Variant report

Variant	nsv889084
Chromosome Location	chr7:117212723-117246315
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:343)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:343 , 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	chr7:117222180-117222830	A549	lung:	n/a	n/a
5	ATF3	chr7:117222102-117222912	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	chr7:117228214-117228853	A549	lung:	n/a	n/a
11	BCL3	chr7:117222062-117223040	A549	lung:	n/a	chr7:117222627-117222634
12	BCL3	chr7:117222144-117222940	A549	lung:	n/a	chr7:117222627-117222634
13	BCL3	chr7:117228101-117228945	A549	lung:	n/a	n/a
14	BCLAF1	chr7:117228370-117228794	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:117243779-117244031	GM12878	blood:	n/a	n/a
16	BHLHE40	chr7:117228373-117228856	GM12878	blood:	n/a	n/a
17	BRCA1	chr7:117222167-117222831	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr7:117228113-117228980	Hela-S3	cervix:	n/a	chr7:117228650-117228657
19	BRCA1	chr7:117245834-117246047	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr7:117222117-117222867	IMR90	lung:	n/a	chr7:117222302-117222313
21	CEBPB	chr7:117212851-117213351	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
22	CEBPB	chr7:117245738-117246078	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr7:117222135-117222657	MCF-7	breast:	n/a	chr7:117222302-117222313
24	CEBPB	chr7:117227809-117228967	Hela-S3	cervix:	n/a	chr7:117228586-117228597
25	CEBPB	chr7:117245562-117246203	A549	lung:	n/a	n/a
26	CEBPB	chr7:117213004-117213146	A549	lung:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
27	CEBPB	chr7:117222236-117222366	HepG2	liver:	n/a	chr7:117222302-117222313
28	CEBPB	chr7:117221920-117222859	A549	lung:	n/a	chr7:117222302-117222313
29	CEBPB	chr7:117228203-117228832	A549	lung:	n/a	chr7:117228586-117228597
30	CEBPB	chr7:117228431-117228821	IMR90	lung:	n/a	chr7:117228586-117228597
31	CEBPB	chr7:117212837-117213239	MCF-7	breast:	n/a	chr7:117213047-117213058 chr7:117213047-117213058 chr7:117213045-117213058 chr7:117213045-117213058
32	CEBPB	chr7:117221884-117223012	A549	lung:	n/a	chr7:117222302-117222313
33	CEBPB	chr7:117222133-117222567	HepG2	liver:	n/a	chr7:117222302-117222313
34	CEBPB	chr7:117228349-117228788	MCF-7	breast:	n/a	chr7:117228586-117228597
35	CEBPB	chr7:117222244-117222431	K562	blood:	n/a	chr7:117222302-117222313
36	CEBPB	chr7:117222054-117222935	A549	lung:	n/a	chr7:117222302-117222313
37	CEBPB	chr7:117228036-117228960	A549	lung:	n/a	chr7:117228586-117228597
38	CEBPB	chr7:117222032-117222940	Hela-S3	cervix:	n/a	chr7:117222302-117222313
39	CHD2	chr7:117222172-117222928	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr7:117228282-117228913	GM12878	blood:	n/a	n/a
41	CHD2	chr7:117228247-117228854	Hela-S3	cervix:	n/a	n/a
42	CREB1	chr7:117222454-117222759	A549	lung:	n/a	n/a
43	CREB1	chr7:117222364-117222750	A549	lung:	n/a	n/a
44	CTCF	chr7:117236439-117236509	Fibrobl	skin:	n/a	n/a
45	CTCF	chr7:117232469-117232518	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:117232437-117232563	A549	lung:	n/a	n/a
47	CTCF	chr7:117236460-117236610	GM12866	blood:	n/a	n/a
48	CTCF	chr7:117242060-117242210	K562	blood:	n/a	n/a
49	CTCF	chr7:117223370-117223403	Lung_OC	lung:	n/a	n/a
50	CTCF	chr7:117232459-117232519	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:117228958-117229008	LNCaP	prostate:	n/a
2	chr7:117228958-117229008	HUVEC	blood vessel:	n/a
3	chr7:117228958-117229008	NT2-D1	testis:	n/a
4	chr7:117228958-117229008	HIPEpiC	eye:	n/a
5	chr7:117228958-117229008	SK-N-SH	brain:	n/a
6	chr7:117228958-117229008	T-47D	breast:	n/a
7	chr7:117228958-117229008	HL-60	blood:	n/a
8	chr7:117228958-117229008	ovcar-3	ovarian:	n/a
9	chr7:117228958-117229008	GM19239	blood:	n/a
10	chr7:117228958-117229008	ProgFib	skin:	n/a
11	chr7:117228958-117229008	IMR90	lung:	fetal
12	chr7:117228958-117229008	AG04450	lung:	fetal
13	chr7:117228958-117229008	HepG2	liver:	n/a
14	chr7:117228958-117229008	A549	lung:	n/a
15	chr7:117228958-117229008	PrEC	prostate:	n/a
16	chr7:117228958-117229008	SAEC	small airway:	n/a
17	chr7:117228958-117229008	NHDF-neo	bronchial:	n/a
18	chr7:117228958-117229008	PFSK-1	brain:	n/a
19	chr7:117228958-117229008	MCF10A-Er-Src	breast:	n/a
20	chr7:117228958-117229008	HRE	kidney:	n/a
21	chr7:117228958-117229008	GM12878	blood:	n/a
22	chr7:117228958-117229008	PANC-1	pancreas:	n/a
23	chr7:117228958-117229008	Jurkat	blood:	n/a
24	chr7:117228958-117229008	HMEC	breast:	n/a
25	chr7:117228958-117229008	HCPEpiC	choroid plexus:	n/a
26	chr7:117228958-117229008	BJ	skin:	n/a
27	chr7:117228958-117229008	H1-hESC	embryonic stem cell:	embryo
28	chr7:117228958-117229008	HCM	heart:	n/a
29	chr7:117228958-117229008	HEEpiC	esophagus:	n/a
30	chr7:117228958-117229008	Hela-S3	cervix:	n/a
31	chr7:117228958-117229008	U87	brain:	n/a
32	chr7:117228958-117229008	AoSMC	blood vessel:	n/a
33	chr7:117228958-117229008	HRPEpiC	eye:	n/a
34	chr7:117228958-117229008	ECC-1	luminal epithelium:	n/a
35	chr7:117228958-117229008	Caco-2	colon:	n/a
36	chr7:117228958-117229008	K562	blood:	n/a
37	chr7:117228958-117229008	AG09309	skin:	n/a
38	chr7:117228958-117229008	HNPCEpiC	eye:	n/a
39	chr7:117228958-117229008	GM12892	blood:	n/a
40	chr7:117228958-117229008	HCF	heart:	n/a
41	chr7:117228958-117229008	AG04449	skin:	fetal
42	chr7:117228958-117229008	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:117228958-117229008	NB4	blood:	n/a
44	chr7:117228958-117229008	MCF-7	breast:	n/a
45	chr7:117228958-117229008	AG10803	skin:	n/a
46	chr7:117228958-117229008	AG09319	gingival:	n/a
47	chr7:117228958-117229008	BE2_C	brain:	n/a
48	chr7:117228958-117229008	GM06990	blood:	n/a
49	chr7:117228958-117229008	SKMC	muscle:	n/a
50	chr7:117228958-117229008	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:117212776..117215963-chr7:117216725..117220462,3	MCF-7	breast:
2	7:115861595-115870968..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
3	7:116754962-116765597..7:117228556-117233275	Hela-S3	cervix:
4	chr12:58237960..58239522-chr7:117246298..117249075,2	MCF-7	breast:
5	chr7:117244166..117245859-chr7:117250473..117252926,2	MCF-7	breast:
6	7:116544149-116547624..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
7	7:117100350-117112126..7:117245849-117249704	H1-hESC	embryonic stem cell:	embryo
8	7:115847372-115857098..7:117228556-117233275	H1-hESC	embryonic stem cell:	embryo
9	7:115861595-115870968..7:117216968-117220729	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
ENSG00000135269	chromatin interactions
ENSG00000001626	chromatin interactions
ENSG00000175215	chromatin interactions
ENSG00000004866	chromatin interactions

Extended variants
information (count: 1320 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs213934	chr7:117212723-117212724	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540034840	chr7:117212846-117212847	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs565418511	chr7:117212871-117212872	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs557480194	chr7:117212903-117212904	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs140584647	chr7:117212904-117212905	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs536911804	chr7:117212929-117212930	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs183123029	chr7:117212987-117212988	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs375803630	chr7:117212988-117212989	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs530925660	chr7:117212994-117212995	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs573537496	chr7:117213015-117213016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs200211298	chr7:117213020-117213021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186871304	chr7:117213072-117213073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146811028	chr7:117213090-117213091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370235798	chr7:117213091-117213092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140989181	chr7:117213102-117213103	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3035687	chr7:117213111-117213112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377103894	chr7:117213112-117213113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs202055944	chr7:117213113-117213114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201586646	chr7:117213114-117213115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541174141	chr7:117213115-117213116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553097561	chr7:117213116-117213117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191232135	chr7:117213136-117213137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183546753	chr7:117213181-117213182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550953994	chr7:117213263-117213264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567679648	chr7:117213281-117213282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532047770	chr7:117213304-117213305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs543736009	chr7:117213317-117213318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs562145507	chr7:117213339-117213340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs555065467	chr7:117213367-117213368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs547531403	chr7:117213368-117213369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565836019	chr7:117213383-117213384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533209746	chr7:117213449-117213450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551174518	chr7:117213463-117213464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187894480	chr7:117213501-117213502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs193185173	