Variant report

Variant	esv3477159
Chromosome Location	chr7:26218731-26221448
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	chr7:26220280-26220634	K562	blood:	n/a	n/a
2	ATF1	chr7:26220269-26220752	K562	blood:	n/a	n/a
3	BACH1	chr7:26221098-26221334	H1-hESC	embryonic stem cell:	n/a	chr7:26221284-26221298
4	BACH1	chr7:26221177-26221372	K562	blood:	n/a	chr7:26221284-26221298
5	BCL3	chr7:26219133-26220180	A549	lung:	n/a	n/a
6	BCL3	chr7:26217644-26229718	A549	lung:	n/a	chr7:26226946-26226953 chr7:26220505-26220512 chr7:26220601-26220614
7	BCL3	chr7:26218186-26218815	A549	lung:	n/a	n/a
8	BHLHE40	chr7:26220351-26220749	K562	blood:	n/a	n/a
9	BRCA1	chr7:26219780-26220043	Hela-S3	cervix:	n/a	n/a
10	CBX3	chr7:26220287-26220741	K562	blood:	n/a	n/a
11	CCNT2	chr7:26219699-26219943	K562	blood:	n/a	n/a
12	CCNT2	chr7:26220342-26220712	K562	blood:	n/a	n/a
13	CEBPB	chr7:26220315-26220738	K562	blood:	n/a	n/a
14	CEBPB	chr7:26220402-26220682	K562	blood:	n/a	n/a
15	CEBPD	chr7:26220285-26220811	K562	blood:	n/a	n/a
16	CEBPD	chr7:26220289-26220788	K562	blood:	n/a	n/a
17	CEBPZ	chr7:26219373-26219781	HepG2	liver:	n/a	n/a
18	CHD2	chr7:26217936-26218818	HepG2	liver:	n/a	n/a
19	CHD2	chr7:26219404-26219658	HepG2	liver:	n/a	n/a
20	CHD2	chr7:26219475-26219753	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr7:26220400-26220707	K562	blood:	n/a	n/a
22	CREB1	chr7:26220168-26220824	K562	blood:	n/a	n/a
23	CREB1	chr7:26220385-26220748	K562	blood:	n/a	n/a
24	CTCF	chr7:26220640-26220790	GM12875	blood:	n/a	n/a
25	CTCF	chr7:26220588-26220670	K562	blood:	n/a	n/a
26	CUX1	chr7:26220264-26220675	K562	blood:	n/a	n/a
27	E2F4	chr7:26220932-26221128	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr7:26220054-26220578	MCF10A-Er-Src	breast:	n/a	n/a
29	ELF1	chr7:26220428-26220726	K562	blood:	n/a	n/a
30	ELF1	chr7:26220326-26220721	A549	lung:	n/a	n/a
31	EP300	chr7:26220056-26220737	K562	blood:	n/a	n/a
32	EP300	chr7:26220358-26220585	K562	blood:	n/a	n/a
33	FOS	chr7:26221008-26221049	MCF10A-Er-Src	breast:	n/a	n/a
34	FOSL2	chr7:26220454-26220878	HepG2	liver:	n/a	n/a
35	FOSL2	chr7:26219270-26220070	HepG2	liver:	n/a	chr7:26220030-26220042
36	FOXA2	chr7:26220472-26220697	HepG2	liver:	n/a	n/a
37	GATA1	chr7:26220210-26220924	K562	blood:	n/a	chr7:26220500-26220516 chr7:26220500-26220516
38	GATA1	chr7:26219638-26221295	PBDE	blood:	n/a	chr7:26220500-26220516 chr7:26220500-26220516
39	GATA2	chr7:26220247-26220761	K562	blood:	n/a	chr7:26220500-26220516 chr7:26220500-26220516
40	HCFC1	chr7:26220420-26220665	K562	blood:	n/a	n/a
41	IRF1	chr7:26221342-26221344	K562	blood:	n/a	n/a
42	IRF1	chr7:26220245-26220674	K562	blood:	n/a	n/a
43	JUND	chr7:26219454-26220569	SK-N-SH	brain:	n/a	chr7:26220030-26220042
44	JUND	chr7:26220607-26220608	HepG2	liver:	n/a	n/a
45	JUND	chr7:26220252-26220764	K562	blood:	n/a	n/a
46	JUND	chr7:26219725-26220042	A549	lung:	n/a	chr7:26220030-26220042
47	MAFF	chr7:26221107-26221813	HepG2	liver:	n/a	chr7:26221285-26221303
48	MAFF	chr7:26221108-26221760	K562	blood:	n/a	chr7:26221285-26221303
49	MAFK	chr7:26221089-26221812	Hela-S3	cervix:	n/a	chr7:26221290-26221301 chr7:26221281-26221301 chr7:26221288-26221297 chr7:26221286-26221301 chr7:26221245-26221256
50	MAFK	chr7:26221123-26221464	H1-hESC	embryonic stem cell:	n/a	chr7:26221290-26221301 chr7:26221281-26221301 chr7:26221288-26221297 chr7:26221286-26221301 chr7:26221245-26221256

No.	Distal block	Cell Line	Cell type
1	chr7:26187762..26202698-chr7:26218693..26233402,42	K562	blood:
2	chr7:26217885..26219634-chr7:26219672..26221889,2	MCF-7	breast:
3	chr7:26218241..26220346-chr7:26316988..26319565,2	K562	blood:
4	chr7:26209588..26214635-chr7:26216506..26225474,18	K562	blood:
5	chr7:26205835..26207422-chr7:26220316..26222090,2	K562	blood:
6	chr7:26212776..26215168-chr7:26216411..26218758,2	MCF-7	breast:
7	chr7:26217885..26219634-chr7:26219672..26221889,2	MCF-7	breast:
8	chr7:26121331..26123679-chr7:26220972..26223224,2	MCF-7	breast:
9	chr7:26129244..26131736-chr7:26219781..26221965,2	K562	blood:
10	chr7:26209015..26211740-chr7:26220518..26222809,3	MCF-7	breast:
11	chr7:26129567..26132077-chr7:26220760..26223665,4	MCF-7	breast:
12	chr7:26220379..26222750-chr7:26324403..26326556,2	MCF-7	breast:
13	chr7:26214375..26216195-chr7:26219360..26221662,2	MCF-7	breast:
14	chr7:26221250..26223290-chr7:26281932..26283761,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000273237	TF binding region
NFE2L3	TF binding region
ENSG00000050344	chromatin interactions
ENSG00000273237	chromatin interactions

Extended variants
information (count: 113 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11272499	chr7:26218769-26218770	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs375427729	chr7:26218772-26218773	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs555423702	chr7:26218800-26218801	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs188313000	chr7:26218820-26218821	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs566962586	chr7:26218826-26218827	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs369956392	chr7:26218854-26218855	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs563906058	chr7:26218863-26218864	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs111353522	chr7:26218872-26218873	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs184247615	chr7:26218886-26218887	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs559939971	chr7:26218946-26218947	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs528873608	chr7:26218979-26218980	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549135754	chr7:26219015-26219016	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs568994003	chr7:26219053-26219054	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs201128349	chr7:26219120-26219121	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs374640249	chr7:26219163-26219164	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs539184898	chr7:26219192-26219193	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs531398790	chr7:26219240-26219241	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs571136223	chr7:26219259-26219260	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs73281517	chr7:26219274-26219275	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs539788350	chr7:26219275-26219276	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs144020425	chr7:26219277-26219278	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs566784536	chr7:26219287-26219288	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs535433543	chr7:26219299-26219300	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs375755738	chr7:26219303-26219304	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs33998608	chr7:26219311-26219312	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs398004099	chr7:26219312-26219313	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs555315483	chr7:26219314-26219315	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs188785508	chr7:26219319-26219320	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs574516996	chr7:26219327-26219328	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs181201787	chr7:26219383-26219384	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs369078204	chr7:26219387-26219388	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs544262300	chr7:26219416-26219417	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs557535430	chr7:26219440-26219441	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs535281445	chr7:26219445-26219446	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs146607892	chr7:26219465-26219466	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs560381344	chr7:26219466-26219467	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs528911026	chr7:26219476-26219477	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs542659311	chr7:26219515-26219516	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs11974650	chr7:26219559-26219560	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs531437210	chr7:26219562-26219563	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs6965743	chr7:26219615-26219616	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs574669524	chr7:26219627-26219628	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs75892499	chr7:26219661-26219662	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs11971002	chr7:26219687-26219688	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs559753928	chr7:26219698-26219699	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs547004367	chr7:26219739-26219740	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs187130025	chr7:26219753-26219754	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs535717067	chr7:26219766-26219767	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs11977822	chr7:26219777-26219778	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs537996635	chr7:26219778-26219779	Weak transcription Enhancers Strong transcription Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Cancer	21183584	CNVD
