Variant report

Variant	esv1839967
Chromosome Location	chr5:9545701-9547129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:124)
CpG islands
(count:428)
Chromatin interactive
region (count:4)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:124 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr5:9544681-9546179	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr5:9546513-9546837	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr5:9546640-9546811	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr5:9546064-9546142	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr5:9546005-9546199	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr5:9546508-9546878	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTBP2	chr5:9544517-9546952	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr5:9546640-9546790	HRPEpiC	eye:	n/a	n/a
9	CTCF	chr5:9546480-9546630	AG09309	skin:	n/a	n/a
10	CTCF	chr5:9546520-9546670	AoAF	blood vessel:	n/a	n/a
11	CTCF	chr5:9546543-9546635	MCF-7	breast:	n/a	n/a
12	CTCF	chr5:9546560-9546710	SAEC	small airway:	n/a	n/a
13	CTCF	chr5:9546582-9546635	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr5:9546440-9546590	GM12864	blood:	n/a	n/a
15	CTCF	chr5:9546500-9546650	AG09319	gingival:	n/a	n/a
16	CTCF	chr5:9546540-9546690	AG04449	skin:	n/a	n/a
17	CTCF	chr5:9546540-9546690	AG09319	gingival:	n/a	n/a
18	CTCF	chr5:9546360-9546510	NHDF-neo	bronchial:	n/a	n/a
19	CTCF	chr5:9546580-9546730	HPF	lung:	n/a	n/a
20	CTCF	chr5:9546520-9546670	GM12867	blood:	n/a	n/a
21	CTCF	chr5:9546500-9546650	AG04450	lung:	n/a	n/a
22	CTCF	chr5:9546460-9546610	HA-sp	spinal cord:	n/a	n/a
23	CTCF	chr5:9546600-9546750	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr5:9546469-9546686	IMR90	lung:	n/a	n/a
25	CTCF	chr5:9546520-9546670	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr5:9546600-9546750	GM12871	blood:	n/a	n/a
27	CTCF	chr5:9546480-9546630	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr5:9546578-9546624	GM12891	blood:	n/a	n/a
29	CTCF	chr5:9546440-9546590	AG09309	skin:	n/a	n/a
30	CTCF	chr5:9546520-9546670	Caco-2	colon:	n/a	n/a
31	CTCF	chr5:9546568-9546647	Fibrobl	skin:	n/a	n/a
32	CTCF	chr5:9546460-9546610	GM06990	blood:	n/a	n/a
33	CTCF	chr5:9546609-9546632	ProgFib	skin:	n/a	n/a
34	CTCF	chr5:9546540-9546690	HRE	kidney:	n/a	n/a
35	CTCF	chr5:9546475-9546669	MCF-7	breast:	n/a	n/a
36	CTCF	chr5:9546000-9546150	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr5:9546580-9546730	AG10803	skin:	n/a	n/a
38	CTCF	chr5:9546500-9546650	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr5:9546562-9546646	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:9546540-9546690	GM12864	blood:	n/a	n/a
41	CTCF	chr5:9546520-9546670	HMEC	breast:	n/a	n/a
42	CTCF	chr5:9546520-9546670	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr5:9546540-9546690	Caco-2	colon:	n/a	n/a
44	CTCF	chr5:9546640-9546790	HFF	foreskin:	n/a	n/a
45	CTCF	chr5:9546540-9546690	HCFaa	heart:	n/a	n/a
46	CTCF	chr5:9546520-9546670	BJ	skin:	n/a	n/a
