Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4222 |
| ensemblid | ENSG00000005102.14 |
| hgncid | 7013 |
| symbol | MEOX1 |
| name | mesenchyme homeobox 1 |
| refseq_nuc | NM_004527.4 |
| refseq_prot | NP_004518.1 |
| ensembl_nuc | ENST00000318579.9 |
| ensembl_prot | ENSP00000321684.4 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 43640389 |
| end | 43661922 |
| strand | - |
| ver | v1.2 |
| region | chr17:43640389-43661922 |
| region5000 | chr17:43635389-43666922 |
| regionname0 | MEOX1_chr17_43640389_43661922 |
| regionname5000 | MEOX1_chr17_43635389_43666922 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 254 | 336 | 55 | 69 | 156 | 10 | 44 | 110 | MEOX1_chr17_43635389_43666922 | MEOX1 | MDPAA others(249): Show |
chr17 | 43635389 | 43666922 |
| a0002 | 0/0 | 254 | 41 | 35 | 4 | 0 | 0 | 2 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | MDPAA others(249): Show |
chr17 | 43635389 | 43666922 |
| a0003 | 0/0 | 254 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | MDPAA others(249): Show |
chr17 | 43635389 | 43666922 |
| a0004 | 0/0 | 254 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | MDPVA others(249): Show |
chr17 | 43635389 | 43666922 |
| a0005 | 0/0 | 254 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | MDPAA others(249): Show |
chr17 | 43635389 | 43666922 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 762 | 323 | 50 | 69 | 150 | 10 | 42 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0001c0003 | 0/0 | 762 | 6 | 0 | 0 | 6 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0001c0004 | 0/0 | 762 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0001c0005 | 0/0 | 762 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0001c0006 | 0/0 | 762 | 2 | 0 | 0 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0002c0002 | 0/0 | 762 | 41 | 35 | 4 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0003c0007 | 0/0 | 762 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0004c0009 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 | ||
| a0005c0008 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | ATGGA others(757): Show |
chr17 | 43635389 | 43666922 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2674 | 239 | 44 | 46 | 111 | 5 | 31 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0002 | 0/0 | 2674 | 63 | 1 | 22 | 35 | 1 | 4 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0003 | 0/0 | 2674 | 6 | 0 | 0 | 0 | 0 | 6 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0004 | 0/0 | 2655 | 6 | 0 | 0 | 2 | 3 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2650): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0005 | 0/0 | 2674 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0006 | 0/0 | 2674 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0007 | 0/0 | 2674 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0009 | 0/0 | 2674 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0010 | 0/0 | 2674 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0011 | 0/0 | 2674 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0014 | 0/0 | 2674 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0001t0015 | 0/0 | 2674 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0003t0001 | 0/0 | 2674 | 6 | 0 | 0 | 6 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0004t0001 | 0/0 | 2674 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0004t0008 | 0/0 | 2674 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0005t0001 | 0/0 | 2674 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0001c0006t0001 | 0/0 | 2674 | 2 | 0 | 0 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0002c0002t0001 | 0/0 | 2674 | 40 | 34 | 4 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0002c0002t0012 | 0/0 | 2674 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0003c0007t0013 | 0/0 | 2674 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0004c0009t0001 | 0/0 | 2674 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| a0005c0008t0001 | 0/0 | 2674 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | AGCCC others(2669): Show |
chr17 | 43635389 | 43666922 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 21 | 0 | 7 | 13 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0002 | 0/0 | 17 | 1 | 1 | 15 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0004 | 1/0 | 7 | 6 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 3 | 1 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0006 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0094 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0003 | 0/0 | 13 | 0 | 4 | 8 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0004g0031 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0005g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0010g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0014g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0001t0015g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0004t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0004t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0001c0006t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0002c0002t0012g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0003c0007t0013g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0004c0009t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| a0005c0008t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0127 | EUR | FIN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0049 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01069 | hp1 | a0003 | c0007 | t0013 | g0120 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0083 | EUR | IBS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0031 | EUR | IBS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0177 | EUR | IBS | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0251 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01934 | hp1 | a0001 | c0001 | t0010 | g0174 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02129 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0254 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0240 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02572 | hp2 | a0001 | c0001 | t0015 | g0264 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0045 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02615 | hp2 | a0001 | c0005 | t0001 | g0052 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0234 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0244 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0258 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0114 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0246 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02970 | hp1 | a0001 | c0005 | t0001 | g0051 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03041 | hp1 | a0004 | c0009 | t0001 | g0262 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0231 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03209 | hp1 | a0002 | c0002 | t0012 | g0257 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0256 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0255 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03486 | hp1 | a0001 | c0004 | t0001 | g0232 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03491 | hp1 | a0001 | c0006 | t0001 | g0021 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03492 | hp2 | a0001 | c0006 | t0001 | g0021 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0243 | AFR | GWD | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0193 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0191 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0182 | SAS | BEB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0018 | AFR | YRI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18995 | hp2 | a0001 | c0001 | t0011 | g0217 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19030 | hp1 | a0001 | c0004 | t0008 | g0233 | AFR | LWK | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19030 | hp2 | a0005 | c0008 | t0001 | g0261 | AFR | LWK | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | YRI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ASW | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ASW | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20752 | hp1 | a0001 | c0001 | t0014 | g0263 | EUR | TSI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0252 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0248 | AFR | MSL | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | USA | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | USA | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0260 | AFR | LWK | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0094 | REF | REF | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | MEOX1_chr17_43635389_43666922 | MEOX1 | chr17 | 43635389 | 43666922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43641948 | C | T | 1 | a0003 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.727G>A | p.Glu243Lys | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 1115/2674 | 727/765 | 243/254 | chr17 | 43641948 | |||
| chr17:43661419 | G | A | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.116C>T | p.Pro39Leu | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 504/2674 | 116/765 | 39/254 | chr17 | 43661419 | |||
| chr17:43661455 | G | A | 3 | a0002 a0004 a0005 |
43 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
missense_variant | MODERATE | c.80C>T | p.Ser27Leu | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 468/2674 | 80/765 | 27/254 | chr17 | 43661455 | |||
| chr17:43661524 | G | A | 1 | a0004 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.11C>T | p.Ala4Val | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 399/2674 | 11/765 | 4/254 | chr17 | 43661524 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43643574 | G | A | 1 | a0001c0006 | 2 | HG03491.hp1 HG03492.hp2 |
synonymous_variant | LOW | c.556C>T | p.Leu186Leu | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/3 | 944/2674 | 556/765 | 186/254 | chr17 | 43643574 | |||
| chr17:43661091 | T | C | 2 | a0001c0004 a0001c0005 |
5 | HG02615.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
synonymous_variant | LOW | c.444A>G | p.Ser148Ser | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 832/2674 | 444/765 | 148/254 | chr17 | 43661091 | |||
