Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 91624 |
| ensemblid | ENSG00000162614.19 |
| hgncid | 29557 |
| symbol | NEXN |
| name | nexilin F-actin binding protein |
| refseq_nuc | NM_144573.4 |
| refseq_prot | NP_653174.3 |
| ensembl_nuc | ENST00000334785.12 |
| ensembl_prot | ENSP00000333938.7 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 77888624 |
| end | 77943895 |
| strand | + |
| ver | v1.2 |
| region | chr1:77888624-77943895 |
| region5000 | chr1:77883624-77948895 |
| regionname0 | NEXN_chr1_77888624_77943895 |
| regionname5000 | NEXN_chr1_77883624_77948895 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 675 | 231 | 73 | 50 | 65 | 8 | 33 | 45 | NEXN_chr1_77883624_77948895 | NEXN | MNDIS others(670): Show |
chr1 | 77883624 | 77948895 |
| a0002 | 0/0 | 675 | 33 | 0 | 9 | 19 | 4 | 1 | 14 | NEXN_chr1_77883624_77948895 | NEXN | MNDIS others(670): Show |
chr1 | 77883624 | 77948895 |
| a0003 | 0/0 | 675 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | MNDIS others(670): Show |
chr1 | 77883624 | 77948895 |
| a0004 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | MNDIS others(670): Show |
chr1 | 77883624 | 77948895 |
| a0005 | 0/0 | 675 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | MNDIS others(670): Show |
chr1 | 77883624 | 77948895 |
| a0006 | 0/0 | 675 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | MNDIS others(670): Show |
chr1 | 77883624 | 77948895 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2025 | 223 | 65 | 50 | 65 | 8 | 33 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0001c0003 | 0/0 | 2025 | 6 | 6 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0001c0008 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0001c0009 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0002c0002 | 0/0 | 2025 | 33 | 0 | 9 | 19 | 4 | 1 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0003c0007 | 0/0 | 2025 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0004c0005 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0005c0004 | 0/0 | 2025 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 | ||
| a0006c0006 | 0/0 | 2025 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | ATGAA others(2020): Show |
chr1 | 77883624 | 77948895 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3282 | 123 | 40 | 37 | 17 | 6 | 21 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0002 | 0/0 | 3282 | 37 | 2 | 8 | 21 | 2 | 4 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0003 | 0/0 | 3275 | 28 | 8 | 0 | 19 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3270): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0004 | 0/0 | 3283 | 12 | 0 | 2 | 3 | 0 | 7 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3278): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0005 | 0/0 | 3283 | 5 | 5 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3278): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0006 | 0/0 | 3282 | 4 | 3 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0007 | 0/0 | 3283 | 4 | 4 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3278): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0008 | 0/0 | 3275 | 3 | 0 | 0 | 3 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3270): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0010 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3278): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0011 | 0/0 | 3276 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3271): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0013 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0014 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0015 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0016 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0001t0017 | 0/0 | 3283 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3278): Show |
chr1 | 77883624 | 77948895 |
| a0001c0003t0004 | 0/0 | 3283 | 4 | 4 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3278): Show |
chr1 | 77883624 | 77948895 |
| a0001c0003t0009 | 0/0 | 3283 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3278): Show |
chr1 | 77883624 | 77948895 |
| a0001c0008t0001 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0001c0009t0012 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0002c0002t0001 | 0/0 | 3282 | 33 | 0 | 9 | 19 | 4 | 1 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0003c0007t0002 | 0/0 | 3282 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0004c0005t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0005c0004t0001 | 0/0 | 3282 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| a0006c0006t0001 | 0/0 | 3282 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | AGCCA others(3277): Show |
chr1 | 77883624 | 77948895 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0008g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0011g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0016g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0001t0017g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0003t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0008t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0001c0009t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0003c0007t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0004c0005t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0005c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| a0006c0006t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0257 | EUR | GBR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | GBR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | FIN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0241 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0050 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01255 | hp1 | a0001 | c0001 | t0016 | g0010 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01346 | hp2 | a0003 | c0007 | t0002 | g0194 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0252 | AMR | CLM | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0059 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0239 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | IBS | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0214 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01952 | hp2 | a0001 | c0001 | t0015 | g0115 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02040 | hp2 | a0004 | c0005 | t0001 | g0082 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02056 | hp1 | a0001 | c0001 | t0011 | g0102 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02145 | hp2 | a0001 | c0009 | t0012 | g0163 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CDX | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02258 | hp1 | a0001 | c0001 | t0014 | g0202 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0166 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0149 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02615 | hp2 | a0001 | c0008 | t0001 | g0068 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0187 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02818 | hp2 | a0001 | c0003 | t0009 | g0160 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0210 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0207 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0206 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03098 | hp2 | a0001 | c0003 | t0004 | g0159 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03130 | hp2 | a0005 | c0004 | t0001 | g0064 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0256 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03453 | hp1 | a0001 | c0003 | t0004 | g0161 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ESN | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0157 | AFR | GWD | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0251 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0234 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0254 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0132 | SAS | BEB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0253 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | CHB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0209 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0041 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18946 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18969 | hp1 | a0006 | c0006 | t0001 | g0220 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0258 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0153 | AFR | LWK | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19060 | hp2 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19065 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | YRI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ASW | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0240 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | GIH | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG06807 | hp1 | a0001 | c0003 | t0009 | g0162 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| NA20300 | hp2 | a0001 | c0003 | t0004 | g0201 | AFR | USA | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0121 | REF | REF | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0145 | REF | REF | NEXN_chr1_77883624_77948895 | NEXN | chr1 | 77883624 | 77948895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77917990 | G | A | 1 | a0005 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.250G>A | p.Glu84Lys | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 4/13 | 438/3282 | 250/2028 | 84/675 | chr1 | 77917990 | |||
| chr1:77926436 | T | C | 1 | a0004 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.512T>C | p.Ile171Thr | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 7/13 | 700/3282 | 512/2028 | 171/675 | chr1 | 77926436 | |||
| chr1:77926761 | G | A | 2 | a0002 a0006 |
34 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
missense_variant | MODERATE | c.733G>A | p.Gly245Arg | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/13 | 921/3282 | 733/2028 | 245/675 | chr1 | 77926761 | |||
| chr1:77936006 | C | T | 1 | a0003 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1435C>T | p.Leu479Phe | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/13 | 1623/3282 | 1435/2028 | 479/675 | chr1 | 77936006 | |||
| chr1:77942623 | G | A | 1 | a0006 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1822G>A | p.Glu608Lys | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 2010/3282 | 1822/2028 | 608/675 | chr1 | 77942623 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77917694 | C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.156C>T | p.Asp52Asp | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 3/13 | 344/3282 | 156/2028 | 52/675 | chr1 | 77917694 | |||
| chr1:77918189 | G | A | 1 | a0001c0003 | 6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
synonymous_variant | LOW | c.363G>A | p.Thr121Thr | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/13 | 551/3282 | 363/2028 | 121/675 | chr1 | 77918189 | |||
| chr1:77926805 | A | G | 2 | a0001c0008 a0005c0004 |
2 | HG02615.hp2 HG03130.hp2 |
synonymous_variant | LOW | c.777A>G | p.Gln259Gln | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/13 | 965/3282 | 777/2028 | 259/675 | chr1 | 77926805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77888661 | G | A | 1 | a0001c0001t0010 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-151G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/13 | 27446 | chr1 | 77888661 | ||||||
| chr1:77942851 | C | G | 6 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(3): Show |
46 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*22C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 22 | chr1 | 77942851 | ||||||
| chr1:77943108 | G | A | 1 | a0001c0001t0006 | 4 | HG01109.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*279G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 279 | chr1 | 77943108 | ||||||
| chr1:77943143 | A | C | 1 | a0001c0003t0009 | 2 | HG02818.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*314A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 314 | chr1 | 77943143 | ||||||
| chr1:77943237 | C | CA | 4 | a0001c0001t0004 a0001c0001t0011 a0001c0003t0004 others(1): Show |
19 | HG01255.hp2 HG01496.hp2 HG02056.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*418dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 419 | INFO_REALIGN_3_PRIME | chr1 | 77943237 | |||||
| chr1:77943246 | A | AC | 3 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0017 |
7 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*417_*418insC | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 418 | chr1 | 77943246 | ||||||
| chr1:77943289 | T | A | 1 | a0001c0009t0012 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*460T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 460 | chr1 | 77943289 | ||||||
