Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9368 |
| ensemblid | ENSG00000109062.12 |
| hgncid | 11075 |
| symbol | NHERF1 |
| name | NHERF family PDZ scaffold protein 1 |
| refseq_nuc | NM_004252.5 |
| refseq_prot | NP_004243.1 |
| ensembl_nuc | ENST00000262613.10 |
| ensembl_prot | ENSP00000262613.5 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 74748628 |
| end | 74769353 |
| strand | + |
| ver | v1.2 |
| region | chr17:74748628-74769353 |
| region5000 | chr17:74743628-74774353 |
| regionname0 | NHERF1_chr17_74748628_74769353 |
| regionname5000 | NHERF1_chr17_74743628_74774353 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 358 | 364 | 85 | 75 | 139 | 17 | 46 | 108 | NHERF1_chr17_74743628_74774353 | NHERF1 | MSADA others(353): Show |
chr17 | 74743628 | 74774353 |
| a0002 | 0/0 | 358 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | MSADA others(353): Show |
chr17 | 74743628 | 74774353 |
| a0003 | 0/0 | 358 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | MSADA others(353): Show |
chr17 | 74743628 | 74774353 |
| a0004 | 0/0 | 358 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | MSADA others(353): Show |
chr17 | 74743628 | 74774353 |
| a0005 | 0/0 | 358 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | MSADA others(353): Show |
chr17 | 74743628 | 74774353 |
| a0006 | 0/0 | 358 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | MSADA others(353): Show |
chr17 | 74743628 | 74774353 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1074 | 335 | 77 | 60 | 138 | 15 | 44 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0001c0002 | 0/1 | 1074 | 23 | 7 | 13 | 0 | 0 | 2 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0001c0003 | 0/0 | 1074 | 3 | 0 | 1 | 0 | 2 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0001c0007 | 0/0 | 1074 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0001c0008 | 0/0 | 1074 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0001c0011 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0002c0004 | 0/0 | 1074 | 2 | 2 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0003c0009 | 0/0 | 1074 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0004c0005 | 0/0 | 1074 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0005c0010 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 | ||
| a0006c0006 | 0/0 | 1074 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | ATGAG others(1069): Show |
chr17 | 74743628 | 74774353 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1993 | 162 | 37 | 21 | 67 | 10 | 26 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0002 | 0/0 | 1993 | 118 | 25 | 30 | 51 | 4 | 8 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0003 | 0/0 | 1993 | 20 | 0 | 0 | 18 | 0 | 2 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0004 | 0/0 | 1993 | 20 | 8 | 5 | 1 | 0 | 6 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0005 | 0/0 | 1993 | 6 | 5 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0007 | 0/0 | 1993 | 3 | 2 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0008 | 0/0 | 1993 | 2 | 0 | 1 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0009 | 0/0 | 1993 | 2 | 0 | 1 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0011 | 0/0 | 1993 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0001t0013 | 0/0 | 1993 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0002t0002 | 0/1 | 1993 | 21 | 6 | 12 | 0 | 0 | 2 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0002t0004 | 0/0 | 1993 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0002t0012 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0003t0006 | 0/0 | 1993 | 3 | 0 | 1 | 0 | 2 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0007t0001 | 0/0 | 1993 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0008t0002 | 0/0 | 1993 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0001c0011t0002 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0002c0004t0002 | 0/0 | 1993 | 2 | 2 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0003c0009t0002 | 0/0 | 1993 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0004c0005t0003 | 0/0 | 1993 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0005c0010t0010 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| a0006c0006t0001 | 0/0 | 1993 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | AGACG others(1988): Show |
chr17 | 74743628 | 74774353 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 46 | 3 | 8 | 22 | 5 | 8 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0003 | 1/0 | 19 | 11 | 2 | 1 | 1 | 3 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0002 | 0/0 | 23 | 0 | 8 | 10 | 1 | 4 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0008 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0012 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0009 | 0/0 | 5 | 2 | 2 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0005g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0007g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0008g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0009g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0011g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0026 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0002t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0003t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0003t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0003t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0007t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0008t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0001c0011t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0002c0004t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0003c0009t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0004c0005t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0005c0010t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| a0006c0006t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | FIN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | FIN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0013 | EUR | FIN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | CHS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00733 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00733 | hp2 | a0003 | c0009 | t0002 | g0107 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0087 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0142 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0052 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01346 | hp1 | a0001 | c0003 | t0006 | g0046 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0057 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01516 | hp2 | a0001 | c0003 | t0006 | g0143 | EUR | IBS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01517 | hp1 | a0001 | c0003 | t0006 | g0075 | EUR | IBS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01891 | hp2 | a0001 | c0002 | t0012 | g0062 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02015 | hp1 | a0004 | c0005 | t0003 | g0001 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0004 | AMR | PEL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02630 | hp1 | a0002 | c0004 | t0002 | g0047 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02630 | hp2 | a0001 | c0011 | t0002 | g0066 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0020 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0004 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0093 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0116 | SAS | PJL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03831 | hp1 | a0001 | c0001 | t0013 | g0001 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0026 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0020 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | CHB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | CHB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | YRI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | YRI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18977 | hp1 | a0001 | c0008 | t0002 | g0178 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19043 | hp1 | a0002 | c0004 | t0002 | g0047 | AFR | LWK | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0171 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | TSI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20805 | hp1 | a0006 | c0006 | t0001 | g0001 | EUR | TSI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | GIH | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02559 | hp1 | a0005 | c0010 | t0010 | g0078 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | USA | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | USA | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | LWK | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0026 | REF | REF | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0003 | REF | REF | NHERF1_chr17_74743628_74774353 | NHERF1 | chr17 | 74743628 | 74774353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74748976 | C | G | 1 | a0002 | 2 | HG02630.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.130C>G | p.Pro44Ala | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 349/1993 | 130/1077 | 44/358 | chr17 | 74748976 | |||
| chr17:74749000 | G | A | 1 | a0004 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.154G>A | p.Gly52Arg | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 373/1993 | 154/1077 | 52/358 | chr17 | 74749000 | |||
| chr17:74749049 | A | C | 1 | a0005 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.203A>C | p.Glu68Ala | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 422/1993 | 203/1077 | 68/358 | chr17 | 74749049 | |||
| chr17:74749174 | C | G | 1 | a0003 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.328C>G | p.Leu110Val | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 547/1993 | 328/1077 | 110/358 | chr17 | 74749174 | |||
| chr17:74762028 | G | A | 1 | a0006 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.458G>A | p.Arg153Gln | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/6 | 677/1993 | 458/1077 | 153/358 | chr17 | 74762028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74748978 | C | T | 1 | a0001c0011 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.132C>T | p.Pro44Pro | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 351/1993 | 132/1077 | 44/358 | chr17 | 74748978 | |||
| chr17:74762071 | C | T | 3 | a0001c0002 a0001c0011 a0005c0010 |
25 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(22): Show |
synonymous_variant | LOW | c.501C>T | p.Asn167Asn | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/6 | 720/1993 | 501/1077 | 167/358 | chr17 | 74762071 | |||
| chr17:74763390 | G | A | 1 | a0001c0003 | 3 | HG01346.hp1 HG01516.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.627G>A | p.Gly209Gly | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/6 | 846/1993 | 627/1077 | 209/358 | chr17 | 74763390 | |||
| chr17:74763429 | C | T | 1 | a0001c0008 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.666C>T | p.Gly222Gly | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/6 | 885/1993 | 666/1077 | 222/358 | chr17 | 74763429 | |||
| chr17:74763447 | G | A | 1 | a0001c0007 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.684G>A | p.Leu228Leu | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/6 | 903/1993 | 684/1077 | 228/358 | chr17 | 74763447 | |||
| chr17:74763448 | C | T | 1 | a0001c0007 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.685C>T | p.Leu229Leu | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/6 | 904/1993 | 685/1077 | 229/358 | chr17 | 74763448 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74748659 | G | C | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0011 others(9): Show |
171 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
5_prime_UTR_variant | MODIFIER | c.-188G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 188 | chr17 | 74748659 | ||||||
| chr17:74748666 | C | T | 1 | a0001c0002t0012 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-181C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 181 | chr17 | 74748666 | ||||||
| chr17:74748772 | G | A | 1 | a0001c0003t0006 | 3 | HG01346.hp1 HG01516.hp2 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-75G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 75 | chr17 | 74748772 | ||||||
| chr17:74748804 | C | A | 1 | a0001c0001t0008 | 2 | HG00741.hp1 HG03669.hp2 |
5_prime_UTR_variant | MODIFIER | c.-43C>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 43 | chr17 | 74748804 | ||||||
| chr17:74748837 | G | T | 1 | a0001c0002t0012 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/6 | 10 | chr17 | 74748837 | ||||||
| chr17:74768822 | A | G | 1 | a0001c0001t0011 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*166A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 6/6 | 166 | chr17 | 74768822 | ||||||
| chr17:74768874 | T | A | 1 | a0001c0001t0007 | 3 | HG01099.hp2 HG03041.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*218T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 6/6 | 218 | chr17 | 74768874 | ||||||
| chr17:74768902 | G | T | 1 | a0001c0001t0005 | 6 | HG00733.hp1 HG01884.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*246G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 6/6 | 246 | chr17 | 74768902 | ||||||
| chr17:74768925 | T | G | 1 | a0001c0001t0013 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*269T>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 6/6 | 269 | chr17 | 74768925 | ||||||
| chr17:74768928 | G | T | 1 | a0005c0010t0010 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 6/6 | 272 | chr17 | 74768928 | ||||||
| chr17:74769076 | C | T | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(12): Show |
183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*420C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 6/6 | 420 | chr17 | 74769076 | ||||||
| chr17:74769262 | C | T | 1 | a0001c0001t0009 | 2 | HG00323.hp1 HG02300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*606C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 6/6 | 606 | chr17 | 74769262 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:74749294 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00280.hp2 | splice_region_variant&intron_variant | LOW | c.441+7G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74749294 | |||||||
