Variant report
Variant | nsv465646 |
---|---|
Chromosome Location | chr8:43198953-43358947 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:450)
- CpG islands (count:183)
- Chromatin interactive region (count:4)
- LncRNA region (count:8)
- 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 | CEBPB | chr8:43352248-43352856 | Hela-S3 | cervix: | n/a | n/a |
2 | CEBPB | chr8:43317791-43318030 | A549 | lung: | n/a | chr8:43317903-43317914 chr8:43317902-43317915 |
3 | CEBPB | chr8:43222991-43222998 | HepG2 | liver: | n/a | n/a |
4 | CEBPB | chr8:43306476-43306804 | HepG2 | liver: | n/a | chr8:43306646-43306657 chr8:43306657-43306668 |
5 | CEBPB | chr8:43306491-43306829 | A549 | lung: | n/a | chr8:43306646-43306657 chr8:43306657-43306668 |
6 | CEBPB | chr8:43221416-43221477 | A549 | lung: | n/a | n/a |
7 | CEBPB | chr8:43317774-43318025 | HepG2 | liver: | n/a | chr8:43317903-43317914 chr8:43317902-43317915 |
8 | CEBPB | chr8:43306612-43306676 | K562 | blood: | n/a | chr8:43306646-43306657 chr8:43306657-43306668 |
9 | CEBPB | chr8:43303234-43303525 | HepG2 | liver: | n/a | chr8:43303409-43303422 chr8:43303410-43303421 |
10 | CEBPB | chr8:43302895-43303465 | A549 | lung: | n/a | chr8:43303409-43303422 chr8:43303410-43303421 |
11 | CEBPB | chr8:43306501-43306786 | IMR90 | lung: | n/a | chr8:43306646-43306657 chr8:43306657-43306668 |
12 | CEBPB | chr8:43352224-43352840 | A549 | lung: | n/a | n/a |
13 | CEBPB | chr8:43221409-43221449 | HepG2 | liver: | n/a | n/a |
14 | CTCF | chr8:43291260-43291410 | GM12871 | blood: | n/a | n/a |
15 | CTCF | chr8:43291160-43291310 | GM12873 | blood: | n/a | n/a |
16 | CTCF | chr8:43291180-43291330 | GM06990 | blood: | n/a | n/a |
17 | CTCF | chr8:43291221-43291327 | MCF-7 | breast: | n/a | n/a |
18 | CTCF | chr8:43291260-43291410 | GM12870 | blood: | n/a | n/a |
19 | CTCF | chr8:43291200-43291350 | HFF | foreskin: | n/a | n/a |
20 | CTCF | chr8:43291180-43291330 | HMEC | breast: | n/a | n/a |
21 | CTCF | chr8:43290840-43290990 | BJ | skin: | n/a | n/a |
22 | CTCF | chr8:43342598-43342646 | GM13977 | blood: | n/a | n/a |
23 | CTCF | chr8:43286240-43286390 | GM12866 | blood: | n/a | n/a |
24 | CTCF | chr8:43286300-43286450 | GM12864 | blood: | n/a | n/a |
25 | CTCF | chr8:43265040-43265190 | NHEK | skin: | n/a | n/a |
26 | CTCF | chr8:43286218-43286419 | HepG2 | liver: | n/a | n/a |
27 | CTCF | chr8:43291136-43291409 | HepG2 | liver: | n/a | n/a |
28 | CTCF | chr8:43265040-43265190 | SAEC | small airway: | n/a | n/a |
29 | CTCF | chr8:43291207-43291389 | GM10248 | blood: | n/a | n/a |
30 | CTCF | chr8:43265020-43265170 | GM12875 | blood: | n/a | n/a |
31 | CTCF | chr8:43291200-43291350 | BJ | skin: | n/a | n/a |
32 | CTCF | chr8:43291280-43291430 | HepG2 | liver: | n/a | n/a |
33 | CTCF | chr8:43291145-43291400 | LNCaP | prostate: | n/a | n/a |
34 | CTCF | chr8:43303040-43303190 | A549 | lung: | n/a | n/a |
35 | CTCF | chr8:43291163-43291423 | T-47D | breast: | n/a | n/a |
36 | CTCF | chr8:43303180-43303330 | HPAF | blood vessel: | n/a | n/a |
37 | CTCF | chr8:43303280-43303430 | GM12873 | blood: | n/a | n/a |
38 | CTCF | chr8:43291191-43291390 | GM13977 | blood: | n/a | n/a |
39 | CTCF | chr8:43286308-43286397 | NHEK | skin: | n/a | n/a |
40 | CTCF | chr8:43303280-43303430 | HPAF | blood vessel: | n/a | n/a |
41 | CTCF | chr8:43291220-43291370 | GM12872 | blood: | n/a | n/a |
42 | CTCF | chr8:43291160-43291310 | NHEK | skin: | n/a | n/a |
43 | CTCF | chr8:43291220-43291370 | HEK293 | kidney: | n/a | n/a |
44 | CTCF | chr8:43265160-43265310 | GM12872 | blood: | n/a | n/a |
45 | CTCF | chr8:43291200-43291350 | Hela-S3 | cervix: | n/a | n/a |
46 | CTCF | chr8:43291220-43291370 | HCFaa | heart: | n/a | n/a |
47 | CTCF | chr8:43291220-43291370 | SK-N-SH_RA | brain: | n/a | n/a |
48 | CTCF | chr8:43276132-43276171 | Kidney_OC | kidney: | n/a | n/a |
49 | CTCF | chr8:43286220-43286370 | GM12864 | blood: | n/a | n/a |
50 | CTCF | chr8:43291200-43291350 | AG04450 | lung: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:43213875-43213925 | Hela-S3 | cervix: | n/a |
2 | chr8:43275453-43275503 | HMEC | breast: | n/a |
3 | chr8:43275453-43275503 | MCF10A-Er-Src | breast: | n/a |
4 | chr8:43275453-43275503 | HUVEC | blood vessel: | n/a |
5 | chr8:43213875-43213925 | NHBE | bronchial: | n/a |
6 | chr8:43213875-43213925 | PANC-1 | pancreas: | n/a |
7 | chr8:43213875-43213925 | SAEC | small airway: | n/a |
8 | chr8:43278783-43278833 | HMEC | breast: | n/a |
9 | chr8:43278783-43278833 | PANC-1 | pancreas: | n/a |
10 | chr8:43213875-43213925 | HUVEC | blood vessel: | n/a |
11 | chr8:43278783-43278833 | HL-60 | blood: | n/a |
12 | chr8:43275453-43275503 | Jurkat | blood: | n/a |
13 | chr8:43213875-43213925 | AoSMC | blood vessel: | n/a |
14 | chr8:43213875-43213925 | HRE | kidney: | n/a |
15 | chr8:43278783-43278833 | GM06990 | blood: | n/a |
16 | chr8:43278783-43278833 | HPAEpiC | pulmonary alveolar: | n/a |
17 | chr8:43213875-43213925 | ProgFib | skin: | n/a |
18 | chr8:43213875-43213925 | HEK293 | kidney: | embryo |
19 | chr8:43275453-43275503 | K562 | blood: | n/a |
20 | chr8:43213875-43213925 | Caco-2 | colon: | n/a |
21 | chr8:43275453-43275503 | T-47D | breast: | n/a |
22 | chr8:43278783-43278833 | NH-A | brain: | n/a |
23 | chr8:43278783-43278833 | SAEC | small airway: | n/a |
24 | chr8:43275453-43275503 | NHBE | bronchial: | n/a |
25 | chr8:43213875-43213925 | H1-hESC | embryonic stem cell: | embryo |
26 | chr8:43213875-43213925 | HEEpiC | esophagus: | n/a |
27 | chr8:43213875-43213925 | HCM | heart: | n/a |
28 | chr8:43213875-43213925 | GM19239 | blood: | n/a |
29 | chr8:43278783-43278833 | PrEC | prostate: | n/a |
30 | chr8:43213875-43213925 | AG09319 | gingival: | n/a |
31 | chr8:43278783-43278833 | HEEpiC | esophagus: | n/a |
32 | chr8:43278783-43278833 | HCM | heart: | n/a |
33 | chr8:43275453-43275503 | GM12878 | blood: | n/a |
34 | chr8:43278783-43278833 | GM12891 | blood: | n/a |
35 | chr8:43275453-43275503 | HRCEpiC | kidney: | n/a |
36 | chr8:43278783-43278833 | AG04449 | skin: | fetal |
37 | chr8:43278783-43278833 | BJ | skin: | n/a |
38 | chr8:43213875-43213925 | GM12891 | blood: | n/a |
39 | chr8:43278783-43278833 | HCT-116 | colon: | n/a |
40 | chr8:43278783-43278833 | Caco-2 | colon: | n/a |
41 | chr8:43278783-43278833 | HRE | kidney: | n/a |
42 | chr8:43275453-43275503 | HCPEpiC | choroid plexus: | n/a |
43 | chr8:43275453-43275503 | HAEpiC | amniotic membrane: | n/a |
44 | chr8:43213875-43213925 | SK-N-MC | brain: | n/a |
45 | chr8:43213875-43213925 | K562 | blood: | n/a |
46 | chr8:43278783-43278833 | K562 | blood: | n/a |
47 | chr8:43213875-43213925 | NB4 | blood: | n/a |
48 | chr8:43275453-43275503 | HCM | heart: | n/a |
49 | chr8:43213875-43213925 | SKMC | muscle: | n/a |
50 | chr8:43213875-43213925 | NT2-D1 | testis: | n/a |
(count:4 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:42947579..42949100-chr8:43300446..43303387,2 | MCF-7 | breast: | |
2 | chr8:42948115..42950146-chr8:43255758..43258426,2 | K562 | blood: | |
3 | chr8:42948083..42948640-chr8:43285913..43286769,2 | MCF-7 | breast: | |
4 | chr5:82184309..82184963-chr8:43234719..43235395,2 | MCF-7 | breast: |
(count:8 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-HGSNAT-6 | chr8:43236787-43237091 | NONHSAT126355 |
2 | lnc-HGSNAT-7 | chr8:43298045-43298224 | NONHSAT126356 |
3 | lnc-HGSNAT-7 | chr8:43306599-43306780 | NONHSAT126356 |
4 | lnc-HGSNAT-7 | chr8:43299491-43299558 | NONHSAT126356 |
5 | lnc-HGSNAT-7 | chr8:43303948-43304047 | NONHSAT126356 |
6 | lnc-HGSNAT-5 | chr8:43233441-43233652 | NONHSAT126354 |
7 | lnc-HGSNAT-7 | chr8:43307943-43308055 | NONHSAT126356 |
