Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7469 |
| ensemblid | ENSG00000185049.16 |
| hgncid | 12768 |
| symbol | NELFA |
| name | negative elongation factor complex member A |
| refseq_nuc | NM_005663.5 |
| refseq_prot | NP_005654.4 |
| ensembl_nuc | ENST00000382882.9 |
| ensembl_prot | ENSP00000372335.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 1982723 |
| end | 2008974 |
| strand | - |
| ver | v1.2 |
| region | chr4:1982723-2008974 |
| region5000 | chr4:1977723-2013974 |
| regionname0 | NELFA_chr4_1982723_2008974 |
| regionname5000 | NELFA_chr4_1977723_2013974 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 528 | 352 | 69 | 80 | 146 | 14 | 41 | 115 | NELFA_chr4_1977723_2013974 | NELFA | MASMR others(523): Show |
chr4 | 1977723 | 2013974 |
| a0002 | 0/0 | 528 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | NELFA_chr4_1977723_2013974 | NELFA | MASMR others(523): Show |
chr4 | 1977723 | 2013974 |
| a0003 | 0/0 | 528 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | MASMR others(523): Show |
chr4 | 1977723 | 2013974 |
| a0004 | 0/0 | 528 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | MASMR others(523): Show |
chr4 | 1977723 | 2013974 |
| a0005 | 0/0 | 528 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | MASMR others(523): Show |
chr4 | 1977723 | 2013974 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1584 | 238 | 60 | 61 | 72 | 11 | 32 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0001c0002 | 0/0 | 1584 | 97 | 0 | 16 | 71 | 2 | 8 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0001c0003 | 0/0 | 1584 | 10 | 7 | 1 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0001c0005 | 0/0 | 1584 | 3 | 2 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0001c0006 | 0/0 | 1584 | 2 | 0 | 1 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0001c0007 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0001c0010 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0002c0004 | 0/0 | 1584 | 5 | 0 | 0 | 5 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0003c0008 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0004c0009 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 | ||
| a0005c0011 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | ATGGC others(1579): Show |
chr4 | 1977723 | 2013974 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2198 | 133 | 47 | 29 | 26 | 4 | 26 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0001c0001t0002 | 0/0 | 2202 | 82 | 8 | 21 | 46 | 2 | 5 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2197): Show |
chr4 | 1977723 | 2013974 |
| a0001c0001t0003 | 0/1 | 2206 | 17 | 0 | 11 | 0 | 4 | 1 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2201): Show |
chr4 | 1977723 | 2013974 |
| a0001c0001t0004 | 0/0 | 2198 | 3 | 3 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0001c0001t0005 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2197): Show |
chr4 | 1977723 | 2013974 |
| a0001c0001t0006 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0001c0001t0007 | 0/0 | 2202 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2197): Show |
chr4 | 1977723 | 2013974 |
| a0001c0002t0001 | 0/0 | 2198 | 96 | 0 | 16 | 70 | 2 | 8 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0001c0002t0002 | 0/0 | 2202 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2197): Show |
chr4 | 1977723 | 2013974 |
| a0001c0003t0001 | 0/0 | 2198 | 10 | 7 | 1 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0001c0005t0002 | 0/0 | 2202 | 3 | 2 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2197): Show |
chr4 | 1977723 | 2013974 |
| a0001c0006t0002 | 0/0 | 2202 | 2 | 0 | 1 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2197): Show |
chr4 | 1977723 | 2013974 |
| a0001c0007t0001 | 0/0 | 2198 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0001c0010t0001 | 0/0 | 2198 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0002c0004t0001 | 0/0 | 2198 | 5 | 0 | 0 | 5 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0003c0008t0001 | 0/0 | 2198 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| a0004c0009t0002 | 0/0 | 2202 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2197): Show |
chr4 | 1977723 | 2013974 |
| a0005c0011t0001 | 0/0 | 2198 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | GCGCT others(2193): Show |
chr4 | 1977723 | 2013974 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 14 | 0 | 3 | 10 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0005 | 0/0 | 5 | 1 | 0 | 0 | 1 | 3 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0008 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0011 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0018 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0010 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0004 | 0/1 | 5 | 0 | 2 | 0 | 2 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0001 | 0/0 | 22 | 0 | 3 | 18 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0005t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0005t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0005t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0006t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0006t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0001c0010t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0002c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0002c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0002c0004t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0002c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0002c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0003c0008t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0004c0009t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| a0005c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0045 | EUR | GBR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0090 | EUR | FIN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00544 | hp2 | a0001 | c0010 | t0001 | g0115 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00597 | hp2 | a0002 | c0004 | t0001 | g0147 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | CHS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01099 | hp2 | a0001 | c0006 | t0002 | g0237 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0078 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0061 | EUR | IBS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01516 | hp2 | a0001 | c0006 | t0002 | g0190 | EUR | IBS | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0253 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0254 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01975 | hp2 | a0001 | c0005 | t0002 | g0232 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0177 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0100 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0037 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0035 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0036 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0170 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0095 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0094 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0233 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0196 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | ESN | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03540 | hp1 | a0001 | c0005 | t0002 | g0206 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | BEB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04204 | hp1 | a0001 | c0007 | t0001 | g0260 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04204 | hp2 | a0004 | c0009 | t0002 | g0215 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0133 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | YRI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18940 | hp2 | a0002 | c0004 | t0001 | g0092 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18942 | hp1 | a0002 | c0004 | t0001 | g0149 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18954 | hp1 | a0002 | c0004 | t0001 | g0146 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19000 | hp1 | a0005 | c0011 | t0001 | g0098 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | LWK | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19075 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19075 | hp2 | a0002 | c0004 | t0001 | g0148 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ASW | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ASW | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0169 | EUR | TSI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0197 | EUR | TSI | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | GIH | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | GIH | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02559 | hp1 | a0003 | c0008 | t0001 | g0180 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | USA | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | USA | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0004 | REF | REF | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | NELFA_chr4_1977723_2013974 | NELFA | chr4 | 1977723 | 2013974 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1984047 | G | A | 1 | a0004 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1103C>T | p.Ala368Val | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 9/11 | 1118/2198 | 1103/1587 | 368/528 | chr4 | 1984047 | |||
| chr4:1984841 | A | C | 1 | a0002 | 5 | HG00597.hp2 NA18940.hp2 NA18942.hp1 others(2): Show |
missense_variant | MODERATE | c.1003T>G | p.Ser335Ala | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 8/11 | 1018/2198 | 1003/1587 | 335/528 | chr4 | 1984841 | |||
| chr4:1986376 | C | G | 1 | a0003 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.661G>C | p.Ala221Pro | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 5/11 | 676/2198 | 661/1587 | 221/528 | chr4 | 1986376 | |||
| chr4:1989734 | G | A | 1 | a0005 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.518C>T | p.Thr173Met | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/11 | 533/2198 | 518/1587 | 173/528 | chr4 | 1989734 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1983860 | G | A | 1 | a0001c0006 | 2 | HG01099.hp2 HG01516.hp2 |
synonymous_variant | LOW | c.1290C>T | p.Asn430Asn | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 9/11 | 1305/2198 | 1290/1587 | 430/528 | chr4 | 1983860 | |||
| chr4:1983941 | G | A | 2 | a0001c0003 a0005c0011 |
11 | HG01167.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
synonymous_variant | LOW | c.1209C>T | p.Val403Val | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 9/11 | 1224/2198 | 1209/1587 | 403/528 | chr4 | 1983941 | |||
| chr4:1984815 | C | T | 3 | a0001c0002 a0001c0010 a0002c0004 |
103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
synonymous_variant | LOW | c.1029G>A | p.Thr343Thr | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 8/11 | 1044/2198 | 1029/1587 | 343/528 | chr4 | 1984815 | |||
| chr4:1985800 | G | A | 1 | a0001c0005 | 3 | HG01975.hp2 HG03209.hp1 HG03540.hp1 |
synonymous_variant | LOW | c.900C>T | p.Tyr300Tyr | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/11 | 915/2198 | 900/1587 | 300/528 | chr4 | 1985800 | |||
| chr4:1986392 | T | C | 1 | a0001c0010 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.645A>G | p.Lys215Lys | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 5/11 | 660/2198 | 645/1587 | 215/528 | chr4 | 1986392 | |||
| chr4:1989853 | C | T | 1 | a0001c0007 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.399G>A | p.Ala133Ala | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/11 | 414/2198 | 399/1587 | 133/528 | chr4 | 1989853 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1982757 | T | C | 1 | a0001c0001t0007 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*562A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 11/11 | 562 | chr4 | 1982757 | ||||||
| chr4:1982787 | A | ACTGT | 1 | a0001c0001t0003 | 16 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*528_*531dupACAG | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 11/11 | 531 | chr4 | 1982787 | ||||||
| chr4:1982865 | C | T | 1 | a0001c0001t0006 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 11/11 | 454 | chr4 | 1982865 | ||||||
| chr4:1982875 | G | A | 1 | a0001c0001t0004 | 3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*444C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 11/11 | 444 | chr4 | 1982875 | ||||||
| chr4:1983005 | T | TAACA | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(5): Show |
107 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*310_*313dupTGTT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 11/11 | 313 | chr4 | 1983005 | ||||||
| chr4:1983295 | C | T | 1 | a0001c0001t0005 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 11/11 | 24 | chr4 | 1983295 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:1983530 | G | A | 66 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0182 others(63): Show |
91 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1403-27C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 10/10 | chr4 | 1983530 | |||||||
| chr4:1983547 | G | A | 1 | a0001c0001t0002g0030 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1403-44C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 10/10 | chr4 | 1983547 | |||||||
| chr4:1983702 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | splice_region_variant&intron_variant | LOW | c.1303-7G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 9/10 | chr4 | 1983702 | |||||||
| chr4:1983766 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0175 a0001c0001t0003g0061 |
4 | HG00140.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303-71G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 9/10 | chr4 | 1983766 | |||||||
| chr4:1984343 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1037-230G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 8/10 | chr4 | 1984343 | |||||||
| chr4:1984567 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0224 |
2 | HG02027.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1036+241C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 8/10 | chr4 | 1984567 | |||||||
| chr4:1985023 | C | G | 3 | a0001c0001t0007g0038 a0001c0003t0001g0037 a0001c0003t0001g0094 |
3 | HG02622.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.925-104G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985023 | |||||||
| chr4:1985056 | C | T | 1 | a0001c0001t0002g0028 | 2 | HG00408.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.925-137G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985056 | |||||||
| chr4:1985211 | G | A | 180 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0021 others(177): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.925-292C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985211 | |||||||
| chr4:1985245 | A | G | 96 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0211 others(93): Show |
127 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.925-326T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985245 | |||||||
| chr4:1985383 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.924+393C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985383 | |||||||
| chr4:1985491 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.924+285G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985491 | |||||||
| chr4:1985570 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.924+206G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985570 | |||||||
| chr4:1985590 | A | G | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0248 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+186T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985590 | |||||||
| chr4:1985591 | T | C | 4 | a0001c0001t0001g0053 a0001c0001t0001g0066 a0001c0001t0001g0071 others(1): Show |
4 | HG02922.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.924+185A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985591 | |||||||
| chr4:1985600 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0003c0008t0001g0180 |
3 | HG02559.hp1 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.924+176G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985600 | |||||||