| chr1:77943338 | T | TA | 1 | a0001c0001t0007 | 4 | HG02897.hp2 HG02922.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*511dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 512 | INFO_REALIGN_3_PRIME | chr1 | 77943338 | |||||
| chr1:77943345 | T | C | 1 | a0001c0001t0013 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*516T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 516 | chr1 | 77943345 | ||||||
| chr1:77943482 | A | G | 1 | a0001c0001t0015 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*653A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 653 | chr1 | 77943482 | ||||||
| chr1:77943524 | G | A | 1 | a0001c0001t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*695G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 695 | chr1 | 77943524 | ||||||
| chr1:77943535 | CAGTGTTG | C | 3 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*716_*722delTGTTGA others(1): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 716 | INFO_REALIGN_3_PRIME | chr1 | 77943535 | |||||
| chr1:77943588 | T | A | 1 | a0001c0003t0009 | 2 | HG02818.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*759T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 759 | chr1 | 77943588 | ||||||
| chr1:77943674 | C | T | 1 | a0001c0001t0017 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*845C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 845 | chr1 | 77943674 | ||||||
| chr1:77943846 | A | G | 1 | a0001c0001t0008 | 3 | NA18946.hp2 NA19060.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1017A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 1017 | chr1 | 77943846 | ||||||
| chr1:77943849 | T | A | 1 | a0001c0001t0016 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1020T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 13/13 | 1020 | chr1 | 77943849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:77888790 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-53+31G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888790 | |||||||
| chr1:77888795 | T | G | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(3): Show |
6 | HG01255.hp1 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+36T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888795 | |||||||
| chr1:77888843 | C | A | 1 | a0001c0001t0002g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+84C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888843 | |||||||
| chr1:77888900 | G | T | 64 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(61): Show |
65 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.-53+141G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888900 | |||||||
| chr1:77888907 | G | C | 1 | a0001c0001t0003g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+148G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888907 | |||||||
| chr1:77888908 | C | G | 1 | a0001c0001t0003g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+149C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888908 | |||||||
| chr1:77888987 | C | G | 1 | a0001c0001t0002g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+228C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888987 | |||||||
| chr1:77888988 | G | C | 1 | a0001c0001t0002g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+229G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77888988 | |||||||
| chr1:77889117 | A | T | 1 | a0001c0003t0004g0201 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-53+358A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889117 | |||||||
| chr1:77889310 | T | TC | 47 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0191 others(44): Show |
48 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-53+559dupC | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77889310 | ||||||
| chr1:77889319 | A | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG00621.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.-53+560A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889319 | |||||||
| chr1:77889353 | C | A | 1 | a0001c0001t0003g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+594C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889353 | |||||||
| chr1:77889355 | CT | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(206): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.-53+612delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77889355 | ||||||
| chr1:77889356 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-53+597T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889356 | |||||||
| chr1:77889756 | A | T | 1 | a0001c0001t0002g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+997A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77889756 | |||||||
| chr1:77890034 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-53+1275C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890034 | |||||||
| chr1:77890097 | G | A | 1 | a0001c0001t0017g0166 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-53+1338G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890097 | |||||||
| chr1:77890117 | A | G | 3 | a0001c0001t0002g0155 a0001c0001t0002g0197 a0001c0001t0002g0198 |
3 | HG00609.hp1 NA19078.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-53+1358A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890117 | |||||||
| chr1:77890180 | A | T | 1 | a0001c0001t0002g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+1421A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890180 | |||||||
| chr1:77890679 | AGCGGCCT others(5): Show |
A | 1 | a0001c0001t0001g0019 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-53+1922_-53+1933d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77890679 | ||||||
| chr1:77890716 | A | T | 1 | a0001c0001t0002g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+1957A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890716 | |||||||
| chr1:77890717 | T | A | 1 | a0001c0001t0002g0016 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-53+1958T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890717 | |||||||
| chr1:77890727 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-53+1968C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890727 | |||||||
| chr1:77890871 | G | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-53+2112G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890871 | |||||||
| chr1:77890999 | C | T | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(254): Show |
265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.-53+2240C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77890999 | |||||||
| chr1:77891747 | T | TA | 12 | a0001c0001t0002g0016 a0001c0001t0002g0146 a0001c0001t0002g0147 others(9): Show |
12 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.-53+3011dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | ||||||
| chr1:77891747 | TA | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(15): Show |
18 | HG00639.hp1 HG00735.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.-53+3011delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | ||||||
| chr1:77891747 | TAA | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(6): Show |
9 | HG00438.hp1 HG01175.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-53+3010_-53+3011d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | ||||||
| chr1:77891747 | TAAA | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(183): Show |
193 | HG00099.hp1 HG00099.hp2 HG00597.hp1 others(190): Show |
intron_variant | MODIFIER | c.-53+3009_-53+3011d others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77891747 | ||||||
| chr1:77892061 | C | T | 1 | a0002c0002t0001g0257 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-53+3302C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892061 | |||||||
| chr1:77892062 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(211): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.-53+3303A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892062 | |||||||
| chr1:77892082 | C | CA | 26 | a0001c0001t0002g0155 a0001c0001t0002g0176 a0001c0001t0002g0232 others(23): Show |
27 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.-53+3335dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77892082 | ||||||
| chr1:77892244 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-53+3485C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892244 | |||||||
| chr1:77892411 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-53+3652C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892411 | |||||||
| chr1:77892583 | T | C | 6 | a0001c0001t0005g0020 a0001c0001t0005g0148 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53+3824T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892583 | |||||||
| chr1:77892607 | A | G | 1 | a0003c0007t0002g0194 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-53+3848A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892607 | |||||||
| chr1:77892778 | A | G | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+4019A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892778 | |||||||
| chr1:77892793 | T | C | 1 | a0001c0003t0004g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-53+4034T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892793 | |||||||
| chr1:77892884 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-53+4125T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77892884 | |||||||
| chr1:77893141 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53+4382A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893141 | |||||||
| chr1:77893344 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(209): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-53+4585T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893344 | |||||||
| chr1:77893434 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(10): Show |
13 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-53+4675G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893434 | |||||||
| chr1:77893526 | C | T | 2 | a0001c0001t0002g0232 a0002c0002t0001g0231 |
2 | NA18947.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-53+4767C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893526 | |||||||
| chr1:77893977 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-53+5218G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77893977 | |||||||
| chr1:77894273 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-53+5514C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77894273 | |||||||
| chr1:77894581 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-53+5822C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77894581 | |||||||
| chr1:77894935 | C | T | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-53+6176C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77894935 | |||||||
| chr1:77895029 | A | AT | 35 | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0191 others(32): Show |
36 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-53+6303dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0010g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-53+6291_-53+6303d others(15): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0017g0166 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-53+6286_-53+6303d others(20): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | AT | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0019 others(54): Show |
61 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.-53+6303delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATT | A | 29 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0076 others(26): Show |
31 | HG00099.hp2 HG00639.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.-53+6302_-53+6303d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTT | A | 16 | a0001c0001t0001g0027 a0001c0001t0001g0040 a0001c0001t0001g0065 others(13): Show |
16 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-53+6301_-53+6303d others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTTT | A | 9 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG02280.hp1 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53+6300_-53+6303d others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0002g0192 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+6293_-53+6303d others(13): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTTTTTT others(5): Show |
A | 8 | a0001c0001t0001g0031 a0001c0003t0004g0157 a0001c0003t0004g0159 others(5): Show |
8 | HG02145.hp2 HG02818.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53+6292_-53+6303d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTTTTTT others(6): Show |
A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0062 a0001c0001t0001g0158 others(1): Show |
4 | HG01261.hp2 HG03492.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+6291_-53+6303d others(15): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTTTTTT others(7): Show |
A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
