Variant report

Variant	esv3422728
Chromosome Location	chr10:44788646-44792944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:366)
Chromatin interactive
region (count:6)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr10:44790521-44790815	GM12878	blood:	n/a	n/a
2	BCL3	chr10:44790369-44790780	GM12878	blood:	n/a	n/a
3	BHLHE40	chr10:44791083-44791469	GM12878	blood:	n/a	n/a
4	BHLHE40	chr10:44788804-44788974	GM12878	blood:	n/a	n/a
5	CEBPB	chr10:44790789-44790979	HepG2	liver:	n/a	n/a
6	CEBPB	chr10:44789236-44789628	IMR90	lung:	n/a	n/a
7	CHD1	chr10:44788827-44788830	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr10:44790424-44790440	GM12878	blood:	n/a	n/a
9	CHD2	chr10:44791241-44791467	GM12878	blood:	n/a	n/a
10	CHD2	chr10:44788814-44788936	GM12878	blood:	n/a	n/a
11	CTCF	chr10:44790260-44790410	GM12873	blood:	n/a	n/a
12	CTCF	chr10:44790326-44790428	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr10:44790647-44790685	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr10:44788844-44788873	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr10:44791205-44791216	GM19239	blood:	n/a	n/a
16	CTCF	chr10:44788700-44788850	GM12873	blood:	n/a	n/a
17	CTCF	chr10:44790606-44790727	GM19239	blood:	n/a	n/a
18	EBF1	chr10:44788629-44789008	GM12878	blood:	n/a	n/a
19	EP300	chr10:44788681-44788924	GM12878	blood:	n/a	n/a
20	EP300	chr10:44791201-44791526	GM12878	blood:	n/a	n/a
21	EP300	chr10:44791113-44791554	GM12878	blood:	n/a	n/a
22	EP300	chr10:44788748-44788899	GM12878	blood:	n/a	n/a
23	EP300	chr10:44791130-44791519	GM12878	blood:	n/a	n/a
24	GTF2F1	chr10:44788858-44788883	H1-hESC	embryonic stem cell:	n/a	n/a
25	MAFK	chr10:44792154-44792250	HepG2	liver:	n/a	n/a
26	MAFK	chr10:44792194-44792256	HepG2	liver:	n/a	n/a
27	MAX	chr10:44790417-44790711	K562	blood:	n/a	n/a
28	MYC	chr10:44790614-44790746	MCF-7	breast:	n/a	n/a
29	MYC	chr10:44790911-44790971	MCF-7	breast:	n/a	n/a
30	MYC	chr10:44788789-44788826	GM12878	blood:	n/a	n/a
31	MYC	chr10:44790622-44790675	MCF-7	breast:	n/a	n/a
32	MYC	chr10:44790761-44790771	MCF-7	breast:	n/a	n/a
33	MYC	chr10:44788779-44788781	GM12878	blood:	n/a	n/a
34	MYC	chr10:44790591-44790620	MCF-7	breast:	n/a	n/a
35	PAX5	chr10:44790918-44791451	GM12878	blood:	n/a	chr10:44791411-44791420
36	POLR2A	chr10:44788993-44789163	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr10:44791040-44791054	Gliobla	brain:	n/a	n/a
38	POLR2A	chr10:44788687-44789713	U87	brain:	n/a	n/a
39	POLR2A	chr10:44788814-44788829	Gliobla	brain:	n/a	n/a
40	POLR2A	chr10:44790894-44791036	Gliobla	brain:	n/a	n/a
41	POLR2A	chr10:44790797-44790808	A549	lung:	n/a	n/a
42	POLR2A	chr10:44788910-44788919	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr10:44790658-44790784	A549	lung:	n/a	n/a
44	POLR2A	chr10:44790566-44790620	Gliobla	brain:	n/a	n/a
45	POLR2A	chr10:44789249-44789681	U87	brain:	n/a	n/a
46	POLR2A	chr10:44789239-44789708	U87	brain:	n/a	n/a
47	POLR2A	chr10:44788795-44788811	Gliobla	brain:	n/a	n/a
48	RUNX3	chr10:44790953-44791457	GM12878	blood:	n/a	chr10:44791218-44791233 chr10:44791199-44791214
49	RUNX3	chr10:44791011-44791435	GM12878	blood:	n/a	chr10:44791218-44791233 chr10:44791199-44791214
