Variant report

Variant	nsv1045690
Chromosome Location	chr10:43550567-43592346
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	chr10:43574500-43574650	WERI-Rb-1	eye:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
5	CTCF	chr10:43574480-43574630	K562	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
6	CTCF	chr10:43571800-43571950	MCF-7	breast:	n/a	n/a
7	CTCF	chr10:43571000-43571227	K562	blood:	n/a	n/a
8	CTCF	chr10:43571060-43571210	RPTEC	kidney:	n/a	n/a
9	CTCF	chr10:43574500-43574650	HMF	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
10	CTCF	chr10:43574352-43574772	MCF-7	breast:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
11	CTCF	chr10:43571043-43571207	GM12878	blood:	n/a	n/a
12	CTCF	chr10:43571060-43571210	NHDF-neo	bronchial:	n/a	n/a
13	CTCF	chr10:43566200-43566350	K562	blood:	n/a	n/a
14	CTCF	chr10:43573800-43573950	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr10:43566140-43566290	HepG2	liver:	n/a	n/a
16	CTCF	chr10:43574419-43574702	A549	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
17	CTCF	chr10:43571065-43571191	HepG2	liver:	n/a	n/a
18	CTCF	chr10:43573920-43574070	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr10:43574500-43574650	HepG2	liver:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
20	CTCF	chr10:43574480-43574630	HPAF	blood vessel:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
21	CTCF	chr10:43574380-43574530	BE2_C	brain:	n/a	n/a
22	CTCF	chr10:43574460-43574610	AG09319	gingival:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
23	CTCF	chr10:43574304-43574760	HCT-116	colon:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
24	CTCF	chr10:43574481-43574635	GM13976	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
25	CTCF	chr10:43566200-43566350	A549	lung:	n/a	n/a
26	CTCF	chr10:43588902-43589085	A549	lung:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
27	CTCF	chr10:43574431-43574670	LNCaP	prostate:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
28	CTCF	chr10:43571020-43571170	HMF	breast:	n/a	n/a
29	CTCF	chr10:43571020-43571170	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr10:43588954-43589111	K562	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
31	CTCF	chr10:43571026-43571234	LNCaP	prostate:	n/a	n/a
32	CTCF	chr10:43571060-43571210	Caco-2	colon:	n/a	n/a
33	CTCF	chr10:43574520-43574670	GM12869	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
34	CTCF	chr10:43574477-43574637	Kidney_OC	kidney:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
35	CTCF	chr10:43588921-43589150	Fibrobl	skin:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
36	CTCF	chr10:43574500-43574650	HAc	cerebellar:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
37	CTCF	chr10:43571049-43571229	MCF-7	breast:	n/a	n/a
38	CTCF	chr10:43574500-43574650	AG04450	lung:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
39	CTCF	chr10:43589060-43589210	HRE	kidney:	n/a	chr10:43589162-43589175
40	CTCF	chr10:43566220-43566370	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr10:43571040-43571190	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr10:43574525-43574601	GM10248	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
43	CTCF	chr10:43588897-43589166	K562	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
44	CTCF	chr10:43571040-43571190	GM12870	blood:	n/a	n/a
45	CTCF	chr10:43574520-43574670	HL-60	blood:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552
46	CTCF	chr10:43566240-43566390	K562	blood:	n/a	n/a
47	CTCF	chr10:43588960-43589110	GM12871	blood:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
48	CTCF	chr10:43588914-43589149	Gliobla	brain:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
49	CTCF	chr10:43588900-43589050	NHDF-neo	bronchial:	n/a	chr10:43589022-43589043 chr10:43589027-43589045
50	CTCF	chr10:43574480-43574630	HVMF	connective:	n/a	chr10:43574535-43574553 chr10:43574530-43574551 chr10:43574537-43574550 chr10:43574536-43574552

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43569045-43569095	HEEpiC	esophagus:	n/a
2	chr10:43569045-43569095	HEEpiC	esophagus:	n/a
3	chr10:43573332-43573382	HEEpiC	esophagus:	n/a
4	chr10:43572359-43572409	AG09309	skin:	n/a
5	chr10:43575142-43575192	Hela-S3	cervix:	n/a
6	chr10:43572244-43572294	HUVEC	blood vessel:	n/a
7	chr10:43571169-43571219	PrEC	prostate:	n/a
8	chr10:43572621-43572671	HCT-116	colon:	n/a
9	chr10:43577025-43577075	HIPEpiC	eye:	n/a
10	chr10:43572413-43572463	HL-60	blood:	n/a
11	chr10:43577025-43577075	HRPEpiC	eye:	n/a
12	chr10:43572413-43572463	GM12892	blood:	n/a
13	chr10:43573332-43573382	GM06990	blood:	n/a
14	chr10:43572467-43572517	HIPEpiC	eye:	n/a
15	chr10:43572621-43572671	Caco-2	colon:	n/a
16	chr10:43585188-43585238	U87	brain:	n/a
17	chr10:43572244-43572294	AG09319	gingival:	n/a
18	chr10:43585188-43585238	NHDF-neo	bronchial:	n/a
19	chr10:43572065-43572115	HCT-116	colon:	n/a
20	chr10:43569045-43569095	H1-hESC	embryonic stem cell:	embryo
21	chr10:43569045-43569095	K562	blood:	n/a
22	chr10:43572424-43572474	HepG2	liver:	n/a
23	chr10:43562544-43562594	ProgFib	skin:	n/a
24	chr10:43572430-43572480	GM12878	blood:	n/a
25	chr10:43572359-43572409	LNCaP	prostate:	n/a
26	chr10:43571169-43571219	ECC-1	luminal epithelium:	n/a
27	chr10:43572621-43572671	HUVEC	blood vessel:	n/a
28	chr10:43572413-43572463	RPTEC	kidney:	n/a
29	chr10:43572065-43572115	HEEpiC	esophagus:	n/a
30	chr10:43575142-43575192	LNCaP	prostate:	n/a
31	chr10:43577025-43577075	HCM	heart:	n/a
32	chr10:43572424-43572474	H1-hESC	embryonic stem cell:	embryo
33	chr10:43575142-43575192	AG04449	skin:	fetal
34	chr10:43569045-43569095	SK-N-SH_RA	brain:	n/a
35	chr10:43562813-43562863	GM12891	blood:	n/a
36	chr10:43572430-43572480	AG09309	skin:	n/a
37	chr10:43572795-43572845	MCF10A-Er-Src	breast:	n/a
38	chr10:43572244-43572294	GM19239	blood:	n/a
39	chr10:43573319-43573369	T-47D	breast:	n/a
40	chr10:43573319-43573369	ovcar-3	ovarian:	n/a
41	chr10:43585188-43585238	HEEpiC	esophagus:	n/a
42	chr10:43571169-43571219	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:43572430-43572480	AG09319	gingival:	n/a
44	chr10:43571169-43571219	GM19239	blood:	n/a
45	chr10:43572244-43572294	GM12891	blood:	n/a
46	chr10:43572621-43572671	SAEC	small airway:	n/a
47	chr10:43572795-43572845	BJ	skin:	n/a
48	chr10:43572795-43572845	HMEC	breast:	n/a
49	chr10:43572621-43572671	MCF-7	breast:	n/a
50	chr10:43572795-43572845	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:43361921..43363073-chr10:43574052..43574909,5	MCF-7	breast:
2	chr10:43549704..43551367-chr10:43558936..43561777,2	MCF-7	breast:
3	chr10:43556705..43558416-chr10:43560624..43562176,2	MCF-7	breast:
4	chr10:43571757..43578165-chr10:43578692..43585292,10	MCF-7	breast:
5	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
6	chr10:43563405..43565262-chr10:43578421..43580080,2	K562	blood:
7	chr10:43572567..43574576-chr10:43871912..43874300,2	MCF-7	breast:
8	chr10:43557710..43559940-chr10:43561579..43563313,2	K562	blood:
9	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
10	chr10:43521855..43522376-chr10:43577254..43578134,2	MCF-7	breast:
11	chr10:43555354..43557716-chr10:43558344..43560863,2	K562	blood:
12	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
13	chr10:43540640..43543554-chr10:43558547..43560903,3	MCF-7	breast:
14	chr10:43588801..43589617-chr10:43600178..43601154,2	MCF-7	breast:
15	chr10:43521611..43522326-chr10:43577256..43578049,6	MCF-7	breast:
16	chr10:43521503..43524600-chr10:43558785..43561738,3	MCF-7	breast:
17	chr10:43561322..43565766-chr10:43567124..43571353,6	K562	blood:
18	chr10:43563253..43566538-chr10:43567124..43569938,3	K562	blood:
19	chr10:43578754..43580371-chr10:43586605..43589212,2	MCF-7	breast:
20	chr10:43589175..43591364-chr10:43599200..43601057,2	MCF-7	breast:
21	chr10:43562026..43563048-chr17:73389362..73390234,5	MCF-7	breast:
22	chr10:43574441..43574987-chr10:43601035..43601611,2	K562	blood:
23	chr10:43521561..43522442-chr10:43555766..43556576,3	MCF-7	breast:
24	chr10:43539794..43541332-chr10:43557128..43559148,2	MCF-7	breast:
25	chr10:43370478..43372425-chr10:43586111..43588010,2	MCF-7	breast:
26	chr10:43521523..43522449-chr10:43577293..43578240,8	MCF-7	breast:
27	chr10:43589023..43591875-chr10:43596909..43598786,2	MCF-7	breast:
28	chr10:43553627..43556215-chr10:43562865..43565687,3	MCF-7	breast:
29	chr10:43571954..43575948-chr10:43588456..43593172,4	MCF-7	breast:
30	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
31	chr10:43574755..43578524-chr10:43632183..43633949,3	MCF-7	breast:
32	chr10:43585387..43587338-chr10:43587452..43589523,2	K562	blood:
33	chr10:43517701..43518324-chr10:43573585..43574127,2	MCF-7	breast:
34	chr10:43551076..43553051-chr10:43554800..43557668,3	MCF-7	breast:
35	chr10:43583134..43585872-chr10:43588187..43591197,3	MCF-7	breast:
36	chr10:43588758..43591392-chr10:43592644..43594640,2	MCF-7	breast:
37	chr10:43522999..43525382-chr10:43554403..43557112,2	MCF-7	breast:
38	chr10:43581616..43582507-chr10:43605989..43606921,3	MCF-7	breast:
39	chr10:43561322..43565766-chr10:43567124..43571353,6	K562	blood:
40	chr10:43521600..43522503-chr10:43589625..43590206,2	MCF-7	breast:
41	chr10:43533504..43534088-chr10:43577355..43578166,2	MCF-7	breast:
42	chr10:43561623..43563408-chr10:43565036..43569380,4	MCF-7	breast:
43	chr10:43520913..43524676-chr10:43563115..43566179,5	MCF-7	breast:
44	chr10:43567330..43568843-chr10:43570636..43572926,2	MCF-7	breast:
45	chr10:43553627..43556215-chr10:43562865..43565687,3	MCF-7	breast:
46	chr10:43521899..43522422-chr10:43563847..43564568,2	MCF-7	breast:
47	chr10:43576471..43578600-chr10:43587847..43590261,2	MCF-7	breast:
48	chr10:43575206..43579107-chr10:43583018..43585750,4	K562	blood:
49	chr10:43556494..43558733-chr10:43559960..43563613,3	MCF-7	breast:
50	chr10:43579643..43581967-chr10:43583481..43585726,2	MCF-7	breast:

Variant related genes	Relation type
RET	TF binding region
RET	CpG island
ENSG00000234944	chromatin interactions
ENSG00000177885	chromatin interactions
ENSG00000169826	chromatin interactions
ENSG00000229630	chromatin interactions
ENSG00000273008	chromatin interactions
ENSG00000165731	chromatin interactions
ENSG00000265342	chromatin interactions

Extended variants
information (count: 1627 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1627 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4948701	chr10:43550567-43550568	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs527389520	chr10:43550613-43550614	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs545849057	chr10:43550646-43550647	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs551938437	chr10:43550665-43550666	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs570671699	chr10:43550694-43550695	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs559304969	chr10:43550738-43550739	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs546201115	chr10:43550759-43550760	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs116193694	chr10:43550821-43550822	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs139116951	chr10:43550837-43550838	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs374763949	chr10:43550853-43550854	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs535717467	chr10:43550855-43550856	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs554225998	chr10:43550859-43550860	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs565896715	chr10:43550862-43550863	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs539928310	chr10:43550875-43550876	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs557970070	chr10:43550914-43550915	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs142301847	chr10:43550924-43550925	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs375857675	chr10:43550945-43550946	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs568005321	chr10:43550960-43550961	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs192987028	chr10:43550964-43550965	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs574017777	chr10:43550978-43550979	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs530083251	chr10:43550990-43550991	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs541285810	chr10:43551039-43551040	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs560095723	chr10:43551057-43551058	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs145972579	chr10:43551101-43551102	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs201247299	chr10:43551147-43551148	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs139511034	chr10:43551197-43551198	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs531562356	chr10:43551199-43551200	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs114829910	chr10:43551226-43551227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113243355	chr10:43551230-43551231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549766656	chr10:43551261-43551262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569995987	chr10:43551290-43551291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189292750	chr10:43551304-43551305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547330375	chr10:43551345-43551346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149731996	chr10:43551357-43551358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs539443647	chr10:43551380-43551381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34351370	chr10:43551425-43551426	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs144537477	chr10:43551430-43551431	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs113233044	chr10:43551514-43551515	