Item | Value |
---|---|
geneid | 64844 |
ensemblid | ENSG00000136536.15 |
hgncid | 17393 |
symbol | MARCHF7 |
name | membrane associated ring-CH-type finger 7 |
refseq_nuc | NM_001282805.2 |
refseq_prot | NP_001269734.1 |
ensembl_nuc | ENST00000409175.6 |
ensembl_prot | ENSP00000386830.1 |
mane_status | MANE Select |
chr | chr2 |
start | 159712506 |
end | 159771027 |
strand | + |
ver | v1.2 |
region | chr2:159712506-159771027 |
region5000 | chr2:159707506-159776027 |
regionname0 | MARCHF7_chr2_159712506_159771027 |
regionname5000 | MARCHF7_chr2_159707506_159776027 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 704 | 295 | 70 | 49 | 145 | 10 | 20 | 116 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0002 | 0/0 | 704 | 28 | 0 | 0 | 28 | 0 | 0 | 22 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0003 | 0/1 | 704 | 11 | 0 | 5 | 4 | 0 | 1 | 3 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0004 | 0/0 | 704 | 9 | 3 | 1 | 0 | 3 | 2 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0005 | 0/0 | 704 | 8 | 0 | 7 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0006 | 0/0 | 704 | 6 | 3 | 0 | 2 | 0 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0007 | 0/0 | 704 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0008 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0009 | 0/0 | 704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0010 | 0/0 | 704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0011 | 0/0 | 704 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0012 | 0/0 | 704 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
a0013 | 0/0 | 704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | MESKP others(699): Show |
chr2 | 159707506 | 159776027 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2112 | 102 | 32 | 12 | 44 | 4 | 10 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0001c0002 | 0/0 | 2112 | 102 | 1 | 31 | 63 | 3 | 4 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0001c0003 | 1/0 | 2112 | 47 | 2 | 1 | 38 | 2 | 3 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0001c0004 | 0/0 | 2112 | 42 | 35 | 5 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0001c0011 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0001c0014 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0002c0005 | 0/0 | 2112 | 28 | 0 | 0 | 28 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0003c0006 | 0/1 | 2112 | 11 | 0 | 5 | 4 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0004c0007 | 0/0 | 2112 | 9 | 3 | 1 | 0 | 3 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0005c0008 | 0/0 | 2112 | 7 | 0 | 6 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0005c0017 | 0/0 | 2112 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0006c0009 | 0/0 | 2112 | 6 | 3 | 0 | 2 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0007c0018 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0008c0013 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0009c0012 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0010c0015 | 0/0 | 2112 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0011c0010 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0012c0016 | 0/0 | 2112 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 | ||
a0013c0019 | 0/0 | 2112 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | ATGGA others(2107): Show |
chr2 | 159707506 | 159776027 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6044 | 68 | 6 | 11 | 39 | 3 | 9 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0006 | 0/0 | 6044 | 14 | 14 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0012 | 0/0 | 6044 | 6 | 6 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0014 | 0/0 | 6045 | 3 | 3 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6040): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0015 | 0/0 | 6046 | 3 | 0 | 0 | 1 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6041): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0016 | 0/0 | 6044 | 3 | 0 | 0 | 3 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0020 | 0/0 | 6044 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0029 | 0/0 | 6044 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0033 | 0/0 | 6045 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6040): Show |
chr2 | 159707506 | 159776027 |
a0001c0001t0038 | 0/0 | 6044 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0002t0001 | 0/0 | 6043 | 86 | 1 | 31 | 47 | 3 | 4 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0002t0007 | 0/0 | 6043 | 11 | 0 | 0 | 11 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0002t0019 | 0/0 | 6043 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0002t0021 | 0/0 | 6043 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0002t0034 | 0/0 | 6045 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6040): Show |
chr2 | 159707506 | 159776027 |
a0001c0003t0003 | 0/0 | 6047 | 9 | 0 | 0 | 9 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0001c0003t0004 | 1/0 | 6043 | 33 | 2 | 1 | 24 | 2 | 3 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0003t0024 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0003t0027 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0003t0030 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0003t0031 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0003t0032 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0003 | 0/0 | 6047 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0005 | 0/0 | 6043 | 14 | 13 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0008 | 0/0 | 6046 | 10 | 9 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6041): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0009 | 0/0 | 6047 | 4 | 4 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0013 | 0/0 | 6046 | 4 | 2 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6041): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0018 | 0/0 | 6052 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6047): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0022 | 0/0 | 6046 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6041): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0023 | 0/0 | 6040 | 2 | 0 | 0 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6035): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0028 | 0/0 | 6054 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6049): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0037 | 0/0 | 6051 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6046): Show |
chr2 | 159707506 | 159776027 |
a0001c0004t0040 | 0/0 | 6040 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6035): Show |
chr2 | 159707506 | 159776027 |
a0001c0011t0002 | 0/0 | 6044 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0001c0014t0002 | 0/0 | 6044 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0002c0005t0003 | 0/0 | 6047 | 23 | 0 | 0 | 23 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0002c0005t0009 | 0/0 | 6047 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0002c0005t0017 | 0/0 | 6049 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6044): Show |
chr2 | 159707506 | 159776027 |
a0002c0005t0025 | 0/0 | 6047 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0002c0005t0026 | 0/0 | 6047 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0003c0006t0010 | 0/1 | 6044 | 10 | 0 | 5 | 3 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6039): Show |
chr2 | 159707506 | 159776027 |
a0003c0006t0039 | 0/0 | 5995 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(5990): Show |
chr2 | 159707506 | 159776027 |
a0004c0007t0011 | 0/0 | 6045 | 9 | 3 | 1 | 0 | 3 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6040): Show |
chr2 | 159707506 | 159776027 |
a0005c0008t0003 | 0/0 | 6047 | 7 | 0 | 6 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0005c0017t0003 | 0/0 | 6047 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTGC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0006c0009t0009 | 0/0 | 6047 | 4 | 1 | 0 | 2 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0006c0009t0035 | 0/0 | 6047 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0006c0009t0036 | 0/0 | 6049 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6044): Show |
chr2 | 159707506 | 159776027 |
a0007c0018t0004 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0008c0013t0014 | 0/0 | 6045 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6040): Show |
chr2 | 159707506 | 159776027 |
a0009c0012t0004 | 0/0 | 6043 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0010c0015t0009 | 0/0 | 6047 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6042): Show |
chr2 | 159707506 | 159776027 |
a0011c0010t0004 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0012c0016t0001 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6038): Show |
chr2 | 159707506 | 159776027 |
a0013c0019t0018 | 0/0 | 6052 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | GGTTC others(6047): Show |
chr2 | 159707506 | 159776027 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0012g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0014g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0014g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0014g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0015g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0015g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0015g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0016g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0016g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0016g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0020g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0020g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0029g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0033g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0001t0038g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0001 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0019g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0019g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0021g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0021g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0002t0034g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0024g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0027g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0030g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0031g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0003t0032g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0013g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0013g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0013g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0018g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0022g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0022g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0023g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0028g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0037g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0004t0040g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0011t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0001c0014t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0009g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0017g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0017g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0025g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0002c0005t0026g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0010g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0003c0006t0039g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0004c0007t0011g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0008t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0005c0017t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0035g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0006c0009t0036g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0007c0018t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0008c0013t0014g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0009c0012t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0010c0015t0009g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0011c0010t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0012c0016t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
a0013c0019t0018g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0004 | g0021 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0151 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0246 | EUR | GBR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00280 | hp1 | a0004 | c0007 | t0011 | g0020 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00280 | hp2 | a0001 | c0001 | t0015 | g0033 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0098 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00323 | hp2 | a0001 | c0011 | t0002 | g0002 | EUR | FIN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00408 | hp2 | a0002 | c0005 | t0003 | g0053 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00438 | hp1 | a0006 | c0009 | t0009 | g0044 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00544 | hp1 | a0007 | c0018 | t0004 | g0187 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00558 | hp1 | a0001 | c0003 | t0004 | g0201 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00597 | hp1 | a0001 | c0003 | t0003 | g0094 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00597 | hp2 | a0002 | c0005 | t0003 | g0071 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00609 | hp1 | a0001 | c0003 | t0004 | g0198 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00639 | hp1 | a0001 | c0004 | t0008 | g0294 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00735 | hp1 | a0003 | c0006 | t0010 | g0169 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00738 | hp1 | a0005 | c0008 | t0003 | g0068 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01074 | hp2 | a0004 | c0007 | t0011 | g0175 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01106 | hp2 | a0001 | c0001 | t0029 | g0261 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01168 | hp1 | a0001 | c0004 | t0013 | g0035 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01169 | hp2 | a0001 | c0004 | t0013 | g0035 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0145 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01175 | hp2 | a0001 | c0003 | t0004 | g0193 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0144 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01257 | hp2 | a0003 | c0006 | t0010 | g0019 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01258 | hp2 | a0003 | c0006 | t0010 | g0019 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01261 | hp2 | a0001 | c0004 | t0005 | g0214 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01358 | hp2 | a0003 | c0006 | t0010 | g0018 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01361 | hp2 | a0001 | c0004 | t0040 | g0212 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01433 | hp1 | a0005 | c0008 | t0003 | g0073 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01515 | hp2 | a0005 | c0008 | t0003 | g0072 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01516 | hp1 | a0001 | c0003 | t0004 | g0037 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01516 | hp2 | a0004 | c0007 | t0011 | g0176 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01517 | hp2 | a0004 | c0007 | t0011 | g0177 | EUR | IBS | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01934 | hp2 | a0005 | c0008 | t0003 | g0057 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01952 | hp1 | a0005 | c0017 | t0003 | g0058 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01975 | hp2 | a0005 | c0008 | t0003 | g0056 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02040 | hp2 | a0001 | c0003 | t0003 | g0087 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0223 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02055 | hp2 | a0001 | c0004 | t0005 | g0222 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0088 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02071 | hp1 | a0001 | c0003 | t0003 | g0092 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02080 | hp1 | a0002 | c0005 | t0009 | g0097 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02080 | hp2 | a0001 | c0003 | t0004 | g0190 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02083 | hp1 | a0002 | c0005 | t0003 | g0064 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02132 | hp1 | a0001 | c0003 | t0003 | g0090 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02135 | hp1 | a0003 | c0006 | t0010 | g0168 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02135 | hp2 | a0002 | c0005 | t0003 | g0063 | EAS | KHV | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02145 | hp1 | a0001 | c0001 | t0006 | g0287 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02145 | hp2 | a0001 | c0001 | t0014 | g0164 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | CDX | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02155 | hp2 | a0002 | c0005 | t0003 | g0052 | EAS | CDX | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02257 | hp2 | a0001 | c0004 | t0008 | g0005 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02258 | hp1 | a0006 | c0009 | t0036 | g0047 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02258 | hp2 | a0001 | c0004 | t0005 | g0007 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02273 | hp2 | a0005 | c0008 | t0003 | g0055 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02280 | hp1 | a0006 | c0009 | t0035 | g0045 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02293 | hp1 | a0005 | c0008 | t0003 | g0054 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02300 | hp1 | a0003 | c0006 | t0010 | g0171 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02451 | hp1 | a0001 | c0004 | t0009 | g0085 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02451 | hp2 | a0008 | c0013 | t0014 | g0283 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02572 | hp2 | a0001 | c0004 | t0013 | g0291 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02615 | hp2 | a0001 | c0004 | t0005 | g0007 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02622 | hp2 | a0001 | c0004 | t0008 | g0298 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0238 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02630 | hp2 | a0001 | c0004 | t0022 | g0295 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02647 | hp1 | a0001 | c0001 | t0020 | g0173 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02647 | hp2 | a0001 | c0004 | t0009 | g0086 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02717 | hp1 | a0001 | c0001 | t0020 | g0172 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02717 | hp2 | a0001 | c0004 | t0005 | g0213 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02738 | hp2 | a0004 | c0007 | t0011 | g0180 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02809 | hp1 | a0001 | c0004 | t0013 | g0292 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02809 | hp2 | a0004 | c0007 | t0011 | g0174 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02895 | hp1 | a0001 | c0004 | t0005 | g0220 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0242 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02896 | hp1 | a0001 | c0004 | t0005 | g0219 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02896 | hp2 | a0001 | c0004 | t0008 | g0005 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0027 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02897 | hp2 | a0001 | c0004 | t0008 | g0005 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0211 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02965 | hp1 | a0001 | c0001 | t0014 | g0282 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02965 | hp2 | a0004 | c0007 | t0011 | g0179 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02970 | hp1 | a0001 | c0004 | t0005 | g0215 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03041 | hp2 | a0001 | c0004 | t0008 | g0005 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03098 | hp1 | a0001 | c0004 | t0008 | g0290 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03139 | hp2 | a0001 | c0004 | t0008 | g0293 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03195 | hp1 | a0006 | c0009 | t0009 | g0046 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0241 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03209 | hp1 | a0001 | c0001 | t0033 | g0165 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03209 | hp2 | a0004 | c0007 | t0011 | g0178 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03225 | hp1 | a0001 | c0004 | t0008 | g0297 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03225 | hp2 | a0001 | c0004 | t0037 | g0218 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03239 | hp2 | a0009 | c0012 | t0004 | g0208 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03453 | hp2 | a0001 | c0004 | t0003 | g0060 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03491 | hp1 | a0001 | c0003 | t0004 | g0184 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0272 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03492 | hp2 | a0001 | c0003 | t0004 | g0183 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03516 | hp1 | a0001 | c0004 | t0005 | g0217 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03516 | hp2 | a0001 | c0001 | t0014 | g0281 | AFR | ESN | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03540 | hp2 | a0001 | c0003 | t0004 | g0224 | AFR | GWD | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03579 | hp1 | a0001 | c0004 | t0003 | g0061 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03579 | hp2 | a0001 | c0004 | t0005 | g0221 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03654 | hp1 | a0006 | c0009 | t0009 | g0048 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03654 | hp2 | a0001 | c0004 | t0023 | g0025 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03704 | hp2 | a0001 | c0014 | t0002 | g0253 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03710 | hp2 | a0010 | c0015 | t0009 | g0288 | SAS | PJL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03834 | hp2 | a0001 | c0004 | t0023 | g0025 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03927 | hp2 | a0001 | c0003 | t0004 | g0186 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | BEB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04199 | hp1 | a0003 | c0006 | t0010 | g0018 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04199 | hp2 | a0001 | c0001 | t0015 | g0267 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG04204 | hp2 | a0004 | c0007 | t0011 | g0020 | SAS | STU | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18612 | hp1 | a0001 | c0002 | t0019 | g0013 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18612 | hp2 | a0001 | c0003 | t0024 | g0204 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18747 | hp1 | a0001 | c0003 | t0032 | g0022 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | CHB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18940 | hp2 | a0001 | c0003 | t0004 | g0197 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18942 | hp1 | a0001 | c0003 | t0004 | g0209 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18942 | hp2 | a0001 | c0001 | t0016 | g0248 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18943 | hp1 | a0001 | c0003 | t0003 | g0084 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18944 | hp1 | a0001 | c0003 | t0027 | g0207 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18944 | hp2 | a0001 | c0002 | t0007 | g0004 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18946 | hp2 | a0001 | c0003 | t0004 | g0024 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18948 | hp2 | a0002 | c0005 | t0003 | g0076 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18950 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18950 | hp2 | a0001 | c0003 | t0004 | g0202 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18951 | hp2 | a0001 | c0002 | t0007 | g0004 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18953 | hp1 | a0001 | c0001 | t0015 | g0300 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18953 | hp2 | a0001 | c0003 | t0004 | g0203 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18954 | hp1 | a0001 | c0002 | t0007 | g0004 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18954 | hp2 | a0001 | c0003 | t0003 | g0093 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18957 | hp2 | a0002 | c0005 | t0003 | g0010 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18960 | hp1 | a0001 | c0002 | t0007 | g0128 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18960 | hp2 | a0002 | c0005 | t0003 | g0066 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18961 | hp1 | a0002 | c0005 | t0026 | g0065 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18961 | hp2 | a0003 | c0006 | t0010 | g0167 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18962 | hp2 | a0011 | c0010 | t0004 | g0023 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18964 | hp1 | a0012 | c0016 | t0001 | g0105 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18964 | hp2 | a0001 | c0003 | t0004 | g0022 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18965 | hp1 | a0001 | c0002 | t0007 | g0117 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18965 | hp2 | a0001 | c0003 | t0004 | g0199 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18968 | hp1 | a0001 | c0002 | t0021 | g0104 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18968 | hp2 | a0001 | c0003 | t0004 | g0195 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18969 | hp2 | a0001 | c0003 | t0004 | g0021 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18970 | hp1 | a0002 | c0005 | t0003 | g0069 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18972 | hp1 | a0001 | c0003 | t0004 | g0181 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18973 | hp1 | a0002 | c0005 | t0025 | g0059 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18977 | hp1 | a0002 | c0005 | t0003 | g0080 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18978 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18979 | hp1 | a0001 | c0003 | t0004 | g0194 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18980 | hp1 | a0001 | c0001 | t0016 | g0252 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18980 | hp2 | a0001 | c0003 | t0004 | g0024 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18981 | hp2 | a0001 | c0003 | t0004 | g0196 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18983 | hp2 | a0001 | c0003 | t0030 | g0206 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18985 | hp1 | a0002 | c0005 | t0003 | g0074 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18987 | hp1 | a0002 | c0005 | t0003 | g0041 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18989 | hp1 | a0002 | c0005 | t0003 | g0050 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18989 | hp2 | a0001 | c0003 | t0004 | g0205 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18990 | hp2 | a0001 | c0003 | t0003 | g0089 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18994 | hp2 | a0001 | c0003 | t0004 | g0200 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18998 | hp2 | a0002 | c0005 | t0003 | g0070 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18999 | hp2 | a0001 | c0002 | t0019 | g0157 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19000 | hp2 | a0001 | c0002 | t0007 | g0118 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19003 | hp2 | a0002 | c0005 | t0003 | g0082 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19004 | hp2 | a0002 | c0005 | t0017 | g0010 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19005 | hp1 | a0002 | c0005 | t0003 | g0078 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19006 | hp2 | a0001 | c0003 | t0004 | g0210 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19030 | hp1 | a0001 | c0004 | t0022 | g0296 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19043 | hp1 | a0001 | c0004 | t0005 | g0007 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19043 | hp2 | a0001 | c0004 | t0005 | g0036 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19055 | hp2 | a0001 | c0002 | t0034 | g0134 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19058 | hp1 | a0001 | c0002 | t0007 | g0004 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19058 | hp2 | a0001 | c0003 | t0003 | g0091 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19060 | hp2 | a0002 | c0005 | t0003 | g0075 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19064 | hp1 | a0002 | c0005 | t0017 | g0079 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19066 | hp1 | a0002 | c0005 | t0003 | g0051 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19066 | hp2 | a0001 | c0003 | t0004 | g0023 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19068 | hp1 | a0001 | c0003 | t0004 | g0192 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19070 | hp1 | a0002 | c0005 | t0003 | g0062 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19070 | hp2 | a0003 | c0006 | t0010 | g0017 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19074 | hp2 | a0001 | c0003 | t0004 | g0188 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19076 | hp2 | a0001 | c0002 | t0007 | g0111 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19078 | hp1 | a0001 | c0003 | t0031 | g0191 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19078 | hp2 | a0002 | c0005 | t0003 | g0081 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19081 | hp1 | a0001 | c0001 | t0016 | g0249 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19082 | hp1 | a0006 | c0009 | t0009 | g0049 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19084 | hp1 | a0001 | c0002 | t0007 | g0004 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19084 | hp2 | a0001 | c0003 | t0004 | g0189 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19085 | hp1 | a0002 | c0005 | t0003 | g0077 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19087 | hp2 | a0002 | c0005 | t0003 | g0067 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19088 | hp1 | a0001 | c0002 | t0021 | g0136 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19088 | hp2 | a0002 | c0005 | t0003 | g0083 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19090 | hp2 | a0001 | c0003 | t0004 | g0185 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19091 | hp2 | a0003 | c0006 | t0039 | g0017 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19240 | hp1 | a0001 | c0004 | t0018 | g0225 | AFR | YRI | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA19240 | hp2 | a0001 | c0004 | t0005 | g0216 | AFR | YRI | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA20129 | hp1 | a0001 | c0004 | t0009 | g0042 | AFR | ASW | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA20129 | hp2 | a0001 | c0004 | t0028 | g0227 | AFR | ASW | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0162 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0237 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03471 | hp1 | a0001 | c0004 | t0009 | g0043 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0240 | AFR | MSL | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG06807 | hp1 | a0001 | c0004 | t0008 | g0289 | AFR | USA | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | USA | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA18955 | hp2 | a0001 | c0001 | t0038 | g0008 | EAS | JPT | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0027 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
NA21309 | hp2 | a0013 | c0019 | t0018 | g0226 | AFR | LWK | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
homoSapiens | chm13v2 | a0003 | c0006 | t0010 | g0170 | REF | REF | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
homoSapiens | grch38p0 | a0001 | c0003 | t0004 | g0182 | REF | REF | MARCHF7_chr2_159707506_159776027 | MARCHF7 | chr2 | 159707506 | 159776027 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159729057 | T | C | 1 | a0011 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.35T>C | p.Ile12Thr | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/12 | 278/6043 | 35/2115 | 12/704 | chr2 | 159729057 | |||
chr2:159743206 | C | G | 1 | a0003 | 10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
missense_variant | MODERATE | c.299C>G | p.Thr100Ser | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/12 | 542/6043 | 299/2115 | 100/704 | chr2 | 159743206 | |||
chr2:159743209 | C | T | 1 | a0013 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.302C>T | p.Thr101Ile | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/12 | 545/6043 | 302/2115 | 101/704 | chr2 | 159743209 | |||
chr2:159747861 | A | G | 1 | a0007 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.571A>G | p.Met191Val | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 814/6043 | 571/2115 | 191/704 | chr2 | 159747861 | |||
chr2:159747868 | C | T | 2 | a0002 a0005 |
36 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(33): Show |
missense_variant | MODERATE | c.578C>T | p.Thr193Ile | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 821/6043 | 578/2115 | 193/704 | chr2 | 159747868 | |||
chr2:159748003 | C | T | 2 | a0006 a0010 |
7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
missense_variant | MODERATE | c.713C>T | p.Thr238Met | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 956/6043 | 713/2115 | 238/704 | chr2 | 159748003 | |||
chr2:159748030 | G | A | 1 | a0010 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.740G>A | p.Ser247Asn | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 983/6043 | 740/2115 | 247/704 | chr2 | 159748030 | |||
chr2:159748183 | G | C | 1 | a0012 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.893G>C | p.Arg298Thr | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1136/6043 | 893/2115 | 298/704 | chr2 | 159748183 | |||
chr2:159748257 | G | A | 1 | a0005 | 8 | HG00738.hp1 HG01433.hp1 HG01515.hp2 others(5): Show |
missense_variant | MODERATE | c.967G>A | p.Ala323Thr | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1210/6043 | 967/2115 | 323/704 | chr2 | 159748257 | |||
chr2:159748425 | G | A | 1 | a0004 | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
missense_variant | MODERATE | c.1135G>A | p.Gly379Ser | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1378/6043 | 1135/2115 | 379/704 | chr2 | 159748425 | |||
chr2:159748498 | G | C | 1 | a0008 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1208G>C | p.Arg403Pro | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1451/6043 | 1208/2115 | 403/704 | chr2 | 159748498 | |||
chr2:159748615 | G | A | 1 | a0009 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.1325G>A | p.Gly442Glu | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1568/6043 | 1325/2115 | 442/704 | chr2 | 159748615 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159743084 | G | A | 1 | a0001c0011 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.177G>A | p.Ala59Ala | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/12 | 420/6043 | 177/2115 | 59/704 | chr2 | 159743084 | |||
chr2:159747941 | C | T | 2 | a0001c0002 a0012c0016 |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
synonymous_variant | LOW | c.651C>T | p.Asp217Asp | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 894/6043 | 651/2115 | 217/704 | chr2 | 159747941 | |||
chr2:159748301 | C | T | 4 | a0001c0001 a0001c0011 a0001c0014 others(1): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
synonymous_variant | LOW | c.1011C>T | p.Pro337Pro | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1254/6043 | 1011/2115 | 337/704 | chr2 | 159748301 | |||
chr2:159748655 | C | T | 1 | a0001c0014 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1365C>T | p.Ser455Ser | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1608/6043 | 1365/2115 | 455/704 | chr2 | 159748655 | |||
chr2:159748757 | T | C | 15 | a0001c0001 a0001c0002 a0001c0004 others(12): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
synonymous_variant | LOW | c.1467T>C | p.Pro489Pro | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/12 | 1710/6043 | 1467/2115 | 489/704 | chr2 | 159748757 | |||
chr2:159752543 | A | G | 1 | a0005c0017 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.1755A>G | p.Lys585Lys | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/12 | 1998/6043 | 1755/2115 | 585/704 | chr2 | 159752543 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159712509 | T | G | 9 | a0001c0003t0003 a0001c0003t0024 a0001c0004t0003 others(6): Show |
47 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-240T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/12 | 16514 | chr2 | 159712509 | ||||||
chr2:159712556 | C | G | 1 | a0001c0001t0016 | 3 | NA18942.hp2 NA18980.hp1 NA19081.hp1 |
5_prime_UTR_variant | MODIFIER | c.-193C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/12 | 16467 | chr2 | 159712556 | ||||||
chr2:159715750 | T | A | 1 | a0001c0003t0027 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-31T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/12 | 13273 | chr2 | 159715750 | ||||||
chr2:159767565 | A | G | 1 | a0002c0005t0026 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 223 | chr2 | 159767565 | ||||||
chr2:159767736 | ACTT | A | 2 | a0001c0004t0023 a0001c0004t0040 |
3 | HG01361.hp2 HG03654.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*395_*397delCTT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 395 | chr2 | 159767736 | ||||||
chr2:159767848 | G | A | 3 | a0001c0004t0018 a0001c0004t0028 a0013c0019t0018 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*506G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 506 | chr2 | 159767848 | ||||||
chr2:159767872 | A | T | 1 | a0001c0004t0022 | 2 | HG02630.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*530A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 530 | chr2 | 159767872 | ||||||
chr2:159768178 | T | G | 2 | a0001c0004t0008 a0001c0004t0022 |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*836T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 836 | chr2 | 159768178 | ||||||
chr2:159768239 | C | CT | 2 | a0003c0006t0010 a0003c0006t0039 |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*902dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 903 | INFO_REALIGN_3_PRIME | chr2 | 159768239 | |||||
chr2:159768331 | G | A | 1 | a0001c0001t0029 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*989G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 989 | chr2 | 159768331 | ||||||
chr2:159768368 | C | G | 1 | a0001c0002t0007 | 11 | NA18944.hp2 NA18950.hp1 NA18951.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1026C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1026 | chr2 | 159768368 | ||||||
chr2:159768606 | G | T | 1 | a0001c0001t0038 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1264G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1264 | chr2 | 159768606 | ||||||
chr2:159769026 | T | C | 1 | a0001c0003t0030 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1684 | chr2 | 159769026 | ||||||
chr2:159769092 | G | C | 1 | a0001c0003t0031 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1750G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1750 | chr2 | 159769092 | ||||||
chr2:159769216 | C | G | 7 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(4): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1874C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1874 | chr2 | 159769216 | ||||||
chr2:159769330 | T | C | 3 | a0001c0004t0008 a0001c0004t0013 a0001c0004t0022 |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1988T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 1988 | chr2 | 159769330 | ||||||
chr2:159769381 | G | T | 1 | a0002c0005t0025 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2039G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2039 | chr2 | 159769381 | ||||||
chr2:159769469 | C | G | 1 | a0001c0001t0012 | 6 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2127C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2127 | chr2 | 159769469 | ||||||
chr2:159769581 | G | T | 1 | a0001c0002t0021 | 2 | NA18968.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2239G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2239 | chr2 | 159769581 | ||||||
chr2:159769641 | A | G | 46 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(43): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*2299A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2299 | chr2 | 159769641 | ||||||
chr2:159769643 | C | CAT | 17 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(14): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*2315_*2316dupTA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | |||||
chr2:159769643 | C | CATAT | 15 | a0001c0001t0015 a0001c0003t0003 a0001c0004t0003 others(12): Show |
60 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2313_*2316dupTATA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | |||||
chr2:159769643 | C | CATATAT | 3 | a0001c0004t0028 a0002c0005t0017 a0006c0009t0036 |
4 | HG02258.hp1 NA19004.hp2 NA19064.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2311_*2316dupTATA others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | |||||
chr2:159769643 | C | CATATATA others(3): Show |
1 | a0001c0004t0037 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2307_*2316dupTATA others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2317 | INFO_REALIGN_3_PRIME | chr2 | 159769643 | |||||
chr2:159769712 | A | G | 1 | a0001c0004t0022 | 2 | HG02630.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2370A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2370 | chr2 | 159769712 | ||||||
chr2:159769787 | A | T | 1 | a0001c0004t0040 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2445A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2445 | chr2 | 159769787 | ||||||
chr2:159769936 | G | T | 1 | a0001c0003t0032 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2594G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2594 | chr2 | 159769936 | ||||||
chr2:159770111 | C | T | 8 | a0001c0002t0001 a0001c0002t0007 a0001c0002t0019 others(5): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*2769C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2769 | chr2 | 159770111 | ||||||
chr2:159770120 | C | T | 1 | a0001c0001t0033 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2778C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2778 | chr2 | 159770120 | ||||||
chr2:159770126 | AT | A | 17 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(14): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*2792delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2792 | INFO_REALIGN_3_PRIME | chr2 | 159770126 | |||||
chr2:159770231 | T | TATCA | 3 | a0001c0004t0018 a0001c0004t0028 a0013c0019t0018 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2892_*2895dupCAAT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 2896 | INFO_REALIGN_3_PRIME | chr2 | 159770231 | |||||