abnormal development	18461090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Breast cancer	18852474	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26196600-26222000	Weak transcription	Left Ventricle	heart
2	chr7:26198800-26222000	Weak transcription	Spleen	Spleen
3	chr7:26199400-26222000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:26199400-26230200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:26200000-26227200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:26206600-26219600	Weak transcription	K562	blood
7	chr7:26206600-26220600	Weak transcription	Right Atrium	heart
8	chr7:26206600-26227600	Weak transcription	Esophagus	oesophagus
9	chr7:26206800-26226000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:26207000-26220200	Weak transcription	Right Ventricle	heart
11	chr7:26207000-26226800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:26207000-26227400	Weak transcription	Gastric	stomach
13	chr7:26207000-26227600	Weak transcription	Primary hematopoietic stem cells	blood
14	chr7:26207000-26228000	Weak transcription	Primary monocytes fromperipheralblood	blood
15	chr7:26207200-26224600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr7:26207200-26227000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr7:26207200-26228200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr7:26207400-26219800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr7:26207400-26221800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr7:26207400-26224800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr7:26207400-26227800	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr7:26207600-26227000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr7:26207600-26227400	Weak transcription	Primary T cells from cord blood	blood
24	chr7:26207800-26223200	Weak transcription	Fetal Thymus	thymus
25	chr7:26208000-26226000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr7:26208000-26227400	Weak transcription	Brain Substantia Nigra	brain
27	chr7:26208600-26222400	Weak transcription	Lung	lung
28	chr7:26208800-26227600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr7:26209000-26222000	Weak transcription	Placenta	Placenta
30	chr7:26209200-26226000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:26209600-26219600	Weak transcription	Brain Hippocampus Middle	brain
32	chr7:26210200-26227000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr7:26210200-26227000	Weak transcription	Small Intestine	intestine
34	chr7:26210400-26222000	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr7:26210800-26223800	Weak transcription	GM12878-XiMat	blood
36	chr7:26210800-26224800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr7:26210800-26226000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:26211000-26220000	Weak transcription	A549	lung
39	chr7:26211000-26226000	Weak transcription	Thymus	Thymus
40	chr7:26211200-26219200	Weak transcription	Primary B cells from peripheral blood	blood
41	chr7:26211400-26222000	Weak transcription	Skeletal Muscle Female	skeletal muscle
42	chr7:26211600-26224600	Weak transcription	Psoas Muscle	Psoas
43	chr7:26212200-26227400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr7:26213800-26223800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr7:26213800-26228400	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr7:26214400-26228200	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr7:26215600-26228800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr7:26217200-26219400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr7:26217200-26228000	Weak transcription	Fetal Brain Male	brain
50	chr7:26217400-26219000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood

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