Variant report
Variant | nsv1029702 |
---|---|
Chromosome Location | chr8:43367207-43786790 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:1404)
- CpG islands (count:918)
- Chromatin interactive region (count:5)
- LncRNA region (count:4)
- 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 | ATF1 | chr8:43786577-43787136 | K562 | blood: | n/a | n/a |
2 | ATF1 | chr8:43785555-43785668 | K562 | blood: | n/a | n/a |
3 | BACH1 | chr8:43717526-43717725 | K562 | blood: | n/a | n/a |
4 | BACH1 | chr8:43654724-43654750 | K562 | blood: | n/a | n/a |
5 | BACH1 | chr8:43572418-43572443 | K562 | blood: | n/a | n/a |
6 | BACH1 | chr8:43779446-43779599 | K562 | blood: | n/a | n/a |
7 | BATF | chr8:43760193-43760718 | GM12878 | blood: | n/a | n/a |
8 | BATF | chr8:43770392-43770728 | GM12878 | blood: | n/a | n/a |
9 | BATF | chr8:43761295-43761752 | GM12878 | blood: | n/a | n/a |
10 | BATF | chr8:43761208-43761764 | GM12878 | blood: | n/a | n/a |
11 | BATF | chr8:43785488-43786069 | GM12878 | blood: | n/a | n/a |
12 | BATF | chr8:43771212-43771629 | GM12878 | blood: | n/a | n/a |
13 | BATF | chr8:43764727-43764995 | GM12878 | blood: | n/a | n/a |
14 | BATF | chr8:43771808-43772466 | GM12878 | blood: | n/a | n/a |
15 | BATF | chr8:43760917-43761158 | GM12878 | blood: | n/a | n/a |
16 | BATF | chr8:43772038-43772467 | GM12878 | blood: | n/a | n/a |
17 | BATF | chr8:43776273-43776586 | GM12878 | blood: | n/a | n/a |
18 | BATF | chr8:43760280-43760716 | GM12878 | blood: | n/a | n/a |
19 | BATF | chr8:43759902-43760143 | GM12878 | blood: | n/a | n/a |
20 | BATF | chr8:43783535-43783800 | GM12878 | blood: | n/a | n/a |
21 | BATF | chr8:43778905-43779151 | GM12878 | blood: | n/a | n/a |
22 | BATF | chr8:43785460-43785804 | GM12878 | blood: | n/a | n/a |
23 | BATF | chr8:43781687-43781911 | GM12878 | blood: | n/a | n/a |
24 | BATF | chr8:43783610-43783797 | GM12878 | blood: | n/a | n/a |
25 | BATF | chr8:43781686-43781952 | GM12878 | blood: | n/a | n/a |
26 | BATF | chr8:43782910-43783364 | GM12878 | blood: | n/a | n/a |
27 | BATF | chr8:43771245-43771622 | GM12878 | blood: | n/a | n/a |
28 | BCL11A | chr8:43761282-43761722 | GM12878 | blood: | n/a | n/a |
29 | BCL11A | chr8:43785261-43786095 | GM12878 | blood: | n/a | n/a |
30 | BCL11A | chr8:43772033-43772507 | GM12878 | blood: | n/a | n/a |
31 | BCL11A | chr8:43785837-43785995 | GM12878 | blood: | n/a | n/a |
32 | BCL11A | chr8:43759939-43760150 | GM12878 | blood: | n/a | n/a |
33 | BCL11A | chr8:43760267-43760707 | GM12878 | blood: | n/a | n/a |
34 | BCL11A | chr8:43783550-43783791 | GM12878 | blood: | n/a | n/a |
35 | BCL11A | chr8:43782626-43783058 | GM12878 | blood: | n/a | n/a |
36 | BCL11A | chr8:43761170-43762049 | GM12878 | blood: | n/a | n/a |
37 | BCL11A | chr8:43785334-43785462 | GM12878 | blood: | n/a | n/a |
38 | BCL11A | chr8:43760155-43760933 | GM12878 | blood: | n/a | n/a |
39 | BCL11A | chr8:43771913-43772498 | GM12878 | blood: | n/a | n/a |
40 | BCL11A | chr8:43783542-43783935 | GM12878 | blood: | n/a | n/a |
41 | BCL11A | chr8:43771282-43771511 | GM12878 | blood: | n/a | n/a |
42 | BCL11A | chr8:43771195-43771641 | GM12878 | blood: | n/a | n/a |
43 | BCL11A | chr8:43781665-43782001 | GM12878 | blood: | n/a | n/a |
44 | BCL11A | chr8:43785511-43785821 | GM12878 | blood: | n/a | n/a |
45 | BCL11A | chr8:43778827-43779220 | GM12878 | blood: | n/a | n/a |
46 | BHLHE40 | chr8:43779571-43779620 | K562 | blood: | n/a | n/a |
47 | BHLHE40 | chr8:43779289-43779754 | HepG2 | liver: | n/a | n/a |
48 | BHLHE40 | chr8:43773624-43773792 | HepG2 | liver: | n/a | n/a |
49 | BHLHE40 | chr8:43761169-43761764 | HepG2 | liver: | n/a | n/a |
50 | BHLHE40 | chr8:43768074-43768375 | HepG2 | liver: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:43406314-43406364 | GM19239 | blood: | n/a |
2 | chr8:43406411-43406461 | CMK | blood: | n/a |
