Variant report
Variant | esv20376 |
---|---|
Chromosome Location | chr8:47725589-47775860 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:320)
- CpG islands (count:305)
- Chromatin interactive region (count:0)
- LncRNA region (count:84)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No. | Transcrition factor | Chromosome Location | Cell Line | Cell type | Cell Stage | Matched TF binding sites |
---|---|---|---|---|---|---|
1 | BACH1 | chr8:47770297-47770313 | H1-hESC | embryonic stem cell: | n/a | n/a |
2 | BACH1 | chr8:47750627-47750683 | H1-hESC | embryonic stem cell: | n/a | n/a |
3 | BATF | chr8:47738438-47738681 | GM12878 | blood: | n/a | chr8:47738534-47738545 |
4 | BATF | chr8:47741055-47741204 | GM12878 | blood: | n/a | n/a |
5 | BATF | chr8:47742552-47742702 | GM12878 | blood: | n/a | n/a |
6 | BATF | chr8:47742543-47742780 | GM12878 | blood: | n/a | n/a |
7 | BATF | chr8:47742058-47742352 | GM12878 | blood: | n/a | n/a |
8 | BATF | chr8:47742166-47742315 | GM12878 | blood: | n/a | n/a |
9 | BCL11A | chr8:47741063-47741196 | GM12878 | blood: | n/a | n/a |
10 | BCL11A | chr8:47742011-47742327 | GM12878 | blood: | n/a | n/a |
11 | BCL11A | chr8:47742493-47742715 | GM12878 | blood: | n/a | n/a |
12 | BCL11A | chr8:47742173-47742308 | GM12878 | blood: | n/a | n/a |
13 | BCL11A | chr8:47742558-47742696 | GM12878 | blood: | n/a | n/a |
14 | BCL11A | chr8:47741045-47741214 | GM12878 | blood: | n/a | n/a |
15 | BHLHE40 | chr8:47741998-47742438 | HepG2 | liver: | n/a | n/a |
16 | BHLHE40 | chr8:47741043-47741216 | HepG2 | liver: | n/a | n/a |
17 | BHLHE40 | chr8:47742538-47742866 | HepG2 | liver: | n/a | n/a |
18 | CEBPB | chr8:47769177-47769401 | A549 | lung: | n/a | n/a |
19 | CEBPB | chr8:47771800-47772967 | A549 | lung: | n/a | chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977 |
20 | CEBPB | chr8:47726154-47726589 | A549 | lung: | n/a | n/a |
21 | CEBPB | chr8:47755769-47755984 | A549 | lung: | n/a | n/a |
22 | CEBPB | chr8:47750993-47751208 | A549 | lung: | n/a | chr8:47751033-47751044 |
23 | CEBPB | chr8:47737694-47737724 | HepG2 | liver: | n/a | n/a |
24 | CEBPB | chr8:47773617-47773955 | IMR90 | lung: | n/a | n/a |
25 | CEBPB | chr8:47760243-47760576 | K562 | blood: | n/a | chr8:47760422-47760435 chr8:47760424-47760433 chr8:47760423-47760434 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760424-47760433 chr8:47760422-47760435 chr8:47760422-47760433 chr8:47760422-47760435 chr8:47760422-47760433 |
26 | CEBPB | chr8:47766240-47766570 | A549 | lung: | n/a | chr8:47766390-47766401 |
27 | CEBPB | chr8:47728521-47729026 | HepG2 | liver: | n/a | n/a |
28 | CEBPB | chr8:47770771-47771000 | A549 | lung: | n/a | chr8:47770927-47770938 |
29 | CEBPB | chr8:47752209-47752790 | A549 | lung: | n/a | n/a |
30 | CEBPB | chr8:47735917-47736098 | HepG2 | liver: | n/a | n/a |
31 | CEBPB | chr8:47767893-47768218 | HepG2 | liver: | n/a | n/a |
32 | CEBPB | chr8:47753716-47755048 | A549 | lung: | n/a | n/a |
33 | CEBPB | chr8:47773629-47774333 | HepG2 | liver: | n/a | n/a |
34 | CEBPB | chr8:47729582-47729782 | IMR90 | lung: | n/a | chr8:47729734-47729745 |
35 | CEBPB | chr8:47757331-47758282 | HepG2 | liver: | n/a | n/a |
36 | CEBPB | chr8:47754786-47755004 | H1-hESC | embryonic stem cell: | n/a | n/a |
37 | CEBPB | chr8:47754666-47755099 | MCF-7 | breast: | n/a | n/a |
38 | CEBPB | chr8:47752678-47752878 | K562 | blood: | n/a | n/a |
