Variant report

Variant	nsv1050305
Chromosome Location	chr10:43568887-43591057
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	chr10:43571080-43571230	GM12867	blood:	n/a	n/a
5	CTCF	chr10:43571000-43571150	HepG2	liver:	n/a	n/a
6	CTCF	chr10:43588940-43589090	BE2_C	brain:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
7	CTCF	chr10:43574419-43574702	A549	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
8	CTCF	chr10:43571040-43571190	WERI-Rb-1	eye:	n/a	n/a
9	CTCF	chr10:43574420-43574570	GM12870	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
10	CTCF	chr10:43571040-43571190	WI-38	lung:	n/a	n/a
11	CTCF	chr10:43571040-43571228	A549	lung:	n/a	n/a
12	CTCF	chr10:43574480-43574630	GM12873	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
13	CTCF	chr10:43574480-43574630	SK-N-SH_RA	brain:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
14	CTCF	chr10:43588980-43589130	HBMEC	blood vessel:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
15	CTCF	chr10:43571220-43571370	GM12872	blood:	n/a	n/a
16	CTCF	chr10:43572480-43572630	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr10:43571880-43572030	HUVEC	blood vessel:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
18	CTCF	chr10:43574520-43574670	GM12871	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
19	CTCF	chr10:43574480-43574630	HBMEC	blood vessel:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
20	CTCF	chr10:43588953-43589117	ProgFib	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
21	CTCF	chr10:43588940-43589090	SK-N-SH_RA	brain:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
22	CTCF	chr10:43574480-43574630	Hela-S3	cervix:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
23	CTCF	chr10:43571040-43571190	GM12864	blood:	n/a	n/a
24	CTCF	chr10:43574414-43574709	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
25	CTCF	chr10:43571060-43571210	HVMF	connective:	n/a	n/a
26	CTCF	chr10:43588960-43589110	HA-sp	spinal cord:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
27	CTCF	chr10:43571120-43571270	GM12865	blood:	n/a	n/a
28	CTCF	chr10:43574341-43574661	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
29	CTCF	chr10:43571640-43571790	A549	lung:	n/a	n/a
30	CTCF	chr10:43588899-43589185	IMR90	lung:	n/a	chr10:43589022-43589043 chr10:43589162-43589175 chr10:43589027-43589045
31	CTCF	chr10:43574438-43574610	ECC-1	luminal epithelium:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
32	CTCF	chr10:43588960-43589110	AG04449	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
33	CTCF	chr10:43574448-43574606	A549	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
34	CTCF	chr10:43574460-43574610	HCPEpiC	choroid plexus:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
35	CTCF	chr10:43574480-43574630	HMF	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
36	CTCF	chr10:43574477-43574637	Kidney_OC	kidney:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
37	CTCF	chr10:43588940-43589090	AG04449	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
38	CTCF	chr10:43574500-43574650	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
39	CTCF	chr10:43588800-43589234	K562	blood:	n/a	chr10:43589022-43589043 chr10:43589162-43589175 chr10:43589027-43589045
40	CTCF	chr10:43571080-43571230	GM12866	blood:	n/a	n/a
41	CTCF	chr10:43574207-43574807	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
42	CTCF	chr10:43574540-43574690	GM12868	blood:	n/a	n/a
43	CTCF	chr10:43574500-43574650	WERI-Rb-1	eye:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
44	CTCF	chr10:43570993-43571330	K562	blood:	n/a	n/a
45	CTCF	chr10:43571916-43572036	MCF-7	breast:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
46	CTCF	chr10:43574481-43574635	GM13976	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
47	CTCF	chr10:43571860-43572010	NHEK	skin:	n/a	chr10:43571958-43571971 chr10:43571942-43571955
48	CTCF	chr10:43571040-43571190	HCM	heart:	n/a	n/a
49	CTCF	chr10:43574431-43574670	LNCaP	prostate:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
50	CTCF	chr10:43571000-43571150	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43572413-43572463	HRE	kidney:	n/a
2	chr10:43572424-43572474	HAEpiC	amniotic membrane:	n/a
3	chr10:43572413-43572463	HRE	kidney:	n/a
4	chr10:43572424-43572474	HAEpiC	amniotic membrane:	n/a
5	chr10:43572621-43572671	AG10803	skin:	n/a
6	chr10:43577025-43577075	SAEC	small airway:	n/a
7	chr10:43572413-43572463	HMEC	breast:	n/a
8	chr10:43569045-43569095	PANC-1	pancreas:	n/a
9	chr10:43572359-43572409	ProgFib	skin:	n/a
10	chr10:43572413-43572463	LNCaP	prostate:	n/a
11	chr10:43569045-43569095	HCM	heart:	n/a
12	chr10:43575142-43575192	MCF10A-Er-Src	breast:	n/a
13	chr10:43572795-43572845	HRPEpiC	eye:	n/a
14	chr10:43573319-43573369	HRPEpiC	eye:	n/a
15	chr10:43572430-43572480	HRCEpiC	kidney:	n/a
