Variant report

Variant	esv2830430
Chromosome Location	chr1:79310760-79555593
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:825)
CpG islands
(count:854)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:825 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr1:79507696-79508185	GM12878	blood:	n/a	n/a
2	ATF2	chr1:79505821-79506890	GM12878	blood:	n/a	n/a
3	ATF2	chr1:79506114-79506881	GM12878	blood:	n/a	n/a
4	ATF2	chr1:79350690-79350993	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr1:79507719-79508191	GM12878	blood:	n/a	n/a
6	BACH1	chr1:79472315-79472519	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr1:79545497-79545905	H1-hESC	embryonic stem cell:	n/a	chr1:79545669-79545683
8	BACH1	chr1:79508075-79508122	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr1:79507950-79508076	K562	blood:	n/a	n/a
10	BATF	chr1:79506304-79506770	GM12878	blood:	n/a	n/a
11	BATF	chr1:79507747-79508138	GM12878	blood:	n/a	n/a
12	BATF	chr1:79506383-79506726	GM12878	blood:	n/a	n/a
13	BATF	chr1:79507758-79508057	GM12878	blood:	n/a	n/a
14	BATF	chr1:79320756-79321223	GM12878	blood:	n/a	chr1:79320825-79320834
15	BCL11A	chr1:79507836-79508150	GM12878	blood:	n/a	n/a
16	BCL11A	chr1:79507862-79508010	GM12878	blood:	n/a	n/a
17	BCL11A	chr1:79506346-79506753	GM12878	blood:	n/a	n/a
18	BCL3	chr1:79507766-79508061	GM12878	blood:	n/a	n/a
19	BCL3	chr1:79506306-79506801	GM12878	blood:	n/a	n/a
20	BCLAF1	chr1:79506260-79506789	GM12878	blood:	n/a	n/a
21	BCLAF1	chr1:79507869-79508207	GM12878	blood:	n/a	n/a
22	BHLHE40	chr1:79405513-79405527	GM12878	blood:	n/a	n/a
23	BHLHE40	chr1:79320988-79321254	GM12878	blood:	n/a	n/a
24	BRCA1	chr1:79509475-79509505	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr1:79415111-79415262	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr1:79459804-79459831	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:79310676-79310947	HepG2	liver:	n/a	chr1:79310824-79310837 chr1:79310825-79310836
28	CEBPB	chr1:79470648-79470928	HepG2	liver:	n/a	chr1:79470789-79470800
29	CEBPB	chr1:79377749-79377922	H1-hESC	embryonic stem cell:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
30	CEBPB	chr1:79379678-79379999	IMR90	lung:	n/a	n/a
31	CEBPB	chr1:79357252-79357448	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr1:79453639-79453775	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr1:79490048-79490150	H1-hESC	embryonic stem cell:	n/a	chr1:79490066-79490077
34	CEBPB	chr1:79507830-79508119	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr1:79490003-79490203	A549	lung:	n/a	chr1:79490066-79490077
36	CEBPB	chr1:79350645-79351099	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr1:79378071-79378234	K562	blood:	n/a	n/a
38	CEBPB	chr1:79409258-79409472	A549	lung:	n/a	chr1:79409399-79409408 chr1:79409398-79409409 chr1:79409397-79409408
39	CEBPB	chr1:79405681-79405919	HepG2	liver:	n/a	n/a
40	CEBPB	chr1:79377650-79378354	IMR90	lung:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
41	CEBPB	chr1:79483498-79483817	HepG2	liver:	n/a	chr1:79483669-79483680
42	CEBPB	chr1:79379745-79379945	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr1:79334884-79335172	IMR90	lung:	n/a	chr1:79334994-79335005
44	CEBPB	chr1:79482686-79482859	HepG2	liver:	n/a	chr1:79482727-79482740 chr1:79482727-79482738 chr1:79482727-79482740
45	CEBPB	chr1:79451150-79451399	K562	blood:	n/a	chr1:79451261-79451272 chr1:79451259-79451270 chr1:79451259-79451272 chr1:79451201-79451214
46	CEBPB	chr1:79470712-79470946	A549	lung:	n/a	chr1:79470789-79470800
47	CEBPB	chr1:79470706-79470922	Hela-S3	cervix:	n/a	chr1:79470789-79470800