| chr17:74749301 | A | G | 22 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0024 others(19): Show |
37 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.441+14A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74749301 | |||||||
| chr17:74749697 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.441+410C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74749697 | |||||||
| chr17:74749988 | A | C | 7 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(4): Show |
7 | HG02451.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+701A>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74749988 | |||||||
| chr17:74750039 | G | A | 1 | a0001c0001t0002g0050 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.441+752G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74750039 | |||||||
| chr17:74750567 | G | T | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441+1280G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74750567 | |||||||
| chr17:74750617 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.441+1330C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74750617 | |||||||
| chr17:74750711 | G | A | 13 | a0001c0001t0001g0054 a0001c0002t0002g0005 a0001c0002t0002g0026 others(10): Show |
20 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.441+1424G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74750711 | |||||||
| chr17:74750722 | C | CT | 8 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(5): Show |
8 | HG02071.hp2 HG02074.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+1453dupT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74750722 | ||||||
| chr17:74750722 | CT | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0063 a0001c0001t0002g0008 others(20): Show |
40 | HG00639.hp2 HG00738.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.441+1453delT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74750722 | ||||||
| chr17:74750862 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0157 |
3 | NA18954.hp2 NA18963.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.441+1575C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74750862 | |||||||
| chr17:74750906 | G | A | 1 | a0001c0001t0002g0027 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.441+1619G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74750906 | |||||||
| chr17:74751024 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0156 |
2 | NA18942.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.441+1737C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751024 | |||||||
| chr17:74751092 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.441+1805G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751092 | |||||||
| chr17:74751472 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.441+2185G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751472 | |||||||
| chr17:74751484 | G | A | 1 | a0001c0011t0002g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+2197G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751484 | |||||||
| chr17:74751568 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441+2281G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751568 | |||||||
| chr17:74751737 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.441+2450C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751737 | |||||||
| chr17:74751808 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.441+2521G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751808 | |||||||
| chr17:74751872 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.441+2585A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751872 | |||||||
| chr17:74751966 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.441+2679C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751966 | |||||||
| chr17:74751968 | G | A | 1 | a0001c0007t0001g0052 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.441+2681G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74751968 | |||||||
| chr17:74752161 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.441+2874G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74752161 | |||||||
| chr17:74752189 | C | G | 1 | a0001c0002t0002g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.441+2902C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74752189 | |||||||
| chr17:74752282 | CT | C | 9 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01168.hp1 HG01517.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.441+3007delT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74752282 | ||||||
| chr17:74752397 | G | A | 21 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0024 others(18): Show |
36 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.441+3110G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74752397 | |||||||
| chr17:74752555 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.441+3268G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74752555 | |||||||
| chr17:74752752 | C | T | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441+3465C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74752752 | |||||||
| chr17:74752810 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.441+3523T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74752810 | |||||||
| chr17:74753069 | C | G | 3 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0060 |
3 | HG02486.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.441+3782C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74753069 | |||||||
| chr17:74753131 | C | T | 1 | a0001c0001t0002g0027 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.441+3844C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74753131 | |||||||
| chr17:74753242 | G | A | 3 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0002c0004t0002g0047 |
4 | HG02630.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+3955G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74753242 | |||||||
| chr17:74753252 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.441+3965T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74753252 | |||||||
| chr17:74753493 | T | C | 4 | a0001c0002t0002g0028 a0001c0002t0002g0079 a0001c0002t0012g0062 others(1): Show |
5 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+4206T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74753493 | |||||||
| chr17:74754165 | A | G | 2 | a0001c0002t0002g0028 a0001c0002t0002g0079 |
3 | HG02258.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.441+4878A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754165 | |||||||
| chr17:74754188 | A | C | 1 | a0001c0011t0002g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+4901A>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754188 | |||||||
| chr17:74754316 | A | C | 4 | a0001c0001t0002g0046 a0001c0003t0006g0046 a0001c0003t0006g0075 others(1): Show |
