Variant report
Variant | nsv548669 |
---|---|
Chromosome Location | chr1:194292509-194330700 |
allele | n/a |
Outlinks | Ensembl   UCSC |
- TF binding region (count:262)
- CpG islands (count:61)
- Chromatin interactive region (count:18)
- LncRNA region (count:5)
- 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 | chr1:194309672-194309782 | A549 | lung: | n/a | n/a |
4 | CEBPB | chr1:194330514-194330873 | Hela-S3 | cervix: | n/a | chr1:194330728-194330739 |
5 | CEBPB | chr1:194330540-194330888 | HepG2 | liver: | n/a | chr1:194330728-194330739 |
6 | CEBPB | chr1:194330473-194330868 | IMR90 | lung: | n/a | chr1:194330728-194330739 |
7 | CEBPB | chr1:194312110-194312319 | A549 | lung: | n/a | n/a |
8 | CEBPB | chr1:194330550-194330806 | A549 | lung: | n/a | chr1:194330728-194330739 |
9 | CEBPB | chr1:194330573-194330832 | K562 | blood: | n/a | chr1:194330728-194330739 |
10 | CREB1 | chr1:194312007-194312285 | H1-hESC | embryonic stem cell: | n/a | n/a |
11 | CTCF | chr1:194311895-194312367 | HCT-116 | colon: | n/a | n/a |
12 | CTCF | chr1:194312065-194312291 | MCF-7 | breast: | n/a | n/a |
13 | CTCF | chr1:194312080-194312230 | HAc | cerebellar: | n/a | n/a |
14 | CTCF | chr1:194312100-194312250 | SK-N-SH_RA | brain: | n/a | n/a |
15 | CTCF | chr1:194312140-194312290 | GM12871 | blood: | n/a | n/a |
16 | CTCF | chr1:194312105-194312253 | NHEK | skin: | n/a | n/a |
17 | CTCF | chr1:194312093-194312197 | GM13976 | blood: | n/a | n/a |
18 | CTCF | chr1:194311780-194311930 | GM06990 | blood: | n/a | n/a |
19 | CTCF | chr1:194318107-194318138 | Spleen_OC | spleen: | n/a | n/a |
20 | CTCF | chr1:194312080-194312267 | A549 | lung: | n/a | n/a |
21 | CTCF | chr1:194312010-194312315 | K562 | blood: | n/a | n/a |
22 | CTCF | chr1:194312066-194312284 | GM12891 | blood: | n/a | n/a |
23 | CTCF | chr1:194312032-194312346 | HepG2 | liver: | n/a | n/a |
24 | CTCF | chr1:194312080-194312230 | GM12864 | blood: | n/a | n/a |
25 | CTCF | chr1:194312120-194312270 | HEK293 | kidney: | n/a | n/a |
26 | CTCF | chr1:194312140-194312290 | Hela-S3 | cervix: | n/a | n/a |
27 | CTCF | chr1:194312060-194312210 | HBMEC | blood vessel: | n/a | n/a |
28 | CTCF | chr1:194312120-194312270 | GM12873 | blood: | n/a | n/a |
29 | CTCF | chr1:194312115-194312208 | HUVEC | blood vessel: | n/a | n/a |
30 | CTCF | chr1:194311960-194312110 | GM12870 | blood: | n/a | n/a |
31 | CTCF | chr1:194312047-194312299 | MCF-7 | breast: | n/a | n/a |
32 | CTCF | chr1:194312040-194312190 | MCF-7 | breast: | n/a | n/a |
33 | CTCF | chr1:194312039-194312301 | HepG2 | liver: | n/a | n/a |
34 | CTCF | chr1:194312120-194312270 | GM12870 | blood: | n/a | n/a |
35 | CTCF | chr1:194312100-194312250 | HUVEC | blood vessel: | n/a | n/a |
36 | CTCF | chr1:194312030-194312294 | A549 | lung: | n/a | n/a |
37 | CTCF | chr1:194312120-194312270 | GM12864 | blood: | n/a | n/a |
38 | CTCF | chr1:194311940-194312318 | MCF-7 | breast: | n/a | n/a |
39 | CTCF | chr1:194312120-194312270 | HRPEpiC | eye: | n/a | n/a |
40 | CTCF | chr1:194312020-194312170 | HCT-116 | colon: | n/a | n/a |
41 | CTCF | chr1:194311993-194312349 | GM12878 | blood: | n/a | n/a |
42 | CTCF | chr1:194312155-194312230 | GM10266 | blood: | n/a | n/a |
43 | CTCF | chr1:194312080-194312230 | MCF-7 | breast: | n/a | n/a |
44 | CTCF | chr1:194312140-194312290 | HPAF | blood vessel: | n/a | n/a |
45 | CTCF | chr1:194312020-194312170 | GM12868 | blood: | n/a | n/a |
46 | CTCF | chr1:194312080-194312230 | GM12875 | blood: | n/a | n/a |
47 | CTCF | chr1:194312086-194312273 | GM19240 | blood: | n/a | n/a |
48 | CTCF | chr1:194312060-194312210 | GM12870 | blood: | n/a | n/a |
49 | CTCF | chr1:194312070-194312274 | A549 | lung: | n/a | n/a |
50 | CTCF | chr1:194311769-194311773 | MCF-7 | breast: | n/a | n/a |
No. | Chromosome Location | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:194327715-194327765 | HAEpiC | amniotic membrane: | n/a |
