Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51497 |
| ensemblid | ENSG00000101158.15 |
| hgncid | 15934 |
| symbol | NELFCD |
| name | negative elongation factor complex member C/D |
| refseq_nuc | NM_198976.4 |
| refseq_prot | NP_945327.3 |
| ensembl_nuc | ENST00000652272.2 |
| ensembl_prot | ENSP00000499018.1 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 58981256 |
| end | 58995113 |
| strand | + |
| ver | v1.2 |
| region | chr20:58981256-58995113 |
| region5000 | chr20:58976256-59000113 |
| regionname0 | NELFCD_chr20_58981256_58995113 |
| regionname5000 | NELFCD_chr20_58976256_59000113 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 581 | 437 | 94 | 78 | 197 | 16 | 50 | 150 | NELFCD_chr20_58976256_59000113 | NELFCD | MDEDY others(576): Show |
chr20 | 58976256 | 59000113 |
| a0002 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | MDEDY others(576): Show |
chr20 | 58976256 | 59000113 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1743 | 359 | 88 | 66 | 156 | 11 | 37 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0002 | 0/0 | 1743 | 54 | 3 | 10 | 29 | 2 | 10 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0003 | 0/1 | 1743 | 7 | 0 | 2 | 0 | 1 | 3 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0004 | 0/0 | 1743 | 6 | 0 | 0 | 6 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0005 | 0/0 | 1743 | 4 | 0 | 0 | 4 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0006 | 0/0 | 1743 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0007 | 0/0 | 1743 | 2 | 0 | 0 | 0 | 2 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0009 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0010 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0001c0011 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 | ||
| a0002c0008 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGGA others(1738): Show |
chr20 | 58976256 | 59000113 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2237 | 182 | 68 | 29 | 62 | 6 | 16 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0001t0002 | 0/0 | 2237 | 166 | 11 | 35 | 94 | 5 | 21 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0001t0004 | 0/0 | 2237 | 7 | 7 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0001t0005 | 0/0 | 2237 | 4 | 2 | 2 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0002t0003 | 0/0 | 2237 | 51 | 1 | 10 | 28 | 2 | 10 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0002t0004 | 0/0 | 2237 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0002t0006 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0003t0001 | 0/1 | 2237 | 7 | 0 | 2 | 0 | 1 | 3 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0004t0002 | 0/0 | 2237 | 6 | 0 | 0 | 6 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0005t0002 | 0/0 | 2237 | 4 | 0 | 0 | 4 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0006t0002 | 0/0 | 2237 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0007t0001 | 0/0 | 2237 | 2 | 0 | 0 | 0 | 2 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0009t0001 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0010t0002 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0001c0011t0001 | 0/0 | 2237 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| a0002c0008t0002 | 0/0 | 2237 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | ATGCG others(2232): Show |
chr20 | 58976256 | 59000113 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 62 | 18 | 11 | 27 | 2 | 4 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0017 | 0/0 | 4 | 2 | 0 | 1 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0020 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0038 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0129 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0002 | 0/0 | 39 | 1 | 10 | 23 | 0 | 5 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0003 | 0/0 | 32 | 2 | 7 | 16 | 3 | 4 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0005 | 0/0 | 17 | 0 | 5 | 11 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0006 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0011 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0030 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0031 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0047 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0004g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0005g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0004 | 0/0 | 17 | 0 | 6 | 5 | 2 | 4 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0007 | 0/0 | 9 | 0 | 3 | 4 | 0 | 2 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0002t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0003t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0003t0001g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0004t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0005t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0005t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0006t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0007t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0009t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0010t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0001c0011t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| a0002c0008t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0004 | EUR | GBR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00323 | hp1 | a0001 | c0003 | t0001 | g0060 | EUR | FIN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0092 | EUR | FIN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00438 | hp1 | a0001 | c0004 | t0002 | g0013 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00597 | hp1 | a0002 | c0008 | t0002 | g0002 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0053 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01167 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01358 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | IBS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01516 | hp2 | a0001 | c0007 | t0001 | g0009 | EUR | IBS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01517 | hp2 | a0001 | c0007 | t0001 | g0009 | EUR | IBS | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0151 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02074 | hp2 | a0001 | c0002 | t0003 | g0149 