Variant report

Variant	nsv916262
Chromosome Location	chr8:51322341-51437077
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	ARID3A	chr8:51351100-51351279	HepG2	liver:	n/a	n/a
2	BACH1	chr8:51380375-51380444	K562	blood:	n/a	n/a
3	BACH1	chr8:51360829-51360868	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr8:51322783-51322854	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr8:51417299-51417672	IMR90	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
6	CEBPB	chr8:51340892-51341151	H1-hESC	embryonic stem cell:	n/a	chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341046-51341057 chr8:51341047-51341056 chr8:51341045-51341056
7	CEBPB	chr8:51340868-51341197	IMR90	lung:	n/a	chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341046-51341057 chr8:51341047-51341056 chr8:51341045-51341056
8	CEBPB	chr8:51330350-51330820	HepG2	liver:	n/a	chr8:51330522-51330533
9	CEBPB	chr8:51417365-51417636	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
10	CEBPB	chr8:51417301-51417674	HepG2	liver:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
11	CEBPB	chr8:51417314-51417678	A549	lung:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
12	CEBPB	chr8:51379026-51379129	A549	lung:	n/a	n/a
13	CEBPB	chr8:51417303-51417661	K562	blood:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
14	CEBPB	chr8:51417307-51417674	H1-hESC	embryonic stem cell:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
15	CEBPB	chr8:51340880-51341177	HepG2	liver:	n/a	chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341056 chr8:51341045-51341058 chr8:51341047-51341056 chr8:51341045-51341058 chr8:51341046-51341057 chr8:51341047-51341056 chr8:51341045-51341056
16	CEBPB	chr8:51330470-51330673	H1-hESC	embryonic stem cell:	n/a	chr8:51330522-51330533
17	CEBPB	chr8:51417321-51417664	Hela-S3	cervix:	n/a	chr8:51417510-51417521 chr8:51417479-51417490
18	CEBPB	chr8:51388326-51388344	A549	lung:	n/a	n/a
19	CEBPB	chr8:51330385-51330704	IMR90	lung:	n/a	chr8:51330522-51330533
20	CEBPB	chr8:51384894-51385137	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:51330359-51330662	A549	lung:	n/a	chr8:51330522-51330533
22	CTCF	chr8:51426020-51426170	NB4	blood:	n/a	n/a
23	CTCF	chr8:51426040-51426190	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:51429179-51429252	Kidney_OC	kidney:	n/a	n/a
25	CTCF	chr8:51326180-51326330	NHDF-neo	bronchial:	n/a	n/a
26	CTCF	chr8:51426060-51426210	GM12872	blood:	n/a	n/a
27	CTCF	chr8:51426040-51426190	HepG2	liver:	n/a	n/a
28	CTCF	chr8:51426020-51426170	GM12872	blood:	n/a	n/a
29	CTCF	chr8:51324375-51324437	H1-hESC	embryonic stem cell:	n/a	chr8:51324394-51324403
30	CTCF	chr8:51426000-51426150	GM12864	blood:	n/a	n/a
31	CTCF	chr8:51426060-51426210	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr8:51426080-51426230	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr8:51426020-51426170	HEK293	kidney:	n/a	n/a
34	CTCF	chr8:51372276-51372364	GM13977	blood:	n/a	n/a
35	CTCF	chr8:51408340-51408402	MCF-7	breast:	n/a	n/a
36	CTCF	chr8:51340920-51341070	Caco-2	colon:	n/a	n/a
37	CTCF	chr8:51426120-51426270	GM12874	blood:	n/a	n/a
38	CTCF	chr8:51324280-51324430	WERI-Rb-1	eye:	n/a	chr8:51324394-51324403
39	CTCF	chr8:51408333-51408408	MCF-7	breast:	n/a	chr8:51408333-51408341
40	CTCF	chr8:51357036-51357094	GM10248	blood:	n/a	n/a
41	CTCF	chr8:51426394-51426423	GM13976	blood:	n/a	n/a
42	CTCF	chr8:51324398-51324434	MCF-7	breast:	n/a	n/a
43	CTCF	chr8:51426040-51426190	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr8:51408280-51408430	MCF-7	breast:	n/a	chr8:51408333-51408341
45	CTCF	chr8:51397533-51397580	GM13976	blood:	n/a	n/a
46	CTCF	chr8:51324415-51324452	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:51426058-51426145	MCF-7	breast:	n/a	n/a
48	CTCF	chr8:51339260-51339354	GM13976	blood:	n/a	n/a
49	CTCF	chr8:51426060-51426210	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr8:51357211-51357287	GM13977	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:51404066-51404116	HAEpiC	amniotic membrane:	n/a
2	chr8:51404066-51404116	HAEpiC	amniotic membrane:	n/a
3	chr8:51404179-51404229	HCM	heart:	n/a
4	chr8:51404179-51404229	HUVEC	blood vessel:	n/a
5	chr8:51404066-51404116	LNCaP	prostate:	n/a
6	chr8:51404066-51404116	NB4	blood:	n/a
7	chr8:51404179-51404229	SK-N-SH	brain:	n/a
8	chr8:51364244-51364294	K562	blood:	n/a
9	chr8:51404106-51404156	H1-hESC	embryonic stem cell:	embryo
10	chr8:51404066-51404116	Jurkat	blood:	n/a
11	chr8:51364244-51364294	HRCEpiC	kidney:	n/a
12	chr8:51404106-51404156	LNCaP	prostate:	n/a
13	chr8:51404179-51404229	RPTEC	kidney:	n/a
14	chr8:51404066-51404116	AoSMC	blood vessel:	n/a
15	chr8:51404066-51404116	Hela-S3	cervix:	n/a
16	chr8:51404179-51404229	PANC-1	pancreas:	n/a
17	chr8:51404106-51404156	HCPEpiC	choroid plexus:	n/a
18	chr8:51404179-51404229	T-47D	breast:	n/a
