Variant report
Variant | esv2752258 |
---|---|
Chromosome Location | chr8:5761142-5806632 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:139)
- CpG islands (count:122)
- Chromatin interactive region (count:2)
- LncRNA region (count:1)
- 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 | chr8:5765727-5765858 | H1-hESC | embryonic stem cell: | n/a | n/a |
2 | CEBPB | chr8:5766581-5766595 | A549 | lung: | n/a | n/a |
3 | CTCF | chr8:5798357-5798574 | MCF-7 | breast: | n/a | n/a |
4 | CTCF | chr8:5790260-5790410 | GM12869 | blood: | n/a | n/a |
5 | CTCF | chr8:5798326-5798597 | H1-hESC | embryonic stem cell: | n/a | n/a |
6 | CTCF | chr8:5798360-5798510 | BE2_C | brain: | n/a | n/a |
7 | CTCF | chr8:5765000-5765150 | GM12866 | blood: | n/a | n/a |
8 | CTCF | chr8:5790200-5790350 | NHDF-neo | bronchial: | n/a | n/a |
9 | CTCF | chr8:5798480-5798630 | A549 | lung: | n/a | n/a |
10 | CTCF | chr8:5798353-5798573 | MCF-7 | breast: | n/a | n/a |
11 | CTCF | chr8:5790260-5790410 | NB4 | blood: | n/a | n/a |
12 | CTCF | chr8:5790250-5790429 | LNCaP | prostate: | n/a | n/a |
13 | CTCF | chr8:5798420-5798570 | Caco-2 | colon: | n/a | n/a |
14 | CTCF | chr8:5798441-5798516 | Gliobla | brain: | n/a | n/a |
15 | CTCF | chr8:5790220-5790370 | NHEK | skin: | n/a | n/a |
16 | CTCF | chr8:5790240-5790390 | Hela-S3 | cervix: | n/a | n/a |
17 | CTCF | chr8:5798340-5798490 | HFF-Myc | foreskin: | n/a | n/a |
18 | CTCF | chr8:5790180-5790330 | HMF | breast: | n/a | n/a |
19 | CTCF | chr8:5790260-5790410 | NHEK | skin: | n/a | n/a |
20 | CTCF | chr8:5798293-5798586 | MCF-7 | breast: | n/a | n/a |
21 | CTCF | chr8:5790220-5790370 | HMEC | breast: | n/a | n/a |
22 | CTCF | chr8:5790240-5790390 | BJ | skin: | n/a | n/a |
23 | CTCF | chr8:5798329-5798521 | HepG2 | liver: | n/a | n/a |
24 | CTCF | chr8:5790281-5790360 | HepG2 | liver: | n/a | n/a |
25 | CTCF | chr8:5790220-5790370 | GM12866 | blood: | n/a | n/a |
26 | CTCF | chr8:5790254-5790377 | MCF-7 | breast: | n/a | n/a |
27 | CTCF | chr8:5790601-5790700 | Gliobla | brain: | n/a | n/a |
28 | CTCF | chr8:5798203-5798596 | H1-hESC | embryonic stem cell: | n/a | n/a |
29 | CTCF | chr8:5790280-5790430 | HL-60 | blood: | n/a | n/a |
30 | CTCF | chr8:5790235-5790336 | SK-N-SH_RA | brain: | n/a | n/a |
31 | CTCF | chr8:5798400-5798550 | HepG2 | liver: | n/a | n/a |
32 | CTCF | chr8:5790240-5790390 | MCF-7 | breast: | n/a | n/a |
33 | CTCF | chr8:5790222-5790383 | SK-N-SH_RA | brain: | n/a | n/a |
34 | CTCF | chr8:5790260-5790410 | BE2_C | brain: | n/a | n/a |
35 | CTCF | chr8:5790200-5790350 | BJ | skin: | n/a | n/a |
36 | CTCF | chr8:5798374-5798543 | MCF-7 | breast: | n/a | n/a |
37 | CTCF | chr8:5796519-5796555 | LNCaP | prostate: | n/a | n/a |
38 | CTCF | chr8:5790240-5790390 | A549 | lung: | n/a | n/a |
39 | CTCF | chr8:5790269-5790386 | Medullo | brain: | n/a | n/a |
40 | CTCF | chr8:5798280-5798430 | Hela-S3 | cervix: | n/a | n/a |
41 | CTCF | chr8:5798330-5798542 | LNCaP | prostate: | n/a | n/a |
42 | CTCF | chr8:5798380-5798530 | Caco-2 | colon: | n/a | n/a |
43 | CTCF | chr8:5790238-5790466 | LNCaP | prostate: | n/a | n/a |
44 | CTCF | chr8:5790263-5790411 | K562 | blood: | n/a | n/a |
45 | CTCF | chr8:5798340-5798490 | MCF-7 | breast: | n/a | n/a |
46 | CTCF | chr8:5790240-5790390 | BE2_C | brain: | n/a | n/a |
47 | CTCF | chr8:5798372-5798556 | MCF-7 | breast: | n/a | n/a |
48 | CTCF | chr8:5790200-5790350 | SK-N-SH_RA | brain: | n/a | n/a |
49 | CTCF | chr8:5790240-5790390 | WERI-Rb-1 | eye: | n/a | n/a |
50 | CTCF | chr8:5790240-5790390 | HFF | foreskin: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr8:5762990-5763040 | MCF10A-Er-Src | breast: | n/a |
2 | chr8:5762944-5762994 | SK-N-MC | brain: | n/a |
3 | chr8:5762944-5762994 | NHDF-neo | bronchial: | n/a |
4 | chr8:5762944-5762994 | HEEpiC | esophagus: | n/a |
5 | chr8:5762944-5762994 | PANC-1 | pancreas: | n/a |
6 | chr8:5762990-5763040 | HRCEpiC | kidney: | n/a |
7 | chr8:5762944-5762994 | HRPEpiC | eye: | n/a |
8 | chr8:5762944-5762994 | H1-hESC | embryonic stem cell: | embryo |
9 | chr8:5762944-5762994 | GM06990 | blood: | n/a |
10 | chr8:5762990-5763040 | HCF | heart: | n/a |
11 | chr8:5762990-5763040 | HEEpiC | esophagus: | n/a |
12 | chr8:5762944-5762994 | SAEC | small airway: | n/a |
13 | chr8:5762990-5763040 | AG04450 | lung: | fetal |
14 | chr8:5762944-5762994 | Hepatocyte | liver: | n/a |
