Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 152518 |
| ensemblid | ENSG00000170448.12 |
| hgncid | 18726 |
| symbol | NFXL1 |
| name | nuclear transcription factor, X-box binding like 1 |
| refseq_nuc | NM_001278624.2 |
| refseq_prot | NP_001265553.1 |
| ensembl_nuc | ENST00000507489.2 |
| ensembl_prot | ENSP00000422037.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 47847240 |
| end | 47914583 |
| strand | - |
| ver | v1.2 |
| region | chr4:47847240-47914583 |
| region5000 | chr4:47842240-47919583 |
| regionname0 | NFXL1_chr4_47847240_47914583 |
| regionname5000 | NFXL1_chr4_47842240_47919583 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 911 | 205 | 54 | 51 | 66 | 11 | 22 | 52 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0002 | 0/1 | 911 | 162 | 30 | 15 | 93 | 5 | 18 | 72 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0003 | 0/0 | 911 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0004 | 0/0 | 911 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0005 | 0/0 | 911 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEAFW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0006 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0007 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0008 | 0/0 | 911 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0009 | 0/0 | 911 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| a0010 | 0/0 | 911 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | MEASW others(906): Show |
chr4 | 47842240 | 47919583 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 2733 | 109 | 24 | 20 | 51 | 4 | 9 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0001c0003 | 0/0 | 2733 | 89 | 30 | 28 | 12 | 7 | 12 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0001c0004 | 0/0 | 2733 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0001c0006 | 0/0 | 2733 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0001c0009 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0002c0001 | 0/1 | 2733 | 160 | 30 | 15 | 91 | 5 | 18 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0002c0008 | 0/0 | 2733 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0003c0005 | 0/0 | 2733 | 3 | 3 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0004c0007 | 0/0 | 2733 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0005c0015 | 0/0 | 2733 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0006c0012 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0007c0013 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0008c0014 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0009c0011 | 0/0 | 2733 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 | ||
| a0010c0010 | 0/0 | 2733 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | ATGGA others(2728): Show |
chr4 | 47842240 | 47919583 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 3879 | 73 | 13 | 8 | 48 | 0 | 4 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0002t0003 | 1/0 | 3880 | 31 | 7 | 11 | 3 | 4 | 5 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3875): Show |
chr4 | 47842240 | 47919583 |
| a0001c0002t0006 | 0/0 | 3880 | 4 | 4 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3875): Show |
chr4 | 47842240 | 47919583 |
| a0001c0002t0009 | 0/0 | 3879 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0003t0001 | 0/0 | 3879 | 17 | 16 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0003t0002 | 0/0 | 3879 | 59 | 3 | 25 | 12 | 7 | 12 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0003t0004 | 0/0 | 3879 | 7 | 7 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0003t0005 | 0/0 | 3879 | 4 | 4 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0003t0008 | 0/0 | 3879 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0004t0003 | 0/0 | 3880 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3875): Show |
chr4 | 47842240 | 47919583 |
| a0001c0006t0002 | 0/0 | 3879 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0001c0009t0002 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0002c0001t0001 | 0/1 | 3879 | 155 | 28 | 12 | 91 | 5 | 18 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0002c0001t0007 | 0/0 | 3879 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0002c0001t0011 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0002c0001t0012 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0002c0008t0001 | 0/0 | 3879 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0003c0005t0001 | 0/0 | 3879 | 3 | 3 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0004c0007t0001 | 0/0 | 3879 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0005c0015t0002 | 0/0 | 3879 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0006c0012t0001 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0007c0013t0010 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0008c0014t0001 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0009c0011t0001 | 0/0 | 3879 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| a0010c0010t0001 | 0/0 | 3879 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | ACCAC others(3874): Show |
chr4 | 47842240 | 47919583 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0301 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0002t0009g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0008g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0003t0008g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0004t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0004t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0004t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0006t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0006t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0001c0009t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0001 | 0/0 | 18 | 0 | 1 | 14 | 0 | 3 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0002 | 0/0 | 11 | 0 | 1 | 8 | 1 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0007g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0001t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0008t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0002c0008t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0003c0005t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0003c0005t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0004c0007t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0004c0007t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0005c0015t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0006c0012t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0007c0013t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0008c0014t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0009c0011t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| a0010c0010t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0154 | EUR | GBR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0117 | EUR | GBR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00280 | hp1 | a0002 | c0001 | t0001 | g0263 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00280 | hp2 | a0001 | c0003 | t0002 | g0120 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00323 | hp1 | a0002 | c0001 | t0001 | g0260 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0109 | EUR | FIN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00408 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0233 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00558 | hp1 | a0001 | c0006 | t0002 | g0149 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0285 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00597 | hp2 | a0001 | c0006 | t0002 | g0023 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0200 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00621 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00639 | hp1 | a0001 | c0004 | t0003 | g0170 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00639 | hp2 | a0001 | c0003 | t0008 | g0304 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00673 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | CHS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00733 | hp1 | a0001 | c0003 | t0002 | g0101 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00733 | hp2 | a0001 | c0004 | t0003 | g0153 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0057 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00738 | hp1 | a0001 | c0003 | t0002 | g0022 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0112 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0148 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG00741 | hp2 | a0001 | c0002 | t0003 | g0155 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0100 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01070 | hp2 | a0002 | c0001 | t0001 | g0248 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01071 | hp1 | a0001 | c0003 | t0002 | g0138 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01071 | hp2 | a0002 | c0001 | t0001 | g0231 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0137 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01074 | hp2 | a0002 | c0001 | t0001 | g0267 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01081 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0123 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0175 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0161 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0164 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01109 | hp2 | a0002 | c0001 | t0001 | g0001 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01167 | hp2 | a0002 | c0001 | t0001 | g0185 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01169 | hp2 | a0001 | c0003 | t0002 | g0022 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0302 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0103 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0143 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0300 | AMR | PUR | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0273 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0262 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0144 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0111 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0166 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0171 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01346 | hp2 | a0004 | c0007 | t0001 | g0210 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0135 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0114 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0158 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01361 | hp2 | a0001 | c0003 | t0002 | g0115 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01433 | hp1 | a0001 | c0004 | t0003 | g0173 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0086 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01515 | hp1 | a0002 | c0001 | t0001 | g0002 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0024 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0025 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0108 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0113 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01517 | hp2 | a0001 | c0002 | t0003 | g0024 | EUR | IBS | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0213 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0027 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01891 | hp1 | a0003 | c0005 | t0001 | g0031 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01928 | hp1 | a0001 | c0003 | t0002 | g0140 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01928 | hp2 | a0002 | c0001 | t0001 | g0232 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01934 | hp2 | a0001 | c0003 | t0002 | g0150 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01943 | hp1 | a0004 | c0007 | t0001 | g0209 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0146 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01952 | hp1 | a0002 | c0001 | t0007 | g0010 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01952 | hp2 | a0001 | c0003 | t0002 | g0139 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01978 | hp2 | a0001 | c0003 | t0002 | g0021 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01981 | hp2 | a0002 | c0001 | t0007 | g0010 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01993 | hp1 | a0001 | c0002 | t0003 | g0156 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0165 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0212 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0208 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0018 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02055 | hp2 | a0003 | c0005 | t0001 | g0187 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0278 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02056 | hp2 | a0001 | c0003 | t0002 | g0147 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02071 | hp1 | a0005 | c0015 | t0002 | g0297 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02080 | hp2 | a0002 | c0001 | t0001 | g0257 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02083 | hp1 | a0002 | c0001 | t0001 | g0193 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02129 | hp1 | a0002 | c0001 | t0001 | g0253 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02129 | hp2 | a0002 | c0001 | t0001 | g0229 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0136 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0038 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02148 | hp1 | a0002 | c0001 | t0001 | g0195 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02148 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02273 | hp1 | a0002 | c0001 | t0007 | g0010 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0226 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0029 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0107 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02300 | hp2 | a0001 | c0002 | t0009 | g0036 | AMR | PEL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02451 | hp1 | a0001 | c0002 | t0006 | g0039 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02451 | hp2 | a0002 | c0001 | t0001 | g0203 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0228 | EAS | KHV | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0035 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0280 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0215 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02615 | hp2 | a0006 | c0012 | t0001 | g0243 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02630 | hp1 | a0002 | c0001 | t0011 | g0281 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02630 | hp2 | a0007 | c0013 | t0010 | g0246 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0299 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02647 | hp2 | a0002 | c0001 | t0001 | g0189 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0159 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0264 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02717 | hp1 | a0003 | c0005 | t0001 | g0031 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0157 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0202 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0046 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02735 | hp2 | a0008 | c0014 | t0001 | g0294 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0205 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02818 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0183 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02895 | hp1 | a0001 | c0003 | t0004 | g0180 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02895 | hp2 | a0002 | c0001 | t0001 | g0028 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02897 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02897 | hp2 | a0001 | c0002 | t0003 | g0026 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02922 | hp1 | a0001 | c0003 | t0004 | g0027 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0174 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02965 | hp2 | a0009 | c0011 | t0001 | g0206 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02970 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02976 | hp1 | a0002 | c0001 | t0001 | g0030 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02976 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03017 | hp1 | a0001 | c0009 | t0002 | g0142 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03017 | hp2 | a0001 | c0003 | t0002 | g0129 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03041 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0048 | AFR | GWD | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03098 | hp1 | a0001 | c0002 | t0006 | g0040 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0177 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03130 | hp1 | a0002 | c0001 | t0001 | g0223 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0298 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0293 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03209 | hp1 | a0002 | c0001 | t0001 | g0004 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03209 | hp2 | a0001 | c0003 | t0005 | g0033 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0207 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0106 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0272 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03453 | hp2 | a0001 | c0003 | t0004 | g0178 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03486 | hp1 | a0002 | c0001 | t0001 | g0182 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03486 | hp2 | a0001 | c0003 | t0005 | g0033 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03490 | hp1 | a0001 | c0003 | t0002 | g0122 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0018 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0152 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03491 | hp2 | a0001 | c0003 | t0002 | g0128 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0211 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ESN | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03579 | hp2 | a0001 | c0003 | t0005 | g0289 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0124 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03654 | hp2 | a0002 | c0001 | t0001 | g0001 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0254 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03669 | hp2 | a0010 | c0010 | t0001 | g0219 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0241 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0047 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0242 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03710 | hp2 | a0002 | c0001 | t0001 | g0186 | SAS | PJL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03831 | hp1 | a0002 | c0001 | t0001 | g0266 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03831 | hp2 | a0002 | c0001 | t0001 | g0032 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03834 | hp1 | a0002 | c0001 | t0001 | g0230 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0268 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03927 | hp1 | a0001 | c0003 | t0002 | g0119 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0063 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0131 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04184 | hp1 | a0002 | c0001 | t0001 | g0214 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0169 | SAS | BEB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04199 | hp1 | a0002 | c0001 | t0001 | g0274 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0141 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0001 