Variant report

Variant	nsv871152
Chromosome Location	chr1:75152186-75197533
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:662)
CpG islands
(count:61)
Chromatin interactive
region (count:22)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:75195690-75196472	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:75155518-75155998	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:75196885-75197457	K562	blood:	n/a	n/a
4	ARID3A	chr1:75195686-75196262	K562	blood:	n/a	n/a
5	ARID3A	chr1:75181886-75182082	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:75155524-75155836	K562	blood:	n/a	n/a
7	ARID3A	chr1:75196807-75197673	HepG2	liver:	n/a	n/a
8	ATF1	chr1:75195816-75196070	K562	blood:	n/a	n/a
9	ATF2	chr1:75179819-75180524	GM12878	blood:	n/a	n/a
10	ATF2	chr1:75197521-75198276	GM12878	blood:	n/a	n/a
11	ATF2	chr1:75196957-75197766	GM12878	blood:	n/a	n/a
12	ATF2	chr1:75179537-75180570	GM12878	blood:	n/a	n/a
13	BCL3	chr1:75180891-75181329	GM12878	blood:	n/a	n/a
14	BCLAF1	chr1:75180039-75180515	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:75181187-75181214	GM12878	blood:	n/a	n/a
16	BHLHE40	chr1:75195816-75196205	HepG2	liver:	n/a	n/a
17	BHLHE40	chr1:75195809-75196119	K562	blood:	n/a	n/a
18	BHLHE40	chr1:75165240-75165247	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:75155573-75155773	K562	blood:	n/a	n/a
20	CBX3	chr1:75191757-75192081	K562	blood:	n/a	n/a
21	CBX3	chr1:75191679-75192165	K562	blood:	n/a	n/a
22	CCNT2	chr1:75195815-75196162	K562	blood:	n/a	n/a
23	CCNT2	chr1:75197018-75197441	K562	blood:	n/a	chr1:75197248-75197268
24	CEBPB	chr1:75155492-75155866	Hela-S3	cervix:	n/a	chr1:75155493-75155504
25	CEBPB	chr1:75155489-75155872	HepG2	liver:	n/a	chr1:75155493-75155504
26	CEBPB	chr1:75197224-75197716	HepG2	liver:	n/a	n/a
27	CEBPB	chr1:75155493-75155867	A549	lung:	n/a	chr1:75155493-75155504
28	CEBPB	chr1:75195390-75196009	IMR90	lung:	n/a	chr1:75195518-75195535 chr1:75195519-75195532
29	CEBPB	chr1:75191865-75191984	K562	blood:	n/a	n/a
30	CEBPB	chr1:75155513-75155853	MCF-7	breast:	n/a	n/a
31	CEBPB	chr1:75155489-75155873	IMR90	lung:	n/a	chr1:75155493-75155504
32	CEBPB	chr1:75197458-75199569	GM12878	blood:	n/a	n/a
33	CEBPB	chr1:75182563-75182880	Hela-S3	cervix:	n/a	chr1:75182702-75182713
34	CEBPB	chr1:75182537-75182886	A549	lung:	n/a	chr1:75182702-75182713
35	CEBPB	chr1:75182585-75182817	H1-hESC	embryonic stem cell:	n/a	chr1:75182702-75182713
36	CEBPB	chr1:75182521-75182892	IMR90	lung:	n/a	chr1:75182702-75182713
37	CEBPB	chr1:75182534-75182894	K562	blood:	n/a	chr1:75182702-75182713
38	CEBPB	chr1:75155493-75155848	K562	blood:	n/a	chr1:75155493-75155504
39	CEBPB	chr1:75182531-75182894	HepG2	liver:	n/a	chr1:75182702-75182713
40	CEBPB	chr1:75155540-75155849	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr1:75195622-75196207	A549	lung:	n/a	n/a
42	CEBPD	chr1:75196968-75197523	K562	blood:	n/a	n/a
43	CEBPD	chr1:75197032-75197501	K562	blood:	n/a	n/a
44	CEBPD	chr1:75195673-75196191	K562	blood:	n/a	n/a
45	CHD1	chr1:75180484-75180496	GM12878	blood:	n/a	n/a
46	CHD2	chr1:75197213-75198218	GM12878	blood:	n/a	n/a
47	CTCF	chr1:75155660-75155810	HFF	foreskin:	n/a	chr1:75155676-75155694 chr1:75155671-75155692 chr1:75155683-75155691 chr1:75155677-75155693
48	CTCF	chr1:75155600-75155750	HepG2	liver:	n/a	chr1:75155676-75155694 chr1:75155671-75155692 chr1:75155683-75155691 chr1:75155677-75155693
49	CTCF	chr1:75155640-75155790	AG09309	skin:	n/a	chr1:75155676-75155694 chr1:75155671-75155692 chr1:75155683-75155691 chr1:75155677-75155693
50	CTCF	chr1:75155600-75155750	AG10803	skin:	n/a	chr1:75155676-75155694 chr1:75155671-75155692 chr1:75155683-75155691 chr1:75155677-75155693

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:75180368-75180418	IMR90	lung:	fetal
2	chr1:75180368-75180418	NH-A	brain:	n/a
3	chr1:75180368-75180418	K562	blood:	n/a
4	chr1:75180368-75180418	HRPEpiC	eye:	n/a
5	chr1:75180368-75180418	GM12878	blood:	n/a
6	chr1:75180368-75180418	HAEpiC	amniotic membrane:	n/a
