Variant report

Variant	nsv889085
Chromosome Location	chr7:117214089-117246315
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:335)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:117228213-117228911	GM12878	blood:	n/a	n/a
2	ATF2	chr7:117228256-117228885	GM12878	blood:	n/a	n/a
3	ATF3	chr7:117228178-117228937	A549	lung:	n/a	n/a
4	ATF3	chr7:117222102-117222912	A549	lung:	n/a	n/a
5	ATF3	chr7:117222180-117222830	A549	lung:	n/a	n/a
6	BACH1	chr7:117245114-117245164	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr7:117228364-117228827	GM12878	blood:	n/a	chr7:117228615-117228626
8	BCL11A	chr7:117228325-117228839	GM12878	blood:	n/a	n/a
9	BCL3	chr7:117245619-117246225	A549	lung:	n/a	n/a
10	BCL3	chr7:117228101-117228945	A549	lung:	n/a	n/a
11	BCL3	chr7:117222144-117222940	A549	lung:	n/a	chr7:117222627-117222634
12	BCL3	chr7:117222062-117223040	A549	lung:	n/a	chr7:117222627-117222634
13	BCL3	chr7:117228214-117228853	A549	lung:	n/a	n/a
14	BCLAF1	chr7:117228370-117228794	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:117228373-117228856	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:117243779-117244031	GM12878	blood:	n/a	n/a
17	BRCA1	chr7:117228113-117228980	Hela-S3	cervix:	n/a	chr7:117228650-117228657
18	BRCA1	chr7:117222167-117222831	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr7:117245834-117246047	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:117245562-117246203	A549	lung:	n/a	n/a
21	CEBPB	chr7:117227809-117228967	Hela-S3	cervix:	n/a	chr7:117228586-117228597
22	CEBPB	chr7:117221920-117222859	A549	lung:	n/a	chr7:117222302-117222313
23	CEBPB	chr7:117228036-117228960	A549	lung:	n/a	chr7:117228586-117228597
24	CEBPB	chr7:117222032-117222940	Hela-S3	cervix:	n/a	chr7:117222302-117222313
25	CEBPB	chr7:117221884-117223012	A549	lung:	n/a	chr7:117222302-117222313
26	CEBPB	chr7:117222117-117222867	IMR90	lung:	n/a	chr7:117222302-117222313
27	CEBPB	chr7:117228431-117228821	IMR90	lung:	n/a	chr7:117228586-117228597
28	CEBPB	chr7:117222135-117222657	MCF-7	breast:	n/a	chr7:117222302-117222313
29	CEBPB	chr7:117222054-117222935	A549	lung:	n/a	chr7:117222302-117222313
30	CEBPB	chr7:117222133-117222567	HepG2	liver:	n/a	chr7:117222302-117222313
31	CEBPB	chr7:117228349-117228788	MCF-7	breast:	n/a	chr7:117228586-117228597
32	CEBPB	chr7:117245738-117246078	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:117222244-117222431	K562	blood:	n/a	chr7:117222302-117222313
34	CEBPB	chr7:117222236-117222366	HepG2	liver:	n/a	chr7:117222302-117222313
35	CEBPB	chr7:117228203-117228832	A549	lung:	n/a	chr7:117228586-117228597
36	CHD2	chr7:117228247-117228854	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr7:117228282-117228913	GM12878	blood:	n/a	n/a
38	CHD2	chr7:117222172-117222928	Hela-S3	cervix:	n/a	n/a
39	CREB1	chr7:117222364-117222750	A549	lung:	n/a	n/a
40	CREB1	chr7:117222454-117222759	A549	lung:	n/a	n/a
41	CTCF	chr7:117223370-117223403	Lung_OC	lung:	n/a	n/a
42	CTCF	chr7:117232459-117232519	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:117232469-117232518	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:117242060-117242210	K562	blood:	n/a	n/a
45	CTCF	chr7:117232453-117232475	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr7:117236439-117236509	Fibrobl	skin:	n/a	n/a
47	CTCF	chr7:117232488-117232514	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:117232437-117232563	A549	lung:	n/a	n/a
49	CTCF	chr7:117236460-117236610	GM12866	blood:	n/a	n/a
50	CUX1	chr7:117228355-117228961	GM12878	blood:	n/a	chr7:117228518-117228529

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:117228958-117229008	MCF-7	breast:	n/a
2	chr7:117228958-117229008	HCPEpiC	choroid plexus:	n/a
3	chr7:117228958-117229008	SK-N-SH_RA	brain:	n/a
4	chr7:117228958-117229008	ECC-1	luminal epithelium:	n/a
5	chr7:117228958-117229008	AG09319	gingival:	n/a
6	chr7:117228958-117229008	GM12892	blood:	n/a
7	chr7:117228958-117229008	LNCaP	prostate:	n/a
8	chr7:117228958-117229008	HEEpiC	esophagus:	n/a
9	chr7:117228958-117229008	Caco-2	colon:	n/a
10	chr7:117228958-117229008	AG10803	skin:	n/a
11	chr7:117228958-117229008	GM12891	blood:	n/a
12	chr7:117228958-117229008	HUVEC	blood vessel:	n/a
13	chr7:117228958-117229008	K562	blood:	n/a
14	chr7:117228958-117229008	SK-N-MC	brain:	n/a
15	chr7:117228958-117229008	HIPEpiC	eye:	n/a
16	chr7:117228958-117229008	HPAEpiC	pulmonary alveolar:	n/a
17	chr7:117228958-117229008	BE2_C	brain:	n/a
18	chr7:117228958-117229008	MCF10A-Er-Src	breast:	n/a
19	chr7:117228958-117229008	BJ	skin:	n/a
20	chr7:117228958-117229008	CMK	blood:	n/a
21	chr7:117228958-117229008	Jurkat	blood:	n/a
22	chr7:117228958-117229008	GM12878	blood:	n/a
23	chr7:117228958-117229008	HCF	heart:	n/a
24	chr7:117228958-117229008	AG04449	skin:	fetal
25	chr7:117228958-117229008	T-47D	breast:	n/a
26	chr7:117228958-117229008	Hepatocyte	liver:	n/a
27	chr7:117228958-117229008	NH-A	brain:	n/a
28	chr7:117228958-117229008	PANC-1	pancreas:	n/a
29	chr7:117228958-117229008	ovcar-3	ovarian:	n/a
30	chr7:117228958-117229008	HRE	kidney:	n/a
31	chr7:117228958-117229008	AG09309	skin:	n/a
32	chr7:117228958-117229008	PFSK-1	brain:	n/a
33	chr7:117228958-117229008	HNPCEpiC	eye:	n/a
34	chr7:117228958-117229008	PrEC	prostate:	n/a
35	chr7:117228958-117229008	SK-N-SH	brain:	n/a
36	chr7:117228958-117229008	RPTEC	kidney:	n/a
37	chr7:117228958-117229008	HepG2	liver:	n/a
38	chr7:117228958-117229008	HL-60	blood:	n/a
39	chr7:117228958-117229008	HAEpiC	amniotic membrane:	n/a
40	chr7:117228958-117229008	ProgFib	skin:	n/a
41	chr7:117228958-117229008	GM06990	blood:	n/a
42	chr7:117228958-117229008	A549	lung:	n/a
43	chr7:117228958-117229008	NHBE	bronchial:	n/a
44	chr7:117228958-117229008	U87	brain:	n/a
45	chr7:117228958-117229008	HRCEpiC	kidney:	n/a
46	chr7:117228958-117229008	HCT-116	colon:	n/a
47	chr7:117228958-117229008	NHDF-neo	bronchial:	n/a
48	chr7:117228958-117229008	NT2-D1	testis:	n/a
49	chr7:117228958-117229008	H1-hESC	embryonic stem cell:	embryo
50	chr7:117228958-117229008	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:117100350-117112126..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
2	7:115861595-115870968..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
3	7:116544149-116547624..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
4	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
5	chr12:58237960..58239522-chr7:117246298..117249075,2	MCF-7	breast:
6	7:116754962-116765597..7:117228556-117233275	Hela-S3	cervix:
7	7:115861595-115870968..7:117216968-117220729	H1-hESC	embryonic stem cell:	embryo
8	chr7:117244166..117245859-chr7:117250473..117252926,2	MCF-7	breast:
9	7:115847372-115857098..7:117228556-117233275	H1-hESC	embryonic stem cell:	embryo
10	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTTNBP2-1	chr7:117244845-117245043	ENSG00000083622.8
2	lnc-CTTNBP2-4	chr7:117226261-117226470	NONHSAT122949

No data

Variant related genes	Relation type
ENSG00000234001	TF binding region
ENSG00000234001	CpG island
ENSG00000004866	chromatin interactions
ENSG00000001626	chromatin interactions
ENSG00000175215	chromatin interactions
ENSG00000135269	chromatin interactions

