Variant report

Variant	nsv1024940
Chromosome Location	chr7:11276392-11310923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:227)
CpG islands
(count:184)
Chromatin interactive
region (count:22)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:227 , 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	chr7:11287818-11288185	HepG2	liver:	n/a	n/a
2	ATF1	chr7:11295980-11296164	K562	blood:	n/a	n/a
3	BACH1	chr7:11296612-11296698	K562	blood:	n/a	n/a
4	BHLHE40	chr7:11305072-11305074	K562	blood:	n/a	n/a
5	BHLHE40	chr7:11297291-11297301	K562	blood:	n/a	n/a
6	CEBPB	chr7:11287633-11287947	HepG2	liver:	n/a	chr7:11287751-11287762
7	CEBPB	chr7:11300941-11301574	MCF-7	breast:	n/a	n/a
8	CEBPB	chr7:11302619-11302868	A549	lung:	n/a	chr7:11302772-11302785
9	CEBPB	chr7:11294783-11295348	MCF-7	breast:	n/a	n/a
10	CEBPB	chr7:11287597-11288246	MCF-7	breast:	n/a	chr7:11287751-11287762
11	CEBPB	chr7:11301044-11301564	MCF-7	breast:	n/a	n/a
12	CEBPB	chr7:11301110-11301336	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr7:11301080-11301230	HEK293	kidney:	n/a	n/a
14	CTCF	chr7:11282007-11282112	K562	blood:	n/a	n/a
15	CTCF	chr7:11281913-11282186	K562	blood:	n/a	n/a
16	CTCF	chr7:11301080-11301230	BE2_C	brain:	n/a	n/a
17	CTCF	chr7:11301260-11301410	MCF-7	breast:	n/a	n/a
18	CTCF	chr7:11301240-11301390	BE2_C	brain:	n/a	n/a
19	CTCF	chr7:11290710-11290764	ProgFib	skin:	n/a	n/a
20	CTCF	chr7:11292535-11292546	K562	blood:	n/a	n/a
21	CUX1	chr7:11288771-11288842	K562	blood:	n/a	n/a
22	E2F4	chr7:11278642-11279166	MCF10A-Er-Src	breast:	n/a	n/a
23	ELK1	chr7:11305006-11305007	K562	blood:	n/a	n/a
24	EP300	chr7:11304843-11305046	K562	blood:	n/a	n/a
25	EP300	chr7:11300996-11301672	MCF-7	breast:	n/a	n/a
26	EP300	chr7:11282998-11285334	SK-N-SH	brain:	n/a	n/a
27	EP300	chr7:11283334-11284143	SK-N-SH_RA	brain:	n/a	n/a
28	EP300	chr7:11301140-11301318	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr7:11300938-11301511	T-47D	breast:	n/a	chr7:11300982-11300996
30	EP300	chr7:11301105-11301509	T-47D	breast:	n/a	n/a
31	EP300	chr7:11300904-11301564	MCF-7	breast:	n/a	chr7:11300982-11300996
32	EP300	chr7:11301374-11301474	K562	blood:	n/a	n/a
33	EP300	chr7:11283772-11284178	SK-N-SH_RA	brain:	n/a	n/a
34	ESR1	chr7:11300978-11301489	T-47D	breast:	n/a	n/a
35	ESR1	chr7:11301061-11301432	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr7:11301024-11301465	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr7:11301034-11301359	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr7:11300955-11301502	T-47D	breast:	n/a	n/a
39	ESR1	chr7:11300963-11301512	T-47D	breast:	n/a	n/a
40	ESR1	chr7:11301007-11301413	T-47D	breast:	n/a	n/a
41	ESR1	chr7:11301084-11301383	ECC-1	luminal epithelium:	n/a	n/a
42	ESR1	chr7:11300963-11301474	T-47D	breast:	n/a	n/a
43	ESR1	chr7:11300942-11301489	T-47D	breast:	n/a	n/a
44	FOS	chr7:11301130-11301503	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr7:11301096-11301593	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr7:11278984-11279306	MCF10A-Er-Src	breast:	n/a	chr7:11279141-11279150
47	FOS	chr7:11301283-11301472	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr7:11278951-11279343	MCF10A-Er-Src	breast:	n/a	chr7:11279141-11279150
49	FOS	chr7:11293819-11294156	MCF10A-Er-Src	breast:	n/a	chr7:11293969-11293977
50	FOS	chr7:11293849-11294192	MCF10A-Er-Src	breast:	n/a	chr7:11293969-11293977

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11292672-11292722	NHDF-neo	bronchial:	n/a
2	chr7:11292672-11292722	NHDF-neo	bronchial:	n/a
3	chr7:11291686-11291736	Hepatocyte	liver:	n/a
4	chr7:11279531-11279581	NHBE	bronchial:	n/a
5	chr7:11291686-11291736	A549	lung:	n/a
6	chr7:11291686-11291736	GM12891	blood:	n/a
7	chr7:11292672-11292722	HRPEpiC	eye:	n/a
8	chr7:11292672-11292722	SAEC	small airway:	n/a
9	chr7:11291686-11291736	BJ	skin:	n/a
10	chr7:11291686-11291736	Jurkat	blood:	n/a
11	chr7:11292672-11292722	GM19239	blood:	n/a
12	chr7:11279531-11279581	SK-N-SH	brain:	n/a
13	chr7:11279531-11279581	AG04450	lung:	fetal
14	chr7:11292672-11292722	H1-hESC	embryonic stem cell:	embryo
15	chr7:11291686-11291736	HEEpiC	esophagus:	n/a
16	chr7:11292672-11292722	HepG2	liver:	n/a
17	chr7:11292672-11292722	Caco-2	colon:	n/a
18	chr7:11292672-11292722	AG09309	skin:	n/a
19	chr7:11291686-11291736	GM12878	blood:	n/a
20	chr7:11291686-11291736	HAEpiC	amniotic membrane:	n/a
21	chr7:11291686-11291736	HCT-116	colon:	n/a
22	chr7:11279531-11279581	HIPEpiC	eye:	n/a
23	chr7:11292672-11292722	GM12878	blood:	n/a
24	chr7:11291686-11291736	SKMC	muscle:	n/a
25	chr7:11291686-11291736	NHDF-neo	bronchial:	n/a
26	chr7:11291686-11291736	ECC-1	luminal epithelium:	n/a
27	chr7:11279531-11279581	MCF10A-Er-Src	breast:	n/a
28	chr7:11292672-11292722	SK-N-SH	brain:	n/a
29	chr7:11292672-11292722	AG10803	skin:	n/a
30	chr7:11292672-11292722	NT2-D1	testis:	n/a
31	chr7:11291686-11291736	SAEC	small airway:	n/a
32	chr7:11291686-11291736	RPTEC	kidney:	n/a
33	chr7:11291686-11291736	U87	brain:	n/a
34	chr7:11291686-11291736	HUVEC	blood vessel:	n/a
35	chr7:11291686-11291736	AG09319	gingival:	n/a
36	chr7:11279531-11279581	Hepatocyte	liver:	n/a
37	chr7:11292672-11292722	RPTEC	kidney:	n/a
38	chr7:11291686-11291736	NT2-D1	testis:	n/a
39	chr7:11279531-11279581	SAEC	small airway:	n/a
40	chr7:11292672-11292722	LNCaP	prostate:	n/a
41	chr7:11279531-11279581	HRPEpiC	eye:	n/a
42	chr7:11279531-11279581	HRE	kidney:	n/a
43	chr7:11291686-11291736	GM06990	blood:	n/a
44	chr7:11291686-11291736	PrEC	prostate:	n/a
45	chr7:11291686-11291736	PANC-1	pancreas:	n/a
46	chr7:11292672-11292722	AG04450	lung:	fetal
47	chr7:11279531-11279581	K562	blood:	n/a
48	chr7:11291686-11291736	ProgFib	skin:	n/a
49	chr7:11279531-11279581	PrEC	prostate:	n/a
50	chr7:11292672-11292722	HEK293	kidney:	embryo

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:11305179..11307568-chr7:11307740..11310059,2	K562	blood:
2	chr7:11277040..11279683-chr7:11299557..11301437,2	MCF-7	breast:
3	chr7:11300390..11302568-chr7:11306434..11309079,2	K562	blood:
4	chr7:11292499..11294774-chr7:11295925..11298788,3	K562	blood:
5	chr7:11300390..11302568-chr7:11306434..11309079,2	K562	blood:
6	chr7:11277040..11279683-chr7:11299557..11301437,2	MCF-7	breast:
7	chr6:27880639..27883461-chr7:11306851..11309270,2	MCF-7	breast:
8	chr7:11283625..11286458-chr7:11299427..11301201,2	MCF-7	breast:
9	chr7:11271128..11274673-chr7:11275122..11277135,3	MCF-7	breast:
10	chr7:11287653..11289211-chr7:11291988..11294174,2	MCF-7	breast:
11	chr7:11283625..11286458-chr7:11299427..11301201,2	MCF-7	breast:
12	chr7:11292499..11294774-chr7:11295300..11298788,3	K562	blood:
13	chr7:11305179..11307568-chr7:11307740..11310059,2	K562	blood:
14	chr7:11252043..11254339-chr7:11287708..11289525,2	MCF-7	breast:
15	chr7:11292499..11294774-chr7:11295300..11298788,3	K562	blood:
16	chr7:11271122..11274578-chr7:11276351..11278199,3	MCF-7	breast:
17	chr7:11282275..11284554-chr7:11292723..11294327,2	MCF-7	breast:
18	chr7:11310747..11312959-chr7:11363468..11365814,2	MCF-7	breast:
19	chr7:11270835..11273820-chr7:11282821..11286972,3	MCF-7	breast:
20	chr7:11300668..11301550-chr7:11377175..11377834,2	MCF-7	breast:
21	chr7:11267788..11269326-chr7:11281868..11283883,2	K562	blood:
22	chr7:11292499..11294774-chr7:11295925..11298788,3	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF14-1	chr7:11292257-11293759	NONHSAT119212
2	lnc-PHF14-1	chr7:11283885-11284106	ENSG00000230333.1
3	lnc-PHF14-1	chr7:11283885-11284106	ENSG00000230333.1
4	lnc-PHF14-1	chr7:11293826-11295704	NONHSAT119212
5	lnc-PHF14-1	chr7:11292607-11292852	ENSG00000230333.1
6	lnc-PHF14-1	chr7:11287920-11288002	ENSG00000230333.1
7	lnc-THSD7A-2	chr7:11297308-11298162	NONHSAT119215
8	lnc-PHF14-1	chr7:11292740-11292852	ENSG00000230333.1

No data

Variant related genes	Relation type
NPM1P11	TF binding region
ENSG00000230333	TF binding region
NPM1P11	CpG island
ENSG00000230333	CpG island
ENSG00000226827	chromatin interactions
ENSG00000230333	chromatin interactions