| chr17:43661208 | C | G | 1 | a0001c0005 | 2 | HG02615.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.327G>C | p.Pro109Pro | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 715/2674 | 327/765 | 109/254 | chr17 | 43661208 | |||
| chr17:43661208 | C | T | 1 | a0001c0003 | 6 | HG00544.hp2 HG00621.hp2 HG02071.hp1 others(3): Show |
synonymous_variant | LOW | c.327G>A | p.Pro109Pro | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 715/2674 | 327/765 | 109/254 | chr17 | 43661208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43640445 | C | T | 1 | a0001c0001t0009 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 1465 | chr17 | 43640445 | ||||||
| chr17:43640659 | T | C | 1 | a0001c0001t0010 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1251A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 1251 | chr17 | 43640659 | ||||||
| chr17:43640695 | C | T | 3 | a0001c0001t0002 a0001c0001t0011 a0002c0002t0012 |
65 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1215G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 1215 | chr17 | 43640695 | ||||||
| chr17:43640825 | G | A | 1 | a0001c0001t0011 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1085C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 1085 | chr17 | 43640825 | ||||||
| chr17:43640850 | A | G | 1 | a0001c0001t0015 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1060T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 1060 | chr17 | 43640850 | ||||||
| chr17:43641039 | G | A | 1 | a0002c0002t0012 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*871C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 871 | chr17 | 43641039 | ||||||
| chr17:43641285 | C | A | 1 | a0001c0001t0003 | 6 | HG02698.hp1 HG02738.hp1 HG03654.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*625G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 625 | chr17 | 43641285 | ||||||
| chr17:43641594 | G | T | 1 | a0001c0004t0008 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 316 | chr17 | 43641594 | ||||||
| chr17:43641758 | CCAGGAAT others(12): Show |
C | 1 | a0001c0001t0004 | 6 | HG01515.hp1 HG01515.hp2 HG01517.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*133_*151delAAACTG others(13): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 133 | chr17 | 43641758 | ||||||
| chr17:43641772 | C | A | 1 | a0001c0001t0001 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 138 | chr17 | 43641772 | ||||||
| chr17:43641873 | G | A | 1 | a0003c0007t0013 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 3/3 | 37 | chr17 | 43641873 | ||||||
| chr17:43661551 | G | A | 1 | a0001c0001t0014 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 17 | chr17 | 43661551 | ||||||
| chr17:43661685 | A | C | 1 | a0001c0001t0007 | 1 | HG00423.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151T>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 151 | chr17 | 43661685 | ||||||
| chr17:43661703 | C | G | 1 | a0001c0001t0006 | 1 | NA20300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-169G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 169 | chr17 | 43661703 | ||||||
| chr17:43661852 | T | C | 2 | a0001c0001t0005 a0001c0001t0015 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
5_prime_UTR_variant | MODIFIER | c.-318A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/3 | 318 | chr17 | 43661852 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43642073 | G | A | 1 | a0001c0004t0008g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.643-41C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642073 | |||||||
| chr17:43642109 | C | T | 4 | a0002c0002t0001g0018 a0002c0002t0001g0243 a0002c0002t0001g0244 others(1): Show |
6 | HG02717.hp2 HG02809.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.643-77G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642109 | |||||||
| chr17:43642252 | G | A | 35 | a0001c0001t0001g0093 a0001c0001t0001g0129 a0001c0001t0001g0172 others(32): Show |
42 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.643-220C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642252 | |||||||
| chr17:43642319 | C | T | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.643-287G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642319 | |||||||
| chr17:43642510 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.643-478C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642510 | |||||||
| chr17:43642512 | C | A | 1 | a0001c0001t0002g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.643-480G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642512 | |||||||
| chr17:43642683 | C | CCAAAA | 46 | a0001c0001t0001g0026 a0001c0001t0001g0071 a0001c0001t0001g0093 others(43): Show |
55 | HG00741.hp2 HG01169.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.643-656_643-652dup others(5): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642683 | |||||||
| chr17:43642690 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0123 a0001c0001t0001g0133 others(2): Show |
7 | HG00735.hp2 HG01123.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-658T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642690 | |||||||
| chr17:43642864 | C | T | 35 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0129 others(32): Show |
42 | HG00741.hp2 HG01169.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.642+624G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642864 | |||||||
| chr17:43642880 | G | A | 35 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0129 others(32): Show |
42 | HG00741.hp2 HG01169.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.642+608C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642880 | |||||||
| chr17:43642892 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.642+596C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43642892 | |||||||
| chr17:43643003 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.642+485G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43643003 | |||||||
| chr17:43643021 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.642+467G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43643021 | |||||||
| chr17:43643146 | TA | T | 95 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0071 others(92): Show |
128 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(125): Show |
intron_variant | MODIFIER | c.642+341delT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43643146 | |||||||
| chr17:43643173 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0077 a0001c0001t0002g0017 others(17): Show |
27 | HG00609.hp2 HG01943.hp1 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.642+315G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43643173 | |||||||
| chr17:43643184 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.642+304T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43643184 | |||||||
| chr17:43643262 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.642+226C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43643262 | |||||||
| chr17:43643484 | G | T | 5 | a0001c0001t0001g0218 a0001c0001t0002g0042 a0001c0001t0002g0196 others(2): Show |
6 | HG00639.hp1 HG00738.hp1 HG02273.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.642+4C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 2/2 | chr17 | 43643484 | |||||||
| chr17:43643834 | T | C | 44 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0099 others(41): Show |
53 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.470-174A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43643834 | |||||||
| chr17:43644001 | C | A | 1 | a0002c0002t0012g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.470-341G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644001 | |||||||
| chr17:43644008 | G | A | 1 | a0002c0002t0001g0247 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.470-348C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644008 | |||||||
| chr17:43644060 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.470-400A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644060 | |||||||
| chr17:43644078 | T | G | 1 | a0002c0002t0012g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.470-418A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644078 | |||||||
| chr17:43644084 | C | G | 93 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(90): Show |
126 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(123): Show |
intron_variant | MODIFIER | c.470-424G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644084 | |||||||
| chr17:43644269 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.470-609T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644269 | |||||||
| chr17:43644691 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.470-1031C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644691 | |||||||
| chr17:43644734 | C | T | 1 | a0002c0002t0001g0260 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.470-1074G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644734 | |||||||
| chr17:43644877 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.470-1217A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43644877 | |||||||
| chr17:43645059 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0009g0114 |
2 | HG02145.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.470-1399C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645059 | |||||||
| chr17:43645170 | TC | T | 23 | a0001c0005t0001g0051 a0002c0002t0001g0018 a0002c0002t0001g0019 others(20): Show |
30 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.470-1511delG | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645170 | |||||||
| chr17:43645171 | C | A | 4 | a0002c0002t0001g0238 a0002c0002t0001g0256 a0002c0002t0001g0259 others(1): Show |
4 | HG01243.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-1511G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645171 | |||||||
| chr17:43645171 | C | CT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0022 others(21): Show |
30 | HG00280.hp1 HG00544.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.470-1512dupA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645171 | |||||||
