Variant report
Variant | nsv1009701 |
---|---|
Chromosome Location | chr1:194304618-194335689 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:249)
- CpG islands (count:61)
- Chromatin interactive region (count:20)
- 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 | ATF3 | chr1:194312059-194312295 | H1-hESC | embryonic stem cell: | n/a | n/a |
2 | ATF3 | chr1:194311963-194312358 | H1-hESC | embryonic stem cell: | n/a | n/a |
3 | CEBPB | chr1:194330514-194330873 | Hela-S3 | cervix: | n/a | chr1:194330728-194330739 |
4 | CEBPB | chr1:194309672-194309782 | A549 | lung: | n/a | n/a |
5 | CEBPB | chr1:194334363-194334677 | HepG2 | liver: | n/a | chr1:194334514-194334525 |
6 | CEBPB | chr1:194330573-194330832 | K562 | blood: | n/a | chr1:194330728-194330739 |
7 | CEBPB | chr1:194334367-194334673 | IMR90 | lung: | n/a | chr1:194334514-194334525 |
8 | CEBPB | chr1:194330540-194330888 | HepG2 | liver: | n/a | chr1:194330728-194330739 |
9 | CEBPB | chr1:194312110-194312319 | A549 | lung: | n/a | n/a |
10 | CEBPB | chr1:194334390-194334657 | K562 | blood: | n/a | chr1:194334514-194334525 |
11 | CEBPB | chr1:194330473-194330868 | IMR90 | lung: | n/a | chr1:194330728-194330739 |
12 | CEBPB | chr1:194330550-194330806 | A549 | lung: | n/a | chr1:194330728-194330739 |
13 | CREB1 | chr1:194312007-194312285 | H1-hESC | embryonic stem cell: | n/a | n/a |
14 | CTCF | chr1:194312100-194312250 | GM12867 | blood: | n/a | n/a |
15 | CTCF | chr1:194312140-194312290 | GM12871 | blood: | n/a | n/a |
16 | CTCF | chr1:194312080-194312230 | K562 | blood: | n/a | n/a |
17 | CTCF | chr1:194311780-194311930 | GM06990 | blood: | n/a | n/a |
18 | CTCF | chr1:194312040-194312190 | BE2_C | brain: | n/a | n/a |
19 | CTCF | chr1:194312113-194312269 | Gliobla | brain: | n/a | n/a |
20 | CTCF | chr1:194312060-194312210 | HBMEC | blood vessel: | n/a | n/a |
21 | CTCF | chr1:194312080-194312230 | SK-N-SH_RA | brain: | n/a | n/a |
22 | CTCF | chr1:194312080-194312230 | HAc | cerebellar: | n/a | n/a |
23 | CTCF | chr1:194312140-194312290 | BE2_C | brain: | n/a | n/a |
24 | CTCF | chr1:194311895-194312367 | HCT-116 | colon: | n/a | n/a |
25 | CTCF | chr1:194312120-194312270 | HA-sp | spinal cord: | n/a | n/a |
26 | CTCF | chr1:194312040-194312190 | HA-sp | spinal cord: | n/a | n/a |
27 | CTCF | chr1:194312100-194312250 | HEK293 | kidney: | n/a | n/a |
28 | CTCF | chr1:194312080-194312230 | WERI-Rb-1 | eye: | n/a | n/a |
29 | CTCF | chr1:194312105-194312253 | NHEK | skin: | n/a | n/a |
30 | CTCF | chr1:194311775-194311829 | MCF-7 | breast: | n/a | n/a |
31 | CTCF | chr1:194312071-194312288 | K562 | blood: | n/a | n/a |
32 | CTCF | chr1:194312046-194312292 | MCF-7 | breast: | n/a | n/a |
33 | CTCF | chr1:194311990-194312329 | H1-hESC | embryonic stem cell: | n/a | n/a |
34 | CTCF | chr1:194312060-194312210 | HEEpiC | esophagus: | n/a | n/a |
35 | CTCF | chr1:194312100-194312250 | GM12874 | blood: | n/a | n/a |
36 | CTCF | chr1:194312086-194312273 | GM19240 | blood: | n/a | n/a |
37 | CTCF | chr1:194312115-194312208 | HUVEC | blood vessel: | n/a | n/a |
38 | CTCF | chr1:194312082-194312280 | GM12892 | blood: | n/a | n/a |
39 | CTCF | chr1:194312119-194312200 | GM20000 | blood: | n/a | n/a |
40 | CTCF | chr1:194312140-194312290 | Hela-S3 | cervix: | n/a | n/a |
41 | CTCF | chr1:194312080-194312267 | A549 | lung: | n/a | n/a |
42 | CTCF | chr1:194312100-194312250 | HPAF | blood vessel: | n/a | n/a |
43 | CTCF | chr1:194311954-194312324 | K562 | blood: | n/a | n/a |
44 | CTCF | chr1:194312039-194312301 | HepG2 | liver: | n/a | n/a |
45 | CTCF | chr1:194311769-194311790 | MCF-7 | breast: | n/a | n/a |
46 | CTCF | chr1:194312180-194312330 | GM12801 | blood: | n/a | n/a |
47 | CTCF | chr1:194312080-194312230 | HFF-Myc | foreskin: | n/a | n/a |
48 | CTCF | chr1:194311820-194311970 | GM12867 | blood: | n/a | n/a |
49 | CTCF | chr1:194312120-194312270 | WERI-Rb-1 | eye: | n/a | n/a |
