Variant report

Variant	nsv1015363
Chromosome Location	chr8:89707267-90158090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1944)
CpG islands
(count:427)
Chromatin interactive
region (count:72)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1944 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:89799915-89800095	K562	blood:	n/a	n/a
2	ATF3	chr8:89727774-89728508	HCT-116	colon:	n/a	n/a
3	ATF3	chr8:89952106-89952686	HCT-116	colon:	n/a	n/a
4	ATF3	chr8:89727790-89728557	HCT-116	colon:	n/a	n/a
5	BACH1	chr8:89792855-89792956	K562	blood:	n/a	n/a
6	BACH1	chr8:89895953-89896258	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr8:89851926-89852130	GM12878	blood:	n/a	n/a
8	BATF	chr8:89970029-89970430	GM12878	blood:	n/a	chr8:89970221-89970232
9	BATF	chr8:89851958-89852146	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:89761792-89761832	K562	blood:	n/a	n/a
11	BRCA1	chr8:89994073-89994536	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr8:90112445-90113476	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr8:89971863-89972933	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr8:90077135-90077137	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr8:89952071-89952826	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr8:89969982-89970622	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr8:90111164-90111268	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr8:89727631-89728784	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr8:89976610-89976924	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr8:89960881-89961214	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:89919766-89920287	HCT-116	colon:	n/a	n/a
22	CBX3	chr8:89919781-89920208	HCT-116	colon:	n/a	n/a
23	CBX3	chr8:89969284-89970570	HCT-116	colon:	n/a	n/a
24	CBX3	chr8:90083855-90084736	HCT-116	colon:	n/a	n/a
25	CBX3	chr8:90055621-90056061	HCT-116	colon:	n/a	n/a
26	CBX3	chr8:89952119-89952678	HCT-116	colon:	n/a	n/a
27	CBX3	chr8:89735838-89736363	HCT-116	colon:	n/a	n/a
28	CBX3	chr8:90112663-90113583	HCT-116	colon:	n/a	n/a
29	CBX3	chr8:89735805-89736242	HCT-116	colon:	n/a	n/a
30	CBX3	chr8:89951975-89952816	HCT-116	colon:	n/a	n/a
31	CBX3	chr8:90053181-90053800	HCT-116	colon:	n/a	n/a
32	CBX3	chr8:89727607-89728675	HCT-116	colon:	n/a	n/a
33	CBX3	chr8:90055683-90055952	HCT-116	colon:	n/a	n/a
34	CBX3	chr8:90053094-90053810	HCT-116	colon:	n/a	n/a
35	CBX3	chr8:90122758-90123680	HCT-116	colon:	n/a	n/a
36	CBX3	chr8:89727777-89728562	HCT-116	colon:	n/a	n/a
37	CBX3	chr8:90112878-90113581	HCT-116	colon:	n/a	n/a
38	CCNT2	chr8:90110746-90110939	K562	blood:	n/a	n/a
39	CCNT2	chr8:90089048-90089139	K562	blood:	n/a	n/a
40	CEBPB	chr8:89951893-89952854	HCT-116	colon:	n/a	n/a
41	CEBPB	chr8:90129374-90129589	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:90006034-90006169	A549	lung:	n/a	n/a
43	CEBPB	chr8:89727749-89728333	A549	lung:	n/a	n/a
44	CEBPB	chr8:89884768-89884942	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:89925100-89925558	MCF-7	breast:	n/a	chr8:89925321-89925332
46	CEBPB	chr8:89940706-89940906	A549	lung:	n/a	n/a
47	CEBPB	chr8:89895622-89896257	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr8:89727679-89728671	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr8:90112862-90113517	HCT-116	colon:	n/a	chr8:90113189-90113202
50	CEBPB	chr8:90112590-90113519	Hela-S3	cervix:	n/a	chr8:90113189-90113202

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:89747827-89747877	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:89969235-89969285	NH-A	brain:	n/a
3	chr8:89718417-89718467	HRCEpiC	kidney:	n/a
4	chr8:89718417-89718467	HUVEC	blood vessel:	n/a
5	chr8:90132979-90133029	U87	brain:	n/a
6	chr8:89969235-89969285	GM12891	blood:	n/a
7	chr8:89747827-89747877	PFSK-1	brain:	n/a
8	chr8:89747827-89747877	AG09309	skin:	n/a
9	chr8:89777219-89777269	HRCEpiC	kidney:	n/a
10	chr8:89747827-89747877	Hela-S3	cervix:	n/a
11	chr8:89856205-89856255	NH-A	brain:	n/a
12	chr8:89969235-89969285	AG04450	lung:	fetal
13	chr8:89969235-89969285	HL-60	blood:	n/a
14	chr8:89969235-89969285	AG09319	gingival:	n/a
15	chr8:89969235-89969285	AG09309	skin:	n/a
16	chr8:90132979-90133029	BE2_C	brain:	n/a
17	chr8:89888638-89888688	PANC-1	pancreas:	n/a
18	chr8:89747827-89747877	HUVEC	blood vessel:	n/a
19	chr8:89777219-89777269	BJ	skin:	n/a
20	chr8:89747827-89747877	GM06990	blood:	n/a
21	chr8:89888638-89888688	Jurkat	blood:	n/a
22	chr8:90132979-90133029	HCM	heart:	n/a
23	chr8:90132979-90133029	NT2-D1	testis:	n/a