19	chr8:51404179-51404229	NB4	blood:	n/a
20	chr8:51404066-51404116	HCF	heart:	n/a
21	chr8:51404106-51404156	GM12892	blood:	n/a
22	chr8:51404066-51404116	RPTEC	kidney:	n/a
23	chr8:51404066-51404116	A549	lung:	n/a
24	chr8:51404179-51404229	AG04450	lung:	fetal
25	chr8:51364244-51364294	PrEC	prostate:	n/a
26	chr8:51404066-51404116	AG04450	lung:	fetal
27	chr8:51404106-51404156	CMK	blood:	n/a
28	chr8:51404179-51404229	BE2_C	brain:	n/a
29	chr8:51364244-51364294	HNPCEpiC	eye:	n/a
30	chr8:51404179-51404229	GM12892	blood:	n/a
31	chr8:51404106-51404156	SK-N-MC	brain:	n/a
32	chr8:51364244-51364294	MCF-7	breast:	n/a
33	chr8:51404066-51404116	BJ	skin:	n/a
34	chr8:51404179-51404229	SAEC	small airway:	n/a
35	chr8:51404179-51404229	HPAEpiC	pulmonary alveolar:	n/a
36	chr8:51364244-51364294	SK-N-MC	brain:	n/a
37	chr8:51404066-51404116	HCT-116	colon:	n/a
38	chr8:51404106-51404156	BE2_C	brain:	n/a
39	chr8:51404066-51404116	CMK	blood:	n/a
40	chr8:51404179-51404229	NHDF-neo	bronchial:	n/a
41	chr8:51364244-51364294	BE2_C	brain:	n/a
42	chr8:51404066-51404116	PANC-1	pancreas:	n/a
43	chr8:51404106-51404156	HIPEpiC	eye:	n/a
44	chr8:51404106-51404156	SK-N-SH_RA	brain:	n/a
45	chr8:51364244-51364294	NB4	blood:	n/a
46	chr8:51364244-51364294	U87	brain:	n/a
47	chr8:51404106-51404156	ProgFib	skin:	n/a
48	chr8:51404066-51404116	MCF10A-Er-Src	breast:	n/a
49	chr8:51364244-51364294	Caco-2	colon:	n/a
50	chr8:51404106-51404156	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:
2	chr8:51372315..51374214-chr8:51375832..51377998,2	K562	blood:

Variant related genes	Relation type
ENSG00000254392	TF binding region
ENSG00000254392	CpG island

Extended variants
information (count: 3040 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:3040 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566839998	chr8:51322375-51322376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs569977305	chr8:51322428-51322429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536946951	chr8:51322430-51322431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs371183834	chr8:51322436-51322437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs556144428	chr8:51322507-51322508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568073507	chr8:51322520-51322521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs3919897	chr8:51322548-51322549	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs553822704	chr8:51322580-51322581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115881509	chr8:51322601-51322602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549169353	chr8:51322676-51322677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141129039	chr8:51322679-51322680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs78408466	chr8:51322689-51322690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531483971	chr8:51322701-51322702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576719672	chr8:51322758-51322759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544083046	chr8:51322767-51322768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146087559	chr8:51322815-51322816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189716624	chr8:51322863-51322864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541147377	chr8:51322891-51322892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547089309	chr8:51322934-51322935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112094311	chr8:51322942-51322943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182510724	chr8:51322957-51322958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs187158095	chr8:51322958-51322959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551600683	chr8:51322968-51322969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs569707279	chr8:51322981-51322982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530725796	chr8:51323018-51323019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs1017840	chr8:51323055-51323056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548831292	chr8:51323060-51323061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568138434	chr8:51323067-51323068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569104228	chr8:51323071-51323072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192017395	chr8:51323082-51323083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138913289	chr8:51323084-51323085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567469499	chr8:51323086-51323087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368249583	chr8:51323090-51323091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566203412	chr8:51323110-51323111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs115348002	chr8:51323159-51323160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182793887	