Variant report

Variant	nsv888533
Chromosome Location	chr7:80272568-80289765
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	chr7:80284287-80284555	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:80288875-80289153	HepG2	liver:	n/a	n/a
3	BRCA1	chr7:80288768-80289107	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr7:80272830-80273384	MCF-7	breast:	n/a	n/a
5	CEBPB	chr7:80272790-80273832	ECC-1	luminal epithelium:	n/a	n/a
6	CEBPB	chr7:80272854-80273198	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr7:80272811-80273219	MCF-7	breast:	n/a	n/a
8	CHD1	chr7:80287800-80289162	IMR90	lung:	n/a	n/a
9	CTCF	chr7:80288900-80289050	GM12873	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
10	CTCF	chr7:80289060-80289210	HCM	heart:	n/a	n/a
11	CTCF	chr7:80288896-80289088	GM13977	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
12	CTCF	chr7:80288900-80289050	HRE	kidney:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
13	CTCF	chr7:80288789-80289167	K562	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
14	CTCF	chr7:80288880-80289030	HFF-Myc	foreskin:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
15	CTCF	chr7:80288900-80289050	Caco-2	colon:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
16	CTCF	chr7:80288881-80289080	A549	lung:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
17	CTCF	chr7:80288940-80289090	SK-N-SH_RA	brain:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
18	CTCF	chr7:80288800-80288950	HFF	foreskin:	n/a	n/a
19	CTCF	chr7:80288860-80289010	NHDF-neo	bronchial:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
20	CTCF	chr7:80288909-80289079	LNCaP	prostate:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
21	CTCF	chr7:80288874-80289086	GM10266	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
22	CTCF	chr7:80288880-80289030	HA-sp	spinal cord:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
23	CTCF	chr7:80288560-80288710	GM12873	blood:	n/a	n/a
24	CTCF	chr7:80289160-80289310	K562	blood:	n/a	n/a
25	CTCF	chr7:80288900-80289050	RPTEC	kidney:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
26	CTCF	chr7:80288900-80289050	HMEC	breast:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
27	CTCF	chr7:80288920-80289070	HEEpiC	esophagus:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
28	CTCF	chr7:80287837-80287926	GM10248	blood:	n/a	n/a
29	CTCF	chr7:80288862-80289120	Pancreas_OC	pancreas:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
30	CTCF	chr7:80288900-80289050	HPF	lung:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
31	CTCF	chr7:80288900-80289050	GM12872	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
32	CTCF	chr7:80288876-80289085	SK-N-SH_RA	brain:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
33	CTCF	chr7:80288880-80289030	AoAF	blood vessel:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
34	CTCF	chr7:80288880-80289030	NHDF-neo	bronchial:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
35	CTCF	chr7:80288864-80289130	HUVEC	blood vessel:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
36	CTCF	chr7:80288980-80289130	GM12866	blood:	n/a	n/a
37	CTCF	chr7:80288940-80289090	BJ	skin:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
38	CTCF	chr7:80288880-80289030	AG09309	skin:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
39	CTCF	chr7:80288900-80289050	HCT-116	colon:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
40	CTCF	chr7:80288825-80289119	HepG2	liver:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
41	CTCF	chr7:80288600-80288750	GM12864	blood:	n/a	n/a
42	CTCF	chr7:80288880-80289030	Caco-2	colon:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
43	CTCF	chr7:80288767-80289188	MCF-7	breast:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
44	CTCF	chr7:80288800-80288950	GM12866	blood:	n/a	n/a
45	CTCF	chr7:80288165-80289708	A549	lung:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
46	CTCF	chr7:80288880-80289030	GM12864	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
47	CTCF	chr7:80288880-80289030	GM12867	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
48	CTCF	chr7:80288900-80289050	AG09319	gingival:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986
49	CTCF	chr7:80289160-80289310	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr7:80288920-80289070	GM12801	blood:	n/a	chr7:80288970-80288988 chr7:80288971-80288987 chr7:80288965-80288986

