Variant report
Variant | nsv1024211 |
---|---|
Chromosome Location | chr8:43396560-43824036 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:3946)
- CpG islands (count:978)
- Chromatin interactive region (count:4)
- LncRNA region (count:2)
- 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 | chr8:43792645-43793396 | K562 | blood: | n/a | n/a |
2 | ATF1 | chr8:43819080-43819187 | K562 | blood: | n/a | n/a |
3 | ATF1 | chr8:43786577-43787136 | K562 | blood: | n/a | n/a |
4 | ATF1 | chr8:43785555-43785668 | K562 | blood: | n/a | n/a |
5 | BACH1 | chr8:43790059-43790248 | K562 | blood: | n/a | n/a |
6 | BACH1 | chr8:43717526-43717725 | K562 | blood: | n/a | n/a |
7 | BACH1 | chr8:43779446-43779599 | K562 | blood: | n/a | n/a |
8 | BACH1 | chr8:43654724-43654750 | K562 | blood: | n/a | n/a |
9 | BACH1 | chr8:43818947-43819136 | K562 | blood: | n/a | n/a |
10 | BACH1 | chr8:43572418-43572443 | K562 | blood: | n/a | n/a |
11 | BACH1 | chr8:43820379-43820751 | K562 | blood: | n/a | n/a |
12 | BATF | chr8:43793735-43795027 | GM12878 | blood: | n/a | n/a |
13 | BATF | chr8:43800371-43800565 | GM12878 | blood: | n/a | n/a |
14 | BATF | chr8:43793545-43795103 | GM12878 | blood: | n/a | n/a |
15 | BATF | chr8:43771245-43771622 | GM12878 | blood: | n/a | n/a |
16 | BATF | chr8:43770392-43770728 | GM12878 | blood: | n/a | n/a |
17 | BATF | chr8:43795406-43795581 | GM12878 | blood: | n/a | n/a |
18 | BATF | chr8:43796850-43797049 | GM12878 | blood: | n/a | n/a |
19 | BATF | chr8:43772038-43772467 | GM12878 | blood: | n/a | n/a |
20 | BATF | chr8:43771808-43772466 | GM12878 | blood: | n/a | n/a |
21 | BATF | chr8:43812453-43812698 | GM12878 | blood: | n/a | n/a |
22 | BATF | chr8:43802641-43802856 | GM12878 | blood: | n/a | n/a |
23 | BATF | chr8:43805088-43805295 | GM12878 | blood: | n/a | n/a |
24 | BATF | chr8:43820702-43821198 | GM12878 | blood: | n/a | n/a |
25 | BATF | chr8:43761295-43761752 | GM12878 | blood: | n/a | n/a |
26 | BATF | chr8:43805930-43806139 | GM12878 | blood: | n/a | n/a |
27 | BATF | chr8:43813396-43813769 | GM12878 | blood: | n/a | n/a |
28 | BATF | chr8:43818775-43819235 | GM12878 | blood: | n/a | n/a |
29 | BATF | chr8:43805912-43806229 | GM12878 | blood: | n/a | n/a |
30 | BATF | chr8:43781687-43781911 | GM12878 | blood: | n/a | n/a |
31 | BATF | chr8:43798729-43799230 | GM12878 | blood: | n/a | n/a |
32 | BATF | chr8:43789506-43789826 | GM12878 | blood: | n/a | n/a |
33 | BATF | chr8:43760280-43760716 | GM12878 | blood: | n/a | n/a |
34 | BATF | chr8:43789506-43789769 | GM12878 | blood: | n/a | n/a |
35 | BATF | chr8:43795629-43796232 | GM12878 | blood: | n/a | n/a |
36 | BATF | chr8:43805641-43805845 | GM12878 | blood: | n/a | n/a |
37 | BATF | chr8:43797348-43797784 | GM12878 | blood: | n/a | n/a |
38 | BATF | chr8:43776273-43776586 | GM12878 | blood: | n/a | n/a |
39 | BATF | chr8:43808822-43809213 | GM12878 | blood: | n/a | n/a |
40 | BATF | chr8:43795705-43796262 | GM12878 | blood: | n/a | n/a |
41 | BATF | chr8:43805556-43805832 | GM12878 | blood: | n/a | n/a |
42 | BATF | chr8:43822327-43823068 | GM12878 | blood: | n/a | n/a |
43 | BATF | chr8:43796330-43796659 | GM12878 | blood: | n/a | n/a |
44 | BATF | chr8:43771212-43771629 | GM12878 | blood: | n/a | n/a |
45 | BATF | chr8:43793093-43793491 | GM12878 | blood: | n/a | n/a |
46 | BATF | chr8:43817245-43817428 | GM12878 | blood: | n/a | n/a |
47 | BATF | chr8:43803567-43803962 | GM12878 | blood: | n/a | n/a |
48 | BATF | chr8:43782910-43783364 | GM12878 | blood: | n/a | n/a |
49 | BATF | chr8:43761208-43761764 | GM12878 | blood: | n/a | n/a |
50 | BATF | chr8:43808539-43808737 | GM12878 | blood: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:43417291-43417341 | HCT-116 | colon: | n/a |
2 | chr8:43794595-43794645 | Hepatocyte | liver: | n/a |
3 | chr8:43417291-43417341 | HCT-116 | colon: | n/a |
4 | chr8:43794595-43794645 | Hepatocyte | liver: | n/a |
5 | chr8:43401874-43401924 | GM12891 | blood: | n/a |
6 | chr8:43403277-43403327 | Hela-S3 | cervix: | n/a |
7 | chr8:43406144-43406194 | AG04449 | skin: | fetal |
