Variant report

Variant	esv3693301
Chromosome Location	chr2:55324960-55335045
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	ARID3A	chr2:55324829-55325004	K562	blood:	n/a	n/a
2	ARID3A	chr2:55333339-55333652	K562	blood:	n/a	n/a
3	ARID3A	chr2:55327031-55327942	K562	blood:	n/a	chr2:55327796-55327812
4	ATF1	chr2:55333344-55333688	K562	blood:	n/a	n/a
5	ATF1	chr2:55327022-55327751	K562	blood:	n/a	n/a
6	ATF3	chr2:55326937-55327390	K562	blood:	n/a	n/a
7	ATF3	chr2:55333276-55333643	K562	blood:	n/a	n/a
8	BRCA1	chr2:55326986-55327540	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr2:55324862-55325282	K562	blood:	n/a	n/a
10	CCNT2	chr2:55333403-55333632	K562	blood:	n/a	n/a
11	CEBPB	chr2:55326985-55328061	IMR90	lung:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
12	CEBPB	chr2:55327081-55327354	H1-hESC	embryonic stem cell:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
13	CEBPB	chr2:55329109-55329508	IMR90	lung:	n/a	n/a
14	CEBPB	chr2:55327042-55327431	ECC-1	luminal epithelium:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
15	CEBPB	chr2:55328839-55329536	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:55333241-55333703	K562	blood:	n/a	chr2:55333495-55333506
17	CEBPB	chr2:55333332-55333669	Hela-S3	cervix:	n/a	chr2:55333495-55333506
18	CEBPB	chr2:55327096-55327286	K562	blood:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
19	CEBPB	chr2:55327013-55327408	ECC-1	luminal epithelium:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
20	CEBPB	chr2:55333281-55333658	A549	lung:	n/a	chr2:55333495-55333506
21	CEBPB	chr2:55333333-55333660	HepG2	liver:	n/a	chr2:55333495-55333506
22	CEBPB	chr2:55326821-55328075	Hela-S3	cervix:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
23	CEBPB	chr2:55326888-55327787	A549	lung:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
24	CEBPB	chr2:55327779-55327912	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:55333280-55333596	A549	lung:	n/a	chr2:55333495-55333506
26	CEBPB	chr2:55327013-55328046	K562	blood:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
27	CEBPB	chr2:55326888-55328104	HCT-116	colon:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
28	CEBPB	chr2:55327027-55327400	HepG2	liver:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
29	CEBPB	chr2:55333309-55333691	K562	blood:	n/a	chr2:55333495-55333506
30	CEBPB	chr2:55326958-55327386	A549	lung:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
31	CEBPB	chr2:55326983-55327991	K562	blood:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
32	CEBPB	chr2:55333336-55333671	A549	lung:	n/a	chr2:55333495-55333506
33	CEBPB	chr2:55327008-55328037	A549	lung:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
34	CEBPB	chr2:55333308-55333695	IMR90	lung:	n/a	chr2:55333495-55333506
35	CEBPB	chr2:55333289-55333667	K562	blood:	n/a	chr2:55333495-55333506
36	CEBPD	chr2:55333315-55333789	K562	blood:	n/a	chr2:55333496-55333507
37	CEBPD	chr2:55333255-55333641	K562	blood:	n/a	chr2:55333496-55333507
38	CTCF	chr2:55331080-55331230	GM12873	blood:	n/a	n/a
39	CTCF	chr2:55327721-55327723	K562	blood:	n/a	n/a
40	CTCF	chr2:55327640-55327790	HRE	kidney:	n/a	n/a
41	CUX1	chr2:55324661-55325145	K562	blood:	n/a	n/a
42	CUX1	chr2:55327341-55327782	K562	blood:	n/a	n/a
43	CUX1	chr2:55333261-55333588	K562	blood:	n/a	n/a
44	CUX1	chr2:55325638-55325752	K562	blood:	n/a	n/a
45	CUX1	chr2:55326218-55326555	K562	blood:	n/a	n/a
46	E2F4	chr2:55333359-55333515	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr2:55327062-55327640	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr2:55329168-55329416	MCF10A-Er-Src	breast:	n/a	n/a
49	ELK1	chr2:55327734-55327738	K562	blood:	n/a	n/a
50	EP300	chr2:55326840-55328084	Hela-S3	cervix:	n/a	chr2:55327202-55327216 chr2:55327872-55327886