3 | chr8:43406411-43406461 | A549 | lung: | n/a |
4 | chr8:43406314-43406364 | GM19239 | blood: | n/a |
5 | chr8:43406411-43406461 | CMK | blood: | n/a |
6 | chr8:43406411-43406461 | A549 | lung: | n/a |
7 | chr8:43406411-43406461 | MCF10A-Er-Src | breast: | n/a |
8 | chr8:43406144-43406194 | Caco-2 | colon: | n/a |
9 | chr8:43417050-43417100 | SK-N-SH | brain: | n/a |
10 | chr8:43401874-43401924 | HepG2 | liver: | n/a |
11 | chr8:43402930-43402980 | GM12891 | blood: | n/a |
12 | chr8:43417291-43417341 | A549 | lung: | n/a |
13 | chr8:43406314-43406364 | HEEpiC | esophagus: | n/a |
14 | chr8:43406411-43406461 | SKMC | muscle: | n/a |
15 | chr8:43404458-43404508 | AoSMC | blood vessel: | n/a |
16 | chr8:43401874-43401924 | SAEC | small airway: | n/a |
17 | chr8:43401874-43401924 | ECC-1 | luminal epithelium: | n/a |
18 | chr8:43405687-43405737 | HRE | kidney: | n/a |
19 | chr8:43404214-43404264 | U87 | brain: | n/a |
20 | chr8:43406411-43406461 | NB4 | blood: | n/a |
21 | chr8:43406411-43406461 | HepG2 | liver: | n/a |
22 | chr8:43402930-43402980 | T-47D | breast: | n/a |
23 | chr8:43406314-43406364 | AG09319 | gingival: | n/a |
24 | chr8:43406411-43406461 | PFSK-1 | brain: | n/a |
25 | chr8:43406144-43406194 | AG09309 | skin: | n/a |
26 | chr8:43406411-43406461 | RPTEC | kidney: | n/a |
27 | chr8:43418406-43418456 | A549 | lung: | n/a |
28 | chr8:43406411-43406461 | HCF | heart: | n/a |
29 | chr8:43418721-43418771 | HCPEpiC | choroid plexus: | n/a |
30 | chr8:43404458-43404508 | GM06990 | blood: | n/a |
31 | chr8:43406314-43406364 | Hepatocyte | liver: | n/a |
32 | chr8:43417291-43417341 | K562 | blood: | n/a |
33 | chr8:43417050-43417100 | K562 | blood: | n/a |
34 | chr8:43404458-43404508 | HL-60 | blood: | n/a |
35 | chr8:43406144-43406194 | PANC-1 | pancreas: | n/a |
36 | chr8:43403277-43403327 | MCF10A-Er-Src | breast: | n/a |
37 | chr8:43402930-43402980 | HepG2 | liver: | n/a |
38 | chr8:43401874-43401924 | H1-hESC | embryonic stem cell: | embryo |
39 | chr8:43405687-43405737 | HCM | heart: | n/a |
40 | chr8:43404214-43404264 | HIPEpiC | eye: | n/a |
41 | chr8:43406411-43406461 | MCF-7 | breast: | n/a |
42 | chr8:43418406-43418456 | HPAEpiC | pulmonary alveolar: | n/a |
43 | chr8:43404214-43404264 | Hela-S3 | cervix: | n/a |
44 | chr8:43404214-43404264 | HNPCEpiC | eye: | n/a |
45 | chr8:43402930-43402980 | AG09319 | gingival: | n/a |
46 | chr8:43406314-43406364 | HCM | heart: | n/a |
47 | chr8:43417050-43417100 | CMK | blood: | n/a |
48 | chr8:43404214-43404264 | SK-N-SH | brain: | n/a |
49 | chr8:43405687-43405737 | SKMC | muscle: | n/a |
50 | chr8:43401874-43401924 | GM06990 | blood: | n/a |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr15:63385860..63386443-chr8:43553599..43554374,2 | MCF-7 | breast: | |
2 | chr8:43395245..43397661-chr8:43402500..43405220,3 | K562 | blood: | |
3 | chr8:43370024..43372377-chr8:43374871..43376951,2 | K562 | blood: | |
4 | chr8:43394978..43396738-chr8:43399115..43401110,2 | K562 | blood: | |
5 | chr8:43370024..43372377-chr8:43374871..43376951,2 | K562 | blood: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-HGSNAT-12 | chr8:43527966-43528218 | NONHSAT126367 |
2 | lnc-RNF170-9 | chr8:43529413-43529734 | NONHSAT126368 |
3 | lnc-HGSNAT-9 | chr8:43368786-43369564 | NONHSAT126361 |
4 | lnc-HGSNAT-10 | chr8:43394280-43394615 | NONHSAT126362 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000253195 | TF binding region |
ENSG00000254145 | TF binding region |
CYP4F44P | TF binding region |
ENSG00000221295 | TF binding region |
ENSG00000253845 | TF binding region |
ENSG00000253198 | TF binding region |
ENSG00000253319 | TF binding region |
SNX18P27 | TF binding region |
ENSG00000253195 | CpG island |
ENSG00000254145 | CpG island |
CYP4F44P | CpG island |
ENSG00000221295 | CpG island |
ENSG00000253845 | CpG island |
ENSG00000253198 | CpG island |
