Variant report

Variant	nsv525495
Chromosome Location	chr8:61566655-61568210
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	BCLAF1	chr8:61565977-61566701	GM12878	blood:	n/a	n/a
2	BCLAF1	chr8:61566190-61566705	GM12878	blood:	n/a	n/a
3	CTCF	chr8:61567044-61567068	Lung_OC	lung:	n/a	n/a
4	ELF1	chr8:61565930-61566744	GM12878	blood:	n/a	n/a
5	ELF1	chr8:61565826-61566687	MCF-7	breast:	n/a	n/a
6	ELF1	chr8:61565623-61566786	GM12878	blood:	n/a	n/a
7	EP300	chr8:61566882-61566896	K562	blood:	n/a	n/a
8	FOXM1	chr8:61565801-61566667	GM12878	blood:	n/a	n/a
9	GTF2F1	chr8:61565780-61566965	Hela-S3	cervix:	n/a	n/a
10	HA-E2F1	chr8:61563994-61566764	MCF-7	breast:	n/a	chr8:61564796-61564806 chr8:61564908-61564917 chr8:61564323-61564338 chr8:61564992-61565002 chr8:61564986-61564995 chr8:61564451-61564461 chr8:61564295-61564304 chr8:61565116-61565127 chr8:61564888-61564897
11	HCFC1	chr8:61563509-61566895	Hela-S3	cervix:	n/a	n/a
12	MAX	chr8:61564001-61566715	A549	lung:	n/a	n/a
13	MAX	chr8:61564128-61567062	Hela-S3	cervix:	n/a	n/a
14	MAX	chr8:61563924-61566771	HCT-116	colon:	n/a	n/a
15	MAX	chr8:61565572-61566759	MCF-7	breast:	n/a	n/a
16	MAZ	chr8:61565944-61566684	GM12878	blood:	n/a	n/a
17	MAZ	chr8:61565790-61566714	Hela-S3	cervix:	n/a	n/a
18	MTA3	chr8:61565664-61566800	GM12878	blood:	n/a	n/a
19	MXI1	chr8:61566309-61566964	Hela-S3	cervix:	n/a	n/a
20	MYC	chr8:61566444-61566688	MCF-7	breast:	n/a	n/a
21	MYC	chr8:61566856-61567235	MCF10A-Er-Src	breast:	n/a	n/a
22	NFIC	chr8:61566062-61566713	GM12878	blood:	n/a	n/a
23	NFYB	chr8:61566492-61566743	GM12878	blood:	n/a	n/a
24	PAX5	chr8:61566293-61566742	GM12878	blood:	n/a	n/a
25	PML	chr8:61565858-61566722	GM12878	blood:	n/a	n/a
26	POLR2A	chr8:61565547-61566811	H1-neurons	neurons:	n/a	n/a
27	POLR2A	chr8:61564000-61566738	Raji	blood:	n/a	n/a
28	POLR2A	chr8:61564015-61566861	GM12891	blood:	n/a	n/a
29	POLR2A	chr8:61566620-61566730	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr8:61566123-61566706	GM12892	blood:	n/a	n/a
31	RAD21	chr8:61566255-61566675	Hela-S3	cervix:	n/a	chr8:61566542-61566555
32	RCOR1	chr8:61565729-61566736	Hela-S3	cervix:	n/a	n/a
33	RELA	chr8:61565855-61566677	GM19099	blood:	n/a	n/a
34	RFX5	chr8:61565774-61566741	Hela-S3	cervix:	n/a	n/a
35	RUNX3	chr8:61565496-61566736	GM12878	blood:	n/a	chr8:61566545-61566560
36	RUNX3	chr8:61565885-61566960	GM12878	blood:	n/a	chr8:61566545-61566560
37	SIN3A	chr8:61563812-61566676	H1-hESC	embryonic stem cell:	n/a	chr8:61565138-61565151 chr8:61564928-61564941
38	SMARCB1	chr8:61565626-61566666	Hela-S3	cervix:	n/a	n/a
39	SMC3	chr8:61565731-61566706	Hela-S3	cervix:	n/a	n/a
40	SPI1	chr8:61566251-61566768	GM12878	blood:	n/a	n/a
41	STAT3	chr8:61568170-61568333	MCF10A-Er-Src	breast:	n/a	chr8:61568188-61568200
42	TBP	chr8:61566084-61566692	Hela-S3	cervix:	n/a	n/a
43	TCF12	chr8:61565809-61566925	A549	lung:	n/a	n/a
44	TCF3	chr8:61566345-61566678	GM12878	blood:	n/a	n/a
45	TCF7L2	chr8:61565675-61566793	Hela-S3	cervix:	n/a	n/a
46	TCF7L2	chr8:61565970-61566662	HCT-116	colon:	n/a	n/a
47	ZKSCAN1	chr8:61566072-61566656	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:61562679..61568216-chr8:61588453..61593754,19	K562	blood:
2	chr8:61562616..61568326-chr8:61569044..61575643,11	MCF-7	breast:
3	chr8:61559343..61568621-chr8:61588061..61597189,35	MCF-7	breast:
4	chr8:61563005..61568398-chr8:61588453..61593214,14	K562	blood:
5	chr8:61563711..61566471-chr8:61567487..61569836,4	K562	blood:
6	chr8:61563620..61565259-chr8:61566551..61570060,3	K562	blood:
7	chr8:61567779..61569596-chr8:61570085..61572537,2	K562	blood:
8	chr8:61567081..61569634-chr8:62050277..62052303,2	K562	blood:
9	chr8:61562515..61568989-chr8:61586860..61594946,37	MCF-7	breast:
10	chr8:61562433..61567496-chr8:61571905..61575539,5	K562	blood:

Variant related genes	Relation type
ENSG00000254869	TF binding region
ENSG00000171316	chromatin interactions
ENSG00000255289	chromatin interactions
ENSG00000254869	chromatin interactions

Extended variants
information (count: 51 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:51 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs657718	chr8:61566655-61566656	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191955524	chr8:61566721-61566722	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs542850247	chr8:61566767-61566768	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs79243692	chr8:61566799-61566800	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs76359653	chr8:61566802-61566803	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs62524906	chr8:61566890-61566891	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs565448272	chr8:61566905-61566906	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs150958782	chr8:61566945-61566946	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs184209865	chr8:61567027-61567028	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs187217602	chr8:61567035-61567036	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532999531	chr8:61567060-61567061	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs551373497	chr8:61567076-61567077	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs200574252	chr8:61567084-61567085	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs78723247	chr8:61567090-61567091	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs566805747	chr8:61567091-61567092	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs72597110	chr8:61567096-61567097	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs397971376	chr8:61567097-61567098	Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs78676451	chr8:61567256-61567257	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs190848995	chr8:61567269-61567270	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs182274862	chr8:61567331-61567332	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550822725	chr8:61567458-61567459	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs567299362	chr8:61567530-61567531	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs538344155	chr8:61567567-61567568	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs556421499	chr8:61567591-61567592	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs140757270	chr8:61567597-61567598	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs538676412	chr8:61567604-61567605	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs561238071	chr8:61567620-61567621	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs375776883	chr8:61567669-61567670	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs186888701	chr8:61567676-61567677	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs35155227	chr8:61567711-61567712	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs572422861	chr8:61567775-61567776	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs542886653	chr8:61567807-61567808	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs530375333	chr8:61567892-61567893	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs534175678	chr8:61567918-61567919	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs79738926	chr8:61567927-61567928	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs543987915	chr8:61567952-61567953	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs562471845	chr8:61567966-61567967	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs533042158	chr8:61567974-61567975	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs114333636	chr8:61567983-61567984	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs113905280	chr8:61567990-61567991	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs114209110	chr8:61568046-61568047	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs150249932	chr8:61568060-61568061	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs114316979	chr8:61568079-61568080	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs35085415	chr8:61568127-61568128	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs35659969	chr8:61568131-61568132	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs77460156	chr8:61568132-61568133	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs370437857	chr8:61568134-61568135	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs34676413	chr8:61568177-61568178	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs566790274	chr8:61568185-61568186	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs538715081	chr8:61568188-61568189	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	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
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61563400-61566800	Active TSS	Sigmoid Colon	Sigmoid Colon
2	chr8:61563400-61567200	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr8:61563600-61566800	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr8:61563600-61566800	Active TSS	Placenta Amnion	Placenta Amnion
5	chr8:61563600-61566800	Active TSS	Psoas Muscle	Psoas
6	chr8:61563600-61566800	Active TSS	Right Ventricle	heart
7	chr8:61563800-61566800	Active TSS	Brain Anterior Caudate	brain
8	chr8:61563800-61566800	Active TSS	Brain Hippocampus Middle	brain
9	chr8:61563800-61566800	Active TSS	Brain Substantia Nigra	brain
10	chr8:61563800-61566800	Active TSS	Fetal Intestine Large	intestine
11	chr8:61563800-61566800	Active TSS	GM12878-XiMat	blood
12	chr8:61564000-61566800	Active TSS	Gastric	stomach
13	chr8:61564200-61566800	Active TSS	Primary T helper naive cells from peripheral blood	blood
14	chr8:61564200-61566800	Active TSS	Primary T killer memory cells from peripheral blood	blood
15	chr8:61564400-61566800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr8:61565000-61566800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr8:61565000-61566800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:61565200-61566800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
19	chr8:61565200-61566800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
20	chr8:61565200-61567000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
21	chr8:61565200-61567000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr8:61565200-61567000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
23	chr8:61565400-61566800	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
24	chr8:61565400-61566800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
25	chr8:61565400-61566800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr8:61565400-61566800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
27	chr8:61565400-61567000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:61565600-61566800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
29	chr8:61565600-61566800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
30	chr8:61565600-61566800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
31	chr8:61565600-61566800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
32	chr8:61565600-61566800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
33	chr8:61565600-61566800	Bivalent/Poised TSS	HepG2	liver
34	chr8:61565600-61566800	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
35	chr8:61565600-61567000	Bivalent/Poised TSS	Fetal Kidney	kidney
36	chr8:61565800-61566800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
37	chr8:61565800-61566800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
38	chr8:61565800-61566800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
39	chr8:61565800-61566800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
40	chr8:61565800-61566800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
41	chr8:61565800-61566800	Active TSS	Brain Angular Gyrus	brain
42	chr8:61565800-61566800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
43	chr8:61565800-61567000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr8:61566000-61566800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
45	chr8:61566000-61566800	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
46	chr8:61566000-61566800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr8:61566000-61566800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr8:61566000-61566800	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr8:61566000-61566800	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr8:61566000-61566800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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