4 | HG01070.hp1 HG01346.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+5029A>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754316 | |||||||
| chr17:74754371 | A | ATTTC | 2 | a0001c0001t0002g0168 a0002c0004t0002g0047 |
3 | HG02630.hp1 HG02896.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.441+5112_441+5115d others(6): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74754371 | ||||||
| chr17:74754371 | ATTTC | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(61): Show |
136 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.441+5112_441+5115d others(6): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74754371 | ||||||
| chr17:74754396 | TTTC | T | 34 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0074 others(31): Show |
50 | HG00738.hp2 HG01099.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.441+5112_441+5114d others(5): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74754396 | ||||||
| chr17:74754399 | C | CT | 6 | a0001c0001t0002g0011 a0001c0001t0002g0114 a0001c0001t0002g0115 others(3): Show |
10 | HG00639.hp2 HG01516.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+5132dupT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74754399 | ||||||
| chr17:74754399 | CT | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0027 a0001c0001t0002g0068 others(6): Show |
15 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.441+5132delT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74754399 | ||||||
| chr17:74754400 | T | TTTC | 8 | a0001c0001t0002g0006 a0001c0001t0002g0049 a0001c0001t0002g0081 others(5): Show |
13 | HG00280.hp2 HG00544.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.441+5115_441+5116i others(5): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74754400 | ||||||
| chr17:74754472 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.441+5185G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754472 | |||||||
| chr17:74754633 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.441+5346A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754633 | |||||||
| chr17:74754634 | A | G | 20 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0002g0008 others(17): Show |
36 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.441+5347A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754634 | |||||||
| chr17:74754702 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0001g0113 |
4 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+5415C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754702 | |||||||
| chr17:74754731 | G | A | 1 | a0001c0011t0002g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.441+5444G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754731 | |||||||
| chr17:74754783 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.441+5496T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754783 | |||||||
| chr17:74754862 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.441+5575A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754862 | |||||||
| chr17:74754896 | T | A | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.441+5609T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74754896 | |||||||
| chr17:74755042 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.441+5755G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74755042 | |||||||
| chr17:74755055 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.441+5768T>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74755055 | |||||||
| chr17:74755235 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.441+5948C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74755235 | |||||||
| chr17:74755524 | C | T | 25 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0002g0008 others(22): Show |
43 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.441+6237C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74755524 | |||||||
| chr17:74755874 | G | C | 1 | a0001c0001t0002g0089 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.442-6138G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74755874 | |||||||
| chr17:74755916 | C | T | 1 | a0001c0001t0004g0116 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.442-6096C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74755916 | |||||||
| chr17:74755956 | G | GT | 10 | a0001c0001t0001g0152 a0001c0001t0001g0157 a0001c0001t0002g0110 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.442-6042dupT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74755956 | ||||||
| chr17:74755957 | T | G | 1 | a0001c0001t0005g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.442-6055T>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74755957 | |||||||
| chr17:74756273 | C | CT | 23 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0141 others(20): Show |
35 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.442-5716dupT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74756273 | ||||||
| chr17:74756273 | C | CTT | 37 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0002g0004 others(34): Show |
62 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.442-5717_442-5716d others(4): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74756273 | ||||||
| chr17:74756273 | C | CTTT | 36 | a0001c0001t0001g0154 a0001c0001t0002g0002 a0001c0001t0002g0021 others(33): Show |
66 | HG00099.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.442-5718_442-5716d others(5): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74756273 | ||||||
| chr17:74756273 | C | CTTTT | 7 | a0001c0001t0002g0027 a0001c0001t0002g0106 a0001c0001t0002g0108 others(4): Show |
8 | HG00438.hp2 HG00639.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.442-5719_442-5716d others(6): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74756273 | ||||||
| chr17:74756273 | CT | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0113 others(6): Show |
12 | HG01074.hp2 HG02293.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-5716delT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74756273 | ||||||
| chr17:74756302 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.442-5710G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756302 | |||||||
| chr17:74756315 | A | G | 104 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0054 others(101): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.442-5697A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756315 | |||||||
| chr17:74756348 | G | A | 2 | a0001c0001t0002g0021 a0001c0001t0002g0111 |
4 | HG00609.hp2 NA19068.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-5664G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756348 | |||||||
| chr17:74756364 | C | T | 2 | a0001c0001t0002g0170 a0001c0001t0004g0045 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.442-5648C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756364 | |||||||
| chr17:74756421 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-5591G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756421 | |||||||
| chr17:74756436 | A | C | 3 | a0001c0002t0002g0028 a0001c0002t0002g0079 a0005c0010t0010g0078 |
