Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4841 |
| ensemblid | ENSG00000147140.17 |
| hgncid | 7871 |
| symbol | NONO |
| name | non-POU domain containing octamer binding |
| refseq_nuc | NM_007363.5 |
| refseq_prot | NP_031389.3 |
| ensembl_nuc | ENST00000276079.13 |
| ensembl_prot | ENSP00000276079.8 |
| mane_status | MANE Select |
| chr | chrX |
| start | 71283635 |
| end | 71301168 |
| strand | + |
| ver | v1.2 |
| region | chrX:71283635-71301168 |
| region5000 | chrX:71278635-71306168 |
| regionname0 | NONO_chrX_71283635_71301168 |
| regionname5000 | NONO_chrX_71278635_71306168 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 471 | 225 | 55 | 42 | 93 | 7 | 28 | 64 | NONO_chrX_71278635_71306168 | NONO | MQSNK others(466): Show |
chrX | 71278635 | 71306168 |
| a0002 | 0/0 | 471 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | MQSNK others(466): Show |
chrX | 71278635 | 71306168 |
| a0003 | 0/0 | 471 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | MQSNK others(466): Show |
chrX | 71278635 | 71306168 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1413 | 215 | 47 | 42 | 92 | 7 | 27 | NONO_chrX_71278635_71306168 | NONO | ATGCA others(1408): Show |
chrX | 71278635 | 71306168 | ||
| a0001c0002 | 0/0 | 1413 | 8 | 8 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | ATGCA others(1408): Show |
chrX | 71278635 | 71306168 | ||
| a0001c0004 | 0/0 | 1413 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | ATGCA others(1408): Show |
chrX | 71278635 | 71306168 | ||
| a0001c0005 | 0/0 | 1413 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | ATGCA others(1408): Show |
chrX | 71278635 | 71306168 | ||
| a0002c0003 | 0/0 | 1413 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | ATGCA others(1408): Show |
chrX | 71278635 | 71306168 | ||
| a0003c0006 | 0/0 | 1413 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | ATGCA others(1408): Show |
chrX | 71278635 | 71306168 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2661 | 123 | 46 | 20 | 38 | 7 | 12 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0002 | 0/0 | 2662 | 42 | 1 | 13 | 19 | 0 | 9 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2657): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0003 | 0/0 | 2661 | 37 | 0 | 5 | 26 | 0 | 6 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0004 | 0/0 | 2662 | 3 | 0 | 3 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2657): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0005 | 0/0 | 2661 | 2 | 0 | 1 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0006 | 0/0 | 2662 | 2 | 0 | 0 | 2 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2657): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0007 | 0/0 | 2663 | 2 | 0 | 0 | 2 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2658): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0008 | 0/0 | 2660 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2655): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0009 | 0/0 | 2661 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0010 | 0/0 | 2661 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0001c0001t0011 | 0/0 | 2662 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2657): Show |
chrX | 71278635 | 71306168 |
| a0001c0002t0001 | 0/0 | 2661 | 4 | 4 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0001c0002t0002 | 0/0 | 2662 | 3 | 3 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2657): Show |
chrX | 71278635 | 71306168 |
| a0001c0002t0012 | 0/0 | 2662 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2657): Show |
chrX | 71278635 | 71306168 |
| a0001c0004t0001 | 0/0 | 2661 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0001c0005t0001 | 0/0 | 2661 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0002c0003t0001 | 0/0 | 2661 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| a0003c0006t0001 | 0/0 | 2661 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | GTTTC others(2656): Show |
chrX | 71278635 | 71306168 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 45 | 10 | 10 | 19 | 4 | 2 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0001 | 0/0 | 15 | 0 | 4 | 8 | 0 | 3 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0001 | 0/0 | 22 | 0 | 2 | 18 | 0 | 2 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0005g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0002t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0001c0005t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0002c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| a0003c0006t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | FIN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00408 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0074 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01981 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0088 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02135 | hp1 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02145 | hp1 | a0003 | c0006 | t0001 | g0007 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CDX | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CDX | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02280 | hp1 | a0001 | c0002 | t0012 | g0091 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02523 | hp2 | a0001 | c0001 | t0009 | g0016 | EAS | KHV | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03704 | hp2 | a0001 | c0005 | t0001 | g0003 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CHB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18943 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18986 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19006 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | LWK | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | LWK | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19058 | hp1 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19072 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | NONO_chrX_71278635_71306168 | NONO | chrX | 71278635 | 71306168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71290753 | C | T | 1 | a0003 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.116C>T | p.Pro39Leu | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/12 | 269/2661 | 116/1416 | 39/471 | chrX | 71290753 | |||
