Variant report

Variant	nsv887803
Chromosome Location	chr7:17540804-17650204
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1239)
CpG islands
(count:244)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:17582050-17582722	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17545639-17546113	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:17563515-17564310	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:17639920-17640241	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:17570705-17570973	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:17547356-17547682	HepG2	liver:	n/a	n/a
7	ATF1	chr7:17639533-17639733	K562	blood:	n/a	n/a
8	ATF1	chr7:17556068-17556263	K562	blood:	n/a	n/a
9	ATF2	chr7:17545626-17546038	GM12878	blood:	n/a	n/a
10	ATF2	chr7:17545610-17546051	GM12878	blood:	n/a	n/a
11	ATF3	chr7:17598333-17599109	A549	lung:	n/a	n/a
12	ATF3	chr7:17598348-17598968	A549	lung:	n/a	n/a
13	BATF	chr7:17586358-17586636	GM12878	blood:	n/a	chr7:17586494-17586505 chr7:17586523-17586532
14	BATF	chr7:17545754-17546108	GM12878	blood:	n/a	n/a
15	BCL11A	chr7:17545665-17546083	GM12878	blood:	n/a	n/a
16	BCL3	chr7:17545577-17546157	A549	lung:	n/a	n/a
17	BCL3	chr7:17597307-17597887	A549	lung:	n/a	n/a
18	BCL3	chr7:17598160-17599399	A549	lung:	n/a	chr7:17598247-17598256
19	BCL3	chr7:17598337-17599111	A549	lung:	n/a	n/a
20	BHLHE40	chr7:17547360-17547534	HepG2	liver:	n/a	n/a
21	BHLHE40	chr7:17570680-17570977	GM12878	blood:	n/a	n/a
22	BHLHE40	chr7:17640010-17640130	HepG2	liver:	n/a	n/a
23	BHLHE40	chr7:17639603-17639687	HepG2	liver:	n/a	n/a
24	BHLHE40	chr7:17545645-17546075	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:17586327-17586569	HepG2	liver:	n/a	n/a
26	BHLHE40	chr7:17547300-17547707	HepG2	liver:	n/a	n/a
27	BHLHE40	chr7:17545738-17546036	HepG2	liver:	n/a	n/a
28	BRCA1	chr7:17639276-17640418	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr7:17563951-17564339	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr7:17638505-17638954	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr7:17572366-17573261	HCT-116	colon:	n/a	n/a
32	CBX3	chr7:17572488-17573127	HCT-116	colon:	n/a	n/a
33	CEBPB	chr7:17619815-17620008	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:17586096-17586561	HepG2	liver:	n/a	n/a
35	CEBPB	chr7:17545602-17546014	A549	lung:	n/a	chr7:17545856-17545869 chr7:17545630-17545641 chr7:17545630-17545643 chr7:17545630-17545641 chr7:17545630-17545643
36	CEBPB	chr7:17596998-17597659	IMR90	lung:	n/a	chr7:17597278-17597289 chr7:17597111-17597124 chr7:17597111-17597122
37	CEBPB	chr7:17553858-17554112	H1-hESC	embryonic stem cell:	n/a	chr7:17553987-17553998
38	CEBPB	chr7:17600249-17600430	HepG2	liver:	n/a	n/a
39	CEBPB	chr7:17553900-17554070	Hela-S3	cervix:	n/a	chr7:17553987-17553998
40	CEBPB	chr7:17574007-17574315	Hela-S3	cervix:	n/a	chr7:17574146-17574157
41	CEBPB	chr7:17545738-17545989	A549	lung:	n/a	chr7:17545856-17545869
42	CEBPB	chr7:17575466-17575735	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:17639957-17640257	HepG2	liver:	n/a	n/a
44	CEBPB	chr7:17541720-17541920	K562	blood:	n/a	chr7:17541766-17541777 chr7:17541768-17541779 chr7:17541768-17541777
45	CEBPB	chr7:17639797-17640456	A549	lung:	n/a	n/a
46	CEBPB	chr7:17597031-17597221	Hela-S3	cervix:	n/a	chr7:17597111-17597124 chr7:17597111-17597122
47	CEBPB	chr7:17572264-17573232	HCT-116	colon:	n/a	chr7:17572855-17572868
48	CEBPB	chr7:17639869-17640297	IMR90	lung:	n/a	n/a
49	CEBPB	chr7:17639879-17640319	A549	lung:	n/a	n/a
50	CEBPB	chr7:17572381-17573224	HCT-116	colon:	n/a	chr7:17572855-17572868

