Variant report

Variant	nsv889101
Chromosome Location	chr7:118778802-119177670
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	ARID3A	chr7:118910137-118910320	K562	blood:	n/a	n/a
2	ARID3A	chr7:118910061-118910256	HepG2	liver:	n/a	n/a
3	ATF1	chr7:118877762-118877767	K562	blood:	n/a	n/a
4	ATF1	chr7:118873522-118873551	K562	blood:	n/a	n/a
5	ATF1	chr7:118893858-118893944	K562	blood:	n/a	n/a
6	BACH1	chr7:119122299-119123000	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr7:118838082-118838260	GM12878	blood:	n/a	n/a
8	BHLHE40	chr7:118869566-118869597	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:118816087-118816420	GM12878	blood:	n/a	n/a
10	BHLHE40	chr7:119122424-119122604	GM12878	blood:	n/a	n/a
11	BHLHE40	chr7:118910175-118910370	K562	blood:	n/a	n/a
12	BHLHE40	chr7:118910078-118910336	GM12878	blood:	n/a	n/a
13	BRCA1	chr7:118910149-118910242	HepG2	liver:	n/a	n/a
14	CBX3	chr7:118807512-118807928	HCT-116	colon:	n/a	n/a
15	CCNT2	chr7:118942141-118942206	K562	blood:	n/a	n/a
16	CCNT2	chr7:118882653-118882709	K562	blood:	n/a	n/a
17	CCNT2	chr7:118787886-118788025	K562	blood:	n/a	n/a
18	CCNT2	chr7:119174992-119175057	K562	blood:	n/a	n/a
19	CEBPB	chr7:118981917-118982143	HepG2	liver:	n/a	chr7:118981977-118981988 chr7:118982054-118982065
20	CEBPB	chr7:119024356-119024693	HepG2	liver:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
21	CEBPB	chr7:119112600-119113033	HCT-116	colon:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
22	CEBPB	chr7:119152429-119152660	HepG2	liver:	n/a	chr7:119152514-119152525
23	CEBPB	chr7:118893101-118893316	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:118997471-118997594	K562	blood:	n/a	n/a
25	CEBPB	chr7:118909918-118910257	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr7:118895992-118896335	HepG2	liver:	n/a	n/a
27	CEBPB	chr7:118868762-118868962	HepG2	liver:	n/a	chr7:118868837-118868848
28	CEBPB	chr7:118843973-118844155	A549	lung:	n/a	chr7:118844087-118844098 chr7:118844088-118844097 chr7:118844086-118844097
29	CEBPB	chr7:118843922-118844229	IMR90	lung:	n/a	chr7:118844087-118844098 chr7:118844088-118844097 chr7:118844086-118844097
30	CEBPB	chr7:119078392-119078635	IMR90	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
31	CEBPB	chr7:119043069-119043327	IMR90	lung:	n/a	chr7:119043190-119043203 chr7:119043190-119043201 chr7:119043192-119043203 chr7:119043190-119043203
32	CEBPB	chr7:119024379-119024647	IMR90	lung:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
33	CEBPB	chr7:119024394-119024680	A549	lung:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
34	CEBPB	chr7:118843968-118844253	HepG2	liver:	n/a	chr7:118844087-118844098 chr7:118844088-118844097 chr7:118844086-118844097
35	CEBPB	chr7:119112723-119113013	A549	lung:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
36	CEBPB	chr7:118990943-118991254	HepG2	liver:	n/a	chr7:118991067-118991078
37	CEBPB	chr7:119112687-119113157	MCF-7	breast:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
38	CEBPB	chr7:119078338-119078628	A549	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
39	CEBPB	chr7:118840953-118841173	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr7:118974488-118974690	HepG2	liver:	n/a	chr7:118974654-118974665
41	CEBPB	chr7:119078319-119078656	HepG2	liver:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
42	CEBPB	chr7:118872191-118872407	HepG2	liver:	n/a	chr7:118872300-118872313 chr7:118872301-118872312
43	CEBPB	chr7:119112604-119113132	HCT-116	colon:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913
44	CEBPB	chr7:119139694-119139733	K562	blood:	n/a	chr7:119139713-119139722
45	CEBPB	chr7:118863979-118864179	H1-hESC	embryonic stem cell:	n/a	chr7:118864117-118864128
46	CEBPB	chr7:118863977-118864186	HepG2	liver:	n/a	chr7:118864117-118864128
47	CEBPB	chr7:119078390-119078544	K562	blood:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
48	CEBPB	chr7:119158599-119158739	HepG2	liver:	n/a	chr7:119158656-119158667
49	CEBPB	chr7:118921903-118922151	A549	lung:	n/a	n/a
50	CEBPB	chr7:119112736-119113039	H1-hESC	embryonic stem cell:	n/a	chr7:119112904-119112913 chr7:119112904-119112913 chr7:119112902-119112915 chr7:119112904-119112913 chr7:119112902-119112913 chr7:119112903-119112914 chr7:119112902-119112915 chr7:119112904-119112913

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119121235-119121285	GM12892	blood:	n/a
2	chr7:119175916-119175966	HL-60	blood:	n/a
3	chr7:119175916-119175966	Hepatocyte	liver:	n/a
4	chr7:119121235-119121285	Caco-2	colon:	n/a
5	chr7:119175916-119175966	HRCEpiC	kidney:	n/a
6	chr7:119121235-119121285	SKMC	muscle:	n/a
