Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25920 |
| ensemblid | ENSG00000188986.9 |
| hgncid | 24324 |
| symbol | NELFB |
| name | negative elongation factor complex member B |
| refseq_nuc | NM_015456.5 |
| refseq_prot | NP_056271.3 |
| ensembl_nuc | ENST00000343053.6 |
| ensembl_prot | ENSP00000339495.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 137255327 |
| end | 137273542 |
| strand | + |
| ver | v1.2 |
| region | chr9:137255327-137273542 |
| region5000 | chr9:137250327-137278542 |
| regionname0 | NELFB_chr9_137255327_137273542 |
| regionname5000 | NELFB_chr9_137250327_137278542 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1884 | 196 | 50 | 35 | 76 | 8 | 26 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0002 | 1/0 | 1884 | 141 | 40 | 23 | 63 | 4 | 10 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0003 | 0/0 | 1884 | 7 | 0 | 7 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0004 | 0/0 | 1884 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0005 | 0/0 | 1884 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0006 | 0/0 | 1884 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0007 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0008 | 0/0 | 1884 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0009 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0010 | 0/0 | 1884 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0011 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0012 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0013 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0014 | 0/0 | 1884 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0015 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0016 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0017 | 0/0 | 1884 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0018 | 0/0 | 1884 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 | ||
| a0001c0019 | 0/0 | 1884 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | CTGGC others(1879): Show |
chr9 | 137250327 | 137278542 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2540 | 190 | 47 | 34 | 76 | 8 | 24 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0001t0009 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0001t0010 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0001t0013 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0001t0014 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0001t0015 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0001t0016 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0002t0002 | 1/0 | 2540 | 128 | 30 | 21 | 62 | 4 | 10 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0002t0003 | 0/0 | 2540 | 5 | 4 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0002t0004 | 0/0 | 2540 | 2 | 1 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0002t0006 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0002t0007 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0002t0011 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0002t0012 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0003t0001 | 0/0 | 2540 | 7 | 0 | 7 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0004t0001 | 0/0 | 2540 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0005t0001 | 0/0 | 2540 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0006t0005 | 0/0 | 2540 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0007t0002 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0008t0001 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0009t0001 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0010t0001 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0011t0002 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0012t0002 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0013t0001 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0014t0002 | 0/0 | 2540 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0015t0002 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0016t0001 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0017t0001 | 0/0 | 2540 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0018t0001 | 0/0 | 2540 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| a0001c0019t0008 | 0/0 | 2540 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | GGCTG others(2535): Show |
chr9 | 137250327 | 137278542 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 31 | 7 | 7 | 13 | 1 | 3 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0003 | 0/0 | 11 | 7 | 2 | 1 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0004 | 0/0 | 8 | 2 | 1 | 5 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0001t0016g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0002 | 0/0 | 13 | 1 | 6 | 6 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0010 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0007g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0002t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0003t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0004t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0005t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0006t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0006t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0007t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0008t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0009t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0011t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0012t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0013t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0014t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0015t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0016t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0017t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0018t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| a0001c0019t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00741 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01081 | hp1 | a0001 | c0009 | t0001 | g0009 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0081 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0203 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01168 | hp2 | a0001 | c0001 | t0015 | g0001 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0168 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01361 | hp1 | a0001 | c0017 | t0001 | g0035 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0199 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0018 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01516 | hp2 | a0001 | c0008 | t0001 | g0146 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0018 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01884 | hp2 | a0001 | c0002 | t0011 | g0213 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0202 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01928 | hp2 | a0001 | c0003 | t0001 | g0186 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01975 | hp2 | a0001 | c0002 | t0003 | g0224 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0012 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02004 | hp1 | a0001 | c0002 | t0002 | g0038 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02015 | hp2 | a0001 | c0016 | t0001 | g0001 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02027 | hp1 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02040 | hp2 | a0001 | c0011 | t0002 | g0002 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0024 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0053 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0089 | EAS | KHV | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0221 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0222 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02148 | hp2 | a0001 | c0003 | t0001 | g0185 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02155 | hp1 | a0001 | c0005 | t0001 | g0040 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0060 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02300 | hp1 | a0001 | c0015 | t0002 | g0002 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02300 | hp2 | a0001 | c0003 | t0001 | g0190 | AMR | PEL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02451 | hp1 | a0001 | c0002 | t0007 | g0037 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0128 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02698 | hp2 | a0001 | c0014 | t0002 | g0026 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02735 | hp1 | a0001 | c0001 | t0009 | g0228 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02818 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0116 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0196 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02922 | hp2 | a0001 | c0002 | t0006 | g0208 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03041 | hp2 | a0001 | c0002 | t0003 | g0011 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03130 | hp2 | a0001 | c0002 | t0006 | g0039 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03139 | hp1 | a0001 | c0006 | t0005 | g0077 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03225 | hp1 | a0001 | c0002 | t0007 | g0037 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03239 | hp2 | a0001 | c0010 | t0001 | g0001 