Variant report

Variant	nsv889106
Chromosome Location	chr7:118928231-119197465
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	BACH1	chr7:119122299-119123000	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr7:119122424-119122604	GM12878	blood:	n/a	n/a
3	CBX3	chr7:119185151-119185664	HCT-116	colon:	n/a	n/a
4	CCNT2	chr7:119174992-119175057	K562	blood:	n/a	n/a
5	CCNT2	chr7:118942141-118942206	K562	blood:	n/a	n/a
6	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
7	CEBPB	chr7:119184919-119185504	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr7:119043069-119043327	IMR90	lung:	n/a	chr7:119043190-119043203 chr7:119043190-119043201 chr7:119043192-119043203 chr7:119043190-119043203
9	CEBPB	chr7:119005301-119005424	A549	lung:	n/a	n/a
10	CEBPB	chr7:119183182-119183277	K562	blood:	n/a	chr7:119183252-119183263
11	CEBPB	chr7:119055965-119055997	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr7:118974488-118974690	HepG2	liver:	n/a	chr7:118974654-118974665
13	CEBPB	chr7:118997471-118997594	K562	blood:	n/a	n/a
14	CEBPB	chr7:119024356-119024693	HepG2	liver:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
15	CEBPB	chr7:119043095-119043321	HepG2	liver:	n/a	chr7:119043190-119043203 chr7:119043190-119043201 chr7:119043192-119043203 chr7:119043190-119043203
16	CEBPB	chr7:119112731-119113061	K562	blood:	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
17	CEBPB	chr7:118981917-118982143	HepG2	liver:	n/a	chr7:118981977-118981988 chr7:118982054-118982065
18	CEBPB	chr7:119152429-119152660	HepG2	liver:	n/a	chr7:119152514-119152525
19	CEBPB	chr7:119078319-119078656	HepG2	liver:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
20	CEBPB	chr7:118997442-118997653	A549	lung:	n/a	n/a
21	CEBPB	chr7:119078392-119078635	IMR90	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
22	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
23	CEBPB	chr7:119024371-119024597	K562	blood:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
24	CEBPB	chr7:119139694-119139733	K562	blood:	n/a	chr7:119139713-119139722
25	CEBPB	chr7:119024394-119024680	A549	lung:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
26	CEBPB	chr7:119112728-119113065	IMR90	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
27	CEBPB	chr7:119112798-119112948	HepG2	liver:	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
28	CEBPB	chr7:119078390-119078544	K562	blood:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
29	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
30	CEBPB	chr7:119112634-119113091	HepG2	liver:	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
31	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
32	CEBPB	chr7:119024379-119024647	IMR90	lung:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
33	CEBPB	chr7:119183092-119183422	HepG2	liver:	n/a	chr7:119183252-119183263
34	CEBPB	chr7:119183098-119183415	A549	lung:	n/a	chr7:119183252-119183263
35	CEBPB	chr7:119184879-119185640	A549	lung:	n/a	n/a
36	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
37	CEBPB	chr7:119158599-119158739	HepG2	liver:	n/a	chr7:119158656-119158667
38	CEBPB	chr7:119078338-119078628	A549	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
39	CEBPB	chr7:119112667-119113038	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
40	CEBPB	chr7:118990943-118991254	HepG2	liver:	n/a	chr7:118991067-118991078
41	CHD1	chr7:119083449-119083466	GM12878	blood:	n/a	n/a
42	CTCF	chr7:119122358-119122571	K562	blood:	n/a	n/a
43	CTCF	chr7:119122374-119122574	LNCaP	prostate:	n/a	n/a
44	CTCF	chr7:119122419-119122540	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr7:118960460-118960610	NB4	blood:	n/a	n/a
46	CTCF	chr7:119122360-119122510	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr7:119122440-119122590	BE2_C	brain:	n/a	n/a
48	CTCF	chr7:119122380-119122530	GM12801	blood:	n/a	n/a
49	CTCF	chr7:119122269-119122608	Gliobla	brain:	n/a	n/a
50	CTCF	chr7:119122360-119122510	GM12869	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119175916-119175966	Hela-S3	cervix:	n/a
2	chr7:119175916-119175966	AG04450	lung:	fetal
3	chr7:119175916-119175966	HCM	heart:	n/a
4	chr7:119121235-119121285	AG04450	lung:	fetal
5	chr7:119175916-119175966	GM12878	blood:	n/a
6	chr7:119175916-119175966	SK-N-MC	brain:	n/a
7	chr7:119175916-119175966	NHDF-neo	bronchial:	n/a
8	chr7:119121235-119121285	PANC-1	pancreas:	n/a
9	chr7:119175916-119175966	HUVEC	blood vessel:	n/a
10	chr7:119121235-119121285	HAEpiC	amniotic membrane:	n/a
11	chr7:119121235-119121285	LNCaP	prostate:	n/a
12	chr7:119121235-119121285	BE2_C	brain:	n/a
13	chr7:119121235-119121285	NHDF-neo	bronchial:	n/a
14	chr7:119121235-119121285	IMR90	lung:	fetal
15	chr7:119175916-119175966	AG10803	skin:	n/a
16	chr7:119121235-119121285	PrEC	prostate:	n/a
17	chr7:119121235-119121285	AoSMC	blood vessel:	n/a
18	chr7:119175916-119175966	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:119121235-119121285	CMK	blood:	n/a
20	chr7:119121235-119121285	HCF	heart:	n/a
21	chr7:119121235-119121285	HEK293	kidney:	embryo
22	chr7:119121235-119121285	HIPEpiC	eye:	n/a
23	chr7:119175916-119175966	HRPEpiC	eye:	n/a
24	chr7:119175916-119175966	SK-N-SH	brain:	n/a
25	chr7:119175916-119175966	K562	blood:	n/a
26	chr7:119121235-119121285	HRCEpiC	kidney:	n/a
27	chr7:119121235-119121285	RPTEC	kidney:	n/a
28	chr7:119175916-119175966	PANC-1	pancreas:	n/a
29	chr7:119121235-119121285	ProgFib	skin:	n/a
30	chr7:119175916-119175966	LNCaP	prostate:	n/a
31	chr7:119175916-119175966	HNPCEpiC	eye:	n/a
32	chr7:119121235-119121285	HEEpiC	esophagus:	n/a