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CDX | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CDX | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PEL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02895 | hp1 | a0001 | c0011 | t0001 | g0132 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02976 | hp1 | a0001 | c0002 | t0004 | g0140 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0141 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0053 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0139 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | PJL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0007 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0138 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0015 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0145 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | BEB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0007 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0004 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | STU | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | CHB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | CHB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | YRI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18950 | hp1 | a0001 | c0005 | t0002 | g0012 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18953 | hp2 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18954 | hp1 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18966 | hp2 | a0001 | c0002 | t0006 | g0004 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18974 | hp2 | a0001 | c0005 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18985 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0148 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18993 | hp1 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19002 | hp1 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19030 | hp2 | a0001 | c0009 | t0001 | g0116 | AFR | LWK | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19058 | hp2 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19059 | hp1 | a0001 | c0005 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19059 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0135 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19065 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19080 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19088 | hp1 | a0001 | c0005 | t0002 | g0003 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19090 | hp2 | a0001 | c0004 | t0002 | g0057 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0147 | AFR | ASW | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | GIH | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02486 | hp1 | a0001 | c0010 | t0002 | g0012 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | USA | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18955 | hp1 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | LWK | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0062 | REF | REF | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0129 | REF | REF | NELFCD_chr20_58976256_59000113 | NELFCD | chr20 | 58976256 | 59000113 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58991891 | T | C | 1 | a0002 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1100T>C | p.Val367Ala | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/15 | 1154/2237 | 1100/1746 | 367/581 | chr20 | 58991891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58981348 | C | T | 1 | a0001c0011 | 1 | HG02895.hp1 | synonymous_variant | LOW | c.39C>T | p.Gly13Gly | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/15 | 93/2237 | 39/1746 | 13/581 | chr20 | 58981348 | |||
| chr20:58988922 | G | A | 1 | a0001c0006 | 2 | NA19065.hp1 NA19080.hp1 |
synonymous_variant | LOW | c.405G>A | p.Ala135Ala | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 5/15 | 459/2237 | 405/1746 | 135/581 | chr20 | 58988922 | |||
| chr20:58989015 | C | T | 1 | a0001c0002 | 54 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(51): Show |
synonymous_variant | LOW | c.498C>T | p.Thr166Thr | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 5/15 | 552/2237 | 498/1746 | 166/581 | chr20 | 58989015 | |||
| chr20:58989640 | C | T | 2 | a0001c0003 a0001c0007 |
8 | HG00323.hp1 HG01169.hp1 HG01261.hp1 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.657C>T | p.Ala219Ala | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 6/15 | 711/2237 | 657/1746 | 219/581 | chr20 | 58989640 | |||
| chr20:58990992 | C | T | 1 | a0001c0010 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.871C>T | p.Leu291Leu | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 8/15 | 925/2237 | 871/1746 | 291/581 | chr20 | 58990992 | |||
| chr20:58991009 | G | C | 1 | a0001c0005 | 4 | NA18950.hp1 NA18974.hp2 NA19059.hp1 others(1): Show |
synonymous_variant | LOW | c.888G>C | p.Leu296Leu | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 8/15 | 942/2237 | 888/1746 | 296/581 | chr20 | 58991009 | |||
| chr20:58991317 | C | T | 1 | a0001c0004 | 6 | HG00438.hp1 NA18953.hp2 NA18954.hp1 others(3): Show |
synonymous_variant | LOW | c.960C>T | p.Arg320Arg | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/15 | 1014/2237 | 960/1746 | 320/581 | chr20 | 58991317 | |||
| chr20:58991889 | A | C | 1 | a0001c0007 | 2 | HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.1098A>C | p.Arg366Arg | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/15 | 1152/2237 | 1098/1746 | 366/581 | chr20 | 58991889 | |||
| chr20:58994205 | G | A | 1 | a0001c0009 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1677G>A | p.Thr559Thr | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/15 | 1731/2237 | 1677/1746 | 559/581 | chr20 | 58994205 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58994761 | G | T | 6 | a0001c0001t0002 a0001c0004t0002 a0001c0005t0002 others(3): Show |
180 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*85G>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 15/15 | 85 | chr20 | 58994761 | ||||||
| chr20:58994805 | C | G | 2 | a0001c0002t0003 a0001c0002t0006 |
52 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*129C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 15/15 | 129 | chr20 | 58994805 | ||||||