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55327371-55327421	PFSK-1	brain:	n/a
2	chr2:55327371-55327421	HCF	heart:	n/a
3	chr2:55327371-55327421	HRE	kidney:	n/a
4	chr2:55327371-55327421	AG09319	gingival:	n/a
5	chr2:55327371-55327421	ProgFib	skin:	n/a
6	chr2:55327371-55327421	LNCaP	prostate:	n/a
7	chr2:55327371-55327421	PrEC	prostate:	n/a
8	chr2:55327371-55327421	Hepatocyte	liver:	n/a
9	chr2:55327371-55327421	GM12891	blood:	n/a
10	chr2:55327371-55327421	HAEpiC	amniotic membrane:	n/a
11	chr2:55327371-55327421	SAEC	small airway:	n/a
12	chr2:55327371-55327421	BJ	skin:	n/a
13	chr2:55327371-55327421	AG10803	skin:	n/a
14	chr2:55327371-55327421	H1-hESC	embryonic stem cell:	embryo
15	chr2:55327371-55327421	HCT-116	colon:	n/a
16	chr2:55327371-55327421	Caco-2	colon:	n/a
17	chr2:55327371-55327421	BE2_C	brain:	n/a
18	chr2:55327371-55327421	NB4	blood:	n/a
19	chr2:55327371-55327421	U87	brain:	n/a
20	chr2:55327371-55327421	HUVEC	blood vessel:	n/a
21	chr2:55327371-55327421	HCM	heart:	n/a
22	chr2:55327371-55327421	Hela-S3	cervix:	n/a
23	chr2:55327371-55327421	ECC-1	luminal epithelium:	n/a
24	chr2:55327371-55327421	HepG2	liver:	n/a
25	chr2:55327371-55327421	HL-60	blood:	n/a
26	chr2:55327371-55327421	HIPEpiC	eye:	n/a
27	chr2:55327371-55327421	PANC-1	pancreas:	n/a
28	chr2:55327371-55327421	GM19239	blood:	n/a
29	chr2:55327371-55327421	AG09309	skin:	n/a
30	chr2:55327371-55327421	ovcar-3	ovarian:	n/a
31	chr2:55327371-55327421	CMK	blood:	n/a
32	chr2:55327371-55327421	NHDF-neo	bronchial:	n/a
33	chr2:55327371-55327421	IMR90	lung:	fetal
34	chr2:55327371-55327421	HCPEpiC	choroid plexus:	n/a
35	chr2:55327371-55327421	GM06990	blood:	n/a
36	chr2:55327371-55327421	RPTEC	kidney:	n/a
37	chr2:55327371-55327421	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:55327371-55327421	MCF10A-Er-Src	breast:	n/a
39	chr2:55327371-55327421	MCF-7	breast:	n/a
40	chr2:55327371-55327421	T-47D	breast:	n/a
41	chr2:55327371-55327421	GM12878	blood:	n/a
42	chr2:55327371-55327421	AoSMC	blood vessel:	n/a
43	chr2:55327371-55327421	A549	lung:	n/a
44	chr2:55327371-55327421	GM12892	blood:	n/a
45	chr2:55327371-55327421	NT2-D1	testis:	n/a
46	chr2:55327371-55327421	NH-A	brain:	n/a
47	chr2:55327371-55327421	Jurkat	blood:	n/a
48	chr2:55327371-55327421	NHBE	bronchial:	n/a
49	chr2:55327371-55327421	HMEC	breast:	n/a
50	chr2:55327371-55327421	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:55312676..55314647-chr2:55325733..55328474,2	K562	blood:
2	chr2:55331372..55335609-chr2:55337059..55340698,6	K562	blood:
3	chr2:55276735..55279463-chr2:55327258..55330571,3	K562	blood:
4	chr2:55323307..55326609-chr2:55326695..55329491,3	K562	blood:
5	chr2:55322759..55325369-chr2:55329915..55332847,3	MCF-7	breast:
6	chr2:55274277..55275806-chr2:55323435..55326407,2	K562	blood:
7	chr2:55278300..55281080-chr2:55325086..55327233,3	K562	blood:
8	chr2:55332689..55335529-chr2:55338275..55340328,2	MCF-7	breast:
9	chr2:55287997..55290069-chr2:55324008..55326423,2	K562	blood:
10	chr2:55323589..55325752-chr2:55333096..55335881,2	MCF-7	breast:
11	chr2:55323175..55325737-chr2:55325839..55328414,2	MCF-7	breast:
12	chr2:55323175..55325737-chr2:55325839..55328414,2	MCF-7	breast:
13	chr2:55275100..55278867-chr2:55332257..55335062,4	K562	blood:
14	chr2:55322759..55325369-chr2:55329915..55332847,3	MCF-7	breast:
15	chr2:55325626..55328074-chr2:55345685..55348277,2	K562	blood:
16	chr2:55326388..55330538-chr2:55335061..55337994,3	K562	blood:
17	chr2:55327279..55331330-chr2:55337574..55341174,5	K562	blood:
18	chr2:55276927..55278545-chr2:55322721..55325631,2	K562	blood:
19	chr2:55326463..55328844-chr2:55338475..55342420,4	K562	blood:
20	chr2:55323307..55326609-chr2:55326695..55329491,3	K562	blood:
21	chr2:55317970..55321435-chr2:55328777..55332297,3	K562	blood:

Variant related genes	Relation type
ENSG00000266376	TF binding region
ENSG00000266376	CpG island
ENSG00000115310	chromatin interactions
ENSG00000266376	chromatin interactions

