Variant report

Variant	nsv887716
Chromosome Location	chr7:14933955-15021223
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:123)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 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	BACH1	chr7:14942659-14942800	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr7:14939548-14939801	GM12878	blood:	n/a	n/a
3	CEBPB	chr7:14938661-14939041	Hela-S3	cervix:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
4	CEBPB	chr7:14939715-14939885	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr7:14938702-14939000	A549	lung:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
6	CEBPB	chr7:14939681-14940006	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr7:14938713-14938985	H1-hESC	embryonic stem cell:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
8	CEBPB	chr7:14938711-14939019	HepG2	liver:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
9	CEBPB	chr7:14938706-14938950	A549	lung:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
10	CEBPB	chr7:14938665-14939042	IMR90	lung:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
11	CEBPB	chr7:14949737-14949944	HepG2	liver:	n/a	chr7:14949816-14949827
12	CEBPB	chr7:14949798-14949837	Hela-S3	cervix:	n/a	chr7:14949816-14949827
13	CEBPB	chr7:14938731-14939006	K562	blood:	n/a	chr7:14938848-14938861 chr7:14938849-14938860 chr7:14938848-14938859
14	CEBPB	chr7:14949720-14949986	H1-hESC	embryonic stem cell:	n/a	chr7:14949816-14949827
15	CTBP2	chr7:14942158-14943272	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr7:14964120-14964270	HPF	lung:	n/a	n/a
17	CTCF	chr7:14964180-14964330	AG10803	skin:	n/a	n/a
18	CTCF	chr7:14943020-14943089	Fibrobl	skin:	n/a	n/a
19	CTCF	chr7:14964140-14964290	HPF	lung:	n/a	n/a
20	CTCF	chr7:14964080-14964230	HCM	heart:	n/a	n/a
21	CTCF	chr7:14964108-14964368	IMR90	lung:	n/a	n/a
22	CTCF	chr7:14964150-14964277	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr7:14964140-14964290	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr7:14964280-14964430	NHDF-neo	bronchial:	n/a	n/a
25	CTCF	chr7:14964180-14964330	AG09319	gingival:	n/a	n/a
26	CTCF	chr7:14964120-14964270	AG09309	skin:	n/a	n/a
27	CTCF	chr7:14964160-14964310	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr7:15001180-15001330	GM12866	blood:	n/a	n/a
29	CTCF	chr7:14964160-14964310	BJ	skin:	n/a	n/a
30	CTCF	chr7:14964141-14964305	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr7:14964140-14964290	HMF	breast:	n/a	n/a
32	CTCF	chr7:14980184-14980214	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr7:14964140-14964290	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr7:14964160-14964310	AG10803	skin:	n/a	n/a
35	CTCF	chr7:14964160-14964310	HCFaa	heart:	n/a	n/a
36	CTCF	chr7:14964158-14964335	LNCaP	prostate:	n/a	n/a
37	CTCF	chr7:14964520-14964670	AG10803	skin:	n/a	n/a
38	CTCF	chr7:14964146-14964299	LNCaP	prostate:	n/a	n/a
39	CTCF	chr7:14964152-14964333	GM12878	blood:	n/a	n/a
40	CTCF	chr7:14964240-14964390	RPTEC	kidney:	n/a	n/a
41	CTCF	chr7:14998320-14998470	HPAF	blood vessel:	n/a	chr7:14998380-14998398 chr7:14998387-14998395
42	CTCF	chr7:14964144-14964300	Medullo	brain:	n/a	n/a
43	CTCF	chr7:14964140-14964290	AG09319	gingival:	n/a	n/a
