Variant report

Variant	nsv1028614
Chromosome Location	chr7:11511684-11596934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr7:11565441-11565499	K562	blood:	n/a	n/a
2	BACH1	chr7:11577482-11577521	K562	blood:	n/a	n/a
3	BATF	chr7:11545349-11545529	GM12878	blood:	n/a	n/a
4	BCL11A	chr7:11567439-11567575	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr7:11545701-11545780	GM12878	blood:	n/a	n/a
6	CEBPB	chr7:11578504-11578674	HepG2	liver:	n/a	chr7:11578573-11578584 chr7:11578572-11578585
7	CEBPB	chr7:11579338-11579755	A549	lung:	n/a	chr7:11579405-11579418 chr7:11579475-11579488 chr7:11579624-11579635 chr7:11579405-11579418 chr7:11579625-11579634 chr7:11579623-11579634
8	CEBPB	chr7:11518529-11518885	HepG2	liver:	n/a	chr7:11518698-11518709
9	CEBPB	chr7:11518534-11518805	H1-hESC	embryonic stem cell:	n/a	chr7:11518698-11518709
10	CEBPB	chr7:11553192-11553495	A549	lung:	n/a	n/a
11	CEBPB	chr7:11579442-11579799	IMR90	lung:	n/a	chr7:11579475-11579488 chr7:11579624-11579635 chr7:11579625-11579634 chr7:11579623-11579634
12	CEBPB	chr7:11535611-11535857	HepG2	liver:	n/a	chr7:11535769-11535780
13	CEBPB	chr7:11535627-11535922	IMR90	lung:	n/a	chr7:11535769-11535780
14	CEBPB	chr7:11564102-11564567	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr7:11518518-11518904	Hela-S3	cervix:	n/a	chr7:11518698-11518709
16	CEBPB	chr7:11579437-11579796	HepG2	liver:	n/a	chr7:11579475-11579488 chr7:11579624-11579635 chr7:11579625-11579634 chr7:11579623-11579634
17	CEBPB	chr7:11535643-11535963	A549	lung:	n/a	chr7:11535769-11535780
18	CEBPB	chr7:11518523-11518878	A549	lung:	n/a	chr7:11518698-11518709
19	CEBPB	chr7:11518561-11518878	IMR90	lung:	n/a	chr7:11518698-11518709
20	CEBPB	chr7:11579282-11579818	Hela-S3	cervix:	n/a	chr7:11579405-11579418 chr7:11579475-11579488 chr7:11579624-11579635 chr7:11579405-11579418 chr7:11579625-11579634 chr7:11579623-11579634
21	CEBPB	chr7:11579460-11579780	H1-hESC	embryonic stem cell:	n/a	chr7:11579475-11579488 chr7:11579624-11579635 chr7:11579625-11579634 chr7:11579623-11579634
22	CTCF	chr7:11514960-11515110	AG09319	gingival:	n/a	n/a
23	CTCF	chr7:11525920-11526070	RPTEC	kidney:	n/a	n/a
24	CTCF	chr7:11525840-11526247	MCF-7	breast:	n/a	chr7:11526084-11526105
25	CTCF	chr7:11525960-11526110	A549	lung:	n/a	chr7:11526084-11526105
26	CTCF	chr7:11525960-11526110	NHDF-neo	bronchial:	n/a	chr7:11526084-11526105
27	CTCF	chr7:11526000-11526150	NHDF-neo	bronchial:	n/a	chr7:11526084-11526105
28	CTCF	chr7:11514900-11515050	HA-sp	spinal cord:	n/a	n/a
29	CTCF	chr7:11525981-11526190	Gliobla	brain:	n/a	chr7:11526084-11526105
30	CTCF	chr7:11526000-11526150	HCM	heart:	n/a	chr7:11526084-11526105
31	CTCF	chr7:11526031-11526130	Kidney_OC	kidney:	n/a	chr7:11526084-11526105
32	CTCF	chr7:11526000-11526150	HMF	breast:	n/a	chr7:11526084-11526105
33	CTCF	chr7:11526000-11526150	HCPEpiC	choroid plexus:	n/a	chr7:11526084-11526105
34	CTCF	chr7:11525993-11526131	SK-N-SH_RA	brain:	n/a	chr7:11526084-11526105
35	CTCF	chr7:11525920-11526070	BE2_C	brain:	n/a	n/a
36	CTCF	chr7:11540904-11540950	GM20000	blood:	n/a	n/a
37	CTCF	chr7:11580060-11580210	HUVEC	blood vessel:	n/a	chr7:11580094-11580112
38	CTCF	chr7:11526008-11526171	MCF-7	breast:	n/a	chr7:11526084-11526105
39	CTCF	chr7:11580000-11580150	SK-N-SH_RA	brain:	n/a	chr7:11580094-11580112
40	CTCF	chr7:11514900-11515050	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr7:11526020-11526170	AG09319	gingival:	n/a	chr7:11526084-11526105
42	CTCF	chr7:11514960-11515110	Caco-2	colon:	n/a	n/a
43	CTCF	chr7:11526020-11526170	SK-N-SH_RA	brain:	n/a	chr7:11526084-11526105
44	CTCF	chr7:11536760-11536910	BE2_C	brain:	n/a	n/a
45	CTCF	chr7:11545740-11545890	HEK293	kidney:	n/a	n/a
46	CTCF	chr7:11580060-11580210	HCPEpiC	choroid plexus:	n/a	chr7:11580094-11580112
47	CTCF	chr7:11579840-11579990	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr7:11525978-11526197	HUVEC	blood vessel:	n/a	chr7:11526084-11526105
49	CTCF	chr7:11526025-11526131	LNCaP	prostate:	n/a	chr7:11526084-11526105
50	CTCF	chr7:11515000-11515150	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:11568529-11568579	GM06990	blood:	n/a
2	chr7:11546495-11546545	IMR90	lung:	fetal
3	chr7:11568529-11568579	SK-N-SH_RA	brain:	n/a
4	chr7:11558886-11558936	ovcar-3	ovarian:	n/a
5	chr7:11558886-11558936	HepG2	liver:	n/a
6	chr7:11558886-11558936	Hepatocyte	liver:	n/a
7	chr7:11568529-11568579	IMR90	lung:	fetal
8	chr7:11568529-11568579	ovcar-3	ovarian:	n/a
9	chr7:11558886-11558936	NHBE	bronchial:	n/a
10	chr7:11546495-11546545	HUVEC	blood vessel:	n/a
11	chr7:11546495-11546545	HRPEpiC	eye:	n/a
12	chr7:11558886-11558936	HUVEC	blood vessel:	n/a
13	chr7:11546495-11546545	MCF-7	breast:	n/a
14	chr7:11546495-11546545	HCF	heart:	n/a
15	chr7:11568529-11568579	ProgFib	skin:	n/a
16	chr7:11558886-11558936	HRPEpiC	eye:	n/a
17	chr7:11568529-11568579	NT2-D1	testis:	n/a
18	chr7:11546495-11546545	NT2-D1	testis:	n/a
19	chr7:11558886-11558936	AG10803	skin:	n/a
20	chr7:11546495-11546545	HMEC	breast:	n/a