48	CEBPB	chr1:79377650-79378354	HepG2	liver:	n/a	chr1:79377823-79377834 chr1:79377848-79377859 chr1:79377824-79377833 chr1:79377822-79377835 chr1:79377822-79377833
49	CEBPB	chr1:79521171-79521337	A549	lung:	n/a	n/a
50	CEBPB	chr1:79379712-79379997	A549	lung:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:79350918-79350968	AG09319	gingival:	n/a
2	chr1:79472361-79472411	HL-60	blood:	n/a
3	chr1:79472408-79472458	AG04450	lung:	fetal
4	chr1:79472917-79472967	Hela-S3	cervix:	n/a
5	chr1:79472643-79472693	HepG2	liver:	n/a
6	chr1:79474718-79474768	Jurkat	blood:	n/a
7	chr1:79472536-79472586	H1-hESC	embryonic stem cell:	embryo
8	chr1:79472408-79472458	LNCaP	prostate:	n/a
9	chr1:79473783-79473833	AG04450	lung:	fetal
10	chr1:79472532-79472582	HAEpiC	amniotic membrane:	n/a
11	chr1:79350918-79350968	PrEC	prostate:	n/a
12	chr1:79472408-79472458	CMK	blood:	n/a
13	chr1:79472532-79472582	RPTEC	kidney:	n/a
14	chr1:79472917-79472967	GM12891	blood:	n/a
15	chr1:79472408-79472458	HMEC	breast:	n/a
16	chr1:79474718-79474768	HEK293	kidney:	embryo
17	chr1:79472361-79472411	HRE	kidney:	n/a
18	chr1:79350918-79350968	PANC-1	pancreas:	n/a
19	chr1:79350918-79350968	NT2-D1	testis:	n/a
20	chr1:79350918-79350968	NHDF-neo	bronchial:	n/a
21	chr1:79472917-79472967	GM19239	blood:	n/a
22	chr1:79472532-79472582	ProgFib	skin:	n/a
23	chr1:79472558-79472608	HL-60	blood:	n/a
24	chr1:79472643-79472693	Jurkat	blood:	n/a
25	chr1:79472361-79472411	SK-N-SH_RA	brain:	n/a
26	chr1:79472361-79472411	HCT-116	colon:	n/a
27	chr1:79350918-79350968	AG04449	skin:	fetal
28	chr1:79350918-79350968	Hepatocyte	liver:	n/a
29	chr1:79472452-79472502	SK-N-MC	brain:	n/a
30	chr1:79472643-79472693	Caco-2	colon:	n/a
31	chr1:79472643-79472693	SK-N-SH_RA	brain:	n/a
32	chr1:79474718-79474768	IMR90	lung:	fetal
33	chr1:79471984-79472034	SAEC	small airway:	n/a
34	chr1:79350918-79350968	ECC-1	luminal epithelium:	n/a
35	chr1:79472536-79472586	AG04450	lung:	fetal
36	chr1:79472408-79472458	PFSK-1	brain:	n/a
37	chr1:79473783-79473833	NB4	blood:	n/a
38	chr1:79472558-79472608	AG04449	skin:	fetal
39	chr1:79472452-79472502	NHBE	bronchial:	n/a
40	chr1:79472532-79472582	HUVEC	blood vessel:	n/a
41	chr1:79472282-79472332	HAEpiC	amniotic membrane:	n/a
42	chr1:79472343-79472393	HAEpiC	amniotic membrane:	n/a
43	chr1:79472532-79472582	K562	blood:	n/a
44	chr1:79472532-79472582	HL-60	blood:	n/a
45	chr1:79472558-79472608	GM12878	blood:	n/a
46	chr1:79472536-79472586	GM12878	blood:	n/a
47	chr1:79474718-79474768	CMK	blood:	n/a
48	chr1:79350918-79350968	ProgFib	skin:	n/a
49	chr1:79472343-79472393	MCF10A-Er-Src	breast:	n/a
50	chr1:79472452-79472502	PFSK-1	brain:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:
2	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
3	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
4	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
5	chr1:79527063..79529337-chr1:79533334..79535055,2	K562	blood:
6	chr1:79411840..79414575-chr1:79858123..79860401,2	K562	blood:
7	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
8	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
9	chr1:79536026..79538535-chr1:79539899..79541790,2	K562	blood:
10	chr1:79356582..79358429-chr1:79361774..79364231,2	MCF-7	breast:
11	chr1:79410821..79413576-chr1:79414533..79416679,2	K562	blood:
12	chr1:79484446..79486654-chr1:79486860..79488839,2	MCF-7	breast:
13	chr1:79370114..79372345-chr1:79443530..79445892,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELTD1-2	chr1:79493775-79493876	XLOC_000877
2	lnc-ELTD1-2	chr1:79490858-79491009	XLOC_000877
3	lnc-ELTD1-1	chr1:79351642-79351681	NONHSAT004083
4	lnc-ELTD1-1	chr1:79346569-79346750	NONHSAT004083