ENSG00000253319 | CpG island |
SNX18P27 | CpG island |
ENSG00000253748 | chromatin interactions |
ENSG00000253195 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs142613109 | chr8:43367212-43367213 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
2 | rs187146916 | chr8:43367227-43367228 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs145997152 | chr8:43367228-43367229 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs572168385 | chr8:43367233-43367234 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs534989818 | chr8:43367272-43367273 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs540750762 | chr8:43367323-43367324 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs554332323 | chr8:43367358-43367359 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs574164429 | chr8:43367423-43367424 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs376339150 | chr8:43367431-43367432 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs551816395 | chr8:43367442-43367443 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs571930357 | chr8:43367470-43367471 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs139885038 | chr8:43367487-43367488 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs537752012 | chr8:43367532-43367533 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
14 | rs557415227 | chr8:43367578-43367579 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs191142839 | chr8:43367593-43367594 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs141615992 | chr8:43367627-43367628 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs183689846 | chr8:43367635-43367636 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs150722252 | chr8:43367637-43367638 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs527914183 | chr8:43367688-43367689 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs547569734 | chr8:43367689-43367690 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs560693455 | chr8:43367702-43367703 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs529739878 | chr8:43367711-43367712 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs116527816 | chr8:43367756-43367757 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs569596605 | chr8:43367762-43367763 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs149852154 | chr8:43367784-43367785 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs571827545 | chr8:43367808-43367809 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs552417596 | chr8:43367839-43367840 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs573122042 | chr8:43367841-43367842 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs534845383 | chr8:43367872-43367873 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs369947521 | chr8:43367903-43367904 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs77650378 | chr8:43367951-43367952 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs574232162 | chr8:43367973-43367974 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs536696638 | chr8:43367998-43367999 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs556291090 | chr8:43368013-43368014 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
35 | rs563235220 | chr8:43368015-43368016 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
36 | rs576357546 | chr8:43368016-43368017 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
37 | rs545053531 | chr8:43368022-43368023 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs115989565 | chr8:43368048-43368049 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
39 | rs189139552 | chr8:43368051-43368052 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs541277529 | chr8:43368052-43368053 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
41 | rs561102424 | chr8:43368059-43368060 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
