Variant report

Variant	nsv970820
Chromosome Location	chr7:39797964-39839303
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:312)
CpG islands
(count:488)
Chromatin interactive
region (count:3)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:312 , 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	BATF	chr7:39813857-39814230	GM12878	blood:	n/a	n/a
2	BATF	chr7:39826290-39826567	GM12878	blood:	n/a	n/a
3	BATF	chr7:39826291-39826499	GM12878	blood:	n/a	n/a
4	BATF	chr7:39813917-39814187	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:39837820-39837975	HepG2	liver:	n/a	n/a
6	BHLHE40	chr7:39837834-39837963	K562	blood:	n/a	n/a
7	CBX3	chr7:39831433-39831839	K562	blood:	n/a	n/a
8	CBX3	chr7:39836592-39836899	K562	blood:	n/a	n/a
9	CEBPB	chr7:39825939-39826087	HepG2	liver:	n/a	chr7:39826051-39826062
10	CEBPB	chr7:39816708-39817080	HepG2	liver:	n/a	chr7:39816882-39816893
11	CEBPB	chr7:39810290-39810355	IMR90	lung:	n/a	n/a
12	CEBPB	chr7:39839062-39839260	K562	blood:	n/a	n/a
13	CEBPB	chr7:39816765-39817021	IMR90	lung:	n/a	chr7:39816882-39816893
14	CEBPB	chr7:39821141-39821517	IMR90	lung:	n/a	n/a
15	CEBPB	chr7:39816708-39817032	K562	blood:	n/a	chr7:39816882-39816893
16	CEBPB	chr7:39816783-39817025	A549	lung:	n/a	chr7:39816882-39816893
17	CEBPB	chr7:39825902-39826102	IMR90	lung:	n/a	chr7:39826051-39826062
18	CEBPB	chr7:39825964-39826087	K562	blood:	n/a	chr7:39826051-39826062
19	CTCF	chr7:39834398-39834628	K562	blood:	n/a	chr7:39834550-39834563
20	CTCF	chr7:39834580-39834730	GM12864	blood:	n/a	n/a
21	CTCF	chr7:39831620-39831770	HepG2	liver:	n/a	n/a
22	CTCF	chr7:39831480-39831630	GM12873	blood:	n/a	n/a
23	CTCF	chr7:39830480-39830630	HCT-116	colon:	n/a	n/a
24	CTCF	chr7:39831627-39831789	GM12878	blood:	n/a	n/a
25	CTCF	chr7:39831605-39831783	GM19238	blood:	n/a	n/a
26	CTCF	chr7:39831740-39831890	GM12866	blood:	n/a	n/a
27	CTCF	chr7:39830780-39830930	HCT-116	colon:	n/a	n/a
28	CTCF	chr7:39831620-39831770	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr7:39838314-39838344	GM13976	blood:	n/a	n/a
30	CTCF	chr7:39831620-39831770	HEK293	kidney:	n/a	n/a
31	CTCF	chr7:39831612-39831776	A549	lung:	n/a	n/a
32	CTCF	chr7:39831620-39831770	GM12874	blood:	n/a	n/a
33	CTCF	chr7:39831608-39831782	A549	lung:	n/a	n/a
34	CTCF	chr7:39831532-39831821	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr7:39830576-39830845	K562	blood:	n/a	n/a
36	CTCF	chr7:39837759-39837805	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr7:39831620-39831770	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr7:39832401-39832839	K562	blood:	n/a	n/a
39	CTCF	chr7:39831640-39831790	GM12868	blood:	n/a	n/a
40	CTCF	chr7:39831540-39831690	GM12875	blood:	n/a	n/a
41	CTCF	chr7:39831600-39831750	K562	blood:	n/a	n/a
42	CTCF	chr7:39830760-39830910	HMF	breast:	n/a	n/a
43	CTCF	chr7:39831640-39831790	HCT-116	colon:	n/a	n/a
44	CTCF	chr7:39830521-39830794	K562	blood:	n/a	n/a
45	CTCF	chr7:39830740-39830890	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr7:39830780-39830930	HEK293	kidney:	n/a	n/a
47	CTCF	chr7:39831600-39831750	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr7:39832492-39832654	K562	blood:	n/a	n/a
49	CTCF	chr7:39800120-39800270	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr7:39831540-39831690	HCM	heart:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:39833648-39833698	MCF10A-Er-Src	breast:	n/a
2	chr7:39831928-39831978	LNCaP	prostate:	n/a
3	chr7:39837692-39837742	SKMC	muscle:	n/a
4	chr7:39833648-39833698	HCT-116	colon:	n/a
5	chr7:39833648-39833698	GM12891	blood:	n/a
6	chr7:39833495-39833545	PrEC	prostate:	n/a
7	chr7:39831928-39831978	HPAEpiC	pulmonary alveolar:	n/a
8	chr7:39833944-39833994	SK-N-SH	brain:	n/a
9	chr7:39832738-39832788	Hepatocyte	liver:	n/a
10	chr7:39831642-39831692	ovcar-3	ovarian:	n/a
11	chr7:39833648-39833698	A549	lung:	n/a
12	chr7:39833628-39833678	H1-hESC	embryonic stem cell:	embryo
13	chr7:39833628-39833678	MCF-7	breast:	n/a
14	chr7:39833628-39833678	HRCEpiC	kidney:	n/a
15	chr7:39833628-39833678	BJ	skin:	n/a
16	chr7:39832738-39832788	NH-A	brain:	n/a
17	chr7:39837692-39837742	AG09319	gingival:	n/a
18	chr7:39831642-39831692	HAEpiC	amniotic membrane:	n/a
19	chr7:39832738-39832788	GM06990	blood:	n/a
20	chr7:39831928-39831978	NT2-D1	testis:	n/a
21	chr7:39833628-39833678	PrEC	prostate:	n/a
22	chr7:39833628-39833678	PFSK-1	brain:	n/a
23	chr7:39833648-39833698	HUVEC	blood vessel:	n/a
24	chr7:39837692-39837742	ProgFib	skin:	n/a
25	chr7:39832738-39832788	ECC-1	luminal epithelium:	n/a
26	chr7:39833495-39833545	SK-N-MC	brain:	n/a
27	chr7:39833648-39833698	AG04450	lung:	fetal
28	chr7:39832738-39832788	HEK293	kidney:	embryo
29	chr7:39833628-39833678	HRE	kidney:	n/a
30	chr7:39833944-39833994	HepG2	liver:	n/a
31	chr7:39837692-39837742	NHDF-neo	bronchial:	n/a
32	chr7:39833495-39833545	HEEpiC	esophagus:	n/a
33	chr7:39831642-39831692	NHDF-neo	bronchial:	n/a
34	chr7:39833944-39833994	SKMC	muscle:	n/a
35	chr7:39832738-39832788	AG04449	skin:	fetal
36	chr7:39833495-39833545	IMR90	lung:	fetal
37	chr7:39833648-39833698	HCM	heart:	n/a
38	chr7:39833648-39833698	ECC-1	luminal epithelium:	n/a
39	chr7:39832738-39832788	GM12878	blood:	n/a
