Variant report

Variant	nsv1014209
Chromosome Location	chr1:69710467-69910241
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:550)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:69786005-69786068	K562	blood:	n/a	n/a
2	BACH1	chr1:69778186-69778224	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr1:69771334-69771638	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:69779311-69779356	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:69721786-69721971	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr1:69876991-69877003	K562	blood:	n/a	n/a
7	BATF	chr1:69848192-69848414	GM12878	blood:	n/a	chr1:69848339-69848350
8	BATF	chr1:69848139-69848482	GM12878	blood:	n/a	chr1:69848339-69848350
9	BATF	chr1:69880342-69880584	GM12878	blood:	n/a	chr1:69880486-69880497
10	BHLHE40	chr1:69786393-69786862	GM12878	blood:	n/a	n/a
11	BRCA1	chr1:69841564-69841592	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr1:69853601-69853623	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:69907945-69908096	K562	blood:	n/a	n/a
14	CEBPB	chr1:69898839-69899159	IMR90	lung:	n/a	chr1:69899008-69899017 chr1:69899006-69899017
15	CEBPB	chr1:69729540-69729991	ECC-1	luminal epithelium:	n/a	chr1:69729726-69729737
16	CEBPB	chr1:69729628-69729889	A549	lung:	n/a	chr1:69729726-69729737
17	CEBPB	chr1:69898171-69898387	K562	blood:	n/a	chr1:69898277-69898288 chr1:69898275-69898288 chr1:69898275-69898288
18	CEBPB	chr1:69729574-69729899	IMR90	lung:	n/a	chr1:69729726-69729737
19	CEBPB	chr1:69768342-69768528	H1-hESC	embryonic stem cell:	n/a	chr1:69768474-69768487 chr1:69768474-69768487
20	CEBPB	chr1:69729539-69729882	ECC-1	luminal epithelium:	n/a	chr1:69729726-69729737
21	CEBPB	chr1:69869653-69870044	HepG2	liver:	n/a	n/a
22	CEBPB	chr1:69843186-69843472	K562	blood:	n/a	n/a
23	CEBPB	chr1:69729570-69729872	H1-hESC	embryonic stem cell:	n/a	chr1:69729726-69729737
24	CEBPB	chr1:69729658-69729819	K562	blood:	n/a	chr1:69729726-69729737
25	CEBPB	chr1:69896937-69896996	HepG2	liver:	n/a	n/a
26	CEBPB	chr1:69735151-69735223	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr1:69729555-69729912	HepG2	liver:	n/a	chr1:69729726-69729737
28	CHD2	chr1:69778135-69778273	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr1:69771987-69771993	HepG2	liver:	n/a	n/a
30	CHD2	chr1:69786464-69786687	GM12878	blood:	n/a	n/a
31	CHD2	chr1:69750198-69750464	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr1:69777506-69777510	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr1:69848520-69848670	GM12865	blood:	n/a	n/a
34	CTCF	chr1:69771480-69771630	GM12875	blood:	n/a	n/a
35	CTCF	chr1:69771440-69771590	HCT-116	colon:	n/a	n/a
36	CTCF	chr1:69848620-69848770	GM12866	blood:	n/a	n/a
37	CTCF	chr1:69771360-69771510	GM12874	blood:	n/a	n/a
38	CTCF	chr1:69771400-69771550	GM12871	blood:	n/a	n/a
39	CTCF	chr1:69843351-69843378	LNCaP	prostate:	n/a	n/a
40	CTCF	chr1:69843331-69843397	HepG2	liver:	n/a	n/a
41	CTCF	chr1:69771340-69771490	HCT-116	colon:	n/a	n/a
42	CTCF	chr1:69843245-69843484	K562	blood:	n/a	n/a
43	CTCF	chr1:69771440-69771590	GM12878	blood:	n/a	n/a
44	CTCF	chr1:69725860-69726010	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr1:69771426-69771545	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr1:69771460-69771610	GM12866	blood:	n/a	n/a
47	CTCF	chr1:69850804-69850862	K562	blood:	n/a	n/a
48	CTCF	chr1:69744600-69744750	AG09309	skin:	n/a	n/a
