Variant report

Variant	esv3425803
Chromosome Location	chr13:76208851-76211849
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:370)
CpG islands
(count:366)
Chromatin interactive
region (count:2)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:370 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:76209632-76210184	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:76210544-76210937	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr13:76210410-76210755	GM12878	blood:	n/a	chr13:76210665-76210678
4	BHLHE40	chr13:76209286-76211225	HepG2	liver:	n/a	chr13:76210232-76210248 chr13:76209876-76209885 chr13:76209876-76209885
5	BHLHE40	chr13:76209746-76210008	K562	blood:	n/a	chr13:76209876-76209885 chr13:76209876-76209885
6	BHLHE40	chr13:76209695-76210786	GM12878	blood:	n/a	chr13:76210232-76210248 chr13:76209876-76209885 chr13:76209876-76209885
7	BHLHE40	chr13:76210644-76210946	K562	blood:	n/a	n/a
8	BRCA1	chr13:76210832-76210935	GM12878	blood:	n/a	n/a
9	BRCA1	chr13:76209756-76209956	HepG2	liver:	n/a	n/a
10	CCNT2	chr13:76210212-76210580	K562	blood:	n/a	n/a
11	CEBPB	chr13:76208282-76208887	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:76209805-76210195	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr13:76210513-76210553	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr13:76208318-76208900	HepG2	liver:	n/a	n/a
15	CHD1	chr13:76209769-76213065	IMR90	lung:	n/a	chr13:76211314-76211324 chr13:76210708-76210718
16	CHD1	chr13:76210863-76211074	GM12878	blood:	n/a	n/a
17	CHD1	chr13:76210947-76210948	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr13:76210523-76210961	GM12878	blood:	n/a	chr13:76210708-76210718
19	CHD2	chr13:76210611-76210825	H1-hESC	embryonic stem cell:	n/a	chr13:76210708-76210718
20	CHD2	chr13:76210660-76211179	HepG2	liver:	n/a	chr13:76210708-76210718
21	CHD2	chr13:76211066-76211232	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr13:76209308-76209928	HepG2	liver:	n/a	chr13:76209566-76209576
23	CHD2	chr13:76210130-76210396	HepG2	liver:	n/a	n/a
24	CHD2	chr13:76209977-76210177	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr13:76209746-76209973	GM12878	blood:	n/a	n/a
26	CHD2	chr13:76209851-76210949	Hela-S3	cervix:	n/a	chr13:76210708-76210718
27	CTBP2	chr13:76209655-76210231	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTBP2	chr13:76210449-76211292	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:76210680-76210830	GM12869	blood:	n/a	n/a
30	CTCF	chr13:76209880-76210030	HMEC	breast:	n/a	n/a
31	CTCF	chr13:76209900-76210050	GM12866	blood:	n/a	n/a
32	CTCF	chr13:76209940-76210090	GM12864	blood:	n/a	n/a
33	CTCF	chr13:76209620-76209770	HepG2	liver:	n/a	n/a
34	CTCF	chr13:76210860-76211010	Caco-2	colon:	n/a	n/a
35	CTCF	chr13:76210903-76210978	GM13977	blood:	n/a	n/a
36	CTCF	chr13:76210280-76210430	GM12864	blood:	n/a	n/a
37	CTCF	chr13:76210826-76210988	GM19240	blood:	n/a	n/a
38	CTCF	chr13:76209600-76209750	AG04449	skin:	n/a	n/a
39	CTCF	chr13:76210900-76211050	HepG2	liver:	n/a	n/a
40	CTCF	chr13:76210200-76210350	AG09309	skin:	n/a	n/a
41	CTCF	chr13:76210000-76210150	GM12873	blood:	n/a	n/a
42	CTCF	chr13:76210842-76210994	MCF-7	breast:	n/a	n/a
