Variant report

Variant	nsv527227
Chromosome Location	chr7:25606120-25615221
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	chr7:25608009-25608865	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:25608534-25608799	K562	blood:	n/a	n/a
3	ATF1	chr7:25608157-25608836	K562	blood:	n/a	n/a
4	BACH1	chr7:25608673-25608795	K562	blood:	n/a	n/a
5	BHLHE40	chr7:25608114-25608813	K562	blood:	n/a	n/a
6	BHLHE40	chr7:25608184-25608761	A549	lung:	n/a	n/a
7	BHLHE40	chr7:25608156-25608401	HepG2	liver:	n/a	n/a
8	BHLHE40	chr7:25608186-25608493	HepG2	liver:	n/a	n/a
9	BHLHE40	chr7:25608040-25608849	HepG2	liver:	n/a	n/a
10	BRCA1	chr7:25611641-25611759	GM12878	blood:	n/a	n/a
11	CBX3	chr7:25608095-25608803	K562	blood:	n/a	n/a
12	CBX3	chr7:25608127-25608926	HCT-116	colon:	n/a	n/a
13	CEBPB	chr7:25608502-25608749	K562	blood:	n/a	n/a
14	CHD1	chr7:25608644-25608665	GM12878	blood:	n/a	n/a
15	CREB1	chr7:25608469-25608898	H1-hESC	embryonic stem cell:	n/a	n/a
16	CREB1	chr7:25608148-25608387	A549	lung:	n/a	n/a
17	CREB1	chr7:25608078-25608416	A549	lung:	n/a	n/a
18	CREB1	chr7:25607934-25608880	HepG2	liver:	n/a	n/a
19	CREB1	chr7:25608444-25608890	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr7:25608640-25608790	BJ	skin:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
21	CTCF	chr7:25608620-25608770	GM12873	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
22	CTCF	chr7:25608520-25608670	HFF-Myc	foreskin:	n/a	n/a
23	CTCF	chr7:25608560-25608710	AG09319	gingival:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
24	CTCF	chr7:25608300-25608450	AG10803	skin:	n/a	chr7:25608392-25608400
25	CTCF	chr7:25608594-25608791	GM10266	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
26	CTCF	chr7:25608580-25608730	BJ	skin:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
27	CTCF	chr7:25608640-25608790	HCT-116	colon:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
28	CTCF	chr7:25608660-25608810	HL-60	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
29	CTCF	chr7:25608547-25608843	MCF-7	breast:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
30	CTCF	chr7:25606660-25606810	AG04449	skin:	n/a	n/a
31	CTCF	chr7:25608410-25608885	K562	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
32	CTCF	chr7:25605201-25606159	HepG2	liver:	n/a	chr7:25605699-25605715 chr7:25605661-25605668 chr7:25605693-25605714 chr7:25605654-25605672 chr7:25605700-25605713 chr7:25605649-25605670 chr7:25605655-25605671 chr7:25605698-25605716
33	CTCF	chr7:25608576-25608818	LNCaP	prostate:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
34	CTCF	chr7:25608602-25608822	ProgFib	skin:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
35	CTCF	chr7:25608525-25608776	ECC-1	luminal epithelium:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
36	CTCF	chr7:25606320-25606470	HAc	cerebellar:	n/a	n/a
37	CTCF	chr7:25608485-25608826	A549	lung:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
38	CTCF	chr7:25608476-25608787	H1-hESC	embryonic stem cell:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
39	CTCF	chr7:25608640-25608790	GM12866	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
40	CTCF	chr7:25608640-25608790	GM12873	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
41	CTCF	chr7:25608400-25608550	GM12873	blood:	n/a	n/a
42	CTCF	chr7:25606540-25606690	BJ	skin:	n/a	n/a
43	CTCF	chr7:25608470-25608887	HepG2	liver:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
44	CTCF	chr7:25608605-25608757	Kidney_OC	kidney:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
45	CTCF	chr7:25608620-25608770	HepG2	liver:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
46	CTCF	chr7:25608585-25608808	LNCaP	prostate:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
47	CTCF	chr7:25608620-25608770	Hela-S3	cervix:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
48	CTCF	chr7:25608550-25608822	GM12892	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
49	CTCF	chr7:25608459-25608918	K562	blood:	n/a	chr7:25608687-25608696 chr7:25608682-25608698 chr7:25608681-25608699
50	CTCF	chr7:25607988-25608956	SK-N-SH	brain:	n/a	chr7:25608687-25608696 chr7:25608392-25608400 chr7:25608682-25608698 chr7:25608681-25608699