| chr4:1985602 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.924+174C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 7/10 | chr4 | 1985602 | |||||||
| chr4:1985887 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG03098.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.836-23G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 6/10 | chr4 | 1985887 | |||||||
| chr4:1985911 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.836-47C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 6/10 | chr4 | 1985911 | |||||||
| chr4:1985955 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.836-91C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 6/10 | chr4 | 1985955 | |||||||
| chr4:1986020 | AGCCCTGC others(12): Show |
A | 1 | a0001c0002t0001g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.835+75_835+93delCA others(17): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 6/10 | chr4 | 1986020 | |||||||
| chr4:1986258 | G | T | 1 | a0001c0001t0001g0021 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.765+14C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 5/10 | chr4 | 1986258 | |||||||
| chr4:1986264 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03927.hp2 | splice_region_variant&intron_variant | LOW | c.765+8C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 5/10 | chr4 | 1986264 | |||||||
| chr4:1986461 | C | CCT | 84 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0211 others(81): Show |
110 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.635-60_635-59insAG | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1986461 | |||||||
| chr4:1986466 | T | C | 72 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0211 others(69): Show |
98 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.635-64A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1986466 | |||||||
| chr4:1986530 | A | G | 81 | a0001c0001t0001g0016 a0001c0001t0001g0205 a0001c0001t0001g0211 others(78): Show |
109 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.635-128T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1986530 | |||||||
| chr4:1986588 | G | A | 1 | a0002c0004t0001g0148 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.635-186C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1986588 | |||||||
| chr4:1986774 | C | CCT | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(258): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.635-373_635-372ins others(2): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1986774 | |||||||
| chr4:1986807 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.635-405C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1986807 | |||||||
| chr4:1986871 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.635-469G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1986871 | |||||||
| chr4:1987254 | C | T | 6 | a0001c0002t0001g0013 a0001c0002t0001g0044 a0001c0002t0001g0047 others(3): Show |
8 | HG00408.hp1 HG02074.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.634+664G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987254 | |||||||
| chr4:1987275 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0002g0200 a0001c0001t0002g0217 |
4 | HG02683.hp2 NA18961.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+643G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987275 | |||||||
| chr4:1987451 | G | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0131 |
2 | HG03239.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.634+467C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987451 | |||||||
| chr4:1987463 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.634+455G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987463 | |||||||
| chr4:1987540 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.634+378G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987540 | |||||||
| chr4:1987604 | CTGTCCTC others(33): Show |
C | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0003c0008t0001g0180 |
3 | HG02559.hp1 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.634+274_634+313del others(40): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987604 | |||||||
| chr4:1987617 | C | A | 1 | a0001c0001t0004g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.634+301G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987617 | |||||||
| chr4:1987634 | A | G | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.634+284T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987634 | |||||||
| chr4:1987643 | G | A | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.634+275C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987643 | |||||||
| chr4:1987644 | G | C | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.634+274C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987644 | |||||||
| chr4:1987663 | T | C | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.634+255A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987663 | |||||||
| chr4:1987698 | C | CGGCCCCT others(11): Show |
1 | a0001c0002t0001g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.634+219_634+220ins others(18): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987698 | |||||||
| chr4:1987715 | T | G | 1 | a0001c0002t0001g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.634+203A>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987715 | |||||||
| chr4:1987756 | C | T | 1 | a0005c0011t0001g0098 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.634+162G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987756 | |||||||
| chr4:1987800 | C | G | 1 | a0001c0002t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.634+118G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 4/10 | chr4 | 1987800 | |||||||
| chr4:1988115 | G | A | 1 | a0001c0001t0002g0033 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.545-108C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988115 | |||||||
| chr4:1988212 | G | A | 3 | a0001c0003t0001g0079 a0001c0003t0001g0080 a0005c0011t0001g0098 |
3 | NA18949.hp1 NA19000.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.545-205C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988212 | |||||||
| chr4:1988257 | G | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.545-250C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988257 | |||||||
| chr4:1988257 | G | T | 1 | a0001c0001t0002g0032 | 2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.545-250C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988257 | |||||||
| chr4:1988365 | C | T | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.545-358G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988365 | |||||||
| chr4:1988654 | G | A | 3 | a0001c0002t0001g0096 a0001c0002t0001g0116 a0001c0002t0001g0142 |
3 | NA18951.hp1 NA18978.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.545-647C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988654 | |||||||
| chr4:1988660 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.545-653A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988660 | |||||||
| chr4:1988698 | A | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0051 others(93): Show |
132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.545-691T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988698 | |||||||
| chr4:1988825 | C | T | 10 | a0001c0001t0001g0256 a0001c0002t0001g0012 a0001c0002t0001g0046 others(7): Show |
12 | HG00621.hp1 HG01256.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.545-818G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988825 | |||||||
| chr4:1988886 | C | G | 1 | a0001c0001t0002g0216 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.544+822G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988886 | |||||||
| chr4:1988917 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.544+791C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988917 | |||||||
| chr4:1988946 | G | GT | 12 | a0001c0001t0001g0017 a0001c0001t0001g0087 a0001c0001t0003g0164 others(9): Show |
13 | HG00597.hp2 HG02148.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.544+761dupA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988946 | |||||||
