Variant report

Variant	esv2754706
Chromosome Location	chr10:23477062-23509344
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	chr10:23484547-23484686	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr10:23488894-23489012	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr10:23481438-23481598	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr10:23490348-23490523	HepG2	liver:	n/a	n/a
5	CEBPB	chr10:23500086-23500238	HepG2	liver:	n/a	chr10:23500170-23500181
6	CEBPB	chr10:23500149-23500279	A549	lung:	n/a	chr10:23500170-23500181
7	CHD1	chr10:23488109-23488277	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr10:23488880-23489189	H1-hESC	embryonic stem cell:	n/a	n/a
9	CREB1	chr10:23483844-23484351	H1-hESC	embryonic stem cell:	n/a	chr10:23484145-23484158
10	CREB1	chr10:23483890-23484414	H1-hESC	embryonic stem cell:	n/a	chr10:23484145-23484158
11	CTBP2	chr10:23485887-23486756	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTBP2	chr10:23487514-23489363	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr10:23479936-23482481	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr10:23493861-23493969	Gliobla	brain:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
15	CTCF	chr10:23481540-23481870	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr10:23493868-23494007	K562	blood:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
17	CTCF	chr10:23488340-23488490	GM12874	blood:	n/a	chr10:23488442-23488460
18	CTCF	chr10:23493840-23493990	HRPEpiC	eye:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
19	CTCF	chr10:23493820-23493970	AG04449	skin:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
20	CTCF	chr10:23507119-23507146	MCF-7	breast:	n/a	n/a
21	CTCF	chr10:23481680-23481830	HEK293	kidney:	n/a	n/a
22	CTCF	chr10:23493811-23494029	H1-hESC	embryonic stem cell:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
23	CTCF	chr10:23481623-23481901	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr10:23507095-23507205	MCF-7	breast:	n/a	n/a
25	CTCF	chr10:23481859-23481893	Fibrobl	skin:	n/a	n/a
26	CTCF	chr10:23493861-23493982	Fibrobl	skin:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
27	CTCF	chr10:23497900-23498050	GM12872	blood:	n/a	n/a
28	CTCF	chr10:23493881-23493938	GM19239	blood:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
29	CTCF	chr10:23493800-23493950	GM06990	blood:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
30	CTCF	chr10:23493820-23493970	K562	blood:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
31	CTCF	chr10:23507076-23507218	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr10:23493820-23493970	HepG2	liver:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
33	CTCF	chr10:23481823-23481847	Fibrobl	skin:	n/a	n/a
34	CTCF	chr10:23493883-23493942	GM12891	blood:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
35	CTCF	chr10:23481750-23481858	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr10:23493812-23494025	H1-hESC	embryonic stem cell:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
37	CTCF	chr10:23481640-23481790	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr10:23481680-23481830	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr10:23493820-23493970	HRPEpiC	eye:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
40	CTCF	chr10:23481705-23481880	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr10:23507114-23507190	MCF-7	breast:	n/a	n/a