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:25608634-25608684	AG10803	skin:	n/a
2	chr7:25608323-25608373	SK-N-SH	brain:	n/a
3	chr7:25608323-25608373	GM19239	blood:	n/a
4	chr7:25608634-25608684	SAEC	small airway:	n/a
5	chr7:25608305-25608355	GM19239	blood:	n/a
6	chr7:25608634-25608684	HUVEC	blood vessel:	n/a
7	chr7:25608673-25608723	HCPEpiC	choroid plexus:	n/a
8	chr7:25608673-25608723	A549	lung:	n/a
9	chr7:25608323-25608373	HEK293	kidney:	embryo
10	chr7:25608305-25608355	ECC-1	luminal epithelium:	n/a
11	chr7:25608673-25608723	HCF	heart:	n/a
12	chr7:25608673-25608723	ECC-1	luminal epithelium:	n/a
13	chr7:25608673-25608723	ProgFib	skin:	n/a
14	chr7:25608634-25608684	AoSMC	blood vessel:	n/a
15	chr7:25608634-25608684	K562	blood:	n/a
16	chr7:25608634-25608684	AG09319	gingival:	n/a
17	chr7:25608673-25608723	PFSK-1	brain:	n/a
18	chr7:25608634-25608684	AG04450	lung:	fetal
19	chr7:25608673-25608723	GM12891	blood:	n/a
20	chr7:25608673-25608723	HRCEpiC	kidney:	n/a
21	chr7:25608634-25608684	HepG2	liver:	n/a
22	chr7:25608323-25608373	ovcar-3	ovarian:	n/a
23	chr7:25608305-25608355	AG09309	skin:	n/a
24	chr7:25608673-25608723	SK-N-MC	brain:	n/a
25	chr7:25608673-25608723	NH-A	brain:	n/a
26	chr7:25608634-25608684	RPTEC	kidney:	n/a
27	chr7:25608323-25608373	MCF10A-Er-Src	breast:	n/a
28	chr7:25608323-25608373	AG04450	lung:	fetal
29	chr7:25608634-25608684	MCF-7	breast:	n/a
30	chr7:25608305-25608355	SKMC	muscle:	n/a
31	chr7:25608634-25608684	GM12892	blood:	n/a
32	chr7:25608323-25608373	HCM	heart:	n/a
33	chr7:25608323-25608373	HepG2	liver:	n/a
34	chr7:25608634-25608684	HEEpiC	esophagus:	n/a
35	chr7:25608673-25608723	AG10803	skin:	n/a
36	chr7:25608323-25608373	HCPEpiC	choroid plexus:	n/a
37	chr7:25608305-25608355	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:25608673-25608723	HEEpiC	esophagus:	n/a
39	chr7:25608673-25608723	U87	brain:	n/a
40	chr7:25608634-25608684	GM06990	blood:	n/a
41	chr7:25608323-25608373	MCF-7	breast:	n/a
42	chr7:25608323-25608373	NH-A	brain:	n/a
43	chr7:25608323-25608373	HMEC	breast:	n/a
44	chr7:25608305-25608355	MCF10A-Er-Src	breast:	n/a
45	chr7:25608673-25608723	Jurkat	blood:	n/a
46	chr7:25608305-25608355	Jurkat	blood:	n/a
47	chr7:25608323-25608373	HPAEpiC	pulmonary alveolar:	n/a
48	chr7:25608634-25608684	SK-N-SH	brain:	n/a
49	chr7:25608634-25608684	ovcar-3	ovarian:	n/a
50	chr7:25608634-25608684	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:25605629..25606130-chr7:26404535..26405453,2	K562	blood:
2	chr7:25430634..25431513-chr7:25608350..25609015,3	MCF-7	breast:
3	chr7:25608970..25611945-chr7:25612045..25614894,3	MCF-7	breast:
4	chr7:25299061..25300348-chr7:25608226..25609143,4	K562	blood:
5	chr7:25605406..25606179-chr7:25890948..25891905,5	K562	blood:
6	chr7:25298951..25300126-chr7:25605192..25606795,18	K562	blood:
7	chr7:25430463..25431643-chr7:25605112..25606187,14	K562	blood:
8	chr7:25298973..25299854-chr7:25605283..25606167,4	MCF-7	breast:
9	chr7:25433474..25434141-chr7:25605268..25606353,4	K562	blood:
10	chr7:25429098..25432014-chr7:25608292..25610212,2	K562	blood:
11	chr7:25433157..25433791-chr7:25605378..25606157,2	MCF-7	breast:
12	chr7:25605147..25606187-chr7:25890189..25892015,14	MCF-7	breast:
13	chr7:25298470..25299852-chr7:25605228..25606576,11	MCF-7	breast:
14	chr7:25608198..25609026-chr7:25891099..25891911,6	MCF-7	breast:
15	chr7:25430704..25431525-chr7:25608219..25609114,4	K562	blood:
16	chr7:25428848..25430407-chr7:25605173..25606452,6	MCF-7	breast:
17	chr7:25614579..25616228-chr7:25892925..25895334,2	K562	blood:
18	chr7:25430622..25431559-chr7:25605393..25606130,7	MCF-7	breast:
19	chr7:25429055..25432240-chr7:25604579..25606349,45	MCF-7	breast:
20	chr7:25256547..25257067-chr7:25608230..25609163,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NPVF-4	chr7:25607521-25607592	XLOC_006381

Variant related genes	Relation type
ENSG00000222101	TF binding region
ENSG00000222101	CpG island
ENSG00000222101	chromatin interactions

