Variant report

Variant	nsv897588
Chromosome Location	chr11:57364381-57373478
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:103)
CpG islands
(count:612)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:103 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:57365519-57366056	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:57365577-57366050	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr11:57370562-57370916	K562	blood:	n/a	n/a
4	CBX3	chr11:57370562-57370891	K562	blood:	n/a	n/a
5	CEBPB	chr11:57370776-57370785	IMR90	lung:	n/a	n/a
6	CHD2	chr11:57365286-57365976	H1-hESC	embryonic stem cell:	n/a	n/a
7	CREB1	chr11:57365225-57366034	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr11:57365461-57366106	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTBP2	chr11:57365451-57366071	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr11:57372645-57372712	Medullo	brain:	n/a	n/a
11	CTCF	chr11:57372584-57372787	K562	blood:	n/a	n/a
12	CTCF	chr11:57370557-57370587	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr11:57372572-57372726	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr11:57372636-57372751	K562	blood:	n/a	n/a
15	CTCF	chr11:57372687-57372745	GM12878	blood:	n/a	n/a
16	CTCF	chr11:57372620-57372770	Caco-2	colon:	n/a	n/a
17	EGR1	chr11:57365544-57366110	H1-hESC	embryonic stem cell:	n/a	chr11:57365818-57365831
18	EGR1	chr11:57365670-57366022	H1-hESC	embryonic stem cell:	n/a	chr11:57365818-57365831
19	EP300	chr11:57365276-57365958	H1-hESC	embryonic stem cell:	n/a	n/a
20	EP300	chr11:57365401-57365959	H1-hESC	embryonic stem cell:	n/a	n/a
21	FOS	chr11:57366946-57367131	MCF10A-Er-Src	breast:	n/a	chr11:57366978-57366987
22	FOS	chr11:57366883-57367131	MCF10A-Er-Src	breast:	n/a	chr11:57366978-57366987
23	FOS	chr11:57366926-57367099	MCF10A-Er-Src	breast:	n/a	chr11:57366978-57366987
24	FOS	chr11:57366932-57367036	MCF10A-Er-Src	breast:	n/a	chr11:57366978-57366987
25	FOS	chr11:57370718-57370799	MCF10A-Er-Src	breast:	n/a	n/a
26	FOSL1	chr11:57370660-57370839	K562	blood:	n/a	chr11:57370744-57370755
27	FOSL1	chr11:57370577-57370945	K562	blood:	n/a	chr11:57370744-57370755
28	FOXA1	chr11:57364017-57364394	HepG2	liver:	n/a	n/a
29	GTF2F1	chr11:57365525-57365950	H1-hESC	embryonic stem cell:	n/a	n/a
30	GTF2F1	chr11:57364772-57364774	H1-hESC	embryonic stem cell:	n/a	n/a
31	GTF3C2	chr11:57370634-57371025	K562	blood:	n/a	n/a
32	HDAC2	chr11:57365400-57365573	H1-hESC	embryonic stem cell:	n/a	n/a
33	HDAC2	chr11:57365610-57365949	H1-hESC	embryonic stem cell:	n/a	n/a
34	HDAC2	chr11:57365625-57365904	HepG2	liver:	n/a	n/a
35	HDAC2	chr11:57365653-57365920	H1-hESC	embryonic stem cell:	n/a	n/a
36	JUN	chr11:57370528-57370951	K562	blood:	n/a	n/a
37	JUN	chr11:57365761-57366037	H1-hESC	embryonic stem cell:	n/a	chr11:57365835-57365844
38	JUND	chr11:57365204-57366089	H1-hESC	embryonic stem cell:	n/a	chr11:57365835-57365844 chr11:57365234-57365248
39	JUND	chr11:57370594-57370923	K562	blood:	n/a	n/a
40	JUND	chr11:57365625-57365942	H1-hESC	embryonic stem cell:	n/a	chr11:57365835-57365844
41	JUND	chr11:57365636-57365860	H1-hESC	embryonic stem cell:	n/a	chr11:57365835-57365844
42	MAX	chr11:57365134-57366127	H1-hESC	embryonic stem cell:	n/a	chr11:57365404-57365413 chr11:57365358-57365368 chr11:57365449-57365459
43	MAX	chr11:57371777-57372136	NB4	blood:	n/a	n/a
44	MAX	chr11:57365008-57366064	H1-hESC	embryonic stem cell:	n/a	chr11:57365404-57365413 chr11:57365358-57365368 chr11:57365449-57365459
45	MAZ	chr11:57365458-57365679	K562	blood:	n/a	n/a
46	MAZ	chr11:57365143-57366079	IMR90	lung:	n/a	chr11:57365404-57365413 chr11:57365358-57365368 chr11:57365449-57365459
47	MAZ	chr11:57365546-57365756	HepG2	liver:	n/a	n/a
48	MXI1	chr11:57365398-57365959	H1-hESC	embryonic stem cell:	n/a	n/a
49	MYC	chr11:57371785-57372111	NB4	blood:	n/a	n/a
50	MYC	chr11:57365383-57365576	H1-hESC	embryonic stem cell:	n/a	chr11:57365404-57365413 chr11:57365449-57365459

