Variant report

Variant	nsv1034426
Chromosome Location	chr7:119584151-119655491
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:342)
CpG islands
(count:122)
Chromatin interactive
region (count:68)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:119583732-119584605	K562	blood:	n/a	n/a
2	ARID3A	chr7:119588383-119588467	K562	blood:	n/a	n/a
3	ARID3A	chr7:119633491-119633554	K562	blood:	n/a	n/a
4	ARID3A	chr7:119585975-119586344	K562	blood:	n/a	n/a
5	ARID3A	chr7:119603730-119604003	K562	blood:	n/a	n/a
6	ARID3A	chr7:119604894-119605665	K562	blood:	n/a	n/a
7	ATF1	chr7:119590901-119591026	K562	blood:	n/a	n/a
8	ATF1	chr7:119645327-119645329	K562	blood:	n/a	n/a
9	ATF1	chr7:119604972-119605649	K562	blood:	n/a	n/a
10	ATF3	chr7:119604903-119605339	K562	blood:	n/a	n/a
11	BACH1	chr7:119589003-119589869	K562	blood:	n/a	n/a
12	BATF	chr7:119636646-119637004	GM12878	blood:	n/a	chr7:119636842-119636853 chr7:119636843-119636853
13	BATF	chr7:119636748-119636964	GM12878	blood:	n/a	chr7:119636842-119636853 chr7:119636843-119636853
14	BCL11A	chr7:119636766-119636964	GM12878	blood:	n/a	n/a
15	BCLAF1	chr7:119588928-119590441	K562	blood:	n/a	n/a
16	BHLHE40	chr7:119617761-119617878	K562	blood:	n/a	n/a
17	BRCA1	chr7:119640774-119640835	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr7:119590477-119591189	K562	blood:	n/a	n/a
19	CBX3	chr7:119607208-119607692	K562	blood:	n/a	n/a
20	CBX3	chr7:119604811-119605354	K562	blood:	n/a	n/a
21	CBX3	chr7:119590471-119591130	K562	blood:	n/a	n/a
22	CBX3	chr7:119583855-119584516	K562	blood:	n/a	n/a
23	CBX3	chr7:119603669-119604091	K562	blood:	n/a	n/a
24	CCNT2	chr7:119604745-119605609	K562	blood:	n/a	n/a
25	CEBPB	chr7:119625618-119625783	K562	blood:	n/a	n/a
26	CEBPB	chr7:119624307-119624625	IMR90	lung:	n/a	chr7:119624459-119624470
27	CEBPB	chr7:119599826-119600424	IMR90	lung:	n/a	n/a
28	CEBPB	chr7:119604128-119604426	HepG2	liver:	n/a	n/a
29	CEBPB	chr7:119624323-119624666	HepG2	liver:	n/a	chr7:119624459-119624470
30	CEBPB	chr7:119609912-119610187	A549	lung:	n/a	chr7:119610022-119610035 chr7:119610023-119610034
31	CEBPB	chr7:119614851-119615155	K562	blood:	n/a	n/a
32	CEBPB	chr7:119609909-119610192	HepG2	liver:	n/a	chr7:119610022-119610035 chr7:119610023-119610034
33	CEBPB	chr7:119604219-119604498	IMR90	lung:	n/a	n/a
34	CEBPB	chr7:119609873-119610184	K562	blood:	n/a	chr7:119610022-119610035 chr7:119610023-119610034
35	CEBPB	chr7:119624391-119624637	Hela-S3	cervix:	n/a	chr7:119624459-119624470
36	CEBPB	chr7:119614881-119615151	HepG2	liver:	n/a	n/a
37	CEBPB	chr7:119641488-119641603	HepG2	liver:	n/a	chr7:119641534-119641545
38	CEBPB	chr7:119624321-119624642	K562	blood:	n/a	chr7:119624459-119624470
39	CEBPB	chr7:119609861-119610180	IMR90	lung:	n/a	chr7:119610022-119610035 chr7:119610023-119610034
40	CEBPB	chr7:119603910-119604674	K562	blood:	n/a	chr7:119604016-119604028
41	CEBPD	chr7:119589065-119590443	K562	blood:	n/a	n/a
42	CHD2	chr7:119584212-119584462	K562	blood:	n/a	n/a
43	CHD2	chr7:119589097-119589531	K562	blood:	n/a	n/a
44	CTCF	chr7:119640303-119640329	K562	blood:	n/a	n/a
45	CTCF	chr7:119640280-119640430	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr7:119584240-119584390	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr7:119584320-119584470	RPTEC	kidney:	n/a	n/a
48	CTCF	chr7:119623103-119623218	K562	blood:	n/a	n/a
49	CTCF	chr7:119640240-119640390	AG04450	lung:	n/a	n/a
50	CTCF	chr7:119626240-119626390	Caco-2	colon:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119604878-119604928	GM12878	blood:	n/a
2	chr7:119604878-119604928	Caco-2	colon:	n/a
3	chr7:119604878-119604928	HEK293	kidney:	embryo
4	chr7:119590451-119590501	PrEC	prostate:	n/a
5	chr7:119590451-119590501	AG09319	gingival:	n/a
6	chr7:119604878-119604928	MCF-7	breast:	n/a
7	chr7:119590451-119590501	ECC-1	luminal epithelium:	n/a
8	chr7:119590451-119590501	MCF10A-Er-Src	breast:	n/a
9	chr7:119590451-119590501	GM12892	blood:	n/a
10	chr7:119604878-119604928	U87	brain:	n/a
11	chr7:119604878-119604928	AG09309	skin:	n/a
12	chr7:119604878-119604928	HNPCEpiC	eye:	n/a
13	chr7:119590451-119590501	SK-N-SH_RA	brain:	n/a
14	chr7:119590451-119590501	ProgFib	skin:	n/a
15	chr7:119604878-119604928	ECC-1	luminal epithelium:	n/a
16	chr7:119590451-119590501	AoSMC	blood vessel:	n/a
17	chr7:119604878-119604928	BJ	skin:	n/a
18	chr7:119604878-119604928	Hela-S3	cervix:	n/a
19	chr7:119590451-119590501	LNCaP	prostate:	n/a
20	chr7:119604878-119604928	HMEC	breast:	n/a
21	chr7:119604878-119604928	LNCaP	prostate:	n/a
22	chr7:119604878-119604928	HL-60	blood:	n/a
