Variant report

Variant	nsv887488
Chromosome Location	chr7:7770203-7794484
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:209)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:209 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:7771103-7771852	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:7791039-7791360	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:7772652-7773151	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:7790255-7790319	K562	blood:	n/a	n/a
5	BACH1	chr7:7772801-7772861	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr7:7778842-7779627	GM12878	blood:	n/a	n/a
7	CEBPB	chr7:7792796-7792918	A549	lung:	n/a	n/a
8	CEBPB	chr7:7772108-7772929	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr7:7772275-7772855	HepG2	liver:	n/a	n/a
10	CEBPB	chr7:7771438-7771664	HepG2	liver:	n/a	n/a
11	CEBPB	chr7:7772334-7772370	A549	lung:	n/a	n/a
12	CHD2	chr7:7778844-7779662	GM12878	blood:	n/a	n/a
13	CTCF	chr7:7781958-7781997	Gliobla	brain:	n/a	n/a
14	CTCF	chr7:7782113-7782253	K562	blood:	n/a	n/a
15	CTCF	chr7:7772800-7772950	AG10803	skin:	n/a	n/a
16	CTCF	chr7:7782136-7782202	MCF-7	breast:	n/a	n/a
17	CTCF	chr7:7785640-7785790	GM12867	blood:	n/a	n/a
18	CTCF	chr7:7782060-7782210	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr7:7782168-7782231	K562	blood:	n/a	n/a
20	CTCF	chr7:7782105-7782251	Gliobla	brain:	n/a	n/a
21	CTCF	chr7:7782150-7782231	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr7:7782080-7782230	BE2_C	brain:	n/a	n/a
23	CTCF	chr7:7781879-7782265	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr7:7778340-7778490	HAc	cerebellar:	n/a	n/a
25	CTCF	chr7:7782062-7782357	A549	lung:	n/a	n/a
26	CTCF	chr7:7781920-7782070	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr7:7782040-7782190	BE2_C	brain:	n/a	n/a
28	CTCF	chr7:7782155-7782247	Medullo	brain:	n/a	n/a
29	CTCF	chr7:7781980-7782130	A549	lung:	n/a	n/a
30	CTCF	chr7:7782102-7782256	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:7782151-7782230	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:7781855-7782284	K562	blood:	n/a	n/a
33	CTCF	chr7:7782040-7782190	HMF	breast:	n/a	n/a
34	CTCF	chr7:7772860-7773010	AG10803	skin:	n/a	n/a
35	CTCF	chr7:7781963-7782058	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:7781820-7781970	HEK293	kidney:	n/a	n/a
37	CTCF	chr7:7781883-7782428	HCT-116	colon:	n/a	n/a
38	CTCF	chr7:7782119-7782217	A549	lung:	n/a	n/a
39	CTCF	chr7:7781948-7782056	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr7:7782020-7782170	NB4	blood:	n/a	n/a
41	CTCF	chr7:7782110-7782236	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:7782071-7782260	A549	lung:	n/a	n/a
43	CUX1	chr7:7778723-7779439	GM12878	blood:	n/a	n/a
44	CUX1	chr7:7772462-7772520	K562	blood:	n/a	n/a
45	E2F4	chr7:7774811-7774838	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr7:7775600-7775884	GM12878	blood:	n/a	chr7:7775746-7775759 chr7:7775747-7775758
47	EBF1	chr7:7775605-7775854	GM12878	blood:	n/a	chr7:7775746-7775759 chr7:7775747-7775758
48	EBF1	chr7:7779507-7779751	GM12878	blood:	n/a	n/a
49	EBF1	chr7:7778808-7779214	GM12878	blood:	n/a	n/a