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03491 | hp1 | a0001 | c0001 | t0016 | g0112 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03516 | hp1 | a0001 | c0006 | t0005 | g0078 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0215 | AFR | ESN | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0205 | AFR | GWD | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0065 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0022 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0066 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0092 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0232 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0067 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18941 | hp2 | a0001 | c0007 | t0002 | g0057 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18942 | hp1 | a0001 | c0019 | t0008 | g0100 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18953 | hp2 | a0001 | c0002 | t0012 | g0068 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18954 | hp2 | a0001 | c0012 | t0002 | g0074 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0217 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19080 | hp2 | a0001 | c0005 | t0001 | g0040 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19240 | hp1 | a0001 | c0018 | t0001 | g0086 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0026 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20752 | hp2 | a0001 | c0004 | t0001 | g0005 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0059 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0214 | AFR | ACB | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0080 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0087 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0206 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20300 | hp1 | a0001 | c0002 | t0003 | g0011 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| NA21309 | hp2 | a0001 | c0013 | t0001 | g0161 | AFR | LWK | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0179 | REF | REF | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0010 | REF | REF | NELFB_chr9_137250327_137278542 | NELFB | chr9 | 137250327 | 137278542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137255457 | G | A | 1 | a0001 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.92G>A | p.Gly31Glu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/13 | 131/2540 | 92/1887 | 31/628 | chr9 | 137255457 | |||
| chr9:137266340 | G | A | 1 | a0001 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1153G>A | p.Asp385Asn | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/13 | 1192/2540 | 1153/1887 | 385/628 | chr9 | 137266340 | |||
| chr9:137267074 | A | G | 1 | a0001 | 2 | HG02155.hp1 NA19080.hp2 |
missense_variant | MODERATE | c.1370A>G | p.Glu457Gly | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/13 | 1409/2540 | 1370/1887 | 457/628 | chr9 | 137267074 | |||
| chr9:137267319 | G | T | 1 | a0001 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.1462G>T | p.Ala488Ser | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/13 | 1501/2540 | 1462/1887 | 488/628 | chr9 | 137267319 | |||
| chr9:137272530 | C | T | 1 | a0001 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1655C>T | p.Ala552Val | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 12/13 | 1694/2540 | 1655/1887 | 552/628 | chr9 | 137272530 | |||
| chr9:137272851 | C | A | 1 | a0001 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1810C>A | p.Pro604Thr | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 1849/2540 | 1810/1887 | 604/628 | chr9 | 137272851 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137255587 | G | T | 1 | a0001c0006 | 2 | HG03139.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.222G>T | p.Pro74Pro | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/13 | 261/2540 | 222/1887 | 74/628 | chr9 | 137255587 | |||
| chr9:137255961 | C | T | 1 | a0001c0004 | 3 | HG00741.hp1 HG01952.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.301C>T | p.Leu101Leu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/13 | 340/2540 | 301/1887 | 101/628 | chr9 | 137255961 | |||
| chr9:137256024 | C | T | 1 | a0001c0019 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.364C>T | p.Leu122Leu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/13 | 403/2540 | 364/1887 | 122/628 | chr9 | 137256024 | |||
| chr9:137256386 | C | G | 1 | a0001c0018 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.468C>G | p.Ser156Ser | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/13 | 507/2540 | 468/1887 | 156/628 | chr9 | 137256386 | |||
| chr9:137256928 | C | T | 1 | a0001c0017 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.615C>T | p.Phe205Phe | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/13 | 654/2540 | 615/1887 | 205/628 | chr9 | 137256928 | |||
| chr9:137263126 | G | A | 1 | a0001c0008 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.831G>A | p.Thr277Thr | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/13 | 870/2540 | 831/1887 | 277/628 | chr9 | 137263126 | |||
| chr9:137263127 | C | A | 1 | a0001c0008 | 1 | HG01516.hp2 | synonymous_variant | LOW | c.832C>A | p.Arg278Arg | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/13 | 871/2540 | 832/1887 | 278/628 | chr9 | 137263127 | |||
| chr9:137265946 | G | T | 1 | a0001c0016 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.1110G>T | p.Leu370Leu | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/13 | 1149/2540 | 1110/1887 | 370/628 | chr9 | 137265946 | |||
| chr9:137272145 | G | A | 1 | a0001c0003 | 7 | HG00738.hp2 HG01346.hp2 HG01928.hp2 others(4): Show |
synonymous_variant | LOW | c.1554G>A | p.Ala518Ala | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 11/13 | 1593/2540 | 1554/1887 | 518/628 | chr9 | 137272145 | |||
| chr9:137272193 | C | T | 1 | a0001c0014 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.1602C>T | p.Phe534Phe | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 11/13 | 1641/2540 | 1602/1887 | 534/628 | chr9 | 137272193 | |||
| chr9:137272570 | G | A | 11 | a0001c0001 a0001c0003 a0001c0004 others(8): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
synonymous_variant | LOW | c.1695G>A | p.Pro565Pro | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 12/13 | 1734/2540 | 1695/1887 | 565/628 | chr9 | 137272570 | |||
| chr9:137272871 | G | A | 1 | a0001c0010 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1830G>A | p.Ala610Ala | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 1869/2540 | 1830/1887 | 610/628 | chr9 | 137272871 | |||
| chr9:137272910 | C | T | 1 | a0001c0012 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.1869C>T | p.Pro623Pro | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 1908/2540 | 1869/1887 | 623/628 | chr9 | 137272910 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137272932 | C | A | 1 | a0001c0019t0008 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 4 | chr9 | 137272932 | ||||||
| chr9:137272933 | C | A | 1 | a0001c0019t0008 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 5 | chr9 | 137272933 | ||||||
| chr9:137272947 | C | T | 1 | a0001c0001t0016 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*19C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 19 | chr9 | 137272947 | ||||||
| chr9:137272953 | C | T | 1 | a0001c0001t0015 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 25 | chr9 | 137272953 | ||||||
| chr9:137272965 | C | T | 1 | a0001c0001t0014 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 37 | chr9 | 137272965 | ||||||
| chr9:137272966 | G | A | 1 | a0001c0001t0009 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 38 | chr9 | 137272966 | ||||||
| chr9:137273013 | C | T | 1 | a0001c0002t0007 | 2 | HG02451.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*85C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 85 | chr9 | 137273013 | ||||||
| chr9:137273065 | C | T | 1 | a0001c0001t0013 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 137 | chr9 | 137273065 | ||||||
| chr9:137273098 | G | A | 1 | a0001c0002t0004 | 2 | HG01109.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*170G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 170 | chr9 | 137273098 | ||||||
| chr9:137273252 | G | T | 1 | a0001c0002t0012 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*324G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 324 | chr9 | 137273252 | ||||||
| chr9:137273278 | G | A | 1 | a0001c0002t0003 | 5 | HG01975.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*350G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 350 | chr9 | 137273278 | ||||||
| chr9:137273386 | G | A | 1 | a0001c0001t0010 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*458G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 458 | chr9 | 137273386 | ||||||
| chr9:137273395 | C | T | 1 | a0001c0002t0006 | 2 | HG02922.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*467C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 467 | chr9 | 137273395 | ||||||
| chr9:137273425 | T | G | 19 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(16): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*497T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 497 | chr9 | 137273425 | ||||||
| chr9:137273512 | C | T | 1 | a0001c0002t0011 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 584 | chr9 | 137273512 | ||||||