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17552196-17552246	Caco-2	colon:	n/a
2	chr7:17552196-17552246	ProgFib	skin:	n/a
3	chr7:17598458-17598508	Hela-S3	cervix:	n/a
4	chr7:17582718-17582768	A549	lung:	n/a
5	chr7:17585471-17585521	HRCEpiC	kidney:	n/a
6	chr7:17598458-17598508	SK-N-MC	brain:	n/a
7	chr7:17598458-17598508	NB4	blood:	n/a
8	chr7:17582718-17582768	HCT-116	colon:	n/a
9	chr7:17585471-17585521	NH-A	brain:	n/a
10	chr7:17598458-17598508	K562	blood:	n/a
11	chr7:17598458-17598508	RPTEC	kidney:	n/a
12	chr7:17552196-17552246	SK-N-SH_RA	brain:	n/a
13	chr7:17552196-17552246	SK-N-MC	brain:	n/a
14	chr7:17582718-17582768	PANC-1	pancreas:	n/a
15	chr7:17582718-17582768	Hepatocyte	liver:	n/a
16	chr7:17585471-17585521	PrEC	prostate:	n/a
17	chr7:17585471-17585521	PFSK-1	brain:	n/a
18	chr7:17585471-17585521	NHDF-neo	bronchial:	n/a
19	chr7:17585471-17585521	SKMC	muscle:	n/a
20	chr7:17598458-17598508	NHBE	bronchial:	n/a
21	chr7:17552196-17552246	K562	blood:	n/a
22	chr7:17552196-17552246	CMK	blood:	n/a
23	chr7:17552196-17552246	HUVEC	blood vessel:	n/a
24	chr7:17598458-17598508	CMK	blood:	n/a
25	chr7:17585471-17585521	HepG2	liver:	n/a
26	chr7:17582718-17582768	CMK	blood:	n/a
27	chr7:17582718-17582768	SK-N-SH	brain:	n/a
28	chr7:17582718-17582768	T-47D	breast:	n/a
29	chr7:17552196-17552246	NHDF-neo	bronchial:	n/a
30	chr7:17598458-17598508	H1-hESC	embryonic stem cell:	embryo
31	chr7:17552196-17552246	HRPEpiC	eye:	n/a
32	chr7:17582718-17582768	HEEpiC	esophagus:	n/a
33	chr7:17552196-17552246	PANC-1	pancreas:	n/a
34	chr7:17585471-17585521	AG04449	skin:	fetal
35	chr7:17552196-17552246	HEK293	kidney:	embryo
36	chr7:17585471-17585521	A549	lung:	n/a
37	chr7:17552196-17552246	Jurkat	blood:	n/a
38	chr7:17582718-17582768	HUVEC	blood vessel:	n/a
39	chr7:17598458-17598508	ECC-1	luminal epithelium:	n/a
40	chr7:17552196-17552246	HCT-116	colon:	n/a
41	chr7:17598458-17598508	GM19239	blood:	n/a
42	chr7:17552196-17552246	AG04450	lung:	fetal
43	chr7:17585471-17585521	NT2-D1	testis:	n/a
44	chr7:17582718-17582768	AG04449	skin:	fetal
45	chr7:17582718-17582768	AG10803	skin:	n/a
46	chr7:17582718-17582768	MCF-7	breast:	n/a
47	chr7:17585471-17585521	NHBE	bronchial:	n/a
48	chr7:17582718-17582768	HepG2	liver:	n/a
49	chr7:17582718-17582768	IMR90	lung:	fetal
50	chr7:17552196-17552246	HAEpiC	amniotic membrane:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:17585475..17587800-chr7:17685188..17687624,2	MCF-7	breast:
2	chr7:17595637..17596623-chr7:17657831..17658483,2	MCF-7	breast:
3	chr7:17579664..17581435-chr7:17584339..17586742,2	K562	blood:
4	chr7:17514240..17514759-chr7:17570395..17571281,2	MCF-7	breast:
5	chr7:17558188..17561143-chr7:17568617..17570224,2	MCF-7	breast:
6	chr7:17344294..17345014-chr7:17570513..17571272,2	MCF-7	breast:
7	chr7:17579664..17581435-chr7:17584339..17586742,2	K562	blood:
8	chr7:17337629..17339397-chr7:17596553..17598570,2	MCF-7	breast:
9	chr7:17102519..17103019-chr7:17570516..17571366,2	MCF-7	breast:
10	chr7:16974533..16976554-chr7:17579096..17580960,2	K562	blood:
11	chr7:17536971..17538870-chr7:17540404..17542296,2	K562	blood:
12	chr7:17566122..17568059-chr7:17569390..17571113,2	MCF-7	breast:
13	chr7:17566122..17568059-chr7:17569390..17571113,2	MCF-7	breast:
14	chr7:17558188..17561143-chr7:17568617..17570224,2	MCF-7	breast:
15	chr7:17342140..17343219-chr7:17570441..17571204,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX13-1	chr7:17598376-17598533	ENSG00000226598
2	lnc-SNX13-3	chr7:17619972-17620082	NONHSAT119341
3	lnc-SNX13-4	chr7:17564901-17565058	NONHSAT119333