8 | lnc-HGSNAT-8 | chr8:43349080-43349905 | NONHSAT126357 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000250637 | TF binding region |
ENSG00000201329 | TF binding region |
ENSG00000254342 | TF binding region |
RN7SKP41 | TF binding region |
ENSG00000264094 | TF binding region |
ENSG00000254069 | TF binding region |
ENSG00000250637 | CpG island |
ENSG00000201329 | CpG island |
ENSG00000254342 | CpG island |
RN7SKP41 | CpG island |
ENSG00000264094 | CpG island |
ENSG00000254069 | CpG island |
ENSG00000185900 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs552517514 | chr8:43205222-43205223 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs572783939 | chr8:43205225-43205226 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs115448030 | chr8:43205229-43205230 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs151206024 | chr8:43205232-43205233 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs140280096 | chr8:43205276-43205277 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs544375658 | chr8:43205277-43205278 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs4507807 | chr8:43205279-43205280 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs532618498 | chr8:43205286-43205287 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs137920126 | chr8:43205288-43205289 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs113484568 | chr8:43205294-43205295 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs184316476 | chr8:43205296-43205297 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs528521489 | chr8:43205316-43205317 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs548850911 | chr8:43205321-43205322 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs568617441 | chr8:43205322-43205323 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs537350019 | chr8:43205355-43205356 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs571077870 | chr8:43205358-43205359 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs112734304 | chr8:43205365-43205366 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs539130183 | chr8:43205373-43205374 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs552839746 | chr8:43205379-43205380 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs138480534 | chr8:43205390-43205391 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs113842696 | chr8:43205396-43205397 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs144382641 | chr8:43205405-43205406 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs575423575 | chr8:43205418-43205419 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs558097060 | chr8:43205420-43205421 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs544536155 | chr8:43205430-43205431 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs34996850 | chr8:43205442-43205443 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs370285212 | chr8:43205451-43205452 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
28 | rs189598117 | chr8:43205459-43205460 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
29 | rs182010203 | chr8:43205471-43205472 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
30 | rs577942930 | chr8:43205513-43205514 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
31 | rs373666498 | chr8:43205517-43205518 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
32 | rs112494836 | chr8:43205521-43205522 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
33 | rs141507892 | chr8:43205581-43205582 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
34 | rs528593712 | chr8:43205584-43205585 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
35 | rs114538866 | chr8:43205594-43205595 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
36 | rs568646693 | chr8:43205599-43205600 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