23	chr7:119590451-119590501	T-47D	breast:	n/a
24	chr7:119604878-119604928	HRPEpiC	eye:	n/a
25	chr7:119604878-119604928	HIPEpiC	eye:	n/a
26	chr7:119590451-119590501	AG04449	skin:	fetal
27	chr7:119590451-119590501	NT2-D1	testis:	n/a
28	chr7:119604878-119604928	AG04450	lung:	fetal
29	chr7:119590451-119590501	HNPCEpiC	eye:	n/a
30	chr7:119590451-119590501	GM19239	blood:	n/a
31	chr7:119604878-119604928	GM06990	blood:	n/a
32	chr7:119590451-119590501	HRE	kidney:	n/a
33	chr7:119604878-119604928	SK-N-MC	brain:	n/a
34	chr7:119604878-119604928	PrEC	prostate:	n/a
35	chr7:119590451-119590501	AG04450	lung:	fetal
36	chr7:119590451-119590501	HCM	heart:	n/a
37	chr7:119590451-119590501	Caco-2	colon:	n/a
38	chr7:119590451-119590501	H1-hESC	embryonic stem cell:	embryo
39	chr7:119604878-119604928	BE2_C	brain:	n/a
40	chr7:119604878-119604928	NB4	blood:	n/a
41	chr7:119604878-119604928	HAEpiC	amniotic membrane:	n/a
42	chr7:119604878-119604928	CMK	blood:	n/a
43	chr7:119590451-119590501	HCT-116	colon:	n/a
44	chr7:119604878-119604928	HPAEpiC	pulmonary alveolar:	n/a
45	chr7:119604878-119604928	HCF	heart:	n/a
46	chr7:119590451-119590501	GM12891	blood:	n/a
47	chr7:119590451-119590501	U87	brain:	n/a
48	chr7:119590451-119590501	BE2_C	brain:	n/a
49	chr7:119590451-119590501	NH-A	brain:	n/a
50	chr7:119604878-119604928	HEEpiC	esophagus:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:119575582..119577165-chr7:119582131..119584732,3	K562	blood:
2	chr7:119545928..119547433-chr7:119598260..119601242,2	K562	blood:
3	chr7:119584419..119586838-chr7:119603002..119604856,2	K562	blood:
4	chr7:119599851..119601809-chr7:119612155..119614686,2	K562	blood:
5	chr7:119545841..119548270-chr7:119587214..119590223,3	K562	blood:
6	chr7:119599851..119601809-chr7:119612155..119614686,2	K562	blood:
7	chr7:119609825..119612771-chr7:119797844..119799640,2	K562	blood:
8	chr7:119627874..119630349-chr7:119632523..119634037,2	K562	blood:
9	chr6:26197408..26198395-chr7:119633064..119634048,2	Hela-S3	cervix:
10	chr7:119589512..119591360-chr7:119594151..119597360,3	K562	blood:
11	chr7:119594641..119599063-chr7:119599275..119601348,3	K562	blood:
12	chr7:119590351..119592523-chr7:119610438..119612381,2	K562	blood:
13	chr7:119547567..119549067-chr7:119606535..119609324,2	K562	blood:
14	chr7:119604091..119606659-chr7:119609179..119612506,3	K562	blood:
15	chr7:119623792..119625656-chr7:119627797..119629586,2	K562	blood:
16	chr7:119643152..119644990-chr7:119648554..119650528,2	K562	blood:
17	chr7:119564930..119567525-chr7:119586667..119589307,3	K562	blood:
18	chr7:119601761..119606490-chr7:119613370..119617437,5	K562	blood:
19	chr7:119596097..119599917-chr7:119604166..119607181,3	K562	blood:
20	chr7:119593756..119596259-chr7:119601631..119603821,2	K562	blood:
21	chr17:29421604..29422445-chr7:119633549..119634068,2	Hela-S3	cervix:
22	chr7:119649916..119652698-chr7:119653693..119655972,2	K562	blood:
23	chr7:119613490..119615786-chr7:119615984..119618281,3	K562	blood:
24	chr7:119579726..119581869-chr7:119583415..119586890,3	K562	blood:
25	chr7:119569917..119573770-chr7:119586780..119589332,3	K562	blood:
26	chr7:119596097..119601852-chr7:119602330..119605666,5	K562	blood:
27	chr7:119607984..119609980-chr7:119613441..119615371,3	K562	blood:
28	chr7:119588397..119591015-chr7:120565946..120567892,2	K562	blood:
29	chr16:70557277..70558159-chr7:119633549..119634068,2	Hela-S3	cervix:
30	chr7:119544847..119547589-chr7:119588940..119593130,4	K562	blood:
31	chr6:86388241..86388876-chr7:119633568..119634069,2	Hela-S3	cervix:
32	chr7:119546057..119547613-chr7:119602770..119604500,2	K562	blood:
33	chr7:119607984..119609980-chr7:119613441..119615371,3	K562	blood:
34	chr7:119603198..119605328-chr7:119613370..119615944,2	K562	blood:
35	chr7:119627874..119630349-chr7:119632523..119634037,2	K562	blood:
36	chr7:119546333..119548677-chr7:119583508..119586175,2	K562	blood:
37	chr7:119592860..119595657-chr7:119604147..119608281,6	K562	blood:
38	chr7:119601761..119606490-chr7:119613370..119617437,5	K562	blood:
39	chr7:119605463..119608341-chr7:119623284..119625635,2	K562	blood:
40	chr7:119593756..119596259-chr7:119601631..119603821,2	K562	blood:
41	chr7:119595929..119598016-chr7:119599722..119602227,2	K562	blood:
42	chr7:119623792..119625656-chr7:119627797..119629586,2	K562	blood:
43	chr7:119643152..119644990-chr7:119648554..119650528,2	K562	blood:
44	chr7:119613490..119615786-chr7:119615984..119618281,3	K562	blood:
45	chr7:119548507..119550960-chr7:119636367..119638999,2	K562	blood:
46	chr7:119570997..119574569-chr7:119582922..119586334,5	K562	blood:
47	chr7:119578083..119580196-chr7:119586572..119589192,2	K562	blood:
48	chr7:119596097..119601852-chr7:119602330..119605666,5	K562	blood:
49	chr7:119571307..119574427-chr7:119582065..119585012,4	K562	blood:
50	chr7:119604091..119606659-chr7:119609179..119612506,3	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN12-7	chr7:119653589-119653779	l_3470_chr7:119643807-119654690_testes
2	lnc-TSPAN12-7	chr7:119643808-119644359	l_3470_chr7:119643807-119654690_testes
3	lnc-TSPAN12-7	chr7:119654369-119654690	l_3470_chr7:119643807-119654690_testes

No data

Variant related genes	Relation type
ENSG00000271739	TF binding region
ENSG00000271739	CpG island
ENSG00000115875	chromatin interactions
ENSG00000103051	chromatin interactions
ENSG00000196712	chromatin interactions
ENSG00000225546	chromatin interactions
ENSG00000152147	chromatin interactions
ENSG00000203875	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000189091	chromatin interactions

Extended variants
information (count: 1596 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1596 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575739790	chr7:119584181-119584182	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577208916	chr7:119584216-119584217	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547890502	chr7:119584220-119584221	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs570922299	chr7:119584242-119584243	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs533447993	chr7:119584304-119584305	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs13233786	chr7:119584409-119584410	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs561200679	chr7:119584431-119584432	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375341810	chr7:119584434-119584435	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570059694	chr7:119584448-119584449	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536158970	chr7:119584489-119584490	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184351074	chr7:119584505-119584506	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs114775690	chr7:119584520-119584521	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566287419	chr7:119584524-119584525	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534872977	chr7:119584618-119584619	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558316865	chr7:119584624-119584625	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369707258	chr7:119584648-119584649	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115344689	chr7:119584710-119584711	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530349069	chr7:119584729-119584730	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540558599	chr7:119584743-119584744	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539144323	chr7:119584752-119584753	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567315536	chr7:119584822-119584823	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs188851722	chr7:119584859-119584860	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs148254961	chr7:119584869-119584870	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs542109337	chr7:119584873-119584874	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73485284	chr7:119584923-119584924	Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs367933989	chr7:119584934-119584935	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs572219432	chr7:119584941-119584942	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs540900977	chr7:119584973-119584974	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79071857	chr7:119584984-119584985	Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs193087208	chr7:119585025-119585026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs550285352	chr7:119585034-119585035	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185833858	chr7:119585048-119585049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189096772	chr7:119585062-119585063	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs532585908	chr7:119585110-119585111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549920294	chr7:119585147-119585148	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs36013530	chr7:119585148-119585149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs549668716	chr7:119585214-119585215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs566280091	chr7:119585351-119585352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs141248448	