50	RUNX3	chr10:44788623-44789015	GM12878	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	chr10:44788812-44788862	ovcar-3	ovarian:	n/a
2	chr10:44788627-44788677	HCM	heart:	n/a
3	chr10:44788887-44788937	IMR90	lung:	fetal
4	chr10:44788887-44788937	U87	brain:	n/a
5	chr10:44789589-44789639	ECC-1	luminal epithelium:	n/a
6	chr10:44788887-44788937	PFSK-1	brain:	n/a
7	chr10:44788812-44788862	T-47D	breast:	n/a
8	chr10:44788887-44788937	HNPCEpiC	eye:	n/a
9	chr10:44789077-44789127	NT2-D1	testis:	n/a
10	chr10:44788887-44788937	NHBE	bronchial:	n/a
11	chr10:44789589-44789639	GM12878	blood:	n/a
12	chr10:44789589-44789639	AG09319	gingival:	n/a
13	chr10:44788812-44788862	SK-N-MC	brain:	n/a
14	chr10:44788915-44788965	T-47D	breast:	n/a
15	chr10:44789589-44789639	PANC-1	pancreas:	n/a
16	chr10:44788915-44788965	Hepatocyte	liver:	n/a
17	chr10:44788915-44788965	IMR90	lung:	fetal
18	chr10:44788812-44788862	HAEpiC	amniotic membrane:	n/a
19	chr10:44788915-44788965	HRPEpiC	eye:	n/a
20	chr10:44789589-44789639	SKMC	muscle:	n/a
21	chr10:44788812-44788862	ECC-1	luminal epithelium:	n/a
22	chr10:44788627-44788677	GM19239	blood:	n/a
23	chr10:44788915-44788965	HAEpiC	amniotic membrane:	n/a
24	chr10:44789589-44789639	HUVEC	blood vessel:	n/a
25	chr10:44788627-44788677	HRCEpiC	kidney:	n/a
26	chr10:44788887-44788937	BJ	skin:	n/a
27	chr10:44789589-44789639	GM12891	blood:	n/a
28	chr10:44788915-44788965	HL-60	blood:	n/a
29	chr10:44788887-44788937	NH-A	brain:	n/a
30	chr10:44788915-44788965	CMK	blood:	n/a
31	chr10:44788915-44788965	SK-N-MC	brain:	n/a
32	chr10:44789077-44789127	SKMC	muscle:	n/a
33	chr10:44789077-44789127	HAEpiC	amniotic membrane:	n/a
34	chr10:44788812-44788862	HepG2	liver:	n/a
35	chr10:44789589-44789639	SK-N-SH_RA	brain:	n/a
36	chr10:44788915-44788965	HIPEpiC	eye:	n/a
37	chr10:44788627-44788677	HRE	kidney:	n/a
38	chr10:44788812-44788862	HRCEpiC	kidney:	n/a
39	chr10:44789589-44789639	HAEpiC	amniotic membrane:	n/a
40	chr10:44788812-44788862	HEK293	kidney:	embryo
41	chr10:44788887-44788937	HRCEpiC	kidney:	n/a
42	chr10:44788915-44788965	NH-A	brain:	n/a
43	chr10:44788812-44788862	Caco-2	colon:	n/a
44	chr10:44789589-44789639	NT2-D1	testis:	n/a
45	chr10:44788812-44788862	GM06990	blood:	n/a
46	chr10:44789077-44789127	MCF10A-Er-Src	breast:	n/a
47	chr10:44789589-44789639	A549	lung:	n/a
48	chr10:44788887-44788937	T-47D	breast:	n/a
49	chr10:44789589-44789639	HPAEpiC	pulmonary alveolar:	n/a
50	chr10:44788627-44788677	GM12892	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:44790481..44792534-chr10:44792786..44795587,2	MCF-7	breast:
2	chr10:44790586..44792742-chr10:44798450..44801246,2	K562	blood:
3	chr10:44776762..44778812-chr10:44792922..44795604,2	MCF-7	breast:
4	chr10:44755013..44756692-chr10:44790155..44792136,2	MCF-7	breast:
5	chr10:44790196..44793217-chr10:44793221..44795884,3	MCF-7	breast:
6	chr10:44790481..44792534-chr10:44792786..44795587,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CXCL12-1	chr10:44789285-44789628	XLOC_008795
2	lnc-CXCL12-1	chr10:44788720-44789209	XLOC_008795
3	lnc-CXCL12-1	chr10:44788720-44789157	XLOC_008795
4	lnc-C10orf136-6	chr10:44788752-44789262	NONHSAT013029