28 | HG00621.hp1 HG00621.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.-53+6290_-53+6303d others(16): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-53+6287_-53+6303d others(19): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895029 | ATTTTTTT others(11): Show |
A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+6286_-53+6303d others(20): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77895029 | ||||||
| chr1:77895125 | A | T | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+6366A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895125 | |||||||
| chr1:77895155 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-53+6396C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895155 | |||||||
| chr1:77895543 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-53+6784A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895543 | |||||||
| chr1:77895721 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0148 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-53+6962C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77895721 | |||||||
| chr1:77896170 | C | CAATAAAT others(1): Show |
24 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(21): Show |
26 | HG00438.hp1 HG02165.hp2 HG02622.hp2 others(23): Show |
intron_variant | MODIFIER | c.-53+7433_-53+7440d others(10): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | ||||||
| chr1:77896170 | C | CAATAAAT others(5): Show |
90 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(87): Show |
93 | HG00099.hp1 HG00323.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.-53+7429_-53+7440d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | ||||||
| chr1:77896170 | C | CAATAAAT others(9): Show |
51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(48): Show |
53 | HG00735.hp2 HG00741.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.-53+7425_-53+7440d others(18): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | ||||||
| chr1:77896170 | C | CAATAAAT others(13): Show |
18 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
18 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.-53+7421_-53+7440d others(22): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | ||||||
| chr1:77896170 | C | CAATAAAT others(17): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0158 others(2): Show |
5 | HG00621.hp1 HG00621.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-53+7417_-53+7440d others(26): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896170 | ||||||
| chr1:77896712 | T | C | 3 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG02976.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-53+7953T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77896712 | |||||||
| chr1:77896761 | T | TA | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(3): Show |
6 | HG03130.hp1 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-53+8015dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77896761 | ||||||
| chr1:77896787 | A | G | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(4): Show |
7 | HG00735.hp2 HG02735.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+8028A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77896787 | |||||||
| chr1:77896987 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-53+8228A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77896987 | |||||||
| chr1:77897099 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-53+8340A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897099 | |||||||
| chr1:77897162 | G | A | 7 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(4): Show |
7 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+8403G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897162 | |||||||
| chr1:77897340 | T | C | 1 | a0002c0002t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53+8581T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897340 | |||||||
| chr1:77897341 | G | A | 1 | a0002c0002t0001g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-53+8582G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897341 | |||||||
| chr1:77897661 | G | C | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-53+8902G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897661 | |||||||
| chr1:77897764 | C | T | 7 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(4): Show |
7 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+9005C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77897764 | |||||||
| chr1:77898075 | GCCATACT others(32): Show |
G | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-53+9321_-53+9359d others(41): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77898075 | ||||||
| chr1:77898123 | C | T | 1 | a0001c0001t0005g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-53+9364C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898123 | |||||||
| chr1:77898126 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-53+9367C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898126 | |||||||
| chr1:77898142 | C | T | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-53+9383C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898142 | |||||||
| chr1:77898184 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-53+9425A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898184 | |||||||
| chr1:77898760 | C | T | 26 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0026 others(23): Show |
27 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-53+10001C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898760 | |||||||
| chr1:77898875 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0235 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-53+10116G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898875 | |||||||
| chr1:77898914 | T | A | 1 | a0001c0001t0004g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-53+10155T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898914 | |||||||
| chr1:77898938 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-53+10179A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77898938 | |||||||
| chr1:77899025 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-53+10266G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899025 | |||||||
| chr1:77899157 | G | T | 1 | a0001c0001t0002g0232 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-53+10398G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899157 | |||||||
| chr1:77899272 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(217): Show |
227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-53+10513T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899272 | |||||||
| chr1:77899273 | G | A | 220 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(217): Show |
227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-53+10514G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899273 | |||||||
| chr1:77899450 | T | A | 1 | a0001c0001t0002g0176 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-53+10691T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77899450 | |||||||
| chr1:77900080 | T | G | 1 | a0002c0002t0001g0218 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-53+11321T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900080 | |||||||
| chr1:77900163 | C | T | 2 | a0002c0002t0001g0225 a0002c0002t0001g0226 |
2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.-53+11404C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900163 | |||||||
| chr1:77900251 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-53+11492T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900251 | |||||||
| chr1:77900378 | A | G | 1 | a0001c0003t0004g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-53+11619A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900378 | |||||||
| chr1:77900660 | T | G | 3 | a0001c0001t0007g0206 a0001c0001t0007g0207 a0001c0001t0007g0209 |
3 | HG02922.hp2 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53+11901T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77900660 | |||||||
| chr1:77901027 | A | G | 1 | a0001c0001t0003g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-53+12268A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901027 | |||||||
| chr1:77901209 | A | G | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(209): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-53+12450A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901209 | |||||||
| chr1:77901474 | C | A | 1 | a0001c0001t0002g0155 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-53+12715C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901474 | |||||||
| chr1:77901654 | A | G | 1 | a0001c0001t0003g0028 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-53+12895A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77901654 | |||||||
| chr1:77902119 | T | A | 4 | a0002c0002t0001g0213 a0002c0002t0001g0214 a0002c0002t0001g0215 others(1): Show |
4 | HG01934.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+13360T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902119 | |||||||
| chr1:77902463 | T | TA | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-52-13591dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77902463 | ||||||
| chr1:77902556 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-52-13499T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902556 | |||||||
| chr1:77902707 | T | C | 1 | a0001c0001t0002g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-52-13348T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902707 | |||||||
| chr1:77902973 | G | T | 1 | a0002c0002t0001g0224 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-52-13082G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77902973 | |||||||
| chr1:77903100 | A | T | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-12955A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903100 | |||||||
| chr1:77903480 | G | A | 3 | a0002c0002t0001g0218 a0002c0002t0001g0227 a0006c0006t0001g0220 |
3 | NA18969.hp1 NA19068.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-52-12575G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903480 | |||||||
| chr1:77903527 | T | G | 54 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(51): Show |
58 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(55): Show |
intron_variant | MODIFIER | c.-52-12528T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903527 | |||||||
| chr1:77903761 | C | CA | 20 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(17): Show |
20 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52-12288dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77903761 | ||||||
| chr1:77903819 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0014g0202 |
3 | HG02258.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-52-12236G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903819 | |||||||
| chr1:77903858 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-52-12197G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77903858 | |||||||
| chr1:77903991 | GTTTTTA | G | 20 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(17): Show |
20 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52-12052_-52-1204 others(10): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77903991 | ||||||
| chr1:77904071 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-52-11984C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904071 | |||||||
| chr1:77904235 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-52-11820C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904235 | |||||||
| chr1:77904449 | G | A | 20 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(17): Show |
20 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-52-11606G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904449 | |||||||
| chr1:77904486 | A | G | 1 | a0001c0001t0017g0166 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-52-11569A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904486 | |||||||
| chr1:77904554 | T | A | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-11501T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904554 | |||||||
| chr1:77904558 | G | A | 27 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(24): Show |
27 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-52-11497G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904558 | |||||||
| chr1:77904766 | A | G | 1 | a0001c0009t0012g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-52-11289A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77904766 | |||||||
| chr1:77905057 | A | C | 6 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0017 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-10998A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905057 | |||||||
| chr1:77905133 | G | A | 1 | a0002c0002t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-52-10922G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905133 | |||||||
