Variant report

Variant	esv2752933
Chromosome Location	chr7:17534660-17633760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1053)
CpG islands
(count:246)
Chromatin interactive
region (count:16)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1053 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:17547356-17547682	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:17563515-17564310	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:17545639-17546113	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:17570705-17570973	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:17582050-17582722	HepG2	liver:	n/a	n/a
6	ATF1	chr7:17556068-17556263	K562	blood:	n/a	n/a
7	ATF2	chr7:17545626-17546038	GM12878	blood:	n/a	n/a
8	ATF2	chr7:17545610-17546051	GM12878	blood:	n/a	n/a
9	ATF3	chr7:17598348-17598968	A549	lung:	n/a	n/a
10	ATF3	chr7:17598333-17599109	A549	lung:	n/a	n/a
11	BATF	chr7:17586358-17586636	GM12878	blood:	n/a	chr7:17586494-17586505 chr7:17586523-17586532
12	BATF	chr7:17545754-17546108	GM12878	blood:	n/a	n/a
13	BATF	chr7:17535125-17535567	GM12878	blood:	n/a	chr7:17535357-17535366
14	BCL11A	chr7:17545665-17546083	GM12878	blood:	n/a	n/a
15	BCL3	chr7:17598337-17599111	A549	lung:	n/a	n/a
16	BCL3	chr7:17598160-17599399	A549	lung:	n/a	chr7:17598247-17598256
17	BCL3	chr7:17597307-17597887	A549	lung:	n/a	n/a
18	BCL3	chr7:17545577-17546157	A549	lung:	n/a	n/a
19	BHLHE40	chr7:17545738-17546036	HepG2	liver:	n/a	n/a
20	BHLHE40	chr7:17537267-17537508	GM12878	blood:	n/a	n/a
21	BHLHE40	chr7:17547360-17547534	HepG2	liver:	n/a	n/a
22	BHLHE40	chr7:17570680-17570977	GM12878	blood:	n/a	n/a
23	BHLHE40	chr7:17547300-17547707	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	BRCA1	chr7:17563951-17564339	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr7:17572488-17573127	HCT-116	colon:	n/a	n/a
28	CBX3	chr7:17572366-17573261	HCT-116	colon:	n/a	n/a
29	CEBPB	chr7:17600174-17600508	A549	lung:	n/a	n/a
30	CEBPB	chr7:17573995-17574324	HepG2	liver:	n/a	chr7:17574146-17574157
31	CEBPB	chr7:17572485-17572943	A549	lung:	n/a	chr7:17572855-17572868
32	CEBPB	chr7:17597031-17597221	Hela-S3	cervix:	n/a	chr7:17597111-17597124 chr7:17597111-17597122
33	CEBPB	chr7:17564763-17565167	Hela-S3	cervix:	n/a	chr7:17564977-17564988 chr7:17564977-17564990
34	CEBPB	chr7:17574009-17574267	IMR90	lung:	n/a	chr7:17574146-17574157
35	CEBPB	chr7:17598446-17599042	MCF-7	breast:	n/a	n/a
36	CEBPB	chr7:17575524-17575771	IMR90	lung:	n/a	n/a
37	CEBPB	chr7:17598274-17599125	A549	lung:	n/a	n/a
38	CEBPB	chr7:17553822-17554159	MCF-7	breast:	n/a	chr7:17553987-17553998
39	CEBPB	chr7:17600249-17600430	HepG2	liver:	n/a	n/a
40	CEBPB	chr7:17598451-17598839	A549	lung:	n/a	n/a
41	CEBPB	chr7:17547464-17547677	HepG2	liver:	n/a	n/a
42	CEBPB	chr7:17586151-17586765	IMR90	lung:	n/a	chr7:17586613-17586624 chr7:17586613-17586626 chr7:17586613-17586626
43	CEBPB	chr7:17541619-17541940	HepG2	liver:	n/a	chr7:17541766-17541777 chr7:17541768-17541779 chr7:17541768-17541777
44	CEBPB	chr7:17535318-17535841	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr7:17564955-17565053	HepG2	liver:	n/a	chr7:17564977-17564988 chr7:17564977-17564990
46	CEBPB	chr7:17619815-17620008	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:17596960-17597300	A549	lung:	n/a	chr7:17597278-17597289 chr7:17597111-17597124 chr7:17597111-17597122
48	CEBPB	chr7:17553882-17554198	A549	lung:	n/a	chr7:17553987-17553998
49	CEBPB	chr7:17545732-17546079	HepG2	liver:	n/a	chr7:17545856-17545869
50	CEBPB	chr7:17545661-17546025	A549	lung:	n/a	chr7:17545856-17545869

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:17582718-17582768	HCF	heart:	n/a
2	chr7:17552196-17552246	GM06990	blood:	n/a
3	chr7:17582718-17582768	HCF	heart:	n/a
4	chr7:17552196-17552246	GM06990	blood:	n/a
5	chr7:17585471-17585521	BE2_C	brain:	n/a
6	chr7:17582718-17582768	Caco-2	colon:	n/a
7	chr7:17598458-17598508	GM12878	blood:	n/a
8	chr7:17582718-17582768	SK-N-SH_RA	brain:	n/a
9	chr7:17582718-17582768	SKMC	muscle:	n/a
10	chr7:17598458-17598508	SKMC	muscle:	n/a
11	chr7:17585471-17585521	SAEC	small airway:	n/a
12	chr7:17598458-17598508	MCF10A-Er-Src	breast:	n/a
13	chr7:17582718-17582768	HCPEpiC	choroid plexus:	n/a
14	chr7:17598458-17598508	H1-hESC	embryonic stem cell:	embryo
15	chr7:17582718-17582768	HCT-116	colon:	n/a
16	chr7:17552196-17552246	ProgFib	skin:	n/a
17	chr7:17582718-17582768	HRE	kidney:	n/a
18	chr7:17598458-17598508	HNPCEpiC	eye:	n/a
19	chr7:17598458-17598508	ECC-1	luminal epithelium:	n/a
20	chr7:17598458-17598508	HCT-116	colon:	n/a
21	chr7:17582718-17582768	Hela-S3	cervix:	n/a
22	chr7:17598458-17598508	SAEC	small airway:	n/a