39 | CEBPB | chr8:47771804-47772479 | IMR90 | lung: | n/a | chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977 |
40 | CEBPB | chr8:47733822-47733874 | HepG2 | liver: | n/a | n/a |
41 | CEBPB | chr8:47767024-47767380 | HepG2 | liver: | n/a | chr8:47767152-47767163 |
42 | CEBPB | chr8:47754701-47755059 | IMR90 | lung: | n/a | n/a |
43 | CEBPB | chr8:47726092-47726550 | MCF-7 | breast: | n/a | n/a |
44 | CEBPB | chr8:47730645-47730867 | HepG2 | liver: | n/a | n/a |
45 | CEBPB | chr8:47731371-47731837 | HepG2 | liver: | n/a | n/a |
46 | CEBPB | chr8:47771818-47772113 | K562 | blood: | n/a | chr8:47771968-47771977 chr8:47771966-47771979 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771966-47771977 chr8:47771968-47771977 chr8:47771967-47771978 chr8:47771966-47771979 chr8:47771966-47771979 chr8:47771968-47771977 |
47 | CEBPB | chr8:47767862-47768307 | A549 | lung: | n/a | n/a |
48 | CEBPB | chr8:47752270-47752699 | IMR90 | lung: | n/a | n/a |
49 | CEBPB | chr8:47730627-47730869 | A549 | lung: | n/a | n/a |
50 | CEBPB | chr8:47766223-47766564 | HepG2 | liver: | n/a | chr8:47766390-47766401 |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:47751623-47751673 | NT2-D1 | testis: | n/a |
2 | chr8:47751953-47752003 | U87 | brain: | n/a |
3 | chr8:47748435-47748485 | U87 | brain: | n/a |
4 | chr8:47751953-47752003 | HMEC | breast: | n/a |
5 | chr8:47751953-47752003 | SK-N-SH_RA | brain: | n/a |
6 | chr8:47748435-47748485 | LNCaP | prostate: | n/a |
7 | chr8:47751953-47752003 | T-47D | breast: | n/a |
8 | chr8:47751494-47751544 | AoSMC | blood vessel: | n/a |
9 | chr8:47761906-47761956 | CMK | blood: | n/a |
10 | chr8:47751953-47752003 | AG09309 | skin: | n/a |
11 | chr8:47761906-47761956 | HCPEpiC | choroid plexus: | n/a |
12 | chr8:47761906-47761956 | MCF-7 | breast: | n/a |
13 | chr8:47748435-47748485 | NHDF-neo | bronchial: | n/a |
14 | chr8:47751494-47751544 | GM06990 | blood: | n/a |
15 | chr8:47748435-47748485 | HAEpiC | amniotic membrane: | n/a |
16 | chr8:47751494-47751544 | ECC-1 | luminal epithelium: | n/a |
17 | chr8:47751623-47751673 | SK-N-SH_RA | brain: | n/a |
18 | chr8:47751953-47752003 | HCT-116 | colon: | n/a |
19 | chr8:47748435-47748485 | H1-hESC | embryonic stem cell: | embryo |
20 | chr8:47748435-47748485 | HL-60 | blood: | n/a |
21 | chr8:47751494-47751544 | SK-N-SH | brain: | n/a |
22 | chr8:47748435-47748485 | NT2-D1 | testis: | n/a |
23 | chr8:47748435-47748485 | SK-N-SH_RA | brain: | n/a |
24 | chr8:47751623-47751673 | HPAEpiC | pulmonary alveolar: | n/a |
25 | chr8:47748435-47748485 | K562 | blood: | n/a |
26 | chr8:47751953-47752003 | ECC-1 | luminal epithelium: | n/a |
27 | chr8:47748435-47748485 | RPTEC | kidney: | n/a |
28 | chr8:47751494-47751544 | SK-N-SH_RA | brain: | n/a |
29 | chr8:47748435-47748485 | HCM | heart: | n/a |
30 | chr8:47751623-47751673 | SK-N-SH | brain: | n/a |
31 | chr8:47751623-47751673 | GM19239 | blood: | n/a |
32 | chr8:47761906-47761956 | LNCaP | prostate: | n/a |
33 | chr8:47751953-47752003 | PFSK-1 | brain: | n/a |
34 | chr8:47751494-47751544 | NB4 | blood: | n/a |
35 | chr8:47748435-47748485 | Caco-2 | colon: | n/a |
36 | chr8:47751953-47752003 | AG04449 | skin: | fetal |
37 | chr8:47751953-47752003 | SKMC | muscle: | n/a |
38 | chr8:47751953-47752003 | Hela-S3 | cervix: | n/a |
39 | chr8:47751953-47752003 | MCF-7 | breast: | n/a |