| chrX:71298714 | G | T | 1 | a0002 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.1179G>T | p.Met393Ile | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/12 | 1332/2661 | 1179/1416 | 393/471 | chrX | 71298714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71294241 | A | G | 1 | a0001c0002 | 8 | HG02055.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
synonymous_variant | LOW | c.363A>G | p.Leu121Leu | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/12 | 516/2661 | 363/1416 | 121/471 | chrX | 71294241 | |||
| chrX:71296580 | G | T | 1 | a0001c0005 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.666G>T | p.Val222Val | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 6/12 | 819/2661 | 666/1416 | 222/471 | chrX | 71296580 | |||
| chrX:71296962 | C | T | 1 | a0001c0004 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.858C>T | p.Asp286Asp | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 7/12 | 1011/2661 | 858/1416 | 286/471 | chrX | 71296962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71300203 | C | T | 1 | a0001c0002t0012 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*127C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 127 | chrX | 71300203 | ||||||
| chrX:71300387 | G | GT | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(3): Show |
52 | HG00597.hp1 HG00609.hp1 HG01109.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*325dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 326 | INFO_REALIGN_3_PRIME | chrX | 71300387 | |||||
| chrX:71300387 | G | GTT | 1 | a0001c0001t0007 | 2 | HG00438.hp1 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*324_*325dupTT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 326 | INFO_REALIGN_3_PRIME | chrX | 71300387 | |||||
| chrX:71300387 | GT | G | 1 | a0001c0001t0008 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325delT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 325 | INFO_REALIGN_3_PRIME | chrX | 71300387 | |||||
| chrX:71300410 | T | C | 1 | a0001c0001t0004 | 3 | HG01109.hp1 HG01943.hp1 HG01981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*334T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 334 | chrX | 71300410 | ||||||
| chrX:71300455 | C | T | 1 | a0001c0001t0005 | 2 | HG01993.hp1 NA19072.hp1 |
3_prime_UTR_variant | MODIFIER | c.*379C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 379 | chrX | 71300455 | ||||||
| chrX:71300490 | C | T | 2 | a0001c0001t0003 a0001c0001t0006 |
39 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 414 | chrX | 71300490 | ||||||
| chrX:71300779 | T | C | 1 | a0001c0001t0009 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*703T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 703 | chrX | 71300779 | ||||||
| chrX:71301064 | T | C | 1 | a0001c0001t0010 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*988T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 988 | chrX | 71301064 | ||||||
| chrX:71301104 | G | A | 1 | a0001c0001t0011 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1028G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 12/12 | 1028 | chrX | 71301104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:71284634 | C | T | 1 | a0001c0001t0003g0025 | 2 | HG02602.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-10+181C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71284634 | |||||||
| chrX:71284642 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-10+189A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71284642 | |||||||
| chrX:71285340 | C | CT | 1 | a0001c0002t0002g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10+894dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71285340 | ||||||
| chrX:71285347 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-10+894T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71285347 | |||||||
| chrX:71285423 | T | G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+970T>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71285423 | |||||||
| chrX:71285438 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0026 others(14): Show |
22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-10+985C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71285438 | |||||||
| chrX:71285495 | T | TG | 1 | a0001c0002t0002g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10+1044dupG | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71285495 | ||||||
| chrX:71285623 | T | TG | 1 | a0001c0002t0002g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10+1172dupG | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71285623 | ||||||
| chrX:71285787 | T | TC | 1 | a0001c0002t0002g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10+1336dupC | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71285787 | ||||||
| chrX:71285829 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-10+1376T>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71285829 | |||||||
| chrX:71285965 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0007g0012 |
2 | HG02083.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-10+1512G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71285965 | |||||||
| chrX:71286658 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-10+2205A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71286658 | |||||||
| chrX:71286682 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-10+2229G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71286682 | |||||||
| chrX:71287333 | G | T | 1 | a0001c0001t0002g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-10+2880G>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71287333 | |||||||
| chrX:71287416 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-10+2963C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71287416 | |||||||
| chrX:71287821 | C | G | 1 | a0001c0002t0002g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-9-2808C>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71287821 | |||||||