chr2:159770355 | G | A | 1 | a0006c0009t0035 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3013G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3013 | chr2 | 159770355 | ||||||
chr2:159770360 | GT | G | 4 | a0001c0004t0005 a0001c0004t0023 a0001c0004t0037 others(1): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3020delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3020 | INFO_REALIGN_3_PRIME | chr2 | 159770360 | |||||
chr2:159770373 | T | TATCA | 3 | a0001c0004t0008 a0001c0004t0013 a0001c0004t0022 |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3032_*3035dupATCA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3036 | INFO_REALIGN_3_PRIME | chr2 | 159770373 | |||||
chr2:159770387 | T | C | 8 | a0001c0002t0001 a0001c0002t0007 a0001c0002t0019 others(5): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3045T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3045 | chr2 | 159770387 | ||||||
chr2:159770469 | G | A | 6 | a0001c0002t0001 a0001c0002t0007 a0001c0002t0019 others(3): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3127G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3127 | chr2 | 159770469 | ||||||
chr2:159770539 | GATAATTG others(27): Show |
G | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3199_*3232delTAAT others(30): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3199 | INFO_REALIGN_3_PRIME | chr2 | 159770539 | |||||
chr2:159770579 | T | G | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3237T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3237 | chr2 | 159770579 | ||||||
chr2:159770582 | T | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3240T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3240 | chr2 | 159770582 | ||||||
chr2:159770583 | T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3241T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3241 | chr2 | 159770583 | ||||||
chr2:159770642 | G | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3300G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3300 | chr2 | 159770642 | ||||||
chr2:159770657 | C | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3315C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3315 | chr2 | 159770657 | ||||||
chr2:159770658 | A | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3316A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3316 | chr2 | 159770658 | ||||||
chr2:159770659 | T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3317T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3317 | chr2 | 159770659 | ||||||
chr2:159770661 | T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3319T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3319 | chr2 | 159770661 | ||||||
chr2:159770663 | T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3321T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3321 | chr2 | 159770663 | ||||||
chr2:159770667 | C | CT | 3 | a0001c0004t0018 a0001c0004t0028 a0013c0019t0018 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3326dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3327 | INFO_REALIGN_3_PRIME | chr2 | 159770667 | |||||
chr2:159770669 | G | T | 3 | a0001c0004t0018 a0001c0004t0028 a0013c0019t0018 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3327G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3327 | chr2 | 159770669 | ||||||
chr2:159770677 | T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3335T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3335 | chr2 | 159770677 | ||||||
chr2:159770679 | T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3337T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3337 | chr2 | 159770679 | ||||||
chr2:159770683 | TTTAGATA others(8): Show |
T | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3344_*3358delAGAT others(11): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3344 | INFO_REALIGN_3_PRIME | chr2 | 159770683 | |||||
chr2:159770701 | G | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3359G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3359 | chr2 | 159770701 | ||||||
chr2:159770705 | T | A | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3363T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3363 | chr2 | 159770705 | ||||||
chr2:159770706 | A | C | 1 | a0003c0006t0039 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3364A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3364 | chr2 | 159770706 | ||||||
chr2:159770771 | A | C | 1 | a0001c0002t0019 | 2 | NA18612.hp1 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3429A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3429 | chr2 | 159770771 | ||||||
chr2:159770806 | C | G | 12 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(9): Show |
103 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3464C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3464 | chr2 | 159770806 | ||||||
chr2:159770903 | T | G | 1 | a0004c0007t0011 | 9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3561T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 12/12 | 3561 | chr2 | 159770903 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:159712765 | C | T | 97 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(94): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.-143+159C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712765 | |||||||
chr2:159712834 | G | T | 3 | a0001c0004t0018g0225 a0001c0004t0028g0227 a0013c0019t0018g0226 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-143+228G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712834 | |||||||
chr2:159712943 | A | C | 1 | a0001c0001t0002g0306 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-143+337A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712943 | |||||||
chr2:159712953 | T | C | 1 | a0001c0004t0005g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-143+347T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712953 | |||||||
chr2:159712991 | G | A | 1 | a0001c0003t0004g0037 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-143+385G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159712991 | |||||||
chr2:159713059 | G | C | 3 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0001g0040 |
3 | HG00735.hp2 HG01258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-143+453G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713059 | |||||||
chr2:159713138 | T | C | 59 | a0001c0003t0003g0084 a0001c0003t0003g0087 a0001c0003t0003g0088 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-143+532T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713138 | |||||||
chr2:159713180 | A | G | 9 | a0001c0001t0002g0003 a0001c0001t0002g0299 a0001c0001t0002g0301 others(6): Show |
14 | HG00408.hp1 HG00544.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.-143+574A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713180 | |||||||
chr2:159713311 | C | G | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-143+705C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713311 | |||||||
chr2:159713522 | T | C | 179 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(176): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.-143+916T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713522 | |||||||
chr2:159713620 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-142-937T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159713620 | |||||||
chr2:159713919 | G | GT | 8 | a0001c0003t0003g0087 a0001c0003t0003g0088 a0001c0003t0003g0089 others(5): Show |
8 | HG00597.hp1 HG02040.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-142-631dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 159713919 | ||||||
chr2:159714056 | G | A | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-142-501G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714056 | |||||||
chr2:159714113 | A | G | 2 | a0001c0003t0004g0223 a0001c0003t0004g0224 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-142-444A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714113 | |||||||
chr2:159714117 | A | G | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-142-440A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714117 | |||||||
chr2:159714171 | A | G | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-142-386A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714171 | |||||||
chr2:159714220 | T | A | 3 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 |
6 | HG02257.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-142-337T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714220 | |||||||
chr2:159714408 | T | C | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-142-149T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714408 | |||||||
chr2:159714504 | A | G | 1 | a0001c0001t0006g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-142-53A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 1/11 | chr2 | 159714504 | |||||||
chr2:159714599 | G | A | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
splice_donor_variant&intron_variant | HIGH | c.-101+1G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714599 | |||||||
chr2:159714758 | C | T | 8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-101+160C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714758 | |||||||
chr2:159714798 | A | G | 1 | a0001c0001t0002g0034 | 2 | HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.-101+200A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714798 | |||||||
chr2:159714826 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-101+228C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714826 | |||||||
chr2:159714844 | G | A | 1 | a0001c0002t0001g0096 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-101+246G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159714844 | |||||||
chr2:159715034 | C | T | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-101+436C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715034 | |||||||
chr2:159715161 | A | G | 1 | a0001c0002t0001g0166 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-100-520A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715161 | |||||||
chr2:159715198 | A | G | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-100-483A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715198 | |||||||
chr2:159715272 | ATCT | A | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-100-407_-100-405d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 159715272 | ||||||
chr2:159715343 | A | G | 2 | a0003c0006t0010g0019 a0003c0006t0010g0171 |
3 | HG01257.hp2 HG01258.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.-100-338A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715343 | |||||||
chr2:159715365 | G | A | 17 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(14): Show |
20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-100-316G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715365 | |||||||
chr2:159715370 | T | C | 1 | a0004c0007t0011g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-100-311T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715370 | |||||||
chr2:159715385 | G | C | 1 | a0001c0003t0004g0181 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-100-296G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715385 | |||||||
chr2:159715493 | C | G | 1 | a0001c0002t0001g0162 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-100-188C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 2/11 | chr2 | 159715493 | |||||||
chr2:159715822 | A | G | 1 | a0004c0007t0011g0180 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-15+56A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159715822 | |||||||
chr2:159715992 | T | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+226T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159715992 | |||||||
chr2:159716008 | G | A | 83 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(80): Show |
103 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-15+242G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716008 | |||||||
chr2:159716033 | A | G | 1 | a0001c0002t0001g0231 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+267A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716033 | |||||||
chr2:159716089 | ATATTTT | A | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+325_-15+330del others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716089 | ||||||
chr2:159716138 | C | CT | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+380dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716138 | ||||||
chr2:159716207 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+441A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716207 | |||||||
chr2:159716266 | A | AT | 110 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(107): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-15+511dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716266 | ||||||
chr2:159716326 | T | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+560T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716326 | |||||||
chr2:159716400 | G | A | 1 | a0001c0004t0005g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+634G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716400 | |||||||
chr2:159716424 | A | T | 2 | a0001c0002t0001g0160 a0001c0002t0001g0161 |
2 | NA18984.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.-15+658A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716424 | |||||||
chr2:159716631 | A | G | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15+865A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716631 | |||||||
chr2:159716643 | CA | C | 88 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(85): Show |
108 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.-15+888delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159716643 | ||||||
chr2:159716715 | A | G | 2 | a0001c0004t0009g0085 a0001c0004t0009g0086 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-15+949A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716715 | |||||||
chr2:159716866 | A | G | 2 | a0001c0001t0002g0284 a0001c0001t0002g0285 |
2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-15+1100A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716866 | |||||||
chr2:159716905 | G | C | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+1139G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716905 | |||||||
chr2:159716940 | T | G | 1 | a0001c0001t0002g0245 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+1174T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159716940 | |||||||
chr2:159717089 | G | A | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+1323G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717089 | |||||||
chr2:159717195 | ATT | A | 61 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(58): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-15+1430_-15+1431d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717195 | |||||||
chr2:159717220 | G | C | 1 | a0001c0004t0023g0025 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-15+1454G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717220 | |||||||
chr2:159717260 | C | T | 2 | a0001c0002t0001g0158 a0001c0002t0001g0159 |
2 | NA18977.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-15+1494C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717260 | |||||||
chr2:159717462 | A | G | 2 | a0001c0004t0005g0221 a0001c0004t0005g0222 |
2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+1696A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717462 | |||||||
chr2:159717520 | CTT | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+1756_-15+1757d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159717520 | ||||||
chr2:159717613 | A | T | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+1847A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717613 | |||||||
chr2:159717614 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+1848G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717614 | |||||||
chr2:159717628 | T | TGTAAACC others(45): Show |
1 | a0001c0002t0019g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-15+1880_-15+1881i others(54): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159717628 | ||||||
chr2:159717857 | G | T | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+2091G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159717857 | |||||||
chr2:159718016 | G | C | 2 | a0001c0002t0001g0098 a0001c0002t0001g0099 |
2 | HG00323.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-15+2250G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718016 | |||||||
chr2:159718037 | A | G | 1 | a0001c0004t0005g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+2271A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718037 | |||||||
chr2:159718201 | A | G | 1 | a0001c0001t0002g0280 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-15+2435A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718201 | |||||||
chr2:159718239 | T | C | 4 | a0003c0006t0010g0017 a0003c0006t0010g0167 a0003c0006t0010g0168 others(1): Show |
4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+2473T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718239 | |||||||
chr2:159718715 | A | G | 85 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(82): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.-15+2949A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718715 | |||||||
chr2:159718845 | T | C | 273 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(270): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.-15+3079T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159718845 | |||||||
chr2:159719065 | C | T | 2 | a0001c0003t0004g0209 a0001c0003t0004g0210 |
2 | NA18942.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-15+3299C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719065 | |||||||
chr2:159719099 | C | T | 1 | a0009c0012t0004g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+3333C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719099 | |||||||
chr2:159719122 | G | A | 2 | a0001c0004t0009g0085 a0001c0004t0009g0086 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-15+3356G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719122 | |||||||
chr2:159719165 | A | C | 1 | a0001c0001t0002g0245 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-15+3399A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719165 | |||||||
chr2:159719274 | C | A | 87 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(84): Show |
110 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.-15+3508C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719274 | |||||||
chr2:159719413 | CCTGAAAG others(5): Show |
C | 6 | a0003c0006t0010g0017 a0003c0006t0010g0019 a0003c0006t0010g0167 others(3): Show |
7 | HG01257.hp2 HG01258.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+3649_-15+3660d others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159719413 | ||||||
chr2:159719647 | A | G | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(81): Show |
104 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-15+3881A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719647 | |||||||
chr2:159719653 | C | T | 37 | a0001c0004t0003g0060 a0001c0004t0003g0061 a0002c0005t0003g0010 others(34): Show |
37 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15+3887C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719653 | |||||||
chr2:159719708 | C | G | 1 | a0001c0002t0001g0156 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-15+3942C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719708 | |||||||
chr2:159719770 | G | A | 60 | a0001c0002t0001g0006 a0001c0002t0001g0011 a0001c0002t0001g0012 others(57): Show |
69 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.-15+4004G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719770 | |||||||
chr2:159719954 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-15+4188G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159719954 | |||||||
chr2:159720072 | C | G | 53 | a0001c0004t0003g0060 a0001c0004t0003g0061 a0001c0004t0005g0036 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-15+4306C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720072 | |||||||
chr2:159720099 | C | A | 2 | a0002c0005t0003g0050 a0002c0005t0003g0051 |
2 | NA18989.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-15+4333C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720099 | |||||||
chr2:159720154 | G | A | 1 | a0002c0005t0003g0041 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-15+4388G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720154 | |||||||
chr2:159720171 | A | G | 55 | a0001c0003t0003g0087 a0001c0003t0003g0088 a0001c0003t0003g0089 others(52): Show |
55 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-15+4405A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720171 | |||||||
chr2:159720393 | C | T | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-15+4627C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720393 | |||||||
chr2:159720422 | A | G | 1 | a0001c0001t0002g0276 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-15+4656A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720422 | |||||||
chr2:159720499 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+4733A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720499 | |||||||