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0025 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0133 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0160 | SAS | STU | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18522 | hp1 | a0002 | c0001 | t0001 | g0188 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18522 | hp2 | a0001 | c0002 | t0006 | g0043 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18612 | hp1 | a0002 | c0001 | t0001 | g0239 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18612 | hp2 | a0002 | c0001 | t0001 | g0291 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18747 | hp2 | a0002 | c0001 | t0001 | g0216 | EAS | CHB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0204 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18906 | hp2 | a0002 | c0001 | t0001 | g0030 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18939 | hp1 | a0002 | c0008 | t0001 | g0296 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18940 | hp1 | a0002 | c0001 | t0001 | g0277 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18942 | hp1 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18949 | hp1 | a0002 | c0001 | t0001 | g0259 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18949 | hp2 | a0001 | c0003 | t0002 | g0126 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18952 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18957 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18961 | hp1 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18963 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18965 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0020 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18968 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0234 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0271 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18969 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0240 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18972 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18972 | hp2 | a0002 | c0001 | t0001 | g0275 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18973 | hp2 | a0001 | c0006 | t0002 | g0023 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18974 | hp2 | a0002 | c0001 | t0001 | g0221 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0199 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18981 | hp1 | a0002 | c0001 | t0001 | g0194 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18982 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18986 | hp1 | a0002 | c0001 | t0001 | g0282 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18986 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18987 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18990 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18991 | hp1 | a0002 | c0001 | t0001 | g0198 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18992 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18994 | hp1 | a0002 | c0001 | t0001 | g0224 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18997 | hp1 | a0002 | c0001 | t0001 | g0225 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0196 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19001 | hp1 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19002 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19003 | hp1 | a0002 | c0001 | t0001 | g0270 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19004 | hp1 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19004 | hp2 | a0002 | c0001 | t0001 | g0255 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19005 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0279 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19007 | hp2 | a0002 | c0001 | t0001 | g0256 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0192 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0284 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19011 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19011 | hp2 | a0002 | c0001 | t0001 | g0276 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19030 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0049 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19043 | hp1 | a0001 | c0003 | t0004 | g0181 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0292 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19056 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19056 | hp2 | a0002 | c0001 | t0001 | g0001 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19057 | hp1 | a0002 | c0001 | t0001 | g0227 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19057 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19058 | hp1 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0222 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19062 | hp2 | a0002 | c0001 | t0001 | g0250 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19063 | hp2 | a0001 | c0003 | t0002 | g0125 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19064 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19064 | hp2 | a0002 | c0001 | t0001 | g0235 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0283 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0244 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19075 | hp1 | a0001 | c0003 | t0002 | g0116 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19076 | hp1 | a0002 | c0008 | t0001 | g0295 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19076 | hp2 | a0001 | c0003 | t0002 | g0132 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19078 | hp1 | a0002 | c0001 | t0001 | g0201 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19080 | hp2 | a0001 | c0003 | t0002 | g0020 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19081 | hp2 | a0002 | c0001 | t0001 | g0287 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19082 | hp1 | a0002 | c0001 | t0001 | g0286 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19082 | hp2 | a0001 | c0003 | t0002 | g0104 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19086 | hp2 | a0001 | c0003 | t0002 | g0121 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19087 | hp1 | a0002 | c0001 | t0001 | g0288 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19088 | hp2 | a0002 | c0001 | t0001 | g0217 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19090 | hp1 | a0002 | c0001 | t0001 | g0269 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19090 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0102 | AFR | YRI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20129 | hp1 | a0002 | c0001 | t0001 | g0251 | AFR | ASW | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20129 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | ASW | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0249 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0110 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0265 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20805 | hp2 | a0001 | c0003 | t0002 | g0021 | EUR | TSI | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0130 | SAS | GIH | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20905 | hp2 | a0002 | c0001 | t0001 | g0261 | SAS | GIH | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01123 | hp1 | a0001 | c0003 | t0008 | g0305 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0303 | AMR | CLM | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02109 | hp2 | a0002 | c0001 | t0001 | g0191 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0190 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0167 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG02559 | hp2 | a0001 | c0003 | t0005 | g0290 | AFR | ACB | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| HG03471 | hp2 | a0001 | c0003 | t0004 | g0179 | AFR | MSL | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | USA | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0145 | AFR | USA | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA21309 | hp1 | a0002 | c0001 | t0012 | g0218 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0151 | AFR | LWK | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0258 | REF | REF | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0301 | REF | REF | NFXL1_chr4_47842240_47919583 | NFXL1 | chr4 | 47842240 | 47919583 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47848180 | T | C | 1 | a0003 | 3 | HG01891.hp1 HG02055.hp2 HG02717.hp1 |
missense_variant | MODERATE | c.2719A>G | p.Thr907Ala | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 2940/3880 | 2719/2736 | 907/911 | chr4 | 47848180 | |||
| chr4:47862904 | G | C | 1 | a0010 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.2258C>G | p.Thr753Arg | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/23 | 2479/3880 | 2258/2736 | 753/911 | chr4 | 47862904 | |||
| chr4:47890643 | T | A | 1 | a0009 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1513A>T | p.Asn505Tyr | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/23 | 1734/3880 | 1513/2736 | 505/911 | chr4 | 47890643 | |||
| chr4:47899459 | G | A | 7 | a0002 a0003 a0004 others(4): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
missense_variant | MODERATE | c.737C>T | p.Pro246Leu | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/23 | 958/3880 | 737/2736 | 246/911 | chr4 | 47899459 | |||
| chr4:47903296 | T | C | 1 | a0006 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.544A>G | p.Ile182Val | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/23 | 765/3880 | 544/2736 | 182/911 | chr4 | 47903296 | |||
| chr4:47903310 | G | A | 1 | a0007 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.530C>T | p.Ser177Leu | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/23 | 751/3880 | 530/2736 | 177/911 | chr4 | 47903310 | |||
| chr4:47905303 | A | T | 1 | a0004 | 2 | HG01346.hp2 HG01943.hp1 |
missense_variant | MODERATE | c.450T>A | p.Asn150Lys | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/23 | 671/3880 | 450/2736 | 150/911 | chr4 | 47905303 | |||
| chr4:47914071 | C | A | 1 | a0008 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.133G>T | p.Val45Phe | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/23 | 354/3880 | 133/2736 | 45/911 | chr4 | 47914071 | |||
| chr4:47914193 | G | A | 1 | a0005 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.11C>T | p.Ser4Phe | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/23 | 232/3880 | 11/2736 | 4/911 | chr4 | 47914193 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47885519 | T | C | 13 | a0001c0003 a0001c0006 a0001c0009 others(10): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
synonymous_variant | LOW | c.1803A>G | p.Ala601Ala | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/23 | 2024/3880 | 1803/2736 | 601/911 | chr4 | 47885519 | |||
| chr4:47885558 | T | C | 1 | a0001c0009 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.1764A>G | p.Lys588Lys | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/23 | 1985/3880 | 1764/2736 | 588/911 | chr4 | 47885558 | |||
| chr4:47885974 | G | A | 13 | a0001c0003 a0001c0006 a0001c0009 others(10): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
synonymous_variant | LOW | c.1569C>T | p.Thr523Thr | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 13/23 | 1790/3880 | 1569/2736 | 523/911 | chr4 | 47885974 | |||
| chr4:47899071 | C | T | 1 | a0001c0004 | 3 | HG00639.hp1 HG00733.hp2 HG01433.hp1 |
synonymous_variant | LOW | c.876G>A | p.Lys292Lys | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 7/23 | 1097/3880 | 876/2736 | 292/911 | chr4 | 47899071 | |||
| chr4:47903258 | G | A | 1 | a0001c0006 | 3 | HG00558.hp1 HG00597.hp2 NA18973.hp2 |
synonymous_variant | LOW | c.582C>T | p.Asp194Asp | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/23 | 803/3880 | 582/2736 | 194/911 | chr4 | 47903258 | |||
| chr4:47914171 | G | A | 1 | a0002c0008 | 2 | NA18939.hp1 NA19076.hp1 |
synonymous_variant | LOW | c.33C>T | p.Gly11Gly | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/23 | 254/3880 | 33/2736 | 11/911 | chr4 | 47914171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47847501 | G | A | 1 | a0007c0013t0010 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 662 | chr4 | 47847501 | ||||||
| chr4:47847582 | T | A | 1 | a0002c0001t0011 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 581 | chr4 | 47847582 | ||||||
| chr4:47847585 | G | A | 1 | a0001c0002t0006 | 4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*578C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 578 | chr4 | 47847585 | ||||||
| chr4:47847597 | T | C | 1 | a0002c0001t0007 | 3 | HG01952.hp1 HG01981.hp2 HG02273.hp1 |
3_prime_UTR_variant | MODIFIER | c.*566A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 566 | chr4 | 47847597 | ||||||
| chr4:47847616 | G | A | 1 | a0002c0001t0012 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 547 | chr4 | 47847616 | ||||||
| chr4:47847659 | A | G | 1 | a0001c0003t0004 | 7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*504T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 504 | chr4 | 47847659 | ||||||
| chr4:47847749 | T | A | 5 | a0001c0003t0002 a0001c0003t0008 a0001c0006t0002 others(2): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*414A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 414 | chr4 | 47847749 | ||||||
| chr4:47847814 | G | C | 1 | a0001c0003t0005 | 4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*349C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 349 | chr4 | 47847814 | ||||||
| chr4:47847966 | TA | T | 22 | a0001c0002t0001 a0001c0002t0009 a0001c0003t0001 others(19): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*196delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 23/23 | 196 | chr4 | 47847966 | ||||||
| chr4:47914445 | C | T | 1 | a0001c0002t0009 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-83G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/23 | 242 | chr4 | 47914445 | ||||||
| chr4:47914446 | G | A | 1 | a0001c0003t0008 | 2 | HG00639.hp2 HG01123.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-84C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/23 | chr4 | 47914446 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47848567 | G | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2563-231C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848567 | |||||||
| chr4:47848617 | C | T | 5 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2563-281G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848617 | |||||||
| chr4:47848665 | G | A | 1 | a0002c0001t0001g0252 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2563-329C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848665 | |||||||
| chr4:47848762 | G | A | 1 | a0001c0002t0001g0076 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2563-426C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848762 | |||||||
| chr4:47848806 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2563-470C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848806 | |||||||
| chr4:47848813 | A | G | 1 | a0002c0001t0001g0205 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2563-477T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848813 | |||||||
| chr4:47848845 | C | T | 1 | a0001c0002t0001g0097 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2563-509G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848845 | |||||||
| chr4:47848896 | T | A | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2563-560A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848896 | |||||||
| chr4:47848923 | G | A | 1 | a0001c0002t0003g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2563-587C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848923 | |||||||
| chr4:47848976 | A | G | 11 | a0002c0001t0001g0028 a0002c0001t0001g0029 a0002c0001t0001g0030 others(8): Show |
15 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2563-640T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47848976 | |||||||
| chr4:47849037 | T | C | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2563-701A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849037 | |||||||
| chr4:47849093 | A | T | 2 | a0001c0003t0008g0304 a0001c0003t0008g0305 |
2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2563-757T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849093 | |||||||
| chr4:47849149 | G | T | 1 | a0001c0002t0001g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2563-813C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849149 | |||||||
| chr4:47849191 | T | C | 67 | a0001c0003t0001g0102 a0001c0003t0002g0018 a0001c0003t0002g0019 others(64): Show |
74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2563-855A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849191 | |||||||
| chr4:47849219 | C | T | 1 | a0002c0001t0001g0270 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2563-883G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849219 | |||||||
| chr4:47849334 | G | C | 1 | a0001c0003t0002g0103 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2563-998C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849334 | |||||||
| chr4:47849382 | T | C | 1 | a0001c0002t0003g0152 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2563-1046A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849382 | |||||||
| chr4:47849554 | A | C | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2563-1218T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849554 | |||||||
| chr4:47849624 | G | A | 1 | a0001c0002t0003g0171 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2563-1288C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849624 | |||||||
| chr4:47849927 | C | T | 64 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(61): Show |
74 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.2562+1168G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849927 | |||||||
| chr4:47849952 | A | AT | 5 | a0001c0002t0001g0012 a0001c0002t0001g0041 a0001c0002t0001g0044 others(2): Show |
6 | HG00642.hp2 HG02257.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2562+1142dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849952 | |||||||
| chr4:47849952 | A | T | 2 | a0001c0002t0003g0171 a0001c0002t0003g0175 |
2 | HG01099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2562+1143T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849952 | |||||||
| chr4:47849952 | AT | A | 155 | a0001c0002t0001g0056 a0001c0002t0001g0064 a0001c0002t0009g0036 others(152): Show |
207 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.2562+1142delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849952 | |||||||
| chr4:47849955 | T | A | 51 | a0001c0003t0001g0102 a0001c0003t0002g0018 a0001c0003t0002g0019 others(48): Show |
59 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2562+1140A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849955 | |||||||
| chr4:47849956 | T | A | 152 | a0001c0002t0001g0052 a0001c0003t0001g0011 a0001c0003t0001g0034 others(149): Show |
204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.2562+1139A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849956 | |||||||
| chr4:47849957 | T | A | 2 | a0002c0001t0001g0208 a0006c0012t0001g0243 |
2 | HG02040.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.2562+1138A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849957 | |||||||
| chr4:47849958 | T | A | 40 | a0001c0003t0002g0018 a0001c0003t0002g0019 a0001c0003t0002g0020 others(37): Show |
46 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.2562+1137A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47849958 | |||||||
| chr4:47850003 | T | C | 65 | a0002c0001t0001g0001 a0002c0001t0001g0009 a0002c0001t0001g0028 others(62): Show |