| chrX:71287865 | C | CT | 13 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0079 others(10): Show |
16 | HG01081.hp1 HG01255.hp1 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-2744dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71287865 | ||||||
| chrX:71287865 | CT | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
9 | HG00735.hp1 HG02129.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9-2744delT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71287865 | ||||||
| chrX:71287865 | CTT | C | 7 | a0001c0001t0001g0026 a0001c0002t0001g0024 a0001c0002t0001g0089 others(4): Show |
8 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9-2745_-9-2744del others(2): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71287865 | ||||||
| chrX:71287865 | CTTT | C | 1 | a0001c0002t0001g0087 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9-2746_-9-2744del others(3): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71287865 | ||||||
| chrX:71287885 | T | A | 7 | a0001c0002t0001g0024 a0001c0002t0001g0087 a0001c0002t0001g0089 others(4): Show |
8 | HG02055.hp1 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-2744T>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71287885 | |||||||
| chrX:71288008 | A | AT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0072 others(8): Show |
15 | HG01175.hp1 HG02015.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-2602dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288008 | ||||||
| chrX:71288008 | AT | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(10): Show |
15 | HG01255.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-2602delT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288008 | ||||||
| chrX:71288008 | ATT | A | 5 | a0001c0002t0001g0024 a0001c0002t0001g0087 a0001c0002t0001g0089 others(2): Show |
6 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-2603_-9-2602del others(2): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288008 | ||||||
| chrX:71288008 | ATTT | A | 1 | a0001c0002t0002g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9-2604_-9-2602del others(3): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288008 | ||||||
| chrX:71288042 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
7 | HG01255.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-2587G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71288042 | |||||||
| chrX:71288062 | C | G | 1 | a0001c0001t0002g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-9-2567C>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71288062 | |||||||
| chrX:71288119 | C | CT | 91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
197 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.-9-2489dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288119 | ||||||
| chrX:71288119 | C | CTT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0027 others(6): Show |
11 | HG01928.hp1 HG01981.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9-2490_-9-2489dup others(2): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288119 | ||||||
| chrX:71288119 | C | CTTT | 1 | a0001c0001t0001g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-9-2491_-9-2489dup others(3): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288119 | ||||||
| chrX:71288119 | C | CTTTT | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-2492_-9-2489dup others(4): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71288119 | ||||||
| chrX:71288800 | CAT | C | 1 | a0001c0001t0001g0020 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-9-1828_-9-1827del others(2): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71288800 | |||||||
| chrX:71289378 | G | A | 1 | a0001c0001t0002g0015 | 2 | HG02165.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-9-1251G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71289378 | |||||||
| chrX:71289652 | A | G | 2 | a0001c0002t0002g0088 a0001c0002t0002g0090 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-9-977A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71289652 | |||||||
| chrX:71289723 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-9-906T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71289723 | |||||||
| chrX:71289742 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-9-887C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71289742 | |||||||
| chrX:71289898 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-9-731A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71289898 | |||||||
| chrX:71290106 | C | G | 1 | a0001c0001t0001g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-9-523C>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71290106 | |||||||
| chrX:71290174 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-9-455G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71290174 | |||||||
| chrX:71290255 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-9-374C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71290255 | |||||||
| chrX:71290289 | TCCTCCCA others(6): Show |
T | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-9-332_-9-320delCC others(11): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71290289 | ||||||
| chrX:71290361 | TTTTC | T | 1 | a0001c0002t0001g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-9-264_-9-261delCT others(2): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71290361 | ||||||
| chrX:71290402 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-9-227T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71290402 | |||||||
| chrX:71290425 | AT | A | 2 | a0001c0001t0001g0016 a0001c0001t0009g0016 |
2 | HG02523.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-9-196delT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 71290425 | ||||||
| chrX:71290487 | A | T | 1 | a0001c0001t0003g0034 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-9-142A>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71290487 | |||||||
| chrX:71290553 | C | T | 1 | a0002c0003t0001g0074 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9-76C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 2/11 | chrX | 71290553 | |||||||