| chr4:1988946 | G | GTT | 7 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0002g0228 others(4): Show |
7 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.544+760_544+761dup others(2): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988946 | |||||||
| chr4:1988946 | G | GTTT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0099 others(73): Show |
116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.544+759_544+761dup others(3): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988946 | |||||||
| chr4:1988946 | G | GTTTT | 11 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0108 others(8): Show |
12 | HG01069.hp2 HG01358.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.544+758_544+761dup others(4): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1988946 | |||||||
| chr4:1989147 | T | C | 1 | a0001c0003t0001g0034 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544+561A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1989147 | |||||||
| chr4:1989348 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.544+360C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1989348 | |||||||
| chr4:1989476 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.544+232G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1989476 | |||||||
| chr4:1989505 | C | A | 1 | a0001c0002t0001g0167 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.544+203G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1989505 | |||||||
| chr4:1989624 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.544+84C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1989624 | |||||||
| chr4:1989686 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.544+22C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1989686 | |||||||
| chr4:1989696 | G | A | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.544+12C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 3/10 | chr4 | 1989696 | |||||||
| chr4:1989909 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.383-40G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1989909 | |||||||
| chr4:1989920 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.383-51G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1989920 | |||||||
| chr4:1989937 | C | T | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-68G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1989937 | |||||||
| chr4:1990375 | G | A | 1 | a0003c0008t0001g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.383-506C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990375 | |||||||
| chr4:1990384 | G | A | 1 | a0001c0002t0001g0159 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.383-515C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990384 | |||||||
| chr4:1990414 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0030 |
5 | HG00140.hp2 HG01074.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-545G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990414 | |||||||
| chr4:1990438 | G | C | 1 | a0003c0008t0001g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.383-569C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990438 | |||||||
| chr4:1990564 | C | T | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.383-695G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990564 | |||||||
| chr4:1990574 | G | A | 1 | a0001c0001t0004g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383-705C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990574 | |||||||
| chr4:1990661 | T | C | 2 | a0001c0002t0001g0117 a0001c0002t0001g0160 |
2 | NA18945.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.383-792A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990661 | |||||||
| chr4:1990700 | G | C | 3 | a0001c0002t0001g0118 a0001c0002t0001g0161 a0001c0002t0001g0162 |
3 | NA18959.hp1 NA18969.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.383-831C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990700 | |||||||
| chr4:1990864 | G | A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.382+680C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990864 | |||||||
| chr4:1990914 | A | C | 88 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(85): Show |
129 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.382+630T>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990914 | |||||||
| chr4:1990941 | C | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(79): Show |
123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.382+603G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1990941 | |||||||
| chr4:1991131 | C | T | 1 | a0001c0007t0001g0260 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.382+413G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1991131 | |||||||
| chr4:1991245 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.382+299G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1991245 | |||||||
| chr4:1991245 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.382+299G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1991245 | |||||||
| chr4:1991279 | A | C | 83 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0124 others(80): Show |
124 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.382+265T>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1991279 | |||||||
| chr4:1991336 | C | A | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+208G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 2/10 | chr4 | 1991336 | |||||||
| chr4:1991736 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.211-21C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1991736 | |||||||
| chr4:1991830 | C | G | 1 | a0001c0003t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.211-115G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1991830 | |||||||
| chr4:1991933 | C | T | 2 | a0001c0001t0002g0220 a0001c0001t0002g0230 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.211-218G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1991933 | |||||||
| chr4:1991941 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.211-226C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1991941 | |||||||
| chr4:1991994 | A | ACT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(85): Show |
129 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.211-281_211-280dup others(2): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1991994 | |||||||
| chr4:1992258 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(79): Show |
123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.211-543C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992258 | |||||||
| chr4:1992314 | C | A | 1 | a0001c0002t0001g0168 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211-599G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992314 | |||||||
| chr4:1992375 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(73): Show |
117 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.211-660C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992375 | |||||||
| chr4:1992490 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.211-775C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992490 | |||||||
| chr4:1992523 | G | C | 1 | a0001c0002t0001g0162 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.211-808C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992523 | |||||||
| chr4:1992684 | G | T | 1 | a0001c0001t0002g0210 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.211-969C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992684 | |||||||
| chr4:1992735 | C | A | 1 | a0001c0002t0001g0163 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.211-1020G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992735 | |||||||
| chr4:1992815 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.211-1100C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992815 | |||||||
| chr4:1992936 | C | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0189 a0001c0001t0002g0208 others(1): Show |
8 | HG01123.hp2 HG01192.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.211-1221G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1992936 | |||||||