| chr9:137273533 | T | A | 17 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(14): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*605T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 13/13 | 605 | chr9 | 137273533 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:137255731 | C | T | 1 | a0001c0002t0002g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.246+120C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255731 | |||||||
| chr9:137255829 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.247-78G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255829 | |||||||
| chr9:137255836 | C | T | 5 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0230 others(2): Show |
5 | HG00099.hp1 HG00639.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-71C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255836 | |||||||
| chr9:137255858 | G | A | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.247-49G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 1/12 | chr9 | 137255858 | |||||||
| chr9:137256147 | T | C | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.410+77T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/12 | chr9 | 137256147 | |||||||
| chr9:137256187 | G | C | 1 | a0001c0002t0002g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.410+117G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 2/12 | chr9 | 137256187 | |||||||
| chr9:137256601 | G | A | 2 | a0001c0002t0004g0080 a0001c0002t0004g0081 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.510+173G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/12 | chr9 | 137256601 | |||||||
| chr9:137256627 | G | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-197G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/12 | chr9 | 137256627 | |||||||
| chr9:137256815 | G | C | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.511-9G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 3/12 | chr9 | 137256815 | |||||||
| chr9:137257172 | C | T | 1 | a0001c0005t0001g0040 | 2 | HG02155.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.741+118C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257172 | |||||||
| chr9:137257316 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.741+262C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257316 | |||||||
| chr9:137257338 | T | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.741+284T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257338 | |||||||
| chr9:137257381 | T | G | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.741+327T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257381 | |||||||
| chr9:137257403 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.741+349A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257403 | |||||||
| chr9:137257427 | A | T | 1 | a0001c0002t0002g0225 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.741+373A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257427 | |||||||
| chr9:137257504 | CT | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.741+465delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137257504 | ||||||
| chr9:137257532 | C | T | 1 | a0001c0002t0003g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.741+478C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257532 | |||||||
| chr9:137257569 | C | T | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+515C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257569 | |||||||
| chr9:137257571 | C | T | 8 | a0001c0002t0002g0024 a0001c0002t0002g0070 a0001c0002t0002g0071 others(5): Show |
9 | HG00597.hp2 HG02080.hp1 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.741+517C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257571 | |||||||
| chr9:137257582 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.741+528G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257582 | |||||||
| chr9:137257650 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.741+596G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257650 | |||||||
| chr9:137257660 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.741+606G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257660 | |||||||
| chr9:137257663 | C | T | 2 | a0001c0002t0002g0223 a0001c0002t0002g0225 |
2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.741+609C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257663 | |||||||
| chr9:137257668 | A | C | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+614A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257668 | |||||||
| chr9:137257744 | C | T | 2 | a0001c0002t0004g0080 a0001c0002t0004g0081 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.741+690C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257744 | |||||||
| chr9:137257782 | G | A | 2 | a0001c0002t0002g0042 a0001c0002t0002g0043 |
2 | NA18999.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.741+728G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257782 | |||||||
| chr9:137257791 | C | T | 2 | a0001c0002t0004g0080 a0001c0002t0004g0081 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.741+737C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257791 | |||||||
| chr9:137257800 | CTTTTTTT others(3): Show |
C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.741+761_741+770del others(10): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137257800 | ||||||
| chr9:137257845 | G | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.741+791G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257845 | |||||||
| chr9:137257974 | A | G | 1 | a0001c0003t0001g0190 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.741+920A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137257974 | |||||||
| chr9:137258118 | GT | G | 71 | a0001c0001t0001g0189 a0001c0002t0002g0002 a0001c0002t0002g0012 others(68): Show |
100 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.741+1087delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | ||||||
| chr9:137258118 | GTT | G | 22 | a0001c0001t0001g0035 a0001c0001t0001g0085 a0001c0001t0001g0175 others(19): Show |
22 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.741+1086_741+1087d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | ||||||
| chr9:137258118 | GTTT | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.741+1085_741+1087d others(5): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | ||||||
| chr9:137258118 | GTTTT | G | 9 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(6): Show |
9 | HG00099.hp1 HG00639.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.741+1084_741+1087d others(6): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258118 | ||||||
| chr9:137258238 | C | A | 3 | a0001c0002t0002g0008 a0001c0002t0002g0196 a0001c0002t0002g0205 |
8 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+1184C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258238 | |||||||
| chr9:137258385 | C | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.741+1331C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258385 | |||||||
| chr9:137258407 | T | C | 1 | a0001c0002t0002g0206 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.741+1353T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258407 | |||||||
| chr9:137258413 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.741+1359C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258413 | |||||||
| chr9:137258449 | AT | A | 19 | a0001c0001t0001g0027 a0001c0001t0001g0105 a0001c0001t0001g0106 others(16): Show |
20 | HG00099.hp1 HG01071.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.741+1412delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137258449 | ||||||
| chr9:137258593 | C | T | 19 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.741+1539C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258593 | |||||||
| chr9:137258597 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.741+1543C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258597 | |||||||
| chr9:137258621 | T | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.741+1567T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258621 | |||||||
| chr9:137258653 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.741+1599C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258653 | |||||||
| chr9:137258693 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.741+1639A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258693 | |||||||
| chr9:137258764 | T | A | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+1710T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258764 | |||||||
| chr9:137258844 | A | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.741+1790A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258844 | |||||||
| chr9:137258879 | T | C | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.741+1825T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137258879 | |||||||
| chr9:137259025 | C | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.741+1971C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259025 | |||||||
| chr9:137259053 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.741+1999T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259053 | |||||||
| chr9:137259198 | GA | G | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.741+2154delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137259198 | ||||||