| chrX:71290802 | G | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(1): Show |
4 | HG02109.hp1 HG02723.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+11G>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | chrX | 71290802 | |||||||
| chrX:71290941 | G | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
7 | HG01255.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+150G>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | chrX | 71290941 | |||||||
| chrX:71291405 | G | GT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0026 others(13): Show |
20 | HG00642.hp1 HG01255.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.155-363dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 71291405 | ||||||
| chrX:71291405 | G | GTT | 3 | a0001c0002t0001g0024 a0001c0002t0001g0087 a0001c0002t0001g0089 |
4 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-364_155-363dup others(2): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 71291405 | ||||||
| chrX:71291413 | T | G | 1 | a0001c0001t0001g0017 | 2 | HG01074.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.155-366T>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | chrX | 71291413 | |||||||
| chrX:71291591 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.155-188C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | chrX | 71291591 | |||||||
| chrX:71291739 | A | G | 2 | a0001c0001t0003g0038 a0001c0001t0003g0068 |
2 | NA18955.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.155-40A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | chrX | 71291739 | |||||||
| chrX:71291774 | C | T | 1 | a0001c0001t0003g0083 | 1 | HG02015.hp1 | splice_region_variant&intron_variant | LOW | c.155-5C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 3/11 | chrX | 71291774 | |||||||
| chrX:71292146 | C | G | 3 | a0001c0002t0001g0024 a0001c0002t0001g0087 a0001c0002t0001g0089 |
4 | HG02559.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+174C>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71292146 | |||||||
| chrX:71292201 | C | CT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0093 others(2): Show |
7 | HG01255.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+242dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 71292201 | ||||||
| chrX:71292223 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.348+251G>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71292223 | |||||||
| chrX:71292245 | T | C | 1 | a0001c0001t0001g0010 | 3 | HG02615.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.348+273T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71292245 | |||||||
| chrX:71292646 | C | G | 1 | a0001c0001t0003g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.348+674C>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71292646 | |||||||
| chrX:71292740 | T | C | 1 | a0001c0001t0001g0010 | 3 | HG02615.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.348+768T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71292740 | |||||||
| chrX:71292954 | TA | T | 1 | a0001c0001t0002g0065 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.348+991delA | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 71292954 | ||||||
| chrX:71293283 | T | C | 1 | a0001c0001t0001g0010 | 3 | HG02615.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.349-944T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71293283 | |||||||
| chrX:71293358 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0003c0006t0001g0007 |
5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-869G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71293358 | |||||||
| chrX:71293444 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.349-783A>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71293444 | |||||||
| chrX:71293583 | G | GA | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.349-634dupA | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 71293583 | ||||||
| chrX:71293583 | GA | G | 5 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0036 others(2): Show |
7 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.349-634delA | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 71293583 | ||||||
| chrX:71293638 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349-589T>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71293638 | |||||||
| chrX:71293725 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.349-502G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71293725 | |||||||
| chrX:71293960 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.349-267T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71293960 | |||||||
| chrX:71294125 | G | A | 1 | a0001c0002t0012g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.349-102G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 4/11 | chrX | 71294125 | |||||||
| chrX:71294715 | G | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0026 others(14): Show |
22 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.650+187G>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71294715 | |||||||
| chrX:71294718 | G | A | 2 | a0001c0001t0003g0041 a0001c0001t0003g0049 |
2 | HG02523.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.650+190G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71294718 | |||||||
| chrX:71295052 | CT | C | 1 | a0001c0001t0003g0050 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.650+525delT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71295052 | |||||||
| chrX:71295220 | C | CA | 11 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0064 others(8): Show |
14 | HG00738.hp1 HG01978.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.650+712dupA | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 71295220 | ||||||
| chrX:71295220 | CA | C | 13 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(10): Show |
15 | HG01943.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.650+712delA | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 71295220 | ||||||
| chrX:71295220 | CAA | C | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.650+711_650+712del others(2): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 71295220 | ||||||
