Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 164781 |
| ensemblid | ENSG00000123977.10 |
| hgncid | 26383 |
| symbol | DAW1 |
| name | dynein assembly factor with WD repeats 1 |
| refseq_nuc | NM_178821.3 |
| refseq_prot | NP_849143.1 |
| ensembl_nuc | ENST00000309931.3 |
| ensembl_prot | ENSP00000311899.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 227871631 |
| end | 227924344 |
| strand | + |
| ver | v1.2 |
| region | chr2:227871631-227924344 |
| region5000 | chr2:227866631-227929344 |
| regionname0 | DAW1_chr2_227871631_227924344 |
| regionname5000 | DAW1_chr2_227866631_227929344 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 415 | 284 | 54 | 48 | 144 | 8 | 28 | 111 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0002 | 0/0 | 415 | 38 | 15 | 12 | 2 | 4 | 5 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0003 | 0/0 | 415 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0004 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0005 | 0/0 | 415 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0006 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0007 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0008 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| a0009 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | MKLKS others(410): Show |
chr2 | 227866631 | 227929344 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1245 | 251 | 43 | 44 | 130 | 7 | 25 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0001c0003 | 0/0 | 1245 | 31 | 10 | 4 | 14 | 1 | 2 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0001c0012 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0001c0013 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0002c0002 | 0/0 | 1245 | 36 | 15 | 12 | 0 | 4 | 5 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0002c0005 | 0/0 | 1245 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0003c0004 | 0/0 | 1245 | 12 | 12 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0004c0010 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0005c0009 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0006c0008 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0007c0011 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0008c0007 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 | ||
| a0009c0006 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | ATGAA others(1240): Show |
chr2 | 227866631 | 227929344 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1683 | 250 | 43 | 44 | 130 | 7 | 24 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0001c0001t0005 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0001c0003t0001 | 0/0 | 1683 | 10 | 9 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0001c0003t0002 | 0/0 | 1683 | 21 | 1 | 4 | 14 | 1 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0001c0012t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0001c0013t0001 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0002c0002t0001 | 0/0 | 1683 | 35 | 15 | 12 | 0 | 4 | 4 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0002c0002t0004 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0002c0005t0003 | 0/0 | 1683 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0003c0004t0001 | 0/0 | 1683 | 12 | 12 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0004c0010t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0005c0009t0001 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0006c0008t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0007c0011t0001 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0008c0007t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| a0009c0006t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | GCTGT others(1678): Show |
chr2 | 227866631 | 227929344 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0185 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0012t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0001c0013t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0002t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0005t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0002c0005t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0003c0004t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0004c0010t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0005c0009t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0006c0008t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0007c0011t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0008c0007t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| a0009c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0029 | EUR | GBR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | FIN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0031 | EUR | FIN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00438 | hp1 | a0002 | c0005 | t0003 | g0319 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0155 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0166 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0164 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0167 | AMR | PUR | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0149 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0019 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0297 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0198 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02055 | hp2 | a0003 | c0004 | t0001 | g0189 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0181 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CDX | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02258 | hp1 | a0004 | c0010 | t0001 | g0150 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02280 | hp2 | a0003 | c0004 | t0001 | g0191 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0163 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02572 | hp1 | a0003 | c0004 | t0001 | g0307 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02602 | hp1 | a0005 | c0009 | t0001 | g0118 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0159 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02630 | hp1 | a0003 | c0004 | t0001 | g0190 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0306 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02723 | hp2 | a0006 | c0008 | t0001 | g0320 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0180 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0316 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0162 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0197 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0188 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0311 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02897 | hp1 | a0001 | c0003 | t0001 | g0187 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02970 | hp1 | a0001 | c0012 | t0001 | g0072 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0309 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02976 | hp1 | a0007 | c0011 | t0001 | g0312 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0192 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0193 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0194 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0313 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0196 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0308 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03540 | hp2 | a0003 | c0004 | t0001 | g0310 | AFR | GWD | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0034 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04184 | hp2 | a0001 | c0013 | t0001 | g0256 | SAS | BEB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0153 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04204 | hp1 | a0002 | c0002 | t0004 | g0151 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0315 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18945 | hp2 | a0001 | c0003 | t0002 | g0170 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0172 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18956 | hp1 | a0001 | c0003 | t0002 | g0174 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18968 | hp1 | a0008 | c0007 | t0001 | g0288 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18973 | hp2 | a0001 | c0003 | t0002 | g0173 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18979 | hp2 | a0002 | c0005 | t0003 | g0318 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0169 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18998 | hp1 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19068 | hp1 | a0001 | c0003 | t0002 | g0177 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19074 | hp2 | a0009 | c0006 | t0001 | g0282 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19086 | hp1 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20129 | hp1 | a0003 | c0004 | t0001 | g0186 | AFR | ASW | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0314 | AFR | ASW | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0294 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0165 | EUR | TSI | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | GIH | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | MSL | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0185 | REF | REF | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0077 | REF | REF | DAW1_chr2_227866631_227929344 | DAW1 | chr2 | 227866631 | 227929344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227871709 | T | C | 1 | a0009 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.20T>C | p.Leu7Pro | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/13 | 79/1683 | 20/1248 | 7/415 | chr2 | 227871709 | |||
| chr2:227885390 | C | T | 1 | a0003 | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
missense_variant | MODERATE | c.80C>T | p.Thr27Ile | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/13 | 139/1683 | 80/1248 | 27/415 | chr2 | 227885390 | |||
| chr2:227893796 | T | G | 2 | a0008 a0009 |
2 | NA18968.hp1 NA19074.hp2 |
missense_variant&splice_region_variant | MODERATE | c.319T>G | p.Phe107Val | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 378/1683 | 319/1248 | 107/415 | chr2 | 227893796 | |||
| chr2:227893821 | C | T | 1 | a0007 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.344C>T | p.Thr115Met | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 403/1683 | 344/1248 | 115/415 | chr2 | 227893821 | |||
| chr2:227893838 | A | T | 2 | a0002 a0004 |
37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
missense_variant | MODERATE | c.361A>T | p.Thr121Ser | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 420/1683 | 361/1248 | 121/415 | chr2 | 227893838 | |||
| chr2:227893839 | C | T | 1 | a0002 | 2 | HG00438.hp1 NA18979.hp2 |
missense_variant | MODERATE | c.362C>T | p.Thr121Ile | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 421/1683 | 362/1248 | 121/415 | chr2 | 227893839 | |||
| chr2:227898271 | C | T | 1 | a0004 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.530C>T | p.Thr177Ile | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/13 | 589/1683 | 530/1248 | 177/415 | chr2 | 227898271 | |||
| chr2:227906255 | G | A | 1 | a0006 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.775G>A | p.Gly259Ser | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/13 | 834/1683 | 775/1248 | 259/415 | chr2 | 227906255 | |||
| chr2:227923964 | G | A | 1 | a0005 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1244G>A | p.Arg415His | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 1303/1683 | 1244/1248 | 415/415 | chr2 | 227923964 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227871710 | G | T | 1 | a0001c0013 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.21G>T | p.Leu7Leu | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/13 | 80/1683 | 21/1248 | 7/415 | chr2 | 227871710 | |||
| chr2:227889877 | A | G | 1 | a0001c0012 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.135A>G | p.Val45Val | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/13 | 194/1683 | 135/1248 | 45/415 | chr2 | 227889877 | |||
| chr2:227893864 | G | C | 2 | a0001c0003 a0007c0011 |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
synonymous_variant | LOW | c.387G>C | p.Thr129Thr | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/13 | 446/1683 | 387/1248 | 129/415 | chr2 | 227893864 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227871666 | G | C | 1 | a0002c0005t0003 | 2 | HG00438.hp1 NA18979.hp2 |
5_prime_UTR_variant | MODIFIER | c.-24G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/13 | 24 | chr2 | 227871666 | ||||||
| chr2:227924006 | T | C | 1 | a0001c0003t0002 | 21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*38T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 38 | chr2 | 227924006 | ||||||
| chr2:227924085 | A | G | 1 | a0001c0001t0005 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 117 | chr2 | 227924085 | ||||||
| chr2:227924254 | A | G | 1 | a0002c0002t0004 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*286A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 13/13 | 286 | chr2 | 227924254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:227871778 | C | G | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | NA18979.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.40+49C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871778 | |||||||
| chr2:227871811 | A | G | 139 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0195 others(136): Show |
141 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.40+82A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871811 | |||||||
| chr2:227871849 | A | C | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+120A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871849 | |||||||
| chr2:227871892 | C | T | 139 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0195 others(136): Show |
141 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.40+163C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871892 | |||||||
| chr2:227871999 | A | C | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+270A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227871999 | |||||||
| chr2:227872097 | G | C | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+368G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872097 | |||||||
| chr2:227872110 | T | C | 17 | a0001c0001t0001g0032 a0002c0002t0001g0016 a0002c0002t0001g0017 others(14): Show |
17 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.40+381T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872110 | |||||||
| chr2:227872137 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40+408C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872137 | |||||||
| chr2:227872275 | C | CA | 28 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(25): Show |
28 | HG00423.hp2 HG01106.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.40+563dupA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227872275 | ||||||
| chr2:227872290 | AAAG | A | 10 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0003c0004t0001g0186 others(7): Show |
10 | HG02055.hp2 HG02280.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.40+564_40+566delGA others(1): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227872290 | ||||||
| chr2:227872292 | AG | A | 110 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(107): Show |
112 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.40+564delG | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872292 | |||||||
| chr2:227872293 | G | A | 13 | a0001c0001t0001g0195 a0001c0001t0001g0206 a0001c0001t0001g0230 others(10): Show |
13 | HG00323.hp1 HG01123.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+564G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872293 | |||||||
| chr2:227872297 | A | G | 136 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(133): Show |
138 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.40+568A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872297 | |||||||
| chr2:227872400 | G | T | 1 | a0001c0001t0001g0184 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.40+671G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872400 | |||||||
| chr2:227872531 | T | C | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+802T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872531 | |||||||
| chr2:227872584 | C | T | 1 | a0001c0003t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.40+855C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872584 | |||||||
| chr2:227872586 | A | G | 1 | a0002c0002t0001g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.40+857A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872586 | |||||||
| chr2:227872649 | T | C | 1 | a0001c0001t0001g0004 | 2 | NA18939.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.40+920T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872649 | |||||||
| chr2:227872693 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+964C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872693 | |||||||
| chr2:227872713 | C | T | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+984C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872713 | |||||||
| chr2:227872726 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.40+997C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872726 | |||||||
| chr2:227872794 | G | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.40+1065G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872794 | |||||||
| chr2:227872977 | A | G | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+1248A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872977 | |||||||
| chr2:227872979 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.40+1250G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227872979 | |||||||
| chr2:227873200 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+1471C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873200 | |||||||
| chr2:227873250 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.40+1521A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873250 | |||||||
| chr2:227873276 | T | C | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+1547T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873276 | |||||||
| chr2:227873338 | T | C | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(112): Show |
117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.40+1609T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873338 | |||||||
| chr2:227873427 | G | A | 1 | a0001c0001t0005g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.40+1698G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873427 | |||||||
| chr2:227873456 | A | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.40+1727A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873456 | |||||||
| chr2:227873549 | G | A | 1 | a0001c0003t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.40+1820G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873549 | |||||||
| chr2:227873552 | C | A | 114 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(111): Show |
116 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.40+1823C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873552 | |||||||
| chr2:227873585 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+1856C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873585 | |||||||
| chr2:227873598 | G | T | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40+1869G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873598 | |||||||
| chr2:227873618 | T | C | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+1889T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873618 | |||||||
| chr2:227873672 | A | T | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+1943A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873672 | |||||||
| chr2:227873861 | A | G | 2 | a0003c0004t0001g0309 a0003c0004t0001g0310 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.40+2132A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873861 | |||||||
| chr2:227873889 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40+2160C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873889 | |||||||
| chr2:227873967 | C | T | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+2238C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227873967 | |||||||
| chr2:227874007 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+2278G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874007 | |||||||
| chr2:227874016 | G | T | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+2287G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874016 | |||||||
| chr2:227874073 | ATAATTTT others(14): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+2346_40+2366del others(21): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874073 | ||||||
| chr2:227874156 | T | C | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+2427T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874156 | |||||||
| chr2:227874206 | C | T | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+2477C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874206 | |||||||
| chr2:227874244 | A | G | 13 | a0001c0003t0001g0198 a0001c0003t0002g0197 a0003c0004t0001g0189 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+2515A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874244 | |||||||
| chr2:227874284 | A | G | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+2555A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874284 | |||||||
| chr2:227874330 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+2601T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874330 | |||||||
| chr2:227874419 | G | T | 199 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(196): Show |
205 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.40+2690G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874419 | |||||||
| chr2:227874438 | G | A | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+2709G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874438 | |||||||
| chr2:227874457 | A | G | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+2728A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874457 | |||||||