89 | HG00408.hp1 HG00423.hp2 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.2562+1092A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850003 | |||||||
| chr4:47850166 | A | G | 61 | a0001c0003t0001g0102 a0001c0003t0002g0018 a0001c0003t0002g0019 others(58): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2562+929T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850166 | |||||||
| chr4:47850201 | T | C | 2 | a0001c0002t0001g0067 a0001c0002t0001g0068 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2562+894A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850201 | |||||||
| chr4:47850276 | T | A | 1 | a0002c0001t0001g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2562+819A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850276 | |||||||
| chr4:47850608 | T | C | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2562+487A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850608 | |||||||
| chr4:47850717 | T | C | 1 | a0002c0001t0001g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2562+378A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850717 | |||||||
| chr4:47850786 | G | A | 15 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(12): Show |
20 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2562+309C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 22/22 | chr4 | 47850786 | |||||||
| chr4:47851360 | T | C | 1 | a0002c0001t0001g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2509-212A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851360 | |||||||
| chr4:47851418 | A | T | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2509-270T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851418 | |||||||
| chr4:47851457 | CTT | C | 2 | a0001c0002t0003g0024 a0001c0002t0003g0155 |
3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2509-311_2509-310d others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851457 | |||||||
| chr4:47851464 | T | C | 1 | a0002c0001t0001g0285 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2509-316A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851464 | |||||||
| chr4:47851652 | T | C | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2508+204A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851652 | |||||||
| chr4:47851826 | T | C | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2508+30A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 21/22 | chr4 | 47851826 | |||||||
| chr4:47852137 | A | G | 1 | a0002c0001t0001g0009 | 3 | NA18947.hp1 NA18990.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2422-195T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852137 | |||||||
| chr4:47852355 | A | G | 1 | a0001c0003t0002g0139 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2422-413T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852355 | |||||||
| chr4:47852567 | T | A | 1 | a0001c0003t0002g0128 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2422-625A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852567 | |||||||
| chr4:47852602 | T | C | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2422-660A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852602 | |||||||
| chr4:47852677 | G | A | 10 | a0002c0001t0001g0004 a0002c0001t0001g0008 a0002c0001t0001g0191 others(7): Show |
15 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2422-735C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852677 | |||||||
| chr4:47852726 | T | C | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2422-784A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852726 | |||||||
| chr4:47852744 | C | G | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2422-802G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852744 | |||||||
| chr4:47852756 | C | T | 300 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(297): Show |
373 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.2422-814G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852756 | |||||||
| chr4:47852850 | T | C | 1 | a0002c0001t0001g0009 | 3 | NA18947.hp1 NA18990.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2422-908A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852850 | |||||||
| chr4:47852864 | T | C | 1 | a0002c0001t0001g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2422-922A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852864 | |||||||
| chr4:47852965 | GT | G | 7 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(4): Show |
8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2422-1024delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47852965 | |||||||
| chr4:47853096 | G | A | 1 | a0002c0001t0001g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2422-1154C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853096 | |||||||
| chr4:47853263 | T | C | 2 | a0001c0002t0003g0163 a0001c0002t0003g0165 |
2 | HG02027.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.2422-1321A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853263 | |||||||
| chr4:47853393 | C | T | 1 | a0002c0001t0001g0256 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2422-1451G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853393 | |||||||
| chr4:47853481 | C | T | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2422-1539G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853481 | |||||||
| chr4:47853686 | G | A | 1 | a0001c0003t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2421+1373C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853686 | |||||||
| chr4:47853982 | T | C | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2421+1077A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47853982 | |||||||
| chr4:47854720 | G | A | 1 | a0001c0002t0001g0015 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2421+339C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854720 | |||||||
| chr4:47854846 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2421+213G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854846 | |||||||
| chr4:47854940 | C | CA | 11 | a0001c0002t0001g0293 a0001c0002t0003g0164 a0001c0002t0003g0169 others(8): Show |
12 | HG01109.hp1 HG01346.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.2421+118dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854940 | |||||||
| chr4:47854940 | CA | C | 15 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(12): Show |
16 | HG00323.hp1 HG00642.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2421+118delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47854940 | |||||||
| chr4:47855005 | C | T | 1 | a0002c0001t0001g0237 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2421+54G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47855005 | |||||||
| chr4:47855023 | T | C | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2421+36A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 20/22 | chr4 | 47855023 | |||||||
| chr4:47855168 | A | T | 1 | a0002c0001t0001g0254 | 1 | HG03669.hp1 | splice_region_variant&intron_variant | LOW | c.2317-5T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855168 | |||||||
| chr4:47855470 | T | C | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2317-307A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855470 | |||||||
| chr4:47855562 | G | A | 6 | a0002c0001t0001g0030 a0002c0001t0001g0188 a0002c0001t0001g0189 others(3): Show |
8 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2317-399C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855562 | |||||||
| chr4:47855565 | C | T | 1 | a0002c0001t0001g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2317-402G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855565 | |||||||
| chr4:47855600 | T | C | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2317-437A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855600 | |||||||
| chr4:47855669 | C | T | 269 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(266): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.2317-506G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855669 | |||||||
| chr4:47855987 | G | A | 2 | a0001c0002t0003g0171 a0001c0002t0003g0175 |
2 | HG01099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2317-824C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47855987 | |||||||
| chr4:47856075 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2317-912A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856075 | |||||||
| chr4:47856082 | G | A | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2317-919C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856082 | |||||||
| chr4:47856123 | G | T | 1 | a0002c0001t0001g0279 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2317-960C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856123 | |||||||
| chr4:47856142 | A | G | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2317-979T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856142 | |||||||
| chr4:47856213 | T | C | 1 | a0009c0011t0001g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2317-1050A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856213 | |||||||
| chr4:47856342 | G | C | 1 | a0001c0003t0002g0019 | 2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.2317-1179C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856342 | |||||||
| chr4:47856457 | T | G | 1 | a0001c0003t0001g0048 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2317-1294A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856457 | |||||||
| chr4:47856501 | ATAG | A | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2317-1341_2317-133 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856501 | |||||||
| chr4:47856564 | G | C | 1 | a0002c0001t0001g0253 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2317-1401C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856564 | |||||||
| chr4:47856866 | T | C | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2317-1703A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47856866 | |||||||
| chr4:47857026 | C | T | 1 | a0002c0001t0001g0252 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2317-1863G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857026 | |||||||
| chr4:47857229 | G | A | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2317-2066C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857229 | |||||||
| chr4:47857303 | A | C | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2317-2140T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857303 | |||||||
| chr4:47857324 | T | G | 11 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(8): Show |
15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2317-2161A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857324 | |||||||
| chr4:47857460 | G | A | 1 | a0001c0002t0003g0026 | 2 | HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2317-2297C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857460 | |||||||
| chr4:47857796 | T | A | 1 | a0002c0001t0001g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2317-2633A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857796 | |||||||
| chr4:47857800 | T | TTAGGTTT others(77): Show |
1 | a0001c0003t0002g0020 | 2 | NA18967.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2317-2721_2317-263 others(88): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857800 | |||||||
| chr4:47857812 | T | C | 1 | a0001c0002t0003g0159 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2317-2649A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857812 | |||||||
| chr4:47857884 | G | T | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2317-2721C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47857884 | |||||||
| chr4:47858288 | T | C | 1 | a0001c0003t0002g0126 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2317-3125A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858288 | |||||||
| chr4:47858375 | C | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2317-3212G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858375 | |||||||
| chr4:47858479 | C | A | 1 | a0002c0001t0001g0269 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2317-3316G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858479 | |||||||
| chr4:47858708 | A | C | 1 | a0002c0001t0001g0245 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2317-3545T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858708 | |||||||
| chr4:47858764 | G | A | 1 | a0002c0001t0001g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2317-3601C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47858764 | |||||||
| chr4:47859240 | A | G | 1 | a0002c0001t0001g0285 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2316+3606T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859240 | |||||||
| chr4:47859455 | G | T | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2316+3391C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859455 | |||||||
| chr4:47859715 | G | A | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2316+3131C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859715 | |||||||
| chr4:47859841 | C | CA | 11 | a0001c0002t0001g0044 a0001c0002t0001g0045 a0001c0002t0003g0151 others(8): Show |
11 | HG00741.hp2 HG01109.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2316+3004dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | |||||||
| chr4:47859841 | C | CAAAA | 12 | a0001c0002t0001g0007 a0001c0002t0001g0013 a0001c0002t0001g0014 others(9): Show |
16 | HG02083.hp2 HG02132.hp1 NA18952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2316+3001_2316+300 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | |||||||
| chr4:47859841 | C | CAAAAA | 15 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0055 others(12): Show |
18 | HG00609.hp2 HG00621.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.2316+3000_2316+300 others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | |||||||
| chr4:47859841 | C | CAAAAAA | 12 | a0001c0002t0001g0016 a0001c0002t0001g0053 a0001c0002t0001g0060 others(9): Show |
13 | HG01433.hp2 HG01934.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.2316+2999_2316+300 others(10): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | |||||||
| chr4:47859841 | C | CAAAAAAA others(3): Show |
2 | a0001c0002t0001g0017 a0001c0002t0001g0089 |
3 | HG00423.hp1 NA18940.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.2316+2995_2316+300 others(14): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | |||||||
| chr4:47859841 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0003g0026 | 2 | HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2316+2993_2316+300 others(16): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859841 | |||||||
| chr4:47859854 | AAAAAAAA others(10): Show |
A | 1 | a0001c0003t0002g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2316+2975_2316+299 others(21): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859854 | |||||||
| chr4:47859856 | AAAAAAAA others(8): Show |
A | 2 | a0001c0002t0001g0054 a0001c0002t0001g0070 |
2 | NA18987.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(19): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859856 | |||||||
| chr4:47859857 | AAAAAAAA others(7): Show |
A | 1 | a0001c0002t0001g0082 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2316+2975_2316+298 others(18): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859857 | |||||||
| chr4:47859858 | AAAAAAAA others(6): Show |
A | 3 | a0001c0002t0001g0069 a0001c0002t0001g0075 a0001c0002t0001g0077 |
3 | HG02523.hp1 NA18947.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(17): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859858 | |||||||
| chr4:47859861 | A | C | 1 | a0001c0003t0002g0018 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2316+2985T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859861 | |||||||
| chr4:47859861 | AAAAAAAA others(3): Show |
A | 2 | a0001c0003t0004g0180 a0005c0015t0002g0297 |
2 | HG02071.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(14): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859861 | |||||||
| chr4:47859862 | AAAAAAAA others(2): Show |
A | 124 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(121): Show |
150 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(13): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859862 | |||||||
| chr4:47859863 | AAAAAAAA others(1): Show |
A | 72 | a0001c0003t0001g0011 a0001c0003t0001g0048 a0001c0003t0001g0300 others(69): Show |
94 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(12): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859863 | |||||||
| chr4:47859864 | AAAAAAAC | A | 16 | a0002c0001t0001g0002 a0002c0001t0001g0004 a0002c0001t0001g0008 others(13): Show |
17 | HG00621.hp1 HG00673.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.2316+2975_2316+298 others(11): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859864 | |||||||
| chr4:47859867 | A | C | 1 | a0001c0002t0003g0172 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2316+2979T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859867 | |||||||
| chr4:47859871 | C | A | 45 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(42): Show |
54 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2316+2975G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859871 | |||||||
| chr4:47859940 | G | A | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2316+2906C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859940 | |||||||
| chr4:47859960 | T | C | 1 | a0006c0012t0001g0243 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2316+2886A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47859960 | |||||||
| chr4:47860230 | T | G | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2316+2616A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860230 | |||||||
| chr4:47860459 | G | A | 3 | a0002c0001t0001g0196 a0002c0001t0001g0235 a0002c0001t0001g0239 |
3 | NA18612.hp1 NA19000.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2316+2387C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860459 | |||||||
| chr4:47860464 | T | C | 1 | a0001c0002t0003g0175 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2316+2382A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860464 | |||||||
| chr4:47860576 | C | T | 47 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0005 others(44): Show |
66 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.2316+2270G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860576 | |||||||
| chr4:47860628 | A | C | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2316+2218T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860628 | |||||||
| chr4:47860672 | A | G | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2316+2174T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860672 | |||||||
| chr4:47860746 | G | A | 1 | a0001c0003t0002g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2316+2100C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860746 | |||||||
| chr4:47860775 | T | C | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2316+2071A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860775 | |||||||
| chr4:47860858 | G | GT | 17 | a0001c0003t0002g0132 a0001c0003t0004g0027 a0001c0003t0004g0177 others(14): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2316+1987dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860858 | |||||||
| chr4:47860914 | G | A | 1 | a0001c0003t0002g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2316+1932C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47860914 | |||||||
| chr4:47861018 | A | AT | 189 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(186): Show |
245 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2316+1827dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861018 | |||||||