4 | HG02258.hp1 HG02559.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-5576A>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756436 | |||||||
| chr17:74756446 | T | C | 12 | a0001c0002t0002g0005 a0001c0002t0002g0026 a0001c0002t0002g0051 others(9): Show |
19 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-5566T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756446 | |||||||
| chr17:74756507 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0138 a0001c0001t0003g0092 |
4 | HG01168.hp2 HG02683.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-5505G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756507 | |||||||
| chr17:74756515 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-5497G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756515 | |||||||
| chr17:74756796 | G | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0120 a0001c0001t0003g0016 others(2): Show |
7 | HG00621.hp1 NA18943.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-5216G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756796 | |||||||
| chr17:74756820 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-5192A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74756820 | |||||||
| chr17:74757125 | G | A | 5 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(2): Show |
7 | HG02622.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-4887G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757125 | |||||||
| chr17:74757180 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442-4832G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757180 | |||||||
| chr17:74757210 | G | T | 1 | a0005c0010t0010g0078 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.442-4802G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757210 | |||||||
| chr17:74757261 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.442-4751C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757261 | |||||||
| chr17:74757263 | C | T | 1 | a0001c0011t0002g0066 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.442-4749C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757263 | |||||||
| chr17:74757583 | C | T | 4 | a0001c0002t0002g0028 a0001c0002t0002g0079 a0001c0002t0012g0062 others(1): Show |
5 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-4429C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757583 | |||||||
| chr17:74757785 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.442-4227C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757785 | |||||||
| chr17:74757788 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0119 others(4): Show |
12 | HG02040.hp1 HG02074.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-4224C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74757788 | |||||||
| chr17:74758011 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-4001T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758011 | |||||||
| chr17:74758150 | C | T | 1 | a0001c0001t0002g0037 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.442-3862C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758150 | |||||||
| chr17:74758216 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.442-3796A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758216 | |||||||
| chr17:74758372 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.442-3640G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758372 | |||||||
| chr17:74758690 | T | C | 71 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0122 others(68): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.442-3322T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758690 | |||||||
| chr17:74758724 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG02965.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.442-3288G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758724 | |||||||
| chr17:74758728 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0145 |
4 | HG00642.hp2 HG00735.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-3284C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758728 | |||||||
| chr17:74758785 | G | A | 71 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0122 others(68): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.442-3227G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758785 | |||||||
| chr17:74758843 | C | G | 1 | a0001c0001t0002g0027 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.442-3169C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74758843 | |||||||
| chr17:74759292 | G | C | 1 | a0001c0001t0004g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.442-2720G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74759292 | |||||||
| chr17:74759624 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.442-2388G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74759624 | |||||||
| chr17:74759717 | T | C | 4 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(1): Show |
5 | HG00639.hp1 HG01074.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-2295T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74759717 | |||||||
| chr17:74759781 | T | C | 4 | a0001c0002t0002g0028 a0001c0002t0002g0079 a0001c0002t0012g0062 others(1): Show |
5 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-2231T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74759781 | |||||||
| chr17:74759818 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.442-2194T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74759818 | |||||||
| chr17:74759956 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.442-2056C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74759956 | |||||||
| chr17:74760001 | C | T | 1 | a0001c0001t0002g0103 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.442-2011C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74760001 | |||||||
| chr17:74760204 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-1808C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74760204 | |||||||
| chr17:74760222 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.442-1790G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74760222 | |||||||
| chr17:74760222 | G | T | 1 | a0001c0001t0002g0027 | 2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.442-1790G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74760222 | |||||||
| chr17:74760537 | TC | T | 16 | a0001c0002t0002g0005 a0001c0002t0002g0026 a0001c0002t0002g0028 others(13): Show |
24 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.442-1473delC | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74760537 | ||||||
| chr17:74760979 | C | A | 1 | a0001c0001t0003g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.442-1033C>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74760979 | |||||||
| chr17:74760988 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.442-1024G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74760988 | |||||||
| chr17:74761013 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0002g0082 |
2 | HG01256.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.442-999G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74761013 | |||||||
