Variant report

Variant	nsv888529
Chromosome Location	chr7:80252518-80295701
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	chr7:80272116-80272564	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80284287-80284555	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:80288875-80289153	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:80263770-80264169	HepG2	liver:	n/a	n/a
5	ATF2	chr7:80267373-80268134	GM12878	blood:	n/a	n/a
6	ATF2	chr7:80267578-80268064	GM12878	blood:	n/a	n/a
7	BACH1	chr7:80260910-80260913	K562	blood:	n/a	n/a
8	BATF	chr7:80267647-80267923	GM12878	blood:	n/a	n/a
9	BATF	chr7:80267605-80267988	GM12878	blood:	n/a	n/a
10	BCL11A	chr7:80267588-80268026	GM12878	blood:	n/a	n/a
11	BCL11A	chr7:80267684-80267984	GM12878	blood:	n/a	n/a
12	BCL3	chr7:80267478-80268093	GM12878	blood:	n/a	chr7:80267573-80267582
13	BCLAF1	chr7:80267523-80268057	GM12878	blood:	n/a	chr7:80267573-80267582
14	BHLHE40	chr7:80267457-80267965	GM12878	blood:	n/a	n/a
15	BRCA1	chr7:80263685-80264171	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr7:80288768-80289107	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr7:80272790-80273832	ECC-1	luminal epithelium:	n/a	n/a
18	CEBPB	chr7:80268417-80268679	IMR90	lung:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
19	CEBPB	chr7:80272188-80272426	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
20	CEBPB	chr7:80263757-80264252	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
21	CEBPB	chr7:80263755-80264281	Hela-S3	cervix:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
22	CEBPB	chr7:80263820-80264077	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
23	CEBPB	chr7:80268410-80268678	K562	blood:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
24	CEBPB	chr7:80263777-80264203	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
25	CEBPB	chr7:80267337-80268157	GM12878	blood:	n/a	chr7:80267547-80267560 chr7:80267352-80267363 chr7:80267356-80267367
26	CEBPB	chr7:80263676-80264299	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
27	CEBPB	chr7:80263773-80264293	IMR90	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
28	CEBPB	chr7:80263870-80264032	K562	blood:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
29	CEBPB	chr7:80272830-80273384	MCF-7	breast:	n/a	n/a
30	CEBPB	chr7:80259876-80260239	MCF-7	breast:	n/a	chr7:80260003-80260014
31	CEBPB	chr7:80263803-80264151	MCF-7	breast:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
32	CEBPB	chr7:80263632-80264325	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
33	CEBPB	chr7:80255387-80255390	HepG2	liver:	n/a	n/a
34	CEBPB	chr7:80263785-80264123	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
35	CEBPB	chr7:80272158-80272462	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
36	CEBPB	chr7:80268377-80268683	HepG2	liver:	n/a	chr7:80268544-80268555 chr7:80268542-80268553 chr7:80268544-80268553
37	CEBPB	chr7:80263790-80264179	A549	lung:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
38	CEBPB	chr7:80259785-80260226	MCF-7	breast:	n/a	chr7:80260003-80260014
39	CEBPB	chr7:80252795-80253074	HepG2	liver:	n/a	chr7:80252895-80252908 chr7:80252895-80252906 chr7:80252913-80252926 chr7:80252897-80252908 chr7:80252915-80252926 chr7:80252895-80252908 chr7:80252915-80252926 chr7:80252913-80252926 chr7:80252913-80252924 chr7:80252895-80252908
40	CEBPB	chr7:80262315-80262400	A549	lung:	n/a	chr7:80262334-80262345
41	CEBPB	chr7:80272148-80272537	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
42	CEBPB	chr7:80272144-80272538	HepG2	liver:	n/a	chr7:80272335-80272348 chr7:80272335-80272346
43	CEBPB	chr7:80262200-80262511	Hela-S3	cervix:	n/a	chr7:80262334-80262345
44	CEBPB	chr7:80272854-80273198	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr7:80263869-80264105	ECC-1	luminal epithelium:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
46	CEBPB	chr7:80262186-80262489	HepG2	liver:	n/a	chr7:80262334-80262345
47	CEBPB	chr7:80259836-80260218	Hela-S3	cervix:	n/a	chr7:80260003-80260014
48	CEBPB	chr7:80263864-80264074	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992
49	CEBPB	chr7:80272811-80273219	MCF-7	breast:	n/a	n/a
50	CEBPB	chr7:80263826-80264127	HepG2	liver:	n/a	chr7:80263980-80263991 chr7:80263979-80263992