chr8:51323170-51323171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543635436	chr8:51323171-51323172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10107375	chr8:51323207-51323208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149403181	chr8:51323232-51323233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs565417008	chr8:51323243-51323244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565898441	chr8:51323310-51323311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534849686	chr8:51323320-51323321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34610906	chr8:51323323-51323324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574364327	chr8:51323392-51323393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs551580812	chr8:51323411-51323412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531270683	chr8:51323415-51323416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs559085376	chr8:51323453-51323454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs533051355	chr8:51323455-51323456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79108714	chr8:51323473-51323474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536907491	chr8:51323575-51323576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
22q11 deletion syndrome	20357662	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:133 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:51320600-51343200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr8:51340400-51341200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr8:51340600-51341000	Enhancers	Liver	Liver
4	chr8:51340600-51341200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:51340600-51341200	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr8:51340800-51341200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr8:51341000-51343000	Weak transcription	Liver	Liver
8	chr8:51343000-51343400	ZNF genes & repeats	Liver	Liver
9	chr8:51343200-51343600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:51343400-51343800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
11	chr8:51343800-51347800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr8:51344800-51345200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:51347800-51348000	Enhancers	Liver	Liver
14	chr8:51347800-51348400	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr8:51347800-51349200	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr8:51347800-51349200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr8:51348000-51348200	Flanking Active TSS	Liver	Liver
18	chr8:51348000-51348400	Enhancers	Fetal Intestine Small	intestine
19	chr8:51348200-51348400	Enhancers	Liver	Liver
20	chr8:51348200-51349600	Enhancers	Brain Germinal Matrix	brain
21	chr8:51348400-51348600	Flanking Active TSS	Liver	Liver
22	chr8:51348400-51348800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:51348400-51356200	Weak transcription	Fetal Intestine Small	intestine
24	chr8:51348600-51348800	Enhancers	Liver	Liver
25	chr8:51348800-51350000	Weak transcription	Liver	Liver
26	chr8:51349600-51350600	Weak transcription	Brain Germinal Matrix	brain
27	chr8:51350000-51350600	Enhancers	Liver	Liver
28	chr8:51350600-51350800	Enhancers	Brain Germinal Matrix	brain
29	chr8:51350600-51351400	Flanking Active TSS	Liver	Liver
30	chr8:51350600-51351600	Enhancers	Fetal Intestine Large	intestine
31	chr8:51350800-51351400	Weak transcription	Brain Germinal Matrix	brain
32	chr8:51351400-51352800	Enhancers	Liver	Liver
33	chr8:51351600-51356400	Weak transcription	Fetal Intestine Large	intestine
34	chr8:51352800-51353400	Weak transcription	Liver	Liver
35	chr8:51353400-51354000	Enhancers	Liver	Liver
36	chr8:51354000-51355600	Weak transcription	Liver	Liver
37	chr8:51355600-51356600	Enhancers	Liver	Liver
38	chr8:51356200-51356600	Enhancers	Fetal Intestine Small	intestine
39	chr8:51356400-51357000	Enhancers	Fetal Intestine Large	intestine
40	chr8:51358000-51358400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr8:51360400-51360800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr8:51360600-51361400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr8:51360800-51363200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr8:51361400-51362400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr8:51361600-51362800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr8:51361800-51362800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr8:51361800-51365600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr8:51362000-51362400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:51362200-51362600	Enhancers	H9 Cell Line	embryonic stem cell
50	chr8:51362200-51362600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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