| chr2:227874652 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.40+2923C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874652 | |||||||
| chr2:227874742 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.40+3013A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874742 | |||||||
| chr2:227874758 | C | T | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+3029C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874758 | |||||||
| chr2:227874833 | C | T | 2 | a0001c0001t0001g0302 a0001c0001t0001g0303 |
2 | NA18939.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.40+3104C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874833 | |||||||
| chr2:227874845 | C | T | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG00323.hp1 HG00735.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+3116C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874845 | |||||||
| chr2:227874890 | G | C | 3 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0001c0003t0001g0306 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+3161G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874890 | |||||||
| chr2:227874963 | A | AAAAC | 86 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0062 others(83): Show |
87 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.40+3256_40+3259dup others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | ||||||
| chr2:227874963 | A | AAAACAAA others(1): Show |
37 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(34): Show |
37 | HG00099.hp1 HG00323.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.40+3252_40+3259dup others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | ||||||
| chr2:227874963 | A | AAAACAAA others(5): Show |
35 | a0001c0001t0001g0033 a0001c0001t0001g0175 a0001c0001t0001g0178 others(32): Show |
37 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.40+3248_40+3259dup others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | ||||||
| chr2:227874963 | A | AAAACAAA others(9): Show |
13 | a0001c0003t0001g0153 a0001c0003t0002g0013 a0001c0003t0002g0154 others(10): Show |
15 | HG00438.hp2 HG00642.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+3244_40+3259dup others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874963 | ||||||
| chr2:227874987 | CAGAA | C | 9 | a0001c0001t0001g0281 a0001c0003t0001g0306 a0001c0003t0001g0311 others(6): Show |
9 | HG02717.hp1 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+3260_40+3263del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227874987 | ||||||
| chr2:227874989 | G | A | 130 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(127): Show |
132 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.40+3260G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874989 | |||||||
| chr2:227874991 | A | C | 129 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(126): Show |
131 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.40+3262A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227874991 | |||||||
| chr2:227875067 | G | A | 35 | a0001c0003t0001g0306 a0002c0002t0001g0003 a0002c0002t0001g0012 others(32): Show |
38 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.40+3338G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875067 | |||||||
| chr2:227875069 | A | G | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+3340A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875069 | |||||||
| chr2:227875078 | G | A | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+3349G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875078 | |||||||
| chr2:227875266 | T | C | 22 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0003t0001g0153 others(19): Show |
23 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+3537T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875266 | |||||||
| chr2:227875395 | T | C | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
143 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.40+3666T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875395 | |||||||
| chr2:227875411 | C | A | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.40+3682C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875411 | |||||||
| chr2:227875762 | A | G | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+4033A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227875762 | |||||||
| chr2:227876020 | CT | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0199 others(22): Show |
26 | HG00323.hp1 HG00735.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.40+4304delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227876020 | ||||||
| chr2:227876020 | CTT | C | 117 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0062 others(114): Show |
118 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.40+4303_40+4304del others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227876020 | ||||||
| chr2:227876025 | TTTTTTTT others(50): Show |
T | 1 | a0001c0001t0001g0067 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.40+4299_40+4355del others(57): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227876025 | ||||||
| chr2:227876030 | T | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0201 a0001c0001t0001g0212 others(16): Show |
20 | HG01361.hp1 HG01981.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.40+4301T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876030 | |||||||
| chr2:227876065 | T | C | 11 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0191 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+4336T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876065 | |||||||
| chr2:227876181 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.40+4452A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876181 | |||||||
| chr2:227876186 | A | T | 117 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(114): Show |
119 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.40+4457A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876186 | |||||||
| chr2:227876211 | G | A | 150 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(147): Show |
153 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.40+4482G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876211 | |||||||
| chr2:227876253 | C | A | 1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.40+4524C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876253 | |||||||
| chr2:227876295 | C | A | 1 | a0001c0001t0001g0290 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.40+4566C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876295 | |||||||
| chr2:227876342 | C | T | 1 | a0002c0002t0001g0152 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.40+4613C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876342 | |||||||
| chr2:227876534 | T | A | 117 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(114): Show |
119 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.40+4805T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876534 | |||||||
| chr2:227876565 | A | T | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.40+4836A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876565 | |||||||
| chr2:227876581 | G | C | 14 | a0001c0003t0001g0198 a0001c0003t0002g0197 a0003c0004t0001g0186 others(11): Show |
14 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.40+4852G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876581 | |||||||
| chr2:227876621 | C | G | 1 | a0001c0001t0001g0289 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.40+4892C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876621 | |||||||
| chr2:227876642 | C | T | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.40+4913C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876642 | |||||||
| chr2:227876718 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+4989T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876718 | |||||||
| chr2:227876725 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+4996G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876725 | |||||||
| chr2:227876754 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0145 |
4 | HG02451.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+5025C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876754 | |||||||
| chr2:227876860 | G | T | 1 | a0002c0002t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.40+5131G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227876860 | |||||||
| chr2:227877210 | G | T | 1 | a0001c0001t0001g0279 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.40+5481G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877210 | |||||||
| chr2:227877277 | C | T | 1 | a0002c0002t0004g0151 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.40+5548C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877277 | |||||||
| chr2:227877376 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.40+5647C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877376 | |||||||
| chr2:227877505 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.40+5776T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877505 | |||||||
| chr2:227877506 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.40+5777A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877506 | |||||||
| chr2:227877579 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.40+5850G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877579 | |||||||
| chr2:227877677 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+5948G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877677 | |||||||
| chr2:227877769 | C | G | 1 | a0001c0003t0002g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.40+6040C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877769 | |||||||
| chr2:227877798 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.40+6069G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877798 | |||||||
| chr2:227877809 | C | T | 2 | a0001c0001t0001g0065 a0006c0008t0001g0320 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.40+6080C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877809 | |||||||
| chr2:227877827 | G | C | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+6098G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877827 | |||||||
| chr2:227877854 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.40+6125A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877854 | |||||||
| chr2:227877929 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
264 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.40+6200C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227877929 | |||||||
| chr2:227878073 | T | C | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | NA18979.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.40+6344T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878073 | |||||||
| chr2:227878153 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40+6424A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878153 | |||||||
| chr2:227878554 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.41-6797T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878554 | |||||||
| chr2:227878632 | G | T | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-6719G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878632 | |||||||
| chr2:227878656 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(43): Show |
52 | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.41-6695C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878656 | |||||||
| chr2:227878679 | G | T | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-6672G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878679 | |||||||
| chr2:227878760 | AT | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
264 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.41-6584delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227878760 | ||||||
| chr2:227878809 | ATTTT | A | 140 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(137): Show |
142 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.41-6528_41-6525del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227878809 | ||||||
| chr2:227878827 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41-6524G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878827 | |||||||
| chr2:227878917 | A | G | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.41-6434A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878917 | |||||||
| chr2:227878945 | T | C | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-6406T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227878945 | |||||||
| chr2:227879030 | C | T | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.41-6321C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879030 | |||||||
| chr2:227879051 | A | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-6300A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879051 | |||||||
| chr2:227879202 | A | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-6149A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879202 | |||||||
| chr2:227879207 | G | A | 1 | a0002c0002t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.41-6144G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879207 | |||||||
| chr2:227879344 | T | C | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-6007T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879344 | |||||||
| chr2:227879428 | T | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-5923T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879428 | |||||||
| chr2:227879609 | C | T | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-5742C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879609 | |||||||
| chr2:227879871 | T | G | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-5480T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227879871 | |||||||
| chr2:227880020 | G | A | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.41-5331G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880020 | |||||||
| chr2:227880046 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-5305G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880046 | |||||||
| chr2:227880275 | C | A | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-5076C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880275 | |||||||
| chr2:227880293 | G | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(260): Show |
274 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.41-5058G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880293 | |||||||
| chr2:227880342 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.41-5009T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880342 | |||||||
| chr2:227880360 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41-4991G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880360 | |||||||
| chr2:227880367 | A | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-4984A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880367 | |||||||
| chr2:227880381 | CT | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0001g0063 others(8): Show |
12 | HG01358.hp2 HG02615.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.41-4954delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227880381 | ||||||
| chr2:227880381 | CTT | C | 123 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(120): Show |
125 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(122): Show |
intron_variant | MODIFIER | c.41-4955_41-4954del others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227880381 | ||||||
| chr2:227880381 | CTTT | C | 11 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0191 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-4956_41-4954del others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227880381 | ||||||
| chr2:227880470 | C | G | 23 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0001c0003t0001g0198 others(20): Show |
23 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.41-4881C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880470 | |||||||
| chr2:227880671 | A | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-4680A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880671 | |||||||
| chr2:227880698 | C | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA18942.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.41-4653C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880698 | |||||||
| chr2:227880730 | C | T | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-4621C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880730 | |||||||
| chr2:227880927 | A | G | 1 | a0002c0002t0001g0162 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.41-4424A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227880927 | |||||||
| chr2:227881024 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-4327G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881024 | |||||||
| chr2:227881165 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.41-4186G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881165 | |||||||
| chr2:227881193 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0143 |
4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-4158A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881193 | |||||||
| chr2:227881357 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | NA19074.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.41-3994A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881357 | |||||||
| chr2:227881403 | G | A | 23 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0001c0003t0001g0198 others(20): Show |
23 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.41-3948G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881403 | |||||||
| chr2:227881418 | G | A | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.41-3933G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881418 | |||||||
| chr2:227881439 | A | G | 1 | a0002c0002t0001g0161 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-3912A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881439 | |||||||
| chr2:227881628 | C | T | 1 | a0001c0003t0002g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.41-3723C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881628 | |||||||
| chr2:227881698 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41-3653G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881698 | |||||||
| chr2:227881743 | C | CT | 65 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
68 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.41-3581dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | ||||||
| chr2:227881743 | CT | C | 23 | a0001c0001t0001g0040 a0001c0001t0001g0112 a0001c0001t0001g0175 others(20): Show |
24 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-3581delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | ||||||
| chr2:227881743 | CTTT | C | 12 | a0001c0001t0001g0195 a0001c0001t0001g0267 a0001c0001t0001g0268 others(9): Show |
12 | HG02717.hp1 HG02809.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.41-3583_41-3581del others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | ||||||
| chr2:227881743 | CTTTT | C | 107 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(104): Show |
109 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.41-3584_41-3581del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | ||||||
| chr2:227881743 | CTTTTT | C | 19 | a0001c0001t0001g0065 a0001c0001t0001g0223 a0001c0001t0001g0224 others(16): Show |
19 | HG01099.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.41-3585_41-3581del others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227881743 | ||||||
| chr2:227881751 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.41-3600T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881751 | |||||||
| chr2:227881813 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.41-3538T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881813 | |||||||
| chr2:227881816 | A | G | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(112): Show |
117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.41-3535A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881816 | |||||||
| chr2:227881833 | A | G | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-3518A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881833 | |||||||
| chr2:227881924 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.41-3427G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881924 | |||||||
| chr2:227881967 | A | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
264 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.41-3384A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227881967 | |||||||
| chr2:227882160 | T | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-3191T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882160 | |||||||
| chr2:227882336 | G | A | 142 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(139): Show |
144 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.41-3015G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882336 | |||||||
| chr2:227882383 | C | T | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.41-2968C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882383 | |||||||
| chr2:227882450 | T | C | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.41-2901T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882450 | |||||||
| chr2:227882451 | C | T | 1 | a0002c0002t0001g0161 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.41-2900C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882451 | |||||||
| chr2:227882927 | T | C | 1 | a0002c0002t0001g0003 | 3 | HG01069.hp1 HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.41-2424T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227882927 | |||||||
| chr2:227883419 | G | A | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.41-1932G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883419 | |||||||
| chr2:227883463 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0143 |
4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1888T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883463 | |||||||
| chr2:227883633 | T | C | 159 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(156): Show |
162 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.41-1718T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883633 | |||||||
