Variant report

Variant	nsv1018125
Chromosome Location	chr7:26745074-26789814
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:131)
CpG islands
(count:62)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:131 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:26778811-26778827	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr7:26745210-26745535	A549	lung:	n/a	n/a
3	E2F4	chr7:26786811-26786896	MCF10A-Er-Src	breast:	n/a	n/a
4	E2F4	chr7:26778194-26778264	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F4	chr7:26781732-26781855	MCF10A-Er-Src	breast:	n/a	n/a
6	EP300	chr7:26779877-26780324	T-47D	breast:	n/a	n/a
7	EP300	chr7:26745148-26745487	SK-N-SH_RA	brain:	n/a	n/a
8	EP300	chr7:26745229-26745578	SK-N-SH_RA	brain:	n/a	n/a
9	EP300	chr7:26745116-26745723	SK-N-SH	brain:	n/a	n/a
10	EP300	chr7:26753555-26754077	T-47D	breast:	n/a	n/a
11	ESR1	chr7:26774953-26775402	T-47D	breast:	n/a	n/a
12	ESR1	chr7:26775041-26775349	T-47D	breast:	n/a	n/a
13	ESR1	chr7:26775049-26775335	T-47D	breast:	n/a	n/a
14	FOS	chr7:26745200-26745611	MCF10A-Er-Src	breast:	n/a	chr7:26745267-26745279
15	FOS	chr7:26765863-26765868	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr7:26745233-26745622	MCF10A-Er-Src	breast:	n/a	chr7:26745267-26745279
17	FOS	chr7:26745236-26745594	MCF10A-Er-Src	breast:	n/a	chr7:26745267-26745279
18	FOS	chr7:26745195-26745686	MCF10A-Er-Src	breast:	n/a	chr7:26745673-26745685 chr7:26745267-26745279
19	FOS	chr7:26764948-26764962	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr7:26745182-26745654	HUVEC	blood vessel:	n/a	chr7:26745267-26745279
21	FOSL2	chr7:26745122-26745704	SK-N-SH	brain:	n/a	chr7:26745673-26745685 chr7:26745267-26745279
22	FOSL2	chr7:26745094-26745678	A549	lung:	n/a	chr7:26745267-26745279
23	FOSL2	chr7:26745218-26745609	A549	lung:	n/a	chr7:26745267-26745279
24	FOXA1	chr7:26761558-26761774	T-47D	breast:	n/a	chr7:26761664-26761679
25	FOXA1	chr7:26779869-26780292	T-47D	breast:	n/a	chr7:26780171-26780183
26	FOXA1	chr7:26774924-26775343	T-47D	breast:	n/a	n/a
27	FOXA1	chr7:26775032-26775291	T-47D	breast:	n/a	n/a
28	FOXA1	chr7:26785898-26786198	HepG2	liver:	n/a	chr7:26786037-26786049
29	FOXA1	chr7:26753563-26753937	T-47D	breast:	n/a	n/a
30	FOXA1	chr7:26779947-26780105	T-47D	breast:	n/a	n/a
31	FOXA1	chr7:26745284-26745483	T-47D	breast:	n/a	n/a
32	FOXA1	chr7:26785860-26786157	T-47D	breast:	n/a	chr7:26786037-26786049
33	FOXA1	chr7:26753617-26753942	T-47D	breast:	n/a	n/a
34	FOXA2	chr7:26745080-26745688	A549	lung:	n/a	n/a
35	FOXA2	chr7:26745283-26745460	HepG2	liver:	n/a	n/a
36	FOXA2	chr7:26785851-26786134	A549	lung:	n/a	chr7:26786037-26786049
37	FOXA2	chr7:26745200-26745657	A549	lung:	n/a	n/a
38	GATA2	chr7:26745146-26745568	HUVEC	blood vessel:	n/a	n/a
39	GATA3	chr7:26789530-26789785	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr7:26753564-26753904	T-47D	breast:	n/a	n/a
41	GATA3	chr7:26745029-26745678	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr7:26745100-26745820	A549	lung:	n/a	n/a
43	GATA3	chr7:26782795-26782939	SH-SY5Y	brain:	n/a	n/a
44	GATA3	chr7:26745110-26745707	SK-N-SH	brain:	n/a	n/a
45	GATA3	chr7:26779905-26780245	T-47D	breast:	n/a	chr7:26780154-26780161
46	GATA3	chr7:26753574-26753947	T-47D	breast:	n/a	n/a
47	JUN	chr7:26745101-26745285	K562	blood:	n/a	chr7:26745267-26745279
48	JUN	chr7:26745199-26745611	HUVEC	blood vessel:	n/a	chr7:26745267-26745279
49	JUN	chr7:26763709-26764048	K562	blood:	n/a	n/a
50	JUN	chr7:26764780-26764975	K562	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:26775731-26775781	RPTEC	kidney:	n/a
2	chr7:26775731-26775781	RPTEC	kidney:	n/a
3	chr7:26775731-26775781	HepG2	liver:	n/a
4	chr7:26775731-26775781	NH-A	brain:	n/a
5	chr7:26775731-26775781	Jurkat	blood:	n/a
6	chr7:26775731-26775781	HUVEC	blood vessel:	n/a
7	chr7:26775731-26775781	GM12892	blood:	n/a
8	chr7:26775731-26775781	GM19239	blood:	n/a
9	chr7:26775731-26775781	MCF10A-Er-Src	breast:	n/a
10	chr7:26775731-26775781	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:26775731-26775781	K562	blood:	n/a
12	chr7:26775731-26775781	MCF-7	breast:	n/a
13	chr7:26775731-26775781	AG04449	skin:	fetal
14	chr7:26775731-26775781	Hela-S3	cervix:	n/a
15	chr7:26775731-26775781	NT2-D1	testis:	n/a
16	chr7:26775731-26775781	HEEpiC	esophagus:	n/a
17	chr7:26775731-26775781	U87	brain:	n/a
18	chr7:26775731-26775781	A549	lung:	n/a
19	chr7:26775731-26775781	HRPEpiC	eye:	n/a
20	chr7:26775731-26775781	HCPEpiC	choroid plexus:	n/a
21	chr7:26775731-26775781	LNCaP	prostate:	n/a
22	chr7:26775731-26775781	IMR90	lung:	fetal
23	chr7:26775731-26775781	NB4	blood:	n/a
24	chr7:26775731-26775781	HRE	kidney:	n/a
25	chr7:26775731-26775781	PANC-1	pancreas:	n/a
26	chr7:26775731-26775781	Caco-2	colon:	n/a
27	chr7:26775731-26775781	HL-60	blood:	n/a