| chr1:77905159 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(209): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-52-10896T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905159 | |||||||
| chr1:77905258 | C | CA | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(208): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-52-10786dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77905258 | ||||||
| chr1:77905303 | T | A | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-52-10752T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905303 | |||||||
| chr1:77905306 | C | T | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-10749C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905306 | |||||||
| chr1:77905352 | A | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-10703A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905352 | |||||||
| chr1:77905666 | A | T | 1 | a0001c0001t0011g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-52-10389A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905666 | |||||||
| chr1:77905706 | A | G | 7 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(4): Show |
7 | HG02145.hp2 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-52-10349A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905706 | |||||||
| chr1:77905909 | G | C | 2 | a0001c0003t0004g0157 a0001c0003t0004g0159 |
2 | HG03098.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-52-10146G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77905909 | |||||||
| chr1:77906048 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-10007G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906048 | |||||||
| chr1:77906108 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-52-9947G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906108 | |||||||
| chr1:77906188 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-52-9867G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906188 | |||||||
| chr1:77906592 | T | C | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-9463T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906592 | |||||||
| chr1:77906767 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-52-9288G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77906767 | |||||||
| chr1:77907032 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-52-9023A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907032 | |||||||
| chr1:77907036 | G | C | 1 | a0001c0001t0006g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-52-9019G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907036 | |||||||
| chr1:77907369 | G | A | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-8686G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907369 | |||||||
| chr1:77907372 | G | A | 2 | a0001c0001t0004g0251 a0001c0001t0004g0253 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-52-8683G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907372 | |||||||
| chr1:77907604 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-52-8451C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907604 | |||||||
| chr1:77907608 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-52-8447G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77907608 | |||||||
| chr1:77908008 | G | A | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-8047G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908008 | |||||||
| chr1:77908057 | T | G | 2 | a0001c0008t0001g0068 a0005c0004t0001g0064 |
2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-52-7998T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908057 | |||||||
| chr1:77908065 | A | C | 3 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0249 |
3 | HG00642.hp2 HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-52-7990A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908065 | |||||||
| chr1:77908100 | C | T | 1 | a0001c0003t0004g0157 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52-7955C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908100 | |||||||
| chr1:77908181 | G | T | 2 | a0001c0001t0001g0084 a0001c0001t0004g0132 |
2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-52-7874G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908181 | |||||||
| chr1:77908231 | T | C | 122 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(119): Show |
127 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.-52-7824T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908231 | |||||||
| chr1:77908312 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-52-7743C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908312 | |||||||
| chr1:77908370 | C | T | 2 | a0001c0001t0003g0063 a0001c0001t0003g0073 |
2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-52-7685C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908370 | |||||||
| chr1:77908394 | A | AT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0058 others(13): Show |
17 | HG01099.hp1 HG01255.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.-52-7638dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | ||||||
| chr1:77908394 | A | ATT | 5 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(2): Show |
5 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-7639_-52-7638d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | ||||||
| chr1:77908394 | AT | A | 39 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0027 others(36): Show |
41 | HG00323.hp2 HG00741.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-52-7638delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | ||||||
| chr1:77908394 | ATT | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(9): Show |
12 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-7639_-52-7638d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77908394 | ||||||
| chr1:77908493 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-52-7562C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908493 | |||||||
| chr1:77908513 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-52-7542G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908513 | |||||||
| chr1:77908620 | G | A | 2 | a0001c0001t0005g0020 a0001c0001t0005g0148 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-52-7435G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908620 | |||||||
| chr1:77908716 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-52-7339A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908716 | |||||||
| chr1:77908861 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.-52-7194T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77908861 | |||||||
| chr1:77909335 | G | T | 3 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0190 |
3 | NA18972.hp2 NA18980.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-52-6720G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909335 | |||||||
| chr1:77909440 | A | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0235 a0001c0001t0001g0248 others(10): Show |
13 | HG00621.hp2 HG00735.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52-6615A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909440 | |||||||
| chr1:77909674 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-52-6381A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909674 | |||||||
| chr1:77909965 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-52-6090T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77909965 | |||||||
| chr1:77910116 | G | C | 1 | a0001c0003t0004g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-52-5939G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910116 | |||||||
| chr1:77910238 | CTG | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(10): Show |
13 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52-5816_-52-5815d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910238 | |||||||
| chr1:77910419 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-52-5636T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910419 | |||||||
| chr1:77910615 | G | A | 1 | a0002c0002t0001g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-52-5440G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910615 | |||||||
| chr1:77910748 | C | CA | 34 | a0001c0001t0001g0204 a0001c0001t0002g0007 a0001c0001t0002g0016 others(31): Show |
35 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52-5284dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910748 | ||||||
| chr1:77910748 | C | CAA | 21 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(18): Show |
21 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.-52-5285_-52-5284d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910748 | ||||||
| chr1:77910761 | A | AAAC | 22 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(19): Show |
22 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-52-5292_-52-5291i others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910761 | ||||||
| chr1:77910762 | A | AAC | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-52-5292_-52-5291i others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77910762 | ||||||
| chr1:77910762 | A | AC | 40 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(37): Show |
44 | HG00438.hp1 HG01496.hp2 HG01515.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-5293_-52-5292i others(3): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910762 | |||||||
| chr1:77910763 | A | C | 1 | a0001c0001t0003g0073 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-52-5292A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77910763 | |||||||
| chr1:77911045 | C | T | 3 | a0002c0002t0001g0214 a0002c0002t0001g0215 a0002c0002t0001g0219 |
3 | HG01934.hp2 HG01975.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-52-5010C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911045 | |||||||
| chr1:77911132 | C | T | 1 | a0001c0001t0005g0177 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-52-4923C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911132 | |||||||
| chr1:77911485 | G | A | 1 | a0002c0002t0001g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-52-4570G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911485 | |||||||
| chr1:77911570 | C | T | 2 | a0001c0001t0005g0177 a0001c0001t0017g0166 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-52-4485C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911570 | |||||||
| chr1:77911664 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-52-4391A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911664 | |||||||
| chr1:77911691 | A | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(10): Show |
13 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52-4364A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911691 | |||||||
| chr1:77911739 | T | A | 5 | a0001c0001t0002g0152 a0001c0001t0002g0155 a0001c0001t0002g0195 others(2): Show |
5 | HG00609.hp1 HG02132.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-4316T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911739 | |||||||
| chr1:77911739 | T | TTA | 23 | a0001c0001t0002g0178 a0001c0001t0003g0003 a0001c0001t0003g0025 others(20): Show |
25 | HG00438.hp1 HG02056.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.-52-4295_-52-4294d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77911739 | ||||||
| chr1:77911739 | TTA | T | 34 | a0001c0001t0001g0019 a0001c0001t0001g0081 a0001c0001t0001g0094 others(31): Show |
35 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-52-4295_-52-4294d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77911739 | ||||||
| chr1:77911739 | TTATA | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(150): Show |
157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.-52-4297_-52-4294d others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77911739 | ||||||
| chr1:77911857 | C | T | 5 | a0001c0001t0003g0025 a0001c0001t0003g0071 a0001c0001t0003g0072 others(2): Show |
5 | HG00438.hp1 NA18962.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-4198C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911857 | |||||||
| chr1:77911867 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-52-4188G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911867 | |||||||
| chr1:77911908 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-52-4147G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911908 | |||||||
| chr1:77911936 | G | T | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-4119G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911936 | |||||||
| chr1:77911965 | G | A | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-4090G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77911965 | |||||||
| chr1:77912003 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG02976.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-52-4052C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912003 | |||||||
| chr1:77912004 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-52-4051G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912004 | |||||||
