Variant report

Variant	nsv870775
Chromosome Location	chr1:93481640-93543119
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:791)
CpG islands
(count:61)
Chromatin interactive
region (count:43)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:93527760-93528006	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:93499336-93499582	K562	blood:	n/a	n/a
3	ARID3A	chr1:93527686-93528083	K562	blood:	n/a	n/a
4	ARID3A	chr1:93507823-93508266	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:93498663-93499122	K562	blood:	n/a	n/a
6	ARID3A	chr1:93491188-93491454	K562	blood:	n/a	n/a
7	ATF1	chr1:93521045-93521187	K562	blood:	n/a	n/a
8	ATF1	chr1:93491196-93491529	K562	blood:	n/a	n/a
9	ATF1	chr1:93499357-93499646	K562	blood:	n/a	n/a
10	ATF1	chr1:93498514-93499041	K562	blood:	n/a	n/a
11	ATF2	chr1:93507858-93508405	GM12878	blood:	n/a	n/a
12	BACH1	chr1:93491254-93491449	K562	blood:	n/a	n/a
13	BACH1	chr1:93498610-93498936	K562	blood:	n/a	n/a
14	BACH1	chr1:93491328-93491355	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr1:93504202-93504490	GM12878	blood:	n/a	n/a
16	BATF	chr1:93498548-93498905	GM12878	blood:	n/a	chr1:93498749-93498760
17	BATF	chr1:93498592-93498888	GM12878	blood:	n/a	chr1:93498749-93498760
18	BHLHE40	chr1:93481848-93482210	HepG2	liver:	n/a	n/a
19	BHLHE40	chr1:93491068-93491491	K562	blood:	n/a	n/a
20	BHLHE40	chr1:93499202-93499757	GM12878	blood:	n/a	n/a
21	BHLHE40	chr1:93481904-93482182	K562	blood:	n/a	n/a
22	BHLHE40	chr1:93499348-93499736	K562	blood:	n/a	n/a
23	BHLHE40	chr1:93527861-93528165	K562	blood:	n/a	n/a
24	CBX3	chr1:93517382-93517903	K562	blood:	n/a	n/a
25	CBX3	chr1:93536510-93536875	K562	blood:	n/a	n/a
26	CCNT2	chr1:93498606-93499547	K562	blood:	n/a	chr1:93498659-93498668
27	CEBPB	chr1:93541804-93542170	K562	blood:	n/a	chr1:93541985-93541996
28	CEBPB	chr1:93499289-93499863	K562	blood:	n/a	n/a
29	CEBPB	chr1:93481872-93482188	HepG2	liver:	n/a	n/a
30	CEBPB	chr1:93541807-93542167	HepG2	liver:	n/a	chr1:93541985-93541996
31	CEBPB	chr1:93521904-93522471	H1-hESC	embryonic stem cell:	n/a	chr1:93522154-93522167 chr1:93522342-93522353
32	CEBPB	chr1:93483072-93483222	A549	lung:	n/a	n/a
33	CEBPB	chr1:93541812-93542154	A549	lung:	n/a	chr1:93541985-93541996
34	CEBPB	chr1:93537685-93537791	K562	blood:	n/a	n/a
35	CEBPB	chr1:93541821-93542166	IMR90	lung:	n/a	chr1:93541985-93541996
36	CEBPB	chr1:93541851-93542110	K562	blood:	n/a	chr1:93541985-93541996
37	CEBPB	chr1:93481920-93482199	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr1:93512050-93512314	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:93481868-93482205	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:93522197-93522511	K562	blood:	n/a	chr1:93522342-93522353
41	CEBPB	chr1:93483074-93483280	K562	blood:	n/a	n/a
42	CEBPB	chr1:93517511-93517851	K562	blood:	n/a	n/a
43	CEBPB	chr1:93512126-93512219	A549	lung:	n/a	n/a
44	CEBPB	chr1:93541763-93542150	K562	blood:	n/a	chr1:93541985-93541996
45	CEBPB	chr1:93522190-93522512	IMR90	lung:	n/a	chr1:93522342-93522353
46	CEBPB	chr1:93495816-93496028	HepG2	liver:	n/a	chr1:93495973-93495985
47	CEBPB	chr1:93491250-93491450	K562	blood:	n/a	n/a
48	CEBPB	chr1:93522287-93522532	A549	lung:	n/a	chr1:93522342-93522353
49	CEBPB	chr1:93522209-93522507	HepG2	liver:	n/a	chr1:93522342-93522353
50	CEBPB	chr1:93541824-93542128	Hela-S3	cervix:	n/a	chr1:93541985-93541996

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:93542483-93542533	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:93542483-93542533	PANC-1	pancreas:	n/a
3	chr1:93542483-93542533	GM06990	blood:	n/a
4	chr1:93542483-93542533	PFSK-1	brain:	n/a
5	chr1:93542483-93542533	SAEC	small airway:	n/a
6	chr1:93542483-93542533	NB4	blood:	n/a
7	chr1:93542483-93542533	Hela-S3	cervix:	n/a
8	chr1:93542483-93542533	ovcar-3	ovarian:	n/a
9	chr1:93542483-93542533	HRE	kidney:	n/a
10	chr1:93542483-93542533	BE2_C	brain:	n/a
11	chr1:93542483-93542533	AG09319	gingival:	n/a
12	chr1:93542483-93542533	HAEpiC	amniotic membrane:	n/a
13	chr1:93542483-93542533	Caco-2	colon:	n/a
14	chr1:93542483-93542533	HRPEpiC	eye:	n/a
15	chr1:93542483-93542533	GM12891	blood:	n/a
16	chr1:93542483-93542533	ProgFib	skin:	n/a
17	chr1:93542483-93542533	GM12878	blood:	n/a
18	chr1:93542483-93542533	MCF10A-Er-Src	breast:	n/a
19	chr1:93542483-93542533	HL-60	blood:	n/a
20	chr1:93542483-93542533	NHBE	bronchial:	n/a
