Variant report

Variant	esv3450265
Chromosome Location	chr1:85747914-85749962
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:85749034-85749344	HepG2	liver:	n/a	chr1:85749276-85749287
2	CEBPB	chr1:85749112-85749470	Hela-S3	cervix:	n/a	chr1:85749276-85749287
3	CEBPB	chr1:85749110-85749721	HepG2	liver:	n/a	chr1:85749276-85749287
4	CEBPB	chr1:85749119-85749404	A549	lung:	n/a	chr1:85749276-85749287
5	CEBPB	chr1:85749188-85749508	MCF-7	breast:	n/a	chr1:85749276-85749287
6	CEBPB	chr1:85749091-85749470	K562	blood:	n/a	chr1:85749276-85749287
7	CEBPB	chr1:85749170-85749356	HepG2	liver:	n/a	chr1:85749276-85749287
8	CEBPB	chr1:85749096-85749471	HepG2	liver:	n/a	chr1:85749276-85749287
9	CEBPB	chr1:85749071-85749458	ECC-1	luminal epithelium:	n/a	chr1:85749276-85749287
10	CEBPB	chr1:85748919-85749601	HCT-116	colon:	n/a	chr1:85749276-85749287
11	CEBPB	chr1:85749088-85749355	K562	blood:	n/a	chr1:85749276-85749287
12	CEBPB	chr1:85749102-85749407	H1-hESC	embryonic stem cell:	n/a	chr1:85749276-85749287
13	CEBPB	chr1:85749043-85749409	K562	blood:	n/a	chr1:85749276-85749287
14	CEBPB	chr1:85749072-85749454	ECC-1	luminal epithelium:	n/a	chr1:85749276-85749287
15	CEBPB	chr1:85747833-85748061	HepG2	liver:	n/a	chr1:85747915-85747926
16	CTCF	chr1:85748300-85748450	MCF-7	breast:	n/a	chr1:85748353-85748362
17	CTCF	chr1:85748140-85748290	HPF	lung:	n/a	n/a
18	CTCF	chr1:85748280-85748430	HRE	kidney:	n/a	chr1:85748353-85748362
19	CTCF	chr1:85748320-85748470	HFF-Myc	foreskin:	n/a	chr1:85748353-85748362
20	CTCF	chr1:85748360-85748510	AG04450	lung:	n/a	n/a
21	CTCF	chr1:85748129-85748401	K562	blood:	n/a	chr1:85748353-85748362
22	CTCF	chr1:85748240-85748390	HepG2	liver:	n/a	chr1:85748353-85748362
23	CTCF	chr1:85748096-85748386	K562	blood:	n/a	chr1:85748353-85748362
24	CTCF	chr1:85748240-85748390	NHEK	skin:	n/a	chr1:85748353-85748362
25	CTCF	chr1:85748198-85748403	Hela-S3	cervix:	n/a	chr1:85748353-85748362
26	CTCF	chr1:85748200-85748350	GM12878	blood:	n/a	n/a
27	CTCF	chr1:85748200-85748350	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:85748240-85748390	AG10803	skin:	n/a	chr1:85748353-85748362
29	CTCF	chr1:85748200-85748350	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr1:85748240-85748390	MCF-7	breast:	n/a	chr1:85748353-85748362
31	CTCF	chr1:85748260-85748410	HRE	kidney:	n/a	chr1:85748353-85748362
32	CTCF	chr1:85748090-85748515	H1-hESC	embryonic stem cell:	n/a	chr1:85748353-85748362
33	CTCF	chr1:85748220-85748370	Caco-2	colon:	n/a	chr1:85748353-85748362
34	CTCF	chr1:85748120-85748270	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr1:85748180-85748330	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr1:85748360-85748510	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr1:85748160-85748310	GM06990	blood:	n/a	n/a
38	CTCF	chr1:85748221-85748361	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:85748120-85748418	HepG2	liver:	n/a	chr1:85748353-85748362
40	CTCF	chr1:85748140-85748290	BJ	skin:	n/a	n/a
41	CTCF	chr1:85748240-85748390	BE2_C	brain:	n/a	chr1:85748353-85748362
42	CTCF	chr1:85748240-85748390	HRPEpiC	eye:	n/a	chr1:85748353-85748362
43	CTCF	chr1:85748003-85748623	HCT-116	colon:	n/a	chr1:85748353-85748362
44	CTCF	chr1:85748180-85748330	HMF	breast:	n/a	n/a
45	CTCF	chr1:85748184-85748414	HepG2	liver:	n/a	chr1:85748353-85748362
46	CTCF	chr1:85748160-85748310	GM12865	blood:	n/a	n/a
47	CTCF	chr1:85748140-85748390	A549	lung:	n/a	chr1:85748353-85748362
48	CTCF	chr1:85748260-85748410	GM12878	blood:	n/a	chr1:85748353-85748362
49	CTCF	chr1:85748200-85748350	GM12869	blood:	n/a	n/a
50	CTCF	chr1:85748300-85748450	GM12865	blood:	n/a	chr1:85748353-85748362

