Variant report

Variant	nsv1038706
Chromosome Location	chr10:43569959-43591617
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	BHLHE40	chr10:43574476-43574611	K562	blood:	n/a	n/a
2	BHLHE40	chr10:43574377-43574555	HepG2	liver:	n/a	n/a
3	BRCA1	chr10:43574519-43574717	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr10:43588980-43589130	WERI-Rb-1	eye:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
5	CTCF	chr10:43574500-43574650	RPTEC	kidney:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
6	CTCF	chr10:43570960-43571110	MCF-7	breast:	n/a	n/a
7	CTCF	chr10:43571220-43571370	GM12866	blood:	n/a	n/a
8	CTCF	chr10:43570937-43571324	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr10:43588960-43589110	NHDF-neo	bronchial:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
10	CTCF	chr10:43588940-43589090	NHEK	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
11	CTCF	chr10:43574500-43574650	GM12865	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
12	CTCF	chr10:43571080-43571230	HPF	lung:	n/a	n/a
13	CTCF	chr10:43574360-43574510	HVMF	connective:	n/a	n/a
14	CTCF	chr10:43573800-43573950	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr10:43574423-43574701	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
16	CTCF	chr10:43572719-43572729	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr10:43571043-43571207	GM12878	blood:	n/a	n/a
18	CTCF	chr10:43571009-43571203	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr10:43574480-43574630	RPTEC	kidney:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
20	CTCF	chr10:43574480-43574630	BJ	skin:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
21	CTCF	chr10:43588986-43589073	GM10266	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
22	CTCF	chr10:43588940-43589090	HMF	breast:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
23	CTCF	chr10:43589002-43589104	GM19240	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
24	CTCF	chr10:43574480-43574630	GM12865	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
25	CTCF	chr10:43574460-43574610	HA-sp	spinal cord:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
26	CTCF	chr10:43570980-43571130	GM12874	blood:	n/a	n/a
27	CTCF	chr10:43588940-43589090	AG04449	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
28	CTCF	chr10:43574417-43574728	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
29	CTCF	chr10:43574480-43574630	AG04449	skin:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
30	CTCF	chr10:43588960-43589110	AG09319	gingival:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
31	CTCF	chr10:43571820-43571970	BE2_C	brain:	n/a	chr10:43571942-43571955
32	CTCF	chr10:43571060-43571210	HCT-116	colon:	n/a	n/a
33	CTCF	chr10:43591140-43591290	A549	lung:	n/a	n/a
34	CTCF	chr10:43581040-43581190	HEK293	kidney:	n/a	n/a
35	CTCF	chr10:43574409-43574689	GM19240	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
36	CTCF	chr10:43574480-43574630	AG09319	gingival:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
37	CTCF	chr10:43571140-43571290	SAEC	small airway:	n/a	n/a
38	CTCF	chr10:43574400-43574550	NHEK	skin:	n/a	chr10:43574537-43574550
39	CTCF	chr10:43589126-43589129	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr10:43574460-43574610	HRE	kidney:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
41	CTCF	chr10:43588980-43589130	HepG2	liver:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
42	CTCF	chr10:43574520-43574670	WI-38	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
43	CTCF	chr10:43574346-43574733	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
44	CTCF	chr10:43574480-43574630	HBMEC	blood vessel:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
45	CTCF	chr10:43574500-43574650	BE2_C	brain:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
46	CTCF	chr10:43588920-43589070	HCM	heart:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
47	CTCF	chr10:43571020-43571170	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr10:43588900-43589166	LNCaP	prostate:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
49	CTCF	chr10:43573920-43574070	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr10:43588960-43589110	HMEC	breast:	n/a	chr10:43589022-43589043 chr10:43589027-43589045

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43585188-43585238	HCT-116	colon:	n/a
2	chr10:43585188-43585238	HCT-116	colon:	n/a
3	chr10:43572413-43572463	AoSMC	blood vessel:	n/a
4	chr10:43572430-43572480	Hepatocyte	liver:	n/a
5	chr10:43573319-43573369	Hepatocyte	liver:	n/a
6	chr10:43585188-43585238	NHBE	bronchial:	n/a
