Variant report

Variant	nsv889100
Chromosome Location	chr7:118744450-119247571
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	chr7:118910061-118910256	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:118910137-118910320	K562	blood:	n/a	n/a
3	ATF1	chr7:118893858-118893944	K562	blood:	n/a	n/a
4	ATF1	chr7:118873522-118873551	K562	blood:	n/a	n/a
5	ATF1	chr7:118877762-118877767	K562	blood:	n/a	n/a
6	BACH1	chr7:119122299-119123000	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr7:119235049-119235354	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr7:118910078-118910336	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	chr7:118869566-118869597	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:118838082-118838260	GM12878	blood:	n/a	n/a
14	BRCA1	chr7:118910149-118910242	HepG2	liver:	n/a	n/a
15	BRCA1	chr7:118747696-118747725	GM12878	blood:	n/a	n/a
16	CBX3	chr7:119185151-119185664	HCT-116	colon:	n/a	n/a
17	CBX3	chr7:118807512-118807928	HCT-116	colon:	n/a	n/a
18	CCNT2	chr7:119201981-119202070	K562	blood:	n/a	n/a
19	CCNT2	chr7:118882653-118882709	K562	blood:	n/a	n/a
20	CCNT2	chr7:118942141-118942206	K562	blood:	n/a	n/a
21	CCNT2	chr7:119174992-119175057	K562	blood:	n/a	n/a
22	CCNT2	chr7:119233909-119234326	K562	blood:	n/a	n/a
23	CCNT2	chr7:118787886-118788025	K562	blood:	n/a	n/a
24	CEBPB	chr7:118981917-118982143	HepG2	liver:	n/a	chr7:118981977-118981988 chr7:118982054-118982065
25	CEBPB	chr7:118843973-118844155	A549	lung:	n/a	chr7:118844087-118844098 chr7:118844088-118844097 chr7:118844086-118844097
26	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
27	CEBPB	chr7:118893101-118893316	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:118997442-118997653	A549	lung:	n/a	n/a
29	CEBPB	chr7:119139694-119139733	K562	blood:	n/a	chr7:119139713-119139722
30	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
31	CEBPB	chr7:119184919-119185504	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:118895992-118896335	HepG2	liver:	n/a	n/a
33	CEBPB	chr7:118887915-118887985	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr7:118840953-118841173	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr7:119183182-119183277	K562	blood:	n/a	chr7:119183252-119183263
36	CEBPB	chr7:119152429-119152660	HepG2	liver:	n/a	chr7:119152514-119152525
37	CEBPB	chr7:119043069-119043327	IMR90	lung:	n/a	chr7:119043190-119043203 chr7:119043190-119043201 chr7:119043192-119043203 chr7:119043190-119043203
38	CEBPB	chr7:118863979-118864179	H1-hESC	embryonic stem cell:	n/a	chr7:118864117-118864128
39	CEBPB	chr7:119078338-119078628	A549	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
40	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
41	CEBPB	chr7:119078392-119078635	IMR90	lung:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
42	CEBPB	chr7:119078390-119078544	K562	blood:	n/a	chr7:119078478-119078489 chr7:119078476-119078487 chr7:119078476-119078489 chr7:119078478-119078487
43	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
44	CEBPB	chr7:118997471-118997594	K562	blood:	n/a	n/a
45	CEBPB	chr7:119024356-119024693	HepG2	liver:	n/a	chr7:119024519-119024532 chr7:119024520-119024531
46	CEBPB	chr7:119043095-119043321	HepG2	liver:	n/a	chr7:119043190-119043203 chr7:119043190-119043201 chr7:119043192-119043203 chr7:119043190-119043203
47	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
48	CEBPB	chr7:119201365-119201423	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:118921903-118922151	A549	lung:	n/a	n/a
50	CEBPB	chr7:119024394-119024680	A549	lung:	n/a	chr7:119024519-119024532 chr7:119024520-119024531

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119175916-119175966	AG09319	gingival:	n/a
2	chr7:119121235-119121285	GM12878	blood:	n/a
3	chr7:119175916-119175966	NH-A	brain:	n/a
4	chr7:119121235-119121285	HEK293	kidney:	embryo
5	chr7:119175916-119175966	Hepatocyte	liver:	n/a
6	chr7:119121235-119121285	HUVEC	blood vessel:	n/a
7	chr7:119121235-119121285	AG04450	lung:	fetal
8	chr7:119121235-119121285	PrEC	prostate:	n/a
9	chr7:119121235-119121285	NT2-D1	testis:	n/a
10	chr7:119175916-119175966	SAEC	small airway:	n/a
11	chr7:119175916-119175966	Caco-2	colon:	n/a
12	chr7:119175916-119175966	HL-60	blood:	n/a
13	chr7:119175916-119175966	HAEpiC	amniotic membrane:	n/a
14	chr7:119121235-119121285	IMR90	lung:	fetal
15	chr7:119175916-119175966	MCF-7	breast:	n/a
16	chr7:119121235-119121285	Caco-2	colon:	n/a
17	chr7:119121235-119121285	ovcar-3	ovarian:	n/a
18	chr7:119175916-119175966	LNCaP	prostate:	n/a
19	chr7:119121235-119121285	NB4	blood:	n/a
20	chr7:119175916-119175966	HEEpiC	esophagus:	n/a
21	chr7:119121235-119121285	HL-60	blood:	n/a
22	chr7:119121235-119121285	HCPEpiC	choroid plexus:	n/a
23	chr7:119121235-119121285	AG10803	skin:	n/a
24	chr7:119121235-119121285	AG04449	skin:	fetal
25	chr7:119175916-119175966	BE2_C	brain:	n/a
26	chr7:119121235-119121285	NH-A	brain:	n/a
27	chr7:119175916-119175966	PrEC	prostate:	n/a
28	chr7:119175916-119175966	GM19239	blood:	n/a
29	chr7:119121235-119121285	NHBE	bronchial:	n/a
30	chr7:119121235-119121285	MCF-7	breast:	n/a
31	chr7:119175916-119175966	T-47D	breast:	n/a
32	chr7:119175916-119175966	HPAEpiC	pulmonary alveolar:	n/a
33	chr7:119175916-119175966	HCT-116	colon:	n/a
34	chr7:119121235-119121285	HNPCEpiC	eye:	n/a
35	chr7:119121235-119121285	U87	brain:	n/a
36	chr7:119121235-119121285	SAEC	small airway:	n/a
37	chr7:119121235-119121285	ECC-1	luminal epithelium:	n/a
38	chr7:119175916-119175966	HCPEpiC	choroid plexus:	n/a
39	chr7:119121235-119121285	HAEpiC	amniotic membrane:	n/a
40	chr7:119175916-119175966	RPTEC	kidney:	n/a
41	chr7:119175916-119175966	HMEC	breast:	n/a
42	chr7:119175916-119175966	HNPCEpiC	eye:	n/a
43	chr7:119175916-119175966	GM12891	blood:	n/a
44	chr7:119175916-119175966	ECC-1	luminal epithelium:	n/a
45	chr7:119121235-119121285	HepG2	liver:	n/a
46	chr7:119175916-119175966	AG04449	skin:	fetal
47	chr7:119121235-119121285	ProgFib	skin:	n/a
48	chr7:119175916-119175966	HIPEpiC	eye:	n/a
49	chr7:119121235-119121285	RPTEC	kidney:	n/a