50	ELF1	chr7:7771336-7771633	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7776115-7776165	SK-N-SH	brain:	n/a
2	chr7:7776115-7776165	HRPEpiC	eye:	n/a
3	chr7:7776115-7776165	PFSK-1	brain:	n/a
4	chr7:7776115-7776165	Caco-2	colon:	n/a
5	chr7:7776115-7776165	HEEpiC	esophagus:	n/a
6	chr7:7776115-7776165	H1-hESC	embryonic stem cell:	embryo
7	chr7:7776115-7776165	HRE	kidney:	n/a
8	chr7:7776115-7776165	ovcar-3	ovarian:	n/a
9	chr7:7776115-7776165	T-47D	breast:	n/a
10	chr7:7776115-7776165	BJ	skin:	n/a
11	chr7:7776115-7776165	MCF10A-Er-Src	breast:	n/a
12	chr7:7776115-7776165	Hepatocyte	liver:	n/a
13	chr7:7776115-7776165	HCF	heart:	n/a
14	chr7:7776115-7776165	IMR90	lung:	fetal
15	chr7:7776115-7776165	SKMC	muscle:	n/a
16	chr7:7776115-7776165	AG04450	lung:	fetal
17	chr7:7776115-7776165	GM12878	blood:	n/a
18	chr7:7776115-7776165	RPTEC	kidney:	n/a
19	chr7:7776115-7776165	A549	lung:	n/a
20	chr7:7776115-7776165	HCT-116	colon:	n/a
21	chr7:7776115-7776165	AG04449	skin:	fetal
22	chr7:7776115-7776165	NHDF-neo	bronchial:	n/a
23	chr7:7776115-7776165	HUVEC	blood vessel:	n/a
24	chr7:7776115-7776165	GM19239	blood:	n/a
25	chr7:7776115-7776165	ECC-1	luminal epithelium:	n/a
26	chr7:7776115-7776165	K562	blood:	n/a
27	chr7:7776115-7776165	GM12892	blood:	n/a
28	chr7:7776115-7776165	Hela-S3	cervix:	n/a
29	chr7:7776115-7776165	SAEC	small airway:	n/a
30	chr7:7776115-7776165	AoSMC	blood vessel:	n/a
31	chr7:7776115-7776165	HEK293	kidney:	embryo
32	chr7:7776115-7776165	Jurkat	blood:	n/a
33	chr7:7776115-7776165	HPAEpiC	pulmonary alveolar:	n/a
34	chr7:7776115-7776165	CMK	blood:	n/a
35	chr7:7776115-7776165	MCF-7	breast:	n/a
36	chr7:7776115-7776165	BE2_C	brain:	n/a
37	chr7:7776115-7776165	GM06990	blood:	n/a
38	chr7:7776115-7776165	NH-A	brain:	n/a
39	chr7:7776115-7776165	AG09309	skin:	n/a
40	chr7:7776115-7776165	PANC-1	pancreas:	n/a
41	chr7:7776115-7776165	HRCEpiC	kidney:	n/a
42	chr7:7776115-7776165	ProgFib	skin:	n/a
43	chr7:7776115-7776165	U87	brain:	n/a
44	chr7:7776115-7776165	HNPCEpiC	eye:	n/a
45	chr7:7776115-7776165	AG09319	gingival:	n/a
46	chr7:7776115-7776165	NT2-D1	testis:	n/a
47	chr7:7776115-7776165	HIPEpiC	eye:	n/a
48	chr7:7776115-7776165	SK-N-SH_RA	brain:	n/a
49	chr7:7776115-7776165	GM12891	blood:	n/a
50	chr7:7776115-7776165	HMEC	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:7766237..7767895-chr7:7769478..7771266,2	K562	blood:
2	chr7:7756124..7759013-chr7:7778482..7780690,2	K562	blood:
3	chr7:7789196..7791456-chr7:7796401..7799287,2	K562	blood:
4	chr7:7775020..7777800-chr7:7778182..7779689,2	K562	blood:
5	chr7:7777111..7778841-chr7:7780789..7783193,3	MCF-7	breast:
6	chr7:7769666..7772016-chr7:7775806..7779623,3	MCF-7	breast:
7	chr7:7780753..7782943-chr7:7783996..7785680,2	K562	blood:
8	chr7:7742121..7744210-chr7:7768171..7770972,2	MCF-7	breast:
9	chr7:7772333..7774684-chr7:7827758..7829772,2	MCF-7	breast:
10	chr7:7776217..7779160-chr7:7788471..7790651,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPA3-2	chr7:7780317-7780751	ENSG00000234718.5
2	lnc-RPA3-2	chr7:7778270-7778615	ENSG00000234718.5
3	lnc-RPA3-1	chr7:7775374-7776482	NONHSAT119131