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80291794-80291844	HUVEC	blood vessel:	n/a
2	chr7:80267619-80267669	BE2_C	brain:	n/a
3	chr7:80252533-80252583	AoSMC	blood vessel:	n/a
4	chr7:80275870-80275920	BJ	skin:	n/a
5	chr7:80275870-80275920	HRE	kidney:	n/a
6	chr7:80291794-80291844	HEK293	kidney:	embryo
7	chr7:80252533-80252583	SKMC	muscle:	n/a
8	chr7:80252533-80252583	A549	lung:	n/a
9	chr7:80267619-80267669	SKMC	muscle:	n/a
10	chr7:80266930-80266980	Hela-S3	cervix:	n/a
11	chr7:80291832-80291882	PANC-1	pancreas:	n/a
12	chr7:80266930-80266980	HCPEpiC	choroid plexus:	n/a
13	chr7:80275870-80275920	NB4	blood:	n/a
14	chr7:80275870-80275920	SAEC	small airway:	n/a
15	chr7:80267619-80267669	BJ	skin:	n/a
16	chr7:80291794-80291844	HNPCEpiC	eye:	n/a
17	chr7:80267943-80267993	SK-N-MC	brain:	n/a
18	chr7:80252533-80252583	HEK293	kidney:	embryo
19	chr7:80266930-80266980	K562	blood:	n/a
20	chr7:80274687-80274737	RPTEC	kidney:	n/a
21	chr7:80267619-80267669	HRCEpiC	kidney:	n/a
22	chr7:80267943-80267993	HRCEpiC	kidney:	n/a
23	chr7:80266930-80266980	NB4	blood:	n/a
24	chr7:80267943-80267993	MCF10A-Er-Src	breast:	n/a
25	chr7:80252533-80252583	HUVEC	blood vessel:	n/a
26	chr7:80291794-80291844	HMEC	breast:	n/a
27	chr7:80266930-80266980	HMEC	breast:	n/a
28	chr7:80291794-80291844	HIPEpiC	eye:	n/a
29	chr7:80267619-80267669	PFSK-1	brain:	n/a
30	chr7:80252533-80252583	MCF10A-Er-Src	breast:	n/a
31	chr7:80252533-80252583	SK-N-MC	brain:	n/a
32	chr7:80274460-80274510	HIPEpiC	eye:	n/a
33	chr7:80274460-80274510	HCF	heart:	n/a
34	chr7:80267943-80267993	ECC-1	luminal epithelium:	n/a
35	chr7:80291832-80291882	HUVEC	blood vessel:	n/a
36	chr7:80275870-80275920	ProgFib	skin:	n/a
37	chr7:80274460-80274510	CMK	blood:	n/a
38	chr7:80275870-80275920	SK-N-SH	brain:	n/a
39	chr7:80274460-80274510	Caco-2	colon:	n/a
40	chr7:80252533-80252583	GM19239	blood:	n/a
41	chr7:80274460-80274510	HMEC	breast:	n/a
42	chr7:80266930-80266980	HL-60	blood:	n/a
43	chr7:80291794-80291844	Hela-S3	cervix:	n/a
44	chr7:80267943-80267993	HNPCEpiC	eye:	n/a
45	chr7:80266930-80266980	SK-N-SH_RA	brain:	n/a
46	chr7:80274687-80274737	HCPEpiC	choroid plexus:	n/a
47	chr7:80274687-80274737	AG04449	skin:	fetal
48	chr7:80275870-80275920	HL-60	blood:	n/a
49	chr7:80274687-80274737	SKMC	muscle:	n/a
50	chr7:80291794-80291844	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:80263049..80265695-chr7:80267263..80270319,3	K562	blood:
2	chr7:80291053..80291665-chr7:81099051..81099939,2	MCF-7	breast:
3	chr7:80057471..80058066-chr7:80288234..80289022,3	MCF-7	breast:
4	chr7:80288156..80289657-chr7:80291382..80293831,2	K562	blood:
5	chr7:80057613..80058392-chr7:80288390..80289288,3	MCF-7	breast:
6	chr7:80290704..80291673-chr7:80310324..80310826,2	MCF-7	breast:
7	chr7:80254055..80256546-chr7:80258500..80261458,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-5	chr7:80275968-80276042	NONHSAT121746
2	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121745
3	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121746
4	lnc-GNAI1-4	chr7:80253211-80253506	NONHSAT121747
5	lnc-GNAI1-5	chr7:80275968-80276531	NONHSAT121745
6	lnc-GNAI1-5	chr7:80266148-80266319	NONHSAT121746
7	lnc-GNAI1-4	chr7:80262513-80262678	NONHSAT121747

Variant related genes	Relation type
CD36	TF binding region
ENSG00000229436	TF binding region
CD36	CpG island
ENSG00000229436	CpG island
ENSG00000229436	chromatin interactions
ENSG00000135218	chromatin interactions