2 | chr1:194327715-194327765 | AG10803 | skin: | n/a |
3 | chr1:194327715-194327765 | ECC-1 | luminal epithelium: | n/a |
4 | chr1:194327715-194327765 | ProgFib | skin: | n/a |
5 | chr1:194327715-194327765 | HCF | heart: | n/a |
6 | chr1:194327715-194327765 | AG04449 | skin: | fetal |
7 | chr1:194327715-194327765 | PANC-1 | pancreas: | n/a |
8 | chr1:194327715-194327765 | HUVEC | blood vessel: | n/a |
9 | chr1:194327715-194327765 | SAEC | small airway: | n/a |
10 | chr1:194327715-194327765 | MCF10A-Er-Src | breast: | n/a |
11 | chr1:194327715-194327765 | HNPCEpiC | eye: | n/a |
12 | chr1:194327715-194327765 | SK-N-MC | brain: | n/a |
13 | chr1:194327715-194327765 | AG09319 | gingival: | n/a |
14 | chr1:194327715-194327765 | H1-hESC | embryonic stem cell: | embryo |
15 | chr1:194327715-194327765 | HCM | heart: | n/a |
16 | chr1:194327715-194327765 | SK-N-SH | brain: | n/a |
17 | chr1:194327715-194327765 | RPTEC | kidney: | n/a |
18 | chr1:194327715-194327765 | SK-N-SH_RA | brain: | n/a |
19 | chr1:194327715-194327765 | LNCaP | prostate: | n/a |
20 | chr1:194327715-194327765 | HepG2 | liver: | n/a |
21 | chr1:194327715-194327765 | NT2-D1 | testis: | n/a |
22 | chr1:194327715-194327765 | HMEC | breast: | n/a |
23 | chr1:194327715-194327765 | Hela-S3 | cervix: | n/a |
24 | chr1:194327715-194327765 | AG04450 | lung: | fetal |
25 | chr1:194327715-194327765 | HCT-116 | colon: | n/a |
26 | chr1:194327715-194327765 | Caco-2 | colon: | n/a |
27 | chr1:194327715-194327765 | U87 | brain: | n/a |
28 | chr1:194327715-194327765 | HEEpiC | esophagus: | n/a |
29 | chr1:194327715-194327765 | AoSMC | blood vessel: | n/a |
30 | chr1:194327715-194327765 | GM12878 | blood: | n/a |
31 | chr1:194327715-194327765 | IMR90 | lung: | fetal |
32 | chr1:194327715-194327765 | NHDF-neo | bronchial: | n/a |
33 | chr1:194327715-194327765 | HRE | kidney: | n/a |
34 | chr1:194327715-194327765 | BJ | skin: | n/a |
35 | chr1:194327715-194327765 | HPAEpiC | pulmonary alveolar: | n/a |
36 | chr1:194327715-194327765 | BE2_C | brain: | n/a |
37 | chr1:194327715-194327765 | NH-A | brain: | n/a |
38 | chr1:194327715-194327765 | HL-60 | blood: | n/a |
39 | chr1:194327715-194327765 | MCF-7 | breast: | n/a |
40 | chr1:194327715-194327765 | NB4 | blood: | n/a |
41 | chr1:194327715-194327765 | AG09309 | skin: | n/a |
42 | chr1:194327715-194327765 | SKMC | muscle: | n/a |
43 | chr1:194327715-194327765 | CMK | blood: | n/a |
44 | chr1:194327715-194327765 | GM06990 | blood: | n/a |
45 | chr1:194327715-194327765 | T-47D | breast: | n/a |
46 | chr1:194327715-194327765 | GM19239 | blood: | n/a |
47 | chr1:194327715-194327765 | NHBE | bronchial: | n/a |
48 | chr1:194327715-194327765 | A549 | lung: | n/a |
49 | chr1:194327715-194327765 | PFSK-1 | brain: | n/a |
50 | chr1:194327715-194327765 | HEK293 | kidney: | embryo |
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr1:194290793..194293350-chr1:194303671..194305841,2 | K562 | blood: | |
2 | chr1:193587120..193589760-chr1:194326578..194328851,2 | K562 | blood: | |
3 | chr1:194315945..194318461-chr1:194337918..194339837,2 | K562 | blood: | |
4 | chr1:194317795..194320009-chr1:194323102..194324851,2 | K562 | blood: | |
5 | chr1:194308962..194311330-chr4:127715408..127718280,2 | MCF-7 | breast: | |
6 | chr1:194306516..194309030-chr1:194325392..194327548,2 | K562 | blood: | |
7 | chr1:194320848..194323111-chr1:194332698..194335480,2 | K562 | blood: | |
8 | chr1:194307530..194310929-chr1:194324369..194327548,3 | K562 | blood: | |
9 | chr1:194286927..194289015-chr1:194296923..194299296,2 | K562 | blood: | |
10 | chr1:194328262..194330986-chr1:194334081..194336171,2 | K562 | blood: | |
11 | chr1:194290793..194293350-chr1:194303671..194305841,2 | K562 | blood: | |
12 | chr1:194306516..194309030-chr1:194325392..194327548,2 | K562 | blood: | |
13 | chr1:194317795..194320009-chr1:194323102..194324851,2 | K562 | blood: | |
14 | chr1:194315164..194317998-chr1:194319254..194321893,3 | K562 | blood: | |