chr2:159720764 | A | G | 3 | a0001c0004t0018g0225 a0001c0004t0028g0227 a0013c0019t0018g0226 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-15+4998A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720764 | |||||||
chr2:159720939 | C | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0274 a0001c0001t0002g0275 others(1): Show |
6 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+5173C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159720939 | |||||||
chr2:159721018 | C | T | 1 | a0001c0004t0005g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-15+5252C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721018 | |||||||
chr2:159721019 | G | A | 1 | a0001c0001t0014g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-15+5253G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721019 | |||||||
chr2:159721023 | A | AT | 91 | a0001c0001t0002g0163 a0001c0001t0002g0274 a0001c0001t0002g0275 others(88): Show |
94 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.-15+5272dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159721023 | ||||||
chr2:159721056 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-15+5290G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721056 | |||||||
chr2:159721309 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-15+5543T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721309 | |||||||
chr2:159721404 | C | T | 1 | a0001c0002t0001g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-15+5638C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721404 | |||||||
chr2:159721641 | C | G | 1 | a0001c0003t0004g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15+5875C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721641 | |||||||
chr2:159721671 | T | A | 1 | a0001c0004t0040g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15+5905T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721671 | |||||||
chr2:159721783 | C | T | 3 | a0001c0004t0013g0035 a0001c0004t0013g0291 a0001c0004t0013g0292 |
4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+6017C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721783 | |||||||
chr2:159721906 | A | T | 53 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-15+6140A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159721906 | |||||||
chr2:159722079 | A | G | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-15+6313A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722079 | |||||||
chr2:159722162 | A | G | 3 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0002g0273 |
3 | HG01109.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-15+6396A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722162 | |||||||
chr2:159722361 | C | T | 1 | a0008c0013t0014g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15+6595C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722361 | |||||||
chr2:159722399 | G | T | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-6610G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722399 | |||||||
chr2:159722467 | G | A | 1 | a0006c0009t0009g0044 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-14-6542G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722467 | |||||||
chr2:159722573 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-6436A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722573 | |||||||
chr2:159722617 | G | C | 1 | a0001c0004t0009g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-14-6392G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722617 | |||||||
chr2:159722706 | T | A | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-6303T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722706 | |||||||
chr2:159722878 | C | T | 7 | a0001c0004t0005g0007 a0001c0004t0005g0211 a0001c0004t0005g0219 others(4): Show |
9 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-14-6131C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159722878 | |||||||
chr2:159723067 | A | G | 1 | a0001c0001t0002g0273 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-14-5942A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723067 | |||||||
chr2:159723165 | C | T | 1 | a0001c0002t0001g0154 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-14-5844C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723165 | |||||||
chr2:159723179 | T | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-5830T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723179 | |||||||
chr2:159723286 | G | A | 1 | a0001c0002t0001g0100 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-14-5723G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723286 | |||||||
chr2:159723381 | G | T | 8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-5628G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723381 | |||||||
chr2:159723451 | G | C | 3 | a0001c0004t0018g0225 a0001c0004t0028g0227 a0013c0019t0018g0226 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-14-5558G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723451 | |||||||
chr2:159723514 | C | T | 1 | a0001c0004t0028g0227 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-14-5495C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723514 | |||||||
chr2:159723540 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-14-5469C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723540 | |||||||
chr2:159723570 | A | G | 3 | a0001c0002t0001g0138 a0001c0002t0001g0139 a0001c0002t0001g0140 |
3 | NA18747.hp2 NA18955.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-14-5439A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723570 | |||||||
chr2:159723646 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-14-5363C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723646 | |||||||
chr2:159723653 | C | T | 5 | a0001c0004t0009g0042 a0001c0004t0009g0043 a0001c0004t0018g0225 others(2): Show |
5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-5356C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723653 | |||||||
chr2:159723654 | T | C | 8 | a0001c0003t0003g0087 a0001c0003t0003g0088 a0001c0003t0003g0089 others(5): Show |
8 | HG00597.hp1 HG02040.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14-5355T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723654 | |||||||
chr2:159723814 | A | G | 1 | a0001c0002t0019g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-14-5195A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723814 | |||||||
chr2:159723861 | A | G | 2 | a0001c0004t0009g0085 a0001c0004t0009g0086 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-14-5148A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723861 | |||||||
chr2:159723876 | C | CATGT | 61 | a0001c0003t0003g0084 a0001c0003t0003g0087 a0001c0003t0003g0088 others(58): Show |
61 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-14-5132_-14-5129d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159723876 | ||||||
chr2:159723900 | C | G | 266 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(263): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.-14-5109C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159723900 | |||||||
chr2:159724088 | G | T | 5 | a0001c0004t0009g0042 a0001c0004t0009g0043 a0001c0004t0018g0225 others(2): Show |
5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-4921G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724088 | |||||||
chr2:159724216 | G | T | 2 | a0001c0004t0009g0085 a0001c0004t0009g0086 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-14-4793G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724216 | |||||||
chr2:159724225 | G | A | 1 | a0001c0004t0008g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-4784G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724225 | |||||||
chr2:159724278 | C | T | 1 | a0001c0002t0001g0137 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-14-4731C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724278 | |||||||
chr2:159724354 | T | A | 1 | a0001c0004t0008g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-14-4655T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724354 | |||||||
chr2:159724356 | G | T | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-4653G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724356 | |||||||
chr2:159724480 | A | T | 1 | a0001c0004t0009g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14-4529A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724480 | |||||||
chr2:159724721 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-4288C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724721 | |||||||
chr2:159724790 | G | A | 2 | a0001c0004t0022g0295 a0001c0004t0022g0296 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-14-4219G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159724790 | |||||||
chr2:159724868 | TC | T | 10 | a0002c0005t0003g0041 a0002c0005t0003g0075 a0002c0005t0003g0076 others(7): Show |
10 | NA18948.hp2 NA18977.hp1 NA18987.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-4138delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159724868 | ||||||
chr2:159725288 | C | T | 1 | a0001c0001t0006g0244 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-14-3721C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725288 | |||||||
chr2:159725302 | A | G | 1 | a0001c0004t0013g0292 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-3707A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725302 | |||||||
chr2:159725454 | T | C | 1 | a0001c0001t0002g0274 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-14-3555T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725454 | |||||||
chr2:159725464 | G | A | 1 | a0001c0002t0019g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-14-3545G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725464 | |||||||
chr2:159725509 | C | T | 90 | a0001c0001t0002g0032 a0001c0001t0002g0163 a0001c0001t0002g0246 others(87): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-14-3500C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725509 | |||||||
chr2:159725535 | A | AT | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-3468dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159725535 | ||||||
chr2:159725593 | G | A | 1 | a0001c0004t0005g0213 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-14-3416G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725593 | |||||||
chr2:159725673 | A | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-3336A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725673 | |||||||
chr2:159725685 | C | T | 17 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(14): Show |
20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-14-3324C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725685 | |||||||
chr2:159725918 | C | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-3091C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159725918 | |||||||
chr2:159726103 | G | T | 1 | a0001c0003t0027g0207 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-14-2906G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726103 | |||||||
chr2:159726217 | A | AGGTTT | 8 | a0001c0002t0001g0011 a0001c0002t0001g0012 a0001c0002t0001g0102 others(5): Show |
10 | NA18968.hp1 NA18979.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-2791_-14-2787d others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726217 | ||||||
chr2:159726218 | G | GGTTTGGT others(3): Show |
1 | a0001c0002t0001g0101 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-14-2787_-14-2786i others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | ||||||
chr2:159726218 | GGTTTT | G | 113 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0013 others(110): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-14-2735_-14-2731d others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | ||||||
chr2:159726218 | GGTTTTGT others(3): Show |
G | 73 | a0001c0001t0002g0029 a0001c0001t0002g0250 a0001c0001t0002g0251 others(70): Show |
77 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-14-2740_-14-2731d others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | ||||||
chr2:159726218 | GGTTTTGT others(8): Show |
G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(76): Show |
99 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.-14-2745_-14-2731d others(17): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | ||||||
chr2:159726218 | GGTTTTGT others(13): Show |
G | 17 | a0001c0001t0002g0304 a0001c0004t0005g0036 a0001c0004t0005g0213 others(14): Show |
20 | HG00639.hp1 HG01261.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-2750_-14-2731d others(22): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | ||||||
chr2:159726218 | GGTTTTGT others(18): Show |
G | 6 | a0001c0001t0002g0266 a0001c0001t0002g0268 a0001c0001t0014g0164 others(3): Show |
8 | HG02145.hp2 HG02258.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-2755_-14-2731d others(27): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726218 | ||||||
chr2:159726223 | T | G | 7 | a0001c0002t0001g0132 a0001c0002t0001g0133 a0001c0002t0001g0135 others(4): Show |
7 | HG01071.hp1 HG01978.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-14-2786T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726223 | |||||||
chr2:159726228 | T | G | 70 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0013 others(67): Show |
85 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-14-2781T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726228 | |||||||
chr2:159726233 | T | G | 43 | a0001c0002t0001g0016 a0001c0002t0001g0040 a0001c0002t0001g0130 others(40): Show |
44 | HG00438.hp1 HG00597.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-14-2776T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726233 | |||||||
chr2:159726238 | T | G | 4 | a0001c0001t0002g0271 a0001c0002t0001g0131 a0002c0005t0003g0050 others(1): Show |
4 | HG01109.hp2 NA18989.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-2771T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726238 | |||||||
chr2:159726243 | T | G | 1 | a0002c0005t0003g0083 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-14-2766T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726243 | |||||||
chr2:159726312 | G | C | 53 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.-14-2697G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726312 | |||||||
chr2:159726353 | C | T | 1 | a0008c0013t0014g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14-2656C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726353 | |||||||
chr2:159726363 | C | T | 39 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(36): Show |
39 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-14-2646C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726363 | |||||||
chr2:159726365 | C | A | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-14-2644C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726365 | |||||||
chr2:159726397 | G | A | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-2612G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726397 | |||||||
chr2:159726497 | T | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-2512T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726497 | |||||||
chr2:159726510 | C | CCT | 8 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(5): Show |
10 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-14-2497_-14-2496d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159726510 | ||||||
chr2:159726551 | C | T | 29 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(26): Show |
36 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.-14-2458C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726551 | |||||||
chr2:159726558 | G | C | 1 | a0001c0003t0004g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-14-2451G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726558 | |||||||
chr2:159726756 | T | C | 1 | a0001c0002t0001g0132 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-14-2253T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159726756 | |||||||
chr2:159727021 | C | G | 1 | a0002c0005t0003g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-14-1988C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727021 | |||||||
chr2:159727095 | A | G | 6 | a0001c0001t0002g0033 a0001c0001t0002g0279 a0001c0001t0015g0033 others(3): Show |
6 | HG00280.hp2 HG01496.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-1914A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727095 | |||||||
chr2:159727114 | A | G | 2 | a0001c0001t0002g0275 a0001c0001t0002g0286 |
2 | HG02109.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-14-1895A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727114 | |||||||
chr2:159727173 | C | T | 47 | a0001c0004t0003g0060 a0001c0004t0003g0061 a0001c0004t0009g0085 others(44): Show |
47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-14-1836C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727173 | |||||||
chr2:159727215 | G | A | 1 | a0012c0016t0001g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-14-1794G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727215 | |||||||
chr2:159727353 | C | T | 2 | a0001c0001t0006g0028 a0001c0001t0006g0235 |
3 | HG02922.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-14-1656C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727353 | |||||||
chr2:159727537 | G | A | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-14-1472G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727537 | |||||||
chr2:159727587 | C | CA | 4 | a0001c0001t0002g0299 a0001c0001t0006g0232 a0001c0001t0006g0236 others(1): Show |
4 | HG02109.hp2 HG03098.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-1421dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 159727587 | ||||||
chr2:159727589 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-1420G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727589 | |||||||
chr2:159727621 | C | T | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-1388C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727621 | |||||||
chr2:159727762 | A | C | 61 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(58): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-14-1247A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727762 | |||||||
chr2:159727812 | A | G | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-14-1197A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727812 | |||||||
chr2:159727836 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-1173G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159727836 | |||||||
chr2:159728250 | T | C | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-759T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728250 | |||||||
chr2:159728284 | A | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-725A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728284 | |||||||
chr2:159728314 | A | G | 1 | a0008c0013t0014g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-14-695A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728314 | |||||||
chr2:159728408 | A | G | 2 | a0001c0003t0004g0223 a0001c0003t0004g0224 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-14-601A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728408 | |||||||
chr2:159728480 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-529A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728480 | |||||||
chr2:159728533 | A | C | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-476A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728533 | |||||||
chr2:159728724 | A | T | 1 | a0004c0007t0011g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-14-285A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728724 | |||||||
chr2:159728887 | G | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.-14-122G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728887 | |||||||
chr2:159728966 | C | A | 1 | a0001c0002t0001g0106 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-14-43C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728966 | |||||||
chr2:159728998 | T | G | 5 | a0001c0004t0009g0042 a0001c0004t0009g0043 a0001c0004t0018g0225 others(2): Show |
5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.-14-11T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 3/11 | chr2 | 159728998 | |||||||
chr2:159729229 | C | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+54C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729229 | |||||||
chr2:159729349 | T | A | 1 | a0001c0004t0005g0214 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.153+174T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729349 | |||||||
chr2:159729445 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.153+270C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729445 | |||||||
chr2:159729491 | C | T | 2 | a0001c0004t0009g0085 a0001c0004t0009g0086 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.153+316C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729491 | |||||||
chr2:159729672 | C | CA | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(81): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.153+510dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159729672 | ||||||
chr2:159729716 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+541G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729716 | |||||||
chr2:159729752 | A | G | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.153+577A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729752 | |||||||
chr2:159729799 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+624C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729799 | |||||||
