Variant report

Variant	esv3312255
Chromosome Location	chr15:41098714-41100320
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:524)
CpG islands
(count:733)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:41099702-41099968	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:41099675-41099846	K562	blood:	n/a	n/a
3	ATF1	chr15:41099553-41100200	K562	blood:	n/a	n/a
4	ATF2	chr15:41099239-41099937	GM12878	blood:	n/a	n/a
5	ATF2	chr15:41099959-41100403	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr15:41099464-41100368	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr15:41099196-41099971	K562	blood:	n/a	n/a
8	ATF3	chr15:41099594-41099921	HepG2	liver:	n/a	n/a
9	BACH1	chr15:41099800-41100048	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr15:41099037-41100223	GM12878	blood:	n/a	n/a
11	BCLAF1	chr15:41099178-41100058	GM12878	blood:	n/a	n/a
12	BHLHE40	chr15:41099006-41100182	K562	blood:	n/a	n/a
13	BHLHE40	chr15:41099168-41100222	GM12878	blood:	n/a	n/a
14	BRCA1	chr15:41099046-41100314	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr15:41099382-41099659	HepG2	liver:	n/a	n/a
16	BRCA1	chr15:41099231-41099642	GM12878	blood:	n/a	n/a
17	CBX3	chr15:41098799-41100368	K562	blood:	n/a	n/a
18	CCNT2	chr15:41099196-41100058	K562	blood:	n/a	n/a
19	CEBPB	chr15:41099039-41099761	GM12878	blood:	n/a	n/a
20	CEBPB	chr15:41100279-41100502	K562	blood:	n/a	n/a
21	CEBPD	chr15:41099754-41100137	HepG2	liver:	n/a	n/a
22	CHD1	chr15:41099188-41099678	GM12878	blood:	n/a	n/a
23	CHD1	chr15:41100149-41100337	GM12878	blood:	n/a	n/a
24	CHD2	chr15:41099520-41100250	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr15:41099405-41100196	K562	blood:	n/a	n/a
26	CHD2	chr15:41098991-41100084	GM12878	blood:	n/a	n/a
27	CHD2	chr15:41099119-41100195	Hela-S3	cervix:	n/a	n/a
28	CHD2	chr15:41099503-41099932	HepG2	liver:	n/a	n/a
29	CREB1	chr15:41099356-41100303	HepG2	liver:	n/a	n/a
30	CREB1	chr15:41099463-41100202	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr15:41099255-41100276	K562	blood:	n/a	n/a
32	CREB1	chr15:41099462-41100020	ECC-1	luminal epithelium:	n/a	n/a
33	CREB1	chr15:41099572-41100036	A549	lung:	n/a	n/a
34	CREB1	chr15:41098984-41100353	HepG2	liver:	n/a	n/a
35	CREB1	chr15:41099345-41100326	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr15:41099168-41100180	GM12878	blood:	n/a	n/a
37	CREB1	chr15:41099635-41099865	A549	lung:	n/a	n/a
38	CTCF	chr15:41099140-41099290	HVMF	connective:	n/a	n/a
39	CTCF	chr15:41099280-41099430	GM12869	blood:	n/a	n/a
40	CTCF	chr15:41099160-41099310	HRE	kidney:	n/a	n/a
41	CTCF	chr15:41099691-41099895	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr15:41099280-41099430	GM12875	blood:	n/a	n/a
43	CTCF	chr15:41099480-41099630	GM06990	blood:	n/a	n/a
44	CTCF	chr15:41099240-41099390	HFF	foreskin:	n/a	n/a
45	CTCF	chr15:41099250-41099531	GM12878	blood:	n/a	n/a
46	CTCF	chr15:41099240-41099390	HCFaa	heart:	n/a	n/a
47	CTCF	chr15:41099240-41099390	BJ	skin:	n/a	n/a
48	CTCF	chr15:41099041-41099851	K562	blood:	n/a	n/a
49	CTCF	chr15:41099220-41099370	GM12878	blood:	n/a	n/a
50	CTCF	chr15:41099220-41099370	NHLF	lung:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:41099257-41099307	Jurkat	blood:	n/a
2	chr15:41099257-41099307	Jurkat	blood:	n/a
3	chr15:41099895-41099945	HIPEpiC	eye:	n/a