23	chr7:17582718-17582768	AG09319	gingival:	n/a
24	chr7:17585471-17585521	HCPEpiC	choroid plexus:	n/a
25	chr7:17585471-17585521	HPAEpiC	pulmonary alveolar:	n/a
26	chr7:17585471-17585521	HRPEpiC	eye:	n/a
27	chr7:17552196-17552246	A549	lung:	n/a
28	chr7:17598458-17598508	Hela-S3	cervix:	n/a
29	chr7:17552196-17552246	Jurkat	blood:	n/a
30	chr7:17552196-17552246	HL-60	blood:	n/a
31	chr7:17582718-17582768	MCF-7	breast:	n/a
32	chr7:17598458-17598508	GM12892	blood:	n/a
33	chr7:17585471-17585521	AG09309	skin:	n/a
34	chr7:17582718-17582768	AG04450	lung:	fetal
35	chr7:17582718-17582768	ECC-1	luminal epithelium:	n/a
36	chr7:17585471-17585521	GM19239	blood:	n/a
37	chr7:17598458-17598508	SK-N-SH_RA	brain:	n/a
38	chr7:17552196-17552246	PrEC	prostate:	n/a
39	chr7:17585471-17585521	HCT-116	colon:	n/a
40	chr7:17552196-17552246	BE2_C	brain:	n/a
41	chr7:17598458-17598508	PFSK-1	brain:	n/a
42	chr7:17585471-17585521	MCF10A-Er-Src	breast:	n/a
43	chr7:17582718-17582768	PANC-1	pancreas:	n/a
44	chr7:17598458-17598508	AG09309	skin:	n/a
45	chr7:17598458-17598508	RPTEC	kidney:	n/a
46	chr7:17552196-17552246	HCM	heart:	n/a
47	chr7:17598458-17598508	MCF-7	breast:	n/a
48	chr7:17585471-17585521	HCF	heart:	n/a
49	chr7:17598458-17598508	HAEpiC	amniotic membrane:	n/a
50	chr7:17585471-17585521	HRE	kidney:	n/a

(count:16 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 5063 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5063 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114434951	chr7:17534663-17534664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs192433018	chr7:17534674-17534675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10249732	chr7:17534676-17534677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs145478457	chr7:17534702-17534703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184573529	chr7:17534716-17534717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148898035	chr7:17534767-17534768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs115508575	chr7:17534826-17534827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565448412	chr7:17534877-17534878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532692162	chr7:17534891-17534892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143615781	chr7:17534949-17534950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs543283520	chr7:17534983-17534984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559850206	chr7:17534985-17534986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530199790	chr7:17534988-17534989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs548726888	chr7:17534991-17534992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374587278	chr7:17535031-17535032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543621354	chr7:17535044-17535045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188019077	chr7:17535083-17535084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1448660	chr7:17535086-17535087	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148025649	chr7:17535088-17535089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571476563	chr7:17535113-17535114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74885289	chr7:17535114-17535115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181230321	chr7:17535122-17535123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565568013	chr7:17535176-17535177	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535940768	chr7:17535207-17535208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs554286293	chr7:17535218-17535219	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575590809	chr7:17535219-17535220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142180187	chr7:17535220-17535221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545116739	chr7:17535260-17535261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs577483557	chr7:17535358-17535359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565330371	chr7:17535364-17535365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112505876	chr7:17535402-17535403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545541686	chr7:17535483-17535484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542331931	chr7:17535494-17535495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563777149	chr7:17535511-17535512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530908130	chr7:17535537-17535538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552306345	chr7:17535543-17535544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139135766	chr7:17535586-17535587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532284401	