| chr4:1993027 | C | T | 1 | a0001c0002t0001g0168 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211-1312G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993027 | |||||||
| chr4:1993083 | C | G | 1 | a0001c0001t0001g0261 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.211-1368G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993083 | |||||||
| chr4:1993171 | A | T | 5 | a0002c0004t0001g0092 a0002c0004t0001g0146 a0002c0004t0001g0147 others(2): Show |
5 | HG00597.hp2 NA18940.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.211-1456T>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993171 | |||||||
| chr4:1993258 | G | A | 34 | a0001c0001t0002g0003 a0001c0001t0002g0007 a0001c0001t0002g0009 others(31): Show |
54 | HG00408.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.211-1543C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993258 | |||||||
| chr4:1993435 | C | T | 1 | a0001c0003t0001g0034 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.211-1720G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993435 | |||||||
| chr4:1993441 | T | C | 3 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0036 |
3 | HG02630.hp1 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.211-1726A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993441 | |||||||
| chr4:1993520 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.211-1805C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993520 | |||||||
| chr4:1993578 | C | CA | 6 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0069 others(3): Show |
6 | HG00735.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.211-1864dupT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993578 | |||||||
| chr4:1993578 | C | CAA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(72): Show |
116 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.211-1865_211-1864d others(4): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993578 | |||||||
| chr4:1993591 | GAAAGAAA others(12): Show |
G | 1 | a0001c0001t0001g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.211-1895_211-1877d others(21): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993591 | |||||||
| chr4:1993629 | GA | G | 4 | a0001c0002t0001g0043 a0001c0002t0001g0045 a0001c0002t0001g0105 others(1): Show |
4 | HG00099.hp1 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-1915delT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993629 | |||||||
| chr4:1993676 | G | A | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0229 |
3 | HG02630.hp2 HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.211-1961C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993676 | |||||||
| chr4:1993720 | G | A | 4 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0230 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.211-2005C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993720 | |||||||
| chr4:1993776 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.211-2061C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993776 | |||||||
| chr4:1993786 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.211-2071G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993786 | |||||||
| chr4:1993795 | C | CT | 25 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0042 others(22): Show |
28 | HG00597.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.211-2081dupA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993795 | |||||||
| chr4:1993795 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.211-2080G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993795 | |||||||
| chr4:1993795 | CT | C | 78 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(75): Show |
119 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.211-2081delA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993795 | |||||||
| chr4:1993888 | C | A | 1 | a0001c0002t0001g0119 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.211-2173G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1993888 | |||||||
| chr4:1994122 | G | A | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.211-2407C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994122 | |||||||
| chr4:1994261 | T | C | 1 | a0001c0002t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.211-2546A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994261 | |||||||
| chr4:1994557 | T | C | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.211-2842A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994557 | |||||||
| chr4:1994716 | G | A | 3 | a0001c0001t0001g0165 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG00733.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.211-3001C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994716 | |||||||
| chr4:1994806 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.211-3091C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994806 | |||||||
| chr4:1994848 | C | CA | 6 | a0001c0001t0001g0250 a0001c0001t0002g0223 a0001c0001t0002g0224 others(3): Show |
6 | HG02027.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-3134dupT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994848 | |||||||
| chr4:1994848 | CA | C | 16 | a0001c0001t0001g0055 a0001c0001t0001g0085 a0001c0001t0001g0086 others(13): Show |
22 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.211-3134delT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994848 | |||||||
| chr4:1994937 | G | A | 3 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0036 |
3 | HG02630.hp1 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.211-3222C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994937 | |||||||
| chr4:1994943 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(77): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.211-3228C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1994943 | |||||||
| chr4:1995006 | T | A | 1 | a0003c0008t0001g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211-3291A>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995006 | |||||||
| chr4:1995058 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.211-3343A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995058 | |||||||
| chr4:1995080 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.211-3365C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995080 | |||||||
| chr4:1995552 | A | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0202 |
3 | NA18946.hp1 NA18995.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.211-3837T>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995552 | |||||||
| chr4:1995720 | TA | T | 3 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 |
3 | HG02109.hp1 HG02257.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.211-4006delT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995720 | |||||||
| chr4:1995877 | A | AT | 72 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(69): Show |
113 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.211-4163dupA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995877 | |||||||
| chr4:1995877 | AT | A | 12 | a0001c0001t0001g0050 a0001c0001t0001g0071 a0001c0001t0001g0137 others(9): Show |
12 | HG01167.hp2 HG01943.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.211-4163delA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995877 | |||||||
| chr4:1995909 | G | A | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-4194C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1995909 | |||||||
| chr4:1996008 | T | C | 1 | a0001c0002t0001g0168 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.211-4293A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996008 | |||||||
| chr4:1996059 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.211-4344G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996059 | |||||||
| chr4:1996234 | C | A | 1 | a0001c0002t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.211-4519G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996234 | |||||||
| chr4:1996362 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(78): Show |
122 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.211-4647G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996362 | |||||||
| chr4:1996371 | C | G | 11 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0036 others(8): Show |