21	chr7:11558886-11558936	ECC-1	luminal epithelium:	n/a
22	chr7:11558886-11558936	AG04449	skin:	fetal
23	chr7:11568529-11568579	HEK293	kidney:	embryo
24	chr7:11568529-11568579	GM19239	blood:	n/a
25	chr7:11568529-11568579	A549	lung:	n/a
26	chr7:11558886-11558936	PrEC	prostate:	n/a
27	chr7:11568529-11568579	NH-A	brain:	n/a
28	chr7:11568529-11568579	HIPEpiC	eye:	n/a
29	chr7:11568529-11568579	AG10803	skin:	n/a
30	chr7:11558886-11558936	K562	blood:	n/a
31	chr7:11546495-11546545	NB4	blood:	n/a
32	chr7:11546495-11546545	SK-N-SH_RA	brain:	n/a
33	chr7:11546495-11546545	Hela-S3	cervix:	n/a
34	chr7:11546495-11546545	HCPEpiC	choroid plexus:	n/a
35	chr7:11568529-11568579	HNPCEpiC	eye:	n/a
36	chr7:11568529-11568579	BJ	skin:	n/a
37	chr7:11568529-11568579	HPAEpiC	pulmonary alveolar:	n/a
38	chr7:11546495-11546545	SAEC	small airway:	n/a
39	chr7:11558886-11558936	HMEC	breast:	n/a
40	chr7:11568529-11568579	HCT-116	colon:	n/a
41	chr7:11568529-11568579	AoSMC	blood vessel:	n/a
42	chr7:11568529-11568579	HUVEC	blood vessel:	n/a
43	chr7:11558886-11558936	HL-60	blood:	n/a
44	chr7:11546495-11546545	PFSK-1	brain:	n/a
45	chr7:11568529-11568579	HRE	kidney:	n/a
46	chr7:11558886-11558936	GM12892	blood:	n/a
47	chr7:11558886-11558936	AG09309	skin:	n/a
48	chr7:11568529-11568579	BE2_C	brain:	n/a
49	chr7:11546495-11546545	GM06990	blood:	n/a
50	chr7:11546495-11546545	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:11531532..11533937-chr7:11555026..11557667,2	K562	blood:
2	chr7:11531532..11533937-chr7:11555026..11557667,2	K562	blood:
3	chr7:11556711..11559691-chr7:129780287..129783080,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF14-1	chr7:11559679-11559802	ENSG00000230333.1

Variant related genes	Relation type
THSD7A	TF binding region
THSD7A	CpG island
ENSG00000229196	chromatin interactions

Extended variants
information (count: 3756 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:3756 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10950349	chr7:11511684-11511685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373059089	chr7:11511832-11511833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs576983110	chr7:11511851-11511852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190056729	chr7:11511871-11511872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548591088	chr7:11511924-11511925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs548111056	chr7:11511958-11511959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35721763	chr7:11512097-11512098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1029465	chr7:11512114-11512115	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs78681591	chr7:11512149-11512150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181424007	chr7:11512192-11512193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141042947	chr7:11512211-11512212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185276185	chr7:11512222-11512223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373560738	chr7:11512248-11512249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149859169	chr7:11512251-11512252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540109773	chr7:11512278-11512279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1029466	chr7:11512299-11512300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs576412579	chr7:11512321-11512322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545420099	chr7:11512329-11512330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116917154	chr7:11512342-11512343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531475582	chr7:11512352-11512353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547988432	chr7:11512380-11512381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561928693	chr7:11512409-11512410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6979339	chr7:11512425-11512426	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs145857627	chr7:11512426-11512427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148993376	chr7:11512438-11512439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs7811562	chr7:11512486-11512487	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs142899335	chr7:11512512-11512513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs550189123	chr7:11512684-11512685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190914476	chr7:11512700-11512701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535898630	chr7:11512708-11512709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183955649	chr7:11512738-11512739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs16876845	chr7:11512786-11512787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs35507856	chr7:11512790-11512791	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs2189310	chr7:11512824-11512825	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs576771744	chr7:11512835-11512836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs73677714	chr7:11512841-11512842	