| chr4:47861080 | C | T | 1 | a0005c0015t0002g0297 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2316+1766G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861080 | |||||||
| chr4:47861283 | A | G | 1 | a0001c0002t0001g0074 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2316+1563T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861283 | |||||||
| chr4:47861357 | C | T | 1 | a0001c0006t0002g0149 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2316+1489G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861357 | |||||||
| chr4:47861564 | A | G | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2316+1282T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861564 | |||||||
| chr4:47861626 | AT | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2316+1219delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861626 | |||||||
| chr4:47861626 | ATTTAT | A | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2316+1215_2316+121 others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861626 | |||||||
| chr4:47861640 | G | A | 7 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(4): Show |
8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2316+1206C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47861640 | |||||||
| chr4:47862431 | T | G | 7 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(4): Show |
8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2316+415A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862431 | |||||||
| chr4:47862437 | C | T | 1 | a0001c0003t0004g0027 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2316+409G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862437 | |||||||
| chr4:47862588 | T | G | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2316+258A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862588 | |||||||
| chr4:47862605 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2316+241T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862605 | |||||||
| chr4:47862652 | A | C | 9 | a0002c0001t0001g0003 a0002c0001t0001g0194 a0002c0001t0001g0253 others(6): Show |
13 | HG00408.hp2 HG02071.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.2316+194T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862652 | |||||||
| chr4:47862725 | G | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2316+121C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862725 | |||||||
| chr4:47862742 | T | C | 2 | a0001c0003t0002g0111 a0001c0003t0002g0112 |
2 | HG00738.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.2316+104A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 19/22 | chr4 | 47862742 | |||||||
| chr4:47863179 | T | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-264A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863179 | |||||||
| chr4:47863202 | A | C | 2 | a0001c0003t0008g0304 a0001c0003t0008g0305 |
2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2247-287T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863202 | |||||||
| chr4:47863231 | TTATCATT others(1): Show |
T | 11 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(8): Show |
15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2247-324_2247-317d others(10): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863231 | |||||||
| chr4:47863243 | T | C | 125 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(122): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.2247-328A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863243 | |||||||
| chr4:47863284 | A | C | 1 | a0001c0002t0003g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2247-369T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863284 | |||||||
| chr4:47863485 | C | T | 4 | a0001c0002t0001g0072 a0001c0002t0001g0073 a0001c0002t0001g0084 others(1): Show |
4 | HG02080.hp1 HG02083.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-570G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863485 | |||||||
| chr4:47863697 | A | G | 1 | a0002c0001t0001g0262 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2247-782T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863697 | |||||||
| chr4:47863760 | T | G | 1 | a0002c0001t0001g0287 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2247-845A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863760 | |||||||
| chr4:47863872 | G | A | 269 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(266): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.2247-957C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47863872 | |||||||
| chr4:47864148 | TCACCTCT others(9): Show |
T | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-1249_2247-123 others(20): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864148 | |||||||
| chr4:47864283 | T | C | 1 | a0001c0003t0002g0121 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2247-1368A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864283 | |||||||
| chr4:47864298 | T | A | 1 | a0002c0001t0001g0257 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2247-1383A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864298 | |||||||
| chr4:47864676 | G | A | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-1761C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864676 | |||||||
| chr4:47864722 | G | A | 2 | a0001c0002t0003g0024 a0001c0002t0003g0155 |
3 | HG00741.hp2 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2247-1807C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864722 | |||||||
| chr4:47864726 | C | T | 212 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(209): Show |
273 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.2247-1811G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864726 | |||||||
| chr4:47864750 | G | A | 2 | a0001c0002t0003g0171 a0001c0002t0003g0175 |
2 | HG01099.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.2247-1835C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864750 | |||||||
| chr4:47864945 | G | A | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2247-2030C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47864945 | |||||||
| chr4:47865100 | C | T | 1 | a0001c0002t0001g0055 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2247-2185G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865100 | |||||||
| chr4:47865357 | T | C | 2 | a0002c0008t0001g0295 a0002c0008t0001g0296 |
2 | NA18939.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.2247-2442A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865357 | |||||||
| chr4:47865488 | G | GA | 102 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(99): Show |
119 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.2247-2574dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865488 | |||||||
| chr4:47865488 | G | GAA | 6 | a0001c0002t0001g0053 a0001c0002t0001g0062 a0001c0002t0001g0067 others(3): Show |
6 | HG02109.hp1 HG03041.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2247-2575_2247-257 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865488 | |||||||
| chr4:47865488 | GA | G | 67 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(64): Show |
74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2247-2574delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865488 | |||||||
| chr4:47865499 | AAAC | A | 110 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(107): Show |
155 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2247-2587_2247-258 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865499 | |||||||
| chr4:47865500 | AAC | A | 16 | a0002c0001t0001g0028 a0002c0001t0001g0029 a0002c0001t0001g0030 others(13): Show |
20 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2247-2587_2247-258 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865500 | |||||||
| chr4:47865533 | C | T | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-2618G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865533 | |||||||
| chr4:47865571 | A | G | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2247-2656T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865571 | |||||||
| chr4:47865581 | T | G | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247-2666A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865581 | |||||||
| chr4:47865678 | C | A | 1 | a0001c0003t0002g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2247-2763G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865678 | |||||||
| chr4:47865748 | TCGGAGGC others(17): Show |
T | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247-2857_2247-283 others(28): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865748 | |||||||
| chr4:47865782 | A | C | 1 | a0001c0003t0002g0147 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2247-2867T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47865782 | |||||||
| chr4:47866011 | T | G | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2247-3096A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866011 | |||||||
| chr4:47866087 | C | T | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2247-3172G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866087 | |||||||
| chr4:47866096 | G | A | 1 | a0001c0002t0003g0303 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2247-3181C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866096 | |||||||
| chr4:47866255 | G | A | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2247-3340C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866255 | |||||||
| chr4:47866298 | C | G | 1 | a0001c0002t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2247-3383G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866298 | |||||||
| chr4:47866400 | G | A | 1 | a0001c0002t0001g0077 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2247-3485C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866400 | |||||||
| chr4:47866872 | G | A | 269 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(266): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.2247-3957C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47866872 | |||||||
| chr4:47867029 | G | A | 6 | a0001c0003t0002g0107 a0001c0003t0002g0108 a0001c0003t0002g0109 others(3): Show |
6 | HG00323.hp2 HG01358.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247-4114C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867029 | |||||||
| chr4:47867206 | T | C | 2 | a0002c0001t0001g0220 a0002c0001t0001g0224 |
2 | NA18994.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2247-4291A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867206 | |||||||
| chr4:47867241 | G | GA | 67 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(64): Show |
74 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.2247-4327dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867241 | |||||||
| chr4:47867361 | G | A | 1 | a0001c0003t0002g0103 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2247-4446C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867361 | |||||||
| chr4:47867386 | A | G | 1 | a0002c0001t0001g0193 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2247-4471T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867386 | |||||||
| chr4:47867507 | G | C | 2 | a0001c0002t0001g0056 a0001c0002t0001g0064 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2247-4592C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867507 | |||||||
| chr4:47867530 | A | G | 1 | a0001c0002t0001g0090 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2247-4615T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867530 | |||||||
| chr4:47867642 | T | TGGA | 71 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(68): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.2247-4730_2247-472 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867642 | |||||||
| chr4:47867663 | G | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2247-4748C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867663 | |||||||
| chr4:47867766 | G | A | 1 | a0001c0003t0002g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2247-4851C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867766 | |||||||
| chr4:47867829 | T | TTA | 4 | a0001c0002t0003g0166 a0001c0004t0003g0153 a0001c0004t0003g0170 others(1): Show |
4 | HG00639.hp1 HG00733.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-4916_2247-491 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867829 | |||||||
| chr4:47867888 | A | G | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2247-4973T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867888 | |||||||
| chr4:47867929 | G | C | 1 | a0002c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2247-5014C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867929 | |||||||
| chr4:47867952 | T | G | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2247-5037A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47867952 | |||||||
| chr4:47868185 | G | A | 1 | a0001c0002t0001g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2247-5270C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868185 | |||||||
| chr4:47868211 | C | T | 11 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(8): Show |
12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2247-5296G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868211 | |||||||
| chr4:47868250 | C | T | 1 | a0002c0001t0001g0204 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2247-5335G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868250 | |||||||
| chr4:47868268 | G | A | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2247-5353C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868268 | |||||||
| chr4:47868294 | G | A | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2247-5379C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868294 | |||||||
| chr4:47868296 | G | C | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-5381C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868296 | |||||||
| chr4:47868334 | A | G | 4 | a0002c0001t0001g0184 a0002c0001t0001g0221 a0002c0001t0001g0276 others(1): Show |
4 | NA18961.hp2 NA18974.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2247-5419T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868334 | |||||||
| chr4:47868351 | A | G | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2247-5436T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868351 | |||||||
| chr4:47868357 | C | T | 46 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0005 others(43): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.2247-5442G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868357 | |||||||
| chr4:47868456 | C | CAAAAT | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2247-5542_2247-554 others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868456 | |||||||
| chr4:47868537 | G | A | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2247-5622C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868537 | |||||||
| chr4:47868625 | T | C | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2247-5710A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868625 | |||||||
| chr4:47868835 | T | C | 6 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(3): Show |
10 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2247-5920A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868835 | |||||||
| chr4:47868907 | C | T | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2247-5992G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868907 | |||||||
| chr4:47868948 | T | C | 1 | a0002c0001t0001g0272 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2247-6033A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868948 | |||||||
| chr4:47868986 | T | C | 65 | a0002c0001t0001g0001 a0002c0001t0001g0009 a0002c0001t0001g0028 others(62): Show |
89 | HG00408.hp1 HG00423.hp2 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.2247-6071A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47868986 | |||||||
| chr4:47869147 | C | A | 3 | a0001c0002t0003g0026 a0001c0002t0003g0167 a0001c0002t0003g0174 |
4 | HG02559.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246+5980G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869147 | |||||||
| chr4:47869359 | G | A | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2246+5768C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869359 | |||||||
| chr4:47869532 | T | C | 1 | a0002c0001t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2246+5595A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869532 | |||||||
| chr4:47869825 | C | T | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2246+5302G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47869825 | |||||||
| chr4:47870161 | A | T | 4 | a0001c0002t0003g0026 a0001c0002t0003g0157 a0001c0002t0003g0167 others(1): Show |
5 | HG02559.hp1 HG02717.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.2246+4966T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870161 | |||||||
| chr4:47870424 | T | A | 1 | a0002c0001t0001g0216 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2246+4703A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870424 | |||||||
| chr4:47870477 | TAAAG | T | 61 | a0001c0003t0001g0118 a0001c0003t0002g0018 a0001c0003t0002g0019 others(58): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.2246+4646_2246+464 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870477 | |||||||
| chr4:47870536 | A | G | 1 | a0001c0003t0002g0147 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2246+4591T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870536 | |||||||
| chr4:47870604 | GA | G | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2246+4522delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870604 | |||||||
| chr4:47870620 | A | G | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.2246+4507T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870620 | |||||||
| chr4:47870734 | A | G | 3 | a0001c0002t0003g0024 a0001c0002t0003g0154 a0001c0002t0003g0155 |
4 | HG00099.hp1 HG00741.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2246+4393T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870734 | |||||||
| chr4:47870948 | C | T | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2246+4179G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870948 | |||||||
| chr4:47870998 | GGTTGGGA others(11): Show |
G | 5 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(2): Show |
6 | HG00642.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2246+4111_2246+412 others(22): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47870998 | |||||||
| chr4:47871117 | G | A | 269 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(266): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.2246+4010C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871117 | |||||||
| chr4:47871119 | G | C | 1 | a0001c0003t0002g0114 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2246+4008C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871119 | |||||||
| chr4:47871150 | A | C | 2 | a0003c0005t0001g0031 a0003c0005t0001g0187 |
3 | HG01891.hp1 HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2246+3977T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871150 | |||||||
| chr4:47871175 | C | T | 1 | a0001c0003t0002g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2246+3952G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871175 | |||||||
| chr4:47871180 | C | A | 1 | a0001c0002t0001g0041 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2246+3947G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871180 | |||||||
| chr4:47871209 | T | C | 1 | a0002c0001t0001g0195 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2246+3918A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871209 | |||||||
