Variant report

Variant	esv3393958
Chromosome Location	chr1:85857980-85874598
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:85872867-85873214	HepG2	liver:	n/a	n/a
2	CBX3	chr1:85872768-85873303	HCT-116	colon:	n/a	n/a
3	CEBPB	chr1:85859862-85860199	HepG2	liver:	n/a	chr1:85860029-85860040
4	CEBPB	chr1:85862972-85863533	IMR90	lung:	n/a	chr1:85863347-85863358
5	CEBPB	chr1:85859852-85860208	H1-hESC	embryonic stem cell:	n/a	chr1:85860029-85860040
6	CEBPB	chr1:85864308-85864682	A549	lung:	n/a	n/a
7	CEBPB	chr1:85863396-85863507	A549	lung:	n/a	n/a
8	CEBPB	chr1:85859860-85860177	A549	lung:	n/a	chr1:85860029-85860040
9	CEBPB	chr1:85863340-85863379	K562	blood:	n/a	chr1:85863347-85863358
10	CEBPB	chr1:85864339-85864722	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:85864383-85864742	A549	lung:	n/a	n/a
12	CEBPB	chr1:85864308-85864682	IMR90	lung:	n/a	n/a
13	CEBPB	chr1:85864326-85864593	HepG2	liver:	n/a	n/a
14	CEBPB	chr1:85859858-85860184	IMR90	lung:	n/a	chr1:85860029-85860040
15	CEBPB	chr1:85859870-85860153	K562	blood:	n/a	chr1:85860029-85860040
16	CEBPB	chr1:85859999-85860129	Hela-S3	cervix:	n/a	chr1:85860029-85860040
17	CEBPB	chr1:85863216-85863530	HepG2	liver:	n/a	chr1:85863347-85863358
18	CTCF	chr1:85864220-85864370	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr1:85864500-85864650	AG10803	skin:	n/a	n/a
20	CTCF	chr1:85864412-85864734	A549	lung:	n/a	n/a
21	CTCF	chr1:85864520-85864670	SAEC	small airway:	n/a	n/a
22	CTCF	chr1:85864400-85864550	HCT-116	colon:	n/a	n/a
23	CTCF	chr1:85864480-85864630	BJ	skin:	n/a	n/a
24	CTCF	chr1:85864557-85864632	GM13977	blood:	n/a	n/a
25	CTCF	chr1:85864500-85864650	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr1:85864476-85864696	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr1:85864520-85864670	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr1:85864500-85864650	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr1:85864272-85864887	HCT-116	colon:	n/a	n/a
30	CTCF	chr1:85862199-85862232	ProgFib	skin:	n/a	n/a
31	CTCF	chr1:85864460-85864610	BE2_C	brain:	n/a	n/a
32	CTCF	chr1:85864400-85864550	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr1:85861980-85862130	HepG2	liver:	n/a	n/a
34	CTCF	chr1:85864480-85864630	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr1:85864540-85864690	HMEC	breast:	n/a	n/a
36	CTCF	chr1:85864480-85864630	HEK293	kidney:	n/a	n/a
37	CTCF	chr1:85864460-85864610	GM12865	blood:	n/a	n/a
38	CTCF	chr1:85864500-85864650	BE2_C	brain:	n/a	n/a
39	CTCF	chr1:85864450-85864639	GM12878	blood:	n/a	n/a
40	CTCF	chr1:85864511-85864640	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:85864500-85864650	HMF	breast:	n/a	n/a
42	CTCF	chr1:85864540-85864690	HCM	heart:	n/a	n/a
43	CTCF	chr1:85864500-85864650	GM12878	blood:	n/a	n/a
44	CTCF	chr1:85864500-85864650	HepG2	liver:	n/a	n/a
45	CTCF	chr1:85864500-85864650	AG09319	gingival:	n/a	n/a
46	CTCF	chr1:85864486-85864645	HepG2	liver:	n/a	n/a
47	CTCF	chr1:85862020-85862170	GM12874	blood:	n/a	n/a
48	CTCF	chr1:85864520-85864670	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr1:85864540-85864690	GM12872	blood:	n/a	n/a
50	CTCF	chr1:85862000-85862150	WERI-Rb-1	eye:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:85872804-85872854	GM12891	blood:	n/a
2	chr1:85864304-85864354	ProgFib	skin:	n/a
3	chr1:85864304-85864354	CMK	blood:	n/a
4	chr1:85864304-85864354	HCT-116	colon:	n/a
5	chr1:85864304-85864354	RPTEC	kidney:	n/a
6	chr1:85864304-85864354	Jurkat	blood:	n/a
7	chr1:85872804-85872854	AG10803	skin:	n/a
8	chr1:85872804-85872854	RPTEC	kidney:	n/a
9	chr1:85864304-85864354	HRCEpiC	kidney:	n/a
10	chr1:85864304-85864354	HPAEpiC	pulmonary alveolar:	n/a
11	chr1:85864304-85864354	HIPEpiC	eye:	n/a
12	chr1:85872804-85872854	NH-A	brain:	n/a
13	chr1:85864304-85864354	AG09309	skin:	n/a
14	chr1:85872804-85872854	T-47D	breast:	n/a
15	chr1:85864304-85864354	PrEC	prostate:	n/a
16	chr1:85872804-85872854	SK-N-SH_RA	brain:	n/a
17	chr1:85864304-85864354	AG04449	skin:	fetal
18	chr1:85864304-85864354	Hepatocyte	liver:	n/a
19	chr1:85872804-85872854	HMEC	breast:	n/a
20	chr1:85872804-85872854	HNPCEpiC	eye:	n/a
21	chr1:85864304-85864354	U87	brain:	n/a
22	chr1:85864304-85864354	HepG2	liver:	n/a
23	chr1:85872804-85872854	HAEpiC	amniotic membrane:	n/a
24	chr1:85872804-85872854	BJ	skin:	n/a
25	chr1:85864304-85864354	HCF	heart:	n/a
26	chr1:85864304-85864354	NT2-D1	testis:	n/a
27	chr1:85864304-85864354	GM12892	blood:	n/a
28	chr1:85872804-85872854	HUVEC	blood vessel:	n/a
29	chr1:85872804-85872854	GM06990	blood:	n/a
30	chr1:85872804-85872854	SAEC	small airway:	n/a
31	chr1:85864304-85864354	SKMC	muscle:	n/a
32	chr1:85864304-85864354	HNPCEpiC	eye:	n/a
33	chr1:85864304-85864354	HL-60	blood:	n/a
34	chr1:85872804-85872854	NT2-D1	testis:	n/a