33	chr7:119121235-119121285	HUVEC	blood vessel:	n/a
34	chr7:119121235-119121285	HMEC	breast:	n/a
35	chr7:119121235-119121285	K562	blood:	n/a
36	chr7:119121235-119121285	SK-N-MC	brain:	n/a
37	chr7:119175916-119175966	AG09319	gingival:	n/a
38	chr7:119175916-119175966	GM12891	blood:	n/a
39	chr7:119175916-119175966	HRE	kidney:	n/a
40	chr7:119175916-119175966	GM06990	blood:	n/a
41	chr7:119121235-119121285	Hepatocyte	liver:	n/a
42	chr7:119121235-119121285	SK-N-SH_RA	brain:	n/a
43	chr7:119175916-119175966	AoSMC	blood vessel:	n/a
44	chr7:119175916-119175966	HL-60	blood:	n/a
45	chr7:119121235-119121285	HL-60	blood:	n/a
46	chr7:119175916-119175966	HEEpiC	esophagus:	n/a
47	chr7:119175916-119175966	ProgFib	skin:	n/a
48	chr7:119121235-119121285	GM06990	blood:	n/a
49	chr7:119175916-119175966	RPTEC	kidney:	n/a
50	chr7:119175916-119175966	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:
2	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
3	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
4	chr7:119174664..119177243-chr7:119179086..119181541,2	K562	blood:
5	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
6	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
7	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
8	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
9	chr6:81998528..81999232-chr7:119153061..119154054,2	MCF-7	breast:
10	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
11	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
12	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
13	chr7:119101385..119103050-chr7:119105094..119106649,2	K562	blood:
14	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
15	chr7:119184831..119187773-chr7:119262380..119264496,2	MCF-7	breast:
16	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:
17	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
18	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
19	chr7:119192825..119195698-chr7:119199166..119201397,2	K562	blood:
20	chr7:118938874..118939826-chr7:129751362..129752092,2	MCF-7	breast:
21	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
22	chr7:119174664..119177243-chr7:119179086..119181541,2	K562	blood:
23	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
24	chr2:32036680..32037459-chr7:119025565..119026383,2	MCF-7	breast:
25	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
26	chr7:119171216..119174031-chr7:119180101..119182290,2	K562	blood:
27	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
28	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
29	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
30	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
31	chr7:119188506..119190356-chr7:119200793..119202933,2	K562	blood:
32	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
33	chr7:119171216..119174031-chr7:119180101..119182290,2	K562	blood:
34	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
35	chr7:119090628..119092465-chr7:119234986..119236766,2	K562	blood:

Variant related genes	Relation type
ENSG00000263692	TF binding region
ENSG00000263692	CpG island

Extended variants
information (count: 1014 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs308177	chr7:118928231-118928232	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs573762458	chr7:118928277-118928278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542403750	chr7:118928281-118928282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187089044	chr7:118928291-118928292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572779314	chr7:118928319-118928320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78851089	chr7:118928342-118928343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs539612793	chr7:118952214-118952215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367788689	chr7:118952275-118952276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs556045677	chr7:118952280-118952281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs576291771	chr7:118952329-118952330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541732061	chr7:118952332-118952333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561765623	chr7:118952401-118952402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572094274	chr7:118952428-118952429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs371310147	chr7:118952446-118952447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs77682931	chr7:118952457-118952458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs370834315	chr7:118952460-118952461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564234068	chr7:118952463-118952464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574194042	chr7:118952565-118952566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533387783	chr7:118952619-118952620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191405722	chr7:118952621-118952622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563683962	chr7:118952673-118952674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529611688	chr7:118952677-118952678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183765181	chr7:118952739-118952740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549377913	chr7:118952747-118952748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs114452749	chr7:118952749-118952750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs374214560	chr7:118952771-118952772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs187759480	