| chr17:74761038 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-974T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74761038 | |||||||
| chr17:74761247 | TC | T | 3 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0002c0004t0002g0047 |
4 | HG02630.hp1 HG02896.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-761delC | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | 74761247 | ||||||
| chr17:74761372 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.442-640C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74761372 | |||||||
| chr17:74761435 | A | G | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.442-577A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74761435 | |||||||
| chr17:74761462 | T | A | 12 | a0001c0002t0002g0005 a0001c0002t0002g0026 a0001c0002t0002g0051 others(9): Show |
19 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.442-550T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 1/5 | chr17 | 74761462 | |||||||
| chr17:74762214 | C | T | 1 | a0001c0001t0003g0033 | 2 | HG02027.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.603+41C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762214 | |||||||
| chr17:74762348 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.603+175A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762348 | |||||||
| chr17:74762401 | G | A | 4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(1): Show |
5 | HG02622.hp1 HG02630.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+228G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762401 | |||||||
| chr17:74762451 | C | T | 2 | a0001c0001t0002g0170 a0001c0001t0004g0045 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.603+278C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762451 | |||||||
| chr17:74762506 | G | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0077 a0001c0001t0001g0119 others(1): Show |
9 | NA18612.hp1 NA18954.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.603+333G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762506 | |||||||
| chr17:74762560 | G | GT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0073 others(5): Show |
11 | HG00280.hp1 HG00621.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.603+400dupT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr17 | 74762560 | ||||||
| chr17:74762560 | G | GTT | 92 | a0001c0001t0001g0018 a0001c0001t0001g0076 a0001c0001t0001g0122 others(89): Show |
155 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.603+399_603+400dup others(2): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr17 | 74762560 | ||||||
| chr17:74762560 | G | GTTT | 5 | a0001c0001t0002g0011 a0001c0001t0002g0024 a0001c0001t0002g0174 others(2): Show |
11 | HG00639.hp2 HG01106.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.603+398_603+400dup others(3): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr17 | 74762560 | ||||||
| chr17:74762574 | A | T | 13 | a0001c0001t0002g0183 a0001c0002t0002g0005 a0001c0002t0002g0026 others(10): Show |
20 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.603+401A>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762574 | |||||||
| chr17:74762653 | G | A | 1 | a0001c0001t0003g0130 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.603+480G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762653 | |||||||
| chr17:74762692 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.603+519G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762692 | |||||||
| chr17:74762707 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.603+534A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762707 | |||||||
| chr17:74762708 | C | T | 1 | a0001c0001t0002g0036 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.603+535C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762708 | |||||||
| chr17:74762938 | G | C | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.604-429G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74762938 | |||||||
| chr17:74763339 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.604-28G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 2/5 | chr17 | 74763339 | |||||||
| chr17:74763712 | G | A | 1 | a0001c0001t0002g0037 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.757+192G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74763712 | |||||||
| chr17:74763715 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.757+195G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74763715 | |||||||
| chr17:74763737 | T | C | 3 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 |
4 | HG00639.hp1 HG01074.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.757+217T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74763737 | |||||||
| chr17:74763879 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.757+359G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74763879 | |||||||
| chr17:74763990 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.757+470G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74763990 | |||||||
| chr17:74763991 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.757+471G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74763991 | |||||||
| chr17:74764097 | A | C | 2 | a0001c0001t0005g0010 a0001c0001t0005g0090 |
6 | HG00733.hp1 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.757+577A>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74764097 | |||||||
| chr17:74764168 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.757+648C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74764168 | |||||||
| chr17:74764629 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.757+1109C>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74764629 | |||||||
| chr17:74764681 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.757+1161G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74764681 | |||||||
| chr17:74764682 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.757+1162C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74764682 | |||||||
| chr17:74764953 | A | G | 1 | a0001c0001t0003g0044 | 2 | HG02135.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.757+1433A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74764953 | |||||||
| chr17:74765026 | C | A | 1 | a0001c0001t0001g0039 | 2 | NA19074.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.757+1506C>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765026 | |||||||
| chr17:74765056 | C | G | 1 | a0003c0009t0002g0107 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.757+1536C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765056 | |||||||
| chr17:74765103 | T | C | 60 | a0001c0001t0001g0122 a0001c0001t0001g0126 a0001c0001t0002g0002 others(57): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.757+1583T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765103 | |||||||
| chr17:74765171 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0004g0045 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.757+1651G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765171 | |||||||