| chr4:47871346 | G | A | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2246+3781C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871346 | |||||||
| chr4:47871350 | C | CA | 195 | a0001c0002t0001g0078 a0001c0003t0001g0011 a0001c0003t0001g0034 others(192): Show |
255 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.2246+3776dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871350 | |||||||
| chr4:47871350 | C | CAA | 6 | a0001c0003t0002g0131 a0001c0003t0002g0145 a0001c0003t0002g0147 others(3): Show |
6 | HG02056.hp2 HG03486.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.2246+3775_2246+377 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871350 | |||||||
| chr4:47871361 | A | C | 7 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(4): Show |
8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2246+3766T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871361 | |||||||
| chr4:47871365 | C | A | 2 | a0001c0003t0002g0128 a0001c0003t0002g0147 |
2 | HG02056.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.2246+3762G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871365 | |||||||
| chr4:47871385 | A | G | 2 | a0002c0001t0001g0248 a0002c0001t0001g0249 |
2 | HG01070.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2246+3742T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871385 | |||||||
| chr4:47871558 | G | C | 19 | a0001c0003t0002g0018 a0001c0003t0002g0019 a0001c0003t0002g0020 others(16): Show |
22 | HG00735.hp1 HG00741.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.2246+3569C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871558 | |||||||
| chr4:47871744 | T | G | 3 | a0001c0002t0001g0058 a0001c0002t0001g0079 a0001c0002t0009g0036 |
3 | HG02300.hp2 HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2246+3383A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871744 | |||||||
| chr4:47871918 | G | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2246+3209C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47871918 | |||||||
| chr4:47872131 | G | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2246+2996C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872131 | |||||||
| chr4:47872359 | G | A | 65 | a0002c0001t0001g0001 a0002c0001t0001g0009 a0002c0001t0001g0028 others(62): Show |
89 | HG00408.hp1 HG00423.hp2 HG01071.hp2 others(86): Show |
intron_variant | MODIFIER | c.2246+2768C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872359 | |||||||
| chr4:47872394 | A | G | 269 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(266): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.2246+2733T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872394 | |||||||
| chr4:47872461 | CA | C | 190 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(187): Show |
243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.2246+2665delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872461 | |||||||
| chr4:47872461 | CAA | C | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01070.hp1 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2246+2664_2246+266 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872461 | |||||||
| chr4:47872476 | AAG | A | 6 | a0002c0001t0001g0004 a0002c0001t0001g0191 a0002c0001t0001g0202 others(3): Show |
9 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2246+2649_2246+265 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872476 | |||||||
| chr4:47872479 | A | G | 6 | a0002c0001t0001g0004 a0002c0001t0001g0191 a0002c0001t0001g0202 others(3): Show |
9 | HG01255.hp2 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2246+2648T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872479 | |||||||
| chr4:47872528 | G | C | 1 | a0001c0003t0008g0304 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2246+2599C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872528 | |||||||
| chr4:47872560 | G | A | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.2246+2567C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872560 | |||||||
| chr4:47872622 | T | C | 1 | a0002c0001t0001g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2246+2505A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872622 | |||||||
| chr4:47872883 | C | T | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2246+2244G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872883 | |||||||
| chr4:47872909 | T | C | 1 | a0002c0001t0001g0236 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2246+2218A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47872909 | |||||||
| chr4:47873038 | C | T | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2246+2089G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873038 | |||||||
| chr4:47873299 | T | G | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2246+1828A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873299 | |||||||
| chr4:47873337 | G | A | 1 | a0001c0002t0001g0070 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2246+1790C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873337 | |||||||
| chr4:47873470 | C | T | 15 | a0001c0003t0002g0021 a0001c0003t0002g0022 a0001c0003t0002g0057 others(12): Show |
17 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.2246+1657G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873470 | |||||||
| chr4:47873548 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2246+1579A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873548 | |||||||
| chr4:47873653 | T | C | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2246+1474A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873653 | |||||||
| chr4:47873707 | G | A | 1 | a0001c0003t0004g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2246+1420C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873707 | |||||||
| chr4:47873841 | CT | C | 7 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(4): Show |
8 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2246+1285delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873841 | |||||||
| chr4:47873869 | T | C | 2 | a0001c0003t0002g0100 a0001c0003t0002g0138 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2246+1258A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47873869 | |||||||
| chr4:47874069 | T | C | 1 | a0001c0002t0001g0044 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2246+1058A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874069 | |||||||
| chr4:47874278 | T | C | 1 | a0001c0003t0004g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2246+849A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874278 | |||||||
| chr4:47874397 | C | A | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2246+730G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874397 | |||||||
| chr4:47874466 | T | A | 1 | a0002c0001t0001g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2246+661A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874466 | |||||||
| chr4:47874687 | A | T | 1 | a0001c0002t0001g0071 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2246+440T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874687 | |||||||
| chr4:47874710 | A | AAAT | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2246+416_2246+417i others(5): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874710 | |||||||
| chr4:47874744 | A | T | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2246+383T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874744 | |||||||
| chr4:47874791 | A | C | 6 | a0002c0001t0001g0184 a0002c0001t0001g0221 a0002c0001t0001g0222 others(3): Show |
6 | NA18961.hp2 NA18974.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.2246+336T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874791 | |||||||
| chr4:47874906 | T | C | 2 | a0002c0001t0001g0004 a0002c0001t0001g0191 |
5 | HG01255.hp2 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2246+221A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47874906 | |||||||
| chr4:47875045 | C | T | 1 | a0001c0003t0002g0057 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2246+82G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47875045 | |||||||
| chr4:47875107 | T | C | 1 | a0001c0003t0002g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2246+20A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 18/22 | chr4 | 47875107 | |||||||
| chr4:47875296 | G | C | 1 | a0001c0002t0003g0157 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.2080-3C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875296 | |||||||
| chr4:47875507 | T | C | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2080-214A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875507 | |||||||
| chr4:47875579 | G | C | 1 | a0002c0001t0001g0262 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2080-286C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875579 | |||||||
| chr4:47875642 | G | A | 1 | a0006c0012t0001g0243 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2080-349C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875642 | |||||||
| chr4:47875670 | G | A | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2080-377C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875670 | |||||||
| chr4:47875823 | C | A | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.2080-530G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875823 | |||||||
| chr4:47875985 | G | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2080-692C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47875985 | |||||||
| chr4:47876120 | T | C | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2080-827A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876120 | |||||||
| chr4:47876254 | G | A | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2080-961C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876254 | |||||||
| chr4:47876288 | C | T | 116 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(113): Show |
164 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2080-995G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876288 | |||||||
| chr4:47876539 | T | C | 1 | a0002c0001t0001g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2080-1246A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876539 | |||||||
| chr4:47876548 | T | C | 120 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(117): Show |
169 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.2080-1255A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876548 | |||||||
| chr4:47876665 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2080-1372A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876665 | |||||||
| chr4:47876708 | G | C | 11 | a0002c0001t0001g0196 a0002c0001t0001g0233 a0002c0001t0001g0234 others(8): Show |
11 | HG00423.hp2 HG03688.hp2 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.2080-1415C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876708 | |||||||
| chr4:47876785 | T | C | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2080-1492A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876785 | |||||||
| chr4:47876932 | A | G | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2079+1593T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876932 | |||||||
| chr4:47876962 | C | CAAAT | 120 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(117): Show |
169 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.2079+1559_2079+156 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47876962 | |||||||
| chr4:47877526 | C | T | 11 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(8): Show |
12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2079+999G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877526 | |||||||
| chr4:47877537 | C | A | 52 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(49): Show |
61 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.2079+988G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877537 | |||||||
| chr4:47877693 | AAAG | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2079+829_2079+831d others(5): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877693 | |||||||
| chr4:47877987 | G | A | 1 | a0001c0003t0001g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2079+538C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47877987 | |||||||
| chr4:47878132 | T | C | 3 | a0002c0001t0001g0264 a0002c0001t0001g0265 a0002c0001t0001g0267 |
3 | HG01074.hp2 HG02698.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2079+393A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878132 | |||||||
| chr4:47878185 | CAG | C | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2079+338_2079+339d others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878185 | |||||||
| chr4:47878397 | G | T | 1 | a0001c0002t0003g0157 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2079+128C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878397 | |||||||
| chr4:47878477 | G | A | 119 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(116): Show |
168 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.2079+48C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 17/22 | chr4 | 47878477 | |||||||
| chr4:47878725 | T | C | 4 | a0001c0002t0001g0055 a0001c0002t0001g0080 a0001c0002t0001g0081 others(1): Show |
4 | NA18973.hp1 NA18974.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-60A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 16/22 | chr4 | 47878725 | |||||||
| chr4:47878788 | GAATAAT | G | 3 | a0001c0002t0001g0054 a0001c0002t0001g0070 a0001c0002t0001g0082 |
3 | NA18987.hp1 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1939-129_1939-124d others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 16/22 | chr4 | 47878788 | |||||||
| chr4:47879085 | C | G | 1 | a0001c0003t0002g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1938+11G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 16/22 | chr4 | 47879085 | |||||||
| chr4:47879174 | C | T | 119 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(116): Show |
168 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1917-57G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879174 | |||||||
| chr4:47879575 | T | C | 2 | a0001c0002t0001g0087 a0001c0002t0001g0097 |
2 | NA18747.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1917-458A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879575 | |||||||
| chr4:47879742 | G | C | 2 | a0001c0002t0001g0062 a0001c0002t0001g0083 |
2 | HG00609.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1917-625C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879742 | |||||||
| chr4:47879777 | T | C | 11 | a0002c0001t0001g0028 a0002c0001t0001g0029 a0002c0001t0001g0030 others(8): Show |
15 | HG01167.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1917-660A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879777 | |||||||
| chr4:47879849 | C | A | 199 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(196): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1917-732G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47879849 | |||||||
| chr4:47880015 | A | G | 1 | a0002c0001t0001g0217 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1917-898T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880015 | |||||||
| chr4:47880050 | T | C | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-933A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880050 | |||||||
| chr4:47880055 | G | A | 2 | a0002c0001t0001g0284 a0002c0001t0001g0286 |
2 | NA19010.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1917-938C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880055 | |||||||
| chr4:47880057 | C | T | 11 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(8): Show |
12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1917-940G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880057 | |||||||
| chr4:47880082 | A | C | 267 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(264): Show |
337 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(334): Show |
intron_variant | MODIFIER | c.1917-965T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880082 | |||||||
| chr4:47880137 | T | A | 11 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(8): Show |
15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1917-1020A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880137 | |||||||
| chr4:47880151 | T | C | 2 | a0002c0001t0001g0213 a0002c0001t0001g0223 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1917-1034A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880151 | |||||||
| chr4:47880304 | G | C | 2 | a0001c0002t0003g0161 a0001c0002t0003g0164 |
2 | HG01099.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.1917-1187C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880304 | |||||||
| chr4:47880426 | C | CA | 21 | a0001c0002t0001g0012 a0001c0002t0001g0041 a0001c0002t0001g0042 others(18): Show |
22 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1917-1310dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880426 | |||||||
| chr4:47880426 | CA | C | 21 | a0001c0002t0001g0070 a0001c0003t0001g0011 a0001c0003t0001g0034 others(18): Show |
26 | HG01070.hp2 HG01243.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1917-1310delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880426 | |||||||
| chr4:47880473 | G | A | 1 | a0002c0001t0011g0281 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1917-1356C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880473 | |||||||
| chr4:47880720 | G | A | 1 | a0002c0001t0001g0190 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1917-1603C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880720 | |||||||
| chr4:47880748 | G | A | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1917-1631C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880748 | |||||||
| chr4:47880807 | T | TA | 11 | a0001c0002t0001g0041 a0001c0002t0001g0042 a0001c0002t0001g0045 others(8): Show |
11 | HG00733.hp2 HG01109.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-1691dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | |||||||
| chr4:47880807 | TA | T | 121 | a0001c0002t0001g0068 a0001c0002t0001g0085 a0001c0002t0001g0086 others(118): Show |
168 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1917-1691delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | |||||||
| chr4:47880807 | TAA | T | 111 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(108): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1917-1692_1917-169 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | |||||||
| chr4:47880807 | TAAA | T | 7 | a0001c0002t0001g0064 a0001c0003t0001g0011 a0001c0003t0001g0034 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1917-1693_1917-169 others(7): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880807 | |||||||
| chr4:47880820 | A | G | 1 | a0002c0001t0001g0192 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1917-1703T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880820 | |||||||
| chr4:47880824 | A | C | 1 | a0001c0003t0001g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1917-1707T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880824 | |||||||
| chr4:47880916 | T | C | 1 | a0002c0001t0001g0260 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1917-1799A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47880916 | |||||||
| chr4:47881007 | T | C | 125 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(122): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1917-1890A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881007 | |||||||
| chr4:47881066 | T | C | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1917-1949A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881066 | |||||||
| chr4:47881456 | T | C | 3 | a0002c0001t0001g0005 a0002c0001t0001g0252 a0002c0001t0001g0271 |