28	chr7:26775731-26775781	GM12891	blood:	n/a
29	chr7:26775731-26775781	HCM	heart:	n/a
30	chr7:26775731-26775781	AG09319	gingival:	n/a
31	chr7:26775731-26775781	CMK	blood:	n/a
32	chr7:26775731-26775781	NHBE	bronchial:	n/a
33	chr7:26775731-26775781	Hepatocyte	liver:	n/a
34	chr7:26775731-26775781	SK-N-SH_RA	brain:	n/a
35	chr7:26775731-26775781	HEK293	kidney:	embryo
36	chr7:26775731-26775781	SK-N-MC	brain:	n/a
37	chr7:26775731-26775781	SK-N-SH	brain:	n/a
38	chr7:26775731-26775781	HCF	heart:	n/a
39	chr7:26775731-26775781	GM12878	blood:	n/a
40	chr7:26775731-26775781	HMEC	breast:	n/a
41	chr7:26775731-26775781	AG10803	skin:	n/a
42	chr7:26775731-26775781	PFSK-1	brain:	n/a
43	chr7:26775731-26775781	ECC-1	luminal epithelium:	n/a
44	chr7:26775731-26775781	SAEC	small airway:	n/a
45	chr7:26775731-26775781	BE2_C	brain:	n/a
46	chr7:26775731-26775781	T-47D	breast:	n/a
47	chr7:26775731-26775781	HIPEpiC	eye:	n/a
48	chr7:26775731-26775781	ovcar-3	ovarian:	n/a
49	chr7:26775731-26775781	GM06990	blood:	n/a
50	chr7:26775731-26775781	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr7:26750676..26752346-chr7:26755111..26757575,2	K562	blood:
2	chr7:26756456..26759351-chr7:26766039..26768385,2	K562	blood:
3	chr7:26742224..26743986-chr7:26746605..26748111,2	K562	blood:
4	chr7:26750689..26752519-chr7:26757003..26759421,2	MCF-7	breast:
5	chr7:26750676..26752346-chr7:26755111..26757575,2	K562	blood:
6	chr7:26763499..26765113-chr7:26769287..26770896,2	MCF-7	breast:
7	chr7:26756456..26759351-chr7:26766039..26768385,2	K562	blood:
8	chr7:26763499..26765113-chr7:26769287..26770896,2	MCF-7	breast:
9	chr7:26750689..26752519-chr7:26757003..26759421,2	MCF-7	breast:

No data

Variant related genes	Relation type
SKAP2	TF binding region
SKAP2	CpG island

Extended variants
information (count: 1513 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1513 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552661547	chr7:26745080-26745081	Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs188493150	chr7:26745128-26745129	Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541304662	chr7:26745153-26745154	Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193097190	chr7:26745195-26745196	Enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs80110935	chr7:26745210-26745211	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574685020	chr7:26745226-26745227	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569769670	chr7:26745326-26745327	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543613191	chr7:26745333-26745334	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185663418	chr7:26745367-26745368	Weak transcription Enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs145572498	chr7:26745436-26745437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs17154376	chr7:26745464-26745465	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs559758235	chr7:26745518-26745519	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs528539473	chr7:26745529-26745530	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs548714572	chr7:26745618-26745619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs79576245	chr7:26745664-26745665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568334418	chr7:26745699-26745700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs186946083	chr7:26745801-26745802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs191364851	chr7:26745829-26745830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184272759	chr7:26745830-26745831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs116815701	chr7:26745884-26745885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530597272	chr7:26745898-26745899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552677860	chr7:26745926-26745927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs5883043	chr7:26745973-26745974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566130782	chr7:26745993-26745994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148868854	chr7:26746009-26746010	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576826790	chr7:26746018-26746019	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371411725	chr7:26746152-26746153	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372615981	chr7:26746153-26746154	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574988354	chr7:26746199-26746200	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143616694	chr7:26746294-26746295	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs6461962	chr7:26746304-26746305	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs577393389	chr7:26746306-26746307	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545974543	chr7:26746341-26746342	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559500722	