| chr2:227883637 | T | C | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.41-1714T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883637 | |||||||
| chr2:227883675 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.41-1676A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883675 | |||||||
| chr2:227883707 | G | A | 4 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(1): Show |
4 | HG01884.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-1644G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883707 | |||||||
| chr2:227883771 | T | C | 1 | a0003c0004t0001g0189 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.41-1580T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883771 | |||||||
| chr2:227883949 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.41-1402T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883949 | |||||||
| chr2:227883972 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.41-1379G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227883972 | |||||||
| chr2:227884288 | C | A | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-1063C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884288 | |||||||
| chr2:227884381 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.41-970A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884381 | |||||||
| chr2:227884562 | G | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
59 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.41-789G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884562 | |||||||
| chr2:227884862 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.41-489G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227884862 | |||||||
| chr2:227885019 | C | A | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(112): Show |
117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.41-332C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885019 | |||||||
| chr2:227885039 | G | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.41-312G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885039 | |||||||
| chr2:227885052 | T | C | 117 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(114): Show |
119 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.41-299T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885052 | |||||||
| chr2:227885080 | A | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0178 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.41-271A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885080 | |||||||
| chr2:227885120 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.41-231T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885120 | |||||||
| chr2:227885131 | A | G | 1 | a0002c0002t0001g0160 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.41-220A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | chr2 | 227885131 | |||||||
| chr2:227885304 | AG | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0145 |
3 | HG02451.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.41-45delG | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 227885304 | ||||||
| chr2:227885523 | G | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.113+100G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885523 | |||||||
| chr2:227885594 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.113+171T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885594 | |||||||
| chr2:227885651 | T | TA | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.113+235dupA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885651 | ||||||
| chr2:227885783 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.113+360C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885783 | |||||||
| chr2:227885947 | C | T | 13 | a0001c0003t0002g0013 a0001c0003t0002g0154 a0001c0003t0002g0155 others(10): Show |
14 | HG00438.hp2 HG02132.hp1 NA18940.hp1 others(11): Show |
intron_variant | MODIFIER | c.113+524C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227885947 | |||||||
| chr2:227885975 | C | CT | 22 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0065 others(19): Show |
22 | HG01928.hp2 HG02027.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.113+568dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | ||||||
| chr2:227885975 | C | CTT | 75 | a0001c0001t0001g0015 a0001c0001t0001g0062 a0001c0001t0001g0199 others(72): Show |
76 | HG00323.hp1 HG00423.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.113+567_113+568dup others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | ||||||
| chr2:227885975 | C | CTTT | 46 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0195 others(43): Show |
47 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.113+566_113+568dup others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | ||||||
| chr2:227885975 | CTTTTTTT | C | 20 | a0001c0003t0001g0153 a0001c0003t0002g0013 a0001c0003t0002g0154 others(17): Show |
21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.113+562_113+568del others(7): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227885975 | ||||||
| chr2:227886010 | T | C | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.113+587T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886010 | |||||||
| chr2:227886036 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.113+613T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886036 | |||||||
| chr2:227886043 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.113+620C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886043 | |||||||
| chr2:227886069 | A | C | 37 | a0001c0001t0001g0033 a0001c0001t0001g0175 a0001c0001t0001g0178 others(34): Show |
40 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.113+646A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886069 | |||||||
| chr2:227886093 | A | C | 34 | a0002c0002t0001g0003 a0002c0002t0001g0012 a0002c0002t0001g0016 others(31): Show |
37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.113+670A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886093 | |||||||
| chr2:227886344 | T | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
264 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.113+921T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886344 | |||||||
| chr2:227886462 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.113+1039C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886462 | |||||||
| chr2:227886576 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.113+1153T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886576 | |||||||
| chr2:227886636 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0069 |
3 | HG02257.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.113+1213T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886636 | |||||||
| chr2:227886713 | G | A | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.113+1290G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886713 | |||||||
| chr2:227886750 | C | T | 11 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0191 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.113+1327C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886750 | |||||||
| chr2:227886788 | TAAAC | T | 38 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0002c0002t0001g0003 others(35): Show |
41 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+1387_113+1390d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 227886788 | ||||||
| chr2:227886916 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.113+1493A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886916 | |||||||
| chr2:227886952 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0245 |
2 | HG01106.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.113+1529C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227886952 | |||||||
| chr2:227887090 | C | G | 1 | a0003c0004t0001g0194 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113+1667C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887090 | |||||||
| chr2:227887099 | G | T | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(47): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.113+1676G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887099 | |||||||
| chr2:227887157 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0144 others(1): Show |
5 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+1734C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887157 | |||||||
| chr2:227887158 | G | A | 199 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(196): Show |
205 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.113+1735G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887158 | |||||||
| chr2:227887186 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.113+1763T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887186 | |||||||
| chr2:227887321 | T | C | 11 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0191 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.113+1898T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887321 | |||||||
| chr2:227887411 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.113+1988C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887411 | |||||||
| chr2:227887415 | T | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(259): Show |
273 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.113+1992T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887415 | |||||||
| chr2:227887433 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113+2010G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887433 | |||||||
| chr2:227887443 | A | G | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.113+2020A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887443 | |||||||
| chr2:227887524 | T | C | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(112): Show |
117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.113+2101T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887524 | |||||||
| chr2:227887632 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
5 | HG00423.hp2 NA18962.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+2209G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887632 | |||||||
| chr2:227887702 | A | G | 11 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0191 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.114-2154A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887702 | |||||||
| chr2:227887740 | T | A | 3 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0001c0003t0001g0306 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.114-2116T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887740 | |||||||
| chr2:227887988 | G | T | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.114-1868G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227887988 | |||||||
| chr2:227888089 | T | C | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.114-1767T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888089 | |||||||
| chr2:227888317 | T | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.114-1539T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888317 | |||||||
| chr2:227888408 | C | A | 1 | a0001c0001t0001g0009 | 2 | NA18994.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.114-1448C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888408 | |||||||
| chr2:227888440 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.114-1416C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888440 | |||||||
| chr2:227888521 | G | A | 1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.114-1335G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888521 | |||||||
| chr2:227888558 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.114-1298G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888558 | |||||||
| chr2:227888727 | A | G | 1 | a0001c0003t0002g0167 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.114-1129A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888727 | |||||||
| chr2:227888736 | G | A | 254 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(251): Show |
264 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.114-1120G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888736 | |||||||
| chr2:227888751 | T | C | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.114-1105T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888751 | |||||||
| chr2:227888793 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.114-1063C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888793 | |||||||
| chr2:227888794 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0209 |
3 | HG02165.hp1 NA18947.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.114-1062G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888794 | |||||||
| chr2:227888894 | C | A | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114-962C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227888894 | |||||||
| chr2:227889055 | T | C | 20 | a0001c0003t0001g0153 a0001c0003t0002g0013 a0001c0003t0002g0154 others(17): Show |
21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-801T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889055 | |||||||
| chr2:227889234 | A | G | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-622A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889234 | |||||||
| chr2:227889236 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0304 |
2 | HG02559.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.114-620A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889236 | |||||||
| chr2:227889256 | G | A | 37 | a0001c0001t0001g0033 a0001c0001t0001g0175 a0001c0001t0001g0178 others(34): Show |
40 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.114-600G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889256 | |||||||
| chr2:227889272 | G | A | 129 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(126): Show |
131 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(128): Show |
intron_variant | MODIFIER | c.114-584G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889272 | |||||||
| chr2:227889319 | A | G | 160 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(157): Show |
163 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.114-537A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889319 | |||||||
| chr2:227889336 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.114-520C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889336 | |||||||
| chr2:227889340 | G | A | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(112): Show |
117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.114-516G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889340 | |||||||
| chr2:227889433 | G | A | 12 | a0003c0004t0001g0186 a0003c0004t0001g0189 a0003c0004t0001g0190 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-423G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889433 | |||||||
| chr2:227889549 | G | A | 3 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0001c0003t0001g0306 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.114-307G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889549 | |||||||
| chr2:227889567 | A | G | 20 | a0001c0003t0001g0153 a0001c0003t0002g0013 a0001c0003t0002g0154 others(17): Show |
21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.114-289A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889567 | |||||||
| chr2:227889584 | T | C | 1 | a0001c0001t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-272T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889584 | |||||||
| chr2:227889591 | T | A | 12 | a0003c0004t0001g0186 a0003c0004t0001g0189 a0003c0004t0001g0190 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-265T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889591 | |||||||
| chr2:227889633 | A | G | 45 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(42): Show |
46 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.114-223A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889633 | |||||||
| chr2:227889688 | G | T | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.114-168G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889688 | |||||||
| chr2:227889699 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.114-157C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889699 | |||||||
| chr2:227889846 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.114-10T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 2/12 | chr2 | 227889846 | |||||||
| chr2:227890151 | A | G | 34 | a0002c0002t0001g0003 a0002c0002t0001g0012 a0002c0002t0001g0016 others(31): Show |
37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.258+151A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890151 | |||||||
| chr2:227890292 | CT | C | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.258+299delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 227890292 | ||||||
| chr2:227890349 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0264 a0001c0001t0001g0269 |
3 | NA18957.hp1 NA18962.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.258+349C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890349 | |||||||
| chr2:227890350 | G | A | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.258+350G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890350 | |||||||
| chr2:227890383 | T | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+383T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890383 | |||||||
| chr2:227890402 | G | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
5 | HG02258.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+402G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890402 | |||||||
| chr2:227890404 | A | G | 11 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0191 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.258+404A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890404 | |||||||
| chr2:227890480 | C | T | 2 | a0001c0003t0002g0173 a0001c0003t0002g0174 |
2 | NA18956.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.258+480C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890480 | |||||||
| chr2:227890557 | C | G | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.258+557C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890557 | |||||||
| chr2:227890578 | T | G | 4 | a0001c0001t0001g0222 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | NA18961.hp2 NA19000.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+578T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890578 | |||||||
| chr2:227890584 | A | G | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.258+584A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890584 | |||||||
| chr2:227890635 | A | G | 46 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(43): Show |
47 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.259-620A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890635 | |||||||
| chr2:227890639 | G | A | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.259-616G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890639 | |||||||
| chr2:227890639 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.259-616G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890639 | |||||||
| chr2:227890728 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.259-527G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890728 | |||||||
| chr2:227890764 | T | A | 34 | a0002c0002t0001g0003 a0002c0002t0001g0012 a0002c0002t0001g0016 others(31): Show |
37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.259-491T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890764 | |||||||
| chr2:227890870 | C | T | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.259-385C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890870 | |||||||
| chr2:227890871 | A | G | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.259-384A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890871 | |||||||
| chr2:227890872 | T | G | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.259-383T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227890872 | |||||||
| chr2:227891031 | C | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259-224C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 3/12 | chr2 | 227891031 | |||||||
| chr2:227891428 | T | C | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317+115T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891428 | |||||||
| chr2:227891573 | G | A | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.317+260G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891573 | |||||||
| chr2:227891693 | G | A | 34 | a0002c0002t0001g0003 a0002c0002t0001g0012 a0002c0002t0001g0016 others(31): Show |
37 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.317+380G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891693 | |||||||
| chr2:227891784 | A | G | 1 | a0004c0010t0001g0150 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.317+471A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891784 | |||||||
| chr2:227891790 | A | G | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.317+477A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891790 | |||||||
| chr2:227891820 | A | G | 5 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0025 others(2): Show |
5 | HG01884.hp1 HG02615.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.317+507A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891820 | |||||||
| chr2:227891841 | A | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0069 |
3 | HG02257.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.317+528A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891841 | |||||||
| chr2:227891897 | G | T | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.317+584G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891897 | |||||||
| chr2:227891965 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.317+652G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227891965 | |||||||
| chr2:227892059 | C | T | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317+746C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892059 | |||||||
| chr2:227892137 | A | ATTTT | 46 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(43): Show |