21	chr1:93542483-93542533	Jurkat	blood:	n/a
22	chr1:93542483-93542533	AG04450	lung:	fetal
23	chr1:93542483-93542533	HEK293	kidney:	embryo
24	chr1:93542483-93542533	SK-N-MC	brain:	n/a
25	chr1:93542483-93542533	AG04449	skin:	fetal
26	chr1:93542483-93542533	NT2-D1	testis:	n/a
27	chr1:93542483-93542533	SKMC	muscle:	n/a
28	chr1:93542483-93542533	Hepatocyte	liver:	n/a
29	chr1:93542483-93542533	K562	blood:	n/a
30	chr1:93542483-93542533	ECC-1	luminal epithelium:	n/a
31	chr1:93542483-93542533	AG10803	skin:	n/a
32	chr1:93542483-93542533	GM12892	blood:	n/a
33	chr1:93542483-93542533	NH-A	brain:	n/a
34	chr1:93542483-93542533	HRCEpiC	kidney:	n/a
35	chr1:93542483-93542533	A549	lung:	n/a
36	chr1:93542483-93542533	HCF	heart:	n/a
37	chr1:93542483-93542533	AoSMC	blood vessel:	n/a
38	chr1:93542483-93542533	HCT-116	colon:	n/a
39	chr1:93542483-93542533	MCF-7	breast:	n/a
40	chr1:93542483-93542533	HepG2	liver:	n/a
41	chr1:93542483-93542533	AG09309	skin:	n/a
42	chr1:93542483-93542533	NHDF-neo	bronchial:	n/a
43	chr1:93542483-93542533	GM19239	blood:	n/a
44	chr1:93542483-93542533	PrEC	prostate:	n/a
45	chr1:93542483-93542533	HIPEpiC	eye:	n/a
46	chr1:93542483-93542533	T-47D	breast:	n/a
47	chr1:93542483-93542533	HNPCEpiC	eye:	n/a
48	chr1:93542483-93542533	U87	brain:	n/a
49	chr1:93542483-93542533	HUVEC	blood vessel:	n/a
50	chr1:93542483-93542533	HEEpiC	esophagus:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:93324135..93325204-chr1:93527740..93528408,3	MCF-7	breast:
2	chr1:93458381..93461372-chr1:93479810..93482559,2	MCF-7	breast:
3	chr1:93433953..93434929-chr1:93527495..93528205,3	MCF-7	breast:
4	chr1:93487223..93489014-chr1:93543210..93544783,2	K562	blood:
5	chr1:93485980..93488495-chr1:93489742..93491453,2	K562	blood:
6	chr1:93486832..93487777-chr1:93527684..93528337,5	MCF-7	breast:
7	chr1:93296777..93298441-chr1:93527629..93529476,2	K562	blood:
8	chr1:93324004..93325373-chr1:93486850..93487700,5	K562	blood:
9	chr1:93324231..93325146-chr1:93527492..93528386,4	MCF-7	breast:
10	chr1:93493844..93495450-chr1:93525930..93527938,2	K562	blood:
11	chr1:93296273..93298052-chr1:93508524..93510484,2	MCF-7	breast:
12	chr1:93489723..93491874-chr1:93538099..93542009,4	K562	blood:
13	chr1:93485808..93487588-chr1:93526047..93528280,2	MCF-7	breast:
14	chr1:93542830..93545559-chr20:45984443..45987122,2	MCF-7	breast:
15	chr1:93538010..93540261-chr1:93544138..93545672,2	MCF-7	breast:
16	chr1:93516477..93519592-chr1:93550501..93553219,3	K562	blood:
17	chr1:93540301..93542414-chr1:93543108..93545399,2	K562	blood:
18	chr1:93314734..93317720-chr1:93541200..93543967,2	K562	blood:
19	chr1:93493844..93495450-chr1:93525930..93527938,2	K562	blood:
20	chr1:93507541..93509653-chr1:93511685..93513516,2	K562	blood:
21	chr1:93331676..93334164-chr1:93480401..93483353,2	K562	blood:
22	chr1:93509911..93511980-chr1:93544557..93546236,2	K562	blood:
23	chr1:93477075..93479957-chr1:93501163..93503966,2	K562	blood:
24	chr1:93497881..93500258-chr1:93541751..93544329,2	K562	blood:
25	chr1:93486773..93487911-chr1:93527469..93528398,9	K562	blood:
26	chr1:93485808..93487588-chr1:93526047..93528280,2	MCF-7	breast:
27	chr1:93540301..93542286-chr1:93542367..93545700,5	K562	blood:
28	chr1:93308545..93311072-chr1:93527284..93530224,2	K562	blood:
29	chr1:93323848..93325079-chr1:93527454..93528796,12	K562	blood:
30	chr1:93486832..93487777-chr1:93527684..93528337,5	MCF-7	breast:
31	chr1:93543004..93547588-chr1:93644888..93649088,6	K562	blood:
32	chr1:93486773..93487911-chr1:93527469..93528398,9	K562	blood:
33	chr1:93535454..93537816-chr1:93542271..93545501,3	K562	blood:
34	chr1:93497881..93500258-chr1:93541751..93544329,2	K562	blood:
35	chr1:93537729..93540718-chr1:93542326..93545559,3	MCF-7	breast:
36	chr1:93296076..93299049-chr1:93541677..93546567,5	K562	blood:
37	chr1:93543004..93547095-chr1:93643826..93649088,10	K562	blood:
38	chr1:93518072..93519593-chr1:93543100..93545883,2	K562	blood:
39	chr1:93486837..93487799-chr1:94374760..94375360,2	K562	blood:
40	chr1:93296941..93299112-chr1:93527214..93529476,2	K562	blood:
41	chr1:93485980..93488495-chr1:93489742..93491453,2	K562	blood:
42	chr1:93507541..93509653-chr1:93511685..93513516,2	K562	blood:
43	chr1:93510480..93512269-chr1:93543965..93546057,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTF2-2	chr1:93491809-93492099	NONHSAT004479