4	chr15:41099904-41099954	SAEC	small airway:	n/a
5	chr15:41099692-41099742	HUVEC	blood vessel:	n/a
6	chr15:41099719-41099769	HCM	heart:	n/a
7	chr15:41099904-41099954	CMK	blood:	n/a
8	chr15:41099160-41099210	HUVEC	blood vessel:	n/a
9	chr15:41099895-41099945	CMK	blood:	n/a
10	chr15:41099692-41099742	SKMC	muscle:	n/a
11	chr15:41098847-41098897	NT2-D1	testis:	n/a
12	chr15:41099160-41099210	PrEC	prostate:	n/a
13	chr15:41099257-41099307	GM06990	blood:	n/a
14	chr15:41099719-41099769	GM12892	blood:	n/a
15	chr15:41099257-41099307	NHDF-neo	bronchial:	n/a
16	chr15:41100233-41100283	AG04450	lung:	fetal
17	chr15:41099692-41099742	ProgFib	skin:	n/a
18	chr15:41099719-41099769	U87	brain:	n/a
19	chr15:41099160-41099210	Hepatocyte	liver:	n/a
20	chr15:41099719-41099769	A549	lung:	n/a
21	chr15:41100308-41100358	GM12891	blood:	n/a
22	chr15:41099776-41099826	AoSMC	blood vessel:	n/a
23	chr15:41099257-41099307	HepG2	liver:	n/a
24	chr15:41099160-41099210	SKMC	muscle:	n/a
25	chr15:41099257-41099307	BE2_C	brain:	n/a
26	chr15:41100308-41100358	AoSMC	blood vessel:	n/a
27	chr15:41099160-41099210	ECC-1	luminal epithelium:	n/a
28	chr15:41099904-41099954	HRCEpiC	kidney:	n/a
29	chr15:41099650-41099700	MCF10A-Er-Src	breast:	n/a
30	chr15:41099895-41099945	NHDF-neo	bronchial:	n/a
31	chr15:41098847-41098897	HRE	kidney:	n/a
32	chr15:41099650-41099700	HCM	heart:	n/a
33	chr15:41099650-41099700	AG10803	skin:	n/a
34	chr15:41098847-41098897	ECC-1	luminal epithelium:	n/a
35	chr15:41099257-41099307	BJ	skin:	n/a
36	chr15:41099776-41099826	K562	blood:	n/a
37	chr15:41099895-41099945	HCM	heart:	n/a
38	chr15:41099257-41099307	AG09319	gingival:	n/a
39	chr15:41099716-41099766	SK-N-SH_RA	brain:	n/a
40	chr15:41100308-41100358	HCPEpiC	choroid plexus:	n/a
41	chr15:41099716-41099766	IMR90	lung:	fetal
42	chr15:41099692-41099742	AG09319	gingival:	n/a
43	chr15:41100308-41100358	GM12892	blood:	n/a
44	chr15:41099776-41099826	NH-A	brain:	n/a
45	chr15:41099895-41099945	HRPEpiC	eye:	n/a
46	chr15:41099650-41099700	NH-A	brain:	n/a
47	chr15:41100233-41100283	HRE	kidney:	n/a
48	chr15:41099904-41099954	NT2-D1	testis:	n/a
49	chr15:41099776-41099826	GM19239	blood:	n/a
50	chr15:41099692-41099742	LNCaP	prostate:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:41098203..41099826-chr15:41186017..41187981,2	K562	blood:
2	chr15:41068398..41070390-chr15:41097835..41100828,2	K562	blood:
3	chr15:41098099..41100613-chr15:41185742..41188181,3	K562	blood:
4	chr15:41068210..41071185-chr15:41097995..41100691,2	MCF-7	breast:
5	chr15:41098435..41103357-chr15:41133527..41139132,10	MCF-7	breast:
6	chr15:41097893..41103310-chr15:41103796..41109268,7	MCF-7	breast:
7	chr15:41045748..41048901-chr15:41096709..41101394,9	K562	blood:
8	chr15:41098123..41102222-chr15:41134582..41138137,4	K562	blood:
9	chr15:41099271..41102222-chr15:41135281..41137187,2	K562	blood:
10	chr15:41045813..41047463-chr15:41099042..41101691,3	K562	blood:
11	chr15:41053870..41057648-chr15:41097391..41099914,3	K562	blood:
12	chr15:41098827..41099580-chr18:11851185..11852024,2	Hela-S3	cervix:
13	chr15:41099333..41100176-chr9:140099690..140100435,2	Hela-S3	cervix:
14	chr15:41054213..41057951-chr15:41097645..41100150,5	K562	blood:
15	chr15:41095442..41103026-chr15:41134658..41140625,11	MCF-7	breast:

No data

Variant related genes	Relation type
ZFYVE19	TF binding region
DNAJC17	TF binding region
ZFYVE19	CpG island
DNAJC17	CpG island
ENSG00000261183	chromatin interactions
ENSG00000187713	chromatin interactions
ENSG00000104142	chromatin interactions
ENSG00000137824	chromatin interactions
ENSG00000137880	chromatin interactions
ENSG00000188566	chromatin interactions
ENSG00000255112	chromatin interactions
ENSG00000104129	chromatin interactions
ENSG00000166140	chromatin interactions
ENSG00000166145	chromatin interactions

Extended variants
information (count: 92 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:92 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371276066	chr15:41098723-41098724	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs191606692	chr15:41098748-41098749	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs143040357	chr15:41098750-41098751	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs540738925	chr15:41098789-41098790	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs61419467	chr15:41098795-41098796	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs572997718	chr15:41098810-41098811	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs544923544	chr15:41098877-41098878	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs114293944	chr15:41098894-41098895	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs7342642	chr15:41098897-41098898	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs7342644	chr15:41098946-41098947	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs530747784	chr15:41098991-41098992	Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs118079000	chr15:41099032-41099033	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs116935857	chr15:41099059-41099060	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs529705932	chr15:41099069-41099070	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs546683878	chr15:41099076-41099077	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs143430607	chr15:41099078-41099079	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs377728869	chr15:41099079-41099080	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs566903193	chr15:41099106-41099107	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs201933431	chr15:41099110-41099111	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs201297595	chr15:41099112-41099113	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs200009385	chr15:41099117-41099118	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs532734051	chr15:41099120-41099121	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs147021183	chr15:41099144-41099145	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs200173311	chr15:41099147-41099148	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs11858010	chr15:41099163-41099164	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs538563388	chr15:41099175-41099176	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs183588715	chr15:41099223-41099224	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs568476251	chr15:41099254-41099255	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs114485719	chr15:41099258-41099259	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs554237791	chr15:41099286-41099287	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs566666676	chr15:41099313-41099314	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs545172747	chr15:41099314-41099315	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs534039040	chr15:41099315-41099316	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs11070297	chr15:41099349-41099350	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs575167731	chr15:41099351-41099352	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
36	rs544113475	chr15:41099401-41099402	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
37	rs188658422	chr15:41099453-41099454	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
38	rs563171854	chr15:41099471-41099472	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs574375252	chr15:41099476-41099477	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs539893089	chr15:41099500-41099501	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs369149658	chr15:41099514-41099515	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs371715684	chr15:41099532-41099533	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs147737352	chr15:41099577-41099578	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs199831258	chr15:41099596-41099597	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs373968674	chr15:41099602-41099603	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs146679421	chr15:41099627-41099628	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs367751300	chr15:41099642-41099643	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs193102973	chr15:41099662-41099663	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs185533526	chr15:41099706-41099707	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
50	rs369912058	chr15:41099707-41099708	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	21510904	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41079600-41098800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr15:41080000-41099000	Weak transcription	Aorta	Aorta
3	chr15:41080400-41098800	Weak transcription	Brain Angular Gyrus	brain
4	chr15:41080400-41098800	Weak transcription	Brain Anterior Caudate	brain
5	chr15:41082000-41098800	Weak transcription	Fetal Kidney	kidney
6	chr15:41086000-41098800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr15:41086000-41098800	Weak transcription	Esophagus	oesophagus
8	chr15:41086200-41098800	Weak transcription	HSMMtube	muscle
9	chr15:41086200-41098800	Weak transcription	NHDF-Ad	bronchial
10	chr15:41089200-41098800	Weak transcription	Small Intestine	intestine
11	chr15:41089600-41098800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr15:41089600-41098800	Weak transcription	HMEC	breast
13	chr15:41091000-41098800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr15:41091600-41098800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:41092000-41098800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr15:41092000-41098800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr15:41092000-41098800	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr15:41092200-41098800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:41092200-41098800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr15:41092200-41098800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr15:41092400-41098800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr15:41094400-41098800	Weak transcription	Right Atrium	heart
23	chr15:41094800-41098800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr15:41095200-41098800	Weak transcription	Lung	lung
25	chr15:41095200-41098800	Weak transcription	Thymus	Thymus
26	chr15:41096000-41099000	Weak transcription	Ovary	ovary
27	chr15:41096200-41098800	Weak transcription	Left Ventricle	heart
28	chr15:41096200-41098800	Weak transcription	Pancreas	Pancrea
29	chr15:41096800-41098800	Weak transcription	Gastric	stomach
30	chr15:41097600-41098800	Weak transcription	Fetal Stomach	stomach
31	chr15:41097800-41098800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr15:41098200-41098800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr15:41098200-41098800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr15:41098200-41098800	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr15:41098200-41098800	Enhancers	Primary B cells from peripheral blood	blood
36	chr15:41098200-41098800	Enhancers	Primary T cells from cord blood	blood
37	chr15:41098200-41098800	Enhancers	Primary T cells fromperipheralblood	blood
38	chr15:41098200-41098800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr15:41098200-41098800	Enhancers	Primary T helper naive cells from peripheral blood	blood
40	chr15:41098200-41098800	Enhancers	Primary T helper cells fromperipheralblood	blood
41	chr15:41098200-41098800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
42	chr15:41098200-41098800	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr15:41098200-41098800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr15:41098200-41098800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr15:41098200-41098800	Enhancers	Liver	Liver
46	chr15:41098200-41098800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr15:41098200-41098800	Enhancers	Fetal Brain Male	brain
48	chr15:41098200-41098800	Enhancers	Fetal Heart	heart
49	chr15:41098200-41098800	Enhancers	Fetal Intestine Large	intestine
50	chr15:41098200-41098800	Enhancers	Fetal Thymus	thymus

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