6 | NA18942.hp1 NA18969.hp1 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1917-2339A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881456 | |||||||
| chr4:47881529 | T | C | 199 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(196): Show |
258 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.1917-2412A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881529 | |||||||
| chr4:47881736 | A | G | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1916+2610T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881736 | |||||||
| chr4:47881746 | T | C | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1916+2600A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47881746 | |||||||
| chr4:47882143 | ACT | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1916+2201_1916+220 others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882143 | |||||||
| chr4:47882203 | A | G | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1916+2143T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882203 | |||||||
| chr4:47882208 | T | C | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1916+2138A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882208 | |||||||
| chr4:47882327 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1916+2019T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882327 | |||||||
| chr4:47882365 | G | A | 3 | a0001c0002t0003g0026 a0001c0002t0003g0167 a0001c0002t0003g0174 |
4 | HG02559.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1916+1981C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882365 | |||||||
| chr4:47882372 | T | C | 8 | a0001c0002t0001g0017 a0001c0002t0001g0059 a0001c0002t0001g0060 others(5): Show |
9 | HG00423.hp1 HG01934.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1916+1974A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882372 | |||||||
| chr4:47882720 | ATTGT | A | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1916+1622_1916+162 others(8): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882720 | |||||||
| chr4:47882775 | A | C | 1 | a0001c0002t0003g0156 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1916+1571T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882775 | |||||||
| chr4:47882819 | G | A | 1 | a0002c0001t0001g0240 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1916+1527C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47882819 | |||||||
| chr4:47883068 | T | G | 6 | a0001c0003t0002g0022 a0001c0003t0002g0057 a0001c0003t0002g0117 others(3): Show |
7 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1916+1278A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883068 | |||||||
| chr4:47883128 | G | C | 1 | a0001c0002t0001g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1916+1218C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883128 | |||||||
| chr4:47883336 | G | A | 1 | a0001c0002t0001g0066 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1916+1010C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883336 | |||||||
| chr4:47883997 | G | A | 10 | a0002c0001t0001g0248 a0002c0001t0001g0249 a0002c0001t0001g0261 others(7): Show |
10 | HG00280.hp1 HG01070.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1916+349C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47883997 | |||||||
| chr4:47884087 | C | T | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1916+259G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884087 | |||||||
| chr4:47884088 | G | A | 1 | a0001c0003t0002g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1916+258C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884088 | |||||||
| chr4:47884101 | A | C | 9 | a0002c0001t0001g0196 a0002c0001t0001g0233 a0002c0001t0001g0234 others(6): Show |
9 | HG00423.hp2 NA18612.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.1916+245T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884101 | |||||||
| chr4:47884302 | A | C | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1916+44T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884302 | |||||||
| chr4:47884312 | G | T | 3 | a0001c0002t0003g0024 a0001c0002t0003g0154 a0001c0002t0003g0155 |
4 | HG00099.hp1 HG00741.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1916+34C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 15/22 | chr4 | 47884312 | |||||||
| chr4:47884722 | C | G | 60 | a0001c0003t0002g0018 a0001c0003t0002g0019 a0001c0003t0002g0020 others(57): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1825-285G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47884722 | |||||||
| chr4:47884898 | G | A | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1825-461C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47884898 | |||||||
| chr4:47885035 | G | A | 1 | a0001c0003t0002g0292 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1824+463C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885035 | |||||||
| chr4:47885049 | C | G | 68 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(65): Show |
78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1824+449G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885049 | |||||||
| chr4:47885050 | C | T | 1 | a0001c0003t0002g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1824+448G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885050 | |||||||
| chr4:47885119 | C | T | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1824+379G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885119 | |||||||
| chr4:47885188 | T | C | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1824+310A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885188 | |||||||
| chr4:47885376 | C | T | 68 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(65): Show |
78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1824+122G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885376 | |||||||
| chr4:47885491 | C | G | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.1824+7G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 14/22 | chr4 | 47885491 | |||||||
| chr4:47885700 | T | C | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1665-43A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 13/22 | chr4 | 47885700 | |||||||
| chr4:47886024 | A | G | 1 | a0001c0003t0002g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1544-25T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886024 | |||||||
| chr4:47886120 | T | A | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1544-121A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886120 | |||||||
| chr4:47886176 | T | C | 1 | a0002c0001t0001g0266 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1544-177A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886176 | |||||||
| chr4:47886366 | T | C | 10 | a0002c0001t0001g0004 a0002c0001t0001g0008 a0002c0001t0001g0191 others(7): Show |
15 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1544-367A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886366 | |||||||
| chr4:47886508 | C | G | 11 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(8): Show |
15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1544-509G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886508 | |||||||
| chr4:47886640 | T | A | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1544-641A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886640 | |||||||
| chr4:47886641 | G | T | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1544-642C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886641 | |||||||
| chr4:47886647 | G | A | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1544-648C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886647 | |||||||
| chr4:47886798 | C | T | 125 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(122): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1544-799G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886798 | |||||||
| chr4:47886875 | T | C | 68 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(65): Show |
78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1544-876A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886875 | |||||||
| chr4:47886928 | G | T | 1 | a0001c0002t0001g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1544-929C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47886928 | |||||||
| chr4:47887066 | C | T | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.1544-1067G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887066 | |||||||
| chr4:47887234 | A | G | 1 | a0001c0003t0002g0128 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1544-1235T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887234 | |||||||
| chr4:47887340 | T | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1544-1341A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887340 | |||||||
| chr4:47887354 | G | T | 1 | a0001c0002t0003g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1544-1355C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887354 | |||||||
| chr4:47887634 | G | A | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1544-1635C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887634 | |||||||
| chr4:47887725 | G | A | 2 | a0002c0001t0001g0195 a0002c0001t0001g0226 |
2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1544-1726C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887725 | |||||||
| chr4:47887867 | G | A | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1544-1868C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887867 | |||||||
| chr4:47887971 | T | C | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1544-1972A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47887971 | |||||||
| chr4:47888201 | G | T | 1 | a0002c0001t0001g0280 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1544-2202C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888201 | |||||||
| chr4:47888488 | T | C | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543+2125A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888488 | |||||||
| chr4:47888533 | T | C | 1 | a0001c0003t0002g0127 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1543+2080A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888533 | |||||||
| chr4:47888565 | AC | A | 125 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(122): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1543+2047delG | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888565 | |||||||
| chr4:47888692 | AC | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1920delG | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888692 | |||||||
| chr4:47888694 | T | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1919A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888694 | |||||||
| chr4:47888696 | A | T | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1917T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888696 | |||||||
| chr4:47888697 | G | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1916C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888697 | |||||||
| chr4:47888699 | C | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1914G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888699 | |||||||
| chr4:47888701 | C | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1912G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888701 | |||||||
| chr4:47888702 | T | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1911A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888702 | |||||||
| chr4:47888703 | G | A | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1910C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888703 | |||||||
| chr4:47888704 | A | G | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1909T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888704 | |||||||
| chr4:47888705 | G | C | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1908C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888705 | |||||||
| chr4:47888708 | A | C | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1543+1905T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888708 | |||||||
| chr4:47888821 | T | C | 122 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(119): Show |
170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1543+1792A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47888821 | |||||||
| chr4:47889051 | T | A | 2 | a0001c0002t0003g0167 a0001c0002t0003g0174 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1543+1562A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889051 | |||||||
| chr4:47889083 | G | A | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1543+1530C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889083 | |||||||
| chr4:47889768 | A | G | 3 | a0001c0002t0003g0024 a0001c0002t0003g0154 a0001c0002t0003g0155 |
4 | HG00099.hp1 HG00741.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1543+845T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889768 | |||||||
| chr4:47889817 | T | C | 1 | a0001c0003t0001g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1543+796A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889817 | |||||||
| chr4:47889936 | C | T | 125 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(122): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1543+677G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47889936 | |||||||
| chr4:47890013 | A | G | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1543+600T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890013 | |||||||
| chr4:47890299 | T | C | 1 | a0001c0003t0002g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1543+314A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890299 | |||||||
| chr4:47890318 | T | C | 2 | a0001c0003t0002g0122 a0001c0003t0002g0123 |
2 | HG01081.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1543+295A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890318 | |||||||
| chr4:47890467 | C | T | 1 | a0002c0001t0001g0231 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1543+146G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890467 | |||||||
| chr4:47890564 | A | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1543+49T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 12/22 | chr4 | 47890564 | |||||||
| chr4:47891114 | CT | C | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1453-412delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891114 | |||||||
| chr4:47891190 | C | T | 2 | a0001c0002t0001g0045 a0001c0002t0001g0046 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1453-487G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891190 | |||||||
| chr4:47891278 | G | A | 1 | a0002c0001t0001g0279 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1453-575C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891278 | |||||||
| chr4:47891413 | C | T | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-710G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891413 | |||||||
| chr4:47891416 | T | C | 1 | a0001c0003t0001g0035 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1453-713A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891416 | |||||||
| chr4:47891601 | A | G | 1 | a0002c0001t0001g0244 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1453-898T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891601 | |||||||
| chr4:47891624 | T | G | 1 | a0002c0001t0001g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1453-921A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891624 | |||||||
| chr4:47891801 | T | C | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1453-1098A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891801 | |||||||
| chr4:47891807 | G | A | 1 | a0001c0002t0006g0040 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453-1104C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891807 | |||||||
| chr4:47891830 | C | T | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1453-1127G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891830 | |||||||
| chr4:47891831 | G | A | 2 | a0001c0002t0001g0037 a0001c0002t0001g0042 |
2 | HG02280.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1453-1128C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891831 | |||||||
| chr4:47891918 | T | C | 1 | a0002c0001t0001g0227 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1453-1215A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47891918 | |||||||
| chr4:47892390 | C | T | 61 | a0001c0003t0001g0118 a0001c0003t0002g0018 a0001c0003t0002g0019 others(58): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1453-1687G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892390 | |||||||
| chr4:47892427 | G | A | 1 | a0002c0001t0001g0228 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1453-1724C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892427 | |||||||
| chr4:47892660 | A | T | 1 | a0002c0001t0001g0216 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1452+1520T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892660 | |||||||
| chr4:47892662 | T | C | 1 | a0002c0001t0001g0212 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1452+1518A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892662 | |||||||
| chr4:47892667 | C | T | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1452+1513G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892667 | |||||||
| chr4:47892786 | C | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1452+1394G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892786 | |||||||
| chr4:47892868 | A | T | 1 | a0001c0002t0001g0069 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1452+1312T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892868 | |||||||
| chr4:47892932 | C | A | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1452+1248G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47892932 | |||||||
| chr4:47893018 | G | A | 1 | a0002c0001t0001g0229 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1452+1162C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893018 | |||||||
| chr4:47893116 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+1064A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893116 | |||||||
| chr4:47893136 | G | A | 1 | a0002c0001t0001g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1452+1044C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893136 | |||||||
| chr4:47893201 | T | C | 125 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(122): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1452+979A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893201 | |||||||
| chr4:47893449 | A | C | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1452+731T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893449 | |||||||
| chr4:47893564 | G | T | 1 | a0002c0001t0001g0009 | 3 | NA18947.hp1 NA18990.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1452+616C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893564 | |||||||
| chr4:47893636 | A | C | 68 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(65): Show |
78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1452+544T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893636 | |||||||
| chr4:47893708 | AAAAAATG others(11): Show |
A | 1 | a0002c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1452+454_1452+471d others(20): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893708 | |||||||
| chr4:47893912 | CAGTGATC others(6): Show |
C | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1452+255_1452+267d others(15): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893912 | |||||||
| chr4:47893925 | T | TAGTC | 79 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(76): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.1452+254_1452+255i others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893925 | |||||||