| chr9:137259329 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.741+2275G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259329 | |||||||
| chr9:137259341 | G | T | 2 | a0001c0002t0002g0026 a0001c0014t0002g0026 |
2 | HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.741+2287G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259341 | |||||||
| chr9:137259343 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.741+2289C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259343 | |||||||
| chr9:137259344 | G | A | 1 | a0001c0002t0002g0225 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.741+2290G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259344 | |||||||
| chr9:137259472 | G | A | 1 | a0001c0001t0010g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.741+2418G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259472 | |||||||
| chr9:137259649 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0175 |
2 | HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.741+2595T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259649 | |||||||
| chr9:137259728 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.741+2674T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259728 | |||||||
| chr9:137259787 | C | T | 1 | a0001c0002t0002g0024 | 2 | HG00597.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.741+2733C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259787 | |||||||
| chr9:137259810 | C | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.741+2756C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259810 | |||||||
| chr9:137259811 | G | A | 2 | a0001c0002t0004g0080 a0001c0002t0004g0081 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.741+2757G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259811 | |||||||
| chr9:137259818 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0027 others(22): Show |
37 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.741+2764G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259818 | |||||||
| chr9:137259841 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
5 | HG02109.hp1 HG02257.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.741+2787C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259841 | |||||||
| chr9:137259870 | G | A | 1 | a0001c0002t0003g0011 | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.741+2816G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259870 | |||||||
| chr9:137259920 | C | T | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.741+2866C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259920 | |||||||
| chr9:137259931 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.741+2877A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259931 | |||||||
| chr9:137259952 | A | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.741+2898A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137259952 | |||||||
| chr9:137260009 | C | T | 48 | a0001c0001t0001g0169 a0001c0002t0002g0002 a0001c0002t0002g0012 others(45): Show |
69 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.741+2955C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260009 | |||||||
| chr9:137260043 | ATTTATTT others(3): Show |
A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0167 a0001c0003t0001g0005 others(5): Show |
13 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.742-2980_742-2971d others(12): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260043 | ||||||
| chr9:137260106 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.742-2931G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260106 | |||||||
| chr9:137260154 | G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.742-2883G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260154 | |||||||
| chr9:137260157 | C | T | 5 | a0001c0002t0002g0025 a0001c0002t0002g0095 a0001c0002t0002g0096 others(2): Show |
6 | NA18945.hp2 NA18953.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-2880C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260157 | |||||||
| chr9:137260195 | G | GCC | 18 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(15): Show |
21 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.742-2840_742-2839d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260195 | ||||||
| chr9:137260212 | G | C | 1 | a0001c0001t0013g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.742-2825G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260212 | |||||||
| chr9:137260222 | T | C | 1 | a0001c0001t0013g0128 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.742-2815T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260222 | |||||||
| chr9:137260307 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.742-2730C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260307 | |||||||
| chr9:137260346 | G | A | 3 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 |
3 | HG01243.hp1 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.742-2691G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260346 | |||||||
| chr9:137260392 | T | A | 1 | a0001c0002t0002g0199 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.742-2645T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260392 | |||||||
| chr9:137260393 | A | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.742-2644A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260393 | |||||||
| chr9:137260396 | A | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.742-2641A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260396 | |||||||
| chr9:137260401 | T | A | 2 | a0001c0001t0001g0109 a0001c0001t0010g0116 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.742-2636T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260401 | |||||||
| chr9:137260405 | A | ATTTAT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.742-2622_742-2618d others(7): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260405 | ||||||
| chr9:137260457 | ATT | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.742-2568_742-2567d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137260457 | ||||||
| chr9:137260524 | C | G | 1 | a0001c0002t0002g0206 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.742-2513C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260524 | |||||||
| chr9:137260672 | C | T | 2 | a0001c0002t0002g0232 a0001c0019t0008g0100 |
2 | HG03834.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.742-2365C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260672 | |||||||
| chr9:137260680 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.742-2357T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260680 | |||||||
| chr9:137260694 | C | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.742-2343C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260694 | |||||||
| chr9:137260749 | A | G | 5 | a0001c0002t0002g0021 a0001c0002t0002g0061 a0001c0002t0002g0062 others(2): Show |
6 | NA18953.hp2 NA18967.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.742-2288A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260749 | |||||||
| chr9:137260943 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.742-2094C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137260943 | |||||||
| chr9:137261015 | C | T | 1 | a0001c0002t0002g0060 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.742-2022C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261015 | |||||||
| chr9:137261031 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | NA18947.hp1 NA18970.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.742-2006G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261031 | |||||||
| chr9:137261112 | G | T | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.742-1925G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261112 | |||||||
| chr9:137261113 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.742-1924C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261113 | |||||||
| chr9:137261123 | A | T | 2 | a0001c0002t0002g0044 a0001c0002t0002g0059 |
2 | HG01496.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.742-1914A>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261123 | |||||||
| chr9:137261211 | G | A | 1 | a0001c0002t0002g0095 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.742-1826G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261211 | |||||||
| chr9:137261233 | G | C | 1 | a0001c0001t0001g0195 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.742-1804G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261233 | |||||||
| chr9:137261241 | G | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.742-1796G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261241 | |||||||
| chr9:137261266 | G | C | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.742-1771G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261266 | |||||||
| chr9:137261281 | A | G | 1 | a0001c0003t0001g0168 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.742-1756A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261281 | |||||||
| chr9:137261297 | G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.742-1740G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261297 | |||||||
| chr9:137261321 | C | A | 1 | a0001c0002t0002g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.742-1716C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261321 | |||||||