chr2:159729926 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+751A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159729926 | |||||||
chr2:159730569 | G | A | 1 | a0001c0014t0002g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.153+1394G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159730569 | |||||||
chr2:159730618 | T | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+1443T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159730618 | |||||||
chr2:159730893 | G | T | 1 | a0001c0003t0004g0201 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.153+1718G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159730893 | |||||||
chr2:159730925 | CTG | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+1752_153+1753d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159730925 | ||||||
chr2:159731014 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+1839C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731014 | |||||||
chr2:159731038 | A | T | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.153+1863A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731038 | |||||||
chr2:159731580 | C | T | 1 | a0001c0001t0002g0245 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.153+2405C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731580 | |||||||
chr2:159731583 | C | T | 1 | a0001c0002t0001g0129 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.153+2408C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731583 | |||||||
chr2:159731622 | C | T | 1 | a0003c0006t0010g0169 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.153+2447C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731622 | |||||||
chr2:159731686 | G | A | 1 | a0010c0015t0009g0288 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.153+2511G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731686 | |||||||
chr2:159731740 | G | A | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.153+2565G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731740 | |||||||
chr2:159731808 | A | C | 53 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.153+2633A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731808 | |||||||
chr2:159731879 | C | T | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+2704C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731879 | |||||||
chr2:159731894 | G | C | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.153+2719G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731894 | |||||||
chr2:159731955 | T | C | 1 | a0001c0004t0037g0218 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.153+2780T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731955 | |||||||
chr2:159731973 | G | A | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.153+2798G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731973 | |||||||
chr2:159731977 | G | A | 1 | a0001c0004t0008g0289 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.153+2802G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159731977 | |||||||
chr2:159732082 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.153+2907C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732082 | |||||||
chr2:159732083 | G | A | 1 | a0001c0001t0015g0300 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.153+2908G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732083 | |||||||
chr2:159732091 | G | A | 2 | a0001c0002t0001g0107 a0001c0002t0001g0108 |
2 | NA18943.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.153+2916G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732091 | |||||||
chr2:159732266 | T | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3091T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732266 | |||||||
chr2:159732298 | A | T | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.153+3123A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732298 | |||||||
chr2:159732420 | A | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3245A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732420 | |||||||
chr2:159732567 | T | C | 1 | a0001c0001t0012g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.153+3392T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732567 | |||||||
chr2:159732587 | G | A | 1 | a0002c0005t0003g0052 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.153+3412G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732587 | |||||||
chr2:159732642 | A | G | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+3467A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732642 | |||||||
chr2:159732659 | C | T | 1 | a0001c0004t0009g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+3484C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732659 | |||||||
chr2:159732674 | C | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3499C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732674 | |||||||
chr2:159732698 | T | TA | 4 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(1): Show |
4 | HG02040.hp1 HG02083.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.153+3529dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159732698 | ||||||
chr2:159732798 | A | G | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.153+3623A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732798 | |||||||
chr2:159732814 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.153+3639C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732814 | |||||||
chr2:159732832 | T | C | 112 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(109): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.153+3657T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732832 | |||||||
chr2:159732854 | T | G | 1 | a0001c0002t0001g0133 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.153+3679T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732854 | |||||||
chr2:159732869 | T | C | 47 | a0001c0004t0003g0060 a0001c0004t0003g0061 a0001c0004t0009g0085 others(44): Show |
47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.153+3694T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732869 | |||||||
chr2:159732981 | C | A | 61 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(58): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.153+3806C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159732981 | |||||||
chr2:159733005 | A | C | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+3830A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733005 | |||||||
chr2:159733061 | AGTTATAA others(1): Show |
A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3887_153+3894d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733061 | |||||||
chr2:159733062 | G | T | 180 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(177): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.153+3887G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733062 | |||||||
chr2:159733072 | T | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3897T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733072 | |||||||
chr2:159733099 | CATT | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+3931_153+3933d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733099 | ||||||
chr2:159733266 | T | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+4091T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733266 | |||||||
chr2:159733279 | C | T | 3 | a0001c0004t0018g0225 a0001c0004t0028g0227 a0013c0019t0018g0226 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.153+4104C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733279 | |||||||
chr2:159733307 | A | G | 8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+4132A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733307 | |||||||
chr2:159733547 | A | AT | 7 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(4): Show |
8 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.153+4374dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733547 | ||||||
chr2:159733549 | T | TA | 161 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(158): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.153+4390dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733549 | ||||||
chr2:159733549 | T | TAA | 15 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(12): Show |
18 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.153+4389_153+4390d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159733549 | ||||||
chr2:159733550 | A | T | 1 | a0004c0007t0011g0177 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.153+4375A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733550 | |||||||
chr2:159733569 | T | C | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+4394T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159733569 | |||||||
chr2:159734323 | CT | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+5159delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734323 | ||||||
chr2:159734351 | C | T | 4 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0127 others(1): Show |
4 | NA18962.hp1 NA18994.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.153+5176C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734351 | |||||||
chr2:159734402 | ATTAATTT | A | 25 | a0001c0002t0001g0001 a0001c0002t0001g0015 a0001c0002t0001g0016 others(22): Show |
34 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.153+5232_153+5238d others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734402 | ||||||
chr2:159734497 | A | T | 1 | a0001c0002t0001g0154 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.153+5322A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734497 | |||||||
chr2:159734685 | A | G | 1 | a0001c0004t0009g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.153+5510A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734685 | |||||||
chr2:159734812 | A | G | 1 | a0003c0006t0010g0019 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.153+5637A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734812 | |||||||
chr2:159734817 | G | GA | 17 | a0001c0001t0002g0009 a0001c0001t0002g0257 a0001c0001t0002g0274 others(14): Show |
19 | HG00438.hp2 HG00609.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.153+5661dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734817 | ||||||
chr2:159734817 | GAA | G | 52 | a0001c0004t0003g0060 a0001c0004t0003g0061 a0001c0004t0009g0042 others(49): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.153+5660_153+5661d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159734817 | ||||||
chr2:159734856 | A | T | 4 | a0001c0001t0002g0008 a0001c0001t0002g0245 a0001c0001t0002g0264 others(1): Show |
5 | HG01943.hp1 NA18941.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+5681A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159734856 | |||||||
chr2:159735028 | A | G | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.153+5853A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735028 | |||||||
chr2:159735058 | A | G | 1 | a0001c0001t0006g0026 | 2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.153+5883A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735058 | |||||||
chr2:159735137 | T | G | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.153+5962T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735137 | |||||||
chr2:159735240 | A | G | 10 | a0002c0005t0003g0041 a0002c0005t0003g0075 a0002c0005t0003g0076 others(7): Show |
10 | NA18948.hp2 NA18977.hp1 NA18987.hp1 others(7): Show |
intron_variant | MODIFIER | c.153+6065A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735240 | |||||||
chr2:159735307 | G | A | 5 | a0005c0008t0003g0054 a0005c0008t0003g0055 a0005c0008t0003g0056 others(2): Show |
5 | HG01934.hp2 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+6132G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735307 | |||||||
chr2:159735336 | A | G | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+6161A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735336 | |||||||
chr2:159735454 | A | G | 1 | a0008c0013t0014g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.153+6279A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735454 | |||||||
chr2:159735535 | A | T | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.153+6360A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735535 | |||||||
chr2:159735601 | A | G | 2 | a0001c0001t0002g0034 a0001c0001t0002g0263 |
3 | HG00558.hp2 HG02015.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.153+6426A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735601 | |||||||
chr2:159735614 | T | TC | 2 | a0001c0001t0006g0026 a0001c0001t0006g0234 |
3 | HG02486.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.153+6439_153+6440i others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735614 | |||||||
chr2:159735699 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.153+6524A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735699 | |||||||
chr2:159735925 | C | T | 2 | a0001c0001t0002g0255 a0001c0001t0002g0256 |
2 | HG02083.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.153+6750C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159735925 | |||||||
chr2:159736179 | G | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6882G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736179 | |||||||
chr2:159736378 | C | T | 7 | a0006c0009t0009g0044 a0006c0009t0009g0046 a0006c0009t0009g0048 others(4): Show |
7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-6683C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736378 | |||||||
chr2:159736428 | C | T | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.154-6633C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736428 | |||||||
chr2:159736603 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6458G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736603 | |||||||
chr2:159736687 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6374A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736687 | |||||||
chr2:159736806 | A | T | 311 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(308): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.154-6255A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736806 | |||||||
chr2:159736959 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-6102A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159736959 | |||||||
chr2:159737015 | A | G | 4 | a0006c0009t0009g0044 a0006c0009t0009g0048 a0006c0009t0009g0049 others(1): Show |
4 | HG00438.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-6046A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737015 | |||||||
chr2:159737054 | A | C | 1 | a0001c0001t0002g0302 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.154-6007A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737054 | |||||||
chr2:159737264 | T | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-5797T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737264 | |||||||
chr2:159737535 | G | T | 1 | a0001c0003t0004g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.154-5526G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737535 | |||||||
chr2:159737626 | A | C | 1 | a0001c0001t0002g0262 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.154-5435A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737626 | |||||||
chr2:159737649 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-5412A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737649 | |||||||
chr2:159737697 | A | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-5364A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737697 | |||||||
chr2:159737718 | G | A | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-5343G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737718 | |||||||
chr2:159737795 | A | T | 1 | a0001c0001t0002g0270 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.154-5266A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737795 | |||||||
chr2:159737987 | G | A | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-5074G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737987 | |||||||
chr2:159737995 | A | G | 1 | a0001c0004t0009g0085 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.154-5066A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159737995 | |||||||
chr2:159738016 | A | G | 47 | a0001c0003t0003g0084 a0001c0003t0003g0087 a0001c0003t0003g0088 others(44): Show |
47 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.154-5045A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738016 | |||||||
chr2:159738067 | G | T | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.154-4994G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738067 | |||||||
chr2:159738264 | C | T | 7 | a0006c0009t0009g0044 a0006c0009t0009g0046 a0006c0009t0009g0048 others(4): Show |
7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-4797C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738264 | |||||||
chr2:159738338 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.154-4723G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738338 | |||||||
chr2:159738372 | A | G | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-4689A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738372 | |||||||
chr2:159738380 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-4681A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738380 | |||||||
chr2:159738418 | C | A | 4 | a0003c0006t0010g0018 a0003c0006t0010g0019 a0003c0006t0010g0169 others(1): Show |
6 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-4643C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738418 | |||||||
chr2:159738451 | G | A | 89 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(86): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.154-4610G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738451 | |||||||
chr2:159738496 | C | T | 1 | a0004c0007t0011g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.154-4565C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738496 | |||||||
chr2:159738616 | G | A | 120 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(117): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.154-4445G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738616 | |||||||
chr2:159738714 | A | G | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-4347A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738714 | |||||||
chr2:159738811 | C | T | 3 | a0004c0007t0011g0174 a0004c0007t0011g0178 a0004c0007t0011g0179 |
3 | HG02809.hp2 HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.154-4250C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738811 | |||||||
chr2:159738922 | C | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-4139C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738922 | |||||||
chr2:159738954 | T | C | 274 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(271): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.154-4107T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159738954 | |||||||
chr2:159739109 | G | A | 2 | a0001c0002t0001g0096 a0001c0002t0007g0111 |
2 | NA19076.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.154-3952G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739109 | |||||||
chr2:159739199 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-3862A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739199 | |||||||
chr2:159739287 | C | T | 1 | a0001c0002t0019g0157 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.154-3774C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739287 | |||||||
chr2:159739373 | C | T | 5 | a0001c0004t0009g0042 a0001c0004t0009g0043 a0001c0004t0018g0225 others(2): Show |
5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-3688C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739373 | |||||||
chr2:159739392 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-3669A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739392 | |||||||
chr2:159739459 | A | T | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-3602A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739459 | |||||||
chr2:159739532 | A | G | 1 | a0001c0002t0001g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.154-3529A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739532 | |||||||
chr2:159739654 | C | T | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.154-3407C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739654 | |||||||
chr2:159739669 | A | G | 3 | a0006c0009t0009g0046 a0006c0009t0035g0045 a0006c0009t0036g0047 |
3 | HG02258.hp1 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.154-3392A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739669 | |||||||
chr2:159739832 | TAAC | T | 3 | a0001c0004t0013g0035 a0001c0004t0013g0291 a0001c0004t0013g0292 |
4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-3226_154-3224d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159739832 | ||||||
chr2:159739883 | G | A | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(81): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.154-3178G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159739883 | |||||||
chr2:159740088 | G | T | 1 | a0004c0007t0011g0174 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.154-2973G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740088 | |||||||
chr2:159740189 | T | A | 8 | a0001c0003t0004g0021 a0001c0003t0004g0185 a0001c0003t0004g0195 others(5): Show |
8 | HG03239.hp2 NA18942.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.154-2872T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740189 | |||||||
chr2:159740204 | A | G | 61 | a0001c0003t0003g0084 a0001c0003t0003g0087 a0001c0003t0003g0088 others(58): Show |