42	CTCF	chr10:23493858-23494002	Pancreas_OC	pancreas:	n/a	chr10:23493916-23493937 chr10:23493915-23493931
43	E2F4	chr10:23492079-23492154	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F6	chr10:23480648-23481045	H1-hESC	embryonic stem cell:	n/a	n/a
45	E2F6	chr10:23480742-23481213	H1-hESC	embryonic stem cell:	n/a	chr10:23481163-23481172
46	E2F6	chr10:23481362-23482238	H1-hESC	embryonic stem cell:	n/a	n/a
47	E2F6	chr10:23481438-23482266	H1-hESC	embryonic stem cell:	n/a	n/a
48	EGR1	chr10:23481544-23481932	H1-hESC	embryonic stem cell:	n/a	n/a
49	ELK4	chr10:23494998-23495172	HEK293	kidney:	n/a	n/a
50	EP300	chr10:23505822-23505836	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:23484228-23484278	BE2_C	brain:	n/a
2	chr10:23484326-23484376	PANC-1	pancreas:	n/a
3	chr10:23481176-23481226	A549	lung:	n/a
4	chr10:23484228-23484278	BE2_C	brain:	n/a
5	chr10:23484326-23484376	PANC-1	pancreas:	n/a
6	chr10:23481176-23481226	A549	lung:	n/a
7	chr10:23487775-23487825	HPAEpiC	pulmonary alveolar:	n/a
8	chr10:23479410-23479460	HEEpiC	esophagus:	n/a
9	chr10:23481385-23481435	HIPEpiC	eye:	n/a
10	chr10:23489702-23489752	CMK	blood:	n/a
11	chr10:23481389-23481439	HL-60	blood:	n/a
12	chr10:23479410-23479460	HEK293	kidney:	embryo
13	chr10:23480190-23480240	SAEC	small airway:	n/a
14	chr10:23481176-23481226	HRCEpiC	kidney:	n/a
15	chr10:23478530-23478580	HEK293	kidney:	embryo
16	chr10:23487758-23487808	HEK293	kidney:	embryo
17	chr10:23492470-23492520	GM12878	blood:	n/a
18	chr10:23480803-23480853	AG04449	skin:	fetal
19	chr10:23481594-23481644	ovcar-3	ovarian:	n/a
20	chr10:23478530-23478580	RPTEC	kidney:	n/a
21	chr10:23484326-23484376	HepG2	liver:	n/a
22	chr10:23492798-23492848	SAEC	small airway:	n/a
23	chr10:23481594-23481644	PANC-1	pancreas:	n/a
24	chr10:23479993-23480043	HCF	heart:	n/a
25	chr10:23489702-23489752	HIPEpiC	eye:	n/a
26	chr10:23484556-23484606	GM12891	blood:	n/a
27	chr10:23484326-23484376	Caco-2	colon:	n/a
28	chr10:23481594-23481644	AG04450	lung:	fetal
29	chr10:23484556-23484606	NHBE	bronchial:	n/a
30	chr10:23492914-23492964	ECC-1	luminal epithelium:	n/a
31	chr10:23484025-23484075	GM06990	blood:	n/a
32	chr10:23489232-23489282	H1-hESC	embryonic stem cell:	embryo
33	chr10:23487775-23487825	MCF10A-Er-Src	breast:	n/a
34	chr10:23489850-23489900	HL-60	blood:	n/a
35	chr10:23492798-23492848	NH-A	brain:	n/a
36	chr10:23480237-23480287	MCF10A-Er-Src	breast:	n/a
37	chr10:23481786-23481836	HIPEpiC	eye:	n/a
38	chr10:23488272-23488322	SAEC	small airway:	n/a
39	chr10:23484556-23484606	IMR90	lung:	fetal
40	chr10:23480018-23480068	H1-hESC	embryonic stem cell:	embryo
41	chr10:23488272-23488322	AG10803	skin:	n/a
42	chr10:23484326-23484376	K562	blood:	n/a
43	chr10:23481786-23481836	NHDF-neo	bronchial:	n/a
44	chr10:23489850-23489900	HCM	heart:	n/a
45	chr10:23484025-23484075	AG04449	skin:	fetal
46	chr10:23484025-23484075	HepG2	liver:	n/a
47	chr10:23480018-23480068	HL-60	blood:	n/a
48	chr10:23492798-23492848	Jurkat	blood:	n/a
49	chr10:23479993-23480043	Caco-2	colon:	n/a
50	chr10:23484556-23484606	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr10:23476776..23479722-chr10:23481093..23483955,2	MCF-7	breast:
2	chr10:23474176..23477115-chr10:23477275..23479247,2	K562	blood:
3	chr10:23474176..23477115-chr10:23477275..23479247,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf115-2	chr10:23492745-23493184	NR_103721