50	chr7:119175916-119175966	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:119212184..119216632-chr7:119220970..119225768,5	K562	blood:
2	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
3	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:
4	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
5	chr7:118558392..118559287-chr7:118815693..118816489,5	MCF-7	breast:
6	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
7	chr7:119192825..119195698-chr7:119199166..119201397,2	K562	blood:
8	chr7:119114137..119115777-chr7:119118248..119120055,2	K562	blood:
9	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
10	chr7:118792620..118793489-chr9:140473359..140473903,2	Hela-S3	cervix:
11	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
12	chr7:118782215..118784443-chr7:118786067..118788168,2	K562	blood:
13	chr7:118823416..118825410-chr7:118825629..118827229,2	K562	blood:
14	chr7:119119277..119121222-chr7:119136610..119138824,2	K562	blood:
15	chr7:119212184..119214604-chr7:119220970..119224685,3	K562	blood:
16	chr7:119202572..119205180-chr8:103798970..103800546,2	MCF-7	breast:
17	chr7:119174664..119177243-chr7:119179086..119181541,2	K562	blood:
18	chr7:119119681..119121337-chr7:119126080..119128108,2	K562	blood:
19	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
20	chr7:119092010..119093559-chr7:119096407..119098268,2	K562	blood:
21	chr7:118909733..118910708-chr7:145816212..145816735,2	MCF-7	breast:
22	chr7:118829678..118832309-chr7:118833350..118835537,2	MCF-7	breast:
23	chr7:119212184..119214604-chr7:119220970..119224685,3	K562	blood:
24	chr7:118857357..118859002-chr8:11343082..11345568,2	MCF-7	breast:
25	chr7:119174664..119177243-chr7:119179086..119181541,2	K562	blood:
26	chr7:117992682..117993833-chr7:118815599..118816513,3	MCF-7	breast:
27	chr7:118878113..118880101-chr7:118887192..118890136,2	K562	blood:
28	chr7:119088296..119090701-chr7:119093018..119094825,2	K562	blood:
29	chr7:118917919..118920251-chr7:118925221..118926809,2	K562	blood:
30	chr7:119057102..119059266-chr7:119065046..119067833,2	K562	blood:
31	chr7:119090133..119091662-chr7:119125393..119128092,2	K562	blood:
32	chr7:119211056..119214261-chr7:119214480..119218185,4	K562	blood:
33	chr7:119184831..119187773-chr7:119262380..119264496,2	MCF-7	breast:
34	chr7:118910028..118911067-chr7:119729751..119730686,4	MCF-7	breast:
35	chr7:119211056..119214261-chr7:119214480..119218185,4	K562	blood:
36	chr7:119055228..119059267-chr7:119060829..119064124,3	K562	blood:
37	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
38	chr7:118852197..118855111-chr7:118862886..118865559,2	K562	blood:
39	chr7:119188506..119190356-chr7:119200793..119202933,2	K562	blood:
40	chr6:30580881..30583485-chr7:118868073..118870261,2	MCF-7	breast:
41	chr7:119188506..119190356-chr7:119200793..119202933,2	K562	blood:
42	chr7:118852197..118855111-chr7:118862886..118865559,2	K562	blood:
43	chr7:118997927..118999902-chr7:119000028..119001713,2	K562	blood:
44	chr7:118782215..118784443-chr7:118786067..118788168,2	K562	blood:
45	chr7:118800323..118802977-chr7:118807126..118809160,2	K562	blood:
46	chr7:119171216..119174031-chr7:119180101..119182290,2	K562	blood:
47	chr7:119100295..119103050-chr7:119105149..119106900,2	K562	blood:
48	chr7:117992651..117993374-chr7:118815864..118816654,2	MCF-7	breast:
49	chr7:119090473..119092463-chr7:119095710..119098543,2	MCF-7	breast:
50	chr7:118823416..118825410-chr7:118825629..118827229,2	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
ENSG00000256882	TF binding region
ENSG00000270516	CpG island
ENSG00000263692	CpG island
ENSG00000256882	CpG island
ENSG00000148399	chromatin interactions

Extended variants
information (count: 3317 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:3317 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs386717200	chr7:118744450-118744451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs79053647	chr7:118744452-118744453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569048366	chr7:118744468-118744469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs117701779	chr7:118744478-118744479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78163013	chr7:118744517-118744518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs76608933	chr7:118744518-118744519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554621091	chr7:118744560-118744561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs574607245	chr7:118744610-118744611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148244413	chr7:118744622-118744623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74779820	chr7:118744721-118744722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577068778	chr7:118744771-118744772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs192057185	chr7:118744787-118744788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs546068925	chr7:118744805-118744806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs184656105	chr7:118744811-118744812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568749867	chr7:118744817-118744818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531861784	chr7:118744831-118744832	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141703584	chr7:118744962-118744963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189323234	chr7:118745018-118745019	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529701084	chr7:118745025-118745026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs546748118	chr7:118745063-118745064	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182464263	chr7:118745148-118745149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532389262	chr7:118745172-118745173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs552046669	chr7:118745184-118745185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs527937350	chr7:118745249-118745250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185762336	chr7:118745304-118745305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114607957	