| chr4:47893992 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1452+188A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47893992 | |||||||
| chr4:47894040 | T | C | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.1452+140A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47894040 | |||||||
| chr4:47894177 | A | C | 1 | a0002c0001t0001g0202 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.1452+3T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 11/22 | chr4 | 47894177 | |||||||
| chr4:47894309 | G | A | 6 | a0002c0001t0001g0030 a0002c0001t0001g0188 a0002c0001t0001g0189 others(3): Show |
8 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1330-7C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894309 | |||||||
| chr4:47894422 | C | T | 11 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(8): Show |
12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1330-120G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894422 | |||||||
| chr4:47894461 | T | C | 2 | a0002c0001t0001g0280 a0002c0001t0011g0281 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1330-159A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894461 | |||||||
| chr4:47894539 | T | TA | 77 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(74): Show |
88 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1330-238dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894539 | |||||||
| chr4:47894539 | T | TAA | 6 | a0001c0002t0001g0056 a0001c0002t0001g0064 a0001c0002t0001g0065 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-239_1330-238d others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894539 | |||||||
| chr4:47894539 | TA | T | 7 | a0001c0002t0003g0171 a0001c0003t0001g0048 a0001c0003t0001g0049 others(4): Show |
7 | HG01346.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-238delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894539 | |||||||
| chr4:47894575 | AT | A | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1330-274delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894575 | |||||||
| chr4:47894719 | T | G | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1330-417A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894719 | |||||||
| chr4:47894763 | C | G | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1330-461G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894763 | |||||||
| chr4:47894780 | C | T | 1 | a0002c0001t0001g0252 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1330-478G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894780 | |||||||
| chr4:47894909 | G | A | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1330-607C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894909 | |||||||
| chr4:47894917 | C | T | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1330-615G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894917 | |||||||
| chr4:47894990 | A | G | 47 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0005 others(44): Show |
66 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1330-688T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47894990 | |||||||
| chr4:47895100 | G | C | 1 | a0002c0001t0001g0269 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1330-798C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895100 | |||||||
| chr4:47895214 | G | A | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1330-912C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895214 | |||||||
| chr4:47895238 | A | T | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1330-936T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895238 | |||||||
| chr4:47895454 | T | C | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1329+1069A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895454 | |||||||
| chr4:47895507 | C | T | 4 | a0001c0002t0006g0038 a0001c0002t0006g0039 a0001c0002t0006g0040 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1329+1016G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895507 | |||||||
| chr4:47895649 | G | T | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1329+874C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895649 | |||||||
| chr4:47895678 | C | T | 2 | a0001c0002t0001g0067 a0001c0002t0001g0068 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1329+845G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895678 | |||||||
| chr4:47895717 | T | C | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1329+806A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895717 | |||||||
| chr4:47895861 | T | C | 1 | a0002c0001t0001g0230 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1329+662A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47895861 | |||||||
| chr4:47896059 | G | A | 11 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(8): Show |
12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1329+464C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896059 | |||||||
| chr4:47896092 | T | C | 46 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0005 others(43): Show |
65 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.1329+431A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896092 | |||||||
| chr4:47896112 | C | A | 1 | a0001c0006t0002g0149 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1329+411G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896112 | |||||||
| chr4:47896129 | T | C | 1 | a0002c0001t0001g0285 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1329+394A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896129 | |||||||
| chr4:47896217 | G | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1329+306C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896217 | |||||||
| chr4:47896309 | G | A | 1 | a0002c0001t0001g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1329+214C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896309 | |||||||
| chr4:47896339 | T | C | 5 | a0001c0003t0001g0011 a0001c0003t0001g0035 a0001c0003t0001g0298 others(2): Show |
8 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329+184A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896339 | |||||||
| chr4:47896474 | C | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1329+49G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 10/22 | chr4 | 47896474 | |||||||
| chr4:47896702 | A | G | 1 | a0002c0001t0001g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1205-55T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47896702 | |||||||
| chr4:47896738 | C | T | 1 | a0001c0003t0001g0105 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1205-91G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47896738 | |||||||
| chr4:47896868 | C | A | 1 | a0001c0003t0004g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1205-221G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47896868 | |||||||
| chr4:47897309 | C | G | 2 | a0001c0002t0001g0056 a0001c0002t0001g0064 |
2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1204+658G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897309 | |||||||
| chr4:47897352 | G | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1204+615C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897352 | |||||||
| chr4:47897502 | C | T | 1 | a0002c0001t0001g0213 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1204+465G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897502 | |||||||
| chr4:47897546 | C | G | 1 | a0002c0001t0001g0212 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1204+421G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897546 | |||||||
| chr4:47897691 | T | G | 18 | a0001c0003t0002g0021 a0001c0003t0002g0022 a0001c0003t0002g0057 others(15): Show |
21 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1204+276A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897691 | |||||||
| chr4:47897775 | T | A | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1204+192A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897775 | |||||||
| chr4:47897780 | T | C | 1 | a0001c0003t0001g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1204+187A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897780 | |||||||
| chr4:47897824 | G | A | 2 | a0002c0001t0001g0231 a0002c0001t0001g0232 |
2 | HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1204+143C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897824 | |||||||
| chr4:47897825 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1204+142C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897825 | |||||||
| chr4:47897897 | G | A | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1204+70C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 9/22 | chr4 | 47897897 | |||||||
| chr4:47898169 | CAAAT | C | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1090-92_1090-89del others(4): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898169 | |||||||
| chr4:47898320 | A | G | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1090-239T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898320 | |||||||
| chr4:47898452 | A | G | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.1089+305T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898452 | |||||||
| chr4:47898459 | C | T | 5 | a0001c0003t0002g0116 a0001c0003t0002g0121 a0001c0003t0002g0125 others(2): Show |
5 | NA18949.hp2 NA18961.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+298G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898459 | |||||||
| chr4:47898498 | A | G | 1 | a0002c0001t0001g0028 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1089+259T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898498 | |||||||
| chr4:47898542 | A | G | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1089+215T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898542 | |||||||
| chr4:47898708 | G | A | 1 | a0001c0002t0001g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1089+49C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898708 | |||||||
| chr4:47898708 | G | C | 2 | a0001c0003t0002g0114 a0001c0003t0002g0115 |
2 | HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1089+49C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 8/22 | chr4 | 47898708 | |||||||
| chr4:47899138 | C | CA | 11 | a0001c0002t0001g0063 a0001c0002t0001g0091 a0001c0002t0001g0092 others(8): Show |
11 | HG00621.hp2 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.827-19dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | |||||||
| chr4:47899138 | CA | C | 8 | a0001c0002t0001g0066 a0001c0002t0003g0152 a0002c0001t0001g0207 others(5): Show |
8 | HG01346.hp2 HG03225.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-19delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | |||||||
| chr4:47899138 | CAA | C | 128 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(125): Show |
181 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.827-20_827-19delTT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | |||||||
| chr4:47899138 | CAAA | C | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.827-21_827-19delTT others(1): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899138 | |||||||
| chr4:47899159 | A | T | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-39T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899159 | |||||||
| chr4:47899236 | C | T | 1 | a0002c0001t0001g0282 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.827-116G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899236 | |||||||
| chr4:47899242 | G | A | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.827-122C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899242 | |||||||
| chr4:47899298 | A | AT | 5 | a0001c0002t0001g0293 a0001c0003t0005g0033 a0001c0003t0005g0289 others(2): Show |
6 | HG02559.hp2 HG02630.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+71dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899298 | |||||||
| chr4:47899298 | AT | A | 12 | a0001c0002t0003g0168 a0001c0003t0001g0011 a0001c0003t0001g0034 others(9): Show |
16 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.826+71delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 6/22 | chr4 | 47899298 | |||||||
| chr4:47899982 | T | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.648-434A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47899982 | |||||||
| chr4:47900084 | G | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-536C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900084 | |||||||
| chr4:47900204 | A | G | 2 | a0002c0001t0001g0250 a0002c0001t0001g0277 |
2 | NA18940.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.648-656T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900204 | |||||||
| chr4:47900272 | C | T | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.648-724G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900272 | |||||||
| chr4:47900358 | C | T | 10 | a0002c0001t0001g0004 a0002c0001t0001g0008 a0002c0001t0001g0191 others(7): Show |
15 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.648-810G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900358 | |||||||
| chr4:47900594 | C | T | 1 | a0002c0001t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.648-1046G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900594 | |||||||
| chr4:47900595 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.648-1047T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900595 | |||||||
| chr4:47900600 | T | C | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.648-1052A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900600 | |||||||
| chr4:47900621 | C | A | 2 | a0002c0001t0001g0272 a0002c0001t0001g0273 |
2 | HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.648-1073G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900621 | |||||||
| chr4:47900788 | T | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.648-1240A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900788 | |||||||
| chr4:47900791 | C | T | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-1243G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900791 | |||||||
| chr4:47900820 | C | T | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.648-1272G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47900820 | |||||||
| chr4:47901150 | T | G | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.648-1602A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901150 | |||||||
| chr4:47901256 | G | C | 1 | a0001c0002t0006g0038 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.648-1708C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901256 | |||||||
| chr4:47901569 | G | A | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.647+1624C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901569 | |||||||
| chr4:47901907 | C | T | 1 | a0002c0001t0001g0030 | 2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.647+1286G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47901907 | |||||||
| chr4:47902113 | C | T | 1 | a0001c0003t0001g0118 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.647+1080G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902113 | |||||||
| chr4:47902436 | C | T | 68 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(65): Show |
78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.647+757G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902436 | |||||||
| chr4:47902529 | T | C | 1 | a0001c0003t0005g0290 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.647+664A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902529 | |||||||
| chr4:47902577 | C | A | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.647+616G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902577 | |||||||
| chr4:47902588 | G | A | 3 | a0001c0003t0002g0101 a0001c0003t0002g0143 a0001c0003t0002g0144 |
3 | HG00733.hp1 HG01243.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.647+605C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902588 | |||||||
| chr4:47902707 | G | T | 2 | a0002c0001t0001g0248 a0002c0001t0001g0249 |
2 | HG01070.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.647+486C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902707 | |||||||
| chr4:47902930 | G | A | 11 | a0002c0001t0001g0196 a0002c0001t0001g0233 a0002c0001t0001g0234 others(8): Show |
11 | HG00423.hp2 HG03688.hp2 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.647+263C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47902930 | |||||||
| chr4:47903141 | A | G | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.647+52T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 5/22 | chr4 | 47903141 | |||||||
| chr4:47903364 | C | A | 1 | a0001c0002t0003g0169 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.517-41G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903364 | |||||||
| chr4:47903509 | G | A | 1 | a0001c0003t0002g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.517-186C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903509 | |||||||
| chr4:47903548 | G | T | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.517-225C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903548 | |||||||
| chr4:47903654 | T | C | 61 | a0001c0003t0001g0118 a0001c0003t0002g0018 a0001c0003t0002g0019 others(58): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.517-331A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903654 | |||||||
| chr4:47903727 | G | A | 2 | a0002c0001t0001g0272 a0002c0001t0001g0273 |
2 | HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.517-404C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903727 | |||||||
| chr4:47903800 | C | T | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.517-477G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903800 | |||||||
| chr4:47903976 | T | C | 1 | a0002c0001t0001g0244 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.517-653A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47903976 | |||||||
| chr4:47904026 | G | A | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-703C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904026 | |||||||
| chr4:47904089 | C | G | 2 | a0001c0003t0002g0107 a0001c0003t0002g0109 |
2 | HG00323.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.517-766G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904089 | |||||||
| chr4:47904144 | T | A | 1 | a0002c0001t0001g0278 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.517-821A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904144 | |||||||
| chr4:47904444 | A | T | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.516+793T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904444 | |||||||
| chr4:47904447 | C | T | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+790G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904447 | |||||||
| chr4:47904665 | G | A | 1 | a0001c0004t0003g0170 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.516+572C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904665 | |||||||
| chr4:47904741 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+496G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904741 | |||||||
| chr4:47904795 | C | A | 112 | a0002c0001t0001g0001 a0002c0001t0001g0002 a0002c0001t0001g0003 others(109): Show |
155 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.516+442G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904795 | |||||||
| chr4:47904907 | C | CAAACCCA others(2): Show |
205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.516+329_516+330ins others(9): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47904907 | |||||||
| chr4:47905180 | A | G | 1 | a0001c0003t0002g0101 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.516+57T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 4/22 | chr4 | 47905180 | |||||||