40 | chr8:47751494-47751544 | Jurkat | blood: | n/a |
41 | chr8:47751953-47752003 | GM19239 | blood: | n/a |
42 | chr8:47751494-47751544 | HPAEpiC | pulmonary alveolar: | n/a |
43 | chr8:47751623-47751673 | HIPEpiC | eye: | n/a |
44 | chr8:47751623-47751673 | AG10803 | skin: | n/a |
45 | chr8:47751494-47751544 | HCPEpiC | choroid plexus: | n/a |
46 | chr8:47748435-47748485 | AG10803 | skin: | n/a |
47 | chr8:47751623-47751673 | Hela-S3 | cervix: | n/a |
48 | chr8:47751623-47751673 | HCT-116 | colon: | n/a |
49 | chr8:47748435-47748485 | ECC-1 | luminal epithelium: | n/a |
50 | chr8:47748435-47748485 | AG09319 | gingival: | n/a |
No data |
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-RP11-1134I14.8.1-3 | chr8:47754972-47755048 | NONHSAT126420 |
2 | lnc-RP11-1134I14.8.1-3 | chr8:47765729-47765929 | NR_027013 |
3 | lnc-RP11-1134I14.8.1-3 | chr8:47752667-47752748 | ENSG00000253314.1 |
4 | lnc-RP11-1134I14.8.1-3 | chr8:47760406-47761152 | NR_027013 |
5 | lnc-RP11-1134I14.8.1-3 | chr8:47752667-47752748 | NR_027013 |
6 | lnc-RP11-1134I14.8.1-3 | chr8:47765729-47765991 | NONHSAT126420 |
7 | lnc-RP11-1134I14.8.1-3 | chr8:47757651-47757703 | ENSG00000253314.1 |
8 | lnc-RP11-1134I14.8.1-3 | chr8:47752438-47752557 | ENSG00000253314.1 |
9 | lnc-RP11-1134I14.8.1-3 | chr8:47752667-47752748 | ENSG00000253314.1 |
10 | lnc-RP11-1134I14.8.1-3 | chr8:47760406-47761152 | ENSG00000253314.1 |
11 | lnc-RP11-1134I14.8.1-3 | chr8:47759598-47759722 | NR_027013 |
12 | lnc-RP11-1134I14.8.1-3 | chr8:47760406-47760523 | ENSG00000253314.1 |
13 | lnc-RP11-1134I14.8.1-3 | chr8:47752667-47752748 | ENSG00000253314.1 |
14 | lnc-RP11-1134I14.8.1-3 | chr8:47754972-47755048 | NONHSAT126421 |
15 | lnc-RP11-1134I14.8.1-3 | chr8:47762290-47762365 | NONHSAT126423 |
16 | lnc-RP11-1134I14.8.1-3 | chr8:47759598-47759722 | ENSG00000253314.1 |
17 | lnc-RP11-1134I14.8.1-3 | chr8:47759598-47759722 | NONHSAT126419 |
18 | lnc-RP11-350F16.2.1-2 | chr8:47730635-47730705 | XLOC_007078 |
19 | lnc-RP11-1134I14.8.1-3 | chr8:47765729-47765991 | NONHSAT126421 |
20 | lnc-RP11-1134I14.8.1-3 | chr8:47752508-47752557 | NONHSAT126420 |
21 | lnc-RP11-1134I14.8.1-3 | chr8:47766092-47766216 | NONHSAT126421 |
22 | lnc-RP11-1134I14.8.1-3 | chr8:47757651-47757703 | NONHSAT126421 |
23 | lnc-RP11-1134I14.8.1-3 | chr8:47748364-47748420 | ENSG00000253314.1 |
24 | lnc-RP11-1134I14.8.1-3 | chr8:47753899-47753974 | ENSG00000253314.1 |
25 | lnc-RP11-1134I14.8.1-3 | chr8:47757651-47757703 | ENSG00000253314.1 |
26 | lnc-RP11-1134I14.8.1-3 | chr8:47761071-47761815 | NONHSAT126415 |
27 | lnc-RP11-1134I14.8.1-3 | chr8:47754972-47755048 | NONHSAT126419 |
28 | lnc-RP11-1134I14.8.1-3 | chr8:47754972-47755048 | ENSG00000253314.1 |
29 | lnc-RP11-1134I14.8.1-3 | chr8:47762290-47762365 | NONHSAT126421 |
30 | lnc-RP11-1134I14.8.1-3 | chr8:47752508-47752557 | NONHSAT126421 |
31 | lnc-RP11-1134I14.8.1-3 | chr8:47754972-47755048 | ENSG00000253314.1 |
32 | lnc-RP11-1134I14.8.1-3 | chr8:47759598-47759722 | NONHSAT126415 |
33 | lnc-RP11-1134I14.8.1-3 | chr8:47752517-47752557 | ENSG00000253314.1 |
34 | lnc-RP11-1134I14.8.1-3 | chr8:47752508-47752557 | NR_027013 |
35 | lnc-RP11-1134I14.8.1-3 | chr8:47765729-47765833 | ENSG00000253314.1 |
36 | lnc-RP11-1134I14.8.1-3 | chr8:47759598-47759722 | ENSG00000253314.1 |
37 | lnc-RP11-1134I14.8.1-3 | chr8:47760406-47761152 | NONHSAT126420 |
38 | lnc-RP11-1134I14.8.1-3 | chr8:47757651-47757703 | NR_027013 |