47 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.317+833_317+836dup others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 227892137 | ||||||
| chr2:227892198 | T | A | 1 | a0001c0001t0001g0041 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.317+885T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892198 | |||||||
| chr2:227892404 | G | T | 2 | a0001c0001t0001g0065 a0006c0008t0001g0320 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.317+1091G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892404 | |||||||
| chr2:227892446 | T | C | 1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.317+1133T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892446 | |||||||
| chr2:227892460 | T | C | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317+1147T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892460 | |||||||
| chr2:227892517 | C | G | 16 | a0001c0001t0001g0065 a0002c0005t0003g0318 a0002c0005t0003g0319 others(13): Show |
16 | HG00438.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.317+1204C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892517 | |||||||
| chr2:227892604 | G | A | 162 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(159): Show |
165 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.318-1191G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892604 | |||||||
| chr2:227892617 | A | G | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-1178A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892617 | |||||||
| chr2:227892618 | G | A | 2 | a0003c0004t0001g0309 a0003c0004t0001g0310 |
2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.318-1177G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892618 | |||||||
| chr2:227892709 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.318-1086G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892709 | |||||||
| chr2:227892774 | T | C | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318-1021T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227892774 | |||||||
| chr2:227893004 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.318-791G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893004 | |||||||
| chr2:227893094 | C | CCCGT | 16 | a0001c0001t0001g0065 a0002c0005t0003g0318 a0002c0005t0003g0319 others(13): Show |
16 | HG00438.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.318-699_318-698ins others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 227893094 | ||||||
| chr2:227893097 | A | G | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(260): Show |
274 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.318-698A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893097 | |||||||
| chr2:227893140 | C | T | 2 | a0001c0001t0001g0065 a0006c0008t0001g0320 |
2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.318-655C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893140 | |||||||
| chr2:227893143 | A | G | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-652A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893143 | |||||||
| chr2:227893185 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0209 |
3 | HG02165.hp1 NA18947.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.318-610G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893185 | |||||||
| chr2:227893186 | C | A | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-609C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893186 | |||||||
| chr2:227893187 | T | C | 2 | a0001c0003t0001g0313 a0007c0011t0001g0312 |
2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.318-608T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893187 | |||||||
| chr2:227893211 | A | C | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.318-584A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893211 | |||||||
| chr2:227893357 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.318-438A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893357 | |||||||
| chr2:227893367 | T | A | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-428T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893367 | |||||||
| chr2:227893391 | C | T | 47 | a0001c0001t0001g0065 a0001c0003t0001g0153 a0001c0003t0001g0187 others(44): Show |
48 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.318-404C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893391 | |||||||
| chr2:227893447 | C | T | 16 | a0001c0001t0001g0065 a0002c0005t0003g0318 a0002c0005t0003g0319 others(13): Show |
16 | HG00438.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.318-348C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893447 | |||||||
| chr2:227893473 | C | T | 1 | a0003c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.318-322C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893473 | |||||||
| chr2:227893533 | G | A | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(47): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.318-262G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893533 | |||||||
| chr2:227893651 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.318-144G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893651 | |||||||
| chr2:227893662 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18957.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.318-133A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893662 | |||||||
| chr2:227893671 | T | TAAAC | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(42): Show |
51 | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.318-102_318-99dupA others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 227893671 | ||||||
| chr2:227893683 | C | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0012t0001g0072 |
3 | HG01109.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.318-112C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893683 | |||||||
| chr2:227893740 | C | A | 114 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(111): Show |
116 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.318-55C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 4/12 | chr2 | 227893740 | |||||||
| chr2:227893919 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | splice_donor_variant&intron_variant | HIGH | c.440+2T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227893919 | |||||||
| chr2:227894002 | G | A | 11 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0191 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.440+85G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894002 | |||||||
| chr2:227894094 | A | C | 1 | a0001c0001t0001g0276 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.440+177A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894094 | |||||||
| chr2:227894128 | G | T | 1 | a0001c0003t0001g0153 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440+211G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894128 | |||||||
| chr2:227894167 | C | T | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.440+250C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894167 | |||||||
| chr2:227894216 | C | T | 1 | a0002c0002t0001g0027 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.440+299C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894216 | |||||||
| chr2:227894285 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.440+368G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894285 | |||||||
| chr2:227894314 | G | T | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+397G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894314 | |||||||
| chr2:227894461 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0280 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.440+544C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894461 | |||||||
| chr2:227894500 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.440+583G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894500 | |||||||
| chr2:227894553 | C | T | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.440+636C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894553 | |||||||
| chr2:227894700 | T | A | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+783T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894700 | |||||||
| chr2:227894712 | C | A | 2 | a0002c0002t0001g0017 a0002c0002t0001g0018 |
2 | HG01358.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.440+795C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894712 | |||||||
| chr2:227894761 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.440+844T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894761 | |||||||
| chr2:227894801 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.440+884G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894801 | |||||||
| chr2:227894815 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.440+898C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894815 | |||||||
| chr2:227894830 | C | A | 31 | a0001c0003t0001g0153 a0001c0003t0001g0187 a0001c0003t0001g0188 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.440+913C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894830 | |||||||
| chr2:227894838 | T | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(214): Show |
224 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.440+921T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894838 | |||||||
| chr2:227894938 | A | G | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.440+1021A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227894938 | |||||||
| chr2:227895018 | G | A | 1 | a0001c0003t0002g0173 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.440+1101G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895018 | |||||||
| chr2:227895137 | G | A | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.440+1220G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895137 | |||||||
| chr2:227895299 | A | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(68): Show |
75 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.440+1382A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895299 | |||||||
| chr2:227895350 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.440+1433G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895350 | |||||||
| chr2:227895587 | T | C | 1 | a0002c0002t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.440+1670T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895587 | |||||||
| chr2:227895620 | C | T | 32 | a0001c0001t0001g0305 a0001c0003t0001g0153 a0001c0003t0001g0187 others(29): Show |
33 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.440+1703C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895620 | |||||||
| chr2:227895695 | A | T | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.440+1778A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895695 | |||||||
| chr2:227895827 | A | G | 116 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(113): Show |
118 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.440+1910A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895827 | |||||||
| chr2:227895905 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440+1988A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895905 | |||||||
| chr2:227895922 | A | G | 1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.440+2005A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227895922 | |||||||
| chr2:227896027 | G | T | 1 | a0002c0002t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.440+2110G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896027 | |||||||
| chr2:227896198 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.441-1984A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896198 | |||||||
| chr2:227896320 | T | C | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441-1862T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896320 | |||||||
| chr2:227896487 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00673.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.441-1695C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896487 | |||||||
| chr2:227896559 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.441-1623A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896559 | |||||||
| chr2:227896577 | C | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0241 a0001c0001t0001g0274 others(20): Show |
24 | HG00323.hp1 HG00735.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.441-1605C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896577 | |||||||
| chr2:227896593 | A | AGT | 24 | a0001c0001t0001g0178 a0001c0001t0001g0195 a0001c0001t0001g0270 others(21): Show |
24 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.441-1552_441-1551d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | A | AGTGT | 17 | a0001c0001t0001g0033 a0001c0001t0001g0075 a0001c0001t0001g0284 others(14): Show |
18 | HG01074.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.441-1554_441-1551d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | A | AGTGTGT | 11 | a0001c0003t0002g0168 a0001c0003t0002g0174 a0001c0003t0002g0180 others(8): Show |
13 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.441-1556_441-1551d others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | A | AGTGTGTG others(1): Show |
15 | a0001c0003t0002g0013 a0001c0003t0002g0154 a0001c0003t0002g0155 others(12): Show |
16 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.441-1558_441-1551d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | A | AGTGTGTG others(3): Show |
2 | a0001c0003t0002g0177 a0002c0002t0001g0149 |
2 | HG01433.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.441-1560_441-1551d others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | A | AGTGTGTG others(7): Show |
1 | a0001c0003t0002g0172 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.441-1564_441-1551d others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | AGT | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0014 others(115): Show |
122 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.441-1552_441-1551d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | AGTGT | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(44): Show |
53 | HG00099.hp2 HG00673.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.441-1554_441-1551d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | AGTGTGT | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(53): Show |
60 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.441-1556_441-1551d others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | AGTGTGTG others(1): Show |
A | 10 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0082 others(7): Show |
10 | HG02165.hp2 HG02809.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-1558_441-1551d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | AGTGTGTG others(5): Show |
A | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441-1562_441-1551d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.441-1564_441-1551d others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896593 | AGTGTGTG others(11): Show |
A | 1 | a0002c0002t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441-1568_441-1551d others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227896593 | ||||||
| chr2:227896665 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0178 |
2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.441-1517C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896665 | |||||||
| chr2:227896709 | C | T | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.441-1473C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896709 | |||||||
| chr2:227896742 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.441-1440A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896742 | |||||||
| chr2:227896766 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.441-1416T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896766 | |||||||
| chr2:227896947 | A | G | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.441-1235A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227896947 | |||||||
| chr2:227897040 | C | T | 1 | a0003c0004t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.441-1142C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897040 | |||||||
| chr2:227897054 | C | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.441-1128C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897054 | |||||||
| chr2:227897093 | G | GA | 9 | a0001c0001t0001g0066 a0001c0001t0001g0086 a0001c0001t0001g0087 others(6): Show |
9 | HG01975.hp1 HG02027.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.441-1071dupA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227897093 | ||||||
| chr2:227897093 | GA | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(87): Show |
95 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.441-1071delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227897093 | ||||||
| chr2:227897100 | A | G | 10 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0192 others(7): Show |
10 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.441-1082A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897100 | |||||||
| chr2:227897298 | A | G | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-884A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897298 | |||||||
| chr2:227897358 | C | T | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-824C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897358 | |||||||
| chr2:227897401 | G | T | 21 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(18): Show |
22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.441-781G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897401 | |||||||
| chr2:227897484 | T | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0120 |
2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.441-698T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897484 | |||||||
| chr2:227897612 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.441-570C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897612 | |||||||
| chr2:227897614 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
91 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.441-568C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897614 | |||||||
| chr2:227897748 | T | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
91 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.441-434T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897748 | |||||||
| chr2:227897891 | A | G | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-291A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227897891 | |||||||
| chr2:227897951 | CCAAA | C | 31 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0001c0003t0001g0198 others(28): Show |
32 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.441-226_441-223del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 227897951 | ||||||
| chr2:227898017 | C | G | 1 | a0002c0002t0001g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.441-165C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 5/12 | chr2 | 227898017 | |||||||
| chr2:227898470 | G | A | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(112): Show |
117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.540+189G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898470 | |||||||
| chr2:227898603 | A | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.540+322A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898603 | |||||||
| chr2:227898628 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.540+347A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898628 | |||||||
| chr2:227898827 | G | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.540+546G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898827 | |||||||
| chr2:227898850 | T | G | 30 | a0001c0003t0001g0187 a0001c0003t0001g0188 a0001c0003t0001g0198 others(27): Show |
31 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.540+569T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898850 | |||||||
| chr2:227898953 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.540+672A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227898953 | |||||||
| chr2:227899119 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.540+838A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899119 | |||||||
| chr2:227899178 | A | G | 115 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(112): Show |
117 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.540+897A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899178 | |||||||
| chr2:227899187 | C | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(214): Show |
224 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.540+906C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899187 | |||||||
| chr2:227899188 | T | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(214): Show |
224 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(221): Show |
intron_variant | MODIFIER | c.540+907T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899188 | |||||||
| chr2:227899214 | A | C | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.540+933A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899214 | |||||||
| chr2:227899238 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.540+957C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899238 | |||||||
| chr2:227899503 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(247): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.540+1222T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899503 | |||||||
| chr2:227899648 | A | G | 1 | a0001c0003t0002g0177 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.540+1367A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899648 | |||||||
| chr2:227899792 | C | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0241 a0001c0001t0001g0274 others(18): Show |
22 | HG00323.hp1 HG00735.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.540+1511C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899792 | |||||||
| chr2:227899957 | T | C | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.540+1676T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227899957 | |||||||
| chr2:227900122 | A | G | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1841A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900122 | |||||||
| chr2:227900253 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0289 |