50 | CTCF | chr1:194312120-194312270 | GM12870 | blood: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:194327715-194327765 | Hela-S3 | cervix: | n/a |
2 | chr1:194327715-194327765 | HRE | kidney: | n/a |
3 | chr1:194327715-194327765 | AG04449 | skin: | fetal |
4 | chr1:194327715-194327765 | HPAEpiC | pulmonary alveolar: | n/a |
5 | chr1:194327715-194327765 | MCF-7 | breast: | n/a |
6 | chr1:194327715-194327765 | ECC-1 | luminal epithelium: | n/a |
7 | chr1:194327715-194327765 | SK-N-MC | brain: | n/a |
8 | chr1:194327715-194327765 | AG04450 | lung: | fetal |
9 | chr1:194327715-194327765 | PANC-1 | pancreas: | n/a |
10 | chr1:194327715-194327765 | LNCaP | prostate: | n/a |
11 | chr1:194327715-194327765 | HCM | heart: | n/a |
12 | chr1:194327715-194327765 | PFSK-1 | brain: | n/a |
13 | chr1:194327715-194327765 | HUVEC | blood vessel: | n/a |
14 | chr1:194327715-194327765 | AG10803 | skin: | n/a |
15 | chr1:194327715-194327765 | NT2-D1 | testis: | n/a |
16 | chr1:194327715-194327765 | ProgFib | skin: | n/a |
17 | chr1:194327715-194327765 | U87 | brain: | n/a |
18 | chr1:194327715-194327765 | IMR90 | lung: | fetal |
19 | chr1:194327715-194327765 | GM12878 | blood: | n/a |
20 | chr1:194327715-194327765 | GM06990 | blood: | n/a |
21 | chr1:194327715-194327765 | AoSMC | blood vessel: | n/a |
22 | chr1:194327715-194327765 | Caco-2 | colon: | n/a |
23 | chr1:194327715-194327765 | HepG2 | liver: | n/a |
24 | chr1:194327715-194327765 | HEEpiC | esophagus: | n/a |
25 | chr1:194327715-194327765 | HAEpiC | amniotic membrane: | n/a |
26 | chr1:194327715-194327765 | Jurkat | blood: | n/a |
27 | chr1:194327715-194327765 | T-47D | breast: | n/a |
28 | chr1:194327715-194327765 | ovcar-3 | ovarian: | n/a |
29 | chr1:194327715-194327765 | HNPCEpiC | eye: | n/a |
30 | chr1:194327715-194327765 | SKMC | muscle: | n/a |
31 | chr1:194327715-194327765 | BJ | skin: | n/a |
32 | chr1:194327715-194327765 | NH-A | brain: | n/a |
33 | chr1:194327715-194327765 | SK-N-SH_RA | brain: | n/a |
34 | chr1:194327715-194327765 | BE2_C | brain: | n/a |
35 | chr1:194327715-194327765 | K562 | blood: | n/a |
36 | chr1:194327715-194327765 | NB4 | blood: | n/a |
37 | chr1:194327715-194327765 | Hepatocyte | liver: | n/a |
38 | chr1:194327715-194327765 | H1-hESC | embryonic stem cell: | embryo |
39 | chr1:194327715-194327765 | RPTEC | kidney: | n/a |
40 | chr1:194327715-194327765 | HCF | heart: | n/a |
41 | chr1:194327715-194327765 | MCF10A-Er-Src | breast: | n/a |
42 | chr1:194327715-194327765 | PrEC | prostate: | n/a |
43 | chr1:194327715-194327765 | HEK293 | kidney: | embryo |
44 | chr1:194327715-194327765 | AG09319 | gingival: | n/a |
45 | chr1:194327715-194327765 | CMK | blood: | n/a |
46 | chr1:194327715-194327765 | HRPEpiC | eye: | n/a |
47 | chr1:194327715-194327765 | AG09309 | skin: | n/a |
48 | chr1:194327715-194327765 | GM19239 | blood: | n/a |
49 | chr1:194327715-194327765 | HMEC | breast: | n/a |
50 | chr1:194327715-194327765 | A549 | lung: | n/a |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:193587120..193589760-chr1:194326578..194328851,2 | K562 | blood: | |
2 | chr1:194325391..194328027-chr1:194331850..194333464,2 | K562 | blood: | |
3 | chr1:194317795..194320009-chr1:194323102..194324851,2 | K562 | blood: | |
4 | chr1:194328262..194330986-chr1:194334081..194336171,2 | K562 | blood: | |
5 | chr1:194307530..194310929-chr1:194324369..194327548,3 | K562 | blood: | |
6 | chr1:194307530..194310929-chr1:194324369..194327548,3 | K562 | blood: | |
7 | chr1:194325391..194328027-chr1:194331850..194333464,2 | K562 | blood: | |
8 | chr1:194308962..194311330-chr4:127715408..127718280,2 | MCF-7 | breast: | |
9 | chr1:194290793..194293350-chr1:194303671..194305841,2 | K562 | blood: | |
10 | chr1:194306516..194309030-chr1:194325392..194327548,2 | K562 | blood: | |
11 | chr1:194320848..194323111-chr1:194332698..194335480,2 | K562 | blood: | |
12 | chr1:194317795..194320009-chr1:194323102..194324851,2 | K562 | blood: | |
13 | chr1:194315164..194317998-chr1:194319254..194321893,3 | K562 | blood: | |