| chr17:43645171 | C | T | 1 | a0002c0002t0001g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.470-1511G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645171 | |||||||
| chr17:43645171 | CT | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(15): Show |
22 | HG01069.hp2 HG01169.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.470-1512delA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645171 | |||||||
| chr17:43645171 | CTT | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(10): Show |
14 | HG01358.hp1 HG02055.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.470-1513_470-1512d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645171 | |||||||
| chr17:43645171 | CTTT | C | 47 | a0001c0001t0001g0041 a0001c0001t0001g0192 a0001c0001t0001g0199 others(44): Show |
65 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.470-1514_470-1512d others(5): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645171 | |||||||
| chr17:43645172 | T | A | 23 | a0001c0005t0001g0051 a0002c0002t0001g0018 a0002c0002t0001g0019 others(20): Show |
30 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.470-1512A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645172 | |||||||
| chr17:43645173 | T | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0006g0048 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-1513A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645173 | |||||||
| chr17:43645174 | T | A | 1 | a0001c0005t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.470-1514A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645174 | |||||||
| chr17:43645175 | T | A | 3 | a0001c0001t0001g0093 a0001c0001t0006g0048 a0001c0005t0001g0052 |
3 | HG02615.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.470-1515A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645175 | |||||||
| chr17:43645176 | T | A | 1 | a0001c0005t0001g0051 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.470-1516A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645176 | |||||||
| chr17:43645177 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.470-1517A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645177 | |||||||
| chr17:43645199 | T | C | 1 | a0001c0001t0006g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.470-1539A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645199 | |||||||
| chr17:43645200 | G | A | 1 | a0001c0001t0006g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.470-1540C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645200 | |||||||
| chr17:43645219 | A | C | 1 | a0001c0001t0006g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.470-1559T>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645219 | |||||||
| chr17:43645306 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.470-1646T>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645306 | |||||||
| chr17:43645326 | G | A | 5 | a0001c0001t0003g0033 a0001c0001t0003g0189 a0001c0001t0003g0190 others(2): Show |
6 | HG02698.hp1 HG02738.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-1666C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645326 | |||||||
| chr17:43645433 | T | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG02055.hp1 HG02486.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-1773A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645433 | |||||||
| chr17:43645541 | G | A | 43 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0099 others(40): Show |
52 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.470-1881C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645541 | |||||||
| chr17:43645680 | A | G | 95 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(92): Show |
128 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(125): Show |
intron_variant | MODIFIER | c.470-2020T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645680 | |||||||
| chr17:43645760 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.470-2100G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645760 | |||||||
| chr17:43645805 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0102 |
4 | HG02486.hp1 HG03041.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-2145G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645805 | |||||||
| chr17:43645897 | T | G | 46 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0099 others(43): Show |
55 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.470-2237A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43645897 | |||||||
| chr17:43646186 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.470-2526G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646186 | |||||||
| chr17:43646233 | A | G | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.470-2573T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646233 | |||||||
| chr17:43646249 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(36): Show |
67 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.470-2589G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646249 | |||||||
| chr17:43646298 | G | A | 1 | a0002c0002t0001g0260 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.470-2638C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646298 | |||||||
| chr17:43646352 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.470-2692C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646352 | |||||||
| chr17:43646384 | C | G | 4 | a0001c0001t0002g0035 a0001c0001t0002g0207 a0001c0001t0002g0209 others(1): Show |
5 | HG00733.hp2 HG01256.hp2 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-2724G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646384 | |||||||
| chr17:43646500 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0116 |
4 | NA18961.hp1 NA18971.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-2840C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646500 | |||||||
| chr17:43646520 | C | T | 1 | a0002c0002t0012g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.470-2860G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646520 | |||||||
| chr17:43646613 | A | AAAAC | 177 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
246 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(243): Show |
intron_variant | MODIFIER | c.470-2954_470-2953i others(6): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646613 | |||||||
| chr17:43646676 | C | T | 8 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
9 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-3016G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646676 | |||||||
| chr17:43646759 | T | G | 1 | a0001c0001t0002g0202 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.470-3099A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646759 | |||||||
| chr17:43646788 | C | T | 50 | a0001c0001t0001g0041 a0001c0001t0001g0105 a0001c0001t0001g0192 others(47): Show |
74 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.470-3128G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646788 | |||||||
| chr17:43646793 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.470-3133A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646793 | |||||||
| chr17:43646901 | C | A | 44 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0099 others(41): Show |
53 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.470-3241G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646901 | |||||||
| chr17:43646943 | C | T | 13 | a0001c0001t0001g0041 a0001c0001t0002g0017 a0001c0001t0002g0034 others(10): Show |
19 | HG01943.hp1 HG01975.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.470-3283G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43646943 | |||||||
| chr17:43647142 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.470-3482C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647142 | |||||||
| chr17:43647142 | G | C | 1 | a0001c0001t0002g0220 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.470-3482C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647142 | |||||||
| chr17:43647290 | A | C | 95 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(92): Show |
128 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(125): Show |
intron_variant | MODIFIER | c.470-3630T>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647290 | |||||||
| chr17:43647301 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0148 |
2 | HG02257.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.470-3641C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647301 | |||||||
| chr17:43647422 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.470-3762G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647422 | |||||||
| chr17:43647440 | T | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
9 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-3780A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647440 | |||||||
| chr17:43647459 | T | C | 1 | a0002c0002t0012g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.470-3799A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647459 | |||||||
| chr17:43647665 | T | C | 94 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(91): Show |
127 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.470-4005A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647665 | |||||||
| chr17:43647841 | C | T | 4 | a0002c0002t0001g0235 a0002c0002t0001g0245 a0002c0002t0001g0246 others(1): Show |
4 | HG02486.hp2 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-4181G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647841 | |||||||
| chr17:43647901 | G | A | 44 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0099 others(41): Show |
53 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.470-4241C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647901 | |||||||
| chr17:43647944 | A | G | 1 | a0002c0002t0001g0243 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.470-4284T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647944 | |||||||
| chr17:43647991 | A | C | 1 | a0002c0002t0012g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.470-4331T>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43647991 | |||||||
| chr17:43648126 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
117 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.470-4466C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648126 | |||||||