| chrX:71295269 | C | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0094 a0003c0006t0001g0007 |
5 | HG01255.hp1 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.650+741C>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71295269 | |||||||
| chrX:71295275 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.650+747A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71295275 | |||||||
| chrX:71295356 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.650+828G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71295356 | |||||||
| chrX:71295360 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.650+832G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71295360 | |||||||
| chrX:71296114 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.651-451A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71296114 | |||||||
| chrX:71296145 | C | CT | 11 | a0001c0001t0001g0005 a0001c0001t0001g0072 a0001c0001t0001g0092 others(8): Show |
14 | HG01167.hp1 HG02055.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.651-403dupT | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 71296145 | ||||||
| chrX:71296167 | C | G | 4 | a0001c0002t0001g0024 a0001c0002t0001g0087 a0001c0002t0001g0089 others(1): Show |
5 | HG02280.hp1 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.651-398C>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71296167 | |||||||
| chrX:71296182 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.651-383G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71296182 | |||||||
| chrX:71296358 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.651-207C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71296358 | |||||||
| chrX:71296359 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0062 |
2 | NA18942.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.651-206G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 5/11 | chrX | 71296359 | |||||||
| chrX:71296841 | T | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(7): Show |
14 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.747-10T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 6/11 | chrX | 71296841 | |||||||
| chrX:71297229 | G | T | 1 | a0001c0002t0012g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.944-148G>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 7/11 | chrX | 71297229 | |||||||
| chrX:71297502 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0054 a0001c0001t0001g0061 |
3 | HG00735.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1028+41G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 8/11 | chrX | 71297502 | |||||||
| chrX:71297601 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1028+140A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 8/11 | chrX | 71297601 | |||||||
| chrX:71297821 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG02922.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1029-15G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 8/11 | chrX | 71297821 | |||||||
| chrX:71297987 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1131+49C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 9/11 | chrX | 71297987 | |||||||
| chrX:71298084 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0072 a0001c0001t0001g0084 others(1): Show |
6 | HG04199.hp1 NA18747.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1131+146G>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 9/11 | chrX | 71298084 | |||||||
| chrX:71298243 | TC | T | 1 | a0001c0001t0001g0046 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1132-221delC | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 71298243 | ||||||
| chrX:71298396 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0002g0003 a0001c0005t0001g0003 |
6 | HG01069.hp1 HG01071.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132-73T>C | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 9/11 | chrX | 71298396 | |||||||
| chrX:71298953 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0062 |
3 | HG02074.hp1 NA18942.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1281+137C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71298953 | |||||||
| chrX:71299015 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0007g0012 |
2 | HG02083.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1281+199G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299015 | |||||||
| chrX:71299046 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1281+230C>T | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299046 | |||||||
| chrX:71299272 | T | TTGGGAAA | 2 | a0001c0001t0003g0050 a0001c0001t0003g0056 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1281+456_1281+457i others(9): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299272 | |||||||
| chrX:71299275 | C | G | 2 | a0001c0001t0003g0050 a0001c0001t0003g0056 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1281+459C>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299275 | |||||||
| chrX:71299276 | A | AGCACTTT others(3): Show |
2 | a0001c0001t0003g0050 a0001c0001t0003g0056 |
2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1281+460_1281+461i others(12): Show |
NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299276 | |||||||
| chrX:71299285 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0073 |
2 | NA18973.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1281+469G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299285 | |||||||
| chrX:71299395 | G | A | 8 | a0001c0001t0002g0002 a0001c0001t0002g0019 a0001c0001t0002g0021 others(5): Show |
12 | HG01109.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1282-547G>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299395 | |||||||
| chrX:71299690 | C | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0026 others(11): Show |
18 | HG01255.hp1 HG02055.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1282-252C>A | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299690 | |||||||
| chrX:71299829 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1282-113A>G | NONO | ENSG00000147140.17 | transcript | ENST00000276079.13 | protein_coding | 11/11 | chrX | 71299829 |