11 | HG01167.hp1 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.211-4656G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996371 | |||||||
| chr4:1996686 | A | G | 1 | a0002c0004t0001g0146 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.211-4971T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996686 | |||||||
| chr4:1996854 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.211-5139A>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996854 | |||||||
| chr4:1996857 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.211-5142C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996857 | |||||||
| chr4:1996919 | G | A | 1 | a0001c0002t0001g0132 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.211-5204C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996919 | |||||||
| chr4:1996950 | T | TA | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.211-5236dupT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996950 | |||||||
| chr4:1996951 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.211-5236T>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1996951 | |||||||
| chr4:1997136 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.211-5421G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1997136 | |||||||
| chr4:1997254 | C | G | 1 | a0001c0002t0001g0103 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.211-5539G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1997254 | |||||||
| chr4:1997572 | C | T | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG01167.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.211-5857G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1997572 | |||||||
| chr4:1997584 | G | T | 2 | a0001c0003t0001g0077 a0001c0003t0001g0078 |
2 | HG01167.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.211-5869C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1997584 | |||||||
| chr4:1997739 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.211-6024C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1997739 | |||||||
| chr4:1997879 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-6164A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1997879 | |||||||
| chr4:1997986 | G | C | 3 | a0001c0001t0007g0038 a0001c0003t0001g0037 a0001c0003t0001g0094 |
3 | HG02622.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.211-6271C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1997986 | |||||||
| chr4:1998058 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.211-6343G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998058 | |||||||
| chr4:1998074 | C | T | 1 | a0003c0008t0001g0180 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211-6359G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998074 | |||||||
| chr4:1998109 | C | CAAT | 99 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0123 others(96): Show |
140 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.211-6395_211-6394i others(5): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998109 | |||||||
| chr4:1998506 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.211-6791G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998506 | |||||||
| chr4:1998531 | A | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(78): Show |
122 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.211-6816T>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998531 | |||||||
| chr4:1998678 | G | C | 1 | a0001c0001t0002g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.211-6963C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998678 | |||||||
| chr4:1998740 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.211-7025G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998740 | |||||||
| chr4:1998755 | C | T | 1 | a0001c0001t0002g0028 | 2 | HG00408.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.211-7040G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998755 | |||||||
| chr4:1998836 | A | G | 1 | a0001c0002t0001g0102 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.211-7121T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998836 | |||||||
| chr4:1998870 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.211-7155C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998870 | |||||||
| chr4:1998896 | A | T | 1 | a0001c0001t0001g0019 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.211-7181T>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1998896 | |||||||
| chr4:1999124 | C | T | 4 | a0001c0001t0004g0177 a0001c0001t0004g0179 a0001c0001t0004g0184 others(1): Show |
4 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.211-7409G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1999124 | |||||||
| chr4:1999274 | G | A | 1 | a0001c0001t0004g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.211-7559C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1999274 | |||||||
| chr4:1999288 | C | T | 1 | a0001c0001t0002g0201 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.211-7573G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1999288 | |||||||
| chr4:1999385 | T | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(79): Show |
123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.211-7670A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1999385 | |||||||
| chr4:1999870 | C | T | 95 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0050 others(92): Show |
131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.211-8155G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1999870 | |||||||
| chr4:1999953 | T | C | 1 | a0001c0002t0001g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.211-8238A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 1999953 | |||||||
| chr4:2000678 | C | G | 1 | a0001c0001t0002g0027 | 2 | NA19055.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.210+8072G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2000678 | |||||||
| chr4:2000845 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.210+7905T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2000845 | |||||||
| chr4:2001267 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.210+7483T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001267 | |||||||
| chr4:2001326 | G | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0131 |
2 | HG03239.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.210+7424C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001326 | |||||||
| chr4:2001425 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.210+7325T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001425 | |||||||
| chr4:2001644 | T | C | 1 | a0001c0002t0001g0255 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.210+7106A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001644 | |||||||
| chr4:2001674 | A | G | 1 | a0001c0001t0004g0179 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.210+7076T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001674 | |||||||
| chr4:2001907 | G | GA | 86 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(83): Show |
128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+6842dupT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001907 | |||||||
| chr4:2001928 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(80): Show |
125 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.210+6822G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001928 | |||||||
| chr4:2001967 | G | A | 1 | a0001c0005t0002g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.210+6783C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2001967 | |||||||
| chr4:2002057 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.210+6693T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002057 | |||||||
| chr4:2002061 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(83): Show |
127 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.210+6689T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002061 | |||||||
| chr4:2002069 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.210+6681C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002069 | |||||||
| chr4:2002092 | A | C | 2 | a0001c0001t0002g0009 a0001c0001t0002g0199 |