| chr17:43648142 | G | C | 2 | a0002c0002t0001g0241 a0002c0002t0001g0255 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.470-4482C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648142 | |||||||
| chr17:43648193 | G | T | 50 | a0001c0001t0001g0041 a0001c0001t0001g0105 a0001c0001t0001g0192 others(47): Show |
74 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.470-4533C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648193 | |||||||
| chr17:43648241 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.470-4581C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648241 | |||||||
| chr17:43648281 | A | G | 4 | a0001c0001t0002g0039 a0001c0001t0002g0206 a0001c0001t0002g0213 others(1): Show |
5 | HG00609.hp2 NA18612.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-4621T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648281 | |||||||
| chr17:43648296 | C | T | 44 | a0001c0001t0001g0026 a0001c0001t0001g0093 a0001c0001t0001g0099 others(41): Show |
53 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(50): Show |
intron_variant | MODIFIER | c.470-4636G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648296 | |||||||
| chr17:43648400 | C | T | 1 | a0001c0004t0008g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.470-4740G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648400 | |||||||
| chr17:43648466 | C | CA | 8 | a0001c0001t0001g0029 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
9 | HG02071.hp2 HG02132.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-4807dupT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648466 | |||||||
| chr17:43648466 | CA | C | 94 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0041 others(91): Show |
127 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.470-4807delT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648466 | |||||||
| chr17:43648703 | A | T | 5 | a0001c0001t0003g0033 a0001c0001t0003g0189 a0001c0001t0003g0190 others(2): Show |
6 | HG02698.hp1 HG02738.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-5043T>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648703 | |||||||
| chr17:43648708 | C | A | 1 | a0001c0001t0003g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.470-5048G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648708 | |||||||
| chr17:43648763 | T | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0095 others(2): Show |
5 | HG00423.hp1 HG02080.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-5103A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648763 | |||||||
| chr17:43648764 | C | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0095 others(2): Show |
5 | HG00423.hp1 HG02080.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-5104G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648764 | |||||||
| chr17:43648783 | C | A | 1 | a0001c0001t0009g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.470-5123G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648783 | |||||||
| chr17:43648837 | C | A | 33 | a0001c0001t0001g0093 a0001c0001t0001g0173 a0001c0001t0006g0048 others(30): Show |
40 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.470-5177G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648837 | |||||||
| chr17:43648910 | T | G | 5 | a0002c0002t0001g0045 a0002c0002t0001g0237 a0002c0002t0001g0242 others(2): Show |
6 | HG01891.hp1 HG02615.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-5250A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648910 | |||||||
| chr17:43648941 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.470-5281G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648941 | |||||||
| chr17:43648957 | A | G | 94 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(91): Show |
127 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.470-5297T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43648957 | |||||||
| chr17:43649061 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.470-5401C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649061 | |||||||
| chr17:43649117 | G | C | 1 | a0001c0001t0001g0149 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.470-5457C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649117 | |||||||
| chr17:43649121 | A | G | 1 | a0002c0002t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.470-5461T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649121 | |||||||
| chr17:43649137 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.470-5477G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649137 | |||||||
| chr17:43649290 | C | CT | 28 | a0001c0001t0001g0012 a0001c0001t0001g0074 a0001c0001t0001g0089 others(25): Show |
33 | HG00280.hp1 HG00438.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.470-5631dupA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649290 | |||||||
| chr17:43649290 | C | CTTT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0057 others(10): Show |
20 | HG00280.hp2 HG00408.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.470-5633_470-5631d others(5): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649290 | |||||||
| chr17:43649290 | C | CTTTT | 11 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0069 others(8): Show |
12 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.470-5634_470-5631d others(6): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649290 | |||||||
| chr17:43649290 | CT | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(42): Show |
76 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.470-5631delA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649290 | |||||||
| chr17:43649290 | CTT | C | 27 | a0001c0001t0001g0093 a0001c0001t0001g0176 a0001c0001t0001g0184 others(24): Show |
32 | HG00741.hp2 HG01069.hp2 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.470-5632_470-5631d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649290 | |||||||
| chr17:43649290 | CTTT | C | 6 | a0001c0001t0006g0048 a0001c0001t0009g0114 a0001c0005t0001g0051 others(3): Show |
6 | HG02615.hp2 HG02895.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.470-5633_470-5631d others(5): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649290 | |||||||
| chr17:43649331 | T | G | 1 | a0001c0001t0004g0195 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.470-5671A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649331 | |||||||
| chr17:43649359 | T | C | 94 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(91): Show |
127 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.470-5699A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649359 | |||||||
| chr17:43649375 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.470-5715G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649375 | |||||||
| chr17:43649522 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0178 a0001c0001t0001g0185 |
5 | HG02083.hp1 HG03831.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.470-5862C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649522 | |||||||
| chr17:43649549 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.470-5889G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649549 | |||||||
| chr17:43649559 | G | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
9 | HG02055.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-5899C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649559 | |||||||
| chr17:43649600 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.470-5940G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649600 | |||||||
| chr17:43649623 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
118 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.470-5963G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649623 | |||||||
| chr17:43649737 | C | T | 2 | a0002c0002t0001g0019 a0002c0002t0001g0258 |
4 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.470-6077G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649737 | |||||||
| chr17:43649776 | A | G | 94 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(91): Show |
127 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.470-6116T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649776 | |||||||
| chr17:43649848 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0104 a0001c0001t0001g0122 others(4): Show |
8 | HG00639.hp2 HG01074.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-6188G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43649848 | |||||||
| chr17:43650099 | T | C | 94 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(91): Show |
127 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.470-6439A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650099 | |||||||
| chr17:43650212 | A | AAAGTAGA others(2): Show |
50 | a0001c0001t0001g0041 a0001c0001t0001g0105 a0001c0001t0001g0192 others(47): Show |
74 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.470-6561_470-6553d others(11): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650212 | |||||||
| chr17:43650365 | C | T | 50 | a0001c0001t0001g0041 a0001c0001t0001g0105 a0001c0001t0001g0192 others(47): Show |
74 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.470-6705G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650365 | |||||||
| chr17:43650527 | G | T | 1 | a0001c0001t0001g0115 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.470-6867C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650527 | |||||||
| chr17:43650556 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
114 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.470-6896C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650556 | |||||||
| chr17:43650567 | A | G | 1 | a0001c0004t0001g0231 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.470-6907T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650567 | |||||||
| chr17:43650574 | T | C | 1 | a0001c0001t0009g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.470-6914A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650574 | |||||||
| chr17:43650619 | G | A | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.470-6959C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650619 | |||||||
| chr17:43650681 | G | A | 94 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0093 others(91): Show |