| chr17:74765197 | T | G | 1 | a0001c0001t0002g0034 | 2 | HG02602.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.757+1677T>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765197 | |||||||
| chr17:74765262 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0166 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.758-1674T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765262 | |||||||
| chr17:74765501 | G | A | 2 | a0001c0001t0002g0170 a0001c0001t0004g0045 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.758-1435G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765501 | |||||||
| chr17:74765510 | G | A | 13 | a0001c0001t0004g0031 a0001c0002t0002g0005 a0001c0002t0002g0026 others(10): Show |
21 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.758-1426G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765510 | |||||||
| chr17:74765549 | C | T | 4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0004g0164 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.758-1387C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765549 | |||||||
| chr17:74765557 | C | CT | 13 | a0001c0001t0001g0043 a0001c0001t0001g0153 a0001c0001t0001g0157 others(10): Show |
18 | HG00733.hp1 HG01175.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.758-1364dupT | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 74765557 | ||||||
| chr17:74765557 | C | CTT | 6 | a0001c0001t0002g0027 a0001c0001t0002g0096 a0001c0001t0002g0168 others(3): Show |
8 | HG00639.hp1 HG01074.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.758-1365_758-1364d others(4): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 74765557 | ||||||
| chr17:74765569 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.758-1367T>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765569 | |||||||
| chr17:74765659 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.758-1277C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765659 | |||||||
| chr17:74765684 | T | C | 4 | a0001c0002t0002g0028 a0001c0002t0002g0079 a0001c0002t0012g0062 others(1): Show |
5 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.758-1252T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765684 | |||||||
| chr17:74765705 | C | T | 7 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(4): Show |
9 | HG00639.hp1 HG01074.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.758-1231C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765705 | |||||||
| chr17:74765713 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.758-1223G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765713 | |||||||
| chr17:74765749 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.758-1187G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765749 | |||||||
| chr17:74765924 | T | C | 7 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(4): Show |
9 | HG00639.hp1 HG01074.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.758-1012T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74765924 | |||||||
| chr17:74766077 | C | G | 7 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(4): Show |
9 | HG00639.hp1 HG01074.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.758-859C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766077 | |||||||
| chr17:74766077 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.758-859C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766077 | |||||||
| chr17:74766146 | C | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0096 |
2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.758-790C>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766146 | |||||||
| chr17:74766183 | G | T | 7 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(4): Show |
9 | HG00639.hp1 HG01074.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.758-753G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766183 | |||||||
| chr17:74766187 | T | G | 4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0004g0164 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.758-749T>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766187 | |||||||
| chr17:74766187 | T | TTTTTG | 7 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0002g0095 others(4): Show |
11 | HG00639.hp1 HG01074.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.758-723_758-719dup others(5): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr17 | 74766187 | ||||||
| chr17:74766238 | C | T | 1 | a0001c0001t0004g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.758-698C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766238 | |||||||
| chr17:74766258 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.758-678G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766258 | |||||||
| chr17:74766353 | T | C | 4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0004g0164 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.758-583T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766353 | |||||||
| chr17:74766399 | C | T | 1 | a0001c0001t0002g0035 | 2 | HG02129.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.758-537C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766399 | |||||||
| chr17:74766400 | A | G | 1 | a0001c0002t0002g0060 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.758-536A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766400 | |||||||
| chr17:74766431 | A | G | 13 | a0001c0001t0004g0031 a0001c0002t0002g0005 a0001c0002t0002g0026 others(10): Show |
21 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.758-505A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766431 | |||||||
| chr17:74766464 | A | G | 2 | a0001c0001t0005g0010 a0001c0001t0005g0090 |
6 | HG00733.hp1 HG01884.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.758-472A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766464 | |||||||
| chr17:74766488 | C | T | 1 | a0001c0001t0001g0041 | 2 | NA18951.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.758-448C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766488 | |||||||
| chr17:74766507 | C | A | 101 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(98): Show |
179 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.758-429C>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766507 | |||||||
| chr17:74766516 | G | T | 1 | a0001c0008t0002g0178 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.758-420G>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766516 | |||||||
| chr17:74766561 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-375G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766561 | |||||||
| chr17:74766564 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-372A>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766564 | |||||||
| chr17:74766565 | G | C | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-371G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766565 | |||||||
| chr17:74766566 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-370G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766566 | |||||||
| chr17:74766569 | G | A | 1 | a0001c0001t0004g0131 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.758-367G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766569 | |||||||