61 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.154-2857A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740204 | |||||||
chr2:159740423 | G | C | 1 | a0001c0001t0002g0264 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.154-2638G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740423 | |||||||
chr2:159740907 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-2154G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740907 | |||||||
chr2:159740916 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-2145G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159740916 | |||||||
chr2:159741029 | A | G | 3 | a0001c0001t0014g0281 a0001c0001t0014g0282 a0008c0013t0014g0283 |
3 | HG02451.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.154-2032A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741029 | |||||||
chr2:159741144 | G | T | 1 | a0001c0002t0001g0127 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.154-1917G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741144 | |||||||
chr2:159741412 | T | C | 2 | a0001c0004t0009g0042 a0001c0004t0009g0043 |
2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.154-1649T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741412 | |||||||
chr2:159741459 | A | ATCT | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-1600_154-1598d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159741459 | ||||||
chr2:159741467 | C | T | 48 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(45): Show |
48 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.154-1594C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741467 | |||||||
chr2:159741690 | T | C | 1 | a0001c0001t0014g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.154-1371T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741690 | |||||||
chr2:159741796 | A | T | 2 | a0002c0005t0003g0050 a0002c0005t0003g0051 |
2 | NA18989.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.154-1265A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741796 | |||||||
chr2:159741891 | C | G | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-1170C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741891 | |||||||
chr2:159741912 | C | CTG | 4 | a0004c0007t0011g0020 a0004c0007t0011g0175 a0004c0007t0011g0176 others(1): Show |
5 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-1137_154-1136d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159741912 | ||||||
chr2:159741914 | G | C | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-1147G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159741914 | |||||||
chr2:159742254 | T | G | 4 | a0001c0003t0004g0188 a0001c0003t0004g0189 a0001c0003t0004g0190 others(1): Show |
4 | HG00544.hp1 HG02080.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-807T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742254 | |||||||
chr2:159742257 | T | G | 53 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.154-804T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742257 | |||||||
chr2:159742433 | A | G | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-628A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742433 | |||||||
chr2:159742505 | G | A | 2 | a0001c0003t0004g0183 a0001c0003t0004g0184 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.154-556G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742505 | |||||||
chr2:159742548 | T | TA | 24 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(21): Show |
27 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.154-504dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159742548 | ||||||
chr2:159742548 | T | TAA | 61 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(58): Show |
78 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.154-505_154-504dup others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159742548 | ||||||
chr2:159742565 | C | G | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.154-496C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742565 | |||||||
chr2:159742569 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-492G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742569 | |||||||
chr2:159742670 | A | C | 53 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.154-391A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742670 | |||||||
chr2:159742704 | C | T | 1 | a0001c0001t0006g0026 | 2 | HG02486.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.154-357C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742704 | |||||||
chr2:159742763 | CCT | C | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.154-297_154-296del others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742763 | |||||||
chr2:159742928 | C | T | 1 | a0001c0001t0012g0241 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.154-133C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742928 | |||||||
chr2:159742936 | CAAAA | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.154-116_154-113del others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 159742936 | ||||||
chr2:159742982 | A | G | 48 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(45): Show |
48 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.154-79A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 4/11 | chr2 | 159742982 | |||||||
chr2:159743446 | T | C | 1 | a0001c0001t0033g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.346+193T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743446 | |||||||
chr2:159743663 | G | T | 1 | a0003c0006t0010g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.346+410G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743663 | |||||||
chr2:159743682 | T | C | 1 | a0001c0004t0008g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.346+429T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743682 | |||||||
chr2:159743691 | G | A | 2 | a0001c0002t0001g0132 a0001c0002t0034g0134 |
2 | NA19055.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.346+438G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743691 | |||||||
chr2:159743737 | CA | C | 169 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0013 others(166): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.346+497delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743737 | ||||||
chr2:159743747 | A | AAG | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(81): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.346+495_346+496ins others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743747 | ||||||
chr2:159743749 | A | AGAG | 1 | a0001c0001t0002g0009 | 3 | HG02280.hp2 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.346+496_346+497ins others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743749 | |||||||
chr2:159743749 | A | G | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(81): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.346+496A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743749 | |||||||
chr2:159743869 | A | G | 2 | a0001c0004t0009g0042 a0001c0004t0009g0043 |
2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.346+616A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743869 | |||||||
chr2:159743903 | G | A | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.346+650G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743903 | |||||||
chr2:159743927 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+674A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743927 | |||||||
chr2:159743966 | TAGG | T | 4 | a0003c0006t0010g0017 a0003c0006t0010g0167 a0003c0006t0010g0168 others(1): Show |
4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+716_346+718del others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743966 | ||||||
chr2:159743974 | C | CT | 47 | a0001c0002t0001g0006 a0001c0002t0001g0011 a0001c0002t0001g0096 others(44): Show |
52 | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.346+751dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | C | CTT | 11 | a0001c0002t0001g0012 a0001c0002t0001g0110 a0001c0002t0001g0122 others(8): Show |
12 | HG00609.hp2 HG00673.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+750_346+751dup others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | C | CTTT | 7 | a0001c0002t0001g0040 a0001c0002t0001g0124 a0001c0002t0001g0130 others(4): Show |
7 | HG00639.hp2 HG02818.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.346+749_346+751dup others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | C | CTTTT | 6 | a0001c0002t0001g0039 a0001c0002t0001g0098 a0001c0002t0001g0099 others(3): Show |
6 | HG00323.hp1 HG01258.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+748_346+751dup others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | C | CTTTTTTT others(1): Show |
5 | a0001c0002t0001g0016 a0001c0002t0001g0151 a0001c0002t0001g0152 others(2): Show |
6 | HG00099.hp2 HG00140.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+744_346+751dup others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | C | CTTTTTTT others(4): Show |
1 | a0013c0019t0018g0226 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346+741_346+751dup others(11): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | C | CTTTTTTT others(11): Show |
1 | a0001c0004t0009g0042 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.346+734_346+751dup others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | C | CTTTTTTT others(17): Show |
1 | a0001c0004t0009g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.346+728_346+751dup others(24): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743974 | CT | C | 10 | a0001c0003t0003g0087 a0001c0003t0003g0089 a0001c0003t0003g0094 others(7): Show |
11 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(8): Show |
intron_variant | MODIFIER | c.346+751delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159743974 | ||||||
chr2:159743990 | TTTTTTTT others(8): Show |
T | 6 | a0001c0002t0001g0001 a0001c0002t0001g0095 a0001c0002t0001g0143 others(3): Show |
13 | HG00738.hp2 HG00741.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.346+738_346+752del others(15): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159743990 | |||||||
chr2:159744000 | TTTTTG | T | 41 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(38): Show |
53 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.346+748_346+752del others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744000 | |||||||
chr2:159744001 | TTTTG | T | 16 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0247 others(13): Show |
16 | HG00741.hp1 HG01109.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.346+749_346+752del others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744001 | |||||||
chr2:159744002 | TTTG | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0034 a0001c0001t0002g0163 others(64): Show |
74 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.346+750_346+752del others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744002 | |||||||
chr2:159744003 | TTG | T | 39 | a0001c0001t0002g0002 a0001c0001t0002g0032 a0001c0001t0002g0255 others(36): Show |
43 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.346+751_346+752del others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744003 | |||||||
chr2:159744004 | TG | T | 15 | a0001c0001t0002g0030 a0001c0001t0002g0284 a0001c0004t0005g0216 others(12): Show |
17 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+753delG | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 159744004 | ||||||
chr2:159744005 | G | T | 85 | a0001c0002t0001g0006 a0001c0002t0001g0011 a0001c0002t0001g0012 others(82): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.346+752G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744005 | |||||||
chr2:159744009 | A | C | 1 | a0001c0001t0015g0300 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.346+756A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744009 | |||||||
chr2:159744018 | C | T | 1 | a0002c0005t0003g0074 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.346+765C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744018 | |||||||
chr2:159744113 | A | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+860A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744113 | |||||||
chr2:159744133 | G | A | 3 | a0001c0003t0003g0084 a0002c0005t0009g0097 a0002c0005t0025g0059 |
3 | HG02080.hp1 NA18943.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.346+880G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744133 | |||||||
chr2:159744235 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+982A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744235 | |||||||
chr2:159744239 | C | T | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.346+986C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744239 | |||||||
chr2:159744268 | G | A | 13 | a0001c0004t0005g0036 a0001c0004t0008g0005 a0001c0004t0008g0289 others(10): Show |
17 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.346+1015G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744268 | |||||||
chr2:159744278 | G | A | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.346+1025G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744278 | |||||||
chr2:159744301 | A | G | 53 | a0001c0003t0003g0084 a0001c0004t0003g0060 a0001c0004t0003g0061 others(50): Show |
53 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.346+1048A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744301 | |||||||
chr2:159744392 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+1139A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744392 | |||||||
chr2:159744469 | A | G | 5 | a0001c0004t0009g0042 a0001c0004t0009g0043 a0001c0004t0018g0225 others(2): Show |
5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+1216A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744469 | |||||||
chr2:159744496 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.346+1243A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744496 | |||||||
chr2:159744563 | A | G | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.347-1207A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744563 | |||||||
chr2:159744925 | A | G | 8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-845A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159744925 | |||||||
chr2:159745015 | A | G | 61 | a0001c0003t0003g0084 a0001c0003t0003g0087 a0001c0003t0003g0088 others(58): Show |
61 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.347-755A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745015 | |||||||
chr2:159745028 | T | C | 2 | a0001c0004t0003g0060 a0001c0004t0003g0061 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.347-742T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745028 | |||||||
chr2:159745060 | C | T | 2 | a0001c0001t0006g0028 a0001c0001t0006g0235 |
3 | HG02922.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.347-710C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745060 | |||||||
chr2:159745173 | A | T | 27 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(24): Show |
34 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.347-597A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745173 | |||||||
chr2:159745240 | C | T | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.347-530C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745240 | |||||||
chr2:159745278 | A | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-492A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745278 | |||||||
chr2:159745359 | G | A | 213 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(210): Show |
261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.347-411G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745359 | |||||||
chr2:159745377 | C | T | 8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-393C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745377 | |||||||
chr2:159745389 | C | G | 1 | a0001c0001t0016g0252 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.347-381C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745389 | |||||||
chr2:159745397 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-373G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745397 | |||||||
chr2:159745420 | C | T | 6 | a0001c0001t0002g0029 a0001c0001t0002g0031 a0001c0001t0002g0257 others(3): Show |
8 | HG01071.hp2 HG01081.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.347-350C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745420 | |||||||
chr2:159745458 | C | T | 1 | a0001c0001t0015g0300 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.347-312C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745458 | |||||||
chr2:159745467 | C | T | 13 | a0001c0002t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0113 others(10): Show |
13 | HG04184.hp1 NA18747.hp2 NA18941.hp2 others(10): Show |
intron_variant | MODIFIER | c.347-303C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745467 | |||||||
chr2:159745484 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.347-286A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745484 | |||||||
chr2:159745613 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.347-157G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745613 | |||||||
chr2:159745747 | A | G | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.347-23A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 5/11 | chr2 | 159745747 | |||||||
chr2:159746186 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+249C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746186 | |||||||
chr2:159746300 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+363A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746300 | |||||||
chr2:159746370 | T | G | 1 | a0001c0004t0005g0215 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.514+433T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746370 | |||||||
chr2:159746452 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+515G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746452 | |||||||
chr2:159746548 | T | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.514+611T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159746548 | |||||||
chr2:159747084 | A | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.515-721A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747084 | |||||||
chr2:159747128 | C | T | 2 | a0004c0007t0011g0176 a0004c0007t0011g0177 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.515-677C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747128 | |||||||
chr2:159747270 | C | A | 4 | a0006c0009t0009g0044 a0006c0009t0009g0048 a0006c0009t0009g0049 others(1): Show |
4 | HG00438.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.515-535C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747270 | |||||||
chr2:159747477 | A | T | 1 | a0001c0004t0013g0035 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.515-328A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 6/11 | chr2 | 159747477 | |||||||
chr2:159748949 | A | C | 1 | a0001c0001t0002g0305 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1613+46A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748949 | |||||||
chr2:159748959 | C | T | 3 | a0001c0004t0018g0225 a0001c0004t0028g0227 a0013c0019t0018g0226 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1613+56C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748959 | |||||||
chr2:159748973 | C | CT | 14 | a0001c0001t0020g0172 a0001c0004t0005g0007 a0001c0004t0005g0036 others(11): Show |
17 | HG01261.hp2 HG01361.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1613+74dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159748973 | ||||||
chr2:159748973 | C | CTT | 4 | a0001c0001t0020g0173 a0001c0004t0005g0216 a0001c0004t0005g0217 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1613+73_1613+74dup others(2): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159748973 | ||||||
chr2:159748973 | CTTTTCTT others(1): Show |
C | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1613+75_1613+82del others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159748973 | ||||||
chr2:159748977 | TC | T | 138 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(135): Show |
161 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.1613+75delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748977 | |||||||
chr2:159748978 | C | T | 117 | a0001c0001t0002g0009 a0001c0001t0002g0163 a0001c0001t0002g0255 others(114): Show |
140 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1613+75C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748978 | |||||||
chr2:159748980 | T | C | 2 | a0001c0001t0006g0026 a0001c0001t0006g0234 |
3 | HG02486.hp1 HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1613+77T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748980 | |||||||
chr2:159748987 | T | C | 85 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(82): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1613+84T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159748987 | |||||||
chr2:159749002 | G | A | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1613+99G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749002 | |||||||
chr2:159749005 | G | T | 1 | a0001c0004t0008g0293 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1613+102G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749005 | |||||||
chr2:159749013 | C | G | 1 | a0001c0001t0002g0009 | 3 | HG02280.hp2 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1613+110C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749013 | |||||||