35	chr1:85872804-85872854	SK-N-MC	brain:	n/a
36	chr1:85872804-85872854	HepG2	liver:	n/a
37	chr1:85864304-85864354	ovcar-3	ovarian:	n/a
38	chr1:85872804-85872854	Jurkat	blood:	n/a
39	chr1:85864304-85864354	GM12878	blood:	n/a
40	chr1:85872804-85872854	SK-N-SH	brain:	n/a
41	chr1:85872804-85872854	HCM	heart:	n/a
42	chr1:85864304-85864354	HRPEpiC	eye:	n/a
43	chr1:85872804-85872854	Hepatocyte	liver:	n/a
44	chr1:85864304-85864354	HMEC	breast:	n/a
45	chr1:85864304-85864354	Caco-2	colon:	n/a
46	chr1:85864304-85864354	PANC-1	pancreas:	n/a
47	chr1:85872804-85872854	GM12892	blood:	n/a
48	chr1:85864304-85864354	SAEC	small airway:	n/a
49	chr1:85864304-85864354	ECC-1	luminal epithelium:	n/a
50	chr1:85872804-85872854	AG09319	gingival:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:85872823..85874492-chr1:85874813..85877121,2	MCF-7	breast:
2	chr1:85809642..85811064-chr1:85864019..85865015,8	MCF-7	breast:
3	chr1:85773623..85774572-chr1:85864125..85865314,5	MCF-7	breast:
4	chr1:85863358..85866240-chr1:85910699..85913658,2	K562	blood:
5	chr1:85866495..85869056-chr1:86046414..86047968,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYR61-3	chr1:85864140-85865646	ENSG00000223653

No data

Variant related genes	Relation type
DDAH1	TF binding region
DDAH1	CpG island
ENSG00000142871	chromatin interactions
GEN1	miRNA target sites

Extended variants
information (count: 551 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535722466	chr1:85858047-85858048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149498632	chr1:85858099-85858100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565641521	chr1:85858120-85858121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs12033483	chr1:85858123-85858124	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs535830440	chr1:85858124-85858125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554110076	chr1:85858129-85858130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs147192329	chr1:85858131-85858132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs117358352	chr1:85858157-85858158	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs12565015	chr1:85858167-85858168	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370932232	chr1:85858236-85858237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs556916372	chr1:85858246-85858247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576467881	chr1:85858249-85858250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574014988	chr1:85858253-85858254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541864966	chr1:85858273-85858274	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6576761	chr1:85858274-85858275	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs60176254	chr1:85858318-85858319	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541205412	chr1:85858336-85858337	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186132557	chr1:85858368-85858369	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532983515	chr1:85858369-85858370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549630749	chr1:85858394-85858395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs569623557	chr1:85858403-85858404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528813250	chr1:85858455-85858456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11314404	chr1:85858474-85858475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555726454	chr1:85858488-85858489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs56165363	chr1:85858493-85858494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs6576762	chr1:85858494-85858495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369359018	chr1:85858501-85858502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368722074	chr1:85858546-85858547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147359300	chr1:85858552-85858553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565757843	chr1:85858570-85858571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534452865	chr1:85858625-85858626	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554319718	chr1:85858711-85858712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571026798	chr1:85858812-85858813	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6671599	chr1:85858857-85858858	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs148394666	chr1:85858920-85858921	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576810450	chr1:85858948-85858949	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367554885	chr1:85858957-85858958	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544137944	chr1:85858987-85858988	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12754419	chr1:85858993-85858994	