5 | NA18939.hp1 NA18963.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+6658T>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002092 | |||||||
| chr4:2002103 | C | G | 1 | a0001c0005t0002g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.210+6647G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002103 | |||||||
| chr4:2002104 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.210+6646C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002104 | |||||||
| chr4:2002132 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(76): Show |
120 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.210+6618C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002132 | |||||||
| chr4:2002142 | A | G | 1 | a0001c0005t0002g0196 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.210+6608T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002142 | |||||||
| chr4:2002149 | A | G | 2 | a0001c0002t0001g0133 a0001c0005t0002g0196 |
2 | HG03209.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.210+6601T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002149 | |||||||
| chr4:2002154 | C | T | 1 | a0001c0002t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.210+6596G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002154 | |||||||
| chr4:2002155 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.210+6595C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002155 | |||||||
| chr4:2002156 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.210+6594G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002156 | |||||||
| chr4:2002157 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.210+6593C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002157 | |||||||
| chr4:2002183 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.210+6567T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002183 | |||||||
| chr4:2002187 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0074 a0001c0001t0001g0075 others(3): Show |
7 | HG01070.hp1 HG01071.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.210+6563C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002187 | |||||||
| chr4:2002462 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.210+6288G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002462 | |||||||
| chr4:2002538 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(95): Show |
139 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.210+6212G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002538 | |||||||
| chr4:2002625 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(77): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.210+6125C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002625 | |||||||
| chr4:2002706 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0143 |
2 | NA18986.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.210+6044A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2002706 | |||||||
| chr4:2003007 | C | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0134 |
2 | HG01358.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.210+5743G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003007 | |||||||
| chr4:2003033 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(84): Show |
128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+5717C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003033 | |||||||
| chr4:2003185 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.210+5565G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003185 | |||||||
| chr4:2003204 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(96): Show |
140 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.210+5546A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003204 | |||||||
| chr4:2003240 | G | A | 1 | a0001c0002t0001g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.210+5510C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003240 | |||||||
| chr4:2003315 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.210+5435G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003315 | |||||||
| chr4:2003423 | G | A | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | HG00597.hp1 HG03491.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.210+5327C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003423 | |||||||
| chr4:2003541 | C | T | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.210+5209G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003541 | |||||||
| chr4:2003645 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.210+5105C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003645 | |||||||
| chr4:2003675 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.210+5075A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003675 | |||||||
| chr4:2003805 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.210+4945A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003805 | |||||||
| chr4:2003832 | G | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0192 a0001c0001t0002g0193 others(1): Show |
5 | HG01361.hp1 HG01928.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+4918C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003832 | |||||||
| chr4:2003837 | CT | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0089 others(84): Show |
128 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+4912delA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003837 | |||||||
| chr4:2003837 | CTT | C | 6 | a0001c0001t0001g0191 a0001c0001t0001g0236 a0001c0001t0002g0238 others(3): Show |
6 | HG01099.hp2 HG01168.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.210+4911_210+4912d others(4): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003837 | |||||||
| chr4:2003856 | T | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(75): Show |
119 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.210+4894A>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003856 | |||||||
| chr4:2003912 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.210+4838C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003912 | |||||||
| chr4:2003978 | C | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(77): Show |
121 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.210+4772G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2003978 | |||||||
| chr4:2004096 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.210+4654A>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004096 | |||||||
| chr4:2004316 | T | C | 2 | a0001c0003t0001g0037 a0001c0003t0001g0094 |
2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.210+4434A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004316 | |||||||
| chr4:2004336 | C | A | 1 | a0001c0001t0003g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.210+4414G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004336 | |||||||
| chr4:2004342 | C | G | 2 | a0001c0003t0001g0037 a0001c0003t0001g0094 |
2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.210+4408G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004342 | |||||||
| chr4:2004346 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.210+4404A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004346 | |||||||
| chr4:2004432 | C | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.210+4318G>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004432 | |||||||
| chr4:2004474 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+4276A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004474 | |||||||
| chr4:2004491 | T | C | 1 | a0001c0002t0001g0141 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.210+4259A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004491 | |||||||
| chr4:2004513 | G | A | 1 | a0001c0002t0001g0168 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.210+4237C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004513 | |||||||
| chr4:2004776 | C | A | 2 | a0001c0001t0002g0243 a0001c0001t0002g0244 |
2 | NA18972.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.210+3974G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004776 | |||||||
| chr4:2004809 | C | CT | 10 | a0001c0001t0001g0097 a0001c0001t0001g0182 a0001c0001t0001g0248 others(7): Show |