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs562464598	chr7:11512873-11512874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148707903	chr7:11512876-11512877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575950268	chr7:11512878-11512879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs146580479	chr7:11512899-11512900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561780611	chr7:11512920-11512921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs550001497	chr7:11512968-11512969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570268553	chr7:11513019-11513020	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141280922	chr7:11513027-11513028	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145011841	chr7:11513099-11513100	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138829354	chr7:11513124-11513125	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372807719	chr7:11513129-11513130	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572357456	chr7:11513133-11513134	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550212758	chr7:11513142-11513143	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140439651	chr7:11513143-11513144	Weak transcription Enhancers Strong transcription	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
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	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
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Autism	22495309	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11464800-11513400	Weak transcription	Fetal Kidney	kidney
2	chr7:11480400-11523200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:11490800-11515800	Weak transcription	Fetal Stomach	stomach
4	chr7:11498600-11519800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr7:11499200-11513400	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr7:11499200-11513400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr7:11500600-11513000	Weak transcription	Placenta	Placenta
8	chr7:11500600-11513400	Weak transcription	Fetal Lung	lung
9	chr7:11501800-11514000	Weak transcription	Pancreas	Pancrea
10	chr7:11509600-11514000	Weak transcription	Gastric	stomach
11	chr7:11509600-11514000	Weak transcription	Stomach Mucosa	stomach
12	chr7:11509800-11513000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:11511400-11515000	Enhancers	Liver	Liver
14	chr7:11513000-11513800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr7:11513000-11514800	Strong transcription	Placenta	Placenta
16	chr7:11513400-11514000	Strong transcription	Fetal Kidney	kidney
17	chr7:11513400-11514200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr7:11513400-11514200	Strong transcription	Fetal Lung	lung
19	chr7:11513800-11519000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:11514000-11514200	Enhancers	Pancreas	Pancrea
21	chr7:11514000-11515000	Enhancers	Stomach Mucosa	stomach
22	chr7:11514000-11515200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:11514000-11515200	Enhancers	Gastric	stomach
24	chr7:11514000-11520600	Weak transcription	Fetal Kidney	kidney
25	chr7:11514200-11514600	Weak transcription	Pancreas	Pancrea
26	chr7:11514200-11522200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr7:11514200-11531600	Weak transcription	Fetal Lung	lung
28	chr7:11514600-11515200	Enhancers	Pancreas	Pancrea
29	chr7:11514800-11515000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr7:11514800-11523000	Weak transcription	Placenta	Placenta
31	chr7:11515200-11521400	Weak transcription	Pancreas	Pancrea
32	chr7:11518000-11518800	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr7:11518000-11519000	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr7:11518800-11519800	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr7:11519000-11520400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr7:11519800-11520200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr7:11519800-11520200	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr7:11519800-11520200	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr7:11520200-11523600	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr7:11520400-11525000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr7:11521400-11521600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr7:11521400-11521600	ZNF genes & repeats	Pancreas	Pancrea
43	chr7:11521600-11538600	Weak transcription	Pancreas	Pancrea
44	chr7:11522200-11522600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr7:11523600-11524000	Enhancers	H1 Cell Line	embryonic stem cell
46	chr7:11523600-11524000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr7:11525000-11526200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr7:11525200-11525600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr7:11525200-11525600	Enhancers	Brain Anterior Caudate	brain
50	chr7:11526200-11526800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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