2 | HG02615.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.540+1972G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900253 | |||||||
| chr2:227900349 | A | G | 6 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(3): Show |
6 | HG00323.hp1 HG00735.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+2068A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900349 | |||||||
| chr2:227900456 | C | T | 3 | a0001c0001t0001g0219 a0001c0001t0001g0247 a0001c0001t0001g0261 |
3 | HG02735.hp1 HG02738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.540+2175C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900456 | |||||||
| chr2:227900531 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.540+2250G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900531 | |||||||
| chr2:227900558 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG01099.hp1 HG01109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.540+2277C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900558 | |||||||
| chr2:227900674 | G | A | 7 | a0001c0001t0001g0041 a0001c0003t0001g0311 a0001c0003t0001g0313 others(4): Show |
7 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-2328G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900674 | |||||||
| chr2:227900875 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.541-2127G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227900875 | |||||||
| chr2:227901016 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
324 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.541-1986A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901016 | |||||||
| chr2:227901037 | C | T | 1 | a0001c0003t0002g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.541-1965C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901037 | |||||||
| chr2:227901040 | T | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.541-1962T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901040 | |||||||
| chr2:227901138 | C | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
262 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.541-1864C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901138 | |||||||
| chr2:227901178 | A | G | 1 | a0001c0003t0001g0316 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.541-1824A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901178 | |||||||
| chr2:227901179 | G | T | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.541-1823G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901179 | |||||||
| chr2:227901328 | AC | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.541-1673delC | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901328 | |||||||
| chr2:227901411 | G | T | 1 | a0002c0002t0001g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.541-1591G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901411 | |||||||
| chr2:227901491 | A | G | 121 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(118): Show |
123 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.541-1511A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901491 | |||||||
| chr2:227901493 | T | G | 127 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(124): Show |
129 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.541-1509T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901493 | |||||||
| chr2:227901721 | C | A | 25 | a0001c0001t0001g0065 a0001c0001t0001g0305 a0001c0003t0001g0198 others(22): Show |
26 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.541-1281C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901721 | |||||||
| chr2:227901809 | T | C | 1 | a0001c0003t0002g0172 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.541-1193T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901809 | |||||||
| chr2:227901861 | G | A | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.541-1141G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901861 | |||||||
| chr2:227901917 | G | A | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.541-1085G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901917 | |||||||
| chr2:227901938 | C | T | 20 | a0001c0001t0001g0075 a0001c0003t0001g0187 a0001c0003t0001g0188 others(17): Show |
20 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(17): Show |
intron_variant | MODIFIER | c.541-1064C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227901938 | |||||||
| chr2:227902244 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.541-758G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902244 | |||||||
| chr2:227902354 | C | T | 1 | a0001c0003t0002g0154 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.541-648C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902354 | |||||||
| chr2:227902357 | G | T | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.541-645G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902357 | |||||||
| chr2:227902438 | T | C | 2 | a0001c0001t0001g0075 a0003c0004t0001g0186 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.541-564T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902438 | |||||||
| chr2:227902470 | A | G | 1 | a0001c0001t0001g0038 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.541-532A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902470 | |||||||
| chr2:227902479 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.541-523G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902479 | |||||||
| chr2:227902674 | G | A | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | NA18979.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.541-328G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902674 | |||||||
| chr2:227902703 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
59 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.541-299C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902703 | |||||||
| chr2:227902710 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.541-292T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902710 | |||||||
| chr2:227902902 | T | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(304): Show |
324 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(321): Show |
intron_variant | MODIFIER | c.541-100T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902902 | |||||||
| chr2:227902915 | G | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
127 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.541-87G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902915 | |||||||
| chr2:227902992 | TG | T | 1 | a0001c0001t0001g0002 | 3 | HG02622.hp2 HG02630.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.541-9delG | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 6/12 | chr2 | 227902992 | |||||||
| chr2:227903361 | T | C | 1 | a0002c0002t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.648+252T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903361 | |||||||
| chr2:227903441 | T | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
129 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.648+332T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903441 | |||||||
| chr2:227903476 | C | T | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.648+367C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903476 | |||||||
| chr2:227903638 | T | TCTCCCCT others(10): Show |
7 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(4): Show |
7 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.648+582_648+598dup others(17): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 227903638 | ||||||
| chr2:227903638 | TCTCCCCT others(10): Show |
T | 43 | a0001c0001t0001g0033 a0001c0001t0001g0075 a0001c0001t0001g0226 others(40): Show |
46 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.648+582_648+598del others(17): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 227903638 | ||||||
| chr2:227903768 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
131 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.648+659A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903768 | |||||||
| chr2:227903808 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(120): Show |
131 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.648+699G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903808 | |||||||
| chr2:227903835 | C | T | 50 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(47): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.648+726C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903835 | |||||||
| chr2:227903836 | C | A | 1 | a0002c0002t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.648+727C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903836 | |||||||
| chr2:227903943 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.648+834C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227903943 | |||||||
| chr2:227903988 | G | GT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
129 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.648+889dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 227903988 | ||||||
| chr2:227904188 | A | G | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.649-741A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904188 | |||||||
| chr2:227904277 | T | C | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.649-652T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904277 | |||||||
| chr2:227904528 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.649-401T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904528 | |||||||
| chr2:227904718 | T | C | 1 | a0001c0001t0001g0066 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.649-211T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 7/12 | chr2 | 227904718 | |||||||
| chr2:227905215 | C | T | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.755+180C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905215 | |||||||
| chr2:227905510 | A | G | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.755+475A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905510 | |||||||
| chr2:227905583 | C | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
130 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.755+548C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905583 | |||||||
| chr2:227905743 | T | C | 1 | a0003c0004t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.756-493T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905743 | |||||||
| chr2:227905755 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.756-481T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905755 | |||||||
| chr2:227905759 | G | T | 10 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0192 others(7): Show |
10 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.756-477G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905759 | |||||||
| chr2:227905792 | T | TTGCCC | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
61 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.756-443_756-439dup others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 227905792 | ||||||
| chr2:227905823 | C | T | 122 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
130 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.756-413C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905823 | |||||||
| chr2:227905843 | T | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
130 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.756-393T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905843 | |||||||
| chr2:227905847 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(246): Show |
259 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.756-389T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905847 | |||||||
| chr2:227905848 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
129 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.756-388G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905848 | |||||||
| chr2:227905869 | T | C | 111 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(108): Show |
113 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.756-367T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905869 | |||||||
| chr2:227905880 | G | A | 111 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(108): Show |
113 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.756-356G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905880 | |||||||
| chr2:227905882 | T | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
262 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.756-354T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905882 | |||||||
| chr2:227905894 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.756-342A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905894 | |||||||
| chr2:227905904 | A | G | 1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-332A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905904 | |||||||
| chr2:227905915 | T | C | 1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.756-321T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905915 | |||||||
| chr2:227905918 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.756-318C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905918 | |||||||
| chr2:227905956 | G | A | 1 | a0001c0001t0001g0014 | 2 | NA18977.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.756-280G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227905956 | |||||||
| chr2:227906050 | C | T | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.756-186C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227906050 | |||||||
| chr2:227906231 | T | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | NA18961.hp2 NA19004.hp2 |
splice_region_variant&intron_variant | LOW | c.756-5T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 8/12 | chr2 | 227906231 | |||||||
| chr2:227906413 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.858+75A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906413 | |||||||
| chr2:227906417 | A | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.858+79A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906417 | |||||||
| chr2:227906554 | A | G | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.858+216A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906554 | |||||||
| chr2:227906590 | T | C | 1 | a0003c0004t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.858+252T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906590 | |||||||
| chr2:227906707 | A | T | 38 | a0001c0001t0001g0033 a0001c0001t0001g0226 a0001c0001t0001g0260 others(35): Show |
41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.858+369A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906707 | |||||||
| chr2:227906847 | C | G | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.859-291C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227906847 | |||||||
| chr2:227907103 | C | CT | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(10): Show |
13 | HG00642.hp2 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.859-24dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 227907103 | ||||||
| chr2:227907115 | G | T | 2 | a0001c0001t0001g0075 a0003c0004t0001g0186 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.859-23G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227907115 | |||||||
| chr2:227907119 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.859-19T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 9/12 | chr2 | 227907119 | |||||||
| chr2:227907404 | G | C | 1 | a0002c0002t0001g0003 | 3 | HG01069.hp1 HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.973+152G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227907404 | |||||||
| chr2:227907452 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(130): Show |
141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.973+200T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227907452 | |||||||
| chr2:227908097 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.973+845T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908097 | |||||||
| chr2:227908103 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.973+851G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908103 | |||||||
| chr2:227908171 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.973+919G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908171 | |||||||
| chr2:227908199 | G | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(44): Show |
53 | HG00099.hp2 HG00621.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.973+947G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908199 | |||||||
| chr2:227908245 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(130): Show |
141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.973+993T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908245 | |||||||
| chr2:227908363 | C | G | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.973+1111C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908363 | |||||||
| chr2:227908430 | C | T | 9 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0296 others(6): Show |
9 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.973+1178C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908430 | |||||||
| chr2:227908571 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.973+1319T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908571 | |||||||
| chr2:227908581 | A | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.973+1329A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908581 | |||||||
| chr2:227908608 | G | T | 9 | a0003c0004t0001g0189 a0003c0004t0001g0190 a0003c0004t0001g0192 others(6): Show |
9 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.973+1356G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908608 | |||||||
| chr2:227908690 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.973+1438A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908690 | |||||||
| chr2:227908716 | A | G | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.973+1464A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908716 | |||||||
| chr2:227908808 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.973+1556T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908808 | |||||||
| chr2:227908821 | T | C | 5 | a0001c0001t0001g0065 a0001c0001t0001g0305 a0001c0003t0001g0306 others(2): Show |
5 | HG00438.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+1569T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908821 | |||||||
| chr2:227908889 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.973+1637A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908889 | |||||||
| chr2:227908912 | C | T | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+1660C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227908912 | |||||||
| chr2:227909053 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(130): Show |
141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.973+1801T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909053 | |||||||
| chr2:227909232 | T | TTATC | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(114): Show |
124 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.973+2018_973+2021d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | ||||||
| chr2:227909232 | T | TTATCTAT others(1): Show |
91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(88): Show |
98 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.973+2014_973+2021d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | ||||||
| chr2:227909232 | T | TTATCTAT others(5): Show |
53 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0050 others(50): Show |
55 | HG00642.hp2 HG00673.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.973+2010_973+2021d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | ||||||
| chr2:227909232 | T | TTATCTAT others(9): Show |
13 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0062 others(10): Show |
13 | HG00099.hp1 HG00423.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.973+2006_973+2021d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | ||||||
| chr2:227909232 | TTATC | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0003t0001g0198 others(2): Show |
5 | HG01109.hp1 HG01891.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+2018_973+2021d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | ||||||
| chr2:227909232 | TTATCTAT others(1): Show |
T | 19 | a0001c0003t0002g0013 a0001c0003t0002g0154 a0001c0003t0002g0155 others(16): Show |
20 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.973+2014_973+2021d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909232 | ||||||
| chr2:227909258 | A | ATCTGTCT others(9): Show |
1 | a0001c0003t0002g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.973+2009_973+2010i others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909258 | ||||||
| chr2:227909262 | A | G | 1 | a0001c0003t0002g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.973+2010A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909262 | |||||||
| chr2:227909266 | A | G | 20 | a0001c0003t0002g0013 a0001c0003t0002g0154 a0001c0003t0002g0155 others(17): Show |
21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.973+2014A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909266 | |||||||
| chr2:227909270 | A | ATCTG | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(101): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.973+2034_973+2037d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | ||||||
| chr2:227909270 | A | ATCTGTCT others(1): Show |
4 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0002c0002t0001g0019 others(1): Show |
4 | HG01515.hp1 HG01934.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+2030_973+2037d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | ||||||
| chr2:227909270 | A | ATCTGTCT others(9): Show |
1 | a0001c0003t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.973+2022_973+2037d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | ||||||
| chr2:227909270 | A | G | 20 | a0001c0003t0002g0013 a0001c0003t0002g0154 a0001c0003t0002g0155 others(17): Show |
21 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.973+2018A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909270 | |||||||