chr7:119585358-119585359	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs180740315	chr7:119585369-119585370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs150804365	chr7:119585403-119585404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183671000	chr7:119585409-119585410	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs571226296	chr7:119585434-119585435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs139732119	chr7:119585452-119585453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs369653345	chr7:119585543-119585544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555793071	chr7:119585555-119585556	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576009066	chr7:119585634-119585635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs535070821	chr7:119585732-119585733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs77650056	chr7:119585733-119585734	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs75139062	chr7:119585853-119585854	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	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
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119584000-119584800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:119584000-119585000	Flanking Active TSS	K562	blood
3	chr7:119584200-119584800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr7:119585000-119585800	Weak transcription	K562	blood
5	chr7:119585800-119590600	Active TSS	K562	blood
6	chr7:119589000-119589400	Enhancers	Ovary	ovary
7	chr7:119597400-119597600	Active TSS	K562	blood
8	chr7:119597400-119597800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr7:119597400-119597800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr7:119597600-119598000	Enhancers	HMEC	breast
11	chr7:119597600-119603800	Weak transcription	K562	blood
12	chr7:119597800-119598000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr7:119597800-119599400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr7:119598400-119599800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:119599200-119602200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:119599200-119602400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr7:119599400-119599600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr7:119599400-119602200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr7:119599400-119602400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr7:119599600-119600000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:119599600-119601400	Enhancers	HSMM	muscle
22	chr7:119599600-119602200	Enhancers	Osteobl	bone
23	chr7:119599800-119600200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr7:119599800-119600600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr7:119599800-119601200	Enhancers	NHEK	skin
26	chr7:119599800-119601800	Enhancers	NH-A	brain
27	chr7:119600000-119600800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr7:119600200-119600600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:119600200-119605200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr7:119600400-119600600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr7:119600400-119601200	Enhancers	NHDF-Ad	bronchial
32	chr7:119600400-119601200	Enhancers	NHLF	lung
33	chr7:119600600-119604800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr7:119600600-119605000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr7:119601000-119601400	Enhancers	HUVEC	blood vessel
36	chr7:119601200-119604800	Weak transcription	NHDF-Ad	bronchial
37	chr7:119601200-119604800	Weak transcription	NHLF	lung
38	chr7:119601400-119603800	Weak transcription	HSMM	muscle
39	chr7:119601800-119604800	Weak transcription	NH-A	brain
40	chr7:119602200-119603800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr7:119602200-119603800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr7:119602200-119604800	Weak transcription	Osteobl	bone
43	chr7:119602400-119603800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr7:119602400-119603800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr7:119603800-119605000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr7:119603800-119605800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr7:119603800-119605800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr7:119603800-119605800	Enhancers	Muscle Satellite Cultured Cells	--
49	chr7:119603800-119605800	Enhancers	HSMM	muscle
50	chr7:119603800-119605800	Enhancers	HSMMtube	muscle

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