39 | lnc-RP11-1134I14.8.1-3 | chr8:47761071-47761152 | NONHSAT126421 |
40 | lnc-RP11-1134I14.8.1-3 | chr8:47753899-47753974 | ENSG00000253314.1 |
41 | lnc-RP11-1134I14.8.1-3 | chr8:47759598-47759722 | NONHSAT126420 |
42 | lnc-RP11-1134I14.8.1-3 | chr8:47759598-47759688 | ENSG00000253314.1 |
43 | lnc-RP11-1134I14.8.1-3 | chr8:47757651-47757703 | NONHSAT126419 |
44 | lnc-RP11-1134I14.8.1-3 | chr8:47752486-47752557 | NONHSAT126419 |
45 | lnc-RP11-1134I14.8.1-3 | chr8:47733859-47734050 | ENSG00000253314.1 |
46 | lnc-RP11-1134I14.8.1-3 | chr8:47754972-47755048 | NR_027013 |
47 | lnc-RP11-1134I14.8.1-3 | chr8:47765729-47765991 | NONHSAT126424 |
48 | lnc-RP11-1134I14.8.1-3 | chr8:47753899-47753974 | NONHSAT126420 |
49 | lnc-RP11-1134I14.8.1-3 | chr8:47752667-47752748 | NONHSAT126421 |
50 | lnc-RP11-1134I14.8.1-3 | chr8:47752667-47752748 | NONHSAT126420 |
No data |
No data |
Variant related genes | Relation type |
---|---|
MTND1P7 | TF binding region |
MTND6P20 | TF binding region |
LINC00293 | TF binding region |
RNU6-656P | TF binding region |
ENSG00000254118 | TF binding region |
MTND1P7 | CpG island |
MTND6P20 | CpG island |
LINC00293 | CpG island |
RNU6-656P | CpG island |
ENSG00000254118 | CpG island |
USO1 | miRNA target sites |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs145094969 | chr8:47728909-47728910 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
2 | rs551192973 | chr8:47728913-47728914 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
3 | rs566786967 | chr8:47728948-47728949 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
4 | rs191009018 | chr8:47728957-47728958 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
5 | rs551452903 | chr8:47728978-47728979 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
6 | rs150959937 | chr8:47728985-47728986 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
7 | rs375655009 | chr8:47728991-47728992 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
8 | rs181763922 | chr8:47729010-47729011 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
9 | rs140804952 | chr8:47729085-47729086 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
10 | rs557213664 | chr8:47729089-47729090 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
11 | rs186460519 | chr8:47729136-47729137 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
12 | rs191435519 | chr8:47729141-47729142 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
13 | rs183756550 | chr8:47729200-47729201 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
14 | rs73676245 | chr8:47729213-47729214 | Inactive region | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
15 | rs573130181 | chr8:47729217-47729218 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
16 | rs113547297 | chr8:47729219-47729220 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
17 | rs537026267 | chr8:47729256-47729257 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
18 | rs577202851 | chr8:47729267-47729268 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
19 | rs11990120 | chr8:47729355-47729356 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
20 | rs562969216 | chr8:47729365-47729366 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
21 | rs550898568 | chr8:47729368-47729369 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
22 | rs541977560 | chr8:47729385-47729386 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