chr7:118745366-118745367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547667778	chr7:118745421-118745422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146243925	chr7:118745424-118745425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138101286	chr7:118745449-118745450	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533928206	chr7:118745470-118745471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs371653629	chr7:118745518-118745519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78405936	chr7:118745543-118745544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117993469	chr7:118745596-118745597	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189487304	chr7:118745651-118745652	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs77626724	chr7:118745652-118745653	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs150820513	chr7:118745674-118745675	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs113547776	chr7:118745685-118745686	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs71684014	chr7:118745686-118745687	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs113741203	chr7:118745689-118745690	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs542194561	chr7:118745707-118745708	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs181034725	chr7:118745708-118745709	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574534274	chr7:118745842-118745843	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs540225861	chr7:118745855-118745856	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs560298849	chr7:118745920-118745921	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532064636	chr7:118745921-118745922	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs116473438	chr7:118745994-118745995	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs139267327	chr7:118746064-118746065	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs76428127	chr7:118746069-118746070	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs150008190	chr7:118746112-118746113	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs144306062	chr7:118746117-118746118	Enhancers Weak transcription Active TSS	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:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:118740600-118747600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:118741000-118745600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:118742000-118744800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr7:118743200-118744800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr7:118743600-118744600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:118743600-118744800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr7:118743600-118745600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr7:118743800-118745600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr7:118743800-118745600	Weak transcription	Fetal Lung	lung
10	chr7:118743800-118745800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:118743800-118747200	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:118744000-118745400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:118744200-118745000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr7:118744600-118744800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:118744800-118745000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr7:118744800-118745000	Enhancers	H1 Cell Line	embryonic stem cell
17	chr7:118744800-118745200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:118744800-118745200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr7:118745000-118745400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr7:118745200-118745800	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:118745200-118746200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr7:118745400-118746200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr7:118745600-118745800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr7:118745600-118745800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:118745600-118746000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr7:118745600-118746000	Enhancers	Fetal Lung	lung
27	chr7:118745600-118746200	Active TSS	Adipose Nuclei	Adipose
28	chr7:118745800-118746000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr7:118745800-118746600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:118747200-118747600	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr7:118747600-118747800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr7:118750000-118750200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr7:118750200-118750400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr7:118758000-118758200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr7:118758000-118758400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr7:118758000-118758400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:118758000-118759400	Enhancers	Fetal Kidney	kidney
38	chr7:118758400-118765800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:118763400-118764000	Enhancers	Pancreas	Pancrea
40	chr7:118765200-118767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr7:118765600-118766800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr7:118765600-118767000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr7:118765800-118766800	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr7:118765800-118766800	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr7:118765800-118767000	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:118765800-118767000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr7:118766000-118767000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:118773200-118774400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr7:118790600-118792800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr7:118808200-118808800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived

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