Variant report

Variant	nsv429771
Chromosome Location	chr7:70188375-70294296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1774)
CpG islands
(count:1773)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1774 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:70217669-70218032	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:70246580-70246894	HepG2	liver:	n/a	n/a
3	ATF2	chr7:70226556-70227409	GM12878	blood:	n/a	n/a
4	ATF2	chr7:70228852-70229895	GM12878	blood:	n/a	n/a
5	ATF2	chr7:70228752-70229755	GM12878	blood:	n/a	n/a
6	ATF2	chr7:70191802-70192414	GM12878	blood:	n/a	n/a
7	ATF2	chr7:70191740-70192428	GM12878	blood:	n/a	n/a
8	ATF2	chr7:70194222-70194708	GM12878	blood:	n/a	n/a
9	ATF2	chr7:70264860-70265281	GM12878	blood:	n/a	n/a
10	ATF2	chr7:70193730-70194787	GM12878	blood:	n/a	n/a
11	ATF2	chr7:70258518-70258992	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr7:70226427-70227404	GM12878	blood:	n/a	n/a
13	ATF2	chr7:70294118-70294578	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:70294211-70294569	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr7:70277553-70277731	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr7:70195849-70196064	GM12878	blood:	n/a	chr7:70195970-70195981
17	BATF	chr7:70294231-70294607	GM12878	blood:	n/a	n/a
18	BATF	chr7:70264853-70265265	GM12878	blood:	n/a	n/a
19	BATF	chr7:70226797-70227424	GM12878	blood:	n/a	chr7:70227126-70227136 chr7:70227125-70227136
20	BATF	chr7:70192129-70192402	GM12878	blood:	n/a	n/a
21	BATF	chr7:70229142-70229667	GM12878	blood:	n/a	n/a
22	BATF	chr7:70264945-70265249	GM12878	blood:	n/a	n/a
23	BATF	chr7:70226780-70227411	GM12878	blood:	n/a	chr7:70227126-70227136 chr7:70227125-70227136
24	BATF	chr7:70229244-70229678	GM12878	blood:	n/a	n/a
25	BATF	chr7:70191842-70192464	GM12878	blood:	n/a	n/a
26	BATF	chr7:70241512-70241829	GM12878	blood:	n/a	n/a
27	BATF	chr7:70241538-70241996	GM12878	blood:	n/a	n/a
28	BATF	chr7:70195779-70196118	GM12878	blood:	n/a	chr7:70195970-70195981
29	BATF	chr7:70294291-70294547	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:70193763-70194026	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr7:70229020-70229654	GM12878	blood:	n/a	chr7:70229064-70229072
32	BCL11A	chr7:70226689-70227260	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
33	BCL11A	chr7:70194287-70194666	GM12878	blood:	n/a	n/a
34	BCL11A	chr7:70264860-70265214	GM12878	blood:	n/a	n/a
35	BCL11A	chr7:70229154-70229733	GM12878	blood:	n/a	n/a
36	BCL11A	chr7:70226751-70227076	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
37	BCL11A	chr7:70191921-70192224	GM12878	blood:	n/a	chr7:70191981-70191990
38	BCL11A	chr7:70264916-70265214	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:70192090-70192386	GM12878	blood:	n/a	n/a
40	BCL11A	chr7:70241509-70241830	GM12878	blood:	n/a	n/a
41	BCL3	chr7:70226630-70227241	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
42	BCL3	chr7:70191976-70192347	GM12878	blood:	n/a	chr7:70191981-70191990
43	BCL3	chr7:70228999-70229661	GM12878	blood:	n/a	chr7:70229064-70229072
44	BCL3	chr7:70194233-70194787	GM12878	blood:	n/a	n/a
45	BCL3	chr7:70228934-70229775	GM12878	blood:	n/a	chr7:70229064-70229072
46	BCL3	chr7:70191822-70192406	GM12878	blood:	n/a	chr7:70191981-70191990
47	BCLAF1	chr7:70228896-70229709	GM12878	blood:	n/a	chr7:70229064-70229072
48	BCLAF1	chr7:70226582-70227292	GM12878	blood:	n/a	chr7:70226852-70226861 chr7:70226921-70226930
49	BCLAF1	chr7:70194201-70194815	GM12878	blood:	n/a	n/a
50	BCLAF1	chr7:70228851-70229760	GM12878	blood:	n/a	chr7:70228879-70228888 chr7:70229064-70229072