| chr1:77912052 | C | T | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-4003C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912052 | |||||||
| chr1:77912078 | C | CA | 15 | a0001c0001t0001g0042 a0001c0001t0001g0065 a0001c0001t0001g0112 others(12): Show |
15 | HG00621.hp2 HG01175.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-52-3960dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912078 | ||||||
| chr1:77912168 | T | C | 22 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0028 others(19): Show |
24 | HG00438.hp1 HG02056.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.-52-3887T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912168 | |||||||
| chr1:77912213 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0116 |
3 | HG02622.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-52-3842A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912213 | |||||||
| chr1:77912221 | A | T | 1 | a0001c0001t0001g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-52-3834A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912221 | |||||||
| chr1:77912246 | A | ATGTGGAA others(4): Show |
2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-52-3806_-52-3796d others(13): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912246 | ||||||
| chr1:77912295 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-52-3760T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912295 | |||||||
| chr1:77912378 | TC | T | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-3675delC | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912378 | ||||||
| chr1:77912596 | T | TA | 13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(10): Show |
13 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-52-3456dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77912596 | ||||||
| chr1:77912718 | T | C | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0008t0001g0068 others(1): Show |
4 | HG01257.hp2 HG02615.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-3337T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77912718 | |||||||
| chr1:77913152 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-52-2903C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913152 | |||||||
| chr1:77913162 | C | T | 3 | a0001c0008t0001g0068 a0001c0009t0012g0163 a0005c0004t0001g0064 |
3 | HG02145.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-52-2893C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913162 | |||||||
| chr1:77913202 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-52-2853G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913202 | |||||||
| chr1:77913244 | A | G | 1 | a0002c0002t0001g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-52-2811A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913244 | |||||||
| chr1:77913371 | T | C | 1 | a0002c0002t0001g0224 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-52-2684T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913371 | |||||||
| chr1:77913414 | C | CA | 8 | a0001c0001t0001g0113 a0001c0003t0004g0157 a0001c0003t0004g0159 others(5): Show |
8 | HG02071.hp1 HG02818.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2628dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77913414 | ||||||
| chr1:77913721 | T | G | 1 | a0001c0001t0002g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-52-2334T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913721 | |||||||
| chr1:77913815 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-52-2240C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77913815 | |||||||
| chr1:77914074 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-1981T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77914074 | |||||||
| chr1:77914116 | T | G | 3 | a0001c0008t0001g0068 a0001c0009t0012g0163 a0005c0004t0001g0064 |
3 | HG02145.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-52-1939T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77914116 | |||||||
| chr1:77914857 | C | CA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(3): Show |
6 | HG00639.hp1 HG02818.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-1183dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | 77914857 | ||||||
| chr1:77914948 | T | C | 1 | a0001c0001t0005g0148 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-52-1107T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77914948 | |||||||
| chr1:77915001 | C | G | 1 | a0001c0001t0004g0132 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-52-1054C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915001 | |||||||
| chr1:77915367 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-52-688T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915367 | |||||||
| chr1:77915425 | T | G | 1 | a0001c0001t0010g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-52-630T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915425 | |||||||
| chr1:77915664 | A | T | 1 | a0001c0001t0001g0120 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-52-391A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 1/12 | chr1 | 77915664 | |||||||
| chr1:77916290 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.27+157C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916290 | |||||||
| chr1:77916314 | C | T | 1 | a0001c0001t0002g0170 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.27+181C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916314 | |||||||
| chr1:77916333 | T | C | 6 | a0001c0001t0005g0020 a0001c0001t0005g0148 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+200T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916333 | |||||||
| chr1:77916353 | A | C | 24 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0030 others(21): Show |
24 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.27+220A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916353 | |||||||
| chr1:77916907 | C | T | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-659C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | chr1 | 77916907 | |||||||
| chr1:77917475 | AT | A | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.28-85delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr1 | 77917475 | ||||||
| chr1:77917782 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.219+25G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 3/12 | chr1 | 77917782 | |||||||
| chr1:77918378 | A | G | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+105A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918378 | |||||||
| chr1:77918473 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.447+200C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918473 | |||||||
| chr1:77918668 | G | GA | 10 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0003g0100 others(7): Show |
10 | HG02056.hp1 HG02071.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.447+413dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77918668 | ||||||
| chr1:77918668 | GA | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0043 others(35): Show |
39 | HG00621.hp1 HG01099.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.447+413delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77918668 | ||||||
| chr1:77918772 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0111 a0001c0001t0001g0116 |
3 | HG02622.hp1 HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.447+499T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918772 | |||||||
| chr1:77918824 | T | C | 1 | a0001c0001t0006g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.447+551T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918824 | |||||||
| chr1:77918833 | C | T | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+560C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77918833 | |||||||
| chr1:77919075 | G | A | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.447+802G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919075 | |||||||
| chr1:77919302 | G | A | 1 | a0002c0002t0001g0231 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.447+1029G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919302 | |||||||
| chr1:77919318 | A | G | 2 | a0001c0001t0002g0168 a0001c0001t0002g0169 |
2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.447+1045A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919318 | |||||||
| chr1:77919582 | A | AT | 48 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0026 others(45): Show |
51 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.447+1327dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77919582 | ||||||
| chr1:77919582 | AT | A | 7 | a0001c0001t0001g0043 a0001c0003t0004g0157 a0001c0003t0004g0159 others(4): Show |
7 | HG02698.hp1 HG02818.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.447+1327delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77919582 | ||||||
| chr1:77919644 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.447+1371C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919644 | |||||||
| chr1:77919784 | G | C | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+1511G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919784 | |||||||
| chr1:77919845 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.447+1572C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919845 | |||||||
| chr1:77919925 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.447+1652A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919925 | |||||||
| chr1:77919930 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0043 others(29): Show |
33 | HG00621.hp1 HG01099.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.447+1657C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77919930 | |||||||
| chr1:77920024 | C | T | 4 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0242 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+1751C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920024 | |||||||
| chr1:77920153 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.447+1880G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920153 | |||||||
| chr1:77920181 | C | T | 5 | a0001c0001t0003g0025 a0001c0001t0003g0071 a0001c0001t0003g0072 others(2): Show |
5 | HG00438.hp1 NA18962.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+1908C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920181 | |||||||
| chr1:77920364 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.447+2091A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920364 | |||||||
| chr1:77920489 | C | T | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2216C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920489 | |||||||
| chr1:77920555 | A | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0205 |
2 | HG00639.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.447+2282A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920555 | |||||||
| chr1:77920619 | T | TA | 10 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0133 others(7): Show |
10 | HG01109.hp2 HG01168.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.447+2369dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | ||||||
| chr1:77920619 | TA | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(157): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.447+2369delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | ||||||
| chr1:77920619 | TAA | T | 13 | a0001c0001t0001g0021 a0001c0001t0001g0047 a0001c0001t0001g0061 others(10): Show |
13 | HG00323.hp1 HG01256.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.447+2368_447+2369d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | ||||||
| chr1:77920619 | TAAAAAAA others(5): Show |
T | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2358_447+2369d others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920619 | ||||||
| chr1:77920800 | G | T | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2527G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920800 | |||||||
| chr1:77920804 | GAGA | G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.447+2534_447+2536d others(5): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77920804 | ||||||
| chr1:77920938 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+2665C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77920938 | |||||||
| chr1:77921081 | A | C | 1 | a0001c0009t0012g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.447+2808A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921081 | |||||||
| chr1:77921124 | A | G | 1 | a0002c0002t0001g0224 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.447+2851A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921124 | |||||||
| chr1:77921242 | T | C | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.447+2969T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921242 | |||||||
| chr1:77921316 | C | T | 5 | a0002c0002t0001g0218 a0002c0002t0001g0223 a0002c0002t0001g0227 others(2): Show |
5 | NA18947.hp1 NA18969.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.447+3043C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921316 | |||||||