7	chr1:75180368-75180418	HCT-116	colon:	n/a
8	chr1:75180368-75180418	HUVEC	blood vessel:	n/a
9	chr1:75180368-75180418	HPAEpiC	pulmonary alveolar:	n/a
10	chr1:75180368-75180418	NHBE	bronchial:	n/a
11	chr1:75180368-75180418	HCM	heart:	n/a
12	chr1:75180368-75180418	HEEpiC	esophagus:	n/a
13	chr1:75180368-75180418	SK-N-SH	brain:	n/a
14	chr1:75180368-75180418	BE2_C	brain:	n/a
15	chr1:75180368-75180418	RPTEC	kidney:	n/a
16	chr1:75180368-75180418	LNCaP	prostate:	n/a
17	chr1:75180368-75180418	MCF-7	breast:	n/a
18	chr1:75180368-75180418	ECC-1	luminal epithelium:	n/a
19	chr1:75180368-75180418	AG10803	skin:	n/a
20	chr1:75180368-75180418	A549	lung:	n/a
21	chr1:75180368-75180418	HCPEpiC	choroid plexus:	n/a
22	chr1:75180368-75180418	AG09319	gingival:	n/a
23	chr1:75180368-75180418	PANC-1	pancreas:	n/a
24	chr1:75180368-75180418	AG04450	lung:	fetal
25	chr1:75180368-75180418	Hela-S3	cervix:	n/a
26	chr1:75180368-75180418	SK-N-MC	brain:	n/a
27	chr1:75180368-75180418	U87	brain:	n/a
28	chr1:75180368-75180418	NB4	blood:	n/a
29	chr1:75180368-75180418	GM19239	blood:	n/a
30	chr1:75180368-75180418	HEK293	kidney:	embryo
31	chr1:75180368-75180418	MCF10A-Er-Src	breast:	n/a
32	chr1:75180368-75180418	Jurkat	blood:	n/a
33	chr1:75180368-75180418	AG09309	skin:	n/a
34	chr1:75180368-75180418	HIPEpiC	eye:	n/a
35	chr1:75180368-75180418	AG04449	skin:	fetal
36	chr1:75180368-75180418	ProgFib	skin:	n/a
37	chr1:75180368-75180418	HRE	kidney:	n/a
38	chr1:75180368-75180418	HNPCEpiC	eye:	n/a
39	chr1:75180368-75180418	HRCEpiC	kidney:	n/a
40	chr1:75180368-75180418	NHDF-neo	bronchial:	n/a
41	chr1:75180368-75180418	H1-hESC	embryonic stem cell:	embryo
42	chr1:75180368-75180418	GM12892	blood:	n/a
43	chr1:75180368-75180418	PFSK-1	brain:	n/a
44	chr1:75180368-75180418	SAEC	small airway:	n/a
45	chr1:75180368-75180418	SKMC	muscle:	n/a
46	chr1:75180368-75180418	PrEC	prostate:	n/a
47	chr1:75180368-75180418	GM06990	blood:	n/a
48	chr1:75180368-75180418	Hepatocyte	liver:	n/a
49	chr1:75180368-75180418	CMK	blood:	n/a
50	chr1:75180368-75180418	HepG2	liver:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:75176716..75178804-chr1:75183304..75185593,2	K562	blood:
2	chr1:75154629..75156914-chr1:75162681..75164412,2	K562	blood:
3	chr1:75117987..75118877-chr1:75155539..75156443,2	MCF-7	breast:
4	chr1:75176716..75178804-chr1:75183304..75185593,2	K562	blood:
5	chr1:75165629..75168544-chr1:75168897..75171535,2	K562	blood:
6	chr1:75185247..75187667-chr1:75196459..75199563,3	MCF-7	breast:
7	chr1:75184341..75186211-chr1:75195843..75198815,2	K562	blood:
8	chr1:75182455..75184516-chr1:75199218..75200932,2	K562	blood:
9	chr1:75184634..75186342-chr1:75186359..75187995,2	K562	blood:
10	chr1:75165629..75168544-chr1:75168897..75171535,2	K562	blood:
11	chr1:75169904..75171834-chr1:75191758..75194711,2	K562	blood:
12	chr1:75184634..75186342-chr1:75186359..75187995,2	K562	blood:
13	chr1:75146366..75148912-chr1:75156254..75157976,2	K562	blood:
14	chr1:75195743..75197778-chr1:75197921..75199580,2	MCF-7	breast:
15	chr1:75192924..75196422-chr1:75198121..75200705,3	MCF-7	breast:
16	chr1:75154629..75156914-chr1:75162681..75164412,2	K562	blood:
17	chr1:75178320..75181136-chr1:75198418..75199986,2	MCF-7	breast:
18	chr1:75114474..75116619-chr1:75157243..75159501,2	MCF-7	breast:
19	chr1:75166184..75168158-chr1:75197288..75199350,2	MCF-7	breast:
20	chr1:75118268..75118957-chr1:75155576..75156140,2	MCF-7	breast:
21	chr1:75169904..75171834-chr1:75191758..75194711,2	K562	blood:
22	chr1:75197237..75200127-chr1:76254006..76255529,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRYZ-1	chr1:75164453-75165017	ENSG00000272864.1

No data

Variant related genes	Relation type
CRYZ	TF binding region
ENSG00000272864	TF binding region
TYW3	TF binding region
CRYZ	CpG island
ENSG00000272864	CpG island
TYW3	CpG island
ENSG00000201487	chromatin interactions
ENSG00000162623	chromatin interactions
ENSG00000116791	chromatin interactions

Extended variants