15 | chr1:194326093..194330986-chr1:194331715..194336171,7 | K562 | blood: | |
16 | chr1:194325391..194328027-chr1:194331850..194333464,2 | K562 | blood: | |
17 | chr1:194070430..194072677-chr1:194322592..194324190,2 | K562 | blood: | |
18 | chr1:194307530..194310929-chr1:194324369..194327548,3 | K562 | blood: |
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No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-CDC73-4 | chr1:194320593-194321556 | NONHSAT008581 |
2 | lnc-CDC73-4 | chr1:194320073-194320368 | XLOC_000510 |
3 | lnc-B3GALT2-5 | chr1:194296750-194296826 | NONHSAT008580 |
4 | lnc-CDC73-4 | chr1:194320009-194320481 | NONHSAT008581 |
5 | lnc-CDC73-4 | chr1:194321413-194321556 | 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 | rs570878912 | chr1:194296764-194296765 | Inactive region | lncRNA | n/a | Overlapped CNVs | n/a |
2 | rs16836713 | chr1:194300204-194300205 | Active TSS | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
3 | rs185798699 | chr1:194300216-194300217 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
4 | rs540244849 | chr1:194300249-194300250 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
5 | rs117355937 | chr1:194300299-194300300 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
6 | rs17838232 | chr1:194300301-194300302 | Active TSS | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
7 | rs544771307 | chr1:194300312-194300313 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
8 | rs529944952 | chr1:194300327-194300328 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
9 | rs60019237 | chr1:194300344-194300345 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
10 | rs141208926 | chr1:194300348-194300349 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
11 | rs75488372 | chr1:194300386-194300387 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
12 | rs533591129 | chr1:194300400-194300401 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
13 | rs188319841 | chr1:194300418-194300419 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
14 | rs567179898 | chr1:194300421-194300422 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
15 | rs528082782 | chr1:194300428-194300429 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
16 | rs371451240 | chr1:194300459-194300460 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
17 | rs193043334 | chr1:194300461-194300462 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
18 | rs373530323 | chr1:194300466-194300467 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
19 | rs570853037 | chr1:194300472-194300473 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
20 | rs568137333 | chr1:194300474-194300475 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
21 | rs535228661 | chr1:194300497-194300498 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
22 | rs550292507 | chr1:194300529-194300530 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
23 | rs535607834 | chr1:194300539-194300540 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
24 | rs185252264 | chr1:194300550-194300551 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
25 | rs568928634 | chr1:194300559-194300560 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
26 | rs539625243 | chr1:194300565-194300566 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
27 | rs138839519 | chr1:194300571-194300572 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
28 | rs140490495 | chr1:194300579-194300580 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
29 | rs143204689 | chr1:194300581-194300582 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
30 | rs148264512 | chr1:194300586-194300587 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
31 | rs189661386 | chr1:194300589-194300590 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
32 | rs376805057 | chr1:194300592-194300593 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