| chr1:77921585 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.447+3312C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921585 | |||||||
| chr1:77921810 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.448-3378C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921810 | |||||||
| chr1:77921860 | G | A | 4 | a0001c0001t0005g0153 a0001c0001t0005g0177 a0001c0001t0010g0149 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-3328G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77921860 | |||||||
| chr1:77922013 | C | A | 1 | a0001c0001t0001g0052 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.448-3175C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922013 | |||||||
| chr1:77922140 | CT | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.448-3031delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77922140 | ||||||
| chr1:77922344 | T | A | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.448-2844T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922344 | |||||||
| chr1:77922409 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.448-2779G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922409 | |||||||
| chr1:77922420 | C | T | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.448-2768C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922420 | |||||||
| chr1:77922584 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(216): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.448-2604C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922584 | |||||||
| chr1:77922597 | T | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448-2591T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922597 | |||||||
| chr1:77922601 | C | CT | 35 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(32): Show |
39 | HG00438.hp1 HG00735.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.448-2573dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77922601 | ||||||
| chr1:77922616 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448-2572G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922616 | |||||||
| chr1:77922618 | G | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG00735.hp2 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.448-2570G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922618 | |||||||
| chr1:77922762 | A | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.448-2426A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77922762 | |||||||
| chr1:77923003 | C | CT | 30 | a0001c0001t0001g0023 a0001c0001t0001g0027 a0001c0001t0001g0032 others(27): Show |
30 | HG01106.hp1 HG01109.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.448-2163dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923003 | ||||||
| chr1:77923056 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.448-2132C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923056 | |||||||
| chr1:77923060 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.448-2128C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923060 | |||||||
| chr1:77923147 | C | T | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-2041C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923147 | |||||||
| chr1:77923160 | A | AT | 71 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0037 others(68): Show |
75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.448-2009dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923160 | ||||||
| chr1:77923160 | A | ATT | 5 | a0001c0001t0001g0038 a0001c0001t0003g0103 a0001c0001t0004g0253 others(2): Show |
5 | HG00642.hp2 HG03098.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-2010_448-2009d others(4): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923160 | ||||||
| chr1:77923195 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.448-1993C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923195 | |||||||
| chr1:77923214 | G | C | 4 | a0001c0001t0005g0153 a0001c0001t0005g0177 a0001c0001t0010g0149 others(1): Show |
4 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-1974G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923214 | |||||||
| chr1:77923253 | C | A | 1 | a0001c0001t0002g0182 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.448-1935C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923253 | |||||||
| chr1:77923467 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.448-1721A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923467 | |||||||
| chr1:77923679 | CT | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(196): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.448-1489delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77923679 | ||||||
| chr1:77923867 | G | A | 6 | a0001c0001t0005g0020 a0001c0001t0005g0148 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1321G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77923867 | |||||||
| chr1:77924019 | G | A | 6 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0017 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.448-1169G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924019 | |||||||
| chr1:77924097 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0208 a0001c0001t0014g0202 |
3 | HG02258.hp1 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.448-1091C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924097 | |||||||
| chr1:77924135 | G | A | 1 | a0002c0002t0001g0231 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.448-1053G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924135 | |||||||
| chr1:77924144 | T | C | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.448-1044T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924144 | |||||||
| chr1:77924348 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.448-840C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924348 | |||||||
| chr1:77924361 | C | CA | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
142 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.448-816dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77924361 | ||||||
| chr1:77924476 | G | A | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.448-712G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924476 | |||||||
| chr1:77924666 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.448-522T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924666 | |||||||
| chr1:77924667 | C | CT | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(208): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.448-514dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr1 | 77924667 | ||||||
| chr1:77924667 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0077 |
2 | HG01106.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.448-521C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924667 | |||||||
| chr1:77924705 | A | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.448-483A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924705 | |||||||
| chr1:77924744 | G | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(218): Show |
228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.448-444G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 5/12 | chr1 | 77924744 | |||||||
| chr1:77925335 | T | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0065 others(7): Show |
10 | HG01993.hp1 HG02132.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.489+106T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 6/12 | chr1 | 77925335 | |||||||
| chr1:77925591 | C | T | 4 | a0002c0002t0001g0213 a0002c0002t0001g0214 a0002c0002t0001g0215 others(1): Show |
4 | HG01934.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+362C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 6/12 | chr1 | 77925591 | |||||||
| chr1:77926935 | T | G | 1 | a0001c0001t0004g0114 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.864+43T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77926935 | |||||||
| chr1:77927123 | A | G | 8 | a0001c0001t0001g0027 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.864+231A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927123 | |||||||
| chr1:77927182 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.864+290C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927182 | |||||||
| chr1:77927186 | A | G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.864+294A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927186 | |||||||
| chr1:77927197 | C | T | 1 | a0001c0001t0005g0153 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.864+305C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927197 | |||||||
| chr1:77927259 | A | T | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.864+367A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927259 | |||||||
| chr1:77927391 | A | G | 5 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(2): Show |
5 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.864+499A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927391 | |||||||
| chr1:77927600 | GTC | G | 13 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(10): Show |
13 | HG01496.hp2 HG02145.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+710_864+711del others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 77927600 | ||||||
| chr1:77927601 | T | TGA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0060 others(3): Show |
6 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+709_864+710ins others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927601 | |||||||
| chr1:77927602 | C | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(196): Show |
206 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.864+710C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927602 | |||||||
| chr1:77927603 | T | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(177): Show |
187 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.864+711T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927603 | |||||||
| chr1:77927603 | T | TGA | 12 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(9): Show |
12 | HG02280.hp1 HG02809.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.864+712_864+713ins others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr1 | 77927603 | ||||||
| chr1:77927604 | G | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0060 others(3): Show |
6 | HG00323.hp1 HG00733.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+712G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927604 | |||||||
| chr1:77927605 | T | A | 13 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(10): Show |
13 | HG01496.hp2 HG02145.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+713T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927605 | |||||||
| chr1:77927606 | G | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(189): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.864+714G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927606 | |||||||
| chr1:77927607 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.864+715T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927607 | |||||||
| chr1:77927608 | G | C | 13 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(10): Show |
13 | HG01496.hp2 HG02145.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+716G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927608 | |||||||
| chr1:77927610 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.864+718G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927610 | |||||||
| chr1:77927614 | G | T | 6 | a0001c0001t0005g0020 a0001c0001t0005g0148 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+722G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927614 | |||||||
| chr1:77927732 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG00621.hp1 HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.864+840G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927732 | |||||||
| chr1:77927769 | T | C | 1 | a0001c0001t0003g0070 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.864+877T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927769 | |||||||
| chr1:77927936 | T | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.864+1044T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927936 | |||||||
| chr1:77927987 | G | T | 1 | a0001c0001t0002g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.864+1095G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927987 | |||||||
| chr1:77927988 | A | T | 1 | a0001c0001t0002g0146 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.864+1096A>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77927988 | |||||||
| chr1:77928053 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.864+1161A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928053 | |||||||
| chr1:77928068 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.864+1176G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928068 | |||||||