chr2:159749104 | G | A | 1 | a0002c0005t0003g0082 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1613+201G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749104 | |||||||
chr2:159749272 | C | T | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1613+369C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749272 | |||||||
chr2:159749349 | T | G | 86 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(83): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1613+446T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749349 | |||||||
chr2:159749349 | T | TG | 5 | a0001c0004t0009g0042 a0001c0004t0009g0043 a0001c0004t0018g0225 others(2): Show |
5 | HG03471.hp1 NA19240.hp1 NA20129.hp1 others(2): Show |
intron_variant | MODIFIER | c.1613+446_1613+447i others(3): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749349 | |||||||
chr2:159749367 | G | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1613+464G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749367 | |||||||
chr2:159749567 | C | T | 1 | a0001c0004t0005g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1613+664C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749567 | |||||||
chr2:159749736 | G | T | 1 | a0001c0004t0005g0215 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1613+833G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749736 | |||||||
chr2:159749737 | C | CG | 37 | a0001c0002t0001g0095 a0001c0002t0001g0108 a0001c0002t0001g0112 others(34): Show |
38 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1613+842dupG | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159749737 | ||||||
chr2:159749740 | G | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(81): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.1613+837G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749740 | |||||||
chr2:159749740 | G | T | 1 | a0001c0001t0015g0300 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1613+837G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749740 | |||||||
chr2:159749744 | G | T | 3 | a0001c0004t0009g0085 a0001c0004t0009g0086 a0005c0008t0003g0073 |
3 | HG01433.hp1 HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1613+841G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749744 | |||||||
chr2:159749745 | GC | G | 82 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(79): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1613+843delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749745 | |||||||
chr2:159749746 | C | G | 3 | a0001c0001t0002g0255 a0001c0001t0002g0271 a0001c0001t0002g0280 |
3 | HG01109.hp2 NA19000.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1613+843C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749746 | |||||||
chr2:159749789 | T | C | 7 | a0001c0004t0005g0007 a0001c0004t0005g0211 a0001c0004t0005g0219 others(4): Show |
9 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1613+886T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159749789 | |||||||
chr2:159750056 | A | G | 1 | a0001c0002t0001g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1613+1153A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750056 | |||||||
chr2:159750143 | C | A | 1 | a0001c0002t0001g0228 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1613+1240C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750143 | |||||||
chr2:159750249 | C | T | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1613+1346C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750249 | |||||||
chr2:159750261 | T | C | 265 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(262): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1613+1358T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750261 | |||||||
chr2:159750266 | G | A | 8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1613+1363G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750266 | |||||||
chr2:159750355 | T | A | 1 | a0001c0001t0006g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1613+1452T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750355 | |||||||
chr2:159750523 | CAAAATAA others(3): Show |
C | 1 | a0001c0001t0006g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1613+1638_1613+164 others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159750523 | ||||||
chr2:159750608 | G | A | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1613+1705G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750608 | |||||||
chr2:159750646 | A | T | 60 | a0001c0002t0001g0006 a0001c0002t0001g0011 a0001c0002t0001g0012 others(57): Show |
69 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.1613+1743A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750646 | |||||||
chr2:159750649 | A | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1613+1746A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750649 | |||||||
chr2:159750758 | G | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1614-1644G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750758 | |||||||
chr2:159750773 | TTA | T | 36 | a0002c0005t0003g0010 a0002c0005t0003g0041 a0002c0005t0003g0050 others(33): Show |
36 | HG00408.hp2 HG00597.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1614-1624_1614-162 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 159750773 | ||||||
chr2:159750855 | G | A | 1 | a0001c0004t0005g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1614-1547G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750855 | |||||||
chr2:159750925 | T | G | 1 | a0001c0004t0023g0025 | 2 | HG03654.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1614-1477T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750925 | |||||||
chr2:159750976 | C | A | 3 | a0001c0004t0013g0035 a0001c0004t0013g0291 a0001c0004t0013g0292 |
4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614-1426C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159750976 | |||||||
chr2:159751818 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1614-584G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159751818 | |||||||
chr2:159752008 | C | T | 3 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0001g0040 |
3 | HG00735.hp2 HG01258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1614-394C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159752008 | |||||||
chr2:159752111 | A | G | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1614-291A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159752111 | |||||||
chr2:159752264 | G | A | 1 | a0002c0005t0003g0063 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1614-138G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 7/11 | chr2 | 159752264 | |||||||
chr2:159752651 | T | C | 23 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(20): Show |
27 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1783+80T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159752651 | |||||||
chr2:159752947 | C | T | 17 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(14): Show |
20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1783+376C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159752947 | |||||||
chr2:159753189 | G | A | 3 | a0001c0001t0016g0248 a0001c0001t0016g0249 a0001c0001t0016g0252 |
3 | NA18942.hp2 NA18980.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1783+618G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753189 | |||||||
chr2:159753483 | G | A | 1 | a0001c0001t0006g0239 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1783+912G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753483 | |||||||
chr2:159753493 | G | A | 4 | a0006c0009t0009g0044 a0006c0009t0009g0048 a0006c0009t0009g0049 others(1): Show |
4 | HG00438.hp1 HG03654.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1783+922G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753493 | |||||||
chr2:159753550 | C | CA | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1783+992dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159753550 | ||||||
chr2:159753550 | CA | C | 87 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(84): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1783+992delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159753550 | ||||||
chr2:159753644 | A | G | 2 | a0001c0001t0002g0284 a0001c0001t0002g0285 |
2 | NA18963.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1783+1073A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753644 | |||||||
chr2:159753753 | A | G | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1783+1182A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753753 | |||||||
chr2:159753869 | G | A | 267 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(264): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1783+1298G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159753869 | |||||||
chr2:159754047 | A | C | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1783+1476A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754047 | |||||||
chr2:159754656 | C | T | 1 | a0001c0001t0029g0261 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1783+2085C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754656 | |||||||
chr2:159754726 | A | G | 1 | a0003c0006t0010g0169 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1783+2155A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754726 | |||||||
chr2:159754793 | A | G | 7 | a0006c0009t0009g0044 a0006c0009t0009g0046 a0006c0009t0009g0048 others(4): Show |
7 | HG00438.hp1 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1783+2222A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754793 | |||||||
chr2:159754889 | C | T | 12 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(9): Show |
16 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1783+2318C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754889 | |||||||
chr2:159754940 | A | G | 1 | a0001c0004t0008g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1783+2369A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754940 | |||||||
chr2:159754966 | G | A | 52 | a0001c0004t0003g0060 a0001c0004t0003g0061 a0001c0004t0009g0042 others(49): Show |
52 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1783+2395G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754966 | |||||||
chr2:159754972 | A | T | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1783+2401A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754972 | |||||||
chr2:159754992 | C | A | 1 | a0001c0004t0005g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1783+2421C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159754992 | |||||||
chr2:159755192 | C | T | 1 | a0001c0002t0007g0117 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1783+2621C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755192 | |||||||
chr2:159755232 | C | T | 3 | a0001c0001t0006g0232 a0001c0001t0006g0236 a0001c0001t0006g0237 |
3 | HG02109.hp2 HG03098.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1783+2661C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755232 | |||||||
chr2:159755297 | TG | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1783+2728delG | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159755297 | ||||||
chr2:159755339 | T | C | 1 | a0001c0001t0002g0030 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1783+2768T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755339 | |||||||
chr2:159755501 | C | G | 1 | a0005c0017t0003g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1783+2930C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755501 | |||||||
chr2:159755781 | T | C | 54 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0004t0003g0060 others(51): Show |
54 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1783+3210T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755781 | |||||||
chr2:159755852 | T | C | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1783+3281T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159755852 | |||||||
chr2:159756099 | A | T | 5 | a0001c0004t0005g0213 a0001c0004t0005g0214 a0001c0004t0005g0215 others(2): Show |
5 | HG01261.hp2 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1784-3127A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756099 | |||||||
chr2:159756189 | A | G | 2 | a0006c0009t0009g0044 a0006c0009t0009g0049 |
2 | HG00438.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1784-3037A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756189 | |||||||
chr2:159756494 | C | G | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1784-2732C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756494 | |||||||
chr2:159756687 | C | CA | 13 | a0001c0001t0002g0034 a0001c0001t0002g0258 a0001c0003t0003g0088 others(10): Show |
14 | HG00544.hp1 HG00597.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1784-2512dupA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | ||||||
chr2:159756687 | CA | C | 50 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(47): Show |
65 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1784-2512delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | ||||||
chr2:159756687 | CAA | C | 25 | a0001c0001t0002g0264 a0001c0001t0002g0274 a0001c0001t0006g0232 others(22): Show |
27 | HG00438.hp1 HG01943.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1784-2513_1784-251 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | ||||||
chr2:159756687 | CAAA | C | 59 | a0001c0001t0002g0009 a0001c0001t0002g0275 a0001c0001t0002g0286 others(56): Show |
63 | HG00438.hp2 HG00597.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.1784-2514_1784-251 others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | ||||||
chr2:159756687 | CAAAA | C | 28 | a0001c0001t0006g0233 a0001c0001t0006g0234 a0001c0001t0006g0239 others(25): Show |
29 | HG00735.hp1 HG00735.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.1784-2515_1784-251 others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | ||||||
chr2:159756687 | CAAAAA | C | 73 | a0001c0001t0006g0243 a0001c0002t0001g0001 a0001c0002t0001g0006 others(70): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1784-2516_1784-251 others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756687 | ||||||
chr2:159756707 | AAAAAAAA others(1): Show |
A | 11 | a0001c0004t0008g0005 a0001c0004t0008g0290 a0001c0004t0008g0293 others(8): Show |
15 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1784-2517_1784-251 others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756707 | ||||||
chr2:159756714 | A | C | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1784-2512A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756714 | |||||||
chr2:159756766 | C | T | 1 | a0001c0003t0004g0223 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1784-2460C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756766 | |||||||
chr2:159756820 | CAA | C | 13 | a0001c0001t0002g0277 a0001c0004t0008g0005 a0001c0004t0008g0289 others(10): Show |
17 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1784-2403_1784-240 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756820 | ||||||
chr2:159756895 | G | GTTTGTT | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1784-2321_1784-231 others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 159756895 | ||||||
chr2:159756917 | G | A | 8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1784-2309G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159756917 | |||||||
chr2:159757114 | C | T | 3 | a0001c0004t0018g0225 a0001c0004t0028g0227 a0013c0019t0018g0226 |
3 | NA19240.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1784-2112C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757114 | |||||||
chr2:159757505 | G | C | 1 | a0001c0002t0001g0131 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1784-1721G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757505 | |||||||
chr2:159757586 | C | T | 2 | a0001c0001t0014g0164 a0001c0001t0033g0165 |
2 | HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1784-1640C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757586 | |||||||
chr2:159757743 | C | T | 47 | a0001c0004t0003g0060 a0001c0004t0003g0061 a0001c0004t0009g0085 others(44): Show |
47 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1784-1483C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757743 | |||||||
chr2:159757781 | A | G | 1 | a0001c0002t0001g0114 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1784-1445A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757781 | |||||||
chr2:159757812 | C | T | 3 | a0001c0002t0001g0100 a0001c0002t0001g0112 a0001c0002t0001g0116 |
3 | NA18972.hp2 NA18985.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1784-1414C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757812 | |||||||
chr2:159757969 | C | T | 1 | a0001c0001t0002g0258 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1784-1257C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159757969 | |||||||
chr2:159758165 | T | C | 2 | a0002c0005t0003g0064 a0002c0005t0026g0065 |
2 | HG02083.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1784-1061T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758165 | |||||||
chr2:159758247 | A | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1784-979A>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758247 | |||||||
chr2:159758354 | T | A | 1 | a0001c0002t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1784-872T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758354 | |||||||
chr2:159758546 | T | G | 4 | a0001c0002t0001g0125 a0001c0002t0001g0126 a0001c0002t0001g0127 others(1): Show |
4 | NA18962.hp1 NA18994.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784-680T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758546 | |||||||
chr2:159758549 | G | C | 265 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(262): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1784-677G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758549 | |||||||
chr2:159758742 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1784-484C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 8/11 | chr2 | 159758742 | |||||||
chr2:159759503 | A | AT | 33 | a0001c0003t0003g0087 a0001c0003t0003g0088 a0001c0003t0003g0089 others(30): Show |
34 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1893+181dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159759503 | ||||||
chr2:159759503 | AT | A | 86 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(83): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1893+181delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159759503 | ||||||
chr2:159759721 | A | G | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1893+386A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159759721 | |||||||
chr2:159759756 | A | C | 1 | a0001c0001t0002g0264 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1893+421A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159759756 | |||||||
chr2:159759931 | TACA | T | 8 | a0004c0007t0011g0020 a0004c0007t0011g0174 a0004c0007t0011g0175 others(5): Show |
9 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.1893+598_1893+600d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159759931 | ||||||
chr2:159759991 | T | A | 1 | a0001c0004t0005g0214 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1893+656T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159759991 | |||||||
chr2:159760362 | C | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1893+1027C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760362 | |||||||
chr2:159760364 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1893+1029A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760364 | |||||||
chr2:159760464 | T | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1893+1129T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760464 | |||||||
chr2:159760598 | TA | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0270 |
3 | NA18966.hp2 NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1893+1266delA | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159760598 | ||||||
chr2:159760708 | C | CT | 145 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(142): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1893+1379dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159760708 | ||||||
chr2:159760715 | G | T | 266 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(263): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.1893+1380G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760715 | |||||||
chr2:159760724 | T | C | 8 | a0001c0002t0001g0015 a0001c0002t0001g0016 a0001c0002t0001g0142 others(5): Show |
10 | HG00099.hp2 HG00140.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1893+1389T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760724 | |||||||
chr2:159760820 | T | A | 1 | a0002c0005t0003g0066 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1893+1485T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760820 | |||||||
chr2:159760957 | G | C | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1893+1622G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159760957 | |||||||
chr2:159761020 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1893+1685C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761020 | |||||||
chr2:159761027 | A | AT | 66 | a0001c0001t0002g0260 a0001c0001t0014g0281 a0001c0001t0014g0282 others(63): Show |
67 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1893+1709dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761027 | ||||||
chr2:159761027 | AT | A | 6 | a0001c0001t0002g0264 a0001c0002t0001g0113 a0001c0002t0001g0149 others(3): Show |