24	chr8:89777219-89777269	PrEC	prostate:	n/a
25	chr8:89969235-89969285	GM12892	blood:	n/a
26	chr8:90132979-90133029	HEK293	kidney:	embryo
27	chr8:89888638-89888688	HEEpiC	esophagus:	n/a
28	chr8:89856205-89856255	HL-60	blood:	n/a
29	chr8:89969235-89969285	LNCaP	prostate:	n/a
30	chr8:89888638-89888688	SK-N-MC	brain:	n/a
31	chr8:90132979-90133029	GM12892	blood:	n/a
32	chr8:89777219-89777269	HAEpiC	amniotic membrane:	n/a
33	chr8:89718417-89718467	K562	blood:	n/a
34	chr8:89888638-89888688	AG04450	lung:	fetal
35	chr8:89718417-89718467	NB4	blood:	n/a
36	chr8:89888638-89888688	HAEpiC	amniotic membrane:	n/a
37	chr8:89747827-89747877	HEK293	kidney:	embryo
38	chr8:89777219-89777269	NHDF-neo	bronchial:	n/a
39	chr8:89969235-89969285	SAEC	small airway:	n/a
40	chr8:89777219-89777269	U87	brain:	n/a
41	chr8:89888638-89888688	HCM	heart:	n/a
42	chr8:89888638-89888688	HL-60	blood:	n/a
43	chr8:89718417-89718467	HEK293	kidney:	embryo
44	chr8:90132979-90133029	HCF	heart:	n/a
45	chr8:89888638-89888688	HCPEpiC	choroid plexus:	n/a
46	chr8:90132979-90133029	A549	lung:	n/a
47	chr8:89747827-89747877	RPTEC	kidney:	n/a
48	chr8:89718417-89718467	Hela-S3	cervix:	n/a
49	chr8:89856205-89856255	GM06990	blood:	n/a
50	chr8:89856205-89856255	GM12891	blood:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:89725198..89726864-chr8:89729514..89731095,2	MCF-7	breast:
2	chr8:89981805..89984539-chr8:89992447..89994087,2	MCF-7	breast:
3	chr8:89848601..89851264-chr8:89852497..89854514,2	MCF-7	breast:
4	chr8:89690069..89691649-chr8:89726011..89728542,2	MCF-7	breast:
5	chr8:89993652..89996623-chr8:90001684..90003388,2	MCF-7	breast:
6	chr8:89794068..89795764-chr8:89807097..89809455,2	MCF-7	breast:
7	chr8:89877780..89878499-chrX:117700612..117701483,2	MCF-7	breast:
8	chr8:89739274..89741263-chr8:89742331..89745180,2	K562	blood:
9	chr8:89716285..89719319-chr8:89720018..89723186,3	MCF-7	breast:
10	chr8:89304192..89305173-chr8:89823627..89824192,2	MCF-7	breast:
11	chr8:89725334..89726635-chr8:89823867..89824656,3	MCF-7	breast:
12	chr8:89795626..89797821-chr8:89798441..89801193,3	MCF-7	breast:
13	chr8:89725198..89726864-chr8:89729514..89731095,2	MCF-7	breast:
14	chr8:89713917..89716858-chr8:89717587..89721325,3	K562	blood:
15	chr8:89716285..89719319-chr8:89720018..89723186,3	MCF-7	breast:
16	chr21:47742904..47745243-chr8:89801334..89803902,2	MCF-7	breast:
17	chr8:89721490..89723475-chr8:89723913..89725684,2	MCF-7	breast:
18	chr8:89993652..89996623-chr8:90001684..90003388,2	MCF-7	breast:
19	chr8:90014072..90014862-chr8:111171720..111172332,2	MCF-7	breast:
20	chr8:89724996..89725850-chr8:89855566..89856466,2	MCF-7	breast:
21	chr8:90092575..90095200-chr8:90099585..90102136,2	MCF-7	breast:
22	chr8:90092575..90095200-chr8:90099585..90102136,2	MCF-7	breast:
23	chr8:89809461..89810989-chr8:89814329..89816042,2	K562	blood:
24	chr8:89724996..89725850-chr8:89855566..89856466,2	MCF-7	breast:
25	chr8:90120174..90121731-chr8:90128653..90130886,2	MCF-7	breast:
26	chr8:89752103..89756050-chr8:89761305..89763594,3	K562	blood:
27	chr8:89713917..89716858-chr8:89717587..89721325,3	K562	blood:
28	chr8:90010838..90012467-chr8:90027284..90029768,2	MCF-7	breast:
29	chr5:134900665..134901406-chr8:90016865..90017446,2	MCF-7	breast:
30	chr8:89983917..89985937-chr8:89988632..89991497,2	MCF-7	breast:
31	chr8:89340717..89341497-chr8:89823523..89824135,2	MCF-7	breast:
32	chr8:89981805..89984539-chr8:89992447..89994087,2	MCF-7	breast:
33	chr8:89721490..89723475-chr8:89723913..89725684,2	MCF-7	breast:
34	chr8:89795626..89797821-chr8:89798441..89801193,3	MCF-7	breast:
35	chr8:89892387..89896738-chr8:89897046..89901552,4	MCF-7	breast:
36	chr8:89826530..89828949-chr8:89832664..89834256,2	MCF-7	breast:
37	chr8:90067439..90070191-chr8:90075999..90077616,2	MCF-7	breast:
38	chr8:89927938..89930216-chr8:89935264..89937935,2	K562	blood:
39	chr17:66790796..66791327-chr8:90031920..90032588,2	MCF-7	breast:
40	chr8:90074965..90076573-chr8:102340913..102342555,2	MCF-7	breast:
41	chr8:89566591..89567525-chr8:89823590..89824198,2	MCF-7	breast:
42	chr8:89896479..89897988-chr8:89898456..89900553,2	MCF-7	breast:
43	chr8:89983917..89985937-chr8:89988632..89991497,2	MCF-7	breast:
44	chr8:90010838..90012467-chr8:90027284..90029768,2	MCF-7	breast:
45	chr8:90120174..90121731-chr8:90128653..90130886,2	MCF-7	breast:
46	chr8:89794068..89795764-chr8:89807097..89809455,2	MCF-7	breast:
47	chr8:89896479..89897988-chr8:89898456..89900553,2	MCF-7	breast:
48	chr8:89725334..89726635-chr8:89823867..89824656,3	MCF-7	breast:
49	chr8:89809461..89810989-chr8:89814329..89816042,2	K562	blood:
50	chr8:89739274..89741263-chr8:89742331..89745180,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNBD1-4	chr8:89748095-89749363	NONHSAT127604
2	lnc-MMP16-4	chr8:89820547-89821137	ENSG00000271156.1
3	lnc-CNBD1-4	chr8:89712520-89712578	ENSG00000253553.1
4	lnc-CNBD1-4	chr8:89721559-89721956	ENSG00000253553.1
5	lnc-CNBD1-4	chr8:89747954-89749363	ENSG00000253553.1
6	lnc-CNBD1-4	chr8:89712521-89712578	ENSG00000253553.1
7	lnc-CNBD1-4	chr8:89721559-89721920	ENSG00000253553.1
8	lnc-CNBD1-4	chr8:89721559-89721769	ENSG00000253553.1

No data

Variant related genes	Relation type
ENSG00000271156	TF binding region
ENSG00000253553	TF binding region
ENSG00000271156	CpG island
ENSG00000253553	CpG island
ENSG00000160298	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000271156	chromatin interactions
ENSG00000160299	chromatin interactions

Extended variants
information (count: 7987 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:7987 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72660635	chr8:89707560-89707561	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs544708258	chr8:89707604-89707605	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs377618219	chr8:89707647-89707648	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559765994	chr8:89707665-89707666	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs557204019	chr8:89707666-89707667	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs141787979	chr8:89707670-89707671	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs575465437	chr8:89707679-89707680	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs546102218	chr8:89707690-89707691	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs192584487	chr8:89707703-89707704	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs550219077	chr8:89708067-89708068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183499392	chr8:89708081-89708082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs146238066	chr8:89708112-89708113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189205163	chr8:89708124-89708125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs567085740	chr8:89708142-89708143	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs534503604	chr8:89708143-89708144	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs529220605	chr8:89708161-89708162	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs555519215	chr8:89708170-89708171	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs114636623	chr8:89708181-89708182	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs371029629	chr8:89708198-89708199	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs528850345	chr8:89708216-89708217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534017403	chr8:89708233-89708234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs181095602	chr8:89708276-89708277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575526727	chr8:89708304-89708305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184962087	chr8:89708317-89708318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190201933	chr8:89708332-89708333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs201356741	chr8:89708340-89708341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139230590	chr8:89708342-89708343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376533342	chr8:89708345-89708346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs201614944	chr8:89708384-89708385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530038538	chr8:89708385-89708386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs144052130	chr8:89708402-89708403	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75249176	chr8:89708405-89708406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs150947811	chr8:89708433-89708434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75202154	chr8:89708440-89708441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548681407	chr8:89708486-89708487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562209177	chr8:89708488-89708489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562400348	chr8:89708492-89708493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs118046854	chr8:89708534-89708535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560728805	chr8:89708561-89708562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527986953	