42 | rs563746243 | chr8:43368067-43368068 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs529751445 | chr8:43368118-43368119 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
44 | rs182434093 | chr8:43368149-43368150 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs145889077 | chr8:43368160-43368161 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
46 | rs568293156 | chr8:43368169-43368170 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
47 | rs140179626 | chr8:43368178-43368179 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs116388835 | chr8:43368182-43368183 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs543695620 | chr8:43368183-43368184 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs534913007 | chr8:43368194-43368195 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Chronic lymphocytic leukemia | 21546498 | CNVD |
Cancer | 21637783 | CNVD |
Breast cancer | 20837533 | CNVD |
Squamous cell cancer | 21044232 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Cancer | 22429812 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Non-syndromic sensorineural hearing loss | 18471307 | CNVD |
T-cell prolymphocytic leukemia | 19278963 | CNVD |
Colorectal cancer | 20709793 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Basal cell lymphoma | 21115979 | CNVD |
Breast cancer | 21264507 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Oral cancer | 21386901 | CNVD |
Prostate cancer | 21088497 | CNVD |
Prostate cancer | 21965145 | CNVD |
Breast cancer | 20940404 | CNVD |
Colorectal cancer | 19359472 | CNVD |
Embryonal rhabdomyosarcoma | 16790082 | CNVD |
Gastric cancer | 17167181 | CNVD |
Prostate cancer | 16705090 | CNVD |
8p-syndrome | 17576883 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Human rectal carcinomas | 16397240 | CNVD |
Medulloblastoma | 16968546 | CNVD |
Lung adenocarcinoma | 19525976 | CNVD |
Lung cancer | 19525976 | CNVD |
Prostate cancer | 17245344 | CNVD |
Gastrointestinal stromal cancer | 16982739 | CNVD |
Cancer | 16751803 | CNVD |
Wilms tumour | 21544195 | CNVD |
Gastric cancer | 17908304 | CNVD |
Melanoma | 18172304 | CNVD |
Medulloblastoma | 21979893 | 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 |
Acute myeloid leukemia | 20729466 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Seminomas | 18059402 | CNVD |
Immune disease | 21572526 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Kallmann Syndrome 2 | 22470819 | 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 |
Breast cancer | 17603634 | CNVD |
Pancreatic endocrine tumor | 17639061 | CNVD |
Disorders of sex development | 21048976 | CNVD |
Testicular cancer | 18059402 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Bladder cancer | 19088036 | CNVD |
Breast cancer | 17001308 | CNVD |
Breast cancer | 17157792 | CNVD |
Cancer | 17001308 | CNVD |
Cancer | 18840272 | CNVD |
head and neck squamous cell carcinoma | 17671120 | CNVD |
Chordoma | 18071362 | CNVD |
Salivary gland tumor | 18059337 | CNVD |
Breast cancer | 17133270 | CNVD |
Breast cancer | 16608533 | CNVD |
Breast cancer | 21509527 | CNVD |
Breast cancer | 21785460 | CNVD |
Rhabdomyosarcoma | 16790082 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Breast cancer | 21858162 | CNVD |
Acute lymphoblastic leukemia | 21248843 | CNVD |
Cancer | 20164919 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Esophageal cancer | 20955586 | CNVD |
abnormal development | 18461090 | CNVD |
Chronic lymphocytic leukemia | 20421269 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Cancer | 20164920 | CNVD |
Mental retardation | 17124404 | CNVD |
Schizophrenia | 23813976 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Medulloblastoma | 20607354 | CNVD |
Breast cancer | 21364760 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
Breast cancer | 22522925 | CNVD |