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:80274687-80274737	BE2_C	brain:	n/a
2	chr7:80274460-80274510	HRE	kidney:	n/a
3	chr7:80274460-80274510	HUVEC	blood vessel:	n/a
4	chr7:80275870-80275920	HCPEpiC	choroid plexus:	n/a
5	chr7:80275870-80275920	AG04450	lung:	fetal
6	chr7:80274460-80274510	AG04450	lung:	fetal
7	chr7:80274460-80274510	HRCEpiC	kidney:	n/a
8	chr7:80274687-80274737	HMEC	breast:	n/a
9	chr7:80274687-80274737	AoSMC	blood vessel:	n/a
10	chr7:80274460-80274510	NH-A	brain:	n/a
11	chr7:80274687-80274737	HCF	heart:	n/a
12	chr7:80274460-80274510	HCT-116	colon:	n/a
13	chr7:80274460-80274510	ECC-1	luminal epithelium:	n/a
14	chr7:80275870-80275920	HCT-116	colon:	n/a
15	chr7:80274460-80274510	HRPEpiC	eye:	n/a
16	chr7:80275870-80275920	AG04449	skin:	fetal
17	chr7:80275870-80275920	GM12891	blood:	n/a
18	chr7:80275870-80275920	HCF	heart:	n/a
19	chr7:80274460-80274510	SK-N-SH	brain:	n/a
20	chr7:80274460-80274510	U87	brain:	n/a
21	chr7:80274460-80274510	GM19239	blood:	n/a
22	chr7:80274460-80274510	RPTEC	kidney:	n/a
23	chr7:80274460-80274510	Hepatocyte	liver:	n/a
24	chr7:80275870-80275920	AG09319	gingival:	n/a
25	chr7:80274687-80274737	HCT-116	colon:	n/a
26	chr7:80274460-80274510	ProgFib	skin:	n/a
27	chr7:80274687-80274737	NT2-D1	testis:	n/a
28	chr7:80274460-80274510	H1-hESC	embryonic stem cell:	embryo
29	chr7:80274460-80274510	T-47D	breast:	n/a
30	chr7:80275870-80275920	AG10803	skin:	n/a
31	chr7:80274460-80274510	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:80274460-80274510	AG09319	gingival:	n/a
33	chr7:80274460-80274510	Caco-2	colon:	n/a
34	chr7:80274460-80274510	PrEC	prostate:	n/a
35	chr7:80274687-80274737	PFSK-1	brain:	n/a
36	chr7:80274687-80274737	HIPEpiC	eye:	n/a
37	chr7:80274460-80274510	AG09309	skin:	n/a
38	chr7:80274687-80274737	HEEpiC	esophagus:	n/a
39	chr7:80274460-80274510	ovcar-3	ovarian:	n/a
40	chr7:80274460-80274510	PANC-1	pancreas:	n/a
41	chr7:80274460-80274510	NT2-D1	testis:	n/a
42	chr7:80274687-80274737	GM19239	blood:	n/a
43	chr7:80274460-80274510	HAEpiC	amniotic membrane:	n/a
44	chr7:80275870-80275920	SK-N-MC	brain:	n/a
45	chr7:80275870-80275920	HepG2	liver:	n/a
46	chr7:80275870-80275920	PFSK-1	brain:	n/a
47	chr7:80274460-80274510	GM12878	blood:	n/a
48	chr7:80274687-80274737	HUVEC	blood vessel:	n/a
49	chr7:80274460-80274510	SK-N-MC	brain:	n/a
50	chr7:80274687-80274737	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:80057471..80058066-chr7:80288234..80289022,3	MCF-7	breast:
2	chr7:80288156..80289657-chr7:80291382..80293831,2	K562	blood:
3	chr7:80057613..80058392-chr7:80288390..80289288,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNAI1-5	chr7:80275968-80276531	NONHSAT121745
2	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121746
3	lnc-GNAI1-5	chr7:80275404-80275497	NONHSAT121745
4	lnc-GNAI1-5	chr7:80275968-80276042	NONHSAT121746