49	CTCF	chr1:69848620-69848770	GM12873	blood:	n/a	n/a
50	CTCF	chr1:69771420-69771570	HBMEC	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:69778399-69778449	HL-60	blood:	n/a
2	chr1:69778399-69778449	T-47D	breast:	n/a
3	chr1:69778399-69778449	HNPCEpiC	eye:	n/a
4	chr1:69778399-69778449	AG04450	lung:	fetal
5	chr1:69778399-69778449	GM12892	blood:	n/a
6	chr1:69778399-69778449	HCPEpiC	choroid plexus:	n/a
7	chr1:69778399-69778449	HepG2	liver:	n/a
8	chr1:69778399-69778449	AG04449	skin:	fetal
9	chr1:69778399-69778449	SKMC	muscle:	n/a
10	chr1:69778399-69778449	Hela-S3	cervix:	n/a
11	chr1:69778399-69778449	MCF-7	breast:	n/a
12	chr1:69778399-69778449	AoSMC	blood vessel:	n/a
13	chr1:69778399-69778449	HIPEpiC	eye:	n/a
14	chr1:69778399-69778449	NHBE	bronchial:	n/a
15	chr1:69778399-69778449	A549	lung:	n/a
16	chr1:69778399-69778449	SAEC	small airway:	n/a
17	chr1:69778399-69778449	GM12878	blood:	n/a
18	chr1:69778399-69778449	Caco-2	colon:	n/a
19	chr1:69778399-69778449	Jurkat	blood:	n/a
20	chr1:69778399-69778449	HAEpiC	amniotic membrane:	n/a
21	chr1:69778399-69778449	BE2_C	brain:	n/a
22	chr1:69778399-69778449	K562	blood:	n/a
23	chr1:69778399-69778449	U87	brain:	n/a
24	chr1:69778399-69778449	HUVEC	blood vessel:	n/a
25	chr1:69778399-69778449	NB4	blood:	n/a
26	chr1:69778399-69778449	ovcar-3	ovarian:	n/a
27	chr1:69778399-69778449	BJ	skin:	n/a
28	chr1:69778399-69778449	HMEC	breast:	n/a
29	chr1:69778399-69778449	HCT-116	colon:	n/a
30	chr1:69778399-69778449	HCM	heart:	n/a
31	chr1:69778399-69778449	NH-A	brain:	n/a
32	chr1:69778399-69778449	HRPEpiC	eye:	n/a
33	chr1:69778399-69778449	LNCaP	prostate:	n/a
34	chr1:69778399-69778449	MCF10A-Er-Src	breast:	n/a
35	chr1:69778399-69778449	AG10803	skin:	n/a
36	chr1:69778399-69778449	HEEpiC	esophagus:	n/a
37	chr1:69778399-69778449	ProgFib	skin:	n/a
38	chr1:69778399-69778449	NT2-D1	testis:	n/a
39	chr1:69778399-69778449	GM06990	blood:	n/a
40	chr1:69778399-69778449	RPTEC	kidney:	n/a
41	chr1:69778399-69778449	SK-N-SH	brain:	n/a
42	chr1:69778399-69778449	PANC-1	pancreas:	n/a
43	chr1:69778399-69778449	HEK293	kidney:	embryo
44	chr1:69778399-69778449	Hepatocyte	liver:	n/a
45	chr1:69778399-69778449	SK-N-MC	brain:	n/a
46	chr1:69778399-69778449	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:69778399-69778449	HCF	heart:	n/a
48	chr1:69778399-69778449	GM12891	blood:	n/a
49	chr1:69778399-69778449	PFSK-1	brain:	n/a
50	chr1:69778399-69778449	AG09319	gingival:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:69820993..69822577-chr1:70080640..70082316,2	K562	blood:
2	chr1:69905907..69908777-chr1:69910942..69912719,3	K562	blood:
3	chr1:69905842..69908777-chr1:69909714..69912512,3	K562	blood:
4	chr1:69734519..69737300-chr1:69737700..69740274,2	K562	blood:
5	chr1:69842939..69843593-chr1:70202979..70203753,2	K562	blood:
6	chr1:69826184..69828041-chr1:69829694..69831375,2	K562	blood:
7	chr1:69734519..69737300-chr1:69737700..69740274,2	K562	blood:
8	chr1:69905842..69908777-chr1:69909714..69912512,3	K562	blood:
9	chr1:69826184..69828041-chr1:69829694..69831375,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC7-3	chr1:69898938-69898988	XLOC_000243
2	lnc-LRRC7-3	chr1:69898834-69898988	NONHSAT003835
3	lnc-DEPDC1-2	chr1:69714898-69715106	XLOC_000866
4	lnc-LRRC7-3	chr1:69900685-69901092	NONHSAT003835
5	lnc-LRRC7-3	chr1:69900686-69901092	XLOC_000243