| chr1:77928137 | T | C | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-1179T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928137 | |||||||
| chr1:77928236 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.865-1080G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928236 | |||||||
| chr1:77928254 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0235 |
2 | HG02055.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.865-1062C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928254 | |||||||
| chr1:77928708 | A | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.865-608A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928708 | |||||||
| chr1:77928773 | G | A | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.865-543G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928773 | |||||||
| chr1:77928866 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.865-450C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928866 | |||||||
| chr1:77928901 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.865-415C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928901 | |||||||
| chr1:77928944 | G | T | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.865-372G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77928944 | |||||||
| chr1:77929312 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | splice_region_variant&intron_variant | LOW | c.865-4T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 8/12 | chr1 | 77929312 | |||||||
| chr1:77929632 | T | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0030 a0001c0001t0001g0031 others(10): Show |
13 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1053+128T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77929632 | |||||||
| chr1:77929717 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1053+213C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77929717 | |||||||
| chr1:77929877 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1053+373C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77929877 | |||||||
| chr1:77930333 | T | A | 1 | a0001c0001t0002g0197 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1053+829T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930333 | |||||||
| chr1:77930654 | GCT | G | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+1153_1053+115 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77930654 | ||||||
| chr1:77930773 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1053+1269A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930773 | |||||||
| chr1:77930784 | C | T | 2 | a0001c0008t0001g0068 a0005c0004t0001g0064 |
2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1053+1280C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930784 | |||||||
| chr1:77930941 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1053+1437T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77930941 | |||||||
| chr1:77931109 | C | T | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1053+1605C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931109 | |||||||
| chr1:77931158 | C | T | 1 | a0001c0001t0005g0187 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1053+1654C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931158 | |||||||
| chr1:77931231 | C | CA | 10 | a0001c0001t0001g0036 a0001c0001t0002g0016 a0001c0001t0002g0146 others(7): Show |
10 | HG00741.hp2 HG01106.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1053+1760dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CA | C | 19 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0141 others(16): Show |
19 | HG00609.hp1 HG00735.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1053+1760delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAA | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(12): Show |
15 | HG00639.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1053+1759_1053+176 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAA | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0135 a0001c0001t0004g0251 others(5): Show |
8 | HG02300.hp2 HG02615.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1053+1758_1053+176 others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAA | C | 21 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(18): Show |
22 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1053+1757_1053+176 others(8): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAAA | C | 18 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(15): Show |
21 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.1053+1756_1053+176 others(9): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1053+1750_1053+176 others(15): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0038 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1053+1748_1053+176 others(17): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0030 a0001c0001t0005g0187 |
2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1053+1746_1053+176 others(19): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAAAAA others(9): Show |
C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1053+1745_1053+176 others(20): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAAAAA others(11): Show |
C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0055 a0001c0001t0001g0060 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1053+1743_1053+176 others(22): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931231 | CAAAAAAA others(12): Show |
C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(119): Show |
125 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1053+1742_1053+176 others(23): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931231 | ||||||
| chr1:77931412 | CA | C | 21 | a0001c0001t0001g0019 a0001c0001t0001g0077 a0001c0001t0001g0081 others(18): Show |
22 | HG00438.hp2 HG01106.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.1054-1841delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | ||||||
| chr1:77931412 | CAA | C | 45 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0027 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1054-1842_1054-184 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | ||||||
| chr1:77931412 | CAAA | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(121): Show |
127 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.1054-1843_1054-184 others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | ||||||
| chr1:77931412 | CAAAA | C | 33 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0033 others(30): Show |
37 | HG00438.hp1 HG01261.hp2 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1054-1844_1054-184 others(8): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | ||||||
| chr1:77931412 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0005g0020 a0001c0001t0005g0148 a0001c0001t0005g0153 others(2): Show |
5 | HG02451.hp1 HG02615.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1054-1850_1054-184 others(14): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | ||||||
| chr1:77931412 | CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0001g0229 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1054-1854_1054-184 others(18): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77931412 | ||||||
| chr1:77931506 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1054-1776C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931506 | |||||||
| chr1:77931670 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1054-1612T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931670 | |||||||
| chr1:77931856 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1054-1426C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77931856 | |||||||
| chr1:77932028 | C | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(218): Show |
228 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.1054-1254C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77932028 | |||||||
| chr1:77932429 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1054-853C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77932429 | |||||||
| chr1:77932692 | ATTTC | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(12): Show |
15 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1054-586_1054-583d others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr1 | 77932692 | ||||||
| chr1:77932894 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1054-388G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77932894 | |||||||
| chr1:77933046 | A | G | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1054-236A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77933046 | |||||||
| chr1:77933076 | G | A | 2 | a0001c0003t0009g0160 a0001c0003t0009g0162 |
2 | HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1054-206G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 9/12 | chr1 | 77933076 | |||||||
| chr1:77933522 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1251+43C>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77933522 | |||||||
| chr1:77933527 | T | C | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1251+48T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77933527 | |||||||
| chr1:77933581 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1251+102A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77933581 | |||||||
| chr1:77933910 | ACTGCAGC others(32): Show |
A | 1 | a0001c0001t0004g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1251+434_1251+472d others(41): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77933910 | ||||||
| chr1:77934011 | A | AT | 15 | a0001c0001t0001g0011 a0001c0001t0002g0192 a0001c0001t0002g0193 others(12): Show |
15 | HG01496.hp2 HG02451.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1251+548dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | ||||||
| chr1:77934011 | A | ATTTTTT | 33 | a0001c0001t0001g0061 a0001c0001t0001g0084 a0001c0001t0004g0075 others(30): Show |
34 | HG00099.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1251+543_1251+548d others(8): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | ||||||
| chr1:77934011 | A | ATTTTTTT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(95): Show |
100 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.1251+542_1251+548d others(9): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | ||||||
| chr1:77934011 | A | ATTTTTTT others(1): Show |
58 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(55): Show |
61 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.1251+541_1251+548d others(10): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | ||||||
| chr1:77934011 | A | ATTTTTTT others(2): Show |
15 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0040 others(12): Show |
15 | HG00438.hp1 HG00735.hp2 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1251+540_1251+548d others(11): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | ||||||
| chr1:77934011 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1251+539_1251+548d others(12): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934011 | ||||||
| chr1:77934048 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1251+569T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934048 | |||||||
| chr1:77934163 | C | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(2): Show |
5 | HG02258.hp2 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1251+684C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934163 | |||||||
| chr1:77934164 | GATGCCCG others(1021): Show |
G | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1251+711_1252-606d others(2): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr1 | 77934164 | ||||||
| chr1:77934166 | T | G | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1251+687T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934166 | |||||||
| chr1:77934190 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.1251+711G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934190 | |||||||
| chr1:77934230 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1251+751G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934230 | |||||||
| chr1:77934307 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1251+828G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934307 | |||||||
| chr1:77934413 | G | A | 10 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0065 others(7): Show |
10 | HG01993.hp1 HG02132.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1251+934G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934413 | |||||||
| chr1:77934468 | A | C | 3 | a0001c0003t0004g0161 a0001c0003t0009g0160 a0001c0003t0009g0162 |
3 | HG02818.hp2 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1251+989A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934468 | |||||||
| chr1:77934813 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(253): Show |
264 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.1252-1010T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934813 | |||||||