No data

Variant related genes	Relation type
RN7SKP123	TF binding region
ENSG00000251837	TF binding region
MTF2	TF binding region
RN7SKP123	CpG island
ENSG00000251837	CpG island
MTF2	CpG island
ENSG00000122483	chromatin interactions
ENSG00000143033	chromatin interactions
ENSG00000122406	chromatin interactions
ENSG00000023909	chromatin interactions
ENSG00000117500	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000222664	chromatin interactions

Extended variants
information (count: 1948 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1948 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10493865	chr1:93481640-93481641	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs5776166	chr1:93481681-93481682	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs571005881	chr1:93481696-93481697	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs75372693	chr1:93481702-93481703	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs150612204	chr1:93481731-93481732	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs553240931	chr1:93481735-93481736	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs521360	chr1:93481736-93481737	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs138681323	chr1:93481742-93481743	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs556976312	chr1:93481747-93481748	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs149377838	chr1:93481831-93481832	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs596817	chr1:93481832-93481833	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs563734302	chr1:93481856-93481857	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs17131685	chr1:93481859-93481860	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs146322299	chr1:93481862-93481863	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561418690	chr1:93481882-93481883	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538403172	chr1:93481884-93481885	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370770089	chr1:93481889-93481890	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs115442490	chr1:93481938-93481939	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558611087	chr1:93481952-93481953	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570294508	chr1:93481956-93481957	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184398287	chr1:93481980-93481981	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs531234218	chr1:93481981-93481982	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574831177	chr1:93481982-93481983	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189272121	chr1:93482010-93482011	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs374970998	chr1:93482044-93482045	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs595783	chr1:93482086-93482087	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs193223175	chr1:93482091-93482092	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs571981347	chr1:93482110-93482111	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs139724205	chr1:93482146-93482147	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs557108871	chr1:93482164-93482165	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs575495701	chr1:93482175-93482176	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs539696435	chr1:93482179-93482180	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs116311709	chr1:93482191-93482192	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs572527535	chr1:93482233-93482234	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs185613379	chr1:93482282-93482283	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs561457939	chr1:93482343-93482344	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs142936346	chr1:93482345-93482346	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs146167415	chr1:93482351-93482352	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs563886114	chr1:93482360-93482361	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs594408	chr1:93482365-93482366	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs552922087	chr1:93482493-93482494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs564738366	chr1:93482498-93482499	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528495451	