| chr2:227909270 | ATCTG | A | 45 | a0001c0001t0001g0062 a0001c0001t0001g0221 a0001c0001t0001g0222 others(42): Show |
45 | HG00423.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.973+2034_973+2037d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909270 | ||||||
| chr2:227909325 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0108 |
2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.973+2073T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909325 | |||||||
| chr2:227909414 | A | T | 8 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0081 others(5): Show |
8 | HG02165.hp2 NA18941.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.973+2162A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909414 | |||||||
| chr2:227909440 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.973+2188G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909440 | |||||||
| chr2:227909449 | T | TAC | 5 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0003t0001g0187 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+2207_973+2208d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227909449 | ||||||
| chr2:227909461 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+2209T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909461 | |||||||
| chr2:227909513 | A | G | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.973+2261A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909513 | |||||||
| chr2:227909533 | T | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(130): Show |
141 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.973+2281T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909533 | |||||||
| chr2:227909670 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.973+2418G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909670 | |||||||
| chr2:227909727 | G | A | 5 | a0001c0001t0001g0065 a0001c0001t0001g0305 a0001c0003t0001g0306 others(2): Show |
5 | HG00438.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.973+2475G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909727 | |||||||
| chr2:227909756 | A | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+2504A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227909756 | |||||||
| chr2:227910086 | T | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0143 |
4 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+2834T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910086 | |||||||
| chr2:227910146 | G | A | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
8 | HG01106.hp2 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.973+2894G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910146 | |||||||
| chr2:227910165 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.973+2913A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910165 | |||||||
| chr2:227910209 | C | T | 1 | a0002c0002t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+2957C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910209 | |||||||
| chr2:227910326 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.973+3074A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910326 | |||||||
| chr2:227910334 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+3082G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910334 | |||||||
| chr2:227910350 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+3098G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910350 | |||||||
| chr2:227910427 | A | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+3175A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910427 | |||||||
| chr2:227910438 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.973+3186A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910438 | |||||||
| chr2:227910465 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+3213C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910465 | |||||||
| chr2:227910477 | T | G | 21 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(18): Show |
22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.973+3225T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910477 | |||||||
| chr2:227910495 | A | AAC | 46 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0076 others(43): Show |
46 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.973+3272_973+3273d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACAC | 68 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(65): Show |
71 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(68): Show |
intron_variant | MODIFIER | c.973+3270_973+3273d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACAC | 27 | a0001c0001t0001g0047 a0001c0001t0001g0200 a0001c0001t0001g0262 others(24): Show |
27 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.973+3268_973+3273d others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACACA others(1): Show |
33 | a0001c0001t0001g0049 a0001c0001t0001g0226 a0001c0001t0001g0260 others(30): Show |
34 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.973+3266_973+3273d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACACA others(3): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0143 a0001c0001t0001g0287 others(4): Show |
9 | HG01433.hp2 HG01884.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.973+3264_973+3273d others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACACA others(5): Show |
30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0033 others(27): Show |
32 | HG00621.hp2 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.973+3262_973+3273d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACACA others(7): Show |
11 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0059 others(8): Show |
13 | HG00558.hp2 HG01069.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.973+3260_973+3273d others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACACA others(9): Show |
13 | a0001c0001t0001g0112 a0001c0001t0001g0123 a0001c0001t0001g0124 others(10): Show |
13 | HG00735.hp1 HG01175.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.973+3258_973+3273d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACACA others(11): Show |
7 | a0001c0001t0001g0122 a0001c0001t0001g0296 a0001c0001t0001g0297 others(4): Show |
7 | HG00323.hp1 HG01257.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.973+3256_973+3273d others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | A | AACACACA others(13): Show |
1 | a0001c0001t0001g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.973+3254_973+3273d others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910495 | AAC | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0046 others(4): Show |
10 | HG00673.hp1 NA18949.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.973+3272_973+3273d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227910495 | ||||||
| chr2:227910525 | C | CACACACA others(10): Show |
1 | a0001c0001t0001g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.973+3273_973+3274i others(19): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910525 | |||||||
| chr2:227910529 | T | C | 1 | a0002c0002t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+3277T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910529 | |||||||
| chr2:227910661 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.973+3409C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910661 | |||||||
| chr2:227910698 | C | T | 2 | a0001c0001t0001g0075 a0003c0004t0001g0186 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.973+3446C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910698 | |||||||
| chr2:227910730 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.973+3478T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910730 | |||||||
| chr2:227910802 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.973+3550A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227910802 | |||||||
| chr2:227911004 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.973+3752C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911004 | |||||||
| chr2:227911005 | A | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(247): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.973+3753A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911005 | |||||||
| chr2:227911084 | C | A | 36 | a0001c0001t0001g0226 a0001c0001t0001g0260 a0001c0001t0001g0284 others(33): Show |
39 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.973+3832C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911084 | |||||||
| chr2:227911197 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.973+3945T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911197 | |||||||
| chr2:227911225 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.973+3973T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911225 | |||||||
| chr2:227911227 | T | TGTGTATA others(43): Show |
2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.973+4014_973+4015i others(52): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911227 | ||||||
| chr2:227911231 | TATATATA others(1): Show |
T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0063 a0001c0001t0001g0069 |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.973+3997_973+4004d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911231 | ||||||
| chr2:227911239 | C | CATATACA others(5): Show |
1 | a0002c0002t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+3992_973+3993i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911239 | C | CATATATA others(27): Show |
7 | a0001c0001t0001g0064 a0001c0003t0001g0311 a0001c0003t0001g0313 others(4): Show |
7 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.973+3996_973+3997i others(36): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911239 | C | CATATATA others(35): Show |
82 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(79): Show |
87 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.973+4014_973+4015i others(44): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911239 | C | CATATATA others(55): Show |
1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.973+4014_973+4015i others(64): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911239 | C | CATATATA others(57): Show |
7 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(4): Show |
7 | HG00323.hp1 HG00735.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.973+4014_973+4015i others(66): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911239 | C | CATATATA others(77): Show |
4 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
4 | HG00558.hp2 HG01496.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.973+4014_973+4015i others(86): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911239 | C | CATATATA others(99): Show |
1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(108): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911239 | C | CATATATA others(37): Show |
1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(46): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911239 | ||||||
| chr2:227911247 | C | CATATATA others(41): Show |
1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(50): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911247 | ||||||
| chr2:227911249 | T | TATATACA others(13): Show |
2 | a0001c0001t0001g0065 a0001c0001t0001g0079 |
2 | HG02257.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.973+4014_973+4015i others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911249 | ||||||
| chr2:227911249 | TATATACA others(13): Show |
T | 1 | a0001c0001t0001g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.973+4015_973+4034d others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911249 | ||||||
| chr2:227911258 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.973+4006G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911258 | |||||||
| chr2:227911260 | G | GTATATAT others(57): Show |
1 | a0002c0002t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.973+4014_973+4015i others(66): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911260 | ||||||
| chr2:227911266 | A | G | 101 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(98): Show |
103 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(100): Show |
intron_variant | MODIFIER | c.973+4014A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911266 | |||||||
| chr2:227911267 | C | CATATACA others(33): Show |
1 | a0001c0001t0001g0279 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.973+4016_973+4017i others(42): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911267 | ||||||
| chr2:227911267 | C | T | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(301): Show |
321 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(318): Show |
intron_variant | MODIFIER | c.973+4015C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911267 | |||||||
| chr2:227911269 | C | CATATACA others(55): Show |
1 | a0001c0001t0001g0124 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.973+4042_973+4043i others(64): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911269 | ||||||
| chr2:227911269 | C | T | 1 | a0002c0002t0001g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.973+4017C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911269 | |||||||
| chr2:227911295 | T | TACACGTG others(15): Show |
1 | a0001c0001t0001g0113 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.973+4053_973+4054i others(24): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227911295 | ||||||
| chr2:227911299 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.973+4047C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911299 | |||||||
| chr2:227911330 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.973+4078A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911330 | |||||||
| chr2:227911352 | A | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.973+4100A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911352 | |||||||
| chr2:227911367 | C | T | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.973+4115C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911367 | |||||||
| chr2:227911407 | T | C | 3 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0022 |
3 | HG00642.hp2 HG01167.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.973+4155T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911407 | |||||||
| chr2:227911669 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+4417T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911669 | |||||||
| chr2:227911807 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.973+4555G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911807 | |||||||
| chr2:227911933 | A | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0108 |
2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.973+4681A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911933 | |||||||
| chr2:227911955 | T | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+4703T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227911955 | |||||||
| chr2:227912029 | GACA | G | 3 | a0001c0003t0002g0163 a0001c0003t0002g0167 a0001c0003t0002g0180 |
3 | HG01243.hp2 HG02293.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.973+4782_973+4784d others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227912029 | ||||||
| chr2:227912207 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.973+4955T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912207 | |||||||
| chr2:227912222 | A | G | 113 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(110): Show |
115 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.973+4970A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912222 | |||||||
| chr2:227912280 | T | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(129): Show |
140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.973+5028T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912280 | |||||||
| chr2:227912354 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.973+5102G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912354 | |||||||
| chr2:227912512 | A | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+5260A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912512 | |||||||
| chr2:227912732 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(247): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.973+5480C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912732 | |||||||
| chr2:227912825 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+5573T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912825 | |||||||
| chr2:227912845 | C | A | 2 | a0001c0001t0001g0080 a0001c0001t0001g0096 |
2 | HG01496.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.973+5593C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912845 | |||||||
| chr2:227912925 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.973+5673G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912925 | |||||||
| chr2:227912940 | C | T | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.973+5688C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912940 | |||||||
| chr2:227912957 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.973+5705A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227912957 | |||||||
| chr2:227913069 | G | A | 20 | a0001c0001t0001g0226 a0001c0001t0001g0260 a0001c0001t0001g0284 others(17): Show |
23 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.974-5711G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913069 | |||||||
| chr2:227913083 | G | C | 59 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(56): Show |
61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.974-5697G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913083 | |||||||
| chr2:227913086 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.974-5694T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913086 | |||||||
| chr2:227913155 | T | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-5625T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913155 | |||||||
| chr2:227913265 | C | T | 38 | a0001c0001t0001g0033 a0001c0001t0001g0226 a0001c0001t0001g0260 others(35): Show |
41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.974-5515C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913265 | |||||||
| chr2:227913450 | A | C | 2 | a0001c0001t0001g0075 a0003c0004t0001g0186 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.974-5330A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913450 | |||||||
| chr2:227913565 | G | A | 1 | a0003c0004t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.974-5215G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913565 | |||||||
| chr2:227913736 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.974-5044A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913736 | |||||||
| chr2:227913737 | C | G | 21 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(18): Show |
22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.974-5043C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913737 | |||||||
| chr2:227913823 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(63): Show |
70 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.974-4957T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913823 | |||||||
| chr2:227913848 | C | T | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.974-4932C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913848 | |||||||
| chr2:227913849 | C | T | 59 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(56): Show |
61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.974-4931C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913849 | |||||||
| chr2:227913871 | A | ATATC | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0131 others(4): Show |
7 | HG00438.hp1 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-4899_974-4896d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | ||||||
| chr2:227913871 | A | ATATCTAT others(1): Show |
61 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(58): Show |
66 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.974-4903_974-4896d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | ||||||
| chr2:227913871 | A | ATATCTAT others(5): Show |
31 | a0001c0001t0001g0226 a0001c0001t0001g0260 a0001c0001t0001g0284 others(28): Show |
33 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.974-4907_974-4896d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | ||||||
| chr2:227913871 | A | ATATCTAT others(9): Show |
6 | a0001c0003t0001g0306 a0002c0002t0001g0019 a0002c0002t0001g0157 others(3): Show |
6 | HG01515.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-4896_974-4895i others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | ||||||
| chr2:227913871 | A | ATATCTAT others(13): Show |
1 | a0001c0001t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(22): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | ||||||
| chr2:227913871 | A | ATATCTAT others(17): Show |
1 | a0002c0002t0001g0023 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.974-4896_974-4895i others(26): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | ||||||
| chr2:227913871 | ATATC | A | 4 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0315 others(1): Show |
4 | HG02896.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-4899_974-4896d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913871 | ||||||
| chr2:227913881 | A | ATCTATCT others(21): Show |
1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(30): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | ||||||
| chr2:227913881 | A | ATCTATCT others(5): Show |
1 | a0001c0001t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | ||||||
| chr2:227913881 | A | ATCTATCT others(5): Show |
1 | a0001c0001t0001g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.974-4896_974-4895i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | ||||||
| chr2:227913881 | A | ATCTG | 3 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0084 |
4 | HG02257.hp2 HG02965.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-4863_974-4860d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | ||||||
| chr2:227913881 | A | G | 1 | a0001c0003t0001g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.974-4899A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913881 | |||||||
| chr2:227913881 | ATCTG | A | 87 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0032 others(84): Show |