10 | HG01261.hp2 HG01516.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.210+3940dupA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004809 | |||||||
| chr4:2004809 | CT | C | 9 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(6): Show |
9 | HG01070.hp2 HG02145.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.210+3940delA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004809 | |||||||
| chr4:2004818 | T | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG01070.hp1 HG01071.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.210+3932A>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004818 | |||||||
| chr4:2004825 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+3925C>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004825 | |||||||
| chr4:2004869 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.210+3881C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004869 | |||||||
| chr4:2004907 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0191 others(76): Show |
120 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.210+3843C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2004907 | |||||||
| chr4:2005121 | T | A | 1 | a0001c0002t0001g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.210+3629A>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005121 | |||||||
| chr4:2005122 | A | T | 1 | a0001c0001t0007g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.210+3628T>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005122 | |||||||
| chr4:2005143 | AT | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(84): Show |
128 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.210+3606delA | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005143 | |||||||
| chr4:2005197 | T | C | 6 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(3): Show |
6 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+3553A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005197 | |||||||
| chr4:2005227 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.210+3523G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005227 | |||||||
| chr4:2005394 | T | A | 1 | a0001c0002t0002g0154 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.210+3356A>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005394 | |||||||
| chr4:2005498 | C | T | 2 | a0001c0003t0001g0037 a0001c0003t0001g0094 |
2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.210+3252G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005498 | |||||||
| chr4:2005647 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.210+3103C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005647 | |||||||
| chr4:2005688 | G | A | 1 | a0001c0002t0001g0145 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.210+3062C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005688 | |||||||
| chr4:2005722 | A | C | 2 | a0001c0002t0001g0093 a0002c0004t0001g0092 |
2 | HG02015.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.210+3028T>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005722 | |||||||
| chr4:2005997 | T | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0182 others(85): Show |
129 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.210+2753A>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2005997 | |||||||
| chr4:2006472 | A | G | 2 | a0001c0001t0002g0091 a0001c0002t0001g0090 |
2 | HG00280.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.210+2278T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006472 | |||||||
| chr4:2006560 | G | C | 5 | a0001c0002t0001g0150 a0002c0004t0001g0146 a0002c0004t0001g0147 others(2): Show |
5 | HG00597.hp2 NA18940.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.210+2190C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006560 | |||||||
| chr4:2006716 | C | A | 1 | a0001c0002t0001g0151 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.210+2034G>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006716 | |||||||
| chr4:2006747 | T | G | 10 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0004g0177 others(7): Show |
11 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.210+2003A>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006747 | |||||||
| chr4:2006768 | C | CA | 87 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0097 others(84): Show |
120 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.210+1981dupT | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006768 | |||||||
| chr4:2006768 | C | CAA | 20 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0166 others(17): Show |
26 | HG00609.hp1 HG00639.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.210+1980_210+1981d others(4): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006768 | |||||||
| chr4:2006768 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0247 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.210+1968_210+1981d others(16): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006768 | |||||||
| chr4:2006768 | CAAAAAAA others(8): Show |
C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(79): Show |
123 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.210+1967_210+1981d others(17): Show |
NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006768 | |||||||
| chr4:2006987 | A | G | 3 | a0001c0003t0001g0034 a0001c0003t0001g0035 a0001c0003t0001g0036 |
3 | HG02630.hp1 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.210+1763T>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2006987 | |||||||
| chr4:2007175 | C | T | 2 | a0001c0001t0002g0187 a0001c0002t0001g0186 |
2 | HG00423.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.210+1575G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2007175 | |||||||
| chr4:2007368 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(78): Show |
122 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.210+1382G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2007368 | |||||||
| chr4:2007409 | G | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.210+1341C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2007409 | |||||||
| chr4:2007489 | G | A | 1 | a0001c0001t0003g0169 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.210+1261C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2007489 | |||||||
| chr4:2007757 | T | C | 1 | a0001c0002t0001g0170 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.210+993A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2007757 | |||||||
| chr4:2007986 | G | A | 1 | a0001c0002t0001g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.210+764C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2007986 | |||||||
| chr4:2008274 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.210+476G>A | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2008274 | |||||||
| chr4:2008394 | G | C | 1 | a0001c0001t0001g0172 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.210+356C>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2008394 | |||||||
| chr4:2008436 | G | A | 83 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0188 others(80): Show |
124 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.210+314C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2008436 | |||||||
| chr4:2008582 | T | C | 6 | a0001c0001t0001g0256 a0001c0002t0001g0252 a0001c0002t0001g0253 others(3): Show |
6 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.210+168A>G | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2008582 | |||||||
| chr4:2008582 | T | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0024 others(94): Show |
140 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.210+168A>C | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2008582 | |||||||
| chr4:2008656 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.210+94C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2008656 | |||||||
| chr4:2008670 | G | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
8 | HG00741.hp2 HG01070.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.210+80C>T | NELFA | ENSG00000185049.16 | transcript | ENST00000382882.9 | protein_coding | 1/10 | chr4 | 2008670 |