127 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.470-7021C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650681 | |||||||
| chr17:43650862 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.470-7202C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650862 | |||||||
| chr17:43650879 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.470-7219T>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43650879 | |||||||
| chr17:43651029 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.470-7369C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651029 | |||||||
| chr17:43651044 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.470-7384G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651044 | |||||||
| chr17:43651046 | C | A | 1 | a0001c0001t0006g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.470-7386G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651046 | |||||||
| chr17:43651089 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.470-7429G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651089 | |||||||
| chr17:43651175 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.470-7515G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651175 | |||||||
| chr17:43651254 | G | T | 2 | a0001c0005t0001g0051 a0001c0005t0001g0052 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.470-7594C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651254 | |||||||
| chr17:43651297 | C | T | 49 | a0001c0001t0001g0041 a0001c0001t0001g0142 a0001c0001t0001g0192 others(46): Show |
73 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.470-7637G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651297 | |||||||
| chr17:43651399 | C | T | 1 | a0002c0002t0012g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.470-7739G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651399 | |||||||
| chr17:43651482 | G | A | 1 | a0001c0001t0009g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.470-7822C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651482 | |||||||
| chr17:43651513 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.470-7853G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651513 | |||||||
| chr17:43651552 | G | A | 1 | a0001c0001t0002g0202 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.470-7892C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651552 | |||||||
| chr17:43651552 | G | GA | 93 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0099 others(90): Show |
126 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(123): Show |
intron_variant | MODIFIER | c.470-7893dupT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651552 | |||||||
| chr17:43651583 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0112 |
3 | HG01099.hp1 HG01192.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.470-7923C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651583 | |||||||
| chr17:43651611 | T | C | 3 | a0001c0001t0001g0187 a0001c0001t0002g0186 a0001c0001t0002g0197 |
3 | HG00408.hp2 HG02083.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.470-7951A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651611 | |||||||
| chr17:43651700 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.470-8040G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651700 | |||||||
| chr17:43651780 | T | C | 4 | a0002c0002t0001g0235 a0002c0002t0001g0245 a0002c0002t0001g0246 others(1): Show |
4 | HG02486.hp2 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-8120A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651780 | |||||||
| chr17:43651789 | G | A | 93 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0099 others(90): Show |
126 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(123): Show |
intron_variant | MODIFIER | c.470-8129C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651789 | |||||||
| chr17:43651859 | T | G | 43 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(40): Show |
52 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.470-8199A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651859 | |||||||
| chr17:43651892 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.470-8232A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651892 | |||||||
| chr17:43651931 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(36): Show |
67 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.470-8271G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651931 | |||||||
| chr17:43651943 | A | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | NA18952.hp1 NA18970.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.470-8283T>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43651943 | |||||||
| chr17:43652003 | G | A | 1 | a0001c0001t0004g0195 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.470-8343C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652003 | |||||||
| chr17:43652009 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00609.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.470-8349G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652009 | |||||||
| chr17:43652116 | A | G | 5 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
6 | HG02055.hp1 HG02486.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-8456T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652116 | |||||||
| chr17:43652240 | G | T | 96 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0099 others(93): Show |
130 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(127): Show |
intron_variant | MODIFIER | c.470-8580C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652240 | |||||||
| chr17:43652249 | C | T | 1 | a0002c0002t0001g0236 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.470-8589G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652249 | |||||||
| chr17:43652785 | T | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0063 a0001c0001t0001g0099 others(8): Show |
13 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.469+8281A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652785 | |||||||
| chr17:43652817 | T | C | 16 | a0001c0001t0001g0064 a0001c0005t0001g0051 a0001c0005t0001g0052 others(13): Show |
20 | HG01884.hp1 HG02004.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.469+8249A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652817 | |||||||
| chr17:43652825 | C | CT | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(41): Show |
72 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.469+8240dupA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652825 | |||||||
| chr17:43652825 | C | CTT | 13 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0081 others(10): Show |
16 | HG00621.hp1 HG01517.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.469+8239_469+8240d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652825 | |||||||
| chr17:43652825 | CT | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
118 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.469+8240delA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652825 | |||||||
| chr17:43652825 | CTT | C | 41 | a0001c0001t0001g0041 a0001c0001t0001g0100 a0001c0001t0001g0105 others(38): Show |
63 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.469+8239_469+8240d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652825 | |||||||
| chr17:43652825 | CTTT | C | 15 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0102 others(12): Show |
18 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.469+8238_469+8240d others(5): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652825 | |||||||
| chr17:43652828 | T | A | 11 | a0002c0002t0001g0018 a0002c0002t0001g0043 a0002c0002t0001g0044 others(8): Show |
15 | HG01884.hp1 HG02004.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.469+8238A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652828 | |||||||
| chr17:43652830 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.469+8236A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652830 | |||||||
| chr17:43652831 | T | A | 4 | a0001c0001t0001g0173 a0001c0001t0006g0048 a0001c0005t0001g0051 others(1): Show |
4 | HG02615.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+8235A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652831 | |||||||
| chr17:43652855 | G | A | 1 | a0002c0002t0001g0240 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.469+8211C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43652855 | |||||||
| chr17:43653010 | T | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
128 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.469+8056A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653010 | |||||||
| chr17:43653034 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.469+8032C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653034 | |||||||
| chr17:43653067 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.469+7999G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653067 | |||||||
| chr17:43653081 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469+7985G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653081 | |||||||
| chr17:43653141 | C | CT | 63 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0061 others(60): Show |
90 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.469+7924dupA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653141 | |||||||
| chr17:43653166 | A | C | 1 | a0001c0001t0009g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.469+7900T>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653166 | |||||||
| chr17:43653211 | C | T | 1 | a0002c0002t0012g0257 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.469+7855G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653211 | |||||||
| chr17:43653242 | C | T | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+7824G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653242 | |||||||
| chr17:43653247 | T | C | 1 | a0001c0001t0015g0264 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.469+7819A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653247 | |||||||
| chr17:43653267 | T | G | 62 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0099 others(59): Show |
88 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.469+7799A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653267 | |||||||