Schizophrenia | 20967226 | CNVD |
Bipolar disorder | 19214233 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:43362600-43367800 | Weak transcription | Spleen | Spleen |
2 | chr8:43364000-43368000 | Weak transcription | Gastric | stomach |
3 | chr8:43366400-43369200 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
4 | chr8:43366600-43368600 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr8:43367000-43368400 | ZNF genes & repeats | iPS-18 Cell Line | embryonic stem cell |
6 | chr8:43367800-43368200 | ZNF genes & repeats | Spleen | Spleen |
7 | chr8:43368000-43369000 | ZNF genes & repeats | Gastric | stomach |
8 | chr8:43368200-43369400 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
9 | chr8:43368200-43373000 | Weak transcription | Spleen | Spleen |
10 | chr8:43371800-43373600 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
11 | chr8:43373000-43373600 | Enhancers | Spleen | Spleen |
12 | chr8:43375200-43376400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
13 | chr8:43377200-43380000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
14 | chr8:43378400-43379600 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
15 | chr8:43378600-43379600 | Enhancers | HepG2 | liver |
16 | chr8:43378800-43379200 | Enhancers | HMEC | breast |
17 | chr8:43378800-43380000 | Enhancers | Left Ventricle | heart |
18 | chr8:43379000-43379400 | Enhancers | NHEK | skin |
19 | chr8:43379400-43380000 | Enhancers | Spleen | Spleen |
20 | chr8:43379600-43382200 | Weak transcription | HepG2 | liver |
21 | chr8:43379800-43380000 | Enhancers | Lung | lung |
22 | chr8:43381400-43383200 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
23 | chr8:43382200-43382600 | Enhancers | HepG2 | liver |
24 | chr8:43384000-43389600 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
25 | chr8:43388600-43391400 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
26 | chr8:43388800-43389200 | Active TSS | Fetal Heart | heart |
27 | chr8:43388800-43393000 | Weak transcription | Spleen | Spleen |
28 | chr8:43390200-43390400 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
29 | chr8:43390400-43391600 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
30 | chr8:43392400-43392600 | Enhancers | Right Ventricle | heart |
31 | chr8:43392400-43412600 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
32 | chr8:43392600-43393400 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
33 | chr8:43392600-43394000 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
34 | chr8:43392600-43394000 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
35 | chr8:43393000-43393400 | Enhancers | Spleen | Spleen |
36 | chr8:43393400-43396000 | Weak transcription | Spleen | Spleen |
37 | chr8:43394800-43396000 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
38 | chr8:43395600-43399400 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
39 | chr8:43396000-43396200 | Enhancers | Spleen | Spleen |
40 | chr8:43396200-43397200 | Weak transcription | Spleen | Spleen |
41 | chr8:43396600-43396800 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
42 | chr8:43396600-43398000 | ZNF genes & repeats | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
43 | chr8:43397200-43397400 | Enhancers | Spleen | Spleen |
44 | chr8:43401400-43401600 | ZNF genes & repeats | Fetal Brain Female | brain |
45 | chr8:43401800-43406000 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
46 | chr8:43402200-43402400 | ZNF genes & repeats | Brain Germinal Matrix | brain |
47 | chr8:43403000-43404800 | ZNF genes & repeats | Foreskin Fibroblast Primary Cells skin02 | Skin |
48 | chr8:43403200-43403400 | Bivalent/Poised TSS | Skeletal Muscle Male | skeletal muscle |
49 | chr8:43403400-43405000 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
50 | chr8:43403400-43406600 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |