Variant report

Variant	nsv606047
Chromosome Location	chr7:7929851-7946400
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:108)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:108 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:7930377-7930681	A549	lung:	n/a	chr7:7930559-7930570
2	CEBPB	chr7:7931313-7931502	K562	blood:	n/a	chr7:7931359-7931370 chr7:7931461-7931472 chr7:7931465-7931476
3	CEBPB	chr7:7930431-7930664	K562	blood:	n/a	chr7:7930559-7930570
4	CEBPB	chr7:7931285-7931446	IMR90	lung:	n/a	chr7:7931359-7931370
5	CEBPB	chr7:7930422-7930730	IMR90	lung:	n/a	chr7:7930559-7930570
6	CEBPB	chr7:7931303-7931494	HepG2	liver:	n/a	chr7:7931359-7931370 chr7:7931461-7931472 chr7:7931465-7931476
7	CEBPB	chr7:7930459-7930578	H1-hESC	embryonic stem cell:	n/a	chr7:7930559-7930570
8	CEBPB	chr7:7930400-7930739	HepG2	liver:	n/a	chr7:7930559-7930570
9	CTCF	chr7:7930033-7930104	GM19238	blood:	n/a	n/a
10	CTCF	chr7:7929934-7930107	MCF-7	breast:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
11	CTCF	chr7:7939926-7939961	Fibrobl	skin:	n/a	n/a
12	CTCF	chr7:7930033-7930100	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:7931632-7931699	GM20000	blood:	n/a	n/a
14	CTCF	chr7:7935460-7935610	SAEC	small airway:	n/a	n/a
15	CTCF	chr7:7935455-7935640	MCF-7	breast:	n/a	n/a
16	CTCF	chr7:7929980-7930130	MCF-7	breast:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
17	CTCF	chr7:7935458-7935651	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:7929939-7930118	Hela-S3	cervix:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
19	CTCF	chr7:7930031-7930095	MCF-7	breast:	n/a	n/a
20	CTCF	chr7:7936838-7936849	Fibrobl	skin:	n/a	n/a
21	CTCF	chr7:7929997-7930033	ProgFib	skin:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
22	CTCF	chr7:7935380-7935530	HMEC	breast:	n/a	n/a
23	CTCF	chr7:7935460-7935610	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr7:7935503-7935594	LNCaP	prostate:	n/a	n/a
25	CTCF	chr7:7935527-7935613	LNCaP	prostate:	n/a	n/a
26	CTCF	chr7:7929840-7929990	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:7935342-7935715	MCF-7	breast:	n/a	n/a
28	CTCF	chr7:7935494-7935606	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr7:7935460-7935610	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:7929859-7930201	K562	blood:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
31	CTCF	chr7:7930020-7930170	MCF-7	breast:	n/a	n/a
32	CTCF	chr7:7935436-7935656	MCF-7	breast:	n/a	n/a
33	CTCF	chr7:7930040-7930190	HMEC	breast:	n/a	n/a
34	CTCF	chr7:7935420-7935570	SAEC	small airway:	n/a	n/a
35	CTCF	chr7:7935458-7935555	GM12878	blood:	n/a	n/a
36	CTCF	chr7:7929900-7930050	WERI-Rb-1	eye:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
37	CTCF	chr7:7929966-7930043	GM12878	blood:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
38	CTCF	chr7:7929860-7930010	BE2_C	brain:	n/a	n/a
39	CTCF	chr7:7935305-7935673	MCF-7	breast:	n/a	n/a
40	CTCF	chr7:7933560-7933710	GM06990	blood:	n/a	n/a
41	CTCF	chr7:7935455-7935647	MCF-7	breast:	n/a	n/a
42	CTCF	chr7:7929940-7930090	WERI-Rb-1	eye:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
43	CTCF	chr7:7935480-7935630	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr7:7929880-7930030	GM12864	blood:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
45	CTCF	chr7:7935525-7935597	Medullo	brain:	n/a	n/a
46	CTCF	chr7:7935420-7935570	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:7935465-7935640	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:7935517-7935569	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr7:7929920-7930070	BE2_C	brain:	n/a	chr7:7930007-7930028 chr7:7930013-7930029
50	CTCF	chr7:7929960-7930110	K562	blood:	n/a	chr7:7930007-7930028 chr7:7930013-7930029

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:7936962-7937012	AG09319	gingival:	n/a
2	chr7:7936962-7937012	NH-A	brain:	n/a
3	chr7:7936962-7937012	PrEC	prostate:	n/a
4	chr7:7936962-7937012	HCT-116	colon:	n/a
5	chr7:7936962-7937012	GM19239	blood:	n/a
6	chr7:7936962-7937012	HEEpiC	esophagus:	n/a
7	chr7:7936962-7937012	HL-60	blood:	n/a
8	chr7:7936962-7937012	HCM	heart:	n/a
9	chr7:7936962-7937012	NB4	blood:	n/a
10	chr7:7936962-7937012	RPTEC	kidney:	n/a
11	chr7:7936962-7937012	HNPCEpiC	eye:	n/a
12	chr7:7936962-7937012	Hepatocyte	liver:	n/a
13	chr7:7936962-7937012	AG04449	skin:	fetal
14	chr7:7936962-7937012	HIPEpiC	eye:	n/a
15	chr7:7936962-7937012	HAEpiC	amniotic membrane:	n/a
16	chr7:7936962-7937012	SK-N-MC	brain:	n/a
17	chr7:7936962-7937012	HRPEpiC	eye:	n/a
18	chr7:7936962-7937012	SK-N-SH	brain:	n/a
19	chr7:7936962-7937012	GM12878	blood:	n/a
20	chr7:7936962-7937012	ECC-1	luminal epithelium:	n/a
21	chr7:7936962-7937012	PFSK-1	brain:	n/a
22	chr7:7936962-7937012	SK-N-SH_RA	brain:	n/a
23	chr7:7936962-7937012	GM12891	blood:	n/a
24	chr7:7936962-7937012	AG10803	skin:	n/a
25	chr7:7936962-7937012	T-47D	breast:	n/a
26	chr7:7936962-7937012	MCF10A-Er-Src	breast:	n/a
27	chr7:7936962-7937012	Caco-2	colon:	n/a
28	chr7:7936962-7937012	H1-hESC	embryonic stem cell:	embryo
29	chr7:7936962-7937012	Hela-S3	cervix:	n/a
30	chr7:7936962-7937012	AG04450	lung:	fetal
31	chr7:7936962-7937012	HRE	kidney:	n/a
32	chr7:7936962-7937012	HMEC	breast:	n/a
33	chr7:7936962-7937012	Jurkat	blood:	n/a
34	chr7:7936962-7937012	HCPEpiC	choroid plexus:	n/a
35	chr7:7936962-7937012	HEK293	kidney:	embryo
36	chr7:7936962-7937012	BJ	skin:	n/a
37	chr7:7936962-7937012	A549	lung:	n/a
38	chr7:7936962-7937012	MCF-7	breast:	n/a
39	chr7:7936962-7937012	IMR90	lung:	fetal
40	chr7:7936962-7937012	HCF	heart:	n/a
41	chr7:7936962-7937012	U87	brain:	n/a
42	chr7:7936962-7937012	SKMC	muscle:	n/a
43	chr7:7936962-7937012	BE2_C	brain:	n/a
44	chr7:7936962-7937012	K562	blood:	n/a
45	chr7:7936962-7937012	GM12892	blood:	n/a
46	chr7:7936962-7937012	HRCEpiC	kidney:	n/a
47	chr7:7936962-7937012	PANC-1	pancreas:	n/a
48	chr7:7936962-7937012	LNCaP	prostate:	n/a
49	chr7:7936962-7937012	AG09309	skin:	n/a
50	chr7:7936962-7937012	NHDF-neo	bronchial:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:7936554..7939221-chr7:8008179..8010269,3	MCF-7	breast:
2	chr7:7908600..7910763-chr7:7934050..7936742,2	K562	blood:
3	chr7:7930260..7932176-chr7:7966125..7967661,2	K562	blood:
4	chr7:7932645..7934651-chr7:7935237..7938092,2	K562	blood:
5	chr7:7935831..7938842-chr7:8008024..8010603,3	MCF-7	breast:
6	chr7:7932645..7934651-chr7:7935237..7938092,2	K562	blood:
7	chr7:7929818..7931482-chr7:7931522..7933853,2	MCF-7	breast:
8	chr7:7929818..7931482-chr7:7931522..7933853,2	MCF-7	breast:
9	chr7:7935711..7938261-chr7:7941744..7943349,2	K562	blood:
10	chr7:7941789..7943515-chr7:8007285..8009574,2	MCF-7	breast:
11	chr7:7935711..7938261-chr7:7941744..7943349,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLCCI1-6	chr7:7939478-7939517	NONHSAT119135
2	lnc-GLCCI1-6	chr7:7938942-7939427	NONHSAT119135
3	lnc-GLCCI1-6	chr7:7935007-7935362	NONHSAT119135
4	lnc-GLCCI1-6	chr7:7933669-7934024	NONHSAT119135

No data

Variant related genes	Relation type
RNU6-534P	TF binding region
RNU6-534P	CpG island
ENSG00000233108	chromatin interactions
ENSG00000106415	chromatin interactions

Extended variants
information (count: 679 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:679 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10278724	chr7:7929851-7929852	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73045521	chr7:7929909-7929910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs553167132	chr7:7929920-7929921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183951818	chr7:7929934-7929935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs116164896	chr7:7929954-7929955	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145092061	chr7:7929961-7929962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576500730	chr7:7930026-7930027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543794577	chr7:7930027-7930028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561974975	chr7:7930029-7930030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149100613	chr7:7930033-7930034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs114968245	chr7:7930034-7930035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs7804964	chr7:7930058-7930059	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551755615	chr7:7930143-7930144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533361249	chr7:7930157-7930158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144242638	chr7:7930198-7930199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563396219	chr7:7930221-7930222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530549487	chr7:7930222-7930223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs75893031	chr7:7930234-7930235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567284044	chr7:7930299-7930300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370294141	chr7:7930309-7930310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs56008587	chr7:7930313-7930314	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs546915832	chr7:7930314-7930315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs571426208	chr7:7930318-7930319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116695763	chr7:7930324-7930325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561221200	chr7:7930338-7930339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188902769	chr7:7930347-7930348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150322232	chr7:7930374-7930375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141256913	chr7:7930379-7930380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs146953081	chr7:7930380-7930381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192632359	chr7:7930387-7930388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541289923	chr7:7930430-7930431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147998460	chr7:7930435-7930436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs578028625	chr7:7930437-7930438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73674714	chr7:7930450-7930451	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs112857299	chr7:7930493-7930494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563761908	chr7:7930516-7930517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182749644	chr7:7930529-7930530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11971467	chr7:7930535-7930536	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs539649501	chr7:7930547-7930548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186965419	chr7:7930559-7930560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150443633	chr7:7930646-7930647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11973960	chr7:7930676-7930677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs6976269	chr7:7930712-7930713	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114284440	chr7:7930716-7930717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537506583	chr7:7930730-7930731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575354964	chr7:7930763-7930764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555450403	chr7:7930777-7930778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550646059	chr7:7930801-7930802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138333061	chr7:7930862-7930863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552980113	chr7:7930899-7930900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:7897200-7942400	Weak transcription	Aorta	Aorta
2	chr7:7909600-7942400	Weak transcription	Left Ventricle	heart
3	chr7:7911600-7934800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr7:7911600-7934800	Weak transcription	Pancreas	Pancrea
5	chr7:7912200-7930000	Weak transcription	Esophagus	oesophagus
6	chr7:7912200-7934600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr7:7913200-7942400	Weak transcription	Primary T cells from cord blood	blood
8	chr7:7915800-7943000	Weak transcription	Gastric	stomach
9	chr7:7924800-7931200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr7:7924800-7932600	Weak transcription	Primary B cells from cord blood	blood
11	chr7:7924800-7933600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:7928600-7942400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr7:7929000-7934600	Weak transcription	Fetal Thymus	thymus
14	chr7:7929200-7930200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:7930000-7934600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr7:7930200-7951000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:7930400-7934600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr7:7932000-7932200	Enhancers	H9 Cell Line	embryonic stem cell
19	chr7:7932000-7932600	Enhancers	Fetal Brain Male	brain
20	chr7:7932200-7932400	Enhancers	Brain Cingulate Gyrus	brain
21	chr7:7932200-7932400	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr7:7932200-7937600	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr7:7932400-7933800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr7:7932400-7934600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr7:7932600-7933000	Weak transcription	Fetal Brain Male	brain
26	chr7:7932600-7934600	Weak transcription	Fetal Muscle Leg	muscle
27	chr7:7933000-7933400	Enhancers	Fetal Brain Male	brain
28	chr7:7933200-7933400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:7933600-7934600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:7933800-7934000	Enhancers	Brain Cingulate Gyrus	brain
31	chr7:7933800-7934600	Enhancers	Brain Hippocampus Middle	brain
32	chr7:7934000-7934200	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr7:7934000-7934600	Weak transcription	Brain Cingulate Gyrus	brain
34	chr7:7934000-7935600	Enhancers	Brain Germinal Matrix	brain
35	chr7:7934600-7934800	Enhancers	Fetal Heart	heart
36	chr7:7934600-7935000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr7:7934600-7935000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:7934600-7935000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr7:7934600-7935000	Enhancers	Muscle Satellite Cultured Cells	--
40	chr7:7934600-7935000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr7:7934600-7935000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
42	chr7:7934600-7935000	Active TSS	Brain Substantia Nigra	brain
43	chr7:7934600-7935000	Enhancers	Fetal Muscle Leg	muscle
44	chr7:7934600-7935000	Enhancers	Fetal Stomach	stomach
45	chr7:7934600-7935000	Enhancers	Fetal Thymus	thymus
46	chr7:7934600-7935000	Enhancers	Stomach Smooth Muscle	stomach
47	chr7:7934600-7935200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr7:7934600-7935200	Active TSS	Brain Angular Gyrus	brain
49	chr7:7934600-7935200	Active TSS	Brain Cingulate Gyrus	brain
50	chr7:7934600-7935400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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