40	chr7:39831928-39831978	HRE	kidney:	n/a
41	chr7:39832738-39832788	PrEC	prostate:	n/a
42	chr7:39833495-39833545	AG09309	skin:	n/a
43	chr7:39833944-39833994	NHDF-neo	bronchial:	n/a
44	chr7:39831642-39831692	HNPCEpiC	eye:	n/a
45	chr7:39833628-39833678	GM19239	blood:	n/a
46	chr7:39833628-39833678	SAEC	small airway:	n/a
47	chr7:39833648-39833698	GM19239	blood:	n/a
48	chr7:39837692-39837742	NB4	blood:	n/a
49	chr7:39833648-39833698	AG10803	skin:	n/a
50	chr7:39831928-39831978	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:39795664..39798503-chr7:39801228..39803990,2	MCF-7	breast:
2	chr7:39619917..39620450-chr7:39831240..39831746,2	K562	blood:
3	chr7:39795664..39798503-chr7:39801228..39803990,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C7orf11-12	chr7:39828566-39828903	NONHSAT120229
2	lnc-RALA-1	chr7:39821288-39821495	ENSG00000188185
3	lnc-RALA-1	chr7:39820934-39820950	XLOC_006058
4	lnc-RALA-1	chr7:39828081-39828203	ENSG00000188185
5	lnc-RALA-1	chr7:39811849-39812029	XLOC_006057
6	lnc-RALA-1	chr7:39820783-39821484	XLOC_006058
7	lnc-RALA-1	chr7:39828953-39829024	ENSG00000188185
8	lnc-RALA-1	chr7:39822334-39822369	XLOC_006058
9	lnc-RALA-1	chr7:39821343-39821627	XLOC_006058
10	lnc-RALA-1	chr7:39822334-39822398	ENSG00000188185
11	lnc-RALA-1	chr7:39820742-39821484	NONHSAT120225
12	lnc-RALA-1	chr7:39822334-39822369	XLOC_006058
13	lnc-C7orf11-2	chr7:39807001-39807261	XLOC_006416
14	lnc-C7orf11-2	chr7:39803198-39803268	XLOC_006416
15	lnc-RALA-1	chr7:39821161-39821495	XLOC_006058
16	lnc-RALA-1	chr7:39821706-39821711	XLOC_006058
17	lnc-RALA-1	chr7:39822334-39822346	NONHSAT120225
18	lnc-RALA-1	chr7:39818870-39819091	XLOC_006057
19	lnc-RALA-1	chr7:39821161-39821484	XLOC_006058

No data

Variant related genes	Relation type
ENSG00000270797	TF binding region
LINC00265	TF binding region
CICP22	TF binding region
RNU6-719P	TF binding region
ENSG00000270797	CpG island
LINC00265	CpG island
CICP22	CpG island
RNU6-719P	CpG island
ZMYND11	miRNA target sites
SMARCD1	miRNA target sites
CRK	miRNA target sites
TMED10	miRNA target sites

Extended variants
information (count: 1675 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1675 , 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	rs564057077	chr7:39798015-39798016	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs150869790	chr7:39798023-39798024	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs528173377	chr7:39798040-39798041	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs542874400	chr7:39798076-39798077	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs375056445	chr7:39798081-39798082	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs559339910	chr7:39798091-39798092	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs183682413	chr7:39798133-39798134	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs551491852	chr7:39798176-39798177	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs571637671	chr7:39798212-39798213	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs75486801	chr7:39798248-39798249	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs188297949	chr7:39798260-39798261	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs567411964	chr7:39798270-39798271	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs536169683	chr7:39798275-39798276	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs533716632	chr7:39798282-39798283	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs34070652	chr7:39798288-39798289	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs566500332	chr7:39798306-39798307	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs538622644	chr7:39798347-39798348	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs181795651	chr7:39798395-39798396	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs575245540	chr7:39798417-39798418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs139720269	chr7:39798450-39798451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186561675	chr7:39798523-39798524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs374197188	chr7:39798531-39798532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542938050	chr7:39798552-39798553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190220384	chr7:39798573-39798574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559598353	chr7:39798672-39798673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528504607	chr7:39798690-39798691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs559887113	chr7:39798719-39798720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565234414	chr7:39798749-39798750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs530916550	chr7:39798770-39798771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530262233	chr7:39798835-39798836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs551017774	chr7:39798937-39798938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560581889	chr7:39798981-39798982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529892206	chr7:39798988-39798989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546950213	