43	CTCF	chr13:76209880-76210030	GM12869	blood:	n/a	n/a
44	CTCF	chr13:76209980-76210130	GM12867	blood:	n/a	n/a
45	CTCF	chr13:76210260-76210410	GM12875	blood:	n/a	n/a
46	CTCF	chr13:76210560-76210710	GM06990	blood:	n/a	n/a
47	CTCF	chr13:76210160-76210310	GM12869	blood:	n/a	n/a
48	CTCF	chr13:76210826-76210986	GM12892	blood:	n/a	n/a
49	CTCF	chr13:76210861-76210959	MCF-7	breast:	n/a	n/a
50	CTCF	chr13:76210840-76210990	GM12865	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76211251-76211301	HCF	heart:	n/a
2	chr13:76210838-76210888	HEK293	kidney:	embryo
3	chr13:76209541-76209591	NHDF-neo	bronchial:	n/a
4	chr13:76211051-76211101	HRCEpiC	kidney:	n/a
5	chr13:76209457-76209507	HEEpiC	esophagus:	n/a
6	chr13:76209457-76209507	Hepatocyte	liver:	n/a
7	chr13:76209541-76209591	NH-A	brain:	n/a
8	chr13:76209541-76209591	PrEC	prostate:	n/a
9	chr13:76209457-76209507	MCF10A-Er-Src	breast:	n/a
10	chr13:76209541-76209591	GM12891	blood:	n/a
11	chr13:76210838-76210888	Hela-S3	cervix:	n/a
12	chr13:76210054-76210104	HUVEC	blood vessel:	n/a
13	chr13:76211251-76211301	T-47D	breast:	n/a
14	chr13:76209457-76209507	HIPEpiC	eye:	n/a
15	chr13:76209541-76209591	NHBE	bronchial:	n/a
16	chr13:76211051-76211101	HMEC	breast:	n/a
17	chr13:76209457-76209507	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:76210838-76210888	BE2_C	brain:	n/a
19	chr13:76211051-76211101	HNPCEpiC	eye:	n/a
20	chr13:76209541-76209591	AG10803	skin:	n/a
21	chr13:76211051-76211101	AG04450	lung:	fetal
22	chr13:76211051-76211101	MCF-7	breast:	n/a
23	chr13:76211051-76211101	HL-60	blood:	n/a
24	chr13:76209457-76209507	GM12891	blood:	n/a
25	chr13:76209541-76209591	AG04449	skin:	fetal
26	chr13:76210838-76210888	NHDF-neo	bronchial:	n/a
27	chr13:76209457-76209507	HAEpiC	amniotic membrane:	n/a
28	chr13:76211251-76211301	U87	brain:	n/a
29	chr13:76209457-76209507	GM12878	blood:	n/a
30	chr13:76211251-76211301	Jurkat	blood:	n/a
31	chr13:76209541-76209591	HCF	heart:	n/a
32	chr13:76209541-76209591	HRCEpiC	kidney:	n/a
33	chr13:76210054-76210104	GM06990	blood:	n/a
34	chr13:76210838-76210888	HCM	heart:	n/a
35	chr13:76210838-76210888	CMK	blood:	n/a
36	chr13:76211051-76211101	Caco-2	colon:	n/a
37	chr13:76211051-76211101	HEK293	kidney:	embryo
38	chr13:76209457-76209507	HRPEpiC	eye:	n/a
39	chr13:76211051-76211101	BE2_C	brain:	n/a
40	chr13:76211051-76211101	HAEpiC	amniotic membrane:	n/a
41	chr13:76209457-76209507	HCF	heart:	n/a
42	chr13:76211251-76211301	NHDF-neo	bronchial:	n/a
43	chr13:76210054-76210104	HIPEpiC	eye:	n/a
44	chr13:76210054-76210104	PFSK-1	brain:	n/a
45	chr13:76209541-76209591	Jurkat	blood:	n/a
46	chr13:76209541-76209591	SK-N-MC	brain:	n/a
47	chr13:76209457-76209507	GM06990	blood:	n/a
48	chr13:76209457-76209507	PFSK-1	brain:	n/a
49	chr13:76210054-76210104	HRE	kidney:	n/a
50	chr13:76210054-76210104	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:76194856..76197534-chr13:76208958..76210482,2	MCF-7	breast:
2	chr13:76210811..76212641-chr13:76212952..76214964,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COMMD6-2	chr13:76209965-76210130	ENSG00000261105.1
2	lnc-COMMD6-2	chr13:76209965-76210130	ENSG00000261105.1