| chr20:58994883 | A | G | 1 | a0001c0001t0005 | 4 | HG01255.hp2 HG02145.hp2 HG02148.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*207A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 15/15 | 207 | chr20 | 58994883 | ||||||
| chr20:58994955 | G | C | 2 | a0001c0001t0004 a0001c0002t0004 |
9 | HG02109.hp1 HG02257.hp1 HG02965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*279G>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 15/15 | 279 | chr20 | 58994955 | ||||||
| chr20:58995085 | A | G | 1 | a0001c0002t0006 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 15/15 | 409 | chr20 | 58995085 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:58981401 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.60+32G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58981401 | |||||||
| chr20:58981433 | C | T | 28 | a0001c0001t0001g0020 a0001c0001t0001g0055 a0001c0001t0001g0146 others(25): Show |
69 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(66): Show |
intron_variant | MODIFIER | c.60+64C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58981433 | |||||||
| chr20:58981536 | G | C | 1 | a0001c0004t0002g0057 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.60+167G>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58981536 | |||||||
| chr20:58981547 | CCCGGGGT others(15): Show |
C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0034 others(7): Show |
16 | HG00323.hp1 HG01169.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.60+189_60+210delGC others(20): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58981547 | ||||||
| chr20:58981696 | A | AC | 6 | a0001c0001t0001g0021 a0001c0001t0001g0063 a0001c0001t0001g0064 others(3): Show |
8 | HG01361.hp1 HG03831.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+332dupC | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58981696 | ||||||
| chr20:58981914 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(21): Show |
111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.60+545T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58981914 | |||||||
| chr20:58981928 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.60+559C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58981928 | |||||||
| chr20:58981963 | A | ACT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(22): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.60+595_60+596dupCT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58981963 | ||||||
| chr20:58981973 | C | T | 1 | a0001c0001t0002g0133 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.60+604C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58981973 | |||||||
| chr20:58982027 | TC | T | 24 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0025 others(21): Show |
37 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.60+662delC | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982027 | ||||||
| chr20:58982140 | AT | A | 17 | a0001c0001t0001g0020 a0001c0001t0001g0049 a0001c0001t0001g0050 others(14): Show |
36 | HG00738.hp1 HG01192.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.60+804delT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATT | A | 41 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0042 others(38): Show |
76 | HG00140.hp2 HG00642.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.60+803_60+804delTT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATTT | A | 35 | a0001c0001t0001g0009 a0001c0001t0001g0025 a0001c0001t0001g0032 others(32): Show |
75 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.60+802_60+804delTT others(1): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATTTT | A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0073 a0001c0001t0001g0094 others(15): Show |
58 | HG00099.hp1 HG00280.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.60+801_60+804delTT others(2): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATTTTT | A | 13 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0028 others(10): Show |
64 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.60+800_60+804delTT others(3): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATTTTTT | A | 5 | a0001c0001t0002g0027 a0001c0001t0002g0081 a0001c0001t0002g0082 others(2): Show |
7 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+799_60+804delTT others(4): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0038 | 2 | HG02559.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.60+790_60+804delTT others(13): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATTTTTTT others(9): Show |
A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(16): Show |
101 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.60+789_60+804delTT others(14): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982140 | ATTTTTTT others(10): Show |
A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0066 others(1): Show |
8 | HG00140.hp1 HG00280.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.60+788_60+804delTT others(15): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58982140 | ||||||
| chr20:58982217 | C | T | 11 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0019 others(8): Show |
42 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.60+848C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982217 | |||||||
| chr20:58982257 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.60+888A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982257 | |||||||
| chr20:58982389 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.60+1020C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982389 | |||||||
| chr20:58982410 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
3 | HG02572.hp2 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.60+1041T>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982410 | |||||||
| chr20:58982489 | T | C | 24 | a0001c0001t0004g0008 a0001c0002t0003g0004 a0001c0002t0003g0007 others(21): Show |
61 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.60+1120T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982489 | |||||||
| chr20:58982520 | T | G | 1 | a0001c0001t0002g0093 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.60+1151T>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982520 | |||||||
| chr20:58982524 | A | G | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.60+1155A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982524 | |||||||