16	chr10:43569045-43569095	HRCEpiC	kidney:	n/a
17	chr10:43572795-43572845	K562	blood:	n/a
18	chr10:43585188-43585238	ovcar-3	ovarian:	n/a
19	chr10:43573332-43573382	AG09309	skin:	n/a
20	chr10:43569045-43569095	AoSMC	blood vessel:	n/a
21	chr10:43573319-43573369	K562	blood:	n/a
22	chr10:43575142-43575192	BE2_C	brain:	n/a
23	chr10:43572430-43572480	A549	lung:	n/a
24	chr10:43575142-43575192	H1-hESC	embryonic stem cell:	embryo
25	chr10:43585188-43585238	HepG2	liver:	n/a
26	chr10:43572244-43572294	ProgFib	skin:	n/a
27	chr10:43571169-43571219	HepG2	liver:	n/a
28	chr10:43572430-43572480	HAEpiC	amniotic membrane:	n/a
29	chr10:43572065-43572115	SKMC	muscle:	n/a
30	chr10:43572065-43572115	HRE	kidney:	n/a
31	chr10:43572621-43572671	NB4	blood:	n/a
32	chr10:43573319-43573369	HL-60	blood:	n/a
33	chr10:43572359-43572409	AG09319	gingival:	n/a
34	chr10:43572424-43572474	AG04449	skin:	fetal
35	chr10:43572359-43572409	SK-N-SH	brain:	n/a
36	chr10:43571169-43571219	AG09309	skin:	n/a
37	chr10:43573332-43573382	HCT-116	colon:	n/a
38	chr10:43573319-43573369	HIPEpiC	eye:	n/a
39	chr10:43573195-43573245	ProgFib	skin:	n/a
40	chr10:43569045-43569095	HUVEC	blood vessel:	n/a
41	chr10:43572065-43572115	SK-N-SH	brain:	n/a
42	chr10:43572467-43572517	HL-60	blood:	n/a
43	chr10:43572065-43572115	HCPEpiC	choroid plexus:	n/a
44	chr10:43572359-43572409	ovcar-3	ovarian:	n/a
45	chr10:43585188-43585238	T-47D	breast:	n/a
46	chr10:43572244-43572294	HEK293	kidney:	embryo
47	chr10:43572467-43572517	HCT-116	colon:	n/a
48	chr10:43573332-43573382	AG04449	skin:	fetal
49	chr10:43573319-43573369	SK-N-SH_RA	brain:	n/a
50	chr10:43569045-43569095	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43496061..43498951-chr10:43575386..43576961,2	MCF-7	breast:
2	chr10:43588801..43589617-chr10:43600178..43601154,2	MCF-7	breast:
3	chr10:43563253..43566538-chr10:43567124..43569938,3	K562	blood:
4	chr10:43470988..43471723-chr10:43574194..43574824,2	MCF-7	breast:
5	chr10:43578198..43579973-chr10:43594655..43597408,2	MCF-7	breast:
6	chr10:43563405..43565262-chr10:43578421..43580080,2	K562	blood:
7	chr10:43521855..43522376-chr10:43577254..43578134,2	MCF-7	breast:
8	chr10:43574441..43574987-chr10:43601035..43601611,2	K562	blood:
9	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
10	chr10:43533504..43534088-chr10:43577355..43578166,2	MCF-7	breast:
11	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
12	chr10:43322775..43323340-chr10:43574006..43574597,2	MCF-7	breast:
13	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
14	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:
15	chr10:43581616..43582507-chr10:43605989..43606921,3	MCF-7	breast:
16	chr10:43517701..43518324-chr10:43573585..43574127,2	MCF-7	breast:
17	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
18	chr10:43520346..43523029-chr10:43587909..43590894,3	MCF-7	breast:
19	chr10:43476076..43477138-chr10:43577286..43578259,3	MCF-7	breast:
20	chr10:43572567..43574576-chr10:43871912..43874300,2	MCF-7	breast:
21	chr10:43370478..43372425-chr10:43586111..43588010,2	MCF-7	breast:
22	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:
23	chr10:43523482..43525302-chr10:43587306..43589145,2	MCF-7	breast:
24	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
25	chr10:43363801..43367756-chr10:43571423..43575718,4	MCF-7	breast:
26	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
27	chr10:43521523..43522449-chr10:43577293..43578240,8	MCF-7	breast:
28	chr10:43589023..43591875-chr10:43596909..43598786,2	MCF-7	breast:
29	chr10:43361782..43362789-chr10:43574108..43574983,3	K562	blood:
30	chr10:43574755..43578524-chr10:43632183..43633949,3	MCF-7	breast:
31	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
32	chr10:43587904..43589717-chr10:43600959..43603478,2	MCF-7	breast:
33	chr10:43521611..43522326-chr10:43577256..43578049,6	MCF-7	breast:
34	chr10:43476676..43477639-chr10:43581673..43582410,2	MCF-7	breast:
35	chr10:43571757..43578165-chr10:43578692..43585292,10	MCF-7	breast:
36	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
37	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
38	chr10:43588758..43591392-chr10:43592644..43594640,2	MCF-7	breast:
39	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
40	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
41	chr10:43521600..43522503-chr10:43589625..43590206,2	MCF-7	breast:
42	chr10:43577015..43578995-chr10:43604341..43606597,2	MCF-7	breast:
43	chr10:43561322..43565766-chr10:43567124..43571353,6	K562	blood:
44	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
45	chr10:43576417..43579207-chr10:43590495..43592572,2	MCF-7	breast:
46	chr10:43589765..43592695-chr10:43600961..43603100,2	MCF-7	breast:
47	chr10:43362412..43363000-chr10:43573894..43574641,2	MCF-7	breast:
48	chr10:43589175..43591364-chr10:43599200..43601057,2	MCF-7	breast:
49	chr10:43521617..43522540-chr10:43581453..43582423,6	MCF-7	breast:
50	chr10:43571954..43575948-chr10:43588456..43593172,4	MCF-7	breast:

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

Extended variants
information (count: 881 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:881 , 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	rs2505994	chr10:43568887-43568888	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550228103	chr10:43568915-43568916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs568351165	chr10:43568954-43568955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535668706	chr10:43568959-43568960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116755273	chr10:43568971-43568972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374456325	chr10:43569078-43569079	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs142719432	chr10:43569108-43569109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539703813	chr10:43569126-43569127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558308486	chr10:43569136-43569137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34698549	chr10:43569158-43569159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11598548	chr10:43569168-43569169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146093682	chr10:43569185-43569186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3026724	chr10:43569210-43569211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556206229	chr10:43569211-43569212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574548468	chr10:43569214-43569215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542064791	chr10:43569252-43569253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560339564	chr10:43569253-43569254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185880516	chr10:43569284-43569285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140071346	chr10:43569291-43569292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35005636	chr10:43569310-43569311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564353548	chr10:43569357-43569358	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs531717119	chr10:43569363-43569364	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs549874600	chr10:43569371-43569372	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs568237657	chr10:43569372-43569373	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs3026725	chr10:43569505-43569506	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs372370634	chr10:43569565-43569566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565925767	chr10:43569566-43569567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539790445	chr10:43569610-43569611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2505995	chr10:43569653-43569654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189139040	chr10:43569680-43569681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537862013	chr10:43569684-43569685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs555855641	chr10:43569691-43569692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574585257	chr10:43569724-43569725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541939930	chr10:43569740-43569741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369660849	chr10:43569786-43569787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370474445	chr10:43569798-43569799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2505996	chr10:43569810-43569811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs545814949	chr10:43569811-43569812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4948703	chr10:43569838-43569839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564422547	chr10:43569839-43569840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529965391	chr10:43569975-43569976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116653591	chr10:43570020-43570021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549714862	chr10:43570036-43570037	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561706532	chr10:43570076-43570077	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs529388119	chr10:43570162-43570163	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs547482695	chr10:43570168-43570169	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs116717012	chr10:43570175-43570176	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs115987241	chr10:43570188-43570189	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs150065549	chr10:43570196-43570197	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs569794078	chr10:43570292-43570293	Weak transcription Genic enhancers	TF binding region	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:494 , 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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