Variant report

Variant	nsv1025989
Chromosome Location	chr8:20829412-20865838
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	BCL3	chr8:20836598-20836879	GM12878	blood:	n/a	n/a
2	CEBPB	chr8:20852997-20853024	A549	lung:	n/a	n/a
3	CEBPB	chr8:20852513-20852598	HepG2	liver:	n/a	n/a
4	CEBPB	chr8:20846099-20846340	HepG2	liver:	n/a	n/a
5	CEBPB	chr8:20830066-20830350	HepG2	liver:	n/a	chr8:20830220-20830231
6	CEBPB	chr8:20852924-20853124	HepG2	liver:	n/a	n/a
7	CEBPB	chr8:20840086-20840263	HepG2	liver:	n/a	chr8:20840222-20840233
8	CEBPB	chr8:20852958-20853147	K562	blood:	n/a	n/a
9	CEBPB	chr8:20830191-20830296	H1-hESC	embryonic stem cell:	n/a	chr8:20830220-20830231
10	CTCF	chr8:20855084-20855159	LNCaP	prostate:	n/a	chr8:20855100-20855118
11	CTCF	chr8:20855040-20855190	WERI-Rb-1	eye:	n/a	chr8:20855100-20855118
12	CTCF	chr8:20855020-20855170	Hela-S3	cervix:	n/a	chr8:20855100-20855118
13	CTCF	chr8:20854896-20855242	MCF-7	breast:	n/a	chr8:20855100-20855118
14	CTCF	chr8:20854960-20855110	HCT-116	colon:	n/a	n/a
15	CTCF	chr8:20855120-20855270	K562	blood:	n/a	n/a
16	CTCF	chr8:20855034-20855194	MCF-7	breast:	n/a	chr8:20855100-20855118
17	CTCF	chr8:20847954-20847971	GM10248	blood:	n/a	n/a
18	CTCF	chr8:20855120-20855270	GM12875	blood:	n/a	n/a
19	CTCF	chr8:20854984-20855212	K562	blood:	n/a	chr8:20855100-20855118
20	CTCF	chr8:20854980-20855130	GM12873	blood:	n/a	chr8:20855100-20855118
21	CTCF	chr8:20855060-20855210	NB4	blood:	n/a	chr8:20855100-20855118
22	CTCF	chr8:20855020-20855170	GM12875	blood:	n/a	chr8:20855100-20855118
23	CTCF	chr8:20855000-20855150	GM12872	blood:	n/a	chr8:20855100-20855118
24	CTCF	chr8:20855080-20855230	GM06990	blood:	n/a	chr8:20855100-20855118
25	CTCF	chr8:20855070-20855171	Gliobla	brain:	n/a	chr8:20855100-20855118
26	CTCF	chr8:20855039-20855196	A549	lung:	n/a	chr8:20855100-20855118
27	CTCF	chr8:20855000-20855150	RPTEC	kidney:	n/a	chr8:20855100-20855118
28	CTCF	chr8:20855072-20855203	GM13977	blood:	n/a	chr8:20855100-20855118
29	CTCF	chr8:20855042-20855156	Medullo	brain:	n/a	chr8:20855100-20855118
30	CTCF	chr8:20855060-20855210	GM12874	blood:	n/a	chr8:20855100-20855118
31	CTCF	chr8:20855044-20855184	MCF-7	breast:	n/a	chr8:20855100-20855118
32	CTCF	chr8:20855000-20855150	GM12871	blood:	n/a	chr8:20855100-20855118
33	CTCF	chr8:20854960-20855110	GM12878	blood:	n/a	n/a
34	CTCF	chr8:20855040-20855190	NHEK	skin:	n/a	chr8:20855100-20855118
35	CTCF	chr8:20855057-20855201	HepG2	liver:	n/a	chr8:20855100-20855118
36	CTCF	chr8:20855040-20855190	GM12872	blood:	n/a	chr8:20855100-20855118
37	CTCF	chr8:20855012-20855240	H1-hESC	embryonic stem cell:	n/a	chr8:20855100-20855118
38	CTCF	chr8:20855000-20855150	HCT-116	colon:	n/a	chr8:20855100-20855118
39	CTCF	chr8:20855040-20855190	GM12873	blood:	n/a	chr8:20855100-20855118
40	CTCF	chr8:20855040-20855190	BE2_C	brain:	n/a	chr8:20855100-20855118
41	CTCF	chr8:20855020-20855170	RPTEC	kidney:	n/a	chr8:20855100-20855118
42	CTCF	chr8:20855000-20855150	GM12866	blood:	n/a	chr8:20855100-20855118
43	CTCF	chr8:20855031-20855198	HepG2	liver:	n/a	chr8:20855100-20855118
44	CTCF	chr8:20855000-20855150	GM12869	blood:	n/a	chr8:20855100-20855118
45	CTCF	chr8:20855041-20855146	Hela-S3	cervix:	n/a	chr8:20855100-20855118
46	CTCF	chr8:20855060-20855210	GM12871	blood:	n/a	chr8:20855100-20855118
47	CTCF	chr8:20855024-20855209	K562	blood:	n/a	chr8:20855100-20855118
48	CTCF	chr8:20855040-20855190	HepG2	liver:	n/a	chr8:20855100-20855118
49	CTCF	chr8:20855060-20855210	GM12864	blood:	n/a	chr8:20855100-20855118
50	CTCF	chr8:20855020-20855170	GM12873	blood:	n/a	chr8:20855100-20855118