chr8:89708566-89708567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549652240	chr8:89708568-89708569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181688847	chr8:89708595-89708596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377382561	chr8:89708618-89708619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139466768	chr8:89708667-89708668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571680757	chr8:89708668-89708669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78058827	chr8:89708687-89708688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557706704	chr8:89708706-89708707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs572949614	chr8:89708734-89708735	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs377155100	chr8:89708763-89708764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs115306204	chr8:89708774-89708775	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:396 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:89708000-89708600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:89708400-89709600	Enhancers	NH-A	brain
3	chr8:89708400-89709800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr8:89708400-89709800	Enhancers	Adipose Nuclei	Adipose
5	chr8:89708600-89709000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:89708600-89710000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:89708600-89710200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr8:89708600-89710200	Enhancers	HUVEC	blood vessel
9	chr8:89709000-89709800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr8:89709800-89710000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr8:89718000-89718800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:89718000-89719000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:89718000-89719000	Enhancers	Osteobl	bone
14	chr8:89718000-89719800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:89718000-89720000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr8:89718200-89718600	Enhancers	NH-A	brain
17	chr8:89718200-89718800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:89718200-89718800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr8:89718200-89718800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr8:89718200-89719000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr8:89718200-89719000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:89718400-89718800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr8:89718400-89718800	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr8:89718400-89719000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr8:89718400-89719000	Enhancers	Adipose Nuclei	Adipose
26	chr8:89718800-89727600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr8:89719800-89725000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr8:89720000-89725000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:89725000-89725600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:89725000-89728800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:89725200-89726000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:89725200-89728800	Enhancers	Hela-S3	cervix
33	chr8:89725200-89728800	Enhancers	HUVEC	blood vessel
34	chr8:89725400-89725600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr8:89725600-89726000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr8:89725600-89726200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr8:89725600-89726400	Enhancers	Adipose Nuclei	Adipose
38	chr8:89725600-89728800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr8:89725800-89728200	Enhancers	NHDF-Ad	bronchial
40	chr8:89725800-89728600	Enhancers	Osteobl	bone
41	chr8:89726000-89726200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr8:89726000-89728600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr8:89726000-89728800	Enhancers	NH-A	brain
44	chr8:89726200-89726400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:89726200-89726400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr8:89726200-89727200	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr8:89726200-89727200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr8:89726400-89726600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:89726400-89726600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr8:89726400-89727800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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