| chr4:47905507 | G | A | 125 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(122): Show |
174 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.407-161C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905507 | |||||||
| chr4:47905634 | G | C | 1 | a0002c0001t0001g0245 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.407-288C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905634 | |||||||
| chr4:47905685 | T | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.407-339A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905685 | |||||||
| chr4:47905893 | T | C | 1 | a0002c0001t0001g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.407-547A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905893 | |||||||
| chr4:47905933 | TTC | T | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.407-589_407-588del others(2): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905933 | |||||||
| chr4:47905996 | T | A | 11 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(8): Show |
15 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.407-650A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47905996 | |||||||
| chr4:47906038 | G | C | 1 | a0001c0002t0001g0092 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.407-692C>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906038 | |||||||
| chr4:47906079 | T | C | 1 | a0007c0013t0010g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.407-733A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906079 | |||||||
| chr4:47906104 | T | TGAGCAGT others(9): Show |
1 | a0001c0003t0002g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.407-774_407-759dup others(16): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906104 | |||||||
| chr4:47906359 | A | G | 1 | a0001c0003t0002g0124 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.407-1013T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906359 | |||||||
| chr4:47906429 | T | A | 1 | a0001c0002t0001g0093 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.407-1083A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906429 | |||||||
| chr4:47906511 | C | A | 6 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(3): Show |
7 | HG01884.hp2 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.407-1165G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906511 | |||||||
| chr4:47906587 | A | T | 204 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(201): Show |
264 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.407-1241T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906587 | |||||||
| chr4:47906610 | A | C | 1 | a0001c0003t0002g0123 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.407-1264T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906610 | |||||||
| chr4:47906842 | G | T | 1 | a0002c0001t0001g0208 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.407-1496C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906842 | |||||||
| chr4:47906976 | A | C | 1 | a0001c0003t0002g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.407-1630T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47906976 | |||||||
| chr4:47907063 | T | C | 1 | a0001c0003t0004g0027 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.407-1717A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907063 | |||||||
| chr4:47907118 | A | G | 2 | a0001c0003t0008g0304 a0001c0003t0008g0305 |
2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.407-1772T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907118 | |||||||
| chr4:47907275 | A | G | 1 | a0002c0001t0001g0247 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.407-1929T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907275 | |||||||
| chr4:47907418 | C | T | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.407-2072G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907418 | |||||||
| chr4:47907550 | T | C | 3 | a0001c0003t0004g0177 a0001c0003t0004g0180 a0001c0003t0004g0181 |
3 | HG02895.hp1 HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.407-2204A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907550 | |||||||
| chr4:47907686 | A | T | 2 | a0002c0001t0001g0004 a0002c0001t0001g0191 |
5 | HG01255.hp2 HG02109.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-2340T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907686 | |||||||
| chr4:47907773 | C | T | 1 | a0001c0002t0001g0064 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.407-2427G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907773 | |||||||
| chr4:47907788 | G | T | 1 | a0002c0001t0001g0199 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.407-2442C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907788 | |||||||
| chr4:47907818 | A | T | 1 | a0001c0003t0002g0121 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.407-2472T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47907818 | |||||||
| chr4:47908114 | G | A | 1 | a0002c0008t0001g0296 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.406+2710C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908114 | |||||||
| chr4:47908166 | G | A | 1 | a0002c0001t0001g0273 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.406+2658C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908166 | |||||||
| chr4:47908302 | C | T | 1 | a0001c0003t0002g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.406+2522G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908302 | |||||||
| chr4:47908310 | G | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+2514C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908310 | |||||||
| chr4:47908422 | CA | C | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.406+2401delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908422 | |||||||
| chr4:47908507 | T | C | 47 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0005 others(44): Show |
66 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.406+2317A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908507 | |||||||
| chr4:47908510 | TACTA | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.406+2310_406+2313d others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908510 | |||||||
| chr4:47908677 | C | T | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+2147G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908677 | |||||||
| chr4:47908678 | T | G | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.406+2146A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908678 | |||||||
| chr4:47908727 | G | A | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.406+2097C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908727 | |||||||
| chr4:47908731 | G | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0094 a0001c0002t0001g0095 others(1): Show |
6 | NA18944.hp1 NA18952.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+2093C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908731 | |||||||
| chr4:47908759 | T | C | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.406+2065A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908759 | |||||||
| chr4:47908880 | G | A | 1 | a0001c0002t0003g0174 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.406+1944C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908880 | |||||||
| chr4:47908926 | G | A | 132 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(129): Show |
182 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.406+1898C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908926 | |||||||
| chr4:47908953 | G | A | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.406+1871C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908953 | |||||||
| chr4:47908954 | C | CA | 83 | a0001c0002t0001g0044 a0001c0002t0001g0055 a0001c0002t0001g0062 others(80): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.406+1869dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908954 | |||||||
| chr4:47908954 | CA | C | 9 | a0002c0001t0001g0004 a0002c0001t0001g0008 a0002c0001t0001g0191 others(6): Show |
14 | HG01255.hp2 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.406+1869delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47908954 | |||||||
| chr4:47909047 | C | T | 1 | a0001c0003t0002g0106 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.406+1777G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909047 | |||||||
| chr4:47909288 | C | A | 1 | a0002c0001t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.406+1536G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909288 | |||||||
| chr4:47909289 | T | A | 1 | a0002c0001t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.406+1535A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909289 | |||||||
| chr4:47909344 | T | A | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.406+1480A>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909344 | |||||||
| chr4:47909489 | C | T | 1 | a0001c0002t0003g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.406+1335G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909489 | |||||||
| chr4:47909558 | G | A | 1 | a0002c0001t0001g0279 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.406+1266C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909558 | |||||||
| chr4:47909559 | C | T | 3 | a0002c0001t0001g0199 a0002c0001t0001g0200 a0002c0001t0001g0201 |
3 | HG00609.hp1 NA18975.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.406+1265G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909559 | |||||||
| chr4:47909567 | T | C | 2 | a0002c0001t0001g0280 a0002c0001t0011g0281 |
2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.406+1257A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909567 | |||||||
| chr4:47909659 | C | CT | 58 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(55): Show |
67 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.406+1164dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909659 | |||||||
| chr4:47909659 | CT | C | 7 | a0001c0002t0003g0174 a0001c0003t0002g0146 a0002c0001t0001g0282 others(4): Show |
7 | HG00558.hp2 HG01943.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.406+1164delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909659 | |||||||
| chr4:47909941 | G | A | 60 | a0001c0003t0002g0018 a0001c0003t0002g0019 a0001c0003t0002g0020 others(57): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.406+883C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47909941 | |||||||
| chr4:47910148 | G | A | 62 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.406+676C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910148 | |||||||
| chr4:47910229 | G | T | 1 | a0002c0001t0001g0198 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.406+595C>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910229 | |||||||
| chr4:47910236 | A | G | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.406+588T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910236 | |||||||
| chr4:47910263 | A | G | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.406+561T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910263 | |||||||
| chr4:47910313 | C | T | 1 | a0001c0003t0002g0117 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.406+511G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910313 | |||||||
| chr4:47910396 | A | C | 1 | a0001c0003t0002g0116 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.406+428T>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910396 | |||||||
| chr4:47910428 | G | A | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.406+396C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910428 | |||||||
| chr4:47910530 | C | T | 10 | a0001c0003t0002g0106 a0001c0003t0002g0107 a0001c0003t0002g0108 others(7): Show |
10 | HG00323.hp2 HG00738.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.406+294G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910530 | |||||||
| chr4:47910631 | T | C | 1 | a0002c0001t0001g0197 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.406+193A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 3/22 | chr4 | 47910631 | |||||||
| chr4:47911110 | C | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.236-116G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911110 | |||||||
| chr4:47911139 | T | G | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.236-145A>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911139 | |||||||
| chr4:47911234 | G | A | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.236-240C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911234 | |||||||
| chr4:47911459 | C | T | 7 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(4): Show |
11 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.236-465G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911459 | |||||||
| chr4:47911663 | T | C | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.236-669A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47911663 | |||||||
| chr4:47912324 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.236-1330A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912324 | |||||||
| chr4:47912345 | C | A | 68 | a0001c0003t0001g0102 a0001c0003t0001g0118 a0001c0003t0002g0018 others(65): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.236-1351G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912345 | |||||||
| chr4:47912461 | C | CT | 57 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0013 others(54): Show |
66 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.236-1468dupA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912461 | |||||||
| chr4:47912461 | CT | C | 207 | a0001c0002t0001g0045 a0001c0002t0001g0046 a0001c0002t0003g0175 others(204): Show |
267 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.236-1468delA | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912461 | |||||||
| chr4:47912499 | G | A | 1 | a0001c0002t0001g0099 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.235+1470C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912499 | |||||||
| chr4:47912528 | C | T | 205 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(202): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.235+1441G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912528 | |||||||
| chr4:47912607 | T | C | 273 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(270): Show |
343 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.235+1362A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912607 | |||||||
| chr4:47912611 | A | AC | 18 | a0001c0002t0001g0058 a0001c0002t0001g0059 a0001c0002t0001g0060 others(15): Show |
18 | HG00621.hp1 HG01175.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+1357dupG | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912611 | |||||||
| chr4:47912612 | C | T | 1 | a0001c0003t0001g0102 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.235+1357G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912612 | |||||||
| chr4:47912829 | T | TA | 8 | a0001c0003t0002g0150 a0002c0001t0001g0030 a0002c0001t0001g0188 others(5): Show |
10 | HG01891.hp1 HG01934.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+1139dupT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912829 | |||||||
| chr4:47912830 | A | G | 1 | a0001c0003t0002g0101 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.235+1139T>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912830 | |||||||
| chr4:47912880 | G | A | 68 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(65): Show |
78 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.235+1089C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912880 | |||||||
| chr4:47912995 | C | G | 1 | a0001c0002t0001g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.235+974G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47912995 | |||||||
| chr4:47913011 | CA | C | 8 | a0001c0002t0001g0037 a0001c0003t0001g0048 a0001c0003t0002g0147 others(5): Show |
8 | HG00558.hp1 HG00741.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+957delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | |||||||
| chr4:47913011 | CAA | C | 180 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(177): Show |
236 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.235+956_235+957del others(2): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | |||||||
| chr4:47913011 | CAAA | C | 14 | a0001c0003t0002g0100 a0002c0001t0001g0028 a0002c0001t0001g0029 others(11): Show |
18 | HG01070.hp1 HG01167.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.235+955_235+957del others(3): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | |||||||
| chr4:47913011 | CAAAAA | C | 52 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0014 others(49): Show |
60 | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.235+953_235+957del others(5): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | |||||||
| chr4:47913011 | CAAAAAA | C | 5 | a0001c0002t0001g0013 a0001c0002t0001g0052 a0001c0002t0001g0053 others(2): Show |
6 | HG02132.hp1 NA18974.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+952_235+957del others(6): Show |
NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913011 | |||||||
| chr4:47913047 | T | C | 3 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 |
4 | HG02559.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+922A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913047 | |||||||
| chr4:47913174 | C | A | 1 | a0002c0001t0001g0291 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.235+795G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913174 | |||||||
| chr4:47913311 | T | C | 132 | a0001c0003t0004g0027 a0001c0003t0004g0177 a0001c0003t0004g0178 others(129): Show |
182 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.235+658A>G | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913311 | |||||||
| chr4:47913420 | G | A | 126 | a0001c0003t0005g0033 a0001c0003t0005g0289 a0001c0003t0005g0290 others(123): Show |
175 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.235+549C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913420 | |||||||
| chr4:47913532 | A | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+437T>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913532 | |||||||
| chr4:47913547 | C | G | 1 | a0001c0003t0002g0047 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.235+422G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913547 | |||||||
| chr4:47913658 | C | A | 1 | a0001c0003t0002g0292 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.235+311G>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913658 | |||||||
| chr4:47913689 | C | T | 11 | a0001c0002t0001g0012 a0001c0002t0001g0037 a0001c0002t0001g0041 others(8): Show |
12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.235+280G>A | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913689 | |||||||
| chr4:47913955 | G | A | 1 | a0001c0002t0001g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.235+14C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 2/22 | chr4 | 47913955 | |||||||
| chr4:47914216 | GA | G | 6 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(3): Show |
10 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-12delT | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/22 | chr4 | 47914216 | |||||||
| chr4:47914309 | G | A | 6 | a0001c0003t0001g0011 a0001c0003t0001g0034 a0001c0003t0001g0035 others(3): Show |
10 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-3+56C>T | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/22 | chr4 | 47914309 | |||||||
| chr4:47914329 | C | G | 301 | a0001c0002t0001g0006 a0001c0002t0001g0007 a0001c0002t0001g0012 others(298): Show |
374 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.-3+36G>C | NFXL1 | ENSG00000170448.12 | transcript | ENST00000507489.2 | protein_coding | 1/22 | chr4 | 47914329 |