| chr9:137261331 | C | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0033 others(8): Show |
17 | HG00099.hp2 HG00280.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.742-1706C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261331 | |||||||
| chr9:137261332 | T | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.742-1705T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261332 | |||||||
| chr9:137261339 | CA | C | 18 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0033 others(15): Show |
23 | HG00099.hp2 HG00642.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.742-1681delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261339 | ||||||
| chr9:137261339 | CAAAAAA | C | 5 | a0001c0002t0002g0019 a0001c0002t0002g0020 a0001c0002t0002g0058 others(2): Show |
7 | HG02027.hp1 HG02056.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-1686_742-1681d others(8): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261339 | ||||||
| chr9:137261358 | T | TA | 9 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0230 others(6): Show |
12 | HG00741.hp2 HG01175.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-1664dupA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261358 | ||||||
| chr9:137261371 | A | C | 2 | a0001c0002t0002g0020 a0001c0002t0002g0058 |
3 | NA18612.hp1 NA18974.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.742-1666A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261371 | |||||||
| chr9:137261447 | C | T | 1 | a0001c0002t0002g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.742-1590C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261447 | |||||||
| chr9:137261486 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.742-1551C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261486 | |||||||
| chr9:137261502 | C | G | 1 | a0001c0002t0002g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.742-1535C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261502 | |||||||
| chr9:137261508 | A | G | 1 | a0001c0002t0002g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.742-1529A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261508 | |||||||
| chr9:137261588 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0132 others(3): Show |
8 | HG01261.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.742-1449G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261588 | |||||||
| chr9:137261612 | C | T | 3 | a0001c0002t0003g0011 a0001c0002t0003g0224 a0001c0002t0007g0037 |
7 | HG01975.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-1425C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261612 | |||||||
| chr9:137261652 | C | T | 12 | a0001c0002t0002g0017 a0001c0002t0002g0038 a0001c0002t0002g0197 others(9): Show |
15 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.742-1385C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261652 | |||||||
| chr9:137261653 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.742-1384G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261653 | |||||||
| chr9:137261657 | CA | C | 10 | a0001c0002t0002g0055 a0001c0002t0002g0059 a0001c0002t0002g0079 others(7): Show |
10 | HG01975.hp2 HG02015.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-1360delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261657 | ||||||
| chr9:137261657 | CAAAAAAA others(2): Show |
C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.742-1368_742-1360d others(11): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261657 | ||||||
| chr9:137261657 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0115 a0001c0013t0001g0161 |
2 | HG02895.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.742-1369_742-1360d others(12): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261657 | ||||||
| chr9:137261702 | C | T | 5 | a0001c0002t0002g0038 a0001c0002t0002g0199 a0001c0002t0002g0202 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.742-1335C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261702 | |||||||
| chr9:137261720 | T | C | 1 | a0001c0002t0003g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.742-1317T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261720 | |||||||
| chr9:137261730 | G | T | 1 | a0001c0002t0002g0054 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.742-1307G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261730 | |||||||
| chr9:137261733 | C | T | 1 | a0001c0002t0002g0066 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.742-1304C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261733 | |||||||
| chr9:137261767 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.742-1270G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261767 | |||||||
| chr9:137261816 | C | A | 12 | a0001c0002t0002g0017 a0001c0002t0002g0038 a0001c0002t0002g0197 others(9): Show |
15 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.742-1221C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137261816 | |||||||
| chr9:137261979 | C | CAGAG | 129 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(126): Show |
210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.742-1045_742-1042d others(6): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261979 | ||||||
| chr9:137261979 | C | CAGAGAG | 7 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(4): Show |
7 | HG00673.hp2 HG03139.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-1047_742-1042d others(8): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr9 | 137261979 | ||||||
| chr9:137262030 | G | T | 9 | a0001c0002t0002g0013 a0001c0002t0002g0079 a0001c0002t0002g0088 others(6): Show |
11 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.742-1007G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262030 | |||||||
| chr9:137262149 | A | G | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.742-888A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262149 | |||||||
| chr9:137262345 | G | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0132 others(2): Show |
7 | HG01261.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-692G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262345 | |||||||
| chr9:137262511 | G | T | 1 | a0001c0002t0002g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.742-526G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262511 | |||||||
| chr9:137262550 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.742-487G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262550 | |||||||
| chr9:137262611 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.742-426G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262611 | |||||||
| chr9:137262614 | T | A | 1 | a0001c0002t0007g0037 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.742-423T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262614 | |||||||
| chr9:137262798 | C | T | 78 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(75): Show |
105 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(102): Show |
intron_variant | MODIFIER | c.742-239C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262798 | |||||||
| chr9:137262870 | A | G | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.742-167A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262870 | |||||||
| chr9:137262977 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.742-60G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137262977 | |||||||
| chr9:137263004 | G | A | 6 | a0001c0002t0002g0038 a0001c0002t0002g0199 a0001c0002t0002g0200 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.742-33G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137263004 | |||||||
| chr9:137263008 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.742-29T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137263008 | |||||||
| chr9:137263030 | G | A | 10 | a0001c0002t0002g0017 a0001c0002t0002g0038 a0001c0002t0002g0197 others(7): Show |
13 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(10): Show |
splice_region_variant&intron_variant | LOW | c.742-7G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 4/12 | chr9 | 137263030 | |||||||
| chr9:137263249 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.927+27C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263249 | |||||||
| chr9:137263267 | T | TGCTGCCC others(76): Show |
1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.927+63_927+64insCT others(81): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr9 | 137263267 | ||||||
| chr9:137263295 | ACTCCCCG others(77): Show |
A | 1 | a0001c0002t0002g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927+93_927+176delT others(83): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr9 | 137263295 | ||||||
| chr9:137263378 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0154 others(2): Show |
5 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+156C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263378 | |||||||
| chr9:137263382 | C | T | 18 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(15): Show |
21 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.927+160C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263382 | |||||||
| chr9:137263385 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02074.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.927+163C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263385 | |||||||