No data

Variant related genes	Relation type
ENSG00000234718	TF binding region
ENSG00000270314	TF binding region
RPL23AP51	TF binding region
ENSG00000234718	CpG island
ENSG00000270314	CpG island
RPL23AP51	CpG island
ENSG00000234718	chromatin interactions
ENSG00000269721	chromatin interactions
ENSG00000106399	chromatin interactions
ENSG00000270314	chromatin interactions

Extended variants
information (count: 1055 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11971584	chr7:7770203-7770204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs554464009	chr7:7770221-7770222	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs62432611	chr7:7770224-7770225	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs80116149	chr7:7770237-7770238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189556119	chr7:7770254-7770255	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559688145	chr7:7770317-7770318	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554041464	chr7:7770329-7770330	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558618769	chr7:7770343-7770344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112867608	chr7:7770356-7770357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs73352759	chr7:7770357-7770358	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs149264719	chr7:7770365-7770366	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374907476	chr7:7770462-7770463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs142527635	chr7:7770507-7770508	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs369779325	chr7:7770509-7770510	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs563765973	chr7:7770510-7770511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs376101724	chr7:7770523-7770524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs531146773	chr7:7770527-7770528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142543163	chr7:7770531-7770532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs180738776	chr7:7770592-7770593	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs561573139	chr7:7770600-7770601	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576485376	chr7:7770628-7770629	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528755349	chr7:7770672-7770673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs59441244	chr7:7770699-7770700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs144340699	chr7:7770715-7770716	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs186223929	chr7:7770722-7770723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs191101877	chr7:7770786-7770787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs568830969	chr7:7770787-7770788	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs181601536	chr7:7770795-7770796	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554302449	chr7:7770816-7770817	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538384980	chr7:7770817-7770818	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs572840499	chr7:7770820-7770821	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs115633824	chr7:7770823-7770824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369671274	chr7:7770825-7770826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185836984	chr7:7770830-7770831	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs577956923	chr7:7770835-7770836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148760150	chr7:7770872-7770873	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs557452359	chr7:7770892-7770893	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs142478009	chr7:7770910-7770911	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs112387008	chr7:7770959-7770960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543253401	chr7:7770964-7770965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561459047	chr7:7770969-7770970	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528841176	chr7:7770988-7770989	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs113981860	chr7:7771025-7771026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565404611	chr7:7771043-7771044	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs190348024	chr7:7771060-7771061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182888986	chr7:7771075-7771076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs151220268	chr7:7771080-7771081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187632269	chr7:7771095-7771096	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs71523788	chr7:7771097-7771098	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs79127645	chr7:7771101-7771102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
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
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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD

Chromatin state (count:369 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7737600-7778800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr7:7743600-7772800	Weak transcription	Gastric	stomach
3	chr7:7748200-7772200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr7:7749200-7770800	Weak transcription	Small Intestine	intestine
5	chr7:7752600-7790400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr7:7755400-7772800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr7:7757000-7770600	Weak transcription	Pancreas	Pancrea
8	chr7:7759000-7785800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr7:7759400-7772000	Weak transcription	Brain Hippocampus Middle	brain
10	chr7:7759400-7791200	Weak transcription	Esophagus	oesophagus
11	chr7:7759600-7779000	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr7:7759600-7780000	Weak transcription	Primary T cells from cord blood	blood
13	chr7:7759600-7786800	Weak transcription	Aorta	Aorta
14	chr7:7759800-7776800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:7760200-7771000	Weak transcription	HSMMtube	muscle
16	chr7:7760600-7770600	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr7:7760800-7778400	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr7:7760800-7785200	Weak transcription	Primary B cells from cord blood	blood
19	chr7:7761000-7777800	Weak transcription	Thymus	Thymus
20	chr7:7761600-7770800	Weak transcription	Primary B cells from peripheral blood	blood
21	chr7:7765600-7770600	Weak transcription	Left Ventricle	heart
22	chr7:7767400-7771400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr7:7767400-7776400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr7:7769000-7771600	Enhancers	Fetal Muscle Leg	muscle
25	chr7:7769200-7773800	Enhancers	HepG2	liver
26	chr7:7769400-7772000	Weak transcription	Brain Substantia Nigra	brain
27	chr7:7769800-7772400	Enhancers	Stomach Mucosa	stomach
28	chr7:7770000-7772000	Enhancers	Brain Germinal Matrix	brain
29	chr7:7770200-7770600	Weak transcription	Hela-S3	cervix
30	chr7:7770600-7771000	Enhancers	Fetal Muscle Trunk	muscle
31	chr7:7770600-7771000	Enhancers	Left Ventricle	heart
32	chr7:7770600-7771000	Enhancers	Pancreas	Pancrea
33	chr7:7770600-7771600	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr7:7770600-7772000	Enhancers	HUVEC	blood vessel
35	chr7:7770600-7772600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr7:7770600-7773400	Enhancers	Hela-S3	cervix
37	chr7:7770800-7771200	Enhancers	Fetal Intestine Small	intestine
38	chr7:7770800-7771600	Enhancers	Fetal Intestine Large	intestine
39	chr7:7770800-7771600	Enhancers	Ovary	ovary
40	chr7:7770800-7771600	Enhancers	Small Intestine	intestine
41	chr7:7770800-7773200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr7:7771000-7773000	Enhancers	A549	lung
43	chr7:7771000-7773200	Enhancers	HSMMtube	muscle
44	chr7:7771000-7773400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr7:7771000-7773600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:7771000-7773800	Enhancers	Muscle Satellite Cultured Cells	--
47	chr7:7771000-7773800	Enhancers	HSMM	muscle
48	chr7:7771000-7776400	Weak transcription	Fetal Muscle Trunk	muscle
49	chr7:7771000-7785600	Weak transcription	Pancreas	Pancrea
50	chr7:7771200-7772800	Enhancers	Rectal Smooth Muscle	rectum

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