No.	Distal block	Cell Line	Cell type
1	chr8:20297170..20297886-chr8:20854968..20855533,2	MCF-7	breast:
2	chr8:20839365..20841858-chr8:20843930..20846390,2	K562	blood:
3	chr8:20831135..20833950-chr8:20835824..20837842,2	K562	blood:
4	chr8:20856229..20857904-chr8:20875184..20876772,2	K562	blood:
5	chr8:20839365..20841858-chr8:20843930..20846390,2	K562	blood:
6	chr8:20400181..20400690-chr8:20854628..20855500,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATP6V1B2-5	chr8:20843922-20843997	XLOC_006734
2	lnc-ATP6V1B2-5	chr8:20831308-20832033	ENSG00000253199
3	lnc-ATP6V1B2-9	chr8:20856970-20857056	l_3558_chr8:20855416-20870707_testes
4	lnc-ATP6V1B2-5	chr8:20831896-20832033	XLOC_006734
5	lnc-ATP6V1B2-5	chr8:20831497-20832164	XLOC_006734
6	lnc-GFRA2-6	chr8:20853998-20854707	l_3557_chr8:20853997-20856467_brain
7	lnc-ATP6V1B2-5	chr8:20832315-20832540	ENSG00000253199
8	lnc-ATP6V1B2-5	chr8:20852540-20852630	XLOC_006734
9	lnc-ATP6V1B2-5	chr8:20832315-20832531	NONHSAT125421
10	lnc-ATP6V1B2-5	chr8:20832315-20832533	XLOC_006734
11	lnc-ATP6V1B2-5	chr8:20831913-20832033	NONHSAT125421
12	lnc-ATP6V1B2-5	chr8:20831860-20832033	XLOC_006734
13	lnc-ATP6V1B2-5	chr8:20831248-20831509	XLOC_006734
14	lnc-ATP6V1B2-5	chr8:20852291-20852449	XLOC_006734
15	lnc-LZTS1-2	chr8:20831244-20831388	ENSG00000254092
16	lnc-ATP6V1B2-9	chr8:20864572-20864692	l_3558_chr8:20855416-20870707_testes
17	lnc-GFRA2-6	chr8:20856446-20856535	l_3557_chr8:20853997-20856467_brain
18	lnc-ATP6V1B2-5	chr8:20840968-20841617	XLOC_006734
19	lnc-ATP6V1B2-5	chr8:20852291-20852334	XLOC_006734
20	lnc-ATP6V1B2-9	chr8:20855417-20855484	l_3558_chr8:20855416-20870707_testes
21	lnc-ATP6V1B2-5	chr8:20832315-20832514	XLOC_006734
22	lnc-ATP6V1B2-9	chr8:20857476-20857627	l_3558_chr8:20855416-20870707_testes
23	lnc-ATP6V1B2-9	chr8:20855632-20855866	l_3558_chr8:20855416-20870707_testes
24	lnc-ATP6V1B2-5	chr8:20831433-20831509	NONHSAT125421

Variant related genes	Relation type
ENSG00000253199	TF binding region
ENSG00000254092	TF binding region
ENSG00000253199	chromatin interactions
ENSG00000254092	chromatin interactions
BMPR2	miRNA target sites

Extended variants
information (count: 663 )
Associated
traits (count: 117 )