8 | chr8:43404458-43404508 | HIPEpiC | eye: | n/a |
9 | chr8:43401874-43401924 | Caco-2 | colon: | n/a |
10 | chr8:43406314-43406364 | AG10803 | skin: | n/a |
11 | chr8:43405687-43405737 | HRCEpiC | kidney: | n/a |
12 | chr8:43404458-43404508 | HL-60 | blood: | n/a |
13 | chr8:43406314-43406364 | IMR90 | lung: | fetal |
14 | chr8:43417291-43417341 | HCF | heart: | n/a |
15 | chr8:43417291-43417341 | HRCEpiC | kidney: | n/a |
16 | chr8:43405739-43405789 | HepG2 | liver: | n/a |
17 | chr8:43401874-43401924 | ECC-1 | luminal epithelium: | n/a |
18 | chr8:43794595-43794645 | HRPEpiC | eye: | n/a |
19 | chr8:43794595-43794645 | NB4 | blood: | n/a |
20 | chr8:43418721-43418771 | HIPEpiC | eye: | n/a |
21 | chr8:43406314-43406364 | PFSK-1 | brain: | n/a |
22 | chr8:43406411-43406461 | ProgFib | skin: | n/a |
23 | chr8:43404458-43404508 | HMEC | breast: | n/a |
24 | chr8:43405687-43405737 | HCT-116 | colon: | n/a |
25 | chr8:43404214-43404264 | PrEC | prostate: | n/a |
26 | chr8:43402930-43402980 | NH-A | brain: | n/a |
27 | chr8:43401874-43401924 | ProgFib | skin: | n/a |
28 | chr8:43405739-43405789 | HAEpiC | amniotic membrane: | n/a |
29 | chr8:43406144-43406194 | HNPCEpiC | eye: | n/a |
30 | chr8:43405687-43405737 | AG09309 | skin: | n/a |
31 | chr8:43402630-43402680 | HUVEC | blood vessel: | n/a |
32 | chr8:43405687-43405737 | GM12878 | blood: | n/a |
33 | chr8:43406411-43406461 | PFSK-1 | brain: | n/a |
34 | chr8:43418721-43418771 | GM12892 | blood: | n/a |
35 | chr8:43406314-43406364 | LNCaP | prostate: | n/a |
36 | chr8:43405687-43405737 | HCM | heart: | n/a |
37 | chr8:43417050-43417100 | SK-N-SH | brain: | n/a |
38 | chr8:43406314-43406364 | HCT-116 | colon: | n/a |
39 | chr8:43404214-43404264 | HUVEC | blood vessel: | n/a |
40 | chr8:43402930-43402980 | AG09309 | skin: | n/a |
41 | chr8:43406144-43406194 | HEK293 | kidney: | embryo |
42 | chr8:43402630-43402680 | GM12878 | blood: | n/a |
43 | chr8:43418721-43418771 | SK-N-MC | brain: | n/a |
44 | chr8:43406314-43406364 | HepG2 | liver: | n/a |
45 | chr8:43403277-43403327 | H1-hESC | embryonic stem cell: | embryo |
46 | chr8:43405739-43405789 | HRPEpiC | eye: | n/a |
47 | chr8:43794595-43794645 | HL-60 | blood: | n/a |
48 | chr8:43794595-43794645 | LNCaP | prostate: | n/a |
49 | chr8:43402630-43402680 | Hepatocyte | liver: | n/a |
50 | chr8:43403277-43403327 | SK-N-MC | brain: | n/a |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:43395245..43397661-chr8:43402500..43405220,3 | K562 | blood: | |
2 | chr8:43394978..43396738-chr8:43399115..43401110,2 | K562 | blood: | |
3 | chr8:43092429..43093269-chr8:43823893..43824414,2 | MCF-7 | breast: | |
4 | chr15:63385860..63386443-chr8:43553599..43554374,2 | MCF-7 | breast: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-RNF170-9 | chr8:43529413-43529734 | NONHSAT126368 |
2 | lnc-HGSNAT-12 | chr8:43527966-43528218 | NONHSAT126367 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000253195 | TF binding region |
ENSG00000221295 | TF binding region |
ENSG00000253845 | TF binding region |
ENSG00000253198 | TF binding region |
ENSG00000253195 | CpG island |
ENSG00000221295 | CpG island |
ENSG00000253845 | CpG island |
ENSG00000253198 | 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 | rs7464678 | chr8:43396560-43396561 | ZNF genes & repeats Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
2 | rs576075161 | chr8:43396578-43396579 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
3 | rs566778236 | chr8:43396589-43396590 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
4 | rs180683812 | chr8:43396594-43396595 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
5 | rs533530622 | chr8:43396602-43396603 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
6 | rs185356709 | chr8:43396605-43396606 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
7 | rs527956023 | chr8:43396609-43396610 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
8 | rs114679967 | chr8:43396614-43396615 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