information (count: 1808 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1808 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10518473	chr1:75152186-75152187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531748789	chr1:75152217-75152218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549831181	chr1:75152245-75152246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs142666736	chr1:75152267-75152268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535416406	chr1:75152278-75152279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553738790	chr1:75152289-75152290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs187189389	chr1:75152290-75152291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566288192	chr1:75152312-75152313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540104282	chr1:75152358-75152359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191934092	chr1:75152529-75152530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576544488	chr1:75152538-75152539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368290235	chr1:75152556-75152557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs184705413	chr1:75152560-75152561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556248964	chr1:75152561-75152562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568916260	chr1:75152576-75152577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143667271	chr1:75152578-75152579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574495353	chr1:75152593-75152594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541888721	chr1:75152595-75152596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560091497	chr1:75152613-75152614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs35726558	chr1:75152643-75152644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs527619940	chr1:75152664-75152665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs546065333	chr1:75152698-75152699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs371707383	chr1:75152730-75152731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76843636	chr1:75152734-75152735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188001566	chr1:75152777-75152778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs150567801	chr1:75152778-75152779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs663246	chr1:75152868-75152869	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs529341269	chr1:75152870-75152871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs547411976	chr1:75152871-75152872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566049854	chr1:75152875-75152876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562745646	chr1:75152876-75152877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139549721	chr1:75152887-75152888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558401175	chr1:75152898-75152899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570159042	chr1:75152932-75152933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs537603014	chr1:75152951-75152952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192233436	chr1:75152999-75153000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs574632275	chr1:75153002-75153003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs541927773	chr1:75153056-75153057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544956196	chr1:75153145-75153146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544284009	chr1:75153180-75153181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553524787	chr1:75153259-75153260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372621902	chr1:75153262-75153263	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369541457	chr1:75153267-75153268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571976313	chr1:75153270-75153271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545802683	chr1:75153314-75153315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs114754006	chr1:75153339-75153340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529667864	chr1:75153340-75153341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147916604	chr1:75153438-75153439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543258650	chr1:75153448-75153449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185762037	chr1:75153472-75153473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	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