Variant overlapped rSNPs/rCNVs (count:663 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192532618	chr8:20829418-20829419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs150564857	chr8:20829433-20829434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546367648	chr8:20829440-20829441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138417569	chr8:20829444-20829445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532466420	chr8:20829496-20829497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373816804	chr8:20829542-20829543	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545933402	chr8:20829589-20829590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs471425	chr8:20829596-20829597	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs149276848	chr8:20829600-20829601	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs536962508	chr8:20829604-20829605	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs117974781	chr8:20829609-20829610	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs144423841	chr8:20829665-20829666	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs534425291	chr8:20829678-20829679	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs559182380	chr8:20829703-20829704	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs571383484	chr8:20829721-20829722	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs538306710	chr8:20829745-20829746	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs542018941	chr8:20829754-20829755	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs538660575	chr8:20829766-20829767	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs183497169	chr8:20829795-20829796	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs57224972	chr8:20829798-20829799	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs373855831	chr8:20829821-20829822	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs542603387	chr8:20829823-20829824	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs113851725	chr8:20829840-20829841	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs554470290	chr8:20829861-20829862	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs572785395	chr8:20829865-20829866	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs188234555	chr8:20829901-20829902	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs191582637	chr8:20829906-20829907	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs377049005	chr8:20829941-20829942	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs11204144	chr8:20829960-20829961	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs139072873	chr8:20829964-20829965	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs562991268	chr8:20829966-20829967	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs530066035	chr8:20829983-20829984	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs73631068	chr8:20829986-20829987	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs372382194	chr8:20829991-20829992	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs114791904	chr8:20829993-20829994	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs112267427	chr8:20829995-20829996	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs552829676	chr8:20829997-20829998	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs140186356	chr8:20830010-20830011	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs496541	chr8:20830052-20830053	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs556808624	chr8:20830056-20830057	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs62499583	chr8:20830073-20830074	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs77487521	chr8:20830093-20830094	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs554104200	chr8:20830115-20830116	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs142380230	chr8:20830142-20830143	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs370341976	chr8:20830145-20830146	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs540107676	chr8:20830147-20830148	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs184922002	chr8:20830148-20830149	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs62499584	chr8:20830154-20830155	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs576997526	chr8:20830202-20830203	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs544372189	chr8:20830204-20830205	Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:117)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20827600-20831600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:20828600-20830400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr8:20828600-20831000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr8:20829200-20830800	Enhancers	Primary hematopoietic stem cells	blood
5	chr8:20829400-20830000	Enhancers	Primary T cells from cord blood	blood
6	chr8:20829400-20830000	Enhancers	Fetal Thymus	thymus
7	chr8:20829400-20830200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:20829400-20830800	Enhancers	Brain Cingulate Gyrus	brain
9	chr8:20829600-20830000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:20829600-20830000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr8:20829600-20830000	Bivalent Enhancer	Brain Substantia Nigra	brain
12	chr8:20829600-20830600	Enhancers	Brain Anterior Caudate	brain
13	chr8:20829600-20831000	Enhancers	Brain Hippocampus Middle	brain
14	chr8:20829800-20830200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr8:20829800-20830400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr8:20829800-20830400	Enhancers	Brain Angular Gyrus	brain
17	chr8:20829800-20830800	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr8:20829800-20831200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:20830000-20830400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr8:20830000-20830600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:20830000-20830800	Enhancers	Brain Substantia Nigra	brain
22	chr8:20830800-20834600	Weak transcription	Brain Cingulate Gyrus	brain
23	chr8:20833800-20834400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr8:20833800-20835400	Enhancers	Fetal Brain Male	brain
25	chr8:20834000-20834400	Enhancers	Brain Germinal Matrix	brain
26	chr8:20834000-20834800	Enhancers	Fetal Brain Female	brain
27	chr8:20834400-20835400	Enhancers	Spleen	Spleen
28	chr8:20834600-20834800	Enhancers	Brain Hippocampus Middle	brain
29	chr8:20834600-20835400	Enhancers	Brain Cingulate Gyrus	brain
30	chr8:20835000-20835600	Enhancers	Fetal Lung	lung
31	chr8:20835600-20835800	Bivalent Enhancer	Fetal Lung	lung
32	chr8:20840200-20840600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr8:20846000-20846400	Active TSS	Fetal Heart	heart
34	chr8:20852000-20852800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr8:20852000-20852800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr8:20853000-20853400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr8:20853600-20854200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr8:20853800-20855200	Enhancers	Fetal Heart	heart
39	chr8:20854000-20854600	Enhancers	Brain Germinal Matrix	brain
40	chr8:20854000-20855000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr8:20854200-20855000	Enhancers	Placenta	Placenta
42	chr8:20864800-20865800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
43	chr8:20865400-20865800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
44	chr8:20865400-20866000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
45	chr8:20865600-20865800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:20865800-20866000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links