7	chr7:119175916-119175966	T-47D	breast:	n/a
8	chr7:119175916-119175966	BJ	skin:	n/a
9	chr7:119121235-119121285	HRE	kidney:	n/a
10	chr7:119121235-119121285	BJ	skin:	n/a
11	chr7:119175916-119175966	H1-hESC	embryonic stem cell:	embryo
12	chr7:119121235-119121285	SAEC	small airway:	n/a
13	chr7:119175916-119175966	AG09309	skin:	n/a
14	chr7:119175916-119175966	HCM	heart:	n/a
15	chr7:119121235-119121285	NT2-D1	testis:	n/a
16	chr7:119121235-119121285	T-47D	breast:	n/a
17	chr7:119175916-119175966	NH-A	brain:	n/a
18	chr7:119121235-119121285	GM12878	blood:	n/a
19	chr7:119121235-119121285	RPTEC	kidney:	n/a
20	chr7:119121235-119121285	LNCaP	prostate:	n/a
21	chr7:119175916-119175966	NHDF-neo	bronchial:	n/a
22	chr7:119121235-119121285	K562	blood:	n/a
23	chr7:119175916-119175966	GM12878	blood:	n/a
24	chr7:119175916-119175966	HNPCEpiC	eye:	n/a
25	chr7:119175916-119175966	AG09319	gingival:	n/a
26	chr7:119175916-119175966	GM06990	blood:	n/a
27	chr7:119175916-119175966	PANC-1	pancreas:	n/a
28	chr7:119121235-119121285	PrEC	prostate:	n/a
29	chr7:119175916-119175966	LNCaP	prostate:	n/a
30	chr7:119175916-119175966	GM12891	blood:	n/a
31	chr7:119121235-119121285	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:119175916-119175966	Jurkat	blood:	n/a
33	chr7:119175916-119175966	SK-N-MC	brain:	n/a
34	chr7:119175916-119175966	HUVEC	blood vessel:	n/a
35	chr7:119175916-119175966	ProgFib	skin:	n/a
36	chr7:119121235-119121285	PFSK-1	brain:	n/a
37	chr7:119121235-119121285	HRPEpiC	eye:	n/a
38	chr7:119175916-119175966	AoSMC	blood vessel:	n/a
39	chr7:119175916-119175966	NT2-D1	testis:	n/a
40	chr7:119121235-119121285	HMEC	breast:	n/a
41	chr7:119175916-119175966	K562	blood:	n/a
42	chr7:119175916-119175966	SAEC	small airway:	n/a
43	chr7:119121235-119121285	GM06990	blood:	n/a
44	chr7:119175916-119175966	SKMC	muscle:	n/a
45	chr7:119175916-119175966	MCF-7	breast:	n/a
46	chr7:119121235-119121285	AG10803	skin:	n/a
47	chr7:119175916-119175966	RPTEC	kidney:	n/a
48	chr7:119175916-119175966	PFSK-1	brain:	n/a
49	chr7:119121235-119121285	H1-hESC	embryonic stem cell:	embryo
50	chr7:119121235-119121285	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:
2	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
3	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
4	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
5	chr7:118823416..118825410-chr7:118825629..118827229,2	K562	blood:
6	chr7:118510382..118510908-chr7:118815972..118816682,2	MCF-7	breast:
7	chr7:118782215..118784443-chr7:118786067..118788168,2	K562	blood:
8	chr7:118917919..118920251-chr7:118925221..118926809,2	K562	blood:
9	chr7:118288299..118289194-chr7:118816171..118816706,2	MCF-7	breast:
10	chr7:118902822..118906670-chr7:118907606..118911086,3	K562	blood:
11	chr7:118558904..118559746-chr7:118816086..118816731,2	MCF-7	breast:
12	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
13	chr7:118910028..118911067-chr7:119729751..119730686,4	MCF-7	breast:
14	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
15	chr6:30580881..30583485-chr7:118868073..118870261,2	MCF-7	breast:
16	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:
17	chr7:118938874..118939826-chr7:129751362..129752092,2	MCF-7	breast:
18	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
19	chr7:117992682..117993833-chr7:118815599..118816513,3	MCF-7	breast:
20	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
21	chr7:117390803..117391431-chr7:118815895..118816706,2	MCF-7	breast:
22	chr7:118852197..118855111-chr7:118862886..118865559,2	K562	blood:
23	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
24	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
25	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
26	chr7:118852197..118855111-chr7:118862886..118865559,2	K562	blood:
27	chr7:118558340..118559254-chr7:118837696..118838683,4	MCF-7	breast:
28	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
29	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
30	chr7:118823416..118825410-chr7:118825629..118827229,2	K562	blood:
31	chr2:32036680..32037459-chr7:119025565..119026383,2	MCF-7	breast:
32	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
33	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
34	chr7:118909733..118910708-chr7:145816212..145816735,2	MCF-7	breast:
35	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
36	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
37	chr7:119090628..119092465-chr7:119234986..119236766,2	K562	blood:
38	chr7:117992579..117993168-chr7:118815740..118816656,2	K562	blood:
39	chr7:118902822..118906670-chr7:118907606..118911086,3	K562	blood:
40	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
41	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
42	chr7:118792620..118793489-chr9:140473359..140473903,2	Hela-S3	cervix:
43	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
44	chr7:119171216..119174031-chr7:119180101..119182290,2	K562	blood:
45	chr7:117992651..117993374-chr7:118815864..118816654,2	MCF-7	breast:
46	chr7:118910007..118910665-chr7:120194855..120195659,2	MCF-7	breast:
47	chr7:118878113..118880101-chr7:118887192..118890136,2	K562	blood:
48	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
49	chr7:118857357..118859002-chr8:11343082..11345568,2	MCF-7	breast:
50	chr7:118917919..118920251-chr7:118925221..118926809,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTTNBP2-7	chr7:118818231-118819203	NONHSAT122980

Variant related genes	Relation type
ENSG00000270516	TF binding region
ENSG00000263692	TF binding region
ENSG00000270516	CpG island
ENSG00000263692	CpG island
ENSG00000148399	chromatin interactions

Extended variants
information (count: 2319 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537742800	chr7:118790633-118790634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545032502	chr7:118790638-118790639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185674786	chr7:118790666-118790667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568318052	chr7:118790667-118790668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115562417	chr7:118790748-118790749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs554275052	chr7:118790768-118790769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577536641	chr7:118790781-118790782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540067658	chr7:118790787-118790788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112193486	chr7:118790790-118790791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112451931	chr7:118790823-118790824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558078972	chr7:118790831-118790832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73221149	chr7:118790871-118790872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141454375	chr7:118790876-118790877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs7806771	chr7:118790891-118790892	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs191228438	chr7:118790924-118790925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539959019	chr7:118790934-118790935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376935106	chr7:118791024-118791025	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183480033	chr7:118791048-118791049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559841473	chr7:118791056-118791057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188468636	chr7:118791068-118791069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193220253	chr7:118791147-118791148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs369280723	chr7:118791166-118791167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7788545	chr7:118791179-118791180	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs183183919	chr7:118791191-118791192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs58825456	chr7:118791206-118791207	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs560127714	chr7:118791256-118791257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187867529	chr7:118791262-118791263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534156354	chr7:118791270-118791271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370143005	chr7:118791334-118791335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570991963	chr7:118791355-118791356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539931301	chr7:118791386-118791387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191267762	chr7:118791401-118791402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73718386	chr7:118791405-118791406	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs536161154	chr7:118791427-118791428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs183760087	chr7:118791428-118791429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188383140	chr7:118791443-118791444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs539874331	chr7:118791446-118791447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs192709396	chr7:118791476-118791477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs576579635	chr7:118791554-118791555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185160041	chr7:118791569-118791570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562714616	