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

Extended variants
information (count: 729 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1527479	chr7:80272568-80272569	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370540966	chr7:80272571-80272572	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs190166729	chr7:80272650-80272651	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530417220	chr7:80272657-80272658	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs550218631	chr7:80272681-80272682	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs569602282	chr7:80272686-80272687	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs538663304	chr7:80272721-80272722	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs181456840	chr7:80272739-80272740	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs565765012	chr7:80272764-80272765	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs199809789	chr7:80272785-80272786	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs186412713	chr7:80272824-80272825	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs574547579	chr7:80272829-80272830	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs543659060	chr7:80272902-80272903	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs556988405	chr7:80272926-80272927	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs140496605	chr7:80272966-80272967	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs143834933	chr7:80272992-80272993	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs114373079	chr7:80272999-80273000	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs148159817	chr7:80273024-80273025	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs113202681	chr7:80273025-80273026	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs3212159	chr7:80273143-80273144	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs377422261	chr7:80273149-80273150	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs550422859	chr7:80273158-80273159	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570232338	chr7:80273191-80273192	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs189202324	chr7:80273246-80273247	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs180933069	chr7:80273257-80273258	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs573082637	chr7:80273301-80273302	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs3212160	chr7:80273308-80273309	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs534659483	chr7:80273334-80273335	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs554375587	chr7:80273338-80273339	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568210011	chr7:80273346-80273347	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs386715085	chr7:80273358-80273359	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs3212162	chr7:80273359-80273360	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs576710113	chr7:80273423-80273424	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs3212163	chr7:80273433-80273434	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs185779180	chr7:80273447-80273448	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs551263951	chr7:80273527-80273528	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs572109878	chr7:80273539-80273540	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs541093785	chr7:80273594-80273595	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs138726953	chr7:80273619-80273620	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs191459490	chr7:80273635-80273636	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs543641346	chr7:80273684-80273685	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145389366	chr7:80273700-80273701	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs3212164	chr7:80273732-80273733	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs546817981	chr7:80273936-80273937	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs532854002	chr7:80273974-80273975	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs552909563	chr7:80273995-80273996	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs549500532	chr7:80274054-80274055	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs183179714	chr7:80274066-80274067	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs36055469	chr7:80274105-80274106	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs528107542	chr7:80274107-80274108	Active TSS Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	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:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80260400-80273400	Weak transcription	Small Intestine	intestine
2	chr7:80262400-80272600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:80267600-80273200	Active TSS	Adipose Nuclei	Adipose
4	chr7:80268000-80272600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:80269400-80305000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr7:80270400-80272800	Enhancers	Placenta Amnion	Placenta Amnion
7	chr7:80270600-80274000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr7:80271000-80272800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:80271000-80272800	Weak transcription	HSMM	muscle
10	chr7:80271200-80272800	Weak transcription	NHDF-Ad	bronchial
11	chr7:80271200-80274200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:80271400-80272800	Weak transcription	Right Ventricle	heart
13	chr7:80271400-80275400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr7:80271600-80272600	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr7:80271600-80273000	Enhancers	HepG2	liver
16	chr7:80271800-80272800	Enhancers	Fetal Heart	heart
17	chr7:80271800-80273000	Enhancers	Fetal Intestine Small	intestine
18	chr7:80272000-80280400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr7:80272200-80272600	Enhancers	Liver	Liver
20	chr7:80272200-80272600	Enhancers	Placenta	Placenta
21	chr7:80272200-80272600	Flanking Active TSS	Right Atrium	heart
22	chr7:80272200-80272800	Active TSS	Psoas Muscle	Psoas
23	chr7:80272200-80272800	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr7:80272200-80273000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr7:80272200-80273200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
26	chr7:80272200-80273600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr7:80272200-80274200	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr7:80272200-80274200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr7:80272400-80272600	Enhancers	NHLF	lung
30	chr7:80272400-80273000	Active TSS	Left Ventricle	heart
31	chr7:80272400-80273800	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr7:80272600-80272800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr7:80272600-80273600	Enhancers	NHEK	skin
34	chr7:80272600-80273800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr7:80272600-80274200	Active TSS	Right Atrium	heart
36	chr7:80272600-80275400	Weak transcription	Liver	Liver
37	chr7:80272600-80293600	Weak transcription	Placenta	Placenta
38	chr7:80272800-80273000	Flanking Active TSS	Psoas Muscle	Psoas
39	chr7:80272800-80273200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
40	chr7:80272800-80273200	Enhancers	NHDF-Ad	bronchial
41	chr7:80272800-80273400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:80272800-80273400	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr7:80272800-80273400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr7:80272800-80273400	Enhancers	HSMM	muscle
45	chr7:80272800-80273600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr7:80272800-80273600	Enhancers	Right Ventricle	heart
47	chr7:80272800-80282600	Weak transcription	Fetal Heart	heart
48	chr7:80273000-80273200	Active TSS	Psoas Muscle	Psoas
49	chr7:80273000-80275400	Weak transcription	Fetal Intestine Small	intestine
50	chr7:80273000-80275400	Weak transcription	Left Ventricle	heart

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