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:57364939-57364989	PFSK-1	brain:	n/a
2	chr11:57364888-57364938	HRE	kidney:	n/a
3	chr11:57364939-57364989	PFSK-1	brain:	n/a
4	chr11:57364888-57364938	HRE	kidney:	n/a
5	chr11:57364888-57364938	HepG2	liver:	n/a
6	chr11:57365701-57365751	H1-hESC	embryonic stem cell:	embryo
7	chr11:57365701-57365751	U87	brain:	n/a
8	chr11:57364939-57364989	ECC-1	luminal epithelium:	n/a
9	chr11:57365725-57365775	HCPEpiC	choroid plexus:	n/a
10	chr11:57364841-57364891	PFSK-1	brain:	n/a
11	chr11:57365717-57365767	SAEC	small airway:	n/a
12	chr11:57364890-57364940	HIPEpiC	eye:	n/a
13	chr11:57365948-57365998	PrEC	prostate:	n/a
14	chr11:57365725-57365775	Jurkat	blood:	n/a
15	chr11:57365018-57365068	ProgFib	skin:	n/a
16	chr11:57364939-57364989	HCT-116	colon:	n/a
17	chr11:57364939-57364989	GM06990	blood:	n/a
18	chr11:57365725-57365775	Hela-S3	cervix:	n/a
19	chr11:57364939-57364989	Hepatocyte	liver:	n/a
20	chr11:57364841-57364891	GM19239	blood:	n/a
21	chr11:57364841-57364891	H1-hESC	embryonic stem cell:	embryo
22	chr11:57365701-57365751	Hepatocyte	liver:	n/a
23	chr11:57365088-57365138	HEK293	kidney:	embryo
24	chr11:57365948-57365998	HPAEpiC	pulmonary alveolar:	n/a
25	chr11:57364888-57364938	AG09319	gingival:	n/a
26	chr11:57365725-57365775	HEEpiC	esophagus:	n/a
27	chr11:57365948-57365998	AoSMC	blood vessel:	n/a
28	chr11:57365948-57365998	IMR90	lung:	fetal
29	chr11:57364890-57364940	GM19239	blood:	n/a
30	chr11:57365725-57365775	HRE	kidney:	n/a
31	chr11:57365948-57365998	A549	lung:	n/a
32	chr11:57365948-57365998	K562	blood:	n/a
33	chr11:57364888-57364938	AG09309	skin:	n/a
34	chr11:57364841-57364891	ProgFib	skin:	n/a
35	chr11:57364939-57364989	HMEC	breast:	n/a
36	chr11:57365717-57365767	Jurkat	blood:	n/a
37	chr11:57364841-57364891	Caco-2	colon:	n/a
38	chr11:57365948-57365998	HCPEpiC	choroid plexus:	n/a
39	chr11:57365701-57365751	HCPEpiC	choroid plexus:	n/a
40	chr11:57364939-57364989	RPTEC	kidney:	n/a
41	chr11:57365701-57365751	Jurkat	blood:	n/a
42	chr11:57364890-57364940	Hepatocyte	liver:	n/a
43	chr11:57365717-57365767	GM12878	blood:	n/a
44	chr11:57364890-57364940	HMEC	breast:	n/a
45	chr11:57365717-57365767	SK-N-SH_RA	brain:	n/a
46	chr11:57364939-57364989	GM12891	blood:	n/a
47	chr11:57365948-57365998	HNPCEpiC	eye:	n/a
48	chr11:57365701-57365751	ECC-1	luminal epithelium:	n/a
49	chr11:57365717-57365767	H1-hESC	embryonic stem cell:	embryo
50	chr11:57365948-57365998	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:57363269..57366608-chr11:57366625..57370345,5	K562	blood:
2	chr11:57280138..57282809-chr11:57363760..57366213,2	MCF-7	breast:
3	chr11:57363269..57366608-chr11:57366625..57370345,5	K562	blood:

No data

Variant related genes	Relation type
SERPING1	TF binding region
SERPING1	CpG island
ENSG00000149131	chromatin interactions
ENSG00000149150	chromatin interactions