| chr1:77934855 | A | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(78): Show |
83 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1252-968A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934855 | |||||||
| chr1:77934910 | T | A | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-913T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934910 | |||||||
| chr1:77934912 | T | C | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-911T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934912 | |||||||
| chr1:77934913 | G | T | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-910G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934913 | |||||||
| chr1:77934917 | G | T | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-906G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934917 | |||||||
| chr1:77934918 | A | C | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-905A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934918 | |||||||
| chr1:77934919 | C | A | 1 | a0001c0001t0003g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1252-904C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77934919 | |||||||
| chr1:77935265 | C | T | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1252-558C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77935265 | |||||||
| chr1:77935522 | T | C | 40 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(37): Show |
44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1252-301T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77935522 | |||||||
| chr1:77935582 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1252-241T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 10/12 | chr1 | 77935582 | |||||||
| chr1:77936156 | ATACAG | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG01109.hp2 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1473+115_1473+119d others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77936156 | ||||||
| chr1:77936308 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1473+264C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936308 | |||||||
| chr1:77936581 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1473+537G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936581 | |||||||
| chr1:77936602 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1473+558G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936602 | |||||||
| chr1:77936966 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(210): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.1473+922A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936966 | |||||||
| chr1:77936970 | C | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1473+926C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77936970 | |||||||
| chr1:77937080 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1473+1036T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937080 | |||||||
| chr1:77937082 | GGTGGGTC others(6): Show |
G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1473+1040_1473+105 others(17): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77937082 | ||||||
| chr1:77937154 | A | G | 3 | a0002c0002t0001g0240 a0002c0002t0001g0241 a0002c0002t0001g0249 |
3 | HG00642.hp2 HG01175.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1473+1110A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937154 | |||||||
| chr1:77937166 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1473+1122C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937166 | |||||||
| chr1:77937245 | G | A | 1 | a0001c0001t0010g0149 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1473+1201G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937245 | |||||||
| chr1:77937259 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1473+1215G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937259 | |||||||
| chr1:77937400 | T | TA | 40 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(37): Show |
44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1473+1357dupA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77937400 | ||||||
| chr1:77937427 | G | A | 40 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(37): Show |
44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1473+1383G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937427 | |||||||
| chr1:77937452 | G | A | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+1408G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937452 | |||||||
| chr1:77937460 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1473+1416T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937460 | |||||||
| chr1:77937487 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1473+1443C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937487 | |||||||
| chr1:77937596 | G | A | 6 | a0001c0001t0002g0150 a0001c0001t0002g0152 a0001c0001t0002g0155 others(3): Show |
6 | HG00609.hp1 HG00738.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+1552G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937596 | |||||||
| chr1:77937666 | G | C | 1 | a0001c0001t0004g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1622G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937666 | |||||||
| chr1:77937668 | G | GCAGCACA others(32): Show |
1 | a0001c0001t0004g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1624_1473+162 others(43): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937668 | |||||||
| chr1:77937672 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1628G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937672 | |||||||
| chr1:77937675 | C | A | 1 | a0001c0001t0004g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+1631C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937675 | |||||||
| chr1:77937675 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1473+1631C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937675 | |||||||
| chr1:77937693 | A | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.1473+1649A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77937693 | |||||||
| chr1:77938131 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1473+2087G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938131 | |||||||
| chr1:77938171 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1473+2127T>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938171 | |||||||
| chr1:77938230 | A | G | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1473+2186A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938230 | |||||||
| chr1:77938487 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2443A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938487 | |||||||
| chr1:77938513 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1473+2469G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938513 | |||||||
| chr1:77938523 | T | G | 6 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | HG00639.hp2 HG01071.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1473+2479T>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938523 | |||||||
| chr1:77938589 | CA | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1473+2563delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77938589 | ||||||
| chr1:77938589 | CAA | C | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1473+2562_1473+256 others(6): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77938589 | ||||||
| chr1:77938618 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2574A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938618 | |||||||
| chr1:77938643 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1473+2599A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938643 | |||||||
| chr1:77938659 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2615T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938659 | |||||||
| chr1:77938666 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1473+2622A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938666 | |||||||
| chr1:77938722 | CAAG | C | 40 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(37): Show |
44 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1473+2682_1473+268 others(7): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77938722 | ||||||
| chr1:77938802 | A | C | 1 | a0001c0001t0004g0075 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1473+2758A>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77938802 | |||||||
| chr1:77939244 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0038 |
2 | HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1474-2779G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939244 | |||||||
| chr1:77939256 | G | A | 10 | a0001c0001t0002g0147 a0001c0001t0002g0168 a0001c0001t0002g0169 others(7): Show |
10 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1474-2767G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939256 | |||||||
| chr1:77939541 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG00621.hp1 HG02056.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1474-2482T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939541 | |||||||
| chr1:77939749 | T | C | 21 | a0001c0001t0003g0003 a0001c0001t0003g0025 a0001c0001t0003g0028 others(18): Show |
23 | HG00438.hp1 HG02056.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.1474-2274T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939749 | |||||||
| chr1:77939771 | G | GT | 6 | a0001c0001t0004g0251 a0001c0001t0004g0252 a0001c0001t0004g0253 others(3): Show |
6 | HG01496.hp2 HG03239.hp1 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474-2251dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77939771 | ||||||
| chr1:77939799 | G | T | 1 | a0001c0001t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1474-2224G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939799 | |||||||
| chr1:77939848 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1474-2175C>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939848 | |||||||
| chr1:77939931 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1474-2092G>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77939931 | |||||||
| chr1:77940113 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1474-1910T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940113 | |||||||
| chr1:77940270 | C | A | 1 | a0001c0009t0012g0163 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1474-1753C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940270 | |||||||
| chr1:77940428 | G | C | 28 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0005 others(25): Show |
32 | HG00438.hp1 HG02055.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1474-1595G>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940428 | |||||||
| chr1:77940750 | A | G | 6 | a0001c0003t0004g0157 a0001c0003t0004g0159 a0001c0003t0004g0161 others(3): Show |
6 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1474-1273A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940750 | |||||||
| chr1:77940816 | T | C | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1474-1207T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940816 | |||||||
| chr1:77940820 | GT | G | 6 | a0001c0001t0005g0020 a0001c0001t0005g0148 a0001c0001t0005g0153 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1474-1201delT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77940820 | ||||||
| chr1:77940831 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1474-1192C>A | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940831 | |||||||
| chr1:77940946 | T | C | 1 | a0001c0001t0016g0010 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1474-1077T>C | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77940946 | |||||||
| chr1:77941229 | TAGAAACC others(8): Show |
T | 85 | a0001c0001t0002g0007 a0001c0001t0002g0016 a0001c0001t0002g0146 others(82): Show |
90 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1474-777_1474-763d others(17): Show |
NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77941229 | ||||||
| chr1:77941246 | G | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0026 others(7): Show |
11 | HG01099.hp2 HG01175.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.1474-777G>T | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77941246 | |||||||
| chr1:77941824 | C | CT | 37 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(34): Show |
37 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1474-198dupT | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr1 | 77941824 | ||||||
| chr1:77941946 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1474-77A>G | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 11/12 | chr1 | 77941946 | |||||||
| chr1:77942370 | TA | T | 13 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(10): Show |
13 | HG00639.hp1 HG00735.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1660-80delA | NEXN | ENSG00000162614.19 | transcript | ENST00000334785.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr1 | 77942370 |