23 | rs560315851 | chr8:47729389-47729390 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
24 | rs527971019 | chr8:47729395-47729396 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
25 | rs567918025 | chr8:47729397-47729398 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
26 | rs564707967 | chr8:47729435-47729436 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
27 | rs532104821 | chr8:47729468-47729469 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
28 | rs369181047 | chr8:47729483-47729484 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
29 | rs550322255 | chr8:47729504-47729505 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
30 | rs568895172 | chr8:47729515-47729516 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
31 | rs536358134 | chr8:47729600-47729601 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
32 | rs535594107 | chr8:47729626-47729627 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
33 | rs536468925 | chr8:47729631-47729632 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
34 | rs553486698 | chr8:47729632-47729633 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
35 | rs111829014 | chr8:47729650-47729651 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
36 | rs187889526 | chr8:47729662-47729663 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
37 | rs11777235 | chr8:47729693-47729694 | Inactive region | TF binding region | 1 gene(s) | LD-proxies of rSNPOverlapped rCNV | n/a |
38 | rs35969444 | chr8:47729695-47729696 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
39 | rs191558799 | chr8:47729697-47729698 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
40 | rs558841586 | chr8:47729706-47729707 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
41 | rs376330050 | chr8:47729716-47729717 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
42 | rs182171746 | chr8:47729746-47729747 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
43 | rs201952445 | chr8:47729817-47729818 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
44 | rs556290727 | chr8:47729827-47729828 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
45 | rs534748590 | chr8:47729895-47729896 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
46 | rs140382452 | chr8:47729902-47729903 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
47 | rs541961621 | chr8:47729910-47729911 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
48 | rs56844665 | chr8:47729931-47729932 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
49 | rs71239878 | chr8:47729974-47729975 | Inactive region | TF binding region | 1 gene(s) | Overlapped CNVs | n/a |
50 | rs552301524 | chr8:47730669-47730670 | Inactive region | TF binding regionlncRNA | 1 gene(s) | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Cancer | 16751803 | CNVD |
Chronic lymphocytic leukemia | 21546498 | CNVD |
Wilms tumour | 21544195 | CNVD |
Gastric cancer | 17908304 | CNVD |
Melanoma | 18172304 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Autism | 19415332 | CNVD |
Malaria | 21533027 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
Esophageal cancer | 21851588 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Breast cancer | 21245420 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Oral cancer | 21386901 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Seminomas | 18059402 | CNVD |