9 | rs116456412 | chr8:43396633-43396634 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
10 | rs530271580 | chr8:43396634-43396635 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
11 | rs549902623 | chr8:43396680-43396681 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
12 | rs569761688 | chr8:43396707-43396708 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
13 | rs73569617 | chr8:43396708-43396709 | ZNF genes & repeats Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
14 | rs116248368 | chr8:43396720-43396721 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
15 | rs117708652 | chr8:43396753-43396754 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
16 | rs545940506 | chr8:43396764-43396765 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
17 | rs140427883 | chr8:43396768-43396769 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
18 | rs568164737 | chr8:43396782-43396783 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
19 | rs374489316 | chr8:43396833-43396834 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
20 | rs536843830 | chr8:43396835-43396836 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
21 | rs558724683 | chr8:43396882-43396883 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs569206385 | chr8:43396885-43396886 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
23 | rs556279197 | chr8:43396892-43396893 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
24 | rs537940639 | chr8:43396899-43396900 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs576110703 | chr8:43396929-43396930 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs190012983 | chr8:43396935-43396936 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs554680560 | chr8:43396959-43396960 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs114797633 | chr8:43396963-43396964 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs558700750 | chr8:43396974-43396975 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs564314571 | chr8:43397002-43397003 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs541366787 | chr8:43397024-43397025 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs117945301 | chr8:43397035-43397036 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs184049353 | chr8:43397076-43397077 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs187328249 | chr8:43397104-43397105 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs111449494 | chr8:43397112-43397113 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs191788725 | chr8:43397118-43397119 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs76464227 | chr8:43397122-43397123 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs149066244 | chr8:43397123-43397124 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs559095824 | chr8:43397126-43397127 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs114288615 | chr8:43397127-43397128 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs138032063 | chr8:43397130-43397131 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs11996667 | chr8:43397135-43397136 | ZNF genes & repeats Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
43 | rs536878974 | chr8:43397137-43397138 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs183519697 | chr8:43397164-43397165 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs368688132 | chr8:43397189-43397190 | ZNF genes & repeats Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs570283463 | chr8:43397200-43397201 | ZNF genes & repeats Weak transcription Enhancers | n/a | n/a | Overlapped CNVs | n/a |
47 | rs113235387 | chr8:43397206-43397207 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
48 | rs368011942 | chr8:43397256-43397257 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
49 | rs188064105 | chr8:43397289-43397290 | ZNF genes & repeats Enhancers | n/a | n/a | Overlapped CNVs | n/a |
50 | rs538760570 | chr8:43397291-43397292 | ZNF genes & repeats Enhancers | 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 | chr8:43392400-43412600 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr8:43395600-43399400 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