15 | chr8:5762990-5763040 | HEK293 | kidney: | embryo |
16 | chr8:5762944-5762994 | NH-A | brain: | n/a |
17 | chr8:5762990-5763040 | Hepatocyte | liver: | n/a |
18 | chr8:5762990-5763040 | K562 | blood: | n/a |
19 | chr8:5762990-5763040 | HIPEpiC | eye: | n/a |
20 | chr8:5762990-5763040 | PANC-1 | pancreas: | n/a |
21 | chr8:5762944-5762994 | Hela-S3 | cervix: | n/a |
22 | chr8:5762990-5763040 | GM12878 | blood: | n/a |
23 | chr8:5762990-5763040 | HPAEpiC | pulmonary alveolar: | n/a |
24 | chr8:5762990-5763040 | GM06990 | blood: | n/a |
25 | chr8:5762944-5762994 | HPAEpiC | pulmonary alveolar: | n/a |
26 | chr8:5762990-5763040 | NB4 | blood: | n/a |
27 | chr8:5762944-5762994 | GM12892 | blood: | n/a |
28 | chr8:5762944-5762994 | HMEC | breast: | n/a |
29 | chr8:5762944-5762994 | HRCEpiC | kidney: | n/a |
30 | chr8:5762944-5762994 | NT2-D1 | testis: | n/a |
31 | chr8:5762990-5763040 | HRPEpiC | eye: | n/a |
32 | chr8:5762944-5762994 | HAEpiC | amniotic membrane: | n/a |
33 | chr8:5762990-5763040 | HUVEC | blood vessel: | n/a |
34 | chr8:5762944-5762994 | RPTEC | kidney: | n/a |
35 | chr8:5762990-5763040 | ovcar-3 | ovarian: | n/a |
36 | chr8:5762944-5762994 | HIPEpiC | eye: | n/a |
37 | chr8:5762990-5763040 | AG10803 | skin: | n/a |
38 | chr8:5762944-5762994 | A549 | lung: | n/a |
39 | chr8:5762944-5762994 | HCT-116 | colon: | n/a |
40 | chr8:5762990-5763040 | Hela-S3 | cervix: | n/a |
41 | chr8:5762990-5763040 | HAEpiC | amniotic membrane: | n/a |
42 | chr8:5762944-5762994 | GM12878 | blood: | n/a |
43 | chr8:5762990-5763040 | U87 | brain: | n/a |
44 | chr8:5762944-5762994 | LNCaP | prostate: | n/a |
45 | chr8:5762990-5763040 | HCM | heart: | n/a |
46 | chr8:5762990-5763040 | T-47D | breast: | n/a |
47 | chr8:5762990-5763040 | PrEC | prostate: | n/a |
48 | chr8:5762990-5763040 | AG09309 | skin: | n/a |
49 | chr8:5762944-5762994 | AG04449 | skin: | fetal |
50 | chr8:5762944-5762994 | MCF10A-Er-Src | breast: | n/a |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-ANGPT2-12 | chr8:5768467-5768758 | NONHSAT124763 |
No data |
No data |
Variant related genes | Relation type |
---|---|
RN7SKP159 | TF binding region |
RN7SKP159 | CpG island |
ENSG00000246089 | chromatin interactions |
ENSG00000147316 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs34211217 | chr8:5761142-5761143 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs562954483 | chr8:5761144-5761145 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs17075051 | chr8:5761145-5761146 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | mRNA abundance |
4 | rs548494818 | chr8:5761170-5761171 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs549421682 | chr8:5761204-5761205 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs376766843 | chr8:5761233-5761234 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs527739001 | chr8:5761240-5761241 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
8 | rs145958864 | chr8:5761253-5761254 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs570486707 | chr8:5761308-5761309 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs139717055 | chr8:5761319-5761320 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs556457948 | chr8:5761323-5761324 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs568240774 | chr8:5761332-5761333 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs553423308 | chr8:5761342-5761343 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs535685690 | chr8:5761343-5761344 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs116755402 | chr8:5761344-5761345 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs114767942 | chr8:5761360-5761361 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs545866621 | chr8:5761377-5761378 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs187776606 | chr8:5761384-5761385 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs144379060 | chr8:5761389-5761390 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
20 | rs192520637 | chr8:5761398-5761399 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs563244055 | chr8:5761407-5761408 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
22 | rs61590929 | chr8:5761416-5761417 | Enhancers Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
23 | rs2703244 | chr8:5761421-5761422 | Enhancers Weak transcription | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