| chr20:58982589 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.60+1220G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982589 | |||||||
| chr20:58982597 | G | C | 24 | a0001c0001t0004g0008 a0001c0002t0003g0004 a0001c0002t0003g0007 others(21): Show |
61 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.60+1228G>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982597 | |||||||
| chr20:58982860 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.60+1491G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982860 | |||||||
| chr20:58982955 | C | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(155): Show |
434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.60+1586C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982955 | |||||||
| chr20:58982960 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
3 | HG02572.hp2 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.60+1591C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58982960 | |||||||
| chr20:58983130 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.60+1761C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983130 | |||||||
| chr20:58983139 | C | CT | 20 | a0001c0001t0001g0024 a0001c0001t0001g0037 a0001c0001t0001g0039 others(17): Show |
58 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.60+1785dupT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58983139 | ||||||
| chr20:58983139 | CT | C | 7 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0074 others(4): Show |
7 | HG01169.hp2 HG02015.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.60+1785delT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58983139 | ||||||
| chr20:58983203 | C | A | 1 | a0001c0002t0003g0053 | 2 | HG01081.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.60+1834C>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983203 | |||||||
| chr20:58983219 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(148): Show |
423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.60+1850T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983219 | |||||||
| chr20:58983241 | A | G | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.60+1872A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983241 | |||||||
| chr20:58983327 | T | G | 29 | a0001c0001t0001g0039 a0001c0001t0001g0043 a0001c0001t0001g0049 others(26): Show |
69 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(66): Show |
intron_variant | MODIFIER | c.60+1958T>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983327 | |||||||
| chr20:58983426 | G | A | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.60+2057G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983426 | |||||||
| chr20:58983435 | C | CT | 10 | a0001c0001t0001g0023 a0001c0001t0001g0118 a0001c0001t0001g0127 others(7): Show |
12 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.60+2084dupT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58983435 | ||||||
| chr20:58983435 | CT | C | 26 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0071 others(23): Show |
66 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.60+2084delT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | 58983435 | ||||||
| chr20:58983646 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.60+2277G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983646 | |||||||
| chr20:58983746 | AT | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0076 |
4 | HG00741.hp1 HG01099.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-2346delT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983746 | |||||||
| chr20:58983954 | A | G | 2 | a0001c0001t0005g0022 a0001c0001t0005g0070 |
4 | HG01255.hp2 HG02145.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-2139A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58983954 | |||||||
| chr20:58984065 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.61-2028C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984065 | |||||||
| chr20:58984078 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.61-2015C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984078 | |||||||
| chr20:58984275 | G | A | 5 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0103 others(2): Show |
7 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-1818G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984275 | |||||||
| chr20:58984318 | C | T | 5 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0103 others(2): Show |
7 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.61-1775C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984318 | |||||||
| chr20:58984338 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.61-1755A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984338 | |||||||
| chr20:58984575 | A | G | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.61-1518A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984575 | |||||||
| chr20:58984600 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0002t0003g0145 |
4 | HG02572.hp2 HG02622.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-1493C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984600 | |||||||
| chr20:58984622 | A | C | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.61-1471A>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984622 | |||||||
| chr20:58984780 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.61-1313T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984780 | |||||||
| chr20:58984787 | G | A | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.61-1306G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984787 | |||||||
| chr20:58984865 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.61-1228C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984865 | |||||||
| chr20:58984997 | A | G | 2 | a0001c0001t0002g0122 a0001c0001t0002g0133 |
2 | HG00673.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.61-1096A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58984997 | |||||||
| chr20:58985113 | C | T | 1 | a0001c0009t0001g0116 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.61-980C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985113 | |||||||
| chr20:58985178 | T | A | 1 | a0001c0002t0003g0138 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.61-915T>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985178 | |||||||
| chr20:58985229 | CT | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
3 | HG02572.hp2 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.61-863delT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985229 | |||||||
| chr20:58985235 | C | CAGCT | 2 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
3 | HG02572.hp2 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.61-858_61-857insAG others(2): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985235 | |||||||
| chr20:58985376 | A | C | 1 | a0001c0001t0001g0049 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.61-717A>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985376 | |||||||
| chr20:58985625 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.61-468A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985625 | |||||||
| chr20:58985639 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.61-454A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985639 | |||||||
| chr20:58985710 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.61-383G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985710 | |||||||
| chr20:58985722 | C | T | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.61-371C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58985722 | |||||||
| chr20:58986063 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.61-30A>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 1/14 | chr20 | 58986063 | |||||||
| chr20:58986307 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.176+99C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986307 | |||||||
| chr20:58986330 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.176+122G>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986330 | |||||||
| chr20:58986361 | T | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(21): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.176+153T>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986361 | |||||||
| chr20:58986363 | T | A | 1 | a0001c0001t0001g0059 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.176+155T>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986363 | |||||||
| chr20:58986364 | A | T | 2 | a0001c0001t0001g0043 a0001c0001t0002g0002 |
3 | HG02155.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.176+156A>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986364 | |||||||
| chr20:58986404 | C | T | 1 | a0001c0002t0003g0149 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.176+196C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986404 | |||||||
| chr20:58986470 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(82): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.176+262G>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986470 | |||||||
| chr20:58986544 | C | T | 1 | a0001c0002t0003g0144 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.177-210C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 2/14 | chr20 | 58986544 | |||||||
| chr20:58986938 | A | G | 1 | a0001c0001t0001g0049 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.286+75A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58986938 | |||||||
| chr20:58986972 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0095 |
4 | NA18948.hp2 NA18951.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+109T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58986972 | |||||||
| chr20:58987047 | C | G | 11 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
20 | HG00544.hp1 HG00741.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.286+184C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58987047 | |||||||
| chr20:58987114 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.286+251C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58987114 | |||||||
| chr20:58987202 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.286+339G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58987202 | |||||||
| chr20:58987216 | T | C | 3 | a0001c0001t0002g0086 a0001c0001t0002g0096 a0001c0001t0002g0104 |
3 | HG00544.hp2 HG02165.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.286+353T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58987216 | |||||||
| chr20:58987358 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.287-350G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58987358 | |||||||
| chr20:58987365 | T | A | 1 | a0001c0001t0002g0019 | 4 | HG02602.hp1 HG03490.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-343T>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58987365 | |||||||
| chr20:58987422 | A | T | 1 | a0001c0001t0002g0110 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.287-286A>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 3/14 | chr20 | 58987422 | |||||||
| chr20:58988006 | C | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
55 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.396+189C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988006 | |||||||
| chr20:58988181 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.396+364G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988181 | |||||||
| chr20:58988319 | C | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0104 |
2 | HG00544.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.396+502C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988319 | |||||||
| chr20:58988339 | T | C | 1 | a0001c0001t0001g0049 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.396+522T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988339 | |||||||
| chr20:58988354 | C | T | 24 | a0001c0001t0004g0008 a0001c0002t0003g0004 a0001c0002t0003g0007 others(21): Show |
61 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(58): Show |
intron_variant | MODIFIER | c.396+537C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988354 | |||||||
| chr20:58988383 | G | T | 1 | a0001c0001t0002g0091 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.397-531G>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988383 | |||||||
| chr20:58988474 | C | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG00738.hp1 HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.397-440C>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988474 | |||||||