3 | chr8:43396200-43397200 | Weak transcription | Spleen | Spleen |
4 | chr8:43396600-43396800 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
5 | chr8:43396600-43398000 | ZNF genes & repeats | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr8:43397200-43397400 | Enhancers | Spleen | Spleen |
7 | chr8:43401400-43401600 | ZNF genes & repeats | Fetal Brain Female | brain |
8 | chr8:43401800-43406000 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
9 | chr8:43402200-43402400 | ZNF genes & repeats | Brain Germinal Matrix | brain |
10 | chr8:43403000-43404800 | ZNF genes & repeats | Foreskin Fibroblast Primary Cells skin02 | Skin |
11 | chr8:43403200-43403400 | Bivalent/Poised TSS | Skeletal Muscle Male | skeletal muscle |
12 | chr8:43403400-43405000 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
13 | chr8:43403400-43406600 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
14 | chr8:43403800-43404200 | Active TSS | Primary T cells from cord blood | blood |
15 | chr8:43403800-43405600 | ZNF genes & repeats | Fetal Stomach | stomach |
16 | chr8:43405800-43406000 | Enhancers | K562 | blood |
17 | chr8:43410400-43411000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
18 | chr8:43411600-43412200 | Active TSS | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
19 | chr8:43413600-43414000 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
20 | chr8:43413800-43414400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
21 | chr8:43414600-43415000 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
22 | chr8:43415400-43427200 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
23 | chr8:43416400-43417000 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
24 | chr8:43416400-43427200 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
25 | chr8:43417400-43419200 | ZNF genes & repeats | iPS-15b Cell Line | embryonic stem cell |
26 | chr8:43417400-43421000 | ZNF genes & repeats | Fetal Stomach | stomach |
27 | chr8:43417800-43422800 | ZNF genes & repeats | Adipose Nuclei | Adipose |
28 | chr8:43418800-43419200 | ZNF genes & repeats | Colonic Mucosa | Colon |
29 | chr8:43418800-43423600 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
30 | chr8:43419000-43419200 | ZNF genes & repeats | Foreskin Fibroblast Primary Cells skin01 | Skin |
31 | chr8:43419600-43421400 | ZNF genes & repeats | Duodenum Smooth Muscle | Duodenum |
32 | chr8:43419600-43422400 | ZNF genes & repeats | Skeletal Muscle Male | skeletal muscle |
33 | chr8:43420400-43420800 | ZNF genes & repeats | Brain Germinal Matrix | brain |
34 | chr8:43420400-43421000 | ZNF genes & repeats | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
35 | chr8:43420400-43421000 | ZNF genes & repeats | Duodenum Mucosa | Duodenum |
36 | chr8:43420400-43423600 | ZNF genes & repeats | Fetal Adrenal Gland | Adrenal Gland |
37 | chr8:43422800-43425800 | ZNF genes & repeats | Fetal Muscle Trunk | muscle |
38 | chr8:43423800-43427400 | ZNF genes & repeats | Monocytes-CD14+_RO01746 | blood |
39 | chr8:43424600-43426200 | ZNF genes & repeats | Primary hematopoietic stem cells short term culture | blood |
40 | chr8:43426800-43430800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
41 | chr8:43427600-43428400 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
42 | chr8:43429200-43430000 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
43 | chr8:43429400-43430600 | ZNF genes & repeats | Liver | Liver |
44 | chr8:43434000-43435000 | ZNF genes & repeats | Liver | Liver |
45 | chr8:43434000-43454200 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
46 | chr8:43436400-43436800 | ZNF genes & repeats | Liver | Liver |
47 | chr8:43439800-43443800 | ZNF genes & repeats | Adipose Nuclei | Adipose |
48 | chr8:43441000-43453800 | ZNF genes & repeats | Liver | Liver |
49 | chr8:43442400-43446800 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
50 | chr8:43444000-43445000 | Weak transcription | Adipose Nuclei | Adipose |