24 | rs151127411 | chr8:5761429-5761430 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
25 | rs539489634 | chr8:5761431-5761432 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
26 | rs527805618 | chr8:5761446-5761447 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
27 | rs552220807 | chr8:5761483-5761484 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
28 | rs74300032 | chr8:5761494-5761495 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
29 | rs531621509 | chr8:5761495-5761496 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
30 | rs549903189 | chr8:5761513-5761514 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
31 | rs568381974 | chr8:5761517-5761518 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
32 | rs183631823 | chr8:5761525-5761526 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
33 | rs553934825 | chr8:5761539-5761540 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
34 | rs79570452 | chr8:5761556-5761557 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
35 | rs373946587 | chr8:5761557-5761558 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
36 | rs201075935 | chr8:5761567-5761568 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
37 | rs565850370 | chr8:5761587-5761588 | Enhancers Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
38 | rs138628931 | chr8:5761616-5761617 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
39 | rs200685896 | chr8:5761623-5761624 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
40 | rs201912129 | chr8:5761626-5761627 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
41 | rs149876399 | chr8:5761627-5761628 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
42 | rs188437182 | chr8:5761642-5761643 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
43 | rs139984439 | chr8:5761648-5761649 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
44 | rs112475060 | chr8:5761688-5761689 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
45 | rs368970203 | chr8:5761689-5761690 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
46 | rs544388789 | chr8:5761694-5761695 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
47 | rs192697645 | chr8:5761723-5761724 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
48 | rs184994969 | chr8:5761725-5761726 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
49 | rs574948784 | chr8:5761735-5761736 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
50 | rs78465456 | chr8:5761736-5761737 | Weak transcription | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Prostate cancer | 16573809 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Ovarian clear cell carcinoma | 21343371 | CNVD |
abnormal development | 18461090 | CNVD |
Crohn''s disease | 19220326 | CNVD |
Psoriasis | 19220326 | CNVD |
Prostate cancer | 21965145 | CNVD |
Prostate cancer | 18515986 | CNVD |
Chronic obstructive pulmonary disease | 20378733 | CNVD |
Autism | 18414403 | CNVD |
Cancer | 21183584 | CNVD |
Non-syndromic sensorineural hearing loss | 15273396 | CNVD |
Breast cancer | 17603634 | CNVD |
Myeloproliferative neoplasm | 20015882 | CNVD |
Ovarian cancer | 20844748 | CNVD |
Cervical cancer | 17311676 | CNVD |
High-grade prostatic intraepithelial neoplasia | 16573809 | CNVD |
Non-syndromic sensorineural hearing loss | 20606397 | CNVD |
Schizophrenia | 20877625 | CNVD |
Disorders of sex development | 21048976 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Follicular lymphoma | 17170743 | CNVD |
Breast cancer | 17001317 | CNVD |
Thyroid cancer | 19087340 | CNVD |
Multiple myeloma | 16616336 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Heart disease | 21282601 | CNVD |
T-cell lymphomas | 19863542 | CNVD |
Ovarian cancer | 22174824 | CNVD |
Colorectal cancer | 21297112 | CNVD |
Hodgkin''s lymphoma | 18641027 | CNVD |
Salivary gland tumor | 18059337 | CNVD |
Breast cancer | 17133270 | CNVD |
Melanoma | 18172304 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Chronic lymphocytic leukemia | 18922857 | CNVD |
Breast cancer | 17393978 | CNVD |
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 |
Oral cancer | 21386901 | CNVD |
Prostate cancer | 21088497 | 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 |
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 |
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 |
Acute lymphoblastic leukemia | 21248843 | CNVD |
Breast cancer | 21785460 | CNVD |