| chr17:43653271 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.469+7795G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653271 | |||||||
| chr17:43653296 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.469+7770G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653296 | |||||||
| chr17:43653376 | G | C | 1 | a0001c0001t0003g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.469+7690C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653376 | |||||||
| chr17:43653391 | T | C | 97 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0099 others(94): Show |
131 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(128): Show |
intron_variant | MODIFIER | c.469+7675A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653391 | |||||||
| chr17:43653430 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.469+7636C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653430 | |||||||
| chr17:43653511 | C | CT | 10 | a0001c0001t0001g0098 a0001c0001t0001g0108 a0001c0001t0001g0118 others(7): Show |
10 | HG00280.hp1 HG01192.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.469+7554dupA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653511 | |||||||
| chr17:43653511 | CTTT | C | 60 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0099 others(57): Show |
86 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.469+7552_469+7554d others(5): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653511 | |||||||
| chr17:43653571 | T | C | 62 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0099 others(59): Show |
88 | HG00609.hp2 HG00639.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.469+7495A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653571 | |||||||
| chr17:43653733 | T | C | 40 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0008g0233 others(37): Show |
48 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.469+7333A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653733 | |||||||
| chr17:43653760 | G | A | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+7306C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653760 | |||||||
| chr17:43653798 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(35): Show |
52 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.469+7268C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653798 | |||||||
| chr17:43653803 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
11 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.469+7263G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653803 | |||||||
| chr17:43653851 | G | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(2): Show |
6 | HG02055.hp1 HG02486.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+7215C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653851 | |||||||
| chr17:43653904 | G | C | 1 | a0001c0001t0001g0065 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.469+7162C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653904 | |||||||
| chr17:43653979 | A | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(77): Show |
116 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.469+7087T>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43653979 | |||||||
| chr17:43654021 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.469+7045C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654021 | |||||||
| chr17:43654088 | C | A | 1 | a0001c0001t0001g0194 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.469+6978G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654088 | |||||||
| chr17:43654280 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.469+6786C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654280 | |||||||
| chr17:43654306 | C | T | 3 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0008g0233 |
3 | HG03130.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.469+6760G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654306 | |||||||
| chr17:43654456 | C | T | 1 | a0002c0002t0001g0258 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.469+6610G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654456 | |||||||
| chr17:43654586 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0097 others(1): Show |
4 | HG00408.hp1 HG00438.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+6480G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654586 | |||||||
| chr17:43654602 | T | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
11 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.469+6464A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654602 | |||||||
| chr17:43654642 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.469+6424C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654642 | |||||||
| chr17:43654778 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(176): Show |
249 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(246): Show |
intron_variant | MODIFIER | c.469+6288A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654778 | |||||||
| chr17:43654879 | C | T | 1 | a0001c0001t0009g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.469+6187G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654879 | |||||||
| chr17:43654880 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(4): Show |
9 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.469+6186C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654880 | |||||||
| chr17:43654940 | T | C | 3 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0008g0233 |
3 | HG03130.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.469+6126A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654940 | |||||||
| chr17:43654945 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.469+6121C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654945 | |||||||
| chr17:43654960 | G | A | 4 | a0002c0002t0001g0235 a0002c0002t0001g0245 a0002c0002t0001g0246 others(1): Show |
4 | HG02486.hp2 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.469+6106C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654960 | |||||||
| chr17:43654976 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.469+6090G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43654976 | |||||||
| chr17:43655145 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.469+5921C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655145 | |||||||
| chr17:43655199 | A | G | 2 | a0001c0005t0001g0051 a0001c0005t0001g0052 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.469+5867T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655199 | |||||||
| chr17:43655327 | T | C | 26 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0022 others(23): Show |
34 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.469+5739A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655327 | |||||||
| chr17:43655395 | C | T | 1 | a0001c0001t0002g0213 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.469+5671G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655395 | |||||||
| chr17:43655512 | A | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA18959.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.469+5554T>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655512 | |||||||
| chr17:43655550 | A | T | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+5516T>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655550 | |||||||
| chr17:43655551 | T | C | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+5515A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655551 | |||||||
| chr17:43655660 | T | TA | 21 | a0001c0001t0001g0026 a0001c0001t0001g0092 a0001c0001t0001g0192 others(18): Show |
22 | HG00609.hp2 HG00741.hp1 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.469+5405dupT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655660 | |||||||
| chr17:43655660 | TA | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(109): Show |
172 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.469+5405delT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655660 | |||||||
| chr17:43655660 | TAA | T | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0009 others(32): Show |
47 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.469+5404_469+5405d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655660 | |||||||
| chr17:43655660 | TAAAAAAA others(5): Show |
T | 1 | a0003c0007t0013g0120 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.469+5394_469+5405d others(14): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655660 | |||||||
| chr17:43655743 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.469+5323C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655743 | |||||||
| chr17:43655747 | C | A | 44 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(41): Show |
54 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.469+5319G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655747 | |||||||
| chr17:43655897 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0006g0048 a0001c0001t0009g0114 |
3 | HG02145.hp1 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.469+5169C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43655897 | |||||||
| chr17:43656222 | G | A | 3 | a0001c0004t0001g0231 a0001c0004t0001g0232 a0001c0004t0008g0233 |
3 | HG03130.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.469+4844C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656222 | |||||||
| chr17:43656313 | CA | C | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+4752delT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656313 | |||||||
| chr17:43656326 | G | C | 2 | a0001c0005t0001g0051 a0001c0005t0001g0052 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.469+4740C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656326 | |||||||
| chr17:43656371 | G | C | 2 | a0001c0005t0001g0051 a0001c0005t0001g0052 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.469+4695C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656371 | |||||||
| chr17:43656758 | C | T | 35 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0043 others(32): Show |
43 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.469+4308G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656758 | |||||||
| chr17:43656768 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