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555515268	chr1:85859102-85859103	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572067470	chr1:85859143-85859144	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192048492	chr1:85859225-85859226	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376817038	chr1:85859242-85859243	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183426575	chr1:85859264-85859265	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35193119	chr1:85859265-85859266	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs35596907	chr1:85859335-85859336	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6659486	chr1:85859372-85859373	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs6576763	chr1:85859376-85859377	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs142982031	chr1:85859384-85859385	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369260234	chr1:85859454-85859455	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription	n/a	n/a	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
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
small cell lung cancer	20016488	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85839800-85864200	Weak transcription	Aorta	Aorta
2	chr1:85841200-85859800	Weak transcription	NH-A	brain
3	chr1:85845000-85870000	Weak transcription	HSMMtube	muscle
4	chr1:85845800-85859800	Weak transcription	NHLF	lung
5	chr1:85849400-85861600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:85849400-85863400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:85850800-85863600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:85852400-85863400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:85852400-85864200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:85852600-85860000	Weak transcription	Gastric	stomach
11	chr1:85852800-85858800	Weak transcription	HSMM	muscle
12	chr1:85852800-85859800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr1:85853200-85861800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr1:85853600-85861800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:85853800-85858800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:85853800-85861600	Weak transcription	NHDF-Ad	bronchial
17	chr1:85853800-85864200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:85854000-85861800	Weak transcription	Osteobl	bone
19	chr1:85854400-85859000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:85854600-85862800	Weak transcription	Liver	Liver
21	chr1:85854600-85863400	Weak transcription	HUVEC	blood vessel
22	chr1:85855200-85870000	Weak transcription	Fetal Stomach	stomach
23	chr1:85856000-85872800	Weak transcription	Fetal Intestine Small	intestine
24	chr1:85857000-85860000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:85857800-85858200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:85857800-85859400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr1:85857800-85859800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr1:85858200-85858600	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr1:85858600-85858800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr1:85858600-85859000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr1:85858600-85859200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr1:85858600-85859400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr1:85858600-85859600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr1:85858600-85860200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr1:85858600-85860600	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:85858600-85860600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr1:85858800-85859200	Enhancers	Brain Anterior Caudate	brain
38	chr1:85858800-85859400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr1:85858800-85859400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr1:85858800-85859600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:85858800-85861000	Strong transcription	HSMM	muscle
42	chr1:85858800-85863600	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr1:85859000-85859200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr1:85859000-85860600	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr1:85859200-85859400	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr1:85859200-85859600	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr1:85859200-85859600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:85859200-85860000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:85859400-85859600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
50	chr1:85859400-85859600	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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