Extended variants
information (count: 414 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4672016	chr2:55324960-55324961	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557928588	chr2:55324961-55324962	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs79800828	chr2:55325001-55325002	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533944670	chr2:55325044-55325045	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs145839248	chr2:55325121-55325122	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs573811512	chr2:55325133-55325134	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs542909818	chr2:55325189-55325190	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs372691457	chr2:55325245-55325246	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs148558013	chr2:55325257-55325258	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs575275574	chr2:55325297-55325298	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs544284786	chr2:55325338-55325339	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs564268709	chr2:55325339-55325340	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528006452	chr2:55325362-55325363	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs4671239	chr2:55325372-55325373	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs2920875	chr2:55325385-55325386	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs567390574	chr2:55325414-55325415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs536260552	chr2:55325520-55325521	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs373965234	chr2:55325536-55325537	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs188310783	chr2:55325544-55325545	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs191234100	chr2:55325560-55325561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs549699526	chr2:55325580-55325581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs185865077	chr2:55325616-55325617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs142132704	chr2:55325619-55325620	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs190343717	chr2:55325637-55325638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7595814	chr2:55325639-55325640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs570031952	chr2:55325677-55325678	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs533881810	chr2:55325719-55325720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553638179	chr2:55325741-55325742	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146688770	chr2:55325749-55325750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115143863	chr2:55325751-55325752	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs556455841	chr2:55325758-55325759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575212635	chr2:55325839-55325840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs182114437	chr2:55325855-55325856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559166737	chr2:55325863-55325864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572557038	chr2:55325868-55325869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7596128	chr2:55325911-55325912	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs2920876	chr2:55325912-55325913	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs186656081	chr2:55325926-55325927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2920877	chr2:55325927-55325928	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs529536269	chr2:55325942-55325943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190127454	chr2:55325943-55325944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181233653	chr2:55325945-55325946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532067624	chr2:55325947-55325948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551351173	chr2:55325999-55326000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs534095816	chr2:55326017-55326018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571274470	chr2:55326033-55326034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533864703	chr2:55326045-55326046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs573814848	chr2:55326109-55326110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2968810	chr2:55326133-55326134	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs567327549	chr2:55326178-55326179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55316800-55327200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr2:55318400-55329600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:55320000-55327200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr2:55321000-55326600	Weak transcription	HMEC	breast
5	chr2:55321400-55326400	Weak transcription	Primary B cells from cord blood	blood
6	chr2:55321600-55325000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr2:55321600-55327400	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr2:55321600-55339400	Weak transcription	Thymus	Thymus
9	chr2:55321800-55336400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr2:55322000-55326600	Weak transcription	Primary hematopoietic stem cells	blood
11	chr2:55322000-55326600	Weak transcription	NHEK	skin
12	chr2:55322200-55325200	Enhancers	Ovary	ovary
13	chr2:55322600-55327200	Enhancers	HUVEC	blood vessel
14	chr2:55322600-55327800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr2:55322800-55327200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr2:55322800-55327200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:55322800-55327200	Enhancers	Adipose Nuclei	Adipose
18	chr2:55323000-55325200	Enhancers	Pancreas	Pancrea
19	chr2:55323600-55325200	Enhancers	Fetal Brain Male	brain
20	chr2:55323600-55325200	Enhancers	Fetal Heart	heart
21	chr2:55323600-55325200	Enhancers	Rectal Smooth Muscle	rectum
22	chr2:55323600-55325400	Enhancers	Colon Smooth Muscle	Colon
23	chr2:55323600-55325400	Enhancers	Right Atrium	heart
24	chr2:55323600-55325400	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr2:55323600-55325400	Enhancers	Hela-S3	cervix
26	chr2:55323600-55326600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr2:55323600-55326600	Enhancers	HSMMtube	muscle
28	chr2:55323600-55326600	Enhancers	NHLF	lung
29	chr2:55323600-55326800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr2:55323600-55327200	Enhancers	Osteobl	bone
31	chr2:55323600-55328200	Enhancers	K562	blood
32	chr2:55323600-55330000	Enhancers	HSMM	muscle
33	chr2:55323800-55325000	Enhancers	Fetal Stomach	stomach
34	chr2:55323800-55325000	Enhancers	A549	lung
35	chr2:55323800-55325200	Enhancers	Brain Anterior Caudate	brain
36	chr2:55323800-55325200	Enhancers	Brain Cingulate Gyrus	brain
37	chr2:55323800-55325200	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr2:55323800-55325200	Enhancers	Fetal Muscle Leg	muscle
39	chr2:55323800-55325200	Enhancers	Gastric	stomach
40	chr2:55323800-55325200	Enhancers	Left Ventricle	heart
41	chr2:55323800-55325200	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr2:55323800-55325400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr2:55323800-55325400	Enhancers	Brain Substantia Nigra	brain
44	chr2:55323800-55325400	Enhancers	Duodenum Smooth Muscle	Duodenum
45	chr2:55323800-55325400	Enhancers	Psoas Muscle	Psoas
46	chr2:55323800-55325400	Enhancers	Stomach Mucosa	stomach
47	chr2:55323800-55327200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr2:55323800-55327200	Enhancers	Dnd41	blood
49	chr2:55323800-55327400	Enhancers	NHDF-Ad	bronchial
50	chr2:55323800-55327800	Enhancers	Brain Hippocampus Middle	brain

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