247 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(244): Show |
intron_variant | MODIFIER | c.469+4298A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656768 | |||||||
| chr17:43656799 | A | G | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+4267T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656799 | |||||||
| chr17:43656919 | T | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.469+4147A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656919 | |||||||
| chr17:43656920 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.469+4146G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656920 | |||||||
| chr17:43656972 | C | T | 35 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0043 others(32): Show |
43 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.469+4094G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656972 | |||||||
| chr17:43656981 | A | ATTTTCTT others(7): Show |
1 | a0001c0001t0001g0119 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.469+4071_469+4084d others(16): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656981 | |||||||
| chr17:43656981 | ATTTTCTT others(7): Show |
A | 1 | a0002c0002t0001g0234 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.469+4071_469+4084d others(16): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656981 | |||||||
| chr17:43656996 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.469+4070A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656996 | |||||||
| chr17:43656996 | TTTTCTTT others(11): Show |
T | 2 | a0001c0001t0001g0173 a0001c0005t0001g0051 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.469+4052_469+4069d others(20): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656996 | |||||||
| chr17:43656998 | T | C | 2 | a0002c0002t0001g0043 a0002c0002t0001g0260 |
3 | HG02004.hp2 HG03490.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.469+4068A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656998 | |||||||
| chr17:43656998 | TTCTTTCT others(7): Show |
T | 1 | a0001c0005t0001g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.469+4054_469+4067d others(16): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43656998 | |||||||
| chr17:43657002 | TTCTTTCT others(3): Show |
T | 5 | a0001c0001t0001g0026 a0002c0002t0001g0045 a0002c0002t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+4054_469+4063d others(12): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657002 | |||||||
| chr17:43657006 | TTCTTTC | T | 6 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0009g0114 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+4054_469+4059d others(8): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657006 | |||||||
| chr17:43657010 | T | TCTCTTTC others(12): Show |
1 | a0001c0001t0001g0002 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.469+4055_469+4056i others(21): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657010 | |||||||
| chr17:43657010 | TTC | T | 22 | a0001c0001t0001g0099 a0001c0001t0001g0102 a0001c0001t0001g0172 others(19): Show |
22 | HG00741.hp2 HG01243.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.469+4054_469+4055d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657010 | |||||||
| chr17:43657012 | C | CTCTT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.469+4050_469+4053d others(6): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTCTT others(8): Show |
1 | a0001c0001t0003g0189 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.469+4053_469+4054i others(17): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTCTT others(12): Show |
1 | a0001c0001t0001g0092 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.469+4053_469+4054i others(21): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTCTT others(16): Show |
1 | a0001c0001t0001g0134 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.469+4053_469+4054i others(25): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTTCT others(1): Show |
58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(55): Show |
71 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.469+4046_469+4053d others(10): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTTCT others(5): Show |
46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(43): Show |
62 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.469+4042_469+4053d others(14): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTTCT others(9): Show |
26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(23): Show |
31 | HG00280.hp1 HG00558.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.469+4038_469+4053d others(18): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTTCT others(13): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG00544.hp2 HG00621.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.469+4034_469+4053d others(22): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTTCT others(17): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0142 a0001c0003t0001g0020 |
3 | HG02559.hp1 NA18952.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.469+4030_469+4053d others(26): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTCTTTCT others(21): Show |
1 | a0001c0001t0001g0108 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.469+4026_469+4053d others(30): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTT | 9 | a0001c0001t0001g0026 a0001c0001t0005g0047 a0002c0002t0001g0019 others(6): Show |
10 | HG02004.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+4053_469+4054i others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTTTCTT | 9 | a0001c0001t0005g0047 a0002c0002t0001g0018 a0002c0002t0001g0019 others(6): Show |
10 | HG02451.hp1 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+4053_469+4054i others(8): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTTTCTTT others(3): Show |
1 | a0001c0001t0001g0105 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.469+4053_469+4054i others(12): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | CTTTCTTT others(11): Show |
1 | a0001c0001t0015g0264 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.469+4053_469+4054i others(20): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.469+4054G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | CTCTT | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0058 others(5): Show |
10 | HG02040.hp2 HG02132.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.469+4050_469+4053d others(6): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657012 | CTCTTTCT others(5): Show |
C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0074 |
2 | HG00423.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.469+4042_469+4053d others(14): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657012 | |||||||
| chr17:43657016 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.469+4050A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657016 | |||||||
| chr17:43657036 | TTC | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0069 a0001c0001t0001g0070 |
5 | HG00642.hp1 HG02683.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+4028_469+4029d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657036 | |||||||
| chr17:43657047 | T | TTTCTTTC others(20): Show |
1 | a0001c0001t0001g0198 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.469+4018_469+4019i others(29): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657047 | |||||||
| chr17:43657055 | T | TTTCTTTC others(5): Show |
1 | a0001c0001t0004g0195 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.469+4010_469+4011i others(14): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657055 | |||||||
| chr17:43657055 | T | TTTCTTTC others(8): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0194 |
2 | NA18981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.469+4010_469+4011i others(17): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657055 | |||||||
| chr17:43657055 | T | TTTCTTTC others(9): Show |
1 | a0001c0004t0008g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.469+4010_469+4011i others(18): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657055 | |||||||
| chr17:43657058 | C | CTTTCTTT others(11): Show |
1 | a0001c0001t0001g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.469+4007_469+4008i others(20): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657058 | |||||||
| chr17:43657059 | C | T | 62 | a0001c0001t0001g0041 a0001c0001t0001g0100 a0001c0001t0001g0107 others(59): Show |
90 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(87): Show |
intron_variant | MODIFIER | c.469+4007G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657059 | |||||||
| chr17:43657063 | C | T | 2 | a0002c0002t0001g0239 a0002c0002t0001g0240 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.469+4003G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657063 | |||||||
| chr17:43657063 | CTTCCTTC others(1): Show |
C | 4 | a0002c0002t0001g0046 a0002c0002t0001g0253 a0002c0002t0001g0254 others(1): Show |
5 | HG00741.hp2 HG02145.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+3995_469+4002d others(10): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657063 | |||||||
| chr17:43657067 | CTTCT | C | 11 | a0002c0002t0001g0045 a0002c0002t0001g0241 a0002c0002t0001g0247 others(8): Show |
12 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.469+3995_469+3998d others(6): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657067 | |||||||
| chr17:43657071 | T | C | 54 | a0001c0001t0001g0041 a0001c0001t0001g0199 a0001c0001t0001g0218 others(51): Show |
81 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.469+3995A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657071 | |||||||
| chr17:43657075 | T | C | 1 | a0002c0002t0001g0256 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.469+3991A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657075 | |||||||
| chr17:43657079 | TTTTC | T | 9 | a0001c0001t0002g0035 a0001c0001t0002g0037 a0001c0001t0002g0206 others(6): Show |
11 | HG00733.hp2 HG01074.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.469+3983_469+3986d others(6): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657079 | |||||||
| chr17:43657082 | T | C | 35 | a0001c0001t0001g0041 a0001c0001t0001g0199 a0001c0001t0001g0218 others(32): Show |