Autism | 22495311 | CNVD |
Acute lymphoblastic leukemia | 21390130 | CNVD |
Lung cancer | 18438408 | CNVD |
Pancreatic cancer | 21811587 | CNVD |
Multiple myeloma | 16461302 | CNVD |
Developmental delay | 21373258 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Breast cancer | 17603634 | CNVD |
Pancreatic endocrine tumor | 17639061 | CNVD |
Disorders of sex development | 21048976 | CNVD |
Testicular cancer | 18059402 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Salivary gland tumor | 18059337 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 21509527 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Acute lymphoblastic leukemia | 21248843 | CNVD |
Cancer | 20164919 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Esophageal cancer | 20955586 | CNVD |
abnormal development | 18461090 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Cancer | 20164920 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Medulloblastoma | 20607354 | CNVD |
Uveal melanoma | 21693616 | CNVD |
Langer-Giedion syndrome | 22283845 | CNVD |
Cancer | 21637783 | CNVD |
Splenic marginal zone lymphoma | 21957467 | CNVD |
Breast cancer | 20632083 | CNVD |
Breast cancer | 19602461 | CNVD |
Cancer | 22429812 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Oral cancer | 19627613 | CNVD |
Prostate cancer | 21088497 | CNVD |
colon cancer | 17210682 | CNVD |
Breast cancer | 21264507 | CNVD |
Breast cancer | 22028636 | CNVD |
Acute myeloid leukemia | 16864856 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Breast cancer | 20409316 | CNVD |
Esophageal squamous carcinoma | 18350619 | CNVD |
Gastric cancer | 17167181 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Breast cancer | 16461572 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Medulloblastoma | 16968546 | CNVD |
head and neck squamous cell carcinoma | 18028549 | CNVD |
Breast cancer | 17001317 | CNVD |
Ewing''s sarcoma | 17952124 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Tetralogy of Fallot | 22912587 | CNVD |
Non-syndromic sensorineural hearing loss | 18451855 | CNVD |
early-passage human iPS cells | 21368824 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:47733800-47736400 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr8:47751400-47752000 | ZNF genes & repeats | iPS-18 Cell Line | embryonic stem cell |
3 | chr8:47751400-47753800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
4 | chr8:47753200-47753800 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
5 | chr8:47754000-47755000 | Enhancers | Placenta | Placenta |
6 | chr8:47755000-47757000 | Weak transcription | Placenta | Placenta |
7 | chr8:47757000-47758200 | Enhancers | Placenta | Placenta |
8 | chr8:47758200-47759400 | Weak transcription | Placenta | Placenta |
9 | chr8:47759200-47761400 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
10 | chr8:47760000-47760400 | Active TSS | Fetal Heart | heart |
11 | chr8:47761400-47762000 | Weak transcription | Placenta | Placenta |
12 | chr8:47762000-47763400 | Enhancers | Placenta | Placenta |
13 | chr8:47763400-47767400 | Weak transcription | Placenta | Placenta |
14 | chr8:47764200-47764400 | Bivalent Enhancer | HUES6 Cell Line | embryonic stem cell |
15 | chr8:47765200-47765400 | Flanking Bivalent TSS/Enh | HUES6 Cell Line | embryonic stem cell |
16 | chr8:47767400-47767800 | Enhancers | Placenta | Placenta |