| chr20:58988554 | A | C | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.397-360A>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988554 | |||||||
| chr20:58988710 | A | G | 60 | a0001c0001t0001g0029 a0001c0001t0001g0077 a0001c0001t0001g0094 others(57): Show |
188 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.397-204A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988710 | |||||||
| chr20:58988752 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0152 |
2 | HG01261.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.397-162G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 4/14 | chr20 | 58988752 | |||||||
| chr20:58989269 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.505-219G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 5/14 | chr20 | 58989269 | |||||||
| chr20:58989364 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0099 |
3 | HG02080.hp2 NA18963.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.505-124G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 5/14 | chr20 | 58989364 | |||||||
| chr20:58989390 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.505-98A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 5/14 | chr20 | 58989390 | |||||||
| chr20:58989393 | C | T | 26 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(23): Show |
64 | HG00140.hp2 HG01081.hp1 HG01167.hp2 others(61): Show |
intron_variant | MODIFIER | c.505-95C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 5/14 | chr20 | 58989393 | |||||||
| chr20:58989434 | G | A | 36 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0020 others(33): Show |
54 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.505-54G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 5/14 | chr20 | 58989434 | |||||||
| chr20:58989714 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.657+74C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 6/14 | chr20 | 58989714 | |||||||
| chr20:58989769 | G | A | 2 | a0001c0001t0005g0022 a0001c0001t0005g0070 |
4 | HG01255.hp2 HG02145.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-89G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 6/14 | chr20 | 58989769 | |||||||
| chr20:58990056 | G | A | 1 | a0001c0001t0001g0010 | 6 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.788+68G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990056 | |||||||
| chr20:58990135 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.788+147G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990135 | |||||||
| chr20:58990162 | C | T | 1 | a0001c0001t0002g0106 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.788+174C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990162 | |||||||
| chr20:58990176 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.788+188C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990176 | |||||||
| chr20:58990232 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(2): Show |
12 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.788+244G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990232 | |||||||
| chr20:58990291 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.788+303T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990291 | |||||||
| chr20:58990345 | A | G | 1 | a0001c0002t0003g0145 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.788+357A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990345 | |||||||
| chr20:58990400 | CA | C | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(28): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.788+429delA | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr20 | 58990400 | ||||||
| chr20:58990639 | T | C | 1 | a0001c0002t0003g0141 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.789-271T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990639 | |||||||
| chr20:58990724 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(2): Show |
12 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.789-186T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990724 | |||||||
| chr20:58990888 | G | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(125): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.789-22G>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 7/14 | chr20 | 58990888 | |||||||
| chr20:58991107 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(2): Show |
12 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.954+32G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 8/14 | chr20 | 58991107 | |||||||
| chr20:58991275 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.955-37G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 8/14 | chr20 | 58991275 | |||||||
| chr20:58991296 | A | G | 3 | a0001c0002t0003g0136 a0001c0002t0003g0143 a0001c0002t0003g0148 |
3 | NA18943.hp1 NA18991.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.955-16A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 8/14 | chr20 | 58991296 | |||||||
| chr20:58991300 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0131 |
5 | HG02965.hp1 HG03195.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.955-12G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 8/14 | chr20 | 58991300 | |||||||
| chr20:58991473 | A | AT | 5 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(2): Show |
12 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1089+33dupT | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | 58991473 | ||||||
| chr20:58991527 | C | T | 3 | a0001c0001t0002g0030 a0001c0001t0002g0087 a0001c0001t0002g0088 |
5 | HG01975.hp1 HG01978.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+81C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | chr20 | 58991527 | |||||||
| chr20:58991582 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0016 others(80): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1089+136C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | chr20 | 58991582 | |||||||
| chr20:58991594 | A | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(2): Show |
12 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1089+148A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | chr20 | 58991594 | |||||||
| chr20:58991685 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
3 | HG02572.hp2 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1090-196A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | chr20 | 58991685 | |||||||