No data

Variant related genes	Relation type
ENSG00000235446	TF binding region
ENSG00000229639	TF binding region
ENSG00000235446	CpG island
ENSG00000229639	CpG island
ZNF644	miRNA target sites

Extended variants
information (count: 3698 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:3698 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375025930	chr1:69710479-69710480	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs537464853	chr1:69710491-69710492	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527820611	chr1:69710495-69710496	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369560819	chr1:69710505-69710506	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149226322	chr1:69710585-69710586	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111680782	chr1:69710586-69710587	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188494202	chr1:69710587-69710588	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376332264	chr1:69710603-69710604	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71651409	chr1:69710625-69710626	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181441559	chr1:69710631-69710632	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568846326	chr1:69710679-69710680	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186943274	chr1:69710730-69710731	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112657818	chr1:69710740-69710741	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs146899916	chr1:69710756-69710757	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527751063	chr1:69710774-69710775	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552543301	chr1:69710793-69710794	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539629310	chr1:69710813-69710814	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs533607002	chr1:69710828-69710829	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12047547	chr1:69710877-69710878	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567119806	chr1:69710887-69710888	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558370795	chr1:69710898-69710899	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs137923896	chr1:69710920-69710921	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143389029	chr1:69711019-69711020	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116542586	chr1:69711053-69711054	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539223519	chr1:69711158-69711159	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2246312	chr1:69711165-69711166	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs572602397	chr1:69711184-69711185	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191383489	chr1:69711192-69711193	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561448785	chr1:69711204-69711205	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2246316	chr1:69711379-69711380	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568296312	chr1:69711425-69711426	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535805288	chr1:69711434-69711435	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs183705502	chr1:69711449-69711450	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562433564	chr1:69711460-69711461	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562382181	chr1:69711462-69711463	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs186317999	chr1:69711470-69711471	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551266828	chr1:69711528-69711529	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574052997	chr1:69711565-69711566	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544644471	chr1:69711566-69711567	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116966691	chr1:69711599-69711600	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2246327	chr1:69711636-69711637	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs547163707	chr1:69711668-69711669	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs572176049	chr1:69711682-69711683	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191114552	chr1:69711696-69711697	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368249730	chr1:69711719-69711720	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78637554	chr1:69711778-69711779	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs112037961	chr1:69711798-69711799	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12091877	chr1:69711800-69711801	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs569676439	chr1:69711801-69711802	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112782797	chr1:69711860-69711861	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
small cell lung cancer	20016488	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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal cancer	21851588	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:286 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69708200-69710800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:69709200-69710600	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr1:69709200-69712400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
4	chr1:69709400-69710600	Enhancers	H1 Cell Line	embryonic stem cell
5	chr1:69709400-69711000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr1:69709600-69711000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
7	chr1:69710000-69710600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
8	chr1:69710000-69710800	Enhancers	Fetal Brain Female	brain
9	chr1:69710200-69711800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr1:69710200-69711800	Weak transcription	Brain Germinal Matrix	brain
11	chr1:69710400-69711200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chr1:69710400-69712800	Enhancers	Fetal Brain Male	brain
13	chr1:69710800-69711200	Weak transcription	Fetal Brain Female	brain
14	chr1:69710800-69712000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:69710800-69712200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:69711000-69711600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr1:69711000-69712000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr1:69711200-69712000	Enhancers	Fetal Brain Female	brain
19	chr1:69711600-69712000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:69711800-69712400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr1:69711800-69713000	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr1:69711800-69713000	Enhancers	Brain Germinal Matrix	brain
23	chr1:69712000-69712200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr1:69712000-69712400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr1:69712000-69712400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr1:69712000-69712400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr1:69712000-69712400	Flanking Active TSS	Fetal Brain Female	brain
28	chr1:69712000-69712400	Enhancers	Fetal Stomach	stomach
29	chr1:69712000-69713000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:69712000-69713000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr1:69712200-69712400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr1:69712200-69712600	Enhancers	Brain Hippocampus Middle	brain
33	chr1:69712200-69712800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr1:69712400-69712800	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr1:69712400-69712800	Active TSS	Fetal Brain Female	brain
36	chr1:69712400-69714400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr1:69712800-69713000	Flanking Active TSS	Fetal Brain Female	brain
38	chr1:69712800-69714600	Weak transcription	Fetal Brain Male	brain
39	chr1:69713000-69714800	Enhancers	Fetal Brain Female	brain
40	chr1:69714400-69715200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr1:69714600-69715000	Enhancers	Fetal Brain Male	brain
42	chr1:69724000-69724400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr1:69724200-69724800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr1:69724200-69724800	Enhancers	Pancreas	Pancrea
45	chr1:69724200-69725000	Enhancers	Gastric	stomach
46	chr1:69724200-69725000	Enhancers	Stomach Mucosa	stomach
47	chr1:69724800-69729800	Weak transcription	Pancreas	Pancrea
48	chr1:69727400-69727600	Enhancers	Fetal Brain Female	brain
49	chr1:69727600-69730000	Weak transcription	Fetal Brain Female	brain
50	chr1:69728000-69728200	Enhancers	Colon Smooth Muscle	Colon

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