47	CTCF	chr5:9546540-9546690	NHEK	skin:	n/a	n/a
48	CTCF	chr5:9546570-9546632	Gliobla	brain:	n/a	n/a
49	CTCF	chr5:9546540-9546690	HMEC	breast:	n/a	n/a
50	CTCF	chr5:9546500-9546650	HCM	heart:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:9545976-9546026	MCF10A-Er-Src	breast:	n/a
2	chr5:9545976-9546026	MCF10A-Er-Src	breast:	n/a
3	chr5:9546695-9546745	HRCEpiC	kidney:	n/a
4	chr5:9546695-9546745	SK-N-MC	brain:	n/a
5	chr5:9546404-9546454	HIPEpiC	eye:	n/a
6	chr5:9546404-9546454	PrEC	prostate:	n/a
7	chr5:9546755-9546805	HepG2	liver:	n/a
8	chr5:9546695-9546745	AG09309	skin:	n/a
9	chr5:9546347-9546397	PrEC	prostate:	n/a
10	chr5:9545976-9546026	AoSMC	blood vessel:	n/a
11	chr5:9546347-9546397	SAEC	small airway:	n/a
12	chr5:9546335-9546385	ovcar-3	ovarian:	n/a
13	chr5:9546351-9546401	AG10803	skin:	n/a
14	chr5:9546351-9546401	MCF-7	breast:	n/a
15	chr5:9546755-9546805	A549	lung:	n/a
16	chr5:9545976-9546026	NHBE	bronchial:	n/a
17	chr5:9546695-9546745	AoSMC	blood vessel:	n/a
18	chr5:9546351-9546401	HCM	heart:	n/a
19	chr5:9546755-9546805	MCF-7	breast:	n/a
20	chr5:9546335-9546385	CMK	blood:	n/a
21	chr5:9545976-9546026	SKMC	muscle:	n/a
22	chr5:9546695-9546745	Hela-S3	cervix:	n/a
23	chr5:9546351-9546401	PrEC	prostate:	n/a
24	chr5:9546347-9546397	HUVEC	blood vessel:	n/a
25	chr5:9546755-9546805	Hepatocyte	liver:	n/a
26	chr5:9546351-9546401	NT2-D1	testis:	n/a
27	chr5:9545976-9546026	HCF	heart:	n/a
28	chr5:9546347-9546397	NHBE	bronchial:	n/a
29	chr5:9546755-9546805	CMK	blood:	n/a
30	chr5:9546755-9546805	ProgFib	skin:	n/a
31	chr5:9546404-9546454	GM19239	blood:	n/a
32	chr5:9546695-9546745	AG09319	gingival:	n/a
33	chr5:9546404-9546454	AG09319	gingival:	n/a
34	chr5:9546404-9546454	A549	lung:	n/a
35	chr5:9545976-9546026	HCPEpiC	choroid plexus:	n/a
36	chr5:9545976-9546026	Hepatocyte	liver:	n/a
37	chr5:9546335-9546385	H1-hESC	embryonic stem cell:	embryo
38	chr5:9546695-9546745	HCM	heart:	n/a
39	chr5:9546347-9546397	A549	lung:	n/a
40	chr5:9546404-9546454	GM12891	blood:	n/a
41	chr5:9546335-9546385	ProgFib	skin:	n/a
42	chr5:9546351-9546401	Hepatocyte	liver:	n/a
43	chr5:9546335-9546385	NH-A	brain:	n/a
44	chr5:9546351-9546401	ProgFib	skin:	n/a
45	chr5:9546404-9546454	Hela-S3	cervix:	n/a
46	chr5:9546695-9546745	MCF-7	breast:	n/a
47	chr5:9546347-9546397	SK-N-SH	brain:	n/a
48	chr5:9546335-9546385	NHBE	bronchial:	n/a
49	chr5:9546347-9546397	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:9546335-9546385	HL-60	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:9546585..9548880-chr5:9563821..9566752,2	K562	blood:
2	chr5:9546514..9548478-chr5:9550572..9552547,2	K562	blood:
3	chr5:9522895..9524468-chr5:9544584..9546294,2	MCF-7	breast:
4	chr5:9546664..9548240-chr5:9561037..9563217,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCT5-4	chr5:9546312-9546642	ENSG00000250786
2	lnc-CCT5-4	chr5:9546402-9546642	ENSG00000250786
3	lnc-CCT5-4	chr5:9546459-9546642	NONHSAT100369
4	lnc-CCT5-4	chr5:9546312-9546642	NR_045196