90 | HG00438.hp2 HG00558.hp1 HG01070.hp1 others(87): Show |
intron_variant | MODIFIER | c.974-4863_974-4860d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | ||||||
| chr2:227913881 | ATCTGTCT others(1): Show |
A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0264 a0003c0004t0001g0186 |
3 | NA18957.hp1 NA19084.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.974-4867_974-4860d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913881 | ||||||
| chr2:227913885 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0065 others(52): Show |
60 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.974-4895G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913885 | |||||||
| chr2:227913889 | G | A | 57 | a0001c0001t0001g0226 a0001c0001t0001g0260 a0001c0001t0001g0284 others(54): Show |
61 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.974-4891G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913889 | |||||||
| chr2:227913893 | G | A | 25 | a0001c0001t0001g0305 a0001c0003t0001g0306 a0001c0003t0002g0013 others(22): Show |
26 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.974-4887G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913893 | |||||||
| chr2:227913897 | G | A | 1 | a0002c0002t0001g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.974-4883G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913897 | |||||||
| chr2:227913913 | G | A | 7 | a0001c0003t0001g0198 a0001c0003t0001g0311 a0001c0003t0001g0313 others(4): Show |
7 | HG01891.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-4867G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913913 | |||||||
| chr2:227913917 | G | A | 141 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(138): Show |
144 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.974-4863G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913917 | |||||||
| chr2:227913921 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.974-4859A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913921 | |||||||
| chr2:227913924 | TA | T | 8 | a0001c0003t0001g0198 a0001c0003t0001g0311 a0001c0003t0001g0313 others(5): Show |
8 | HG01891.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-4855delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913924 | |||||||
| chr2:227913928 | T | A | 8 | a0001c0003t0001g0198 a0001c0003t0001g0311 a0001c0003t0001g0313 others(5): Show |
8 | HG01891.hp1 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-4852T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913928 | |||||||
| chr2:227913928 | T | TA | 109 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.974-4852_974-4851i others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913928 | |||||||
| chr2:227913931 | A | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.974-4849A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227913931 | |||||||
| chr2:227913988 | ATC | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-4770_974-4769d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227913988 | ||||||
| chr2:227914045 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-4735G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914045 | |||||||
| chr2:227914053 | A | C | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-4727A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914053 | |||||||
| chr2:227914139 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-4641G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914139 | |||||||
| chr2:227914153 | A | G | 4 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | NA18942.hp2 NA18984.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-4627A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914153 | |||||||
| chr2:227914321 | A | G | 39 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0226 others(36): Show |
42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-4459A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914321 | |||||||
| chr2:227914394 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.974-4386C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914394 | |||||||
| chr2:227914474 | C | T | 12 | a0001c0001t0001g0063 a0001c0001t0001g0226 a0001c0001t0001g0260 others(9): Show |
13 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.974-4306C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914474 | |||||||
| chr2:227914503 | T | C | 22 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(19): Show |
23 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.974-4277T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914503 | |||||||
| chr2:227914852 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.974-3928A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914852 | |||||||
| chr2:227914920 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
262 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.974-3860G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227914920 | |||||||
| chr2:227915090 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.974-3690G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915090 | |||||||
| chr2:227915134 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
8 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.974-3646T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915134 | |||||||
| chr2:227915143 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0096 |
2 | HG01496.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.974-3637A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915143 | |||||||
| chr2:227915195 | G | T | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.974-3585G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915195 | |||||||
| chr2:227915212 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-3568A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915212 | |||||||
| chr2:227915229 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-3551T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915229 | |||||||
| chr2:227915242 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0120 |
2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.974-3538A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915242 | |||||||
| chr2:227915243 | T | C | 39 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0226 others(36): Show |
42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-3537T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915243 | |||||||
| chr2:227915355 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
262 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.974-3425G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915355 | |||||||
| chr2:227915356 | T | C | 59 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(56): Show |
61 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.974-3424T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915356 | |||||||
| chr2:227915603 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.974-3177C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915603 | |||||||
| chr2:227915626 | G | C | 5 | a0001c0001t0001g0065 a0001c0001t0001g0305 a0001c0003t0001g0306 others(2): Show |
5 | HG00438.hp1 HG02257.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-3154G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915626 | |||||||
| chr2:227915694 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-3086A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915694 | |||||||
| chr2:227915712 | A | C | 1 | a0001c0003t0001g0187 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.974-3068A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915712 | |||||||
| chr2:227915721 | C | T | 3 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0139 |
3 | HG01258.hp1 HG01261.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.974-3059C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915721 | |||||||
| chr2:227915842 | C | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0305 a0001c0003t0001g0306 |
3 | HG02257.hp1 HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-2938C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915842 | |||||||
| chr2:227915892 | T | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | NA18942.hp2 NA18988.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.974-2888T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227915892 | |||||||
| chr2:227916168 | A | C | 1 | a0001c0001t0001g0061 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.974-2612A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916168 | |||||||
| chr2:227916414 | C | T | 1 | a0003c0004t0001g0310 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.974-2366C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916414 | |||||||
| chr2:227916418 | G | A | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.974-2362G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916418 | |||||||
| chr2:227916475 | C | A | 111 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(108): Show |
113 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.974-2305C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916475 | |||||||
| chr2:227916560 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.974-2220C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916560 | |||||||
| chr2:227916574 | T | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(249): Show |
262 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.974-2206T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916574 | |||||||
| chr2:227916584 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.974-2196G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916584 | |||||||
| chr2:227916715 | T | C | 39 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0226 others(36): Show |
42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-2065T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916715 | |||||||
| chr2:227916756 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.974-2024A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227916756 | |||||||
| chr2:227917047 | A | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(106): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.974-1733A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917047 | |||||||
| chr2:227917087 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.974-1693G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917087 | |||||||
| chr2:227917112 | G | GTATC | 7 | a0001c0001t0001g0208 a0001c0001t0001g0217 a0001c0001t0001g0232 others(4): Show |
7 | HG01081.hp2 HG01106.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-1638_974-1635d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | ||||||
| chr2:227917112 | G | GTATCTAT others(1): Show |
4 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0001g0261 others(1): Show |
4 | HG01975.hp1 HG03017.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1642_974-1635d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | ||||||
| chr2:227917112 | G | GTATCTAT others(5): Show |
2 | a0001c0001t0001g0271 a0001c0001t0001g0281 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.974-1646_974-1635d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | ||||||
| chr2:227917112 | GTATC | G | 6 | a0001c0001t0001g0227 a0001c0001t0001g0243 a0001c0001t0001g0255 others(3): Show |
6 | HG02056.hp1 HG03669.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-1638_974-1635d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | ||||||
| chr2:227917112 | GTATCTAT others(1): Show |
G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0071 others(9): Show |
13 | HG00621.hp1 HG01109.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.974-1642_974-1635d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | ||||||
| chr2:227917112 | GTATCTAT others(5): Show |
G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(50): Show |
58 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(55): Show |
intron_variant | MODIFIER | c.974-1646_974-1635d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | ||||||
| chr2:227917112 | GTATCTAT others(9): Show |
G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0101 |
4 | HG01257.hp1 HG01258.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1650_974-1635d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917112 | ||||||
| chr2:227917126 | A | ATCTG | 7 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0063 others(4): Show |
7 | HG00639.hp1 HG00738.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-1651_974-1650i others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917126 | ||||||
| chr2:227917130 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(126): Show |
137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.974-1650A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917130 | |||||||
| chr2:227917130 | ATCTATCT others(9): Show |
A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0082 a0001c0001t0001g0091 |
3 | HG00099.hp2 HG02165.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.974-1646_974-1631d others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917130 | ||||||
| chr2:227917134 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
130 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.974-1646A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917134 | |||||||
| chr2:227917134 | ATCTATCT others(5): Show |
A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0003t0001g0187 others(1): Show |
4 | HG02647.hp2 HG02895.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-1642_974-1631d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917134 | ||||||
| chr2:227917137 | T | C | 1 | a0002c0002t0001g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.974-1643T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917137 | |||||||
| chr2:227917138 | A | ATCTG | 7 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0001g0239 others(4): Show |
7 | HG00558.hp1 HG01167.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-1639_974-1638i others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917138 | ||||||
| chr2:227917138 | A | G | 6 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(3): Show |
6 | HG00673.hp2 HG01361.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-1642A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917138 | |||||||
| chr2:227917138 | ATCTATCT others(1): Show |
A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
15 | HG01106.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.974-1638_974-1631d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917138 | ||||||
| chr2:227917142 | A | ATCTATCT others(5): Show |
3 | a0001c0001t0001g0233 a0001c0001t0001g0244 a0001c0001t0001g0272 |
3 | HG03579.hp2 NA19065.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.974-1635_974-1634i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | A | ATCTATCT others(9): Show |
1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.974-1635_974-1634i others(18): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | A | ATCTATCT others(1): Show |
5 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0001c0001t0001g0210 others(2): Show |
5 | HG01978.hp1 HG02027.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-1635_974-1634i others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | A | ATCTATCT others(5): Show |
5 | a0001c0001t0001g0195 a0001c0001t0001g0203 a0001c0001t0001g0204 others(2): Show |
5 | HG01928.hp1 NA18947.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-1635_974-1634i others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | A | ATCTG | 13 | a0001c0001t0001g0014 a0001c0001t0001g0200 a0001c0001t0001g0215 others(10): Show |
13 | HG01070.hp1 HG01071.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.974-1602_974-1599d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | A | ATCTGTCT others(1): Show |
5 | a0001c0001t0001g0032 a0001c0001t0001g0214 a0001c0001t0001g0245 others(2): Show |
5 | HG02135.hp2 HG03942.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-1606_974-1599d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | A | G | 48 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0062 others(45): Show |
48 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.974-1638A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917142 | |||||||
| chr2:227917142 | ATCTG | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0049 others(36): Show |
41 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.974-1602_974-1599d others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | ATCTGTCT others(1): Show |
A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0276 a0001c0001t0001g0279 others(1): Show |
4 | HG01243.hp1 HG01978.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-1606_974-1599d others(10): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917142 | ATCTGTCT others(5): Show |
A | 2 | a0002c0002t0001g0159 a0002c0002t0001g0162 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.974-1610_974-1599d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917142 | ||||||
| chr2:227917146 | G | A | 80 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(77): Show |
84 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.974-1634G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917146 | |||||||
| chr2:227917150 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0047 others(18): Show |
24 | HG00423.hp2 HG00438.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.974-1630G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917150 | |||||||
| chr2:227917154 | G | A | 3 | a0001c0001t0001g0241 a0002c0005t0003g0318 a0002c0005t0003g0319 |
3 | HG00438.hp1 HG01074.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.974-1626G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917154 | |||||||
| chr2:227917188 | G | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.974-1592G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917188 | |||||||
| chr2:227917266 | CT | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(126): Show |
137 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.974-1501delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917266 | ||||||
| chr2:227917266 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0110 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.974-1512_974-1501d others(14): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917266 | ||||||
| chr2:227917272 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.974-1508T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917272 | |||||||
| chr2:227917299 | C | T | 111 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(108): Show |
113 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.974-1481C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917299 | |||||||
| chr2:227917330 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-1450A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917330 | |||||||
| chr2:227917346 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-1434C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917346 | |||||||
| chr2:227917347 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-1433A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917347 | |||||||
| chr2:227917389 | T | C | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-1391T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917389 | |||||||
| chr2:227917434 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-1346G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917434 | |||||||
| chr2:227917459 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.974-1321A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917459 | |||||||
| chr2:227917487 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-1293C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917487 | |||||||
| chr2:227917528 | G | A | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-1252G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917528 | |||||||
| chr2:227917561 | A | AT | 38 | a0001c0001t0001g0063 a0001c0001t0001g0226 a0001c0001t0001g0260 others(35): Show |
41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.974-1212dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227917561 | ||||||
| chr2:227917584 | T | G | 39 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0226 others(36): Show |
42 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.974-1196T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917584 | |||||||
| chr2:227917586 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1194C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917586 | |||||||
| chr2:227917587 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1193C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917587 | |||||||
| chr2:227917590 | T | G | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1190T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917590 | |||||||
| chr2:227917591 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1189C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917591 | |||||||
| chr2:227917595 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.974-1185A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917595 | |||||||
| chr2:227917817 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.974-963C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917817 | |||||||
| chr2:227917971 | A | T | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-809A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227917971 | |||||||
| chr2:227918017 | A | G | 1 | a0002c0005t0003g0319 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.974-763A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918017 | |||||||
| chr2:227918038 | G | GT | 3 | a0001c0001t0001g0200 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | NA18939.hp2 NA18967.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.974-737dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918038 | ||||||
| chr2:227918050 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0143 a0002c0002t0001g0179 |
5 | HG02572.hp2 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.974-730C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918050 | |||||||
| chr2:227918122 | C | CTGCATCC others(13): Show |