| chr20:58991725 | T | C | 5 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(2): Show |
12 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1090-156T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | chr20 | 58991725 | |||||||
| chr20:58991777 | T | C | 2 | a0001c0004t0002g0013 a0001c0004t0002g0057 |
6 | HG00438.hp1 NA18953.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.1090-104T>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | chr20 | 58991777 | |||||||
| chr20:58991830 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1090-51A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 9/14 | chr20 | 58991830 | |||||||
| chr20:58992051 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1229+31A>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992051 | |||||||
| chr20:58992070 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1229+50C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992070 | |||||||
| chr20:58992071 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1229+51G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992071 | |||||||
| chr20:58992346 | C | G | 1 | a0001c0001t0001g0049 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1229+326C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992346 | |||||||
| chr20:58992473 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1229+453A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992473 | |||||||
| chr20:58992485 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1229+465A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992485 | |||||||
| chr20:58992488 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(127): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1229+468A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992488 | |||||||
| chr20:58992511 | C | G | 1 | a0001c0011t0001g0132 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1230-487C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992511 | |||||||
| chr20:58992675 | A | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.1230-323A>C | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992675 | |||||||
| chr20:58992675 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1230-323A>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992675 | |||||||
| chr20:58992779 | C | T | 1 | a0001c0011t0001g0132 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1230-219C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | chr20 | 58992779 | |||||||
| chr20:58992848 | C | CA | 39 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0017 others(36): Show |
60 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1230-132dupA | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 58992848 | ||||||
| chr20:58992848 | CAAAAAAA others(1): Show |
C | 3 | a0001c0001t0004g0008 a0001c0002t0004g0140 a0001c0002t0004g0147 |
9 | HG02109.hp1 HG02257.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1230-139_1230-132d others(10): Show |
NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | 58992848 | ||||||
| chr20:58993122 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0094 a0001c0001t0001g0102 others(3): Show |
8 | HG01109.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344+10C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 11/14 | chr20 | 58993122 | |||||||
| chr20:58993406 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1345-43G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 11/14 | chr20 | 58993406 | |||||||
| chr20:58993606 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0071 |
3 | HG02572.hp2 HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1441-18G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 12/14 | chr20 | 58993606 | |||||||
| chr20:58993889 | C | G | 1 | a0001c0001t0001g0034 | 2 | NA18940.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1581+125C>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 13/14 | chr20 | 58993889 | |||||||
| chr20:58994079 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0134 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1582-31G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 13/14 | chr20 | 58994079 | |||||||
| chr20:58994092 | C | T | 2 | a0001c0002t0004g0140 a0001c0002t0004g0147 |
2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1582-18C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 13/14 | chr20 | 58994092 | |||||||
| chr20:58994245 | G | A | 6 | a0001c0002t0003g0014 a0001c0002t0003g0052 a0001c0002t0003g0135 others(3): Show |
11 | HG02040.hp2 NA18612.hp2 NA18941.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1711+6G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | chr20 | 58994245 | |||||||
| chr20:58994289 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0071 a0001c0001t0004g0008 others(2): Show |
12 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1711+50C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | chr20 | 58994289 | |||||||
| chr20:58994372 | C | T | 1 | a0001c0001t0002g0040 | 2 | HG03239.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1711+133C>T | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | chr20 | 58994372 | |||||||
| chr20:58994373 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0063 others(2): Show |
9 | NA18948.hp1 NA18960.hp1 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1711+134G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | chr20 | 58994373 | |||||||
| chr20:58994519 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1712-123G>A | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | chr20 | 58994519 | |||||||
| chr20:58994562 | C | CA | 15 | a0001c0001t0001g0035 a0001c0001t0001g0039 a0001c0001t0001g0049 others(12): Show |
25 | HG00408.hp2 HG00609.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1712-62dupA | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr20 | 58994562 | ||||||
| chr20:58994562 | CA | C | 19 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0066 others(16): Show |
33 | HG00323.hp1 HG00423.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1712-62delA | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr20 | 58994562 | ||||||
| chr20:58994577 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1712-65A>G | NELFCD | ENSG00000101158.15 | transcript | ENST00000652272.2 | protein_coding | 14/14 | chr20 | 58994577 |