small cell lung cancer	20016488	CNVD

Chromatin state (count:1154 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75141800-75179600	Weak transcription	Aorta	Aorta
2	chr1:75147200-75155800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:75147400-75152800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:75148200-75153800	Weak transcription	GM12878-XiMat	blood
5	chr1:75152200-75153800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr1:75152800-75153400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr1:75153000-75153600	Enhancers	Fetal Brain Female	brain
8	chr1:75153400-75155200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:75153600-75154600	Weak transcription	Fetal Brain Female	brain
10	chr1:75153800-75154600	Enhancers	GM12878-XiMat	blood
11	chr1:75153800-75155000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:75153800-75155800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:75154400-75154600	Enhancers	Brain Germinal Matrix	brain
14	chr1:75154600-75155200	Weak transcription	Brain Germinal Matrix	brain
15	chr1:75154600-75156000	Enhancers	Fetal Brain Female	brain
16	chr1:75154600-75156000	Weak transcription	GM12878-XiMat	blood
17	chr1:75154600-75156200	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr1:75154600-75156200	Enhancers	Fetal Brain Male	brain
19	chr1:75155000-75155400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr1:75155200-75156000	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr1:75155200-75156000	Enhancers	Brain Germinal Matrix	brain
22	chr1:75155200-75156000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr1:75155200-75156200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr1:75155200-75156200	Enhancers	Ovary	ovary
25	chr1:75155400-75155600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:75155400-75156000	Enhancers	Liver	Liver
27	chr1:75155400-75156200	Enhancers	Fetal Lung	lung
28	chr1:75155400-75156400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:75155600-75156000	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr1:75155600-75156200	Enhancers	HUVEC	blood vessel
31	chr1:75155600-75156600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr1:75155600-75159200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:75155800-75156000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr1:75155800-75156000	Enhancers	Fetal Heart	heart
35	chr1:75155800-75156000	Enhancers	Fetal Intestine Large	intestine
36	chr1:75155800-75156000	Enhancers	NH-A	brain
37	chr1:75155800-75156200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr1:75155800-75156200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:75155800-75156200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr1:75155800-75156200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:75155800-75156200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr1:75155800-75156200	Enhancers	HepG2	liver
43	chr1:75155800-75156400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr1:75155800-75156400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr1:75156000-75156200	Enhancers	GM12878-XiMat	blood
46	chr1:75156000-75158000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr1:75156000-75158800	Weak transcription	NH-A	brain
48	chr1:75156000-75167600	Weak transcription	Liver	Liver
49	chr1:75156000-75183400	Weak transcription	Fetal Heart	heart
50	chr1:75156200-75159000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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