No data

Variant related genes	Relation type
SNORD123	TF binding region
SNHG18	TF binding region
SEMA5A	TF binding region
SNORD123	CpG island
SNHG18	CpG island
SEMA5A	CpG island
ENSG00000250001	chromatin interactions

Extended variants
information (count: 60 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:60 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548126909	chr5:9545757-9545758	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs575983878	chr5:9545799-9545800	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs568256653	chr5:9545820-9545821	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs537296992	chr5:9545861-9545862	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs576598585	chr5:9545881-9545882	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs550917184	chr5:9545978-9545979	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs62342600	chr5:9546006-9546007	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs539475208	chr5:9546025-9546026	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs2271224	chr5:9546027-9546028	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs572898666	chr5:9546035-9546036	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs535209643	chr5:9546039-9546040	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs369316338	chr5:9546044-9546045	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs2271223	chr5:9546046-9546047	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs112941079	chr5:9546098-9546099	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
15	rs113140904	chr5:9546135-9546136	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	mRNA abundance
16	rs2271222	chr5:9546136-9546137	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs373952775	chr5:9546154-9546155	Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs576807965	chr5:9546216-9546217	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs545927172	chr5:9546222-9546223	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs189132790	chr5:9546228-9546229	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs181074606	chr5:9546252-9546253	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs112536265	chr5:9546307-9546308	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
23	rs186068914	chr5:9546310-9546311	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region	3 gene(s)	Overlapped CNVs	n/a
24	rs561705023	chr5:9546332-9546333	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs530742203	chr5:9546366-9546367	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region CpG island lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs550878497	chr5:9546371-9546372	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region CpG island lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs59758866	chr5:9546372-9546373	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers	TF binding region CpG island lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs7720740	chr5:9546451-9546452	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs546317962	chr5:9546487-9546488	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs115441307	chr5:9546542-9546543	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs2271221	chr5:9546589-9546590	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs568278339	chr5:9546610-9546611	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs2271220	chr5:9546628-9546629	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557232059	chr5:9546634-9546635	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs577161195	chr5:9546635-9546636	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs548012179	chr5:9546658-9546659	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs546487874	chr5:9546664-9546665	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs553047942	chr5:9546674-9546675	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs190925462	chr5:9546707-9546708	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
40	rs541926016	chr5:9546721-9546722	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
41	rs78088505	chr5:9546752-9546753	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs565776957	chr5:9546831-9546832	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs2115243	chr5:9546874-9546875	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs77114189	chr5:9546876-9546877	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs538160021	chr5:9546896-9546897	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs564362209	chr5:9546918-9546919	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs533221208	chr5:9546972-9546973	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs148895718	chr5:9546975-9546976	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs1706986	chr5:9546989-9546990	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs1614229	chr5:9546995-9546996	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:107)

Disease	PMID	Source
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Ovarian cancer	19193619	CNVD
Hepatocellular carcinoma	16785998	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intellectual disability	22102821	CNVD
Myelofibrosis	22110671	CNVD
Cri-du chat syndrome	16773131	CNVD
Cryptorchidism	21048976	CNVD
Glioblastoma multiforme	22286061	CNVD
Cervical cancer	16585170	CNVD
Mental retardation	16773131	CNVD
Non-small cell lung cancer	21829676	CNVD
Cri-du chat syndrome	22470819	CNVD
sporadic birth defects	19047251	CNVD
Lung adenocarcinoma	17982442	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:9542800-9547200	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr5:9542800-9548400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr5:9543000-9547200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr5:9543000-9547200	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr5:9543000-9547800	Active TSS	Brain Hippocampus Middle	brain
6	chr5:9543000-9548200	Active TSS	Aorta	Aorta
7	chr5:9543200-9547200	Active TSS	Brain Angular Gyrus	brain
8	chr5:9543200-9547400	Active TSS	Right Ventricle	heart
9	chr5:9543200-9548200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr5:9543200-9548200	Active TSS	Pancreatic Islets	Pancreatic Islet
11	chr5:9543200-9548200	Active TSS	Right Atrium	heart
12	chr5:9543400-9548000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:9543400-9548400	Active TSS	NHLF	lung
14	chr5:9543600-9547200	Active TSS	Fetal Intestine Large	intestine
15	chr5:9543600-9548400	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr5:9543800-9547800	Active TSS	Fetal Lung	lung
17	chr5:9543800-9548000	Active TSS	Fetal Heart	heart
18	chr5:9543800-9548200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:9543800-9548200	Active TSS	Fetal Kidney	kidney
20	chr5:9543800-9548600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:9543800-9548800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr5:9543800-9548800	Active TSS	Placenta Amnion	Placenta Amnion
23	chr5:9544000-9546000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr5:9544000-9546800	Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr5:9544200-9547000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
26	chr5:9544200-9547000	Bivalent/Poised TSS	Fetal Thymus	thymus
27	chr5:9544200-9547600	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr5:9544200-9548000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:9544200-9548000	Active TSS	Ovary	ovary
30	chr5:9544200-9548400	Active TSS	NHDF-Ad	bronchial
31	chr5:9544400-9546000	Flanking Active TSS	NHEK	skin
32	chr5:9544400-9546200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:9544400-9546200	Flanking Active TSS	Liver	Liver
34	chr5:9544400-9546200	Flanking Active TSS	Stomach Smooth Muscle	stomach
35	chr5:9544400-9546600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr5:9544400-9547200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:9544400-9547200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr5:9544400-9547200	Active TSS	Left Ventricle	heart
39	chr5:9544400-9547400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr5:9544400-9547400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr5:9544400-9547400	Active TSS	Brain Cingulate Gyrus	brain
42	chr5:9544400-9547400	Active TSS	Brain Substantia Nigra	brain
43	chr5:9544400-9547600	Active TSS	Fetal Intestine Small	intestine
44	chr5:9544400-9547800	Active TSS	Pancreas	Pancrea
45	chr5:9544400-9548200	Active TSS	H9 Cell Line	embryonic stem cell
46	chr5:9544400-9548400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr5:9544400-9548400	Active TSS	Osteobl	bone
48	chr5:9544600-9545800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
49	chr5:9544600-9545800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
50	chr5:9544600-9546000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland

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