Variant related genes	Relation type
PTF1A	TF binding region
PTF1A	CpG island
ENSG00000168267	chromatin interactions

Extended variants
information (count: 755 )
Associated
traits (count: 38 )

Variant overlapped rSNPs/rCNVs (count:755 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1408986	chr10:23477062-23477063	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544170673	chr10:23477071-23477072	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs117615239	chr10:23477126-23477127	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs572995942	chr10:23477133-23477134	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185151861	chr10:23477160-23477161	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs189569901	chr10:23477190-23477191	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs559328011	chr10:23477197-23477198	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs1408987	chr10:23477203-23477204	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs551404823	chr10:23477209-23477210	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181225003	chr10:23477221-23477222	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs571494476	chr10:23477231-23477232	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs16923107	chr10:23477249-23477250	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs550556054	chr10:23477284-23477285	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs567261754	chr10:23477304-23477305	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536400189	chr10:23477305-23477306	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs75685809	chr10:23477436-23477437	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs566987800	chr10:23477447-23477448	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11594013	chr10:23477504-23477505	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs559009723	chr10:23477524-23477525	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs144759292	chr10:23477559-23477560	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs145871278	chr10:23477566-23477567	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368243545	chr10:23477567-23477568	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs186301757	chr10:23477579-23477580	Bivalent/Poised TSS Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs58872155	chr10:23477614-23477615	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570794493	chr10:23477629-23477630	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371785542	chr10:23477660-23477661	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs77432387	chr10:23477677-23477678	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572977239	chr10:23477693-23477694	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554108483	chr10:23477698-23477699	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566140691	chr10:23477707-23477708	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs148283326	chr10:23477748-23477749	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191769288	chr10:23477800-23477801	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs543820074	chr10:23477839-23477840	Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs369056478	chr10:23477869-23477870	Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529698940	chr10:23477906-23477907	Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs546393293	chr10:23477916-23477917	Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs566533482	chr10:23477927-23477928	Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs538859231	chr10:23477978-23477979	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs201145348	chr10:23477987-23477988	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs61136507	chr10:23478001-23478002	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs533594215	chr10:23478004-23478005	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs183619542	chr10:23478018-23478019	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs538191871	chr10:23478038-23478039	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs188912584	chr10:23478043-23478044	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs192385660	chr10:23478056-23478057	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533907911	chr10:23478083-23478084	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs5783830	chr10:23478105-23478106	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs61847275	chr10:23478106-23478107	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs61847276	chr10:23478107-23478108	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs59570145	chr10:23478108-23478109	Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:38)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Behavioral abnormalities	21522184	CNVD
Dysmorphic features	21522184	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23475800-23477600	Enhancers	Pancreas	Pancrea
2	chr10:23476600-23478600	Bivalent Enhancer	HepG2	liver
3	chr10:23477000-23477800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr10:23477600-23478200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:23477600-23478200	Flanking Active TSS	Pancreas	Pancrea
6	chr10:23477600-23478400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
7	chr10:23477800-23478000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr10:23477800-23478000	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr10:23477800-23478200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr10:23477800-23478600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
11	chr10:23477800-23478600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
12	chr10:23478000-23478200	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
13	chr10:23478000-23478200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
14	chr10:23478200-23478400	Enhancers	Pancreas	Pancrea
15	chr10:23478400-23478600	Flanking Active TSS	Pancreas	Pancrea
16	chr10:23478600-23479000	Enhancers	Pancreas	Pancrea
17	chr10:23479000-23479200	Weak transcription	Pancreas	Pancrea
18	chr10:23479200-23479600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr10:23479200-23480000	Bivalent Enhancer	HepG2	liver
20	chr10:23479200-23480400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
21	chr10:23479200-23481600	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr10:23479200-23483400	Active TSS	Pancreas	Pancrea
23	chr10:23479400-23479600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr10:23479400-23479800	Bivalent Enhancer	Fetal Brain Male	brain
25	chr10:23479400-23480000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
26	chr10:23479400-23480000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
27	chr10:23479400-23480000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr10:23479400-23480600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
29	chr10:23479600-23479800	Flanking Bivalent TSS/Enh	ES-I3 Cell Line	embryonic stem cell
30	chr10:23479600-23479800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr10:23479600-23479800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
32	chr10:23479600-23480000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
33	chr10:23479600-23480800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
34	chr10:23479600-23481400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr10:23479800-23480000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
36	chr10:23479800-23480200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr10:23479800-23480200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
38	chr10:23479800-23480400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr10:23479800-23480800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr10:23479800-23482600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr10:23480000-23480200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr10:23480000-23480200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
43	chr10:23480000-23480200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
44	chr10:23480000-23480200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
45	chr10:23480000-23480400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
46	chr10:23480000-23480400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr10:23480000-23480600	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr10:23480000-23481000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr10:23480000-23481600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
50	chr10:23480000-23481800	Bivalent Enhancer	Fetal Brain Male	brain

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