(count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70200532-70200582	HPAEpiC	pulmonary alveolar:	n/a
2	chr7:70198123-70198173	NHDF-neo	bronchial:	n/a
3	chr7:70258726-70258776	NH-A	brain:	n/a
4	chr7:70252571-70252621	IMR90	lung:	fetal
5	chr7:70200532-70200582	HPAEpiC	pulmonary alveolar:	n/a
6	chr7:70198123-70198173	NHDF-neo	bronchial:	n/a
7	chr7:70258726-70258776	NH-A	brain:	n/a
8	chr7:70252571-70252621	IMR90	lung:	fetal
9	chr7:70252953-70253003	RPTEC	kidney:	n/a
10	chr7:70294264-70294314	HNPCEpiC	eye:	n/a
11	chr7:70231304-70231354	HNPCEpiC	eye:	n/a
12	chr7:70258649-70258699	AoSMC	blood vessel:	n/a
13	chr7:70254810-70254860	IMR90	lung:	fetal
14	chr7:70238460-70238510	HNPCEpiC	eye:	n/a
15	chr7:70252571-70252621	AoSMC	blood vessel:	n/a
16	chr7:70252953-70253003	HUVEC	blood vessel:	n/a
17	chr7:70257926-70257976	AoSMC	blood vessel:	n/a
18	chr7:70252571-70252621	AG04449	skin:	fetal
19	chr7:70209588-70209638	AG09309	skin:	n/a
20	chr7:70216208-70216258	Jurkat	blood:	n/a
21	chr7:70231304-70231354	HAEpiC	amniotic membrane:	n/a
22	chr7:70216208-70216258	IMR90	lung:	fetal
23	chr7:70256003-70256053	HIPEpiC	eye:	n/a
24	chr7:70255804-70255854	ECC-1	luminal epithelium:	n/a
25	chr7:70258726-70258776	PrEC	prostate:	n/a
26	chr7:70198123-70198173	HCM	heart:	n/a
27	chr7:70209588-70209638	HEEpiC	esophagus:	n/a
28	chr7:70198123-70198173	PFSK-1	brain:	n/a
29	chr7:70257960-70258010	GM12891	blood:	n/a
30	chr7:70255210-70255260	H1-hESC	embryonic stem cell:	embryo
31	chr7:70258753-70258803	ECC-1	luminal epithelium:	n/a
32	chr7:70252953-70253003	AG04449	skin:	fetal
33	chr7:70257960-70258010	MCF-7	breast:	n/a
34	chr7:70294264-70294314	NT2-D1	testis:	n/a
35	chr7:70252662-70252712	SK-N-MC	brain:	n/a
36	chr7:70198123-70198173	AoSMC	blood vessel:	n/a
37	chr7:70254810-70254860	AoSMC	blood vessel:	n/a
38	chr7:70252571-70252621	PrEC	prostate:	n/a
39	chr7:70258753-70258803	HPAEpiC	pulmonary alveolar:	n/a
40	chr7:70255985-70256035	AG10803	skin:	n/a
41	chr7:70216208-70216258	HUVEC	blood vessel:	n/a
42	chr7:70194602-70194652	K562	blood:	n/a
43	chr7:70255332-70255382	RPTEC	kidney:	n/a
44	chr7:70255210-70255260	LNCaP	prostate:	n/a
45	chr7:70209588-70209638	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:70209588-70209638	H1-hESC	embryonic stem cell:	embryo
47	chr7:70255416-70255466	IMR90	lung:	fetal
48	chr7:70231304-70231354	K562	blood:	n/a
49	chr7:70252335-70252385	HCPEpiC	choroid plexus:	n/a
50	chr7:70238460-70238510	LNCaP	prostate:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:70294183..70294797-chr7:71197949..71198693,3	MCF-7	breast:
2	chr7:70212124..70215899-chr7:70217656..70219621,3	K562	blood:
3	chr7:70293870..70294792-chr7:71200529..71201300,6	MCF-7	breast:
4	chr7:70225764..70228069-chr7:70229252..70232083,2	K562	blood:
5	chr7:70294046..70294810-chr7:70321629..70322145,2	MCF-7	breast:
6	chr7:70157661..70160081-chr7:70223262..70226171,2	MCF-7	breast:
7	chr7:70243263..70245358-chr7:70247619..70249234,2	K562	blood:
8	chr7:70174321..70176691-chr7:70186792..70188789,2	MCF-7	breast:
9	chr7:70222449..70225424-chr7:70225544..70227809,2	MCF-7	breast:
10	chr7:70293845..70294790-chr7:71197836..71198902,6	K562	blood:
11	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
12	chr6:39278169..39279933-chr7:70204739..70207119,2	MCF-7	breast:
13	chr7:70182197..70184832-chr7:70191535..70193515,2	MCF-7	breast:
14	chr7:70294117..70295302-chr7:71197788..71199575,6	MCF-7	breast:
15	chr7:70184183..70185798-chr7:70197589..70200298,2	MCF-7	breast:
16	chr7:70266587..70269315-chr7:70270383..70272758,2	K562	blood:
17	chr7:70212124..70215899-chr7:70217656..70219621,3	K562	blood:
18	chr7:70243263..70245358-chr7:70247619..70249234,2	K562	blood:
19	chr7:70222449..70225424-chr7:70225544..70227809,2	MCF-7	breast:
20	chr7:70244569..70247076-chr7:70250539..70253250,4	K562	blood:
21	chr7:69997760..70000305-chr7:70252452..70255075,2	MCF-7	breast:
22	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:
23	chr7:70255328..70258832-chr7:70260648..70264116,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WBSCR17-2	chr7:70233010-70233054	NONHSAT121338
2	lnc-WBSCR17-2	chr7:70236202-70236501	NONHSAT121338

No data

Variant related genes	Relation type
AUTS2	TF binding region
AUTS2	CpG island
ENSG00000158321	chromatin interactions