chr7:17535629-17535630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35537684	chr7:17535637-17535638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs183808319	chr7:17535675-17535676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565529528	chr7:17535702-17535703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563534659	chr7:17535703-17535704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs143150112	chr7:17535733-17535734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540396457	chr7:17535742-17535743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs189119858	chr7:17535751-17535752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs577732950	chr7:17535769-17535770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532224507	chr7:17535779-17535780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138165863	chr7:17535787-17535788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537015062	chr7:17535807-17535808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112111158	chr7:17535815-17535816	Weak transcription Enhancers	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:821 , 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	chr7:17529200-17535800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr7:17532400-17537000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:17532400-17537200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr7:17532600-17535000	Weak transcription	GM12878-XiMat	blood
6	chr7:17532600-17536600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr7:17532800-17535000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr7:17532800-17536600	Weak transcription	NHEK	skin
9	chr7:17532800-17536800	Weak transcription	HMEC	breast
10	chr7:17534200-17540400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:17535000-17535600	Enhancers	Colon Smooth Muscle	Colon
12	chr7:17535000-17535600	Enhancers	Placenta Amnion	Placenta Amnion
13	chr7:17535000-17536000	Enhancers	GM12878-XiMat	blood
14	chr7:17535000-17536200	Enhancers	Hela-S3	cervix
15	chr7:17535000-17537600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr7:17535200-17535600	Enhancers	Rectal Mucosa Donor 29	rectum
17	chr7:17535400-17536200	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr7:17535400-17537400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:17535600-17537600	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:17535800-17536000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr7:17535800-17536000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr7:17535800-17536000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:17535800-17536000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr7:17535800-17536000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr7:17535800-17538800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr7:17536000-17536600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr7:17536000-17537000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:17536000-17537000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr7:17536000-17537200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr7:17536000-17537200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:17536200-17536600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr7:17536200-17537600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr7:17536200-17541400	Weak transcription	Hela-S3	cervix
34	chr7:17536400-17537400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr7:17536600-17537400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr7:17536600-17537600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr7:17536600-17537600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:17536600-17537600	Enhancers	NHDF-Ad	bronchial
39	chr7:17536600-17538200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr7:17536600-17538200	Enhancers	NHEK	skin
41	chr7:17536800-17537600	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:17536800-17537600	Enhancers	Fetal Brain Female	brain
43	chr7:17536800-17537600	Enhancers	Ovary	ovary
44	chr7:17536800-17537800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr7:17536800-17537800	Enhancers	HMEC	breast
46	chr7:17536800-17538200	Enhancers	Stomach Mucosa	stomach
47	chr7:17536800-17538400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr7:17537000-17537400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr7:17537000-17537600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:17537000-17538200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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