| chr17:74766574 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-362T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766574 | |||||||
| chr17:74766600 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-336C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766600 | |||||||
| chr17:74766603 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-333T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766603 | |||||||
| chr17:74766605 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-331T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766605 | |||||||
| chr17:74766614 | A | G | 18 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0024 others(15): Show |
32 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.758-322A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766614 | |||||||
| chr17:74766616 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-320T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766616 | |||||||
| chr17:74766619 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-317T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766619 | |||||||
| chr17:74766620 | C | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-316C>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766620 | |||||||
| chr17:74766622 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-314A>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766622 | |||||||
| chr17:74766625 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-311T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766625 | |||||||
| chr17:74766626 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-310G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766626 | |||||||
| chr17:74766628 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-308C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766628 | |||||||
| chr17:74766635 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-301A>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766635 | |||||||
| chr17:74766642 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-294A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766642 | |||||||
| chr17:74766643 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0153 |
3 | NA18943.hp1 NA18961.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.758-293C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766643 | |||||||
| chr17:74766657 | T | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.758-279T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766657 | |||||||
| chr17:74766744 | C | T | 17 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0013 others(14): Show |
28 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.758-192C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766744 | |||||||
| chr17:74766762 | A | T | 58 | a0001c0001t0001g0128 a0001c0001t0002g0002 a0001c0001t0002g0004 others(55): Show |
106 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.758-174A>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766762 | |||||||
| chr17:74766763 | T | A | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.758-173T>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766763 | |||||||
| chr17:74766771 | A | T | 2 | a0001c0001t0002g0170 a0001c0001t0004g0045 |
3 | HG02622.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.758-165A>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 3/5 | chr17 | 74766771 | |||||||
| chr17:74767022 | C | T | 1 | a0001c0002t0012g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.798+46C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767022 | |||||||
| chr17:74767180 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0134 |
3 | HG03491.hp1 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.798+204C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767180 | |||||||
| chr17:74767274 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.798+298A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767274 | |||||||
| chr17:74767313 | CCT | C | 18 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0024 others(15): Show |
32 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.798+338_798+339del others(2): Show |
NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767313 | |||||||
| chr17:74767324 | T | C | 5 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(2): Show |
7 | HG00639.hp1 HG01074.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.798+348T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767324 | |||||||
| chr17:74767404 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.798+428T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767404 | |||||||
| chr17:74767454 | G | C | 1 | a0001c0001t0002g0183 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.798+478G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767454 | |||||||
| chr17:74767483 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.798+507C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767483 | |||||||
| chr17:74767487 | G | A | 2 | a0001c0001t0002g0048 a0001c0001t0011g0171 |
3 | NA18983.hp1 NA19002.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.798+511G>A | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767487 | |||||||
| chr17:74767577 | G | C | 4 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0004g0164 others(1): Show |
5 | HG02630.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-570G>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767577 | |||||||
| chr17:74767611 | C | G | 5 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(2): Show |
7 | HG00639.hp1 HG01074.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-536C>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767611 | |||||||
| chr17:74767659 | C | T | 55 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0006 others(52): Show |
103 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.799-488C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767659 | |||||||
| chr17:74767776 | C | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0095 a0001c0001t0002g0096 others(2): Show |
7 | HG00639.hp1 HG01074.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.799-371C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767776 | |||||||
| chr17:74767779 | C | T | 1 | a0001c0001t0003g0044 | 2 | HG02135.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.799-368C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767779 | |||||||
| chr17:74767970 | A | G | 6 | a0001c0001t0002g0011 a0001c0001t0002g0024 a0001c0001t0002g0173 others(3): Show |
12 | HG00639.hp2 HG01106.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.799-177A>G | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 4/5 | chr17 | 74767970 | |||||||
| chr17:74768249 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.888+13T>C | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 5/5 | chr17 | 74768249 | |||||||
| chr17:74768437 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.889-31C>T | NHERF1 | ENSG00000109062.12 | transcript | ENST00000262613.10 | protein_coding | 5/5 | chr17 | 74768437 |