T | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893456 | |||||||
| chr22:39893507 | A | C | 1 | a0001c0001t0001g0010 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-156+188T>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893507 | |||||||
| chr22:39893588 | C | G | 1 | a0001c0001t0001g0009 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-156+107G>C | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893588 | |||||||
| chr22:39893604 | C | T | 3 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 |
3 | HG02622.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-156+91G>A | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893604 | |||||||
| chr22:39893623 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-156+72C>G | ENTHD1 | ENSG00000176177.10 | transcript | ENST00000325157.7 | protein_coding | 1/6 | chr22 | 39893623 |