Extended variants
information (count: 1272 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1272 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3808185	chr7:117214089-117214090	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3808184	chr7:117214125-117214126	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs533270392	chr7:117214149-117214150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570965903	chr7:117214195-117214196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192751455	chr7:117214204-117214205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563534852	chr7:117214222-117214223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530611728	chr7:117214274-117214275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2518872	chr7:117214373-117214374	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567452242	chr7:117214396-117214397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534875384	chr7:117214422-117214423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182460	chr7:117214451-117214452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs17547485	chr7:117214471-117214472	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs573575904	chr7:117214543-117214544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs213991	chr7:117214614-117214615	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs183814653	chr7:117214622-117214623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576623162	chr7:117214624-117214625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537250077	chr7:117214625-117214626	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555886625	chr7:117214675-117214676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574264837	chr7:117214749-117214750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542883463	chr7:117214850-117214851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541296483	chr7:117214887-117214888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559348134	chr7:117214891-117214892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188188808	chr7:117214932-117214933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs180803449	chr7:117214942-117214943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs563631285	chr7:117214952-117214953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141952948	chr7:117214955-117214956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548914824	chr7:117214993-117214994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560360685	chr7:117215007-117215008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1366913	chr7:117215025-117215026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138417954	chr7:117215026-117215027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572984530	chr7:117215059-117215060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186444233	chr7:117215157-117215158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs527820846	chr7:117215211-117215212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571303607	chr7:117215273-117215274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529952448	chr7:117215339-117215340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376575323	chr7:117215417-117215418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs34013793	chr7:117215421-117215422	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1429560	chr7:117215484-117215485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs567491371	chr7:117215550-117215551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544921648	chr7:117215571-117215572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536308161	chr7:117215587-117215588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143532442	chr7:117215591-117215592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530993180	chr7:117215603-117215604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4570091	chr7:117215705-117215706	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553243817	chr7:117215706-117215707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35603916	chr7:117215740-117215741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189238645	chr7:117215800-117215801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs545006676	chr7:117215847-117215848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557282769	chr7:117215856-117215857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575665787	chr7:117215956-117215957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Sudden cardiac death	19188705	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117206400-117216800	Weak transcription	Small Intestine	intestine
2	chr7:117206600-117217600	Weak transcription	Duodenum Mucosa	Duodenum
3	chr7:117208600-117232400	Weak transcription	Pancreas	Pancrea
4	chr7:117211400-117214200	Enhancers	Fetal Intestine Large	intestine
5	chr7:117211600-117214200	Enhancers	Fetal Intestine Small	intestine
6	chr7:117212600-117214200	Enhancers	Fetal Heart	heart
7	chr7:117213400-117214400	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr7:117213600-117220400	Weak transcription	A549	lung
9	chr7:117213800-117214800	Enhancers	Stomach Mucosa	stomach
10	chr7:117214000-117228000	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr7:117214200-117216200	Weak transcription	Fetal Intestine Small	intestine
12	chr7:117214200-117216600	Weak transcription	Fetal Intestine Large	intestine
13	chr7:117214400-117228000	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr7:117216200-117217800	Enhancers	Fetal Intestine Small	intestine
15	chr7:117216600-117217400	Enhancers	Fetal Intestine Large	intestine
16	chr7:117216600-117218200	Enhancers	Dnd41	blood
17	chr7:117216800-117217000	Enhancers	Fetal Heart	heart
18	chr7:117216800-117217000	Enhancers	Small Intestine	intestine
19	chr7:117216800-117217200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr7:117216800-117217200	Enhancers	Fetal Thymus	thymus
21	chr7:117216800-117217400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:117216800-117235600	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr7:117217200-117226000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr7:117217400-117222000	Weak transcription	Fetal Intestine Large	intestine
25	chr7:117217400-117222800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:117217600-117218400	Strong transcription	Duodenum Mucosa	Duodenum
27	chr7:117217800-117218200	Weak transcription	Fetal Intestine Small	intestine
28	chr7:117218200-117218800	Strong transcription	Fetal Intestine Small	intestine
29	chr7:117218400-117228000	Weak transcription	Duodenum Mucosa	Duodenum
30	chr7:117218800-117221800	Weak transcription	Fetal Intestine Small	intestine
31	chr7:117220400-117223000	Enhancers	A549	lung
32	chr7:117220600-117223200	Enhancers	Hela-S3	cervix
33	chr7:117221800-117222200	Genic enhancers	Fetal Intestine Small	intestine
34	chr7:117221800-117222200	Enhancers	Placenta	Placenta
35	chr7:117221800-117222400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr7:117221800-117222600	Enhancers	Colon Smooth Muscle	Colon
37	chr7:117221800-117222800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr7:117221800-117223000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr7:117222000-117222200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr7:117222000-117223000	Enhancers	Fetal Intestine Large	intestine
41	chr7:117222200-117222600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr7:117222200-117222800	Enhancers	Fetal Intestine Small	intestine
43	chr7:117222200-117223000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr7:117222200-117223000	Enhancers	Liver	Liver
45	chr7:117222200-117223600	Enhancers	Fetal Heart	heart
46	chr7:117222200-117225800	Weak transcription	Placenta	Placenta
47	chr7:117222400-117222800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:117222400-117222800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr7:117222400-117222800	Enhancers	Aorta	Aorta
50	chr7:117222400-117222800	Enhancers	Fetal Lung	lung

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