chr1:93482506-93482507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544450397	chr1:93482550-93482551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188909681	chr1:93482556-93482557	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs568499811	chr1:93482572-93482573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79161476	chr1:93482579-93482580	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115684765	chr1:93482603-93482604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs4342861	chr1:93482687-93482688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569017435	chr1:93482785-93482786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	22429812	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	16397240	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21922591	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Prostate cancer	19156837	CNVD
Autism	17483303	CNVD
Malignant melanoma	17260012	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93474200-93490600	Weak transcription	K562	blood
2	chr1:93478200-93482600	Enhancers	Fetal Muscle Leg	muscle
3	chr1:93478800-93482400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:93478800-93482400	Enhancers	HSMMtube	muscle
5	chr1:93479000-93482200	Enhancers	HSMM	muscle
6	chr1:93479600-93482200	Enhancers	HUVEC	blood vessel
7	chr1:93479800-93481800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:93480000-93481800	Weak transcription	HepG2	liver
9	chr1:93480400-93491000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr1:93480800-93481800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:93480800-93481800	Weak transcription	Psoas Muscle	Psoas
12	chr1:93480800-93482000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:93480800-93482000	Enhancers	Small Intestine	intestine
14	chr1:93480800-93482400	Enhancers	NHDF-Ad	bronchial
15	chr1:93481000-93482000	Enhancers	Fetal Heart	heart
16	chr1:93481000-93482200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr1:93481000-93482400	Enhancers	Hela-S3	cervix
18	chr1:93481200-93482000	Enhancers	NHEK	skin
19	chr1:93481200-93482400	Enhancers	Adipose Nuclei	Adipose
20	chr1:93481400-93481800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:93481400-93481800	Flanking Active TSS	Osteobl	bone
22	chr1:93481400-93482000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
23	chr1:93481400-93482000	Flanking Active TSS	A549	lung
24	chr1:93481400-93482200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:93481400-93482200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr1:93481400-93482200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr1:93481400-93482200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:93481400-93482200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr1:93481400-93482200	Enhancers	Colon Smooth Muscle	Colon
30	chr1:93481400-93482200	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr1:93481400-93482200	Enhancers	Rectal Smooth Muscle	rectum
32	chr1:93481400-93482200	Enhancers	NH-A	brain
33	chr1:93481400-93482400	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr1:93481400-93482400	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:93481400-93482400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:93481400-93482400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr1:93481400-93482400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:93481400-93482400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr1:93481600-93481800	Flanking Active TSS	NHLF	lung
40	chr1:93481600-93482000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
41	chr1:93481600-93482200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr1:93481600-93482400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr1:93481600-93482400	Enhancers	Liver	Liver
44	chr1:93481600-93482600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr1:93481800-93482000	Flanking Active TSS	HepG2	liver
46	chr1:93481800-93482200	Enhancers	H1 Cell Line	embryonic stem cell
47	chr1:93481800-93482200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr1:93481800-93482200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr1:93481800-93482200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:93481800-93482200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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