7	chr10:43572467-43572517	SK-N-MC	brain:	n/a
8	chr10:43572467-43572517	HAEpiC	amniotic membrane:	n/a
9	chr10:43572467-43572517	GM12892	blood:	n/a
10	chr10:43572413-43572463	CMK	blood:	n/a
11	chr10:43572467-43572517	LNCaP	prostate:	n/a
12	chr10:43573319-43573369	HIPEpiC	eye:	n/a
13	chr10:43575142-43575192	T-47D	breast:	n/a
14	chr10:43585188-43585238	HepG2	liver:	n/a
15	chr10:43572413-43572463	PFSK-1	brain:	n/a
16	chr10:43572424-43572474	GM19239	blood:	n/a
17	chr10:43585188-43585238	GM06990	blood:	n/a
18	chr10:43572065-43572115	HepG2	liver:	n/a
19	chr10:43572795-43572845	GM06990	blood:	n/a
20	chr10:43572430-43572480	AG10803	skin:	n/a
21	chr10:43572244-43572294	H1-hESC	embryonic stem cell:	embryo
22	chr10:43572413-43572463	SK-N-SH_RA	brain:	n/a
23	chr10:43572359-43572409	GM12891	blood:	n/a
24	chr10:43572359-43572409	SK-N-SH	brain:	n/a
25	chr10:43577025-43577075	NHBE	bronchial:	n/a
26	chr10:43573319-43573369	HCT-116	colon:	n/a
27	chr10:43572621-43572671	HRCEpiC	kidney:	n/a
28	chr10:43575142-43575192	GM19239	blood:	n/a
29	chr10:43572359-43572409	AG09319	gingival:	n/a
30	chr10:43575142-43575192	HAEpiC	amniotic membrane:	n/a
31	chr10:43572424-43572474	ProgFib	skin:	n/a
32	chr10:43572467-43572517	CMK	blood:	n/a
33	chr10:43572424-43572474	RPTEC	kidney:	n/a
34	chr10:43575142-43575192	SK-N-SH	brain:	n/a
35	chr10:43572359-43572409	RPTEC	kidney:	n/a
36	chr10:43572413-43572463	HEEpiC	esophagus:	n/a
37	chr10:43573195-43573245	GM06990	blood:	n/a
38	chr10:43573332-43573382	HCPEpiC	choroid plexus:	n/a
39	chr10:43572424-43572474	HIPEpiC	eye:	n/a
40	chr10:43572065-43572115	GM12878	blood:	n/a
41	chr10:43573319-43573369	SAEC	small airway:	n/a
42	chr10:43572359-43572409	SAEC	small airway:	n/a
43	chr10:43577025-43577075	SAEC	small airway:	n/a
44	chr10:43572065-43572115	K562	blood:	n/a
45	chr10:43572413-43572463	HNPCEpiC	eye:	n/a
46	chr10:43572244-43572294	MCF-7	breast:	n/a
47	chr10:43572424-43572474	HEK293	kidney:	embryo
48	chr10:43572467-43572517	MCF-7	breast:	n/a
49	chr10:43572244-43572294	HL-60	blood:	n/a
50	chr10:43572430-43572480	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43571757..43578165-chr10:43578692..43585292,10	MCF-7	breast:
2	chr10:43521600..43522503-chr10:43589625..43590206,2	MCF-7	breast:
3	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
4	chr10:43322775..43323340-chr10:43574006..43574597,2	MCF-7	breast:
5	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
6	chr10:43574755..43578524-chr10:43632183..43633949,3	MCF-7	breast:
7	chr10:43363801..43367756-chr10:43571423..43575718,4	MCF-7	breast:
8	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
9	chr10:43589175..43591364-chr10:43599200..43601057,2	MCF-7	breast:
10	chr10:43521523..43522449-chr10:43577293..43578240,8	MCF-7	breast:
11	chr10:43496061..43498951-chr10:43575386..43576961,2	MCF-7	breast:
12	chr10:43571954..43575948-chr10:43588456..43593172,4	MCF-7	breast:
13	chr10:43361782..43362789-chr10:43574108..43574983,3	K562	blood:
14	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
15	chr10:43523482..43525302-chr10:43587306..43589145,2	MCF-7	breast:
16	chr10:43521617..43522540-chr10:43581453..43582423,6	MCF-7	breast:
17	chr10:43577015..43578995-chr10:43604341..43606597,2	MCF-7	breast:
18	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:
19	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
20	chr10:43574441..43574987-chr10:43601035..43601611,2	K562	blood:
21	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
22	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
23	chr10:43476076..43477138-chr10:43577286..43578259,3	MCF-7	breast:
24	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
25	chr10:43589023..43591875-chr10:43596909..43598786,2	MCF-7	breast:
26	chr10:43588801..43589617-chr10:43600178..43601154,2	MCF-7	breast:
27	chr10:43476676..43477639-chr10:43581673..43582410,2	MCF-7	breast:
28	chr10:43362412..43363000-chr10:43573894..43574641,2	MCF-7	breast:
29	chr10:43578198..43579973-chr10:43594655..43597408,2	MCF-7	breast:
30	chr10:43520346..43523029-chr10:43587909..43590894,3	MCF-7	breast:
31	chr10:43517701..43518324-chr10:43573585..43574127,2	MCF-7	breast:
32	chr10:43370478..43372425-chr10:43586111..43588010,2	MCF-7	breast:
33	chr10:43588758..43591392-chr10:43592644..43594640,2	MCF-7	breast:
34	chr10:43521855..43522376-chr10:43577254..43578134,2	MCF-7	breast:
35	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
36	chr10:43521611..43522326-chr10:43577256..43578049,6	MCF-7	breast:
37	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
38	chr10:43581616..43582507-chr10:43605989..43606921,3	MCF-7	breast:
39	chr10:43589765..43592695-chr10:43600961..43603100,2	MCF-7	breast:
40	chr10:43563405..43565262-chr10:43578421..43580080,2	K562	blood:
41	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
42	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
43	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:
44	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
45	chr10:43561322..43565766-chr10:43567124..43571353,6	K562	blood:
46	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
47	chr10:43533504..43534088-chr10:43577355..43578166,2	MCF-7	breast:
48	chr10:43587904..43589717-chr10:43600959..43603478,2	MCF-7	breast:
49	chr10:43572567..43574576-chr10:43871912..43874300,2	MCF-7	breast:

Variant related genes	Relation type
RET	TF binding region
RET	CpG island
ENSG00000234944	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000229630	chromatin interactions

Extended variants
information (count: 855 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529965391	chr10:43569975-43569976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116653591	chr10:43570020-43570021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549714862	chr10:43570036-43570037	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs561706532	chr10:43570076-43570077	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs529388119	chr10:43570162-43570163	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs547482695	chr10:43570168-43570169	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs116717012	chr10:43570175-43570176	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs115987241	chr10:43570188-43570189	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs150065549	chr10:43570196-43570197	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs569794078	chr10:43570292-43570293	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs537296224	chr10:43570295-43570296	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs371523018	chr10:43570299-43570300	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs114282735	chr10:43570324-43570325	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs116348017	chr10:43570325-43570326	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs73266173	chr10:43570344-43570345	Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs2505997	chr10:43570355-43570356	Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs572013373	chr10:43570374-43570375	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs571339214	chr10:43570390-43570391	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs147737869	chr10:43570393-43570394	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs141963411	chr10:43570395-43570396	Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs553894041	chr10:43570480-43570481	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs576296034	chr10:43570485-43570486	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs567424926	chr10:43570500-43570501	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs536305517	chr10:43570574-43570575	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs543343575	chr10:43570575-43570576	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs180699930	chr10:43570581-43570582	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs561792537	chr10:43570588-43570589	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs573675732	chr10:43570603-43570604	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs114749313	chr10:43570632-43570633	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs185319515	chr10:43570652-43570653	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs144192584	chr10:43570661-43570662	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs568341456	chr10:43570671-43570672	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs533238844	chr10:43570751-43570752	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190133238	chr10:43570770-43570771	Weak transcription Genic enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs35718859	chr10:43570809-43570810	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs3026726	chr10:43570833-43570834	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs563688144	chr10:43570849-43570850	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs531273089	chr10:43570892-43570893	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs200422378	chr10:43570911-43570912	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs181327409	chr10:43570912-43570913	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568099096	chr10:43570916-43570917	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs535460417	