No data

Variant related genes	Relation type
ELTD1	TF binding region
PSAT1P3	TF binding region
ELTD1	CpG island
PSAT1P3	CpG island
IGSF1	miRNA target sites
TCF7L2	miRNA target sites

Extended variants
information (count: 7519 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:7519 , 50 per page) page: 1 2 3 4 5 6 7 ... 151

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78583931	chr1:79310781-79310782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569669115	chr1:79310784-79310785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188251591	chr1:79310810-79310811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374754186	chr1:79310827-79310828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549060672	chr1:79310835-79310836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528684315	chr1:79310881-79310882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567447532	chr1:79310930-79310931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2451103	chr1:79310965-79310966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111486088	chr1:79310967-79310968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs61123767	chr1:79310974-79310975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs2489730	chr1:79311009-79311010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2451104	chr1:79311026-79311027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534499895	chr1:79311033-79311034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs553096073	chr1:79311054-79311055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191357186	chr1:79311060-79311061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs550667701	chr1:79311096-79311097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535232082	chr1:79311113-79311114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373940648	chr1:79311123-79311124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370922580	chr1:79311129-79311130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370789117	chr1:79311130-79311131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2489731	chr1:79311235-79311236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2489732	chr1:79311239-79311240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs59221254	chr1:79311335-79311336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs61768720	chr1:79311936-79311937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202075354	chr1:79311981-79311982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184725367	chr1:79312206-79312207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200118940	chr1:79312672-79312673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376412657	chr1:79312787-79312788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370672445	chr1:79312789-79312790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374241120	chr1:79312804-79312805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377638687	chr1:79312846-79312847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371432376	chr1:79312893-79312894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs375901752	chr1:79312903-79312904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372752967	chr1:79312929-79312930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367723314	chr1:79313038-79313039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557300381	chr1:79313039-79313040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575301720	chr1:79313064-79313065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370087028	chr1:79313068-79313069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs542125250	chr1:79313087-79313088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374841641	chr1:79313161-79313162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs61768721	chr1:79313187-79313188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377344092	chr1:79313195-79313196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs368140514	chr1:79313295-79313296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371604776	chr1:79313300-79313301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375271417	chr1:79313365-79313366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368207450	chr1:79313377-79313378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs201774345	chr1:79313380-79313381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375319730	chr1:79313445-79313446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369220891	chr1:79313449-79313450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554684424	chr1:79313484-79313485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	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
Melanoma	17363583	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
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79307400-79317200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr1:79317200-79317400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr1:79319800-79321200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:79320600-79321400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:79320600-79321400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr1:79320800-79321400	Enhancers	Primary hematopoietic stem cells	blood
7	chr1:79332400-79332600	Enhancers	Fetal Stomach	stomach
8	chr1:79332600-79336400	Weak transcription	Fetal Stomach	stomach
9	chr1:79334200-79335000	Enhancers	Fetal Lung	lung
10	chr1:79335000-79335400	Weak transcription	Fetal Lung	lung
11	chr1:79335400-79336200	Enhancers	Fetal Lung	lung
12	chr1:79336400-79336800	Enhancers	Fetal Stomach	stomach
13	chr1:79336800-79337400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr1:79336800-79337600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
15	chr1:79338200-79339200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr1:79338200-79339200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr1:79338200-79339200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:79338800-79339200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:79346400-79350800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr1:79346600-79350800	Weak transcription	HUVEC	blood vessel
21	chr1:79348400-79348600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr1:79348600-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr1:79350200-79350400	Enhancers	Hela-S3	cervix
24	chr1:79350200-79350600	Enhancers	Colon Smooth Muscle	Colon
25	chr1:79350200-79351000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr1:79350200-79351000	Enhancers	Rectal Smooth Muscle	rectum
27	chr1:79350200-79351200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr1:79350200-79351200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr1:79350200-79351400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:79350200-79351400	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr1:79350400-79350800	Enhancers	Fetal Kidney	kidney
32	chr1:79350400-79351000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr1:79350400-79351000	Enhancers	Fetal Stomach	stomach
34	chr1:79350400-79351200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:79350400-79351200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr1:79350400-79351200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:79350400-79351200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:79350400-79351200	Flanking Active TSS	Hela-S3	cervix
39	chr1:79350400-79351200	Enhancers	NH-A	brain
40	chr1:79350400-79351400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr1:79350400-79351400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:79350400-79351600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:79350600-79351000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:79350600-79351000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr1:79350600-79351000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr1:79350600-79351000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:79350600-79351000	Enhancers	Adipose Nuclei	Adipose
48	chr1:79350600-79351000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:79350600-79351000	Enhancers	Fetal Lung	lung
50	chr1:79350600-79351000	Enhancers	Psoas Muscle	Psoas

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