No.	Distal block	Cell Line	Cell type
1	chr1:85739297..85743309-chr1:85744628..85748559,4	MCF-7	breast:
2	chr1:85740526..85742722-chr1:85746661..85748660,2	MCF-7	breast:
3	chr1:85742187..85745018-chr1:85749555..85753087,3	K562	blood:
4	chr1:85743465..85746291-chr1:85746776..85749038,2	MCF-7	breast:
5	chr1:85747755..85748502-chr1:85773895..85774432,2	MCF-7	breast:
6	chr1:85741905..85744580-chr1:85747619..85751624,6	K562	blood:
7	chr1:85742898..85744863-chr1:85746512..85748542,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000264380	TF binding region
ENSG00000223653	chromatin interactions
ENSG00000142867	chromatin interactions

Extended variants
information (count: 68 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537113918	chr1:85747972-85747973	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs533459225	chr1:85747978-85747979	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs532516317	chr1:85748079-85748080	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs12124457	chr1:85748131-85748132	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs567399906	chr1:85748148-85748149	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs191983871	chr1:85748165-85748166	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs183387310	chr1:85748166-85748167	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs371511199	chr1:85748168-85748169	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs567051205	chr1:85748172-85748173	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs144828422	chr1:85748208-85748209	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs140106161	chr1:85748212-85748213	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs12036224	chr1:85748237-85748238	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541714647	chr1:85748247-85748248	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs143956465	chr1:85748262-85748263	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs372010051	chr1:85748313-85748314	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs75844775	chr1:85748476-85748477	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs115897658	chr1:85748540-85748541	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs202012787	chr1:85748635-85748636	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs200172333	chr1:85748636-85748637	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs529392609	chr1:85748811-85748812	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs373511761	chr1:85748814-85748815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs545458083	chr1:85748893-85748894	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs559506050	chr1:85748947-85748948	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs528325838	chr1:85748948-85748949	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs551673954	chr1:85748949-85748950	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs367661984	chr1:85748950-85748951	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs530498672	chr1:85748997-85748998	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558200898	chr1:85749026-85749027	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs5775830	chr1:85749068-85749069	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs397980683	chr1:85749069-85749070	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs140766727	chr1:85749103-85749104	Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs188451852	chr1:85749252-85749253	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs192632026	chr1:85749271-85749272	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs142338902	chr1:85749298-85749299	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs566285630	chr1:85749299-85749300	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs565289027	chr1:85749326-85749327	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs534973722	chr1:85749357-85749358	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs558013258	chr1:85749368-85749369	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs577945421	chr1:85749393-85749394	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs537044508	chr1:85749425-85749426	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs7410996	chr1:85749438-85749439	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs1466818	chr1:85749450-85749451	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs1466819	chr1:85749469-85749470	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs78614257	chr1:85749483-85749484	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs574006850	chr1:85749490-85749491	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs184614707	chr1:85749536-85749537	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs188046387	chr1:85749547-85749548	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs6693229	chr1:85749561-85749562	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs573007823	chr1:85749563-85749564	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs545253306	chr1:85749580-85749581	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85742800-85763000	Weak transcription	Ovary	ovary
2	chr1:85743000-85749200	Weak transcription	Fetal Stomach	stomach
3	chr1:85743000-85749200	Weak transcription	Psoas Muscle	Psoas
4	chr1:85743000-85773600	Weak transcription	Right Atrium	heart
5	chr1:85743200-85748000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr1:85743200-85748200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:85743200-85752000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:85743400-85748000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:85743400-85748000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr1:85745200-85753600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr1:85745400-85749000	Weak transcription	A549	lung
12	chr1:85745400-85749200	Weak transcription	Colonic Mucosa	Colon
13	chr1:85745400-85749400	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr1:85745600-85748000	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr1:85745600-85748000	Weak transcription	HepG2	liver
16	chr1:85745600-85748200	Weak transcription	Esophagus	oesophagus
17	chr1:85745600-85749000	Weak transcription	Stomach Mucosa	stomach
18	chr1:85745600-85749200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr1:85745600-85749200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:85745600-85749400	Weak transcription	Gastric	stomach
21	chr1:85745600-85749400	Weak transcription	Pancreas	Pancrea
22	chr1:85745800-85749000	Weak transcription	HMEC	breast
23	chr1:85745800-85749200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr1:85745800-85749400	Weak transcription	Lung	lung
25	chr1:85745800-85749600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:85746000-85748000	Weak transcription	NHEK	skin
27	chr1:85746800-85749000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:85746800-85753600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:85747000-85749200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:85747000-85749600	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr1:85747200-85749200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr1:85747600-85749400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr1:85747600-85750200	Weak transcription	Primary B cells from cord blood	blood
34	chr1:85747800-85748600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:85747800-85748600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr1:85747800-85748600	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr1:85747800-85750000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr1:85748000-85748200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr1:85748000-85748400	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr1:85748000-85748600	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr1:85748000-85748600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:85748000-85749200	Enhancers	HepG2	liver
43	chr1:85748000-85749600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:85748000-85749800	Enhancers	H1 Cell Line	embryonic stem cell
45	chr1:85748000-85750000	Enhancers	NHEK	skin
46	chr1:85748200-85748400	Enhancers	Esophagus	oesophagus
47	chr1:85748200-85748600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr1:85748400-85748800	Weak transcription	Esophagus	oesophagus
49	chr1:85748400-85749600	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr1:85748600-85764000	Weak transcription	H9 Cell Line	embryonic stem cell

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