No data

Variant related genes	Relation type
ENSG00000229116	TF binding region
ENSG00000229116	CpG island

Extended variants
information (count: 156 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:156 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368112017	chr10:44788705-44788706	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78550452	chr10:44788714-44788715	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs190399365	chr10:44788717-44788718	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs571973984	chr10:44788719-44788720	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73286694	chr10:44788758-44788759	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs557699960	chr10:44788777-44788778	Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs58189594	chr10:44788826-44788827	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs112582308	chr10:44788834-44788835	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs140407264	chr10:44788837-44788838	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs183443274	chr10:44788888-44788889	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs528621679	chr10:44788898-44788899	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs145407268	chr10:44788917-44788918	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs138014076	chr10:44788954-44788955	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs370275316	chr10:44788959-44788960	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs367662703	chr10:44789005-44789006	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
16	rs551228152	chr10:44789025-44789026	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
17	rs563271470	chr10:44789055-44789056	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
18	rs552197223	chr10:44789062-44789063	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
19	rs548608750	chr10:44789076-44789077	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
20	rs12413395	chr10:44789090-44789091	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs534371137	chr10:44789133-44789134	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs546694315	chr10:44789178-44789179	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs75327503	chr10:44789191-44789192	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs539258019	chr10:44789204-44789205	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs557667062	chr10:44789301-44789302	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs571944019	chr10:44789325-44789326	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs536641291	chr10:44789336-44789337	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs573958625	chr10:44789342-44789343	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs368357860	chr10:44789350-44789351	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs56362529	chr10:44789364-44789365	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs554963173	chr10:44789397-44789398	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs573193283	chr10:44789405-44789406	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs34589147	chr10:44789413-44789414	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs186219089	chr10:44789423-44789424	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs565395404	chr10:44789428-44789429	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs368852588	chr10:44789440-44789441	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs577740498	chr10:44789451-44789452	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs190814093	chr10:44789471-44789472	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs374314246	chr10:44789474-44789475	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs141749672	chr10:44789500-44789501	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs72788791	chr10:44789554-44789555	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs533219597	chr10:44789555-44789556	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs560691153	chr10:44789583-44789584	Bivalent Enhancer Weak transcription Enhancers Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs809601	chr10:44789602-44789603	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs182611882	chr10:44789619-44789620	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs150847373	chr10:44789654-44789655	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs74357308	chr10:44789700-44789701	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs189526062	chr10:44789713-44789714	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs192217140	chr10:44789716-44789717	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
50	rs188047286	chr10:44789735-44789736	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44783000-44788800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr10:44785000-44788800	Weak transcription	Colon Smooth Muscle	Colon
3	chr10:44787800-44788800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr10:44787800-44788800	Active TSS	Brain Anterior Caudate	brain
5	chr10:44787800-44788800	Active TSS	Brain Substantia Nigra	brain
6	chr10:44787800-44789000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
7	chr10:44787800-44789000	Active TSS	Brain Angular Gyrus	brain
8	chr10:44787800-44789200	Active TSS	H9 Cell Line	embryonic stem cell
9	chr10:44787800-44789200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
10	chr10:44787800-44789200	Active TSS	Brain Cingulate Gyrus	brain
11	chr10:44787800-44789200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
12	chr10:44787800-44789200	Bivalent Enhancer	Fetal Brain Male	brain
13	chr10:44787800-44790800	Enhancers	Fetal Heart	heart
14	chr10:44787800-44791600	Enhancers	Ovary	ovary
15	chr10:44788000-44788800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr10:44788000-44788800	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr10:44788000-44788800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr10:44788000-44789000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
19	chr10:44788000-44789200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr10:44788000-44789200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
21	chr10:44788000-44789200	Enhancers	Placenta Amnion	Placenta Amnion
22	chr10:44788000-44789400	Enhancers	Lung	lung
23	chr10:44788200-44788800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
24	chr10:44788200-44788800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:44788200-44788800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr10:44788200-44788800	Active TSS	Brain Hippocampus Middle	brain
27	chr10:44788200-44788800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
28	chr10:44788200-44788800	Active TSS	Right Atrium	heart
29	chr10:44788200-44789000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr10:44788200-44789200	Bivalent Enhancer	Placenta	Placenta
31	chr10:44788200-44790400	Weak transcription	Pancreas	Pancrea
32	chr10:44788200-44790600	Weak transcription	Spleen	Spleen
33	chr10:44788200-44791000	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr10:44788400-44788800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr10:44788400-44788800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
36	chr10:44788400-44788800	Active TSS	Fetal Brain Female	brain
37	chr10:44788400-44789800	Enhancers	Fetal Kidney	kidney
38	chr10:44788600-44788800	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr10:44788600-44788800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr10:44788600-44788800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr10:44788600-44788800	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr10:44788600-44788800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr10:44788600-44788800	Flanking Active TSS	Brain Germinal Matrix	brain
44	chr10:44788600-44788800	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
45	chr10:44788600-44788800	Active TSS	Left Ventricle	heart
46	chr10:44788600-44788800	Active TSS	Right Ventricle	heart
47	chr10:44788600-44788800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
48	chr10:44788600-44788800	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr10:44788600-44788800	Active TSS	Stomach Smooth Muscle	stomach
50	chr10:44788600-44788800	Active TSS	GM12878-XiMat	blood

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