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs537120758	chr10:43551523-43551524	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs555549493	chr10:43551532-43551533	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs573848713	chr10:43551587-43551588	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs538774532	chr10:43551666-43551667	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs541371795	chr10:43551696-43551697	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs553381530	chr10:43551741-43551742	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs572039758	chr10:43551745-43551746	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs148491582	chr10:43551802-43551803	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs564079609	chr10:43551839-43551840	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs116600310	chr10:43551892-43551893	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs200381914	chr10:43551988-43551989	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs543504985	chr10:43552016-43552017	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Breast cancer	22522925	CNVD

Chromatin state (count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43540200-43556600	Weak transcription	Spleen	Spleen
2	chr10:43542400-43553600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:43549000-43553400	Enhancers	Liver	Liver
4	chr10:43550200-43551200	Bivalent Enhancer	HepG2	liver
5	chr10:43551200-43553200	Enhancers	Right Ventricle	heart
6	chr10:43551400-43553200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
7	chr10:43551600-43551800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
8	chr10:43551800-43552400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr10:43551800-43553200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr10:43552000-43552400	Bivalent Enhancer	Fetal Brain Female	brain
11	chr10:43552000-43552400	Enhancers	Lung	lung
12	chr10:43552000-43552400	Enhancers	Pancreas	Pancrea
13	chr10:43552000-43552600	Enhancers	Left Ventricle	heart
14	chr10:43552400-43555600	Weak transcription	Pancreas	Pancrea
15	chr10:43552600-43555400	Weak transcription	Left Ventricle	heart
16	chr10:43552800-43553000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
17	chr10:43553200-43555400	Weak transcription	Right Ventricle	heart
18	chr10:43553400-43554800	Weak transcription	Liver	Liver
19	chr10:43553600-43553800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr10:43553800-43554200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:43554200-43555000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr10:43554400-43554600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr10:43554400-43572000	Weak transcription	Right Atrium	heart
24	chr10:43554600-43555000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:43554800-43557800	Enhancers	Liver	Liver
26	chr10:43555000-43555600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr10:43555000-43560400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr10:43555200-43556200	Enhancers	Duodenum Mucosa	Duodenum
29	chr10:43555200-43556200	Enhancers	Fetal Heart	heart
30	chr10:43555200-43556400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
31	chr10:43555400-43556200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr10:43555400-43556200	Enhancers	Left Ventricle	heart
33	chr10:43555400-43556200	Enhancers	Right Ventricle	heart
34	chr10:43555600-43556200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr10:43555600-43556200	Enhancers	Gastric	stomach
36	chr10:43555600-43556200	Enhancers	Pancreas	Pancrea
37	chr10:43555800-43556200	Enhancers	HMEC	breast
38	chr10:43556200-43559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr10:43556200-43559600	Weak transcription	Left Ventricle	heart
40	chr10:43556600-43556800	Enhancers	Spleen	Spleen
41	chr10:43556800-43563200	Weak transcription	Spleen	Spleen
42	chr10:43557600-43558000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr10:43557800-43558000	Enhancers	Right Ventricle	heart
44	chr10:43558000-43563400	Weak transcription	Right Ventricle	heart
45	chr10:43558800-43559000	Enhancers	Esophagus	oesophagus
46	chr10:43559000-43561400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr10:43559000-43562600	Weak transcription	Esophagus	oesophagus
48	chr10:43559400-43560600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr10:43559600-43560000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr10:43559600-43560000	Enhancers	Left Ventricle	heart

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