No data

Variant related genes	Relation type
ENSG00000261105	TF binding region
LMO7	TF binding region
ENSG00000261105	CpG island
LMO7	CpG island
ENSG00000136153	chromatin interactions

Extended variants
information (count: 96 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:96 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532309974	chr13:76208857-76208858	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs576901541	chr13:76208858-76208859	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541027063	chr13:76208867-76208868	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs200614156	chr13:76208877-76208878	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs375781436	chr13:76208878-76208879	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs188781193	chr13:76208890-76208891	Weak transcription Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs2328957	chr13:76208939-76208940	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs541629860	chr13:76208970-76208971	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs563474223	chr13:76208973-76208974	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs11840797	chr13:76208996-76208997	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs530651790	chr13:76209020-76209021	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs180798068	chr13:76209074-76209075	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201844987	chr13:76209139-76209140	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs149523998	chr13:76209142-76209143	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs3036380	chr13:76209143-76209144	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs377009189	chr13:76209159-76209160	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201869634	chr13:76209164-76209165	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs5804828	chr13:76209168-76209169	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369247024	chr13:76209223-76209224	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374071911	chr13:76209289-76209290	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs547397444	chr13:76209369-76209370	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559586164	chr13:76209370-76209371	Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs569203690	chr13:76209406-76209407	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs150308178	chr13:76209447-76209448	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs371315038	chr13:76209459-76209460	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529740903	chr13:76209489-76209490	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs548631098	chr13:76209517-76209518	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs548203465	chr13:76209551-76209552	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs537289847	chr13:76209555-76209556	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs185371704	chr13:76209580-76209581	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs550005762	chr13:76209600-76209601	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs189351017	chr13:76209723-76209724	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs534561399	chr13:76209749-76209750	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs34444653	chr13:76209779-76209780	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs735821	chr13:76209780-76209781	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs2281763	chr13:76209789-76209790	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs373762505	chr13:76209796-76209797	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs113134031	chr13:76209889-76209890	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557013196	chr13:76209903-76209904	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs735822	chr13:76209961-76209962	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs545682233	chr13:76210017-76210018	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs370378210	chr13:76210073-76210074	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs76973625	chr13:76210114-76210115	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs576941774	chr13:76210145-76210146	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs540999924	chr13:76210170-76210171	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs559301757	chr13:76210192-76210193	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2281764	chr13:76210233-76210234	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548856804	chr13:76210261-76210262	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs2281765	chr13:76210324-76210325	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs531090760	chr13:76210342-76210343	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:504 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76125000-76209600	Weak transcription	Right Ventricle	heart
2	chr13:76148200-76209600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr13:76149800-76209600	Weak transcription	Lung	lung
4	chr13:76159000-76209600	Weak transcription	Brain Hippocampus Middle	brain
5	chr13:76164600-76209400	Weak transcription	Esophagus	oesophagus
6	chr13:76165200-76209200	Weak transcription	Fetal Muscle Leg	muscle
7	chr13:76170800-76209600	Weak transcription	Primary B cells from peripheral blood	blood
8	chr13:76177600-76209400	Weak transcription	Left Ventricle	heart
9	chr13:76177600-76209600	Weak transcription	Fetal Stomach	stomach
10	chr13:76180000-76209600	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr13:76180800-76209200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr13:76180800-76209200	Weak transcription	Adipose Nuclei	Adipose
13	chr13:76180800-76209600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr13:76181000-76209400	Weak transcription	Fetal Thymus	thymus
15	chr13:76181000-76209600	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr13:76181000-76209600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr13:76181200-76209400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr13:76181200-76209600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr13:76182800-76209400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr13:76189600-76209400	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr13:76190600-76209600	Weak transcription	Brain Angular Gyrus	brain
22	chr13:76192000-76209600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:76192200-76209400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr13:76192600-76209600	Weak transcription	Fetal Intestine Small	intestine
25	chr13:76193400-76209400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr13:76197000-76209600	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr13:76197800-76209600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr13:76198800-76209400	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr13:76199800-76209600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr13:76200200-76209400	Weak transcription	Primary T cells from cord blood	blood
31	chr13:76200200-76209400	Weak transcription	Aorta	Aorta
32	chr13:76200200-76209600	Weak transcription	Primary B cells from cord blood	blood
33	chr13:76200200-76209600	Weak transcription	Primary hematopoietic stem cells	blood
34	chr13:76200200-76209600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:76200400-76209400	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr13:76202400-76209400	Weak transcription	Fetal Lung	lung
37	chr13:76203200-76209600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr13:76203800-76209400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr13:76203800-76209400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr13:76204800-76209200	Weak transcription	HSMMtube	muscle
41	chr13:76205400-76209400	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr13:76207600-76209200	Enhancers	HepG2	liver
43	chr13:76207600-76209600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr13:76208000-76209400	Weak transcription	HMEC	breast
45	chr13:76208000-76209400	Weak transcription	NHEK	skin
46	chr13:76208000-76211600	Active TSS	Osteobl	bone
47	chr13:76208200-76209000	Weak transcription	HSMM	muscle
48	chr13:76208200-76209200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr13:76208200-76209200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr13:76208200-76209200	Weak transcription	NH-A	brain

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