Extended variants
information (count: 1691 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1691 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4720950	chr7:11276392-11276393	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556095241	chr7:11276405-11276406	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549216370	chr7:11276453-11276454	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115792652	chr7:11276479-11276480	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs541865536	chr7:11276481-11276482	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12055949	chr7:11276492-11276493	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs527816242	chr7:11276510-11276511	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540399187	chr7:11276549-11276550	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560110737	chr7:11276584-11276585	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532413730	chr7:11276587-11276588	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10233910	chr7:11276602-11276603	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568823779	chr7:11276623-11276624	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs202192575	chr7:11276643-11276644	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs77765117	chr7:11276657-11276658	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs397941881	chr7:11276669-11276670	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190515268	chr7:11276672-11276673	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149955459	chr7:11276674-11276675	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs568134646	chr7:11276679-11276680	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533679865	chr7:11276746-11276747	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs10263230	chr7:11276747-11276748	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs368916617	chr7:11276752-11276753	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571872861	chr7:11276760-11276761	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs10263381	chr7:11276859-11276860	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs181999423	chr7:11276889-11276890	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs374500999	chr7:11276924-11276925	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs11973276	chr7:11276932-11276933	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs113183652	chr7:11276959-11276960	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs576367856	chr7:11276995-11276996	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs10263522	chr7:11277021-11277022	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs77592352	chr7:11277039-11277040	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs368721180	chr7:11277062-11277063	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs572473978	chr7:11277069-11277070	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs541181244	chr7:11277090-11277091	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs149073642	chr7:11277165-11277166	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs577115579	chr7:11277216-11277217	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs187605890	chr7:11277274-11277275	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535495396	chr7:11277279-11277280	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs75744311	chr7:11277303-11277304	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs531673405	chr7:11277320-11277321	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs143091486	chr7:11277325-11277326	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs555178713	chr7:11277354-11277355	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs138704239	chr7:11277371-11277372	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs191541520	chr7:11277401-11277402	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs6460795	chr7:11277413-11277414	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs539635234	chr7:11277427-11277428	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs118153096	chr7:11277430-11277431	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs6460796	chr7:11277475-11277476	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs569992235	chr7:11277483-11277484	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs375997505	chr7:11277496-11277497	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs535766566	chr7:11277504-11277505	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
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
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD

Chromatin state (count:148 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11269200-11276400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:11270800-11276400	Weak transcription	Fetal Kidney	kidney
3	chr7:11271800-11277400	Weak transcription	Right Atrium	heart
4	chr7:11272400-11277400	Weak transcription	Ovary	ovary
5	chr7:11274200-11277400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr7:11274400-11276400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr7:11274400-11276400	Weak transcription	NH-A	brain
8	chr7:11274400-11276600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:11274400-11276600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr7:11274600-11277200	Weak transcription	Duodenum Mucosa	Duodenum
11	chr7:11274600-11277200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr7:11274600-11277400	Weak transcription	Adipose Nuclei	Adipose
13	chr7:11274800-11276600	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr7:11274800-11276800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:11274800-11276800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr7:11274800-11277400	Weak transcription	Fetal Intestine Small	intestine
17	chr7:11274800-11277400	Weak transcription	Gastric	stomach
18	chr7:11274800-11283800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:11275000-11277400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:11275400-11276400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr7:11275400-11276600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr7:11275400-11277000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:11275800-11277000	Enhancers	Fetal Lung	lung
24	chr7:11275800-11277400	Enhancers	Liver	Liver
25	chr7:11276200-11276400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr7:11276200-11277000	Enhancers	Stomach Mucosa	stomach
27	chr7:11276200-11278000	Enhancers	Brain Germinal Matrix	brain
28	chr7:11276400-11276600	Enhancers	Fetal Intestine Large	intestine
29	chr7:11276400-11277000	Enhancers	NH-A	brain
30	chr7:11276400-11277200	Enhancers	Fetal Kidney	kidney
31	chr7:11276400-11277400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr7:11276400-11277400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:11276400-11277800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr7:11276400-11278000	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr7:11276600-11277400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr7:11276600-11277400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr7:11276600-11277800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr7:11276600-11278000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr7:11276800-11277400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:11276800-11277800	Enhancers	H1 Cell Line	embryonic stem cell
41	chr7:11277000-11277200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:11277000-11277200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr7:11277000-11277400	Weak transcription	Fetal Intestine Large	intestine
44	chr7:11277000-11277400	Weak transcription	Left Ventricle	heart
45	chr7:11277000-11292600	Weak transcription	Stomach Mucosa	stomach
46	chr7:11277200-11277400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr7:11277200-11277400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr7:11277200-11277400	Enhancers	Duodenum Mucosa	Duodenum
49	chr7:11277200-11277400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:11277200-11277800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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