chr10:43570921-43570922	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs2505998	chr10:43570925-43570926	Weak transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs3026727	chr10:43571010-43571011	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539120962	chr10:43571083-43571084	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs148845033	chr10:43571117-43571118	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs368876789	chr10:43571118-43571119	Weak transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs576153191	chr10:43571201-43571202	Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs536976179	chr10:43571212-43571213	Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs143569810	chr10:43571216-43571217	Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:495 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43554400-43572000	Weak transcription	Right Atrium	heart
2	chr10:43560800-43570800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr10:43562800-43571800	Weak transcription	Esophagus	oesophagus
4	chr10:43563000-43572000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr10:43566600-43570200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:43570200-43571400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:43570400-43570600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr10:43570400-43570800	Bivalent Enhancer	Fetal Stomach	stomach
9	chr10:43570600-43570800	Bivalent Enhancer	Right Ventricle	heart
10	chr10:43570600-43570800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
11	chr10:43570800-43571200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr10:43571000-43572000	Bivalent Enhancer	Fetal Stomach	stomach
13	chr10:43571200-43571400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
14	chr10:43571200-43571400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr10:43571200-43571400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
16	chr10:43571200-43571400	Bivalent/Poised TSS	Spleen	Spleen
17	chr10:43571200-43571400	Enhancers	A549	lung
18	chr10:43571200-43571800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
19	chr10:43571200-43572000	Bivalent Enhancer	Colonic Mucosa	Colon
20	chr10:43571400-43571600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
21	chr10:43571400-43571600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
22	chr10:43571400-43571600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:43571400-43571600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr10:43571400-43571600	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr10:43571400-43571600	Bivalent Enhancer	A549	lung
26	chr10:43571400-43571800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr10:43571400-43571800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
28	chr10:43571400-43571800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
29	chr10:43571400-43571800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr10:43571400-43571800	Bivalent Enhancer	Brain Anterior Caudate	brain
31	chr10:43571400-43571800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
32	chr10:43571400-43571800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr10:43571400-43571800	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr10:43571400-43571800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
35	chr10:43571400-43571800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
36	chr10:43571400-43572000	Bivalent Enhancer	Brain Germinal Matrix	brain
37	chr10:43571400-43572600	Bivalent Enhancer	Spleen	Spleen
38	chr10:43571400-43573400	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr10:43571600-43571800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
40	chr10:43571600-43571800	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
41	chr10:43571600-43571800	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
42	chr10:43571600-43571800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
43	chr10:43571600-43571800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
44	chr10:43571600-43571800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr10:43571600-43571800	Bivalent Enhancer	Adipose Nuclei	Adipose
46	chr10:43571600-43571800	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
47	chr10:43571600-43571800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
48	chr10:43571600-43571800	Flanking Bivalent TSS/Enh	A549	lung
49	chr10:43571600-43571800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
50	chr10:43571600-43572000	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell

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