| chr9:137263429 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.927+207C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263429 | |||||||
| chr9:137263507 | C | T | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.927+285C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263507 | |||||||
| chr9:137263508 | C | T | 1 | a0001c0002t0002g0219 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.927+286C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263508 | |||||||
| chr9:137263518 | CT | C | 1 | a0001c0002t0003g0011 | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+297delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263518 | |||||||
| chr9:137263562 | C | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.927+340C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263562 | |||||||
| chr9:137263569 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.927+347A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263569 | |||||||
| chr9:137263591 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.927+369T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263591 | |||||||
| chr9:137263600 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0157 a0001c0001t0001g0162 |
5 | HG02602.hp2 HG02735.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.927+378C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263600 | |||||||
| chr9:137263705 | G | A | 13 | a0001c0002t0002g0017 a0001c0002t0002g0038 a0001c0002t0002g0197 others(10): Show |
16 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.927+483G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263705 | |||||||
| chr9:137263749 | C | T | 13 | a0001c0002t0002g0017 a0001c0002t0002g0038 a0001c0002t0002g0197 others(10): Show |
16 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.928-496C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263749 | |||||||
| chr9:137263843 | C | T | 2 | a0001c0002t0002g0091 a0001c0002t0002g0094 |
2 | NA18977.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.928-402C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137263843 | |||||||
| chr9:137264017 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.928-228C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264017 | |||||||
| chr9:137264063 | C | G | 1 | a0001c0002t0002g0099 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.928-182C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264063 | |||||||
| chr9:137264085 | G | A | 1 | a0001c0002t0007g0037 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.928-160G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264085 | |||||||
| chr9:137264198 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.928-47C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 5/12 | chr9 | 137264198 | |||||||
| chr9:137264419 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1040+62T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264419 | |||||||
| chr9:137264475 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1040+118G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264475 | |||||||
| chr9:137264497 | G | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1040+140G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264497 | |||||||
| chr9:137264552 | G | A | 1 | a0001c0002t0002g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1040+195G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264552 | |||||||
| chr9:137264659 | G | T | 2 | a0001c0002t0004g0080 a0001c0002t0004g0081 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1040+302G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264659 | |||||||
| chr9:137264772 | G | A | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1040+415G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264772 | |||||||
| chr9:137264787 | C | G | 1 | a0001c0002t0002g0090 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1040+430C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264787 | |||||||
| chr9:137264793 | C | T | 2 | a0001c0002t0004g0080 a0001c0002t0004g0081 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1040+436C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264793 | |||||||
| chr9:137264799 | C | T | 1 | a0001c0003t0001g0190 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1040+442C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264799 | |||||||
| chr9:137264869 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1040+512T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264869 | |||||||
| chr9:137264953 | G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1040+596G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137264953 | |||||||
| chr9:137265031 | C | CT | 41 | a0001c0002t0002g0013 a0001c0002t0002g0017 a0001c0002t0002g0018 others(38): Show |
48 | HG00544.hp1 HG01167.hp1 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.1040+697dupT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265031 | ||||||
| chr9:137265031 | C | CTT | 40 | a0001c0002t0002g0002 a0001c0002t0002g0019 a0001c0002t0002g0021 others(37): Show |
57 | HG00597.hp2 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1040+696_1040+697d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265031 | ||||||
| chr9:137265031 | C | CTTT | 5 | a0001c0002t0002g0012 a0001c0002t0002g0020 a0001c0002t0002g0061 others(2): Show |
8 | HG00423.hp2 HG01978.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1040+695_1040+697d others(5): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265031 | ||||||
| chr9:137265054 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1040+697T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265054 | |||||||
| chr9:137265054 | T | TC | 18 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0035 others(15): Show |
29 | HG01106.hp1 HG01106.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1040+698dupC | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265054 | ||||||
| chr9:137265109 | A | G | 1 | a0001c0002t0002g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1040+752A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265109 | |||||||
| chr9:137265212 | G | C | 10 | a0001c0002t0002g0017 a0001c0002t0002g0038 a0001c0002t0002g0197 others(7): Show |
13 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1041-665G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265212 | |||||||
| chr9:137265230 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1041-647G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265230 | |||||||
| chr9:137265239 | TCAAA | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | HG00673.hp2 NA18950.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041-630_1041-627d others(6): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265239 | ||||||
| chr9:137265387 | C | CTTTTTTT | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(102): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1041-477_1041-471d others(9): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | ||||||
| chr9:137265387 | C | CTTTTTTT others(1): Show |
21 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0030 others(18): Show |
34 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1041-478_1041-471d others(10): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | ||||||
| chr9:137265387 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0153 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1041-484_1041-471d others(16): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | ||||||
| chr9:137265387 | CT | C | 70 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0013 others(67): Show |
97 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.1041-471delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | ||||||
| chr9:137265387 | CTT | C | 6 | a0001c0002t0002g0048 a0001c0002t0002g0054 a0001c0002t0002g0066 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-472_1041-471d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265387 | ||||||
| chr9:137265533 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1041-344C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265533 | |||||||
| chr9:137265580 | G | C | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1041-297G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265580 | |||||||
| chr9:137265634 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1041-243C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265634 | |||||||
| chr9:137265638 | TCGGCCTG others(36): Show |
T | 48 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(45): Show |
69 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1041-196_1041-154d others(45): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137265638 | ||||||
| chr9:137265673 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1041-204C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265673 | |||||||
| chr9:137265674 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1041-203G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265674 | |||||||
| chr9:137265676 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1041-201C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265676 | |||||||
| chr9:137265721 | C | T | 1 | a0001c0002t0002g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1041-156C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265721 | |||||||