14 | chr1:194326093..194330986-chr1:194331715..194336171,7 | K562 | blood: | |
15 | chr1:194320848..194323111-chr1:194332698..194335480,2 | K562 | blood: | |
16 | chr1:194328262..194330986-chr1:194334081..194336171,2 | K562 | blood: | |
17 | chr1:194306516..194309030-chr1:194325392..194327548,2 | K562 | blood: | |
18 | chr1:194326093..194330986-chr1:194331715..194336171,7 | K562 | blood: | |
19 | chr1:194315945..194318461-chr1:194337918..194339837,2 | K562 | blood: | |
20 | chr1:194070430..194072677-chr1:194322592..194324190,2 | K562 | blood: |
(count:4 , 50 per page) page:
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-CDC73-4 | chr1:194321413-194321556 | XLOC_000510 |
2 | lnc-CDC73-4 | chr1:194320593-194321556 | NONHSAT008581 |
3 | lnc-CDC73-4 | chr1:194320009-194320481 | NONHSAT008581 |
4 | lnc-CDC73-4 | chr1:194320073-194320368 | XLOC_000510 |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000231714 | TF binding region |
ENSG00000231714 | CpG island |
ENSG00000231714 | chromatin interactions |
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | rs370340718 | chr1:194307223-194307224 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
2 | rs561606331 | chr1:194307237-194307238 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
3 | rs556260495 | chr1:194307244-194307245 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
4 | rs571758337 | chr1:194307274-194307275 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
5 | rs115687074 | chr1:194307280-194307281 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
6 | rs374229386 | chr1:194307287-194307288 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
7 | rs12083179 | chr1:194307301-194307302 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
8 | rs568684029 | chr1:194307315-194307316 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
9 | rs114568415 | chr1:194307321-194307322 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
10 | rs551221900 | chr1:194307361-194307362 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
11 | rs140923147 | chr1:194307379-194307380 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
12 | rs574970382 | chr1:194307409-194307410 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
13 | rs189048351 | chr1:194307442-194307443 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
14 | rs181144309 | chr1:194307478-194307479 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
15 | rs538307143 | chr1:194307517-194307518 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
16 | rs556695500 | chr1:194307523-194307524 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
17 | rs578185676 | chr1:194307536-194307537 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
18 | rs369824536 | chr1:194307571-194307572 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
19 | rs10801296 | chr1:194307578-194307579 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
20 | rs572725217 | chr1:194307620-194307621 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
21 | rs539831968 | chr1:194307632-194307633 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
22 | rs185337639 | chr1:194307653-194307654 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
23 | rs190196588 | chr1:194307659-194307660 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
24 | rs550603650 | chr1:194307676-194307677 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
25 | rs562253462 | chr1:194307733-194307734 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
26 | rs532953358 | chr1:194307754-194307755 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
27 | rs551211428 | chr1:194307759-194307760 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
28 | rs529338148 | chr1:194307775-194307776 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
29 | rs12093854 | chr1:194307802-194307803 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