Thoracic aortic aneurysm | 21092924 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Breast cancer | 21509527 | CNVD |
T-cell prolymphocytic leukemia | 17713554 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Epilepsy | 22083797 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
low-grade B-cell lymphoma tumor | 18367492 | CNVD |
Prostate cancer | 18632612 | CNVD |
Breast cancer | 21858162 | CNVD |
lymphocytic leukemia | 21291569 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Autism | 22495311 | CNVD |
Congenital diaphragmatic hernia | 21064195 | CNVD |
Cancer | 20164920 | CNVD |
Oral squamous cell carcinoma | 17134496 | CNVD |
Non-small cell lung cancer | 21829676 | CNVD |
Esophageal squamous carcinoma | 18405350 | CNVD |
Prostate cancer | 17217626 | CNVD |
Developmental delay | 19128483 | CNVD |
Neuroticism | 17667963 | CNVD |
Leukoplakia | 24403051 | CNVD |
Intellectual disability | 22045946 | CNVD |
Malignant fibrous histiocytomas | 21085701 | CNVD |
Breast cancer | 16608533 | CNVD |
Seminomas | 18059402 | CNVD |
Breast cancer | 21364760 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Lung cancer | 18438408 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Colorectal cancer | 16774939 | CNVD |
Lung squamous cell carcinoma | 22363434 | CNVD |
Cancer | 20164919 | CNVD |
Non-syndromic sensorineural hearing loss | 17289997 | CNVD |
Non-syndromic sensorineural hearing loss | 17122850 | CNVD |
Chronic myeloid leukemia | 21384125 | CNVD |
Tetralogy of Fallot | 22912587 | CNVD |
Type 2 diabetes | 21526130 | CNVD |
Medulloblastoma | 16783165 | CNVD |
Schizophrenia | 20967226 | CNVD |
Pancreatic ductal adenocarcinoma | 19077451 | CNVD |
Non-syndromic sensorineural hearing loss | 18451855 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:5760200-5761600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
2 | chr8:5760800-5761600 | Enhancers | H1 Cell Line | embryonic stem cell |
3 | chr8:5761000-5761400 | Enhancers | HUES48 Cell Line | embryonic stem cell |
4 | chr8:5761000-5761600 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
5 | chr8:5761400-5762000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
6 | chr8:5761400-5763400 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
7 | chr8:5761600-5762000 | Weak transcription | H1 Cell Line | embryonic stem cell |
8 | chr8:5761600-5763400 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
9 | chr8:5761600-5763400 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
10 | chr8:5762000-5762200 | Enhancers | H1 Cell Line | embryonic stem cell |
11 | chr8:5762000-5762200 | Genic enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
12 | chr8:5762000-5762400 | Active TSS | H1 Derived Mesenchymal Stem Cells | ES cell derived |
13 | chr8:5762200-5764000 | Weak transcription | H1 Cell Line | embryonic stem cell |
14 | chr8:5762200-5764600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
15 | chr8:5763400-5763600 | Enhancers | H9 Cell Line | embryonic stem cell |
16 | chr8:5763400-5764200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
17 | chr8:5763400-5764600 | Enhancers | HUES48 Cell Line | embryonic stem cell |
18 | chr8:5763400-5765600 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
19 | chr8:5763400-5765800 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
20 | chr8:5763600-5764200 | Enhancers | HUES6 Cell Line | embryonic stem cell |
21 | chr8:5763600-5764600 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
22 | chr8:5763800-5764600 | Weak transcription | H9 Cell Line | embryonic stem cell |
23 | chr8:5764000-5764200 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
24 | chr8:5764000-5764600 | Enhancers | H1 Cell Line | embryonic stem cell |
25 | chr8:5764600-5765000 | Weak transcription | H1 Cell Line | embryonic stem cell |
26 | chr8:5764600-5765400 | Enhancers | H9 Cell Line | embryonic stem cell |
27 | chr8:5764600-5765600 | Enhancers | HUES64 Cell Line | embryonic stem cell |
28 | chr8:5765000-5765600 | Enhancers | H1 Cell Line | embryonic stem cell |
29 | chr8:5772600-5774600 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
30 | chr8:5773000-5774800 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
31 | chr8:5792200-5794800 | Enhancers | Dnd41 | blood |
32 | chr8:5796200-5796600 | Enhancers | Fetal Heart | heart |
33 | chr8:5806600-5809600 | Weak transcription | Fetal Heart | heart |