44	CTCF	chr7:14998280-14998430	SK-N-SH_RA	brain:	n/a	chr7:14998380-14998398 chr7:14998387-14998395
45	CTCF	chr7:14964160-14964310	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr7:14964080-14964230	AoAF	blood vessel:	n/a	n/a
47	CTCF	chr7:14958027-14958081	GM20000	blood:	n/a	n/a
48	CTCF	chr7:14963924-14964343	HCT-116	colon:	n/a	n/a
49	CTCF	chr7:14964240-14964390	HMEC	breast:	n/a	n/a
50	CTCF	chr7:14964120-14964270	HBMEC	blood vessel:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:14942359-14942409	K562	blood:	n/a
2	chr7:14942359-14942409	K562	blood:	n/a
3	chr7:14942815-14942865	Caco-2	colon:	n/a
4	chr7:14942815-14942865	AG10803	skin:	n/a
5	chr7:14942815-14942865	HRCEpiC	kidney:	n/a
6	chr7:14942359-14942409	GM12878	blood:	n/a
7	chr7:14942815-14942865	BE2_C	brain:	n/a
8	chr7:14942359-14942409	HEEpiC	esophagus:	n/a
9	chr7:14942359-14942409	AG10803	skin:	n/a
10	chr7:14942815-14942865	HIPEpiC	eye:	n/a
11	chr7:14942359-14942409	AG04450	lung:	fetal
12	chr7:14942815-14942865	HCT-116	colon:	n/a
13	chr7:14942359-14942409	LNCaP	prostate:	n/a
14	chr7:14942359-14942409	HIPEpiC	eye:	n/a
15	chr7:14942815-14942865	U87	brain:	n/a
16	chr7:14942359-14942409	SKMC	muscle:	n/a
17	chr7:14942359-14942409	NT2-D1	testis:	n/a
18	chr7:14942359-14942409	GM06990	blood:	n/a
19	chr7:14942359-14942409	HMEC	breast:	n/a
20	chr7:14942359-14942409	AG09319	gingival:	n/a
21	chr7:14942359-14942409	NH-A	brain:	n/a
22	chr7:14942815-14942865	LNCaP	prostate:	n/a
23	chr7:14942815-14942865	AG04449	skin:	fetal
24	chr7:14942815-14942865	MCF10A-Er-Src	breast:	n/a
25	chr7:14942359-14942409	ovcar-3	ovarian:	n/a
26	chr7:14942359-14942409	Hepatocyte	liver:	n/a
27	chr7:14942359-14942409	GM12892	blood:	n/a
28	chr7:14942815-14942865	A549	lung:	n/a
29	chr7:14942815-14942865	SK-N-SH_RA	brain:	n/a
30	chr7:14942359-14942409	Hela-S3	cervix:	n/a
31	chr7:14942359-14942409	HepG2	liver:	n/a
32	chr7:14942359-14942409	GM12891	blood:	n/a
33	chr7:14942815-14942865	NB4	blood:	n/a
34	chr7:14942815-14942865	IMR90	lung:	fetal
35	chr7:14942815-14942865	HEK293	kidney:	embryo
36	chr7:14942359-14942409	GM19239	blood:	n/a
37	chr7:14942359-14942409	CMK	blood:	n/a
38	chr7:14942359-14942409	PANC-1	pancreas:	n/a
39	chr7:14942815-14942865	HCM	heart:	n/a
40	chr7:14942359-14942409	HAEpiC	amniotic membrane:	n/a
41	chr7:14942359-14942409	NHDF-neo	bronchial:	n/a
42	chr7:14942815-14942865	HCPEpiC	choroid plexus:	n/a
43	chr7:14942815-14942865	NH-A	brain:	n/a
44	chr7:14942359-14942409	AG04449	skin:	fetal
45	chr7:14942815-14942865	RPTEC	kidney:	n/a
46	chr7:14942815-14942865	GM12891	blood:	n/a
47	chr7:14942359-14942409	BE2_C	brain:	n/a
48	chr7:14942815-14942865	AoSMC	blood vessel:	n/a
49	chr7:14942359-14942409	H1-hESC	embryonic stem cell:	embryo
50	chr7:14942815-14942865	NT2-D1	testis:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:14995312..14997683-chr7:15009030..15011950,2	K562	blood:
2	chr7:15003480..15005257-chr7:15044429..15047091,2	K562	blood:
3	chr7:15002300..15004911-chr7:15009747..15012507,2	MCF-7	breast:
4	chr7:15002300..15004911-chr7:15009747..15012507,2	MCF-7	breast:
5	chr7:14958102..14960838-chr7:14962374..14965166,2	K562	blood:
6	chr7:14995312..14997683-chr7:15009030..15011950,2	K562	blood:
7	chr7:14958102..14960838-chr7:14962374..14965166,2	K562	blood:

No data

Variant related genes	Relation type
DGKB	TF binding region
DGKB	CpG island

Extended variants
information (count: 1938 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1938 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2109396	chr7:14933955-14933956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs575950607	chr7:14933980-14933981	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541474820	chr7:14934030-14934031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185681080	chr7:14934035-14934036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs60810592	chr7:14934036-14934037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112314843	chr7:14934056-14934057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148511375	chr7:14934062-14934063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540421092	chr7:14934063-14934064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190817544	chr7:14934182-14934183	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114736614	chr7:14934189-14934190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191337967	chr7:14934244-14934245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75573133	chr7:14934266-14934267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562859150	chr7:14934270-14934271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs73287436	chr7:14934317-14934318	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs536127105	chr7:14934352-14934353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs183490785	chr7:14934409-14934410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529084446	chr7:14934416-14934417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368651188	chr7:14934436-14934437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs188470844	chr7:14934457-14934458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547609268	chr7:14934476-14934477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193221752	chr7:14934486-14934487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs183190276	chr7:14934493-14934494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6968886	chr7:14934554-14934555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556187770	chr7:14934565-14934566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs543649935	chr7:14934584-14934585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576075892	chr7:14934640-14934641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73680375	chr7:14934653-14934654	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs201233871	chr7:14934672-14934673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375985981	chr7:14934689-14934690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147700363	chr7:14934705-14934706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs560425011	chr7:14934726-14934727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576990708	chr7:14934731-14934732	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546010691	chr7:14934749-14934750	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368138277	chr7:14934798-14934799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs531748402	chr7:14934800-14934801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548555162	chr7:14934814-14934815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561987426	chr7:14934826-14934827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187879794	chr7:14934833-14934834	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529198719	chr7:14934834-14934835	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs542984336	chr7:14934909-14934910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547673461	chr7:14934960-14934961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191270117	chr7:14934976-14934977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533130794	chr7:14934981-14934982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559278941	chr7:14935017-14935018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549735695	chr7:14935066-14935067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs569714498	chr7:14935109-14935110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142520954	chr7:14935154-14935155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537951003	chr7:14935223-14935224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs551423490	chr7:14935274-14935275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs217588	chr7:14935311-14935312	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

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
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
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
Myelofibrosis	22110671	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14929000-14938800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:14929000-14940800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr7:14929200-14935000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr7:14929200-14940800	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr7:14933000-14934000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:14933000-14934000	Weak transcription	HUVEC	blood vessel
7	chr7:14934000-14934600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:14934000-14934800	Enhancers	HUVEC	blood vessel
9	chr7:14934600-14935200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:14935000-14935800	Enhancers	Rectal Smooth Muscle	rectum
11	chr7:14935200-14940600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:14935800-14938400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr7:14937800-14938400	Active TSS	Brain Anterior Caudate	brain
14	chr7:14938200-14938400	Enhancers	Right Atrium	heart
15	chr7:14938200-14938600	Enhancers	Fetal Lung	lung
16	chr7:14938200-14939200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:14938400-14938600	Enhancers	Rectal Smooth Muscle	rectum
18	chr7:14938400-14938800	Enhancers	Osteobl	bone
19	chr7:14938400-14939200	Weak transcription	Brain Anterior Caudate	brain
20	chr7:14938400-14939400	Enhancers	Colon Smooth Muscle	Colon
21	chr7:14938600-14938800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr7:14938600-14939000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr7:14938800-14939400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:14938800-14939600	Weak transcription	Osteobl	bone
25	chr7:14938800-14942000	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr7:14939000-14939400	Enhancers	Rectal Smooth Muscle	rectum
27	chr7:14939200-14939400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr7:14939200-14941400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr7:14939200-14943800	Active TSS	Brain Anterior Caudate	brain
30	chr7:14939400-14940200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr7:14939400-14940600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:14939400-14941600	Weak transcription	Rectal Smooth Muscle	rectum
33	chr7:14939400-14941800	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr7:14939400-14942000	Weak transcription	Colon Smooth Muscle	Colon
35	chr7:14939600-14939800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr7:14939600-14940200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr7:14939600-14940200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:14939600-14940200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr7:14939600-14940200	Enhancers	Osteobl	bone
40	chr7:14939600-14943600	Active TSS	Brain Angular Gyrus	brain
41	chr7:14939600-14943800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
42	chr7:14939800-14940000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:14939800-14940000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:14939800-14940200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr7:14939800-14940200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr7:14939800-14942000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr7:14940000-14940200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr7:14940200-14940800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr7:14940200-14941400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr7:14940200-14941400	Weak transcription	Osteobl	bone

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