Extended variants
information (count: 382 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1972671	chr11:57364381-57364382	Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148787585	chr11:57364429-57364430	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs578128202	chr11:57364435-57364436	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs545552620	chr11:57364516-57364517	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs35288249	chr11:57364521-57364522	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs398016136	chr11:57364542-57364543	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs28445232	chr11:57364548-57364549	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs560623050	chr11:57364582-57364583	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs527972970	chr11:57364585-57364586	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs1549364	chr11:57364600-57364601	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548608285	chr11:57364632-57364633	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs553033211	chr11:57364696-57364697	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs531332004	chr11:57364742-57364743	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs183477448	chr11:57364770-57364771	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs571286970	chr11:57364787-57364788	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs188477249	chr11:57364838-57364839	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs142514305	chr11:57364870-57364871	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs192800779	chr11:57364887-57364888	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs536541489	chr11:57364894-57364895	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs146408333	chr11:57365003-57365004	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs574062976	chr11:57365060-57365061	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs538212843	chr11:57365075-57365076	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs556401140	chr11:57365090-57365091	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs28362939	chr11:57365111-57365112	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs578018379	chr11:57365118-57365119	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs372802721	chr11:57365119-57365120	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs112290300	chr11:57365194-57365195	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs560724929	chr11:57365216-57365217	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs183957596	chr11:57365240-57365241	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs28362940	chr11:57365366-57365367	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs561217386	chr11:57365386-57365387	Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs28362941	chr11:57365437-57365438	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs543365482	chr11:57365446-57365447	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs28362942	chr11:57365510-57365511	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs532231419	chr11:57365543-57365544	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs183507388	chr11:57365549-57365550	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs565866483	chr11:57365576-57365577	Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs28362943	chr11:57365633-57365634	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs548528069	chr11:57365658-57365659	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs569933712	chr11:57365659-57365660	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs182197371	chr11:57365691-57365692	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs28362944	chr11:57365723-57365724	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	disease
43	rs185342631	chr11:57365748-57365749	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs201088164	chr11:57365764-57365765	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs201455616	chr11:57365768-57365769	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs199473715	chr11:57365794-57365795	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs572325752	chr11:57365802-57365803	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs199873764	chr11:57365822-57365823	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs554852233	chr11:57365852-57365853	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs28362945	chr11:57365895-57365896	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:624 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57358600-57365000	Weak transcription	Pancreas	Pancrea
2	chr11:57360600-57364600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:57362400-57364600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:57362400-57364600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:57362600-57364600	Enhancers	Fetal Muscle Leg	muscle
6	chr11:57362800-57364400	Enhancers	Liver	Liver
7	chr11:57363000-57364600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:57363000-57365400	Weak transcription	Fetal Thymus	thymus
9	chr11:57363200-57365000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr11:57363400-57364400	Weak transcription	Fetal Kidney	kidney
11	chr11:57363400-57364600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:57363400-57364600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr11:57363600-57364600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:57363800-57364600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr11:57364000-57364400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr11:57364000-57364400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr11:57364000-57364600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr11:57364000-57364600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr11:57364000-57364600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr11:57364000-57364600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:57364000-57364600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:57364000-57364600	Enhancers	Osteobl	bone
23	chr11:57364000-57364800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr11:57364000-57364800	Enhancers	Fetal Muscle Trunk	muscle
25	chr11:57364000-57365200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr11:57364200-57364400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr11:57364200-57364600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr11:57364200-57364600	Active TSS	HepG2	liver
29	chr11:57364200-57364800	Enhancers	Fetal Stomach	stomach
30	chr11:57364200-57365200	Weak transcription	Lung	lung
31	chr11:57364400-57364600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr11:57364400-57364600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:57364400-57364600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr11:57364400-57364600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr11:57364400-57364600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:57364400-57364600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr11:57364400-57364600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr11:57364400-57364600	Enhancers	Adipose Nuclei	Adipose
39	chr11:57364400-57364600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:57364400-57364600	Enhancers	Colon Smooth Muscle	Colon
41	chr11:57364400-57364600	Enhancers	Fetal Kidney	kidney
42	chr11:57364400-57364600	Enhancers	Right Atrium	heart
43	chr11:57364400-57364600	Enhancers	Stomach Smooth Muscle	stomach
44	chr11:57364400-57364800	Flanking Active TSS	Liver	Liver
45	chr11:57364400-57366800	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chr11:57364600-57364800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr11:57364600-57364800	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr11:57364600-57364800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr11:57364600-57364800	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr11:57364600-57364800	Enhancers	Brain Inferior Temporal Lobe	brain

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