chr7:117213621-117213622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs530392434	chr7:117213725-117213726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6945467	chr7:117213769-117213770	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs185110200	chr7:117213792-117213793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534322916	chr7:117213799-117213800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs552958573	chr7:117213930-117213931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567041604	chr7:117213945-117213946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577822760	chr7:117213948-117213949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545091876	chr7:117213978-117213979	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558406962	chr7:117213991-117213992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs576543413	chr7:117214001-117214002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147109285	chr7:117214016-117214017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190106907	chr7:117214044-117214045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574225109	chr7:117214071-117214072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs3808185	chr7:117214089-117214090	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs3808184	chr7:117214125-117214126	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:117181400-117213400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr7:117206400-117216800	Weak transcription	Small Intestine	intestine
3	chr7:117206600-117217600	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:117208600-117232400	Weak transcription	Pancreas	Pancrea
5	chr7:117211400-117214200	Enhancers	Fetal Intestine Large	intestine
6	chr7:117211600-117214200	Enhancers	Fetal Intestine Small	intestine
7	chr7:117212600-117212800	Active TSS	A549	lung
8	chr7:117212600-117213800	Enhancers	Fetal Lung	lung
9	chr7:117212600-117213800	Weak transcription	Stomach Mucosa	stomach
10	chr7:117212600-117214000	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr7:117212600-117214200	Enhancers	Fetal Heart	heart
12	chr7:117212800-117213000	Flanking Active TSS	A549	lung
13	chr7:117213000-117213600	Enhancers	A549	lung
14	chr7:117213400-117214400	Enhancers	Rectal Mucosa Donor 29	rectum
15	chr7:117213600-117220400	Weak transcription	A549	lung
16	chr7:117213800-117214800	Enhancers	Stomach Mucosa	stomach
17	chr7:117214000-117228000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:117214200-117216200	Weak transcription	Fetal Intestine Small	intestine
19	chr7:117214200-117216600	Weak transcription	Fetal Intestine Large	intestine
20	chr7:117214400-117228000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr7:117216200-117217800	Enhancers	Fetal Intestine Small	intestine
22	chr7:117216600-117217400	Enhancers	Fetal Intestine Large	intestine
23	chr7:117216600-117218200	Enhancers	Dnd41	blood
24	chr7:117216800-117217000	Enhancers	Fetal Heart	heart
25	chr7:117216800-117217000	Enhancers	Small Intestine	intestine
26	chr7:117216800-117217200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr7:117216800-117217200	Enhancers	Fetal Thymus	thymus
28	chr7:117216800-117217400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:117216800-117235600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr7:117217200-117226000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr7:117217400-117222000	Weak transcription	Fetal Intestine Large	intestine
32	chr7:117217400-117222800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:117217600-117218400	Strong transcription	Duodenum Mucosa	Duodenum
34	chr7:117217800-117218200	Weak transcription	Fetal Intestine Small	intestine
35	chr7:117218200-117218800	Strong transcription	Fetal Intestine Small	intestine
36	chr7:117218400-117228000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr7:117218800-117221800	Weak transcription	Fetal Intestine Small	intestine
38	chr7:117220400-117223000	Enhancers	A549	lung
39	chr7:117220600-117223200	Enhancers	Hela-S3	cervix
40	chr7:117221800-117222200	Genic enhancers	Fetal Intestine Small	intestine
41	chr7:117221800-117222200	Enhancers	Placenta	Placenta
42	chr7:117221800-117222400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:117221800-117222600	Enhancers	Colon Smooth Muscle	Colon
44	chr7:117221800-117222800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr7:117221800-117223000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr7:117222000-117222200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr7:117222000-117223000	Enhancers	Fetal Intestine Large	intestine
48	chr7:117222200-117222600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:117222200-117222800	Enhancers	Fetal Intestine Small	intestine
50	chr7:117222200-117223000	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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