6 | HG01168.hp2 HG01943.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.1893+1709delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761027 | ||||||
chr2:159761270 | C | T | 1 | a0001c0004t0040g0212 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1894-1610C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761270 | |||||||
chr2:159761326 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1894-1554G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761326 | |||||||
chr2:159761371 | A | G | 1 | a0001c0001t0002g0269 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1894-1509A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761371 | |||||||
chr2:159761406 | C | CT | 11 | a0001c0003t0004g0197 a0001c0003t0004g0199 a0001c0003t0004g0223 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1894-1449dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | C | CTT | 7 | a0001c0004t0005g0036 a0001c0004t0005g0213 a0001c0004t0005g0214 others(4): Show |
8 | HG01261.hp2 HG01361.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1894-1450_1894-144 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | C | CTTT | 10 | a0001c0004t0005g0217 a0001c0004t0008g0005 a0001c0004t0008g0289 others(7): Show |
14 | HG00639.hp1 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1894-1451_1894-144 others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | C | CTTTT | 23 | a0001c0002t0001g0100 a0001c0002t0001g0106 a0001c0002t0001g0109 others(20): Show |
26 | HG00280.hp1 HG00735.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1894-1452_1894-144 others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | C | CTTTTT | 56 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(53): Show |
69 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1894-1453_1894-144 others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | C | CTTTTTT | 23 | a0001c0002t0001g0038 a0001c0002t0001g0040 a0001c0002t0001g0096 others(20): Show |
28 | HG00673.hp1 HG00735.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.1894-1454_1894-144 others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | CT | C | 6 | a0001c0003t0004g0194 a0001c0003t0004g0209 a0001c0004t0009g0086 others(3): Show |
6 | HG02080.hp1 HG02647.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1894-1449delT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | CTT | C | 51 | a0001c0003t0003g0084 a0001c0003t0003g0087 a0001c0003t0003g0088 others(48): Show |
51 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1894-1450_1894-144 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | CTTT | C | 6 | a0001c0003t0003g0090 a0001c0004t0018g0225 a0001c0004t0028g0227 others(3): Show |
6 | HG02132.hp1 HG02280.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.1894-1451_1894-144 others(7): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | CTTTTT | C | 22 | a0001c0001t0002g0257 a0001c0001t0002g0259 a0001c0001t0002g0274 others(19): Show |
25 | HG02056.hp2 HG02109.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1894-1453_1894-144 others(9): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761406 | CTTTTTT | C | 59 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(56): Show |
76 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1894-1454_1894-144 others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761406 | ||||||
chr2:159761537 | C | CCCAAGTA others(1): Show |
8 | a0003c0006t0010g0017 a0003c0006t0010g0018 a0003c0006t0010g0019 others(5): Show |
10 | HG00735.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1894-1341_1894-133 others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 159761537 | ||||||
chr2:159761574 | C | A | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1894-1306C>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761574 | |||||||
chr2:159761611 | C | T | 2 | a0001c0004t0009g0085 a0001c0004t0009g0086 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1894-1269C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761611 | |||||||
chr2:159761777 | A | G | 1 | a0001c0004t0008g0294 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1894-1103A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761777 | |||||||
chr2:159761875 | A | G | 85 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(82): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1894-1005A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159761875 | |||||||
chr2:159762064 | A | G | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1894-816A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762064 | |||||||
chr2:159762095 | T | C | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1894-785T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762095 | |||||||
chr2:159762444 | T | C | 2 | a0001c0004t0009g0042 a0001c0004t0009g0043 |
2 | HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1894-436T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762444 | |||||||
chr2:159762477 | A | C | 1 | a0001c0002t0001g0135 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1894-403A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762477 | |||||||
chr2:159762558 | T | A | 1 | a0008c0013t0014g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1894-322T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762558 | |||||||
chr2:159762595 | T | A | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1894-285T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762595 | |||||||
chr2:159762719 | A | G | 2 | a0001c0001t0014g0281 a0001c0001t0014g0282 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1894-161A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762719 | |||||||
chr2:159762722 | T | G | 266 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(263): Show |
314 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1894-158T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762722 | |||||||
chr2:159762775 | A | G | 1 | a0001c0003t0004g0196 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1894-105A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762775 | |||||||
chr2:159762793 | A | G | 17 | a0001c0001t0006g0026 a0001c0001t0006g0028 a0001c0001t0006g0232 others(14): Show |
20 | HG02109.hp2 HG02145.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1894-87A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 9/11 | chr2 | 159762793 | |||||||
chr2:159763109 | A | C | 2 | a0005c0008t0003g0072 a0005c0008t0003g0073 |
2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2007+116A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763109 | |||||||
chr2:159763383 | T | A | 1 | a0001c0001t0002g0264 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2007+390T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763383 | |||||||
chr2:159763734 | TC | T | 4 | a0001c0002t0001g0100 a0001c0002t0001g0106 a0001c0002t0001g0112 others(1): Show |
4 | NA18972.hp2 NA18985.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2007+742delC | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763734 | |||||||
chr2:159763853 | C | T | 2 | a0001c0001t0014g0281 a0001c0001t0014g0282 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2008-773C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159763853 | |||||||
chr2:159764211 | T | G | 1 | a0001c0001t0002g0273 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2008-415T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764211 | |||||||
chr2:159764212 | T | TGTGTGTG others(6): Show |
2 | a0001c0003t0003g0084 a0001c0004t0003g0061 |
2 | HG03579.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.2008-414_2008-413i others(15): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764212 | |||||||
chr2:159764212 | T | TTG | 7 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0029 others(4): Show |
8 | HG02280.hp2 HG02300.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2008-371_2008-370d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | T | TTGTG | 15 | a0001c0001t0002g0259 a0001c0001t0002g0262 a0001c0001t0002g0263 others(12): Show |
19 | HG00558.hp2 HG00639.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.2008-373_2008-370d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | T | TTGTGTG | 2 | a0001c0001t0002g0031 a0001c0001t0014g0282 |
3 | HG01081.hp1 HG02965.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2008-375_2008-370d others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | T | TTGTGTGT others(1): Show |
4 | a0001c0001t0002g0257 a0001c0001t0014g0281 a0001c0004t0022g0296 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2008-377_2008-370d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | TTG | T | 29 | a0001c0001t0002g0009 a0001c0001t0002g0246 a0001c0001t0002g0247 others(26): Show |
31 | HG00140.hp2 HG01074.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.2008-371_2008-370d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | TTGTG | T | 19 | a0001c0001t0002g0032 a0001c0001t0002g0254 a0001c0001t0002g0255 others(16): Show |
20 | HG00280.hp1 HG01074.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.2008-373_2008-370d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | TTGTGTG | T | 15 | a0001c0001t0002g0003 a0001c0001t0002g0299 a0001c0001t0002g0301 others(12): Show |
20 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.2008-375_2008-370d others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | TTGTGTGT others(1): Show |
T | 5 | a0001c0001t0014g0164 a0001c0002t0001g0001 a0001c0002t0001g0103 others(2): Show |
5 | HG00673.hp1 HG01943.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.2008-377_2008-370d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | TTGTGTGT others(3): Show |
T | 78 | a0001c0001t0002g0305 a0001c0001t0033g0165 a0001c0002t0001g0001 others(75): Show |
95 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2008-379_2008-370d others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764212 | TTGTGTGT others(5): Show |
T | 4 | a0001c0002t0001g0013 a0001c0002t0001g0096 a0001c0002t0001g0160 others(1): Show |
4 | NA18990.hp1 NA19054.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008-381_2008-370d others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764212 | ||||||
chr2:159764241 | T | TGTGC | 4 | a0003c0006t0010g0017 a0003c0006t0010g0167 a0003c0006t0010g0168 others(1): Show |
4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2008-382_2008-381i others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764241 | ||||||
chr2:159764251 | T | C | 1 | a0010c0015t0009g0288 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2008-375T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764251 | |||||||
chr2:159764253 | T | C | 3 | a0001c0004t0018g0225 a0002c0005t0009g0097 a0010c0015t0009g0288 |
3 | HG02080.hp1 HG03710.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2008-373T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764253 | |||||||
chr2:159764255 | T | C | 40 | a0001c0003t0003g0087 a0001c0003t0003g0088 a0001c0003t0003g0089 others(37): Show |
42 | HG00280.hp1 HG00558.hp1 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.2008-371T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764255 | |||||||
chr2:159764255 | T | TGC | 21 | a0001c0003t0003g0091 a0001c0003t0003g0094 a0001c0003t0004g0021 others(18): Show |
23 | HG00099.hp1 HG00597.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.2008-364_2008-363d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGCGC | 3 | a0001c0003t0004g0194 a0001c0003t0004g0197 a0013c0019t0018g0226 |
3 | NA18940.hp2 NA18979.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2008-366_2008-363d others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGCGCGCG others(1): Show |
4 | a0001c0004t0003g0061 a0005c0008t0003g0054 a0005c0008t0003g0055 others(1): Show |
4 | HG01433.hp1 HG02273.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2008-370_2008-363d others(10): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGC | 3 | a0001c0004t0005g0214 a0001c0004t0005g0220 a0007c0018t0004g0187 |
3 | HG00544.hp1 HG01261.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGCGC | 3 | a0001c0004t0009g0042 a0001c0004t0009g0043 a0006c0009t0035g0045 |
3 | HG02280.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(8): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGCGCG others(5): Show |
1 | a0006c0009t0009g0048 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGCGCG others(7): Show |
1 | a0005c0008t0003g0068 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGCGCG others(9): Show |
1 | a0005c0017t0003g0058 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGCG others(3): Show |
3 | a0002c0005t0003g0076 a0002c0005t0026g0065 a0006c0009t0009g0046 |
3 | HG03195.hp1 NA18948.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(12): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(5): Show |
2 | a0002c0005t0003g0050 a0002c0005t0003g0066 |
2 | NA18960.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(7): Show |
2 | a0002c0005t0003g0069 a0005c0008t0003g0056 |
2 | HG01975.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(5): Show |
1 | a0002c0005t0003g0051 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(14): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(7): Show |
2 | a0002c0005t0003g0063 a0002c0005t0003g0083 |
2 | HG02135.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(9): Show |
3 | a0002c0005t0003g0074 a0005c0008t0003g0057 a0005c0008t0003g0072 |
3 | HG01515.hp2 HG01934.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(7): Show |
1 | a0006c0009t0036g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2008-370_2008-369i others(16): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(9): Show |
7 | a0002c0005t0003g0010 a0002c0005t0003g0062 a0002c0005t0003g0075 others(4): Show |
7 | NA18957.hp2 NA18977.hp1 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.2008-370_2008-369i others(18): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(11): Show |
1 | a0002c0005t0003g0052 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2008-370_2008-369i others(20): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(11): Show |
4 | a0002c0005t0003g0067 a0002c0005t0003g0078 a0002c0005t0003g0081 others(1): Show |
4 | NA18973.hp1 NA19005.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.2008-370_2008-369i others(20): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(13): Show |
5 | a0002c0005t0003g0041 a0002c0005t0003g0053 a0002c0005t0003g0070 others(2): Show |
5 | HG00408.hp2 NA18987.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2008-370_2008-369i others(22): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(15): Show |
2 | a0002c0005t0003g0071 a0006c0009t0009g0044 |
2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.2008-370_2008-369i others(24): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764255 | T | TGTGTGTG others(21): Show |
1 | a0001c0004t0003g0060 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2008-370_2008-369i others(30): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764255 | ||||||
chr2:159764257 | C | CGT | 5 | a0001c0004t0005g0007 a0001c0004t0005g0211 a0001c0004t0005g0219 others(2): Show |
7 | HG02055.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2008-368_2008-367i others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 159764257 | ||||||
chr2:159764257 | C | T | 2 | a0001c0004t0005g0220 a0001c0004t0037g0218 |
2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2008-369C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764257 | |||||||
chr2:159764258 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2008-368G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764258 | |||||||
chr2:159764337 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2008-289G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 10/11 | chr2 | 159764337 | |||||||
chr2:159764747 | A | G | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2056+73A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159764747 | |||||||
chr2:159764843 | G | GT | 176 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(173): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2056+180dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159764843 | ||||||
chr2:159764901 | C | CT | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2056+237dupT | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159764901 | ||||||
chr2:159764911 | T | C | 9 | a0001c0004t0008g0005 a0001c0004t0008g0289 a0001c0004t0008g0290 others(6): Show |
12 | HG00639.hp1 HG02257.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2056+237T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159764911 | |||||||
chr2:159764919 | A | C | 1 | a0001c0001t0006g0233 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2056+245A>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159764919 | |||||||
chr2:159765002 | A | G | 1 | a0001c0002t0001g0149 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2056+328A>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765002 | |||||||
chr2:159765102 | T | C | 1 | a0001c0002t0001g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2056+428T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765102 | |||||||
chr2:159765206 | G | GTT | 81 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(78): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.2056+540_2056+541d others(4): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159765206 | ||||||
chr2:159765206 | G | GTTT | 4 | a0001c0001t0002g0009 a0001c0001t0002g0274 a0001c0001t0002g0275 others(1): Show |
6 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2056+539_2056+541d others(5): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159765206 | ||||||
chr2:159765228 | G | T | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2056+554G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765228 | |||||||
chr2:159765413 | T | G | 23 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(20): Show |
27 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.2056+739T>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765413 | |||||||
chr2:159765414 | G | A | 3 | a0001c0004t0013g0035 a0001c0004t0013g0291 a0001c0004t0013g0292 |
4 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2056+740G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765414 | |||||||
chr2:159765617 | C | G | 1 | a0001c0002t0001g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2056+943C>G | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765617 | |||||||
chr2:159765662 | T | C | 1 | a0001c0002t0001g0098 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2056+988T>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765662 | |||||||
chr2:159765854 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2056+1180C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159765854 | |||||||
chr2:159766057 | CAT | C | 15 | a0001c0004t0005g0007 a0001c0004t0005g0036 a0001c0004t0005g0211 others(12): Show |
18 | HG01261.hp2 HG01361.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2057-1226_2057-122 others(6): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766057 | |||||||
chr2:159766119 | G | C | 97 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(94): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.2057-1165G>C | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766119 | |||||||
chr2:159766119 | G | T | 4 | a0003c0006t0010g0017 a0003c0006t0010g0167 a0003c0006t0010g0168 others(1): Show |
4 | HG02135.hp1 NA18961.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2057-1165G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766119 | |||||||
chr2:159766385 | G | T | 1 | a0008c0013t0014g0283 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2057-899G>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766385 | |||||||
chr2:159766450 | C | T | 93 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0011 others(90): Show |
113 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2057-834C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766450 | |||||||
chr2:159766855 | C | T | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2057-429C>T | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159766855 | |||||||
chr2:159767019 | C | CTTGAACC others(118): Show |
1 | a0001c0001t0033g0165 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2057-250_2057-249i others(127): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159767019 | ||||||
chr2:159767019 | C | CTTGAACC others(120): Show |
1 | a0001c0001t0014g0164 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2057-250_2057-249i others(129): Show |
MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 159767019 | ||||||
chr2:159767041 | T | A | 2 | a0001c0001t0020g0172 a0001c0001t0020g0173 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2057-243T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767041 | |||||||
chr2:159767079 | G | A | 85 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(82): Show |
105 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2057-205G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767079 | |||||||
chr2:159767089 | G | A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0274 a0001c0001t0002g0275 others(1): Show |
6 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2057-195G>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767089 | |||||||
chr2:159767240 | T | A | 1 | a0001c0002t0001g0123 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2057-44T>A | MARCHF7 | ENSG00000136536.15 | transcript | ENST00000409175.6 | protein_coding | 11/11 | chr2 | 159767240 |