| chr9:137265726 | G | T | 2 | a0001c0002t0002g0042 a0001c0002t0002g0043 |
2 | NA18999.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1041-151G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265726 | |||||||
| chr9:137265803 | C | T | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1041-74C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265803 | |||||||
| chr9:137265821 | C | A | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1041-56C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 6/12 | chr9 | 137265821 | |||||||
| chr9:137266027 | G | A | 1 | a0001c0006t0005g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1143+48G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266027 | |||||||
| chr9:137266082 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0133 |
2 | HG01261.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1143+103G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266082 | |||||||
| chr9:137266096 | G | T | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1143+117G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266096 | |||||||
| chr9:137266130 | T | C | 1 | a0001c0002t0003g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1143+151T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266130 | |||||||
| chr9:137266185 | C | T | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1144-146C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266185 | |||||||
| chr9:137266191 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1144-140G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266191 | |||||||
| chr9:137266205 | T | A | 1 | a0001c0002t0002g0094 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1144-126T>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266205 | |||||||
| chr9:137266279 | A | G | 1 | a0001c0003t0001g0190 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1144-52A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 7/12 | chr9 | 137266279 | |||||||
| chr9:137266529 | T | G | 1 | a0001c0002t0002g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1239+103T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266529 | |||||||
| chr9:137266602 | G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1239+176G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266602 | |||||||
| chr9:137266645 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1239+219G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266645 | |||||||
| chr9:137266662 | G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1239+236G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266662 | |||||||
| chr9:137266668 | G | A | 1 | a0001c0001t0014g0144 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1239+242G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266668 | |||||||
| chr9:137266732 | C | T | 1 | a0001c0002t0002g0064 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1240-212C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266732 | |||||||
| chr9:137266749 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1240-195T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266749 | |||||||
| chr9:137266882 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1240-62C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266882 | |||||||
| chr9:137266900 | C | T | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | HG00673.hp2 NA18950.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-44C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266900 | |||||||
| chr9:137266901 | A | G | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
5 | HG00673.hp2 NA18950.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1240-43A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 8/12 | chr9 | 137266901 | |||||||
| chr9:137267125 | C | T | 1 | a0001c0002t0002g0075 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1382+39C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267125 | |||||||
| chr9:137267163 | G | C | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1382+77G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267163 | |||||||
| chr9:137267176 | CGGTGTGG others(4): Show |
C | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1383-62_1383-52del others(11): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr9 | 137267176 | ||||||
| chr9:137267179 | TGTGGGGC others(4): Show |
T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
212 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1383-28_1383-18del others(11): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr9 | 137267179 | ||||||
| chr9:137267179 | TGTGGGGC others(15): Show |
T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0165 |
4 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383-39_1383-18del others(22): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr9 | 137267179 | ||||||
| chr9:137267184 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1383-56G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267184 | |||||||
| chr9:137267190 | G | T | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1383-50G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267190 | |||||||
| chr9:137267195 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1383-45G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267195 | |||||||
| chr9:137267206 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0165 |
4 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383-34G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267206 | |||||||
| chr9:137267226 | C | A | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1383-14C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 9/12 | chr9 | 137267226 | |||||||
| chr9:137267397 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1489+51G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267397 | |||||||
| chr9:137267419 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1489+73C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267419 | |||||||
| chr9:137267457 | G | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1489+111G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267457 | |||||||
| chr9:137267490 | C | CT | 17 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0133 others(14): Show |
17 | HG01106.hp2 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1489+164dupT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137267490 | ||||||
| chr9:137267490 | CT | C | 23 | a0001c0001t0001g0142 a0001c0002t0002g0013 a0001c0002t0002g0025 others(20): Show |
26 | HG00544.hp1 HG00741.hp2 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1489+164delT | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137267490 | ||||||
| chr9:137267492 | T | C | 17 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(14): Show |
20 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.1489+146T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267492 | |||||||
| chr9:137267493 | T | C | 1 | a0001c0002t0002g0232 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1489+147T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267493 | |||||||
| chr9:137267518 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1489+172A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267518 | |||||||
| chr9:137267603 | C | T | 1 | a0001c0012t0002g0074 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1489+257C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267603 | |||||||
| chr9:137267638 | C | T | 1 | a0001c0002t0002g0218 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1489+292C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267638 | |||||||
| chr9:137267822 | T | G | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1489+476T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267822 | |||||||
| chr9:137267889 | G | C | 1 | a0001c0018t0001g0086 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1489+543G>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137267889 | |||||||
| chr9:137268088 | A | G | 85 | a0001c0001t0001g0123 a0001c0002t0002g0002 a0001c0002t0002g0012 others(82): Show |
116 | HG00408.hp1 HG00423.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1489+742A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268088 | |||||||
| chr9:137268181 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
6 | HG01891.hp1 HG02280.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.1489+835C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268181 | |||||||
| chr9:137268212 | G | T | 19 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1489+866G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268212 | |||||||
| chr9:137268227 | T | G | 10 | a0001c0002t0002g0017 a0001c0002t0002g0038 a0001c0002t0002g0197 others(7): Show |
13 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.1489+881T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268227 | |||||||
| chr9:137268243 | A | C | 2 | a0001c0002t0002g0215 a0001c0002t0002g0219 |
2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1489+897A>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268243 | |||||||
| chr9:137268360 | C | T | 1 | a0001c0006t0005g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1489+1014C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268360 | |||||||
| chr9:137268381 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1489+1035C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268381 | |||||||