30 | rs549027024 | chr1:194307971-194307972 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
31 | rs147018845 | chr1:194307980-194307981 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
32 | rs537859257 | chr1:194307989-194307990 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
33 | rs182612084 | chr1:194308034-194308035 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
34 | rs147631944 | chr1:194308048-194308049 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
35 | rs539213108 | chr1:194308075-194308076 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
36 | rs185989492 | chr1:194308093-194308094 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
37 | rs555281058 | chr1:194308104-194308105 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
38 | rs572566891 | chr1:194308109-194308110 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
39 | rs192249242 | chr1:194308128-194308129 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
40 | rs543279165 | chr1:194308167-194308168 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
41 | rs145909617 | chr1:194308619-194308620 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
42 | rs536456269 | chr1:194308633-194308634 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
43 | rs555236184 | chr1:194308636-194308637 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
44 | rs11422773 | chr1:194308648-194308649 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
45 | rs397795052 | chr1:194308655-194308656 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
46 | rs576712399 | chr1:194308672-194308673 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
47 | rs386638121 | chr1:194308707-194308708 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
48 | rs6661290 | chr1:194308708-194308709 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
49 | rs117753770 | chr1:194308741-194308742 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
50 | rs192730851 | chr1:194308805-194308806 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
Disease | PMID | Source |
---|---|---|
Breast cancer | 17603634 | CNVD |
Esophageal squamous carcinoma | 21637470 | CNVD |
HIV/AIDS | 22032296 | CNVD |
Schizophrenia | 19415332 | CNVD |
Autism | 22495311 | CNVD |
Liposarcoma | 21253554 | CNVD |
Burkitt''s lymphoma | 18698080 | CNVD |
Melanoma | 18172304 | CNVD |
Rett syndrome | 21593744 | CNVD |
Cancer | 20164919 | CNVD |
Medulloblastoma | 21979893 | CNVD |
Acute lymphoblastic leukemia | 17443227 | CNVD |
Wilms tumour | 21544195 | CNVD |
Breast cancer | 17133270 | CNVD |
Carcinoma ex pleomorphic adenoma | 18828159 | CNVD |
Non-small cell lung cancer | 21044232 | CNVD |
Cervical cancer | 21063398 | CNVD |
Acute lymphoblastic leukemia | 20435627 | CNVD |
Astrocytoma | 17387387 | CNVD |
Breast cancer | 20632083 | CNVD |
Endometrial cancer | 22040021 | CNVD |
Ewing''s sarcoma | 21437220 | CNVD |
Gastrointestinal stromal cancer | 20470368 | CNVD |
Glioblastoma multiforme | 19960244 | CNVD |
Glioblastoma multiforme | 21080181 | CNVD |
Hepatocellular carcinoma | 22174799 | CNVD |
Medulloblastoma | 21292688 | CNVD |
Phyllodes tumor | 17334353 | CNVD |
Breast cancer | 21264507 | CNVD |
Multiple myeloma | 21628407 | CNVD |
Cancer | 16751803 | CNVD |
Prostate cancer | 16705090 | CNVD |
Neuroblastoma | 19435921 | CNVD |
Breast cancer | 17850661 | CNVD |
Breast cancer | 16461572 | CNVD |
Intracranial tumor | 16823260 | CNVD |
Medulloblastoma | 18056178 | CNVD |
Monoclonal gammopathy of undetermined significance | 17077331 | CNVD |
Primary mediastinal b-cell lymphoma | 17728785 | CNVD |
Colorectal cancer | 16272173 | CNVD |
Acute lymphoblastic leukemia | 21098271 | CNVD |
Neuroblastoma | 21899760 | CNVD |
Ovarian neoplasms | 16753589 | CNVD |
Glioblastoma multiforme | 17002787 | CNVD |
Breast cancer | 21858162 | CNVD |
Non-small cell lung cancer | 21385341 | CNVD |
Acute lymphoblastic leukemia | 21980252 | CNVD |
Breast cancer | 16608533 | CNVD |