chr7:118952783-118952784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547555528	chr7:118952787-118952788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560750780	chr7:118952795-118952796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs199964686	chr7:118965064-118965065	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs376402585	chr7:118965072-118965073	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs181871282	chr7:118965106-118965107	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs186426957	chr7:118965287-118965288	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs545794985	chr7:118965292-118965293	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs147432237	chr7:118965347-118965348	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs576143409	chr7:118965365-118965366	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140686922	chr7:118965366-118965367	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs201247182	chr7:118970615-118970616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs201858999	chr7:118970617-118970618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77217402	chr7:118970627-118970628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530223963	chr7:118970659-118970660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184277941	chr7:118970664-118970665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140110559	chr7:118970667-118970668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574740490	chr7:118970675-118970676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548935544	chr7:118970683-118970684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs35509297	chr7:118970707-118970708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540763803	chr7:118970740-118970741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143833551	chr7:118970750-118970751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190343112	chr7:118970765-118970766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs546010420	chr7:118970767-118970768	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:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118927800-118928400	Enhancers	Fetal Brain Male	brain
2	chr7:118952200-118952800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:118965000-118965200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:118965200-118965400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr7:118970600-118971000	Enhancers	Brain Substantia Nigra	brain
6	chr7:118981600-118984200	Enhancers	Liver	Liver
7	chr7:118990400-118990800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:118991400-118991600	Enhancers	Liver	Liver
9	chr7:118991400-118991600	ZNF genes & repeats	Esophagus	oesophagus
10	chr7:118992200-118992400	Enhancers	Liver	Liver
11	chr7:118996800-118997200	Active TSS	Gastric	stomach
12	chr7:119034600-119034800	Active TSS	Liver	Liver
13	chr7:119034800-119035400	Flanking Active TSS	Liver	Liver
14	chr7:119035400-119035600	Active TSS	Liver	Liver
15	chr7:119035600-119037200	Weak transcription	Liver	Liver
16	chr7:119037200-119037600	Enhancers	Liver	Liver
17	chr7:119037200-119037600	Enhancers	GM12878-XiMat	blood
18	chr7:119044000-119046800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr7:119044800-119045000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:119048200-119048800	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr7:119048200-119049400	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr7:119061600-119062200	Enhancers	Liver	Liver
23	chr7:119089600-119090000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:119112400-119112600	Active TSS	Liver	Liver
25	chr7:119112400-119112600	Enhancers	Fetal Intestine Large	intestine
26	chr7:119112400-119112800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr7:119112600-119112800	Flanking Active TSS	Liver	Liver
28	chr7:119112600-119112800	Enhancers	Pancreas	Pancrea
29	chr7:119112600-119113000	Flanking Active TSS	Fetal Intestine Large	intestine
30	chr7:119112600-119113000	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:119112800-119113000	Enhancers	Liver	Liver
32	chr7:119113000-119113200	Enhancers	Fetal Intestine Large	intestine
33	chr7:119117600-119118000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr7:119118000-119122200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr7:119120800-119121200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:119122000-119122400	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr7:119122000-119122400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr7:119122000-119123000	Enhancers	H1 Cell Line	embryonic stem cell
39	chr7:119122000-119123600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:119122200-119122400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr7:119122200-119122800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr7:119122200-119123000	Enhancers	H9 Cell Line	embryonic stem cell
43	chr7:119122200-119123000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:119122200-119123000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:119122200-119123000	Enhancers	Liver	Liver
46	chr7:119122200-119123200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr7:119123000-119123400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr7:119133400-119134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:119134400-119135400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:119135400-119135800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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