37 | rs552927182 | chr8:43220004-43220005 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
38 | rs145049788 | chr8:43220005-43220006 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
39 | rs79683366 | chr8:43220026-43220027 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
40 | rs73561434 | chr8:43220050-43220051 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
41 | rs73561435 | chr8:43220061-43220062 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
42 | rs138831673 | chr8:43220070-43220071 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
43 | rs558420888 | chr8:43220079-43220080 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
44 | rs149345045 | chr8:43220080-43220081 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
45 | rs143613688 | chr8:43220088-43220089 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
46 | rs73677993 | chr8:43220112-43220113 | ZNF genes & repeats | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
47 | rs148051142 | chr8:43220114-43220115 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
48 | rs542611193 | chr8:43220126-43220127 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
49 | rs562613571 | chr8:43220136-43220137 | ZNF genes & repeats | n/a | n/a | Overlapped CNVs | n/a |
50 | rs368336661 | chr8:43220141-43220142 | 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 |
Myxofibrosarcoma | 16751306 | 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 |
Chronic lymphocytic leukemia | 18922857 | CNVD |
Cutaneous T-cell lymphoma | 21881587 | CNVD |
Breast cancer | 21045282 | CNVD |
Lung cancer | 17925434 | CNVD |
Acute lymphoblastic leukemia | 21248843 | CNVD |
Sezary syndrome | 18413736 | 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 |
Breast cancer | 22522925 | CNVD |
Non-syndromic sensorineural hearing loss | 19587683 | CNVD |
Non-syndromic sensorineural hearing loss | 21293372 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:43205200-43205600 | Enhancers | Dnd41 | blood |
2 | chr8:43220000-43221000 | ZNF genes & repeats | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr8:43220600-43221000 | ZNF genes & repeats | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr8:43251800-43252200 | ZNF genes & repeats | H9 Cell Line | embryonic stem cell |
5 | chr8:43259400-43260600 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
6 | chr8:43261800-43264000 | ZNF genes & repeats | HUES48 Cell Line | embryonic stem cell |
7 | chr8:43263000-43263600 | ZNF genes & repeats | iPS DF 19.11 Cell Line | embryonic stem cell |
8 | chr8:43263200-43264800 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
9 | chr8:43265200-43266200 | ZNF genes & repeats | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
10 | chr8:43273200-43273600 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
11 | chr8:43273800-43274000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
12 | chr8:43295200-43295800 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
13 | chr8:43303200-43303800 | Enhancers | Liver | Liver |
14 | chr8:43321800-43324400 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
15 | chr8:43322000-43322800 | ZNF genes & repeats | ES-UCSF4 Cell Line | embryonic stem cell |
16 | chr8:43333000-43333600 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
17 | chr8:43352000-43352600 | Enhancers | A549 | lung |
18 | chr8:43352000-43353600 | Enhancers | Muscle Satellite Cultured Cells | -- |
19 | chr8:43352200-43353000 | Enhancers | Hela-S3 | cervix |
20 | chr8:43352600-43352800 | Active TSS | A549 | lung |
21 | chr8:43352800-43353000 | Flanking Active TSS | A549 | lung |
22 | chr8:43355400-43355600 | Enhancers | Muscle Satellite Cultured Cells | -- |
23 | chr8:43355600-43355800 | Weak transcription | Aorta | Aorta |