No data

Variant related genes	Relation type
ENSG00000226598	TF binding region
ENSG00000226598	CpG island
ENSG00000106546	chromatin interactions
ENSG00000237773	chromatin interactions

Extended variants
information (count: 5528 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5528 , 50 per page) page: 1 2 3 4 5 6 7 ... 111

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9638747	chr7:17540804-17540805	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564857952	chr7:17540807-17540808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532143975	chr7:17540811-17540812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547177503	chr7:17540828-17540829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565568275	chr7:17540830-17540831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369656332	chr7:17540836-17540837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572458118	chr7:17540837-17540838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535963910	chr7:17540909-17540910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548304410	chr7:17540915-17540916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs569507613	chr7:17540921-17540922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185062310	chr7:17540936-17540937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371069578	chr7:17540953-17540954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201186453	chr7:17540997-17540998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189382744	chr7:17541003-17541004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs202002209	chr7:17541006-17541007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577627632	chr7:17541032-17541033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372410606	chr7:17541033-17541034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561988951	chr7:17541063-17541064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553581426	chr7:17541083-17541084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575023065	chr7:17541106-17541107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541919839	chr7:17541139-17541140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536162628	chr7:17541153-17541154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575521582	chr7:17541168-17541169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546196343	chr7:17541195-17541196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564177963	chr7:17541288-17541289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532253628	chr7:17541303-17541304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540975466	chr7:17541314-17541315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs181835507	chr7:17541333-17541334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559110965	chr7:17541364-17541365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111787129	chr7:17541374-17541375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372707551	chr7:17541401-17541402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78076285	chr7:17541430-17541431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185379745	chr7:17541484-17541485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569751344	chr7:17541507-17541508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530390815	chr7:17541584-17541585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552186907	chr7:17541595-17541596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570489391	chr7:17541611-17541612	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs150418168	chr7:17541612-17541613	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs189017177	chr7:17541667-17541668	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs568515970	chr7:17541676-17541677	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs536068615	chr7:17541693-17541694	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs181376011	chr7:17541694-17541695	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs575680760	chr7:17541739-17541740	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs572830869	chr7:17541763-17541764	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs545924300	chr7:17541776-17541777	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs186333322	chr7:17541797-17541798	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs572944827	chr7:17541888-17541889	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs540885133	chr7:17541897-17541898	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs559224467	chr7:17541898-17541899	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs529819953	chr7:17541902-17541903	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
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
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	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
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Autism	22495309	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17499400-17544600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:17536200-17541400	Weak transcription	Hela-S3	cervix
3	chr7:17537400-17541200	Enhancers	Liver	Liver
4	chr7:17537400-17541400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:17537600-17541600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:17537600-17546400	Weak transcription	Ovary	ovary
7	chr7:17538200-17541200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr7:17538200-17541600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:17538200-17544800	Weak transcription	Stomach Mucosa	stomach
10	chr7:17538400-17543200	Weak transcription	Fetal Intestine Small	intestine
11	chr7:17538600-17543600	Enhancers	NHDF-Ad	bronchial
12	chr7:17538800-17541200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:17538800-17541200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:17538800-17541600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr7:17540200-17542200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:17540400-17541600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:17540600-17541000	Enhancers	Small Intestine	intestine
18	chr7:17540600-17541800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:17540600-17541800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr7:17540600-17542400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr7:17540600-17543000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:17540600-17543400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr7:17540600-17543600	Enhancers	Osteobl	bone
24	chr7:17540800-17541000	Enhancers	Fetal Lung	lung
25	chr7:17540800-17541000	Enhancers	NHLF	lung
26	chr7:17540800-17541800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr7:17540800-17543200	Weak transcription	Fetal Intestine Large	intestine
28	chr7:17540800-17543200	Weak transcription	HepG2	liver
29	chr7:17541000-17541600	Weak transcription	NHLF	lung
30	chr7:17541000-17544600	Weak transcription	Fetal Lung	lung
31	chr7:17541200-17541800	Weak transcription	Liver	Liver
32	chr7:17541200-17541800	Enhancers	NH-A	brain
33	chr7:17541200-17542000	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:17541200-17542200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:17541200-17542200	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr7:17541200-17542800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr7:17541400-17541800	Enhancers	Hela-S3	cervix
38	chr7:17541400-17542200	Enhancers	HSMM	muscle
39	chr7:17541600-17541800	Enhancers	H9 Cell Line	embryonic stem cell
40	chr7:17541600-17542000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr7:17541600-17542000	Enhancers	Duodenum Smooth Muscle	Duodenum
42	chr7:17541600-17542200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:17541600-17542200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:17541600-17542400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:17541600-17542400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:17541600-17542800	Enhancers	NHLF	lung
47	chr7:17541800-17542000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr7:17541800-17542000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:17541800-17542200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:17541800-17542200	Enhancers	Liver	Liver

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