chr7:26746358-26746359	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs138111325	chr7:26746375-26746376	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528605048	chr7:26746391-26746392	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs542197440	chr7:26746397-26746398	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112387009	chr7:26746486-26746487	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142392043	chr7:26746489-26746490	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73686604	chr7:26746515-26746516	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs570533791	chr7:26746583-26746584	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs533201634	chr7:26746609-26746610	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2299099	chr7:26746644-26746645	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113023877	chr7:26746679-26746680	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566192156	chr7:26746738-26746739	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576436279	chr7:26746740-26746741	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541981441	chr7:26746782-26746783	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs535181896	chr7:26746871-26746872	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554916042	chr7:26746893-26746894	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2299100	chr7:26746898-26746899	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26705000-26759600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr7:26729000-26756400	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr7:26729200-26747000	Weak transcription	Primary B cells from cord blood	blood
4	chr7:26729200-26747000	Weak transcription	Primary B cells from peripheral blood	blood
5	chr7:26729600-26750000	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:26730000-26747000	Weak transcription	Fetal Kidney	kidney
7	chr7:26731800-26779200	Weak transcription	Spleen	Spleen
8	chr7:26732200-26765000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr7:26737000-26745200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr7:26740400-26782400	Weak transcription	Fetal Intestine Small	intestine
11	chr7:26740600-26745400	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr7:26741000-26745200	Weak transcription	HepG2	liver
13	chr7:26742800-26750800	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr7:26743400-26745400	Enhancers	Adipose Nuclei	Adipose
15	chr7:26743800-26745200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr7:26743800-26745600	Enhancers	Colon Smooth Muscle	Colon
17	chr7:26743800-26745600	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr7:26743800-26746400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:26743800-26746400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr7:26743800-26747800	Enhancers	NHDF-Ad	bronchial
21	chr7:26743800-26747800	Enhancers	NHLF	lung
22	chr7:26744000-26745200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr7:26744000-26745200	Enhancers	Fetal Lung	lung
24	chr7:26744000-26746000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:26744000-26746200	Enhancers	Stomach Smooth Muscle	stomach
26	chr7:26744200-26745200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr7:26744200-26745200	Enhancers	A549	lung
28	chr7:26744200-26746000	Enhancers	Rectal Smooth Muscle	rectum
29	chr7:26744200-26746200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:26744200-26747600	Enhancers	HUVEC	blood vessel
31	chr7:26744400-26745400	Enhancers	Fetal Muscle Leg	muscle
32	chr7:26744400-26745800	Enhancers	HSMMtube	muscle
33	chr7:26744400-26745800	Enhancers	NH-A	brain
34	chr7:26744400-26746000	Enhancers	HSMM	muscle
35	chr7:26744400-26746200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr7:26744400-26746400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr7:26744600-26745800	Enhancers	Primary hematopoietic stem cells	blood
38	chr7:26745000-26745200	Flanking Active TSS	Osteobl	bone
39	chr7:26745000-26745800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:26745000-26745800	Enhancers	HMEC	breast
41	chr7:26745000-26745800	Enhancers	NHEK	skin
42	chr7:26745000-26780800	Weak transcription	Aorta	Aorta
43	chr7:26745200-26745600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr7:26745200-26745600	Flanking Active TSS	A549	lung
45	chr7:26745200-26745600	Enhancers	HepG2	liver
46	chr7:26745200-26746000	Enhancers	Osteobl	bone
47	chr7:26745200-26746200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr7:26745200-26747200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr7:26745200-26747200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr7:26745200-26750200	Weak transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links