| chr9:137268443 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1489+1097G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268443 | |||||||
| chr9:137268558 | C | T | 1 | a0001c0002t0002g0225 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1489+1212C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268558 | |||||||
| chr9:137268573 | G | A | 1 | a0001c0001t0001g0032 | 2 | HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1489+1227G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268573 | |||||||
| chr9:137268581 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1489+1235G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268581 | |||||||
| chr9:137268676 | G | T | 2 | a0001c0002t0003g0011 a0001c0002t0003g0224 |
5 | HG01975.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489+1330G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268676 | |||||||
| chr9:137268717 | C | T | 1 | a0001c0002t0002g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1489+1371C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268717 | |||||||
| chr9:137268826 | T | C | 1 | a0001c0003t0001g0186 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1489+1480T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268826 | |||||||
| chr9:137268937 | G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1489+1591G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268937 | |||||||
| chr9:137268998 | A | G | 5 | a0001c0002t0002g0039 a0001c0002t0002g0217 a0001c0002t0002g0218 others(2): Show |
5 | HG02922.hp2 HG03130.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1489+1652A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137268998 | |||||||
| chr9:137269024 | A | G | 47 | a0001c0002t0002g0002 a0001c0002t0002g0012 a0001c0002t0002g0018 others(44): Show |
68 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1489+1678A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269024 | |||||||
| chr9:137269081 | G | A | 1 | a0001c0002t0002g0223 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1489+1735G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269081 | |||||||
| chr9:137269139 | C | T | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1489+1793C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269139 | |||||||
| chr9:137269223 | T | G | 3 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 |
3 | HG01243.hp1 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1489+1877T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269223 | |||||||
| chr9:137269261 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1489+1915C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269261 | |||||||
| chr9:137269292 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1489+1946G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269292 | |||||||
| chr9:137269667 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1489+2321G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269667 | |||||||
| chr9:137269676 | C | T | 1 | a0001c0002t0003g0224 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1489+2330C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269676 | |||||||
| chr9:137269803 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | NA18950.hp1 NA18970.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-2278G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269803 | |||||||
| chr9:137269924 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1490-2157C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269924 | |||||||
| chr9:137269992 | G | T | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-2089G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137269992 | |||||||
| chr9:137270031 | G | A | 19 | a0001c0002t0002g0013 a0001c0002t0002g0025 a0001c0002t0002g0026 others(16): Show |
22 | HG00544.hp1 HG02015.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.1490-2050G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270031 | |||||||
| chr9:137270158 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1490-1923G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270158 | |||||||
| chr9:137270195 | C | T | 1 | a0001c0002t0011g0213 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1490-1886C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270195 | |||||||
| chr9:137270205 | T | C | 1 | a0001c0002t0002g0079 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1490-1876T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270205 | |||||||
| chr9:137270237 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(129): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.1490-1844C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270237 | |||||||
| chr9:137270280 | C | CA | 33 | a0001c0001t0001g0083 a0001c0001t0001g0120 a0001c0001t0001g0122 others(30): Show |
37 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1490-1781dupA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137270280 | ||||||
| chr9:137270280 | CA | C | 8 | a0001c0001t0001g0151 a0001c0001t0001g0170 a0001c0002t0002g0073 others(5): Show |
8 | HG01516.hp2 HG02897.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1490-1781delA | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137270280 | ||||||
| chr9:137270346 | T | G | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1735T>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270346 | |||||||
| chr9:137270505 | G | A | 2 | a0001c0006t0005g0077 a0001c0006t0005g0078 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1490-1576G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270505 | |||||||
| chr9:137270571 | C | G | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-1510C>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270571 | |||||||
| chr9:137270651 | G | A | 3 | a0001c0002t0002g0209 a0001c0002t0002g0210 a0001c0002t0002g0211 |
3 | HG01243.hp1 HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1490-1430G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270651 | |||||||
| chr9:137270713 | G | A | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1368G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270713 | |||||||
| chr9:137270714 | A | G | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1367A>G | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270714 | |||||||
| chr9:137270715 | G | T | 1 | a0001c0002t0012g0068 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1490-1366G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270715 | |||||||
| chr9:137270795 | C | T | 1 | a0001c0002t0002g0051 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1490-1286C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137270795 | |||||||
| chr9:137271052 | C | T | 3 | a0001c0002t0002g0008 a0001c0002t0002g0196 a0001c0002t0002g0205 |
8 | HG02258.hp1 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490-1029C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271052 | |||||||
| chr9:137271074 | C | T | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1490-1007C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271074 | |||||||
| chr9:137271115 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1490-966C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271115 | |||||||
| chr9:137271166 | C | T | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-915C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271166 | |||||||
| chr9:137271167 | C | T | 1 | a0001c0002t0002g0048 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1490-914C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271167 | |||||||
| chr9:137271379 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1490-702C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271379 | |||||||
| chr9:137271459 | G | A | 1 | a0001c0019t0008g0100 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1490-622G>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271459 | |||||||
| chr9:137271533 | C | T | 1 | a0001c0002t0002g0050 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1490-548C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271533 | |||||||
| chr9:137271545 | C | T | 1 | a0001c0002t0002g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1490-536C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271545 | |||||||
| chr9:137271606 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1490-475T>C | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271606 | |||||||
| chr9:137271647 | ACT | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0164 |
3 | NA18951.hp2 NA19070.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1490-429_1490-428d others(4): Show |
NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137271647 | ||||||
| chr9:137271672 | G | T | 1 | a0001c0002t0002g0087 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1490-409G>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271672 | |||||||
| chr9:137271918 | C | A | 2 | a0001c0002t0004g0080 a0001c0002t0004g0081 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1490-163C>A | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137271918 | |||||||
| chr9:137272028 | C | T | 1 | a0001c0002t0003g0011 | 4 | HG02630.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-53C>T | NELFB | ENSG00000188986.9 | transcript | ENST00000343053.6 | protein_coding | 10/12 | chr9 | 137272028 |