1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.974-657_974-656ins others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918122 | ||||||
| chr2:227918142 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.974-638G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918142 | |||||||
| chr2:227918142 | G | GTCCATCC others(1): Show |
20 | a0001c0001t0001g0113 a0001c0001t0001g0132 a0001c0001t0001g0300 others(17): Show |
21 | HG00323.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.974-615_974-608dup others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | ||||||
| chr2:227918142 | G | GTCCATCC others(5): Show |
21 | a0001c0001t0001g0010 a0001c0001t0001g0127 a0001c0003t0001g0306 others(18): Show |
22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.974-619_974-608dup others(12): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | ||||||
| chr2:227918142 | G | GTCCATCC others(9): Show |
74 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0047 others(71): Show |
80 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.974-623_974-608dup others(16): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | ||||||
| chr2:227918142 | G | GTCCATCC others(13): Show |
5 | a0001c0001t0001g0068 a0001c0001t0001g0112 a0001c0001t0001g0136 others(2): Show |
5 | HG03491.hp1 HG04204.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-627_974-608dup others(20): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | ||||||
| chr2:227918142 | G | GTCCATCC others(17): Show |
1 | a0002c0002t0001g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.974-631_974-608dup others(24): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918142 | ||||||
| chr2:227918146 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0281 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.974-634A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918146 | |||||||
| chr2:227918148 | C | CCATCCAT others(24): Show |
3 | a0001c0003t0002g0163 a0001c0003t0002g0165 a0001c0003t0002g0169 |
3 | HG02293.hp1 NA18993.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.974-608_974-607ins others(31): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918148 | ||||||
| chr2:227918148 | C | CCATCCAT others(28): Show |
4 | a0001c0001t0001g0305 a0002c0005t0003g0318 a0002c0005t0003g0319 others(1): Show |
4 | HG00438.hp1 HG02723.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.974-608_974-607ins others(35): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918148 | ||||||
| chr2:227918171 | T | TCATC | 41 | a0001c0001t0001g0207 a0001c0001t0001g0221 a0001c0001t0001g0222 others(38): Show |
41 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.974-561_974-558dup others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | ||||||
| chr2:227918171 | T | TCATCCAT others(1): Show |
24 | a0001c0001t0001g0062 a0001c0001t0001g0199 a0001c0001t0001g0200 others(21): Show |
24 | HG00423.hp1 HG00673.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.974-565_974-558dup others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | ||||||
| chr2:227918171 | TCATC | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(66): Show |
75 | HG00099.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.974-561_974-558del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | ||||||
| chr2:227918171 | TCATCCAT others(1): Show |
T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0100 a0001c0001t0001g0101 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-565_974-558del others(8): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918171 | ||||||
| chr2:227918175 | C | CCATCATC others(19): Show |
1 | a0001c0003t0002g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.974-601_974-600ins others(26): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918175 | ||||||
| chr2:227918175 | C | CCATCCAT others(12): Show |
18 | a0001c0003t0001g0198 a0001c0003t0001g0306 a0001c0003t0002g0013 others(15): Show |
19 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.974-603_974-585dup others(19): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918175 | ||||||
| chr2:227918179 | C | CCATCCAT others(8): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0065 a0001c0001t0001g0131 others(1): Show |
4 | HG02055.hp1 HG02257.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-599_974-585dup others(15): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918179 | ||||||
| chr2:227918183 | C | CCATCCAT others(4): Show |
44 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0048 others(41): Show |
47 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.974-595_974-585dup others(11): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918183 | ||||||
| chr2:227918187 | C | CCATCCAT | 18 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0113 others(15): Show |
18 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.974-591_974-585dup others(7): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918187 | ||||||
| chr2:227918191 | C | CCAT | 38 | a0001c0001t0001g0010 a0001c0001t0001g0033 a0001c0001t0001g0063 others(35): Show |
42 | HG00099.hp1 HG00323.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.974-587_974-585dup others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 227918191 | ||||||
| chr2:227918260 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.974-520C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918260 | |||||||
| chr2:227918269 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.974-511C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918269 | |||||||
| chr2:227918418 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.974-362G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918418 | |||||||
| chr2:227918420 | G | T | 3 | a0002c0002t0001g0016 a0002c0002t0001g0021 a0002c0002t0001g0022 |
3 | HG00642.hp2 HG01167.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.974-360G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918420 | |||||||
| chr2:227918473 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.974-307T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918473 | |||||||
| chr2:227918510 | A | G | 2 | a0001c0001t0001g0305 a0001c0003t0001g0306 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.974-270A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918510 | |||||||
| chr2:227918547 | A | G | 37 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0195 others(34): Show |
38 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.974-233A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918547 | |||||||
| chr2:227918648 | A | C | 260 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(257): Show |
271 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.974-132A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918648 | |||||||
| chr2:227918694 | G | T | 21 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(18): Show |
22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.974-86G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918694 | |||||||
| chr2:227918731 | G | C | 19 | a0001c0003t0002g0013 a0001c0003t0002g0154 a0001c0003t0002g0155 others(16): Show |
20 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.974-49G>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918731 | |||||||
| chr2:227918763 | C | A | 60 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0048 others(57): Show |
62 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.974-17C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 10/12 | chr2 | 227918763 | |||||||
| chr2:227919206 | AAAG | A | 117 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0033 others(114): Show |
123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1050+353_1050+355d others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919206 | ||||||
| chr2:227919207 | AAG | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0064 others(8): Show |
13 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1050+353_1050+354d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919207 | ||||||
| chr2:227919209 | GA | G | 100 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(97): Show |
102 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(99): Show |
intron_variant | MODIFIER | c.1050+368delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919209 | ||||||
| chr2:227919209 | GAA | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0211 a0001c0001t0001g0214 others(14): Show |
17 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.1050+367_1050+368d others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919209 | ||||||
| chr2:227919210 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0064 others(8): Show |
13 | HG02055.hp1 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1050+354A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919210 | |||||||
| chr2:227919211 | A | G | 117 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0033 others(114): Show |
123 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1050+355A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919211 | |||||||
| chr2:227919212 | A | G | 3 | a0002c0002t0001g0026 a0002c0002t0001g0161 a0002c0002t0001g0183 |
3 | HG01243.hp1 HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1050+356A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919212 | |||||||
| chr2:227919220 | A | G | 2 | a0002c0005t0003g0318 a0002c0005t0003g0319 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1050+364A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919220 | |||||||
| chr2:227919224 | A | AGCATGCT others(38): Show |
1 | a0001c0001t0001g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1050+369_1050+413d others(47): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227919224 | ||||||
| chr2:227919575 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0069 |
3 | HG02257.hp2 HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1050+719T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919575 | |||||||
| chr2:227919785 | A | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(247): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.1050+929A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919785 | |||||||
| chr2:227919889 | C | T | 21 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(18): Show |
22 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1050+1033C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919889 | |||||||
| chr2:227919990 | G | A | 2 | a0001c0003t0001g0198 a0001c0003t0002g0197 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1050+1134G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227919990 | |||||||
| chr2:227920141 | A | C | 3 | a0003c0004t0001g0192 a0003c0004t0001g0194 a0003c0004t0001g0196 |
3 | HG02976.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1051-1258A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920141 | |||||||
| chr2:227920192 | T | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0245 |
2 | HG01106.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1051-1207T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920192 | |||||||
| chr2:227920260 | G | A | 22 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(19): Show |
23 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1051-1139G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920260 | |||||||
| chr2:227920291 | A | G | 4 | a0001c0003t0002g0013 a0001c0003t0002g0154 a0001c0003t0002g0155 others(1): Show |
5 | HG00438.hp2 NA18943.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1051-1108A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920291 | |||||||
| chr2:227920481 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1051-918T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920481 | |||||||
| chr2:227920676 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1051-723A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920676 | |||||||
| chr2:227920708 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1051-691G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920708 | |||||||
| chr2:227920722 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1051-677G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920722 | |||||||
| chr2:227920775 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1051-624T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920775 | |||||||
| chr2:227920892 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1051-507C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920892 | |||||||
| chr2:227920899 | G | T | 1 | a0003c0004t0001g0191 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1051-500G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920899 | |||||||
| chr2:227920980 | G | T | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1051-419G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227920980 | |||||||
| chr2:227921014 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1051-385A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921014 | |||||||
| chr2:227921015 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1051-384G>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921015 | |||||||
| chr2:227921042 | G | A | 1 | a0001c0003t0001g0306 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1051-357G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921042 | |||||||
| chr2:227921069 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1051-330A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921069 | |||||||
| chr2:227921087 | G | A | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1051-312G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | chr2 | 227921087 | |||||||
| chr2:227921305 | C | CT | 14 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG01928.hp2 HG01934.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051-66dupT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CT | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0061 others(11): Show |
14 | HG00735.hp1 HG00735.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1051-66delT | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CTT | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
82 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1051-67_1051-66del others(2): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CTTT | C | 120 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0032 others(117): Show |
125 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1051-68_1051-66del others(3): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CTTTT | C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(9): Show |
12 | HG00438.hp1 HG00642.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1051-69_1051-66del others(4): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CTTTTT | C | 9 | a0001c0001t0001g0234 a0001c0001t0001g0238 a0001c0003t0002g0163 others(6): Show |
9 | HG00738.hp2 HG01243.hp2 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-70_1051-66del others(5): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CTTTTTT | C | 14 | a0001c0003t0001g0198 a0001c0003t0002g0013 a0001c0003t0002g0154 others(11): Show |
15 | HG00438.hp2 HG01891.hp1 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.1051-71_1051-66del others(6): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CTTTTTTT others(4): Show |
C | 3 | a0003c0004t0001g0192 a0003c0004t0001g0194 a0003c0004t0001g0196 |
3 | HG02976.hp2 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1051-76_1051-66del others(11): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921305 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0073 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1051-78_1051-66del others(13): Show |
DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 227921305 | ||||||
| chr2:227921845 | C | T | 2 | a0001c0001t0001g0075 a0003c0004t0001g0186 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1213+284C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227921845 | |||||||
| chr2:227921887 | C | A | 1 | a0001c0001t0001g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1213+326C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227921887 | |||||||
| chr2:227921954 | C | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(129): Show |
140 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1213+393C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227921954 | |||||||
| chr2:227922146 | C | T | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1213+585C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922146 | |||||||
| chr2:227922196 | A | G | 1 | a0006c0008t0001g0320 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1213+635A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922196 | |||||||
| chr2:227922200 | G | A | 2 | a0001c0001t0001g0075 a0003c0004t0001g0186 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1213+639G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922200 | |||||||
| chr2:227922501 | C | T | 1 | a0003c0004t0001g0186 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1213+940C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922501 | |||||||
| chr2:227922553 | T | G | 1 | a0001c0001t0001g0305 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1213+992T>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922553 | |||||||
| chr2:227922641 | C | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(64): Show |
71 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.1213+1080C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922641 | |||||||
| chr2:227922641 | C | T | 2 | a0001c0003t0001g0187 a0001c0003t0001g0188 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1213+1080C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922641 | |||||||
| chr2:227922723 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1213+1162A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922723 | |||||||
| chr2:227922730 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(257): Show |
271 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.1213+1169G>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922730 | |||||||
| chr2:227922817 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1214-1117A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922817 | |||||||
| chr2:227922875 | A | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
138 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1214-1059A>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922875 | |||||||
| chr2:227922939 | A | C | 1 | a0001c0001t0001g0264 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1214-995A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922939 | |||||||
| chr2:227922945 | C | G | 38 | a0001c0001t0001g0033 a0001c0001t0001g0226 a0001c0001t0001g0260 others(35): Show |
41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1214-989C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227922945 | |||||||
| chr2:227923050 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1214-884A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923050 | |||||||
| chr2:227923245 | C | T | 1 | a0001c0003t0002g0176 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1214-689C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923245 | |||||||
| chr2:227923289 | C | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1214-645C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923289 | |||||||
| chr2:227923485 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1214-449A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923485 | |||||||
| chr2:227923493 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1214-441T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923493 | |||||||
| chr2:227923542 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1214-392C>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923542 | |||||||
| chr2:227923574 | A | G | 36 | a0001c0001t0001g0226 a0001c0001t0001g0260 a0001c0001t0001g0284 others(33): Show |
39 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1214-360A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923574 | |||||||
| chr2:227923615 | A | C | 1 | a0001c0003t0001g0198 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1214-319A>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923615 | |||||||
| chr2:227923665 | C | T | 38 | a0001c0001t0001g0033 a0001c0001t0001g0226 a0001c0001t0001g0260 others(35): Show |
41 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1214-269C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923665 | |||||||
| chr2:227923678 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1214-256C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923678 | |||||||
| chr2:227923730 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1214-204A>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923730 | |||||||
| chr2:227923742 | C | T | 4 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(1): Show |
4 | HG01884.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1214-192C>T | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923742 | |||||||
| chr2:227923745 | GA | G | 26 | a0001c0001t0001g0033 a0001c0001t0001g0089 a0001c0001t0001g0213 others(23): Show |
27 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1214-176delA | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 227923745 | ||||||
| chr2:227923768 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
139 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1214-166T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923768 | |||||||
| chr2:227923776 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0108 |
2 | NA18948.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1214-158C>G | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923776 | |||||||
| chr2:227923896 | T | A | 6 | a0001c0003t0001g0311 a0001c0003t0001g0313 a0001c0003t0001g0314 others(3): Show |
6 | HG02809.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1214-38T>A | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923896 | |||||||
| chr2:227923896 | T | C | 3 | a0001c0001t0001g0305 a0001c0003t0001g0306 a0006c0008t0001g0320 |
3 | HG02717.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1214-38T>C | DAW1 | ENSG00000123977.10 | transcript | ENST00000309931.3 | protein_coding | 12/12 | chr2 | 227923896 |