56 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.469+3984A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657082 | |||||||
| chr17:43657083 | C | T | 35 | a0001c0001t0001g0041 a0001c0001t0001g0199 a0001c0001t0001g0218 others(32): Show |
56 | HG00609.hp2 HG00639.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.469+3983G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657083 | |||||||
| chr17:43657099 | TTC | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0116 |
4 | NA18961.hp1 NA18971.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+3965_469+3966d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657099 | |||||||
| chr17:43657119 | CTCCT | C | 8 | a0001c0001t0001g0105 a0001c0001t0001g0160 a0001c0001t0001g0161 others(5): Show |
8 | HG02145.hp1 HG02895.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.469+3943_469+3946d others(6): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657119 | |||||||
| chr17:43657166 | CTTTCTT | C | 29 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0043 others(26): Show |
37 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.469+3894_469+3899d others(8): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657166 | |||||||
| chr17:43657170 | C | CT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(75): Show |
112 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.469+3895dupA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657170 | |||||||
| chr17:43657170 | CT | C | 117 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
175 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.469+3895delA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657170 | |||||||
| chr17:43657170 | CTTT | C | 9 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
11 | HG02055.hp1 HG02486.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.469+3893_469+3895d others(5): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657170 | |||||||
| chr17:43657182 | T | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.469+3884A>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657182 | |||||||
| chr17:43657317 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.469+3749C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657317 | |||||||
| chr17:43657340 | AT | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
236 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.469+3725delA | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657340 | |||||||
| chr17:43657340 | ATT | A | 42 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(39): Show |
50 | HG00741.hp2 HG01070.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.469+3724_469+3725d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657340 | |||||||
| chr17:43657367 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.469+3699T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657367 | |||||||
| chr17:43657456 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.469+3610C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657456 | |||||||
| chr17:43657588 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0006g0048 a0001c0001t0009g0114 |
3 | HG02145.hp1 HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.469+3478C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657588 | |||||||
| chr17:43657752 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
301 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(298): Show |
intron_variant | MODIFIER | c.469+3314A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657752 | |||||||
| chr17:43657933 | A | G | 34 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0043 others(31): Show |
42 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.469+3133T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657933 | |||||||
| chr17:43657979 | G | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(196): Show |
290 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(287): Show |
intron_variant | MODIFIER | c.469+3087C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43657979 | |||||||
| chr17:43658156 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.469+2910G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658156 | |||||||
| chr17:43658168 | T | C | 2 | a0001c0005t0001g0051 a0001c0005t0001g0052 |
2 | HG02615.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.469+2898A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658168 | |||||||
| chr17:43658217 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.469+2849A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658217 | |||||||
| chr17:43658240 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA18959.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.469+2826C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658240 | |||||||
| chr17:43658325 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(156): Show |
242 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.469+2741C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658325 | |||||||
| chr17:43658336 | G | A | 1 | a0001c0001t0009g0114 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.469+2730C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658336 | |||||||
| chr17:43658345 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.469+2721T>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658345 | |||||||
| chr17:43658370 | G | C | 1 | a0001c0001t0002g0228 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.469+2696C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658370 | |||||||
| chr17:43658379 | C | T | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+2687G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658379 | |||||||
| chr17:43658442 | G | A | 3 | a0002c0002t0001g0019 a0002c0002t0001g0258 a0002c0002t0001g0259 |
5 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+2624C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658442 | |||||||
| chr17:43658506 | C | CA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
114 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.469+2559dupT | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658506 | |||||||
| chr17:43658506 | C | CAA | 37 | a0001c0001t0001g0041 a0001c0001t0001g0170 a0001c0001t0001g0171 others(34): Show |
58 | HG00609.hp2 HG00733.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.469+2558_469+2559d others(4): Show |
MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658506 | |||||||
| chr17:43658642 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.469+2424C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658642 | |||||||
| chr17:43658695 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.469+2371A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658695 | |||||||
| chr17:43658943 | C | A | 35 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0043 others(32): Show |
43 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.469+2123G>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43658943 | |||||||
| chr17:43659282 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.469+1784A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659282 | |||||||
| chr17:43659361 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0098 |
3 | HG01081.hp2 HG01361.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.469+1705A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659361 | |||||||
| chr17:43659420 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.469+1646A>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659420 | |||||||
| chr17:43659491 | A | T | 1 | a0002c0002t0001g0234 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.469+1575T>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659491 | |||||||
| chr17:43659503 | G | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0099 |
3 | HG02486.hp1 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.469+1563C>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659503 | |||||||
| chr17:43659516 | G | C | 2 | a0001c0001t0005g0047 a0001c0001t0015g0264 |
3 | HG02559.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.469+1550C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659516 | |||||||
| chr17:43659525 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.469+1541C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659525 | |||||||
| chr17:43659784 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.469+1282G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659784 | |||||||
| chr17:43659942 | G | A | 35 | a0002c0002t0001g0018 a0002c0002t0001g0019 a0002c0002t0001g0043 others(32): Show |
43 | HG00741.hp2 HG01243.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.469+1124C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659942 | |||||||
| chr17:43659991 | T | C | 1 | a0002c0002t0001g0260 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469+1075A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43659991 | |||||||
| chr17:43660077 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.469+989G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43660077 | |||||||
| chr17:43660153 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.469+913C>T | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43660153 | |||||||
| chr17:43660395 | G | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
123 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.469+671C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43660395 | |||||||
| chr17:43660664 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.469+402G>A | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43660664 | |||||||
| chr17:43660719 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(205): Show |
301 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(298): Show |
intron_variant | MODIFIER | c.469+347C>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43660719 | |||||||
| chr17:43660848 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(197): Show |
291 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(288): Show |
intron_variant | MODIFIER | c.469+218A>G | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43660848 | |||||||
| chr17:43660968 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.469+98G>C | MEOX1 | ENSG00000005102.14 | transcript | ENST00000318579.9 | protein_coding | 1/2 | chr17 | 43660968 |