Extended variants
information (count: 4294 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4294 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10265371	chr7:70188375-70188376	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541404957	chr7:70188421-70188422	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530511146	chr7:70188426-70188427	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552295579	chr7:70188434-70188435	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76948375	chr7:70188674-70188675	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570304335	chr7:70188676-70188677	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12698921	chr7:70188690-70188691	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568851043	chr7:70188715-70188716	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113511499	chr7:70188763-70188764	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371644576	chr7:70188863-70188864	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185991027	chr7:70188971-70188972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556131547	chr7:70188974-70188975	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535778014	chr7:70188976-70188977	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190988512	chr7:70189003-70189004	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182697218	chr7:70189027-70189028	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185370679	chr7:70189036-70189037	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376265944	chr7:70189043-70189044	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs111461109	chr7:70189130-70189131	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs55741329	chr7:70189222-70189223	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs12666137	chr7:70189223-70189224	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs555368441	chr7:70189236-70189237	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542751592	chr7:70189267-70189268	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs28536677	chr7:70189301-70189302	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs9638591	chr7:70189312-70189313	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs541325759	chr7:70189338-70189339	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562739669	chr7:70189363-70189364	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539693824	chr7:70189368-70189369	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561076596	chr7:70189428-70189429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373353092	chr7:70189429-70189430	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs71077675	chr7:70189449-70189450	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9638592	chr7:70189462-70189463	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs551540915	chr7:70189480-70189481	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10229143	chr7:70189488-70189489	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs528045519	chr7:70189492-70189493	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs28432049	chr7:70189577-70189578	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs561701528	chr7:70189588-70189589	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10239618	chr7:70189633-70189634	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs137954358	chr7:70189662-70189663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149445145	chr7:70189667-70189668	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs4717545	chr7:70189682-70189683	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs4718986	chr7:70189684-70189685	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs565803138	chr7:70189720-70189721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534065966	chr7:70189722-70189723	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555329843	chr7:70189756-70189757	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573741248	chr7:70189759-70189760	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538099420	chr7:70189767-70189768	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76342480	chr7:70189794-70189795	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs578084030	chr7:70189822-70189823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545604000	chr7:70189855-70189856	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142224157	chr7:70189890-70189891	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Dyslexia	22102821	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2517 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70161800-70191200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr7:70162200-70201600	Weak transcription	Primary B cells from cord blood	blood
3	chr7:70176200-70201600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr7:70176400-70189800	Weak transcription	Fetal Intestine Large	intestine
5	chr7:70176400-70192000	Weak transcription	HMEC	breast
6	chr7:70176400-70193800	Weak transcription	NH-A	brain
7	chr7:70179800-70190200	Weak transcription	Brain Angular Gyrus	brain
8	chr7:70179800-70192000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:70179800-70201600	Weak transcription	Rectal Smooth Muscle	rectum
10	chr7:70180000-70192200	Weak transcription	Aorta	Aorta
11	chr7:70180200-70190400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:70180200-70193800	Weak transcription	Fetal Intestine Small	intestine
13	chr7:70182600-70190400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr7:70182600-70194000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr7:70183000-70194000	Weak transcription	Fetal Stomach	stomach
16	chr7:70183000-70201600	Weak transcription	Fetal Muscle Leg	muscle
17	chr7:70183200-70188400	Weak transcription	Lung	lung
18	chr7:70183200-70190000	Weak transcription	Brain Substantia Nigra	brain
19	chr7:70183200-70190200	Weak transcription	Esophagus	oesophagus
20	chr7:70183200-70191800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr7:70183200-70193800	Weak transcription	Thymus	Thymus
22	chr7:70183200-70194000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:70183200-70200200	Weak transcription	Ovary	ovary
24	chr7:70183200-70201800	Weak transcription	Pancreas	Pancrea
25	chr7:70183400-70193800	Weak transcription	Fetal Muscle Trunk	muscle
26	chr7:70183400-70194000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:70183400-70195400	Weak transcription	HSMM	muscle
28	chr7:70183600-70197600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:70184200-70190200	Weak transcription	Gastric	stomach
30	chr7:70184400-70189600	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr7:70184400-70195200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr7:70184600-70193000	Enhancers	Liver	Liver
33	chr7:70185600-70190200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:70185800-70189600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:70185800-70189800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr7:70185800-70190200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:70185800-70190200	Weak transcription	Fetal Lung	lung
38	chr7:70185800-70191600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr7:70185800-70191600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr7:70185800-70192000	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr7:70185800-70197600	Weak transcription	HSMMtube	muscle
42	chr7:70186000-70189200	Enhancers	GM12878-XiMat	blood
43	chr7:70186000-70189800	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr7:70186000-70191400	Weak transcription	Fetal Heart	heart
45	chr7:70186000-70191600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr7:70186000-70195400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr7:70186200-70190000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:70186200-70190200	Weak transcription	Psoas Muscle	Psoas
49	chr7:70186400-70190400	Weak transcription	Fetal Brain Male	brain
50	chr7:70186400-70198200	Weak transcription	Dnd41	blood

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