chr7:39799029-39799030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs566762942	chr7:39799097-39799098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538685247	chr7:39799108-39799109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368526881	chr7:39799160-39799161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370315847	chr7:39799164-39799165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558590058	chr7:39799197-39799198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs75935107	chr7:39799211-39799212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs568795759	chr7:39799324-39799325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs78712564	chr7:39799333-39799334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549075249	chr7:39799355-39799356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554622174	chr7:39799393-39799394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4461800	chr7:39799425-39799426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs368159788	chr7:39799454-39799455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs553295107	chr7:39799466-39799467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115795097	chr7:39799530-39799531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116153439	chr7:39799532-39799533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs6977471	chr7:39799539-39799540	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
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
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Gastric cancer	24379144	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39774200-39807400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr7:39775800-39807000	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr7:39775800-39811200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr7:39776600-39820400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr7:39782400-39809000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:39784800-39802600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr7:39785000-39831800	Weak transcription	Primary B cells from cord blood	blood
8	chr7:39789600-39807200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr7:39793400-39799800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:39793400-39802000	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:39794000-39830800	Weak transcription	Pancreas	Pancrea
12	chr7:39794200-39799800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:39794200-39801200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr7:39794200-39820800	Weak transcription	Ovary	ovary
15	chr7:39794200-39837400	Weak transcription	Stomach Smooth Muscle	stomach
16	chr7:39794600-39800800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:39794600-39808800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr7:39794600-39810200	Weak transcription	Fetal Stomach	stomach
19	chr7:39794600-39830800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr7:39795000-39802600	Weak transcription	NHDF-Ad	bronchial
21	chr7:39795000-39802800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr7:39795200-39802400	Weak transcription	NH-A	brain
23	chr7:39795200-39807400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:39795400-39813000	Weak transcription	GM12878-XiMat	blood
25	chr7:39795400-39833400	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr7:39795800-39811400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:39796400-39798000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr7:39796400-39798200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
29	chr7:39796400-39798800	Enhancers	HMEC	breast
30	chr7:39796600-39798000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:39796600-39798000	Enhancers	NHEK	skin
32	chr7:39796800-39798800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr7:39797000-39798000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr7:39797000-39798200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr7:39797000-39798200	Enhancers	Colon Smooth Muscle	Colon
36	chr7:39797000-39799000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr7:39797200-39799000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr7:39797400-39798200	Enhancers	Brain Anterior Caudate	brain
39	chr7:39797400-39798200	Enhancers	Brain Hippocampus Middle	brain
40	chr7:39797600-39798000	Enhancers	Fetal Muscle Leg	muscle
41	chr7:39797600-39798000	Enhancers	Rectal Smooth Muscle	rectum
42	chr7:39797600-39798000	Enhancers	Stomach Mucosa	stomach
43	chr7:39797600-39798200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:39797600-39798200	Enhancers	Left Ventricle	heart
45	chr7:39797600-39798400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:39797600-39798400	Enhancers	Brain Substantia Nigra	brain
47	chr7:39797600-39798600	Enhancers	Brain Cingulate Gyrus	brain
48	chr7:39797600-39801400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr7:39797800-39798000	Enhancers	Fetal Muscle Trunk	muscle
50	chr7:39797800-39798200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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