chr7:118791599-118791600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531373070	chr7:118791614-118791615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564754388	chr7:118791630-118791631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146343266	chr7:118791640-118791641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561992648	chr7:118791719-118791720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs527569067	chr7:118791766-118791767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs368829578	chr7:118791779-118791780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541022933	chr7:118791787-118791788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139067688	chr7:118791793-118791794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570812479	chr7:118791797-118791798	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Schizophrenia	21346763	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118790600-118792800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:118808200-118808800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr7:118808400-118809000	ZNF genes & repeats	Aorta	Aorta
4	chr7:118811800-118815800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:118814000-118814600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:118814000-118816600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr7:118814200-118814400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:118814400-118814600	Enhancers	Brain Angular Gyrus	brain
9	chr7:118814400-118818200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:118814600-118816000	Weak transcription	Brain Angular Gyrus	brain
11	chr7:118814600-118818000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:118815800-118816000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr7:118815800-118816000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr7:118815800-118816200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr7:118815800-118816200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:118815800-118816200	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr7:118815800-118816200	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr7:118815800-118816200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr7:118815800-118816200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:118815800-118816400	Enhancers	Dnd41	blood
21	chr7:118816000-118816200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:118816000-118816200	Enhancers	Adipose Nuclei	Adipose
23	chr7:118816000-118816200	Enhancers	Brain Angular Gyrus	brain
24	chr7:118816000-118816200	Enhancers	Brain Anterior Caudate	brain
25	chr7:118816000-118816200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr7:118816000-118816200	Enhancers	Brain Substantia Nigra	brain
27	chr7:118816000-118816200	Enhancers	Esophagus	oesophagus
28	chr7:118816000-118816200	Enhancers	Right Atrium	heart
29	chr7:118816000-118816200	Enhancers	Stomach Smooth Muscle	stomach
30	chr7:118816000-118817800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr7:118816000-118818200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr7:118816200-118818000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr7:118816200-118818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr7:118816200-118818200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr7:118816200-118818200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr7:118816200-118818400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr7:118816200-118829600	Weak transcription	Right Atrium	heart
38	chr7:118817800-118818000	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr7:118818000-118818800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr7:118818000-118819400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr7:118818000-118819400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr7:118818000-118819600	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr7:118818200-118818400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr7:118818200-118819200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr7:118818200-118819400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr7:118818200-118819400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr7:118818200-118819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr7:118818400-118818800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr7:118818400-118819000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr7:118818800-118819400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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