Extended variants
information (count: 1763 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1763 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4545029	chr7:80252518-80252519	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555784977	chr7:80252522-80252523	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs182767739	chr7:80252534-80252535	Weak transcription Enhancers Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs527499776	chr7:80252550-80252551	Weak transcription Enhancers Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs537012250	chr7:80252578-80252579	Weak transcription Enhancers Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs137984792	chr7:80252668-80252669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs71518997	chr7:80252669-80252670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563772185	chr7:80252670-80252671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35634523	chr7:80252671-80252672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556981485	chr7:80252673-80252674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576945044	chr7:80252676-80252677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs57312550	chr7:80252695-80252696	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs150910922	chr7:80252707-80252708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139392752	chr7:80252737-80252738	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs538316924	chr7:80252748-80252749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs59637606	chr7:80252807-80252808	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs143214130	chr7:80252816-80252817	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs77785157	chr7:80252819-80252820	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs200075828	chr7:80252820-80252821	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs201228786	chr7:80252821-80252822	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs533315418	chr7:80252868-80252869	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs578091410	chr7:80252872-80252873	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561799434	chr7:80252878-80252879	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs150036635	chr7:80252981-80252982	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs540861011	chr7:80252992-80252993	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs544127682	chr7:80253052-80253053	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs62461694	chr7:80253053-80253054	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs146620201	chr7:80253076-80253077	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs140124230	chr7:80253086-80253087	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs559801176	chr7:80253146-80253147	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs528651321	chr7:80253187-80253188	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs113593539	chr7:80253234-80253235	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs188032671	chr7:80253237-80253238	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs191300729	chr7:80253254-80253255	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs142483567	chr7:80253257-80253258	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs568597304	chr7:80253258-80253259	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs537721626	chr7:80253268-80253269	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs551345068	chr7:80253326-80253327	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs570418685	chr7:80253328-80253329	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs539441086	chr7:80253331-80253332	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs2151916	chr7:80253383-80253384	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs2366855	chr7:80253455-80253456	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs367779823	chr7:80253504-80253505	Enhancers Flanking Active TSS Weak transcription	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs549148874	chr7:80253586-80253587	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs555515627	chr7:80253593-80253594	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs143305265	chr7:80253604-80253605	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs562694644	chr7:80253721-80253722	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs146688103	chr7:80253793-80253794	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs531745411	chr7:80253838-80253839	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs564049535	chr7:80253845-80253846	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Medulloblastoma	21979893	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
Acute lymphoblastic leukemia	20067559	CNVD
Biliary cancer	19435499	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
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
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Neurodevelopmental disorder	22521361	CNVD
Williams Syndrome	20824207	CNVD
Metanephric adenoma	20802469	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Williams-beuren syndrome	16826523	CNVD
Olfactory neuroblastoma	18408657	CNVD
Wilms tumour	19318497	CNVD
Multiple myeloma	16616336	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Breast cancer	21611746	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80242200-80252800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr7:80244400-80253000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr7:80244800-80253000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:80246800-80254000	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr7:80251000-80253400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:80251200-80253000	Enhancers	Adipose Nuclei	Adipose
7	chr7:80251200-80253600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:80251200-80255800	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr7:80251400-80252600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr7:80251400-80252600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr7:80251400-80253400	Enhancers	NHDF-Ad	bronchial
12	chr7:80251400-80253400	Enhancers	NHLF	lung
13	chr7:80251600-80253200	Enhancers	HSMMtube	muscle
14	chr7:80251600-80253200	Enhancers	Osteobl	bone
15	chr7:80251600-80253400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr7:80251600-80253400	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr7:80251600-80253400	Enhancers	HSMM	muscle
18	chr7:80251600-80253600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr7:80251600-80253600	Enhancers	HMEC	breast
20	chr7:80251800-80253000	Weak transcription	Left Ventricle	heart
21	chr7:80251800-80253200	Weak transcription	Psoas Muscle	Psoas
22	chr7:80251800-80253400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:80251800-80253400	Enhancers	Fetal Heart	heart
24	chr7:80251800-80253400	Enhancers	NHEK	skin
25	chr7:80251800-80260000	Weak transcription	Right Ventricle	heart
26	chr7:80252000-80253000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr7:80252000-80253000	Weak transcription	Right Atrium	heart
28	chr7:80252000-80260000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:80252200-80252600	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr7:80252200-80252800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr7:80252200-80252800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr7:80252400-80252800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr7:80252400-80252800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr7:80252400-80254400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:80252600-80253000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr7:80252600-80253000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr7:80252600-80253400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr7:80252600-80253600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr7:80252800-80253000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr7:80252800-80253400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:80252800-80253400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr7:80252800-80253400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:80253000-80253200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr7:80253000-80253200	Enhancers	Duodenum Mucosa	Duodenum
45	chr7:80253000-80253200	Enhancers	HepG2	liver
46	chr7:80253000-80253200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr7:80253000-80253400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:80253000-80253400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr7:80253000-80253400	Enhancers	Fetal Lung	lung
50	chr7:80253000-80253400	Enhancers	Right Atrium	heart

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