Extended variants
information (count: 408 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2952524	chr7:25606120-25606121	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs75965819	chr7:25606152-25606153	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116207386	chr7:25606208-25606209	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs556059670	chr7:25606211-25606212	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs576027897	chr7:25606223-25606224	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs2999577	chr7:25606273-25606274	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs80151297	chr7:25606337-25606338	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs577995890	chr7:25606387-25606388	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs540703273	chr7:25606443-25606444	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs560419644	chr7:25606463-25606464	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs2938115	chr7:25606484-25606485	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs139631490	chr7:25606485-25606486	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562394694	chr7:25606503-25606504	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs111241694	chr7:25606511-25606512	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532339187	chr7:25606569-25606570	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs551299655	chr7:25606590-25606591	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552134585	chr7:25606595-25606596	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs17727166	chr7:25606612-25606613	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs547452875	chr7:25606654-25606655	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs572199824	chr7:25606656-25606657	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs567264510	chr7:25606659-25606660	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs145303000	chr7:25606696-25606697	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs73693126	chr7:25606731-25606732	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs77850212	chr7:25606735-25606736	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs538535385	chr7:25606748-25606749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558517712	chr7:25606792-25606793	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs12531920	chr7:25606871-25606872	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs114258296	chr7:25606881-25606882	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs560608365	chr7:25606914-25606915	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147629622	chr7:25606916-25606917	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs372376699	chr7:25606917-25606918	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs2960821	chr7:25606956-25606957	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190116789	chr7:25606960-25606961	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs531446468	chr7:25607021-25607022	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs142005589	chr7:25607024-25607025	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs12534642	chr7:25607045-25607046	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs527246117	chr7:25607081-25607082	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs80226696	chr7:25607138-25607139	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs553837610	chr7:25607139-25607140	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs117625209	chr7:25607140-25607141	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs529744866	chr7:25607152-25607153	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs142055231	chr7:25607155-25607156	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs569453509	chr7:25607156-25607157	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs538477098	chr7:25607179-25607180	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558457672	chr7:25607186-25607187	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs573306742	chr7:25607204-25607205	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs28394819	chr7:25607205-25607206	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs181647164	chr7:25607224-25607225	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs553887010	chr7:25607232-25607233	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs574017552	chr7:25607240-25607241	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Lung adenocarcinoma	17086460	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17086460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25604000-25606200	Enhancers	Fetal Lung	lung
2	chr7:25604600-25608200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:25604800-25608200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:25605200-25606400	Weak transcription	Fetal Stomach	stomach
5	chr7:25605200-25606800	Enhancers	Fetal Kidney	kidney
6	chr7:25605400-25607000	Enhancers	Stomach Mucosa	stomach
7	chr7:25605600-25606800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:25606000-25606400	Weak transcription	Colon Smooth Muscle	Colon
9	chr7:25606000-25607400	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr7:25606200-25608000	Weak transcription	Fetal Lung	lung
11	chr7:25606400-25606600	Enhancers	Fetal Stomach	stomach
12	chr7:25606600-25607000	Enhancers	Gastric	stomach
13	chr7:25606800-25607000	Enhancers	Rectal Smooth Muscle	rectum
14	chr7:25607000-25607800	Weak transcription	Stomach Mucosa	stomach
15	chr7:25607400-25608000	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr7:25607800-25608800	Enhancers	Stomach Mucosa	stomach
17	chr7:25608000-25608200	Enhancers	Liver	Liver
18	chr7:25608000-25608200	Enhancers	Colon Smooth Muscle	Colon
19	chr7:25608000-25608200	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr7:25608000-25608200	Enhancers	HepG2	liver
21	chr7:25608000-25608200	Enhancers	K562	blood
22	chr7:25608000-25608400	Enhancers	Fetal Heart	heart
23	chr7:25608000-25608400	Enhancers	Fetal Lung	lung
24	chr7:25608000-25608600	Flanking Active TSS	A549	lung
25	chr7:25608000-25608800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
26	chr7:25608200-25608400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:25608200-25608400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
28	chr7:25608200-25608600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr7:25608200-25608600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr7:25608200-25608600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr7:25608200-25608600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr7:25608200-25608600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr7:25608200-25608600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr7:25608200-25608600	Flanking Active TSS	Liver	Liver
35	chr7:25608200-25608600	Enhancers	Placenta	Placenta
36	chr7:25608200-25608600	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr7:25608200-25608600	Flanking Active TSS	HepG2	liver
38	chr7:25608200-25608600	Flanking Active TSS	K562	blood
39	chr7:25608200-25608800	Enhancers	Pancreas	Pancrea
40	chr7:25608200-25609000	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr7:25608400-25608600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr7:25608400-25608600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr7:25608400-25609200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:25608400-25613400	Weak transcription	Fetal Lung	lung
45	chr7:25608600-25608800	Enhancers	Liver	Liver
46	chr7:25608600-25608800	Active TSS	A549	lung
47	chr7:25608600-25608800	Active TSS	HepG2	liver
48	chr7:25608600-25608800	Active TSS	K562	blood
49	chr7:25609400-25609600	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr7:25609400-25609600	Enhancers	Primary T helper cells PMA-I stimulated	--

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