33 | rs181306102 | chr1:194300595-194300596 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
34 | rs3065312 | chr1:194300596-194300597 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
35 | rs60636442 | chr1:194300600-194300601 | Active TSS | n/a | n/a | Overlapped CNVs | n/a |
36 | rs370340718 | chr1:194307223-194307224 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
37 | rs561606331 | chr1:194307237-194307238 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
38 | rs556260495 | chr1:194307244-194307245 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
39 | rs571758337 | chr1:194307274-194307275 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
40 | rs115687074 | chr1:194307280-194307281 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
41 | rs374229386 | chr1:194307287-194307288 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
42 | rs12083179 | chr1:194307301-194307302 | Enhancers | n/a | n/a | LD-proxies of rSNPOverlapped rCNV | n/a |
43 | rs568684029 | chr1:194307315-194307316 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
44 | rs114568415 | chr1:194307321-194307322 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
45 | rs551221900 | chr1:194307361-194307362 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
46 | rs140923147 | chr1:194307379-194307380 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
47 | rs574970382 | chr1:194307409-194307410 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
48 | rs189048351 | chr1:194307442-194307443 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
49 | rs181144309 | chr1:194307478-194307479 | Enhancers | n/a | n/a | Overlapped CNVs | n/a |
50 | rs538307143 | chr1:194307517-194307518 | 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 | chr1:194300200-194300600 | Active TSS | ES-UCSF4 Cell Line | embryonic stem cell |
2 | chr1:194300200-194300600 | Active TSS | Breast Myoepithelial Primary Cells | Breast |
3 | chr1:194307200-194308000 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr1:194307400-194307800 | Enhancers | Brain Hippocampus Middle | brain |
5 | chr1:194307400-194307800 | Enhancers | Brain Substantia Nigra | brain |
6 | chr1:194307400-194308000 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
7 | chr1:194307400-194308200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
8 | chr1:194308600-194309000 | Enhancers | Fetal Brain Female | brain |
9 | chr1:194311600-194311800 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
10 | chr1:194311600-194311800 | Active TSS | iPS-15b Cell Line | embryonic stem cell |
11 | chr1:194311600-194312000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
12 | chr1:194311600-194312200 | Enhancers | H1 Cell Line | embryonic stem cell |
13 | chr1:194311800-194312000 | Flanking Active TSS | iPS-15b Cell Line | embryonic stem cell |
14 | chr1:194311800-194312000 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
15 | chr1:194311800-194312200 | Active TSS | ES-I3 Cell Line | embryonic stem cell |
16 | chr1:194311800-194312200 | Enhancers | H9 Cell Line | embryonic stem cell |
17 | chr1:194311800-194312200 | Active TSS | HUES48 Cell Line | embryonic stem cell |
18 | chr1:194312000-194312200 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
19 | chr1:194315600-194316600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
20 | chr1:194316200-194316800 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
21 | chr1:194316400-194316600 | Enhancers | Fetal Heart | heart |
22 | chr1:194316400-194317000 | Enhancers | HMEC | breast |
23 | chr1:194325000-194325200 | ZNF genes & repeats | Right Atrium | heart |
24 | chr1:194325200-194327000 | Active TSS | K562 | blood |
25 | chr1:194325200-194329000 | Weak transcription | Right Atrium | heart |
26 | chr1:194327400-194327800 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
27 | chr1:194330400-194332400 | Enhancers | Fetal Heart | heart |