Ewing''s sarcoma | 22429812 | CNVD |
Acute promyelocytic leukemia | 19109227 | CNVD |
Hepatocellular carcinoma | 18803288 | CNVD |
Basal cell lymphoma | 16317097 | CNVD |
Diffuse large b-cell lymphoma | 16317097 | CNVD |
Breast cancer | 17001317 | CNVD |
Acute myeloid leukemia | 21251322 | CNVD |
Multiple myeloma | 17550852 | CNVD |
Prostate cancer | 18632612 | CNVD |
Acute myeloid leukemia | 20729466 | CNVD |
Hodgkin''s lymphoma | 17606441 | CNVD |
Testicular germ cell tumor | 18059402 | CNVD |
Ependymoma | 18628472 | CNVD |
Leukemia | 18628472 | CNVD |
Neuroblastoma | 18923191 | CNVD |
Acute lymphoblastic leukemia | 19100363 | CNVD |
Breast cancer | 21509527 | CNVD |
Endometrioid adenocarcinoma | 16974079 | CNVD |
Lung cancer | 18438408 | CNVD |
Metanephric adenoma | 20802469 | CNVD |
Melanoma | 20688739 | CNVD |
small cell lung cancer | 20016488 | CNVD |
Breast cancer | 21611746 | CNVD |
primary effusion lymphomas | 17116491 | CNVD |
Breast cancer | 17393978 | CNVD |
Hepatocellular carcinoma | 16750200 | CNVD |
Acute lymphoblastic leukemia | 22237106 | CNVD |
Non-small cell lung cancer | 19010865 | CNVD |
Mental retardation | 17847001 | CNVD |
Basal cell lymphoma | 17170743 | CNVD |
Follicular lymphoma | 17170743 | CNVD |
Trisomy 5 syndrome | 21098271 | CNVD |
Glioblastoma multiforme | 22286061 | CNVD |
Urothelial carcinoma | 21177765 | CNVD |
Myelofibrosis | 22110671 | CNVD |
Breast cancer | 16272173 | CNVD |
Mental retardation | 21062444 | CNVD |
Liver carcinoma | 19366792 | CNVD |
Acute lymphoblastic leukemia | 20067559 | CNVD |
Chordoma | 18071362 | CNVD |
Pancreatic cancer | 17952125 | CNVD |
T-cell lymphomas | 22341440 | CNVD |
Non-syndromic sensorineural hearing loss | 22037309 | CNVD |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:194307200-194308000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr1:194307400-194307800 | Enhancers | Brain Hippocampus Middle | brain |
3 | chr1:194307400-194307800 | Enhancers | Brain Substantia Nigra | brain |
4 | chr1:194307400-194308000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr1:194307400-194308200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
6 | chr1:194308600-194309000 | Enhancers | Fetal Brain Female | brain |
7 | chr1:194311600-194311800 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
8 | chr1:194311600-194311800 | Active TSS | iPS-15b Cell Line | embryonic stem cell |
9 | chr1:194311600-194312000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
10 | chr1:194311600-194312200 | Enhancers | H1 Cell Line | embryonic stem cell |
11 | chr1:194311800-194312000 | Flanking Active TSS | iPS-15b Cell Line | embryonic stem cell |
12 | chr1:194311800-194312000 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
13 | chr1:194311800-194312200 | Active TSS | ES-I3 Cell Line | embryonic stem cell |
14 | chr1:194311800-194312200 | Enhancers | H9 Cell Line | embryonic stem cell |
15 | chr1:194311800-194312200 | Active TSS | HUES48 Cell Line | embryonic stem cell |
16 | chr1:194312000-194312200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
17 | chr1:194315600-194316600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
18 | chr1:194316200-194316800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
19 | chr1:194316400-194316600 | Enhancers | Fetal Heart | heart |
20 | chr1:194316400-194317000 | Enhancers | HMEC | breast |
21 | chr1:194325000-194325200 | ZNF genes & repeats | Right Atrium | heart |
22 | chr1:194325200-194327000 | Active TSS | K562 | blood |
23 | chr1:194325200-194329000 | Weak transcription | Right Atrium | heart |
24 | chr1:194327400-194327800 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
25 | chr1:194330400-194332400 | Enhancers | Fetal Heart | heart |
26 | chr1:194335400-194336000 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
27 | chr1:194335400-194336200 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
28 | chr1:194335600-194339200 | Enhancers | HMEC | breast |