Variant report

Variant	nsv8625
Chromosome Location	chr10:43046814-43052296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:1222)
Chromatin interactive
region (count:5)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:43048220-43048891	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:43048312-43048668	K562	blood:	n/a	n/a
3	ATF1	chr10:43048147-43048550	K562	blood:	n/a	n/a
4	ATF3	chr10:43048166-43048482	K562	blood:	n/a	n/a
5	BCLAF1	chr10:43048131-43048562	GM12878	blood:	n/a	n/a
6	BCLAF1	chr10:43048079-43048628	GM12878	blood:	n/a	n/a
7	BHLHE40	chr10:43047423-43047809	K562	blood:	n/a	n/a
8	BHLHE40	chr10:43047425-43048669	GM12878	blood:	n/a	n/a
9	BHLHE40	chr10:43048282-43048608	K562	blood:	n/a	n/a
10	CBX3	chr10:43047384-43048810	K562	blood:	n/a	n/a
11	CBX3	chr10:43048210-43048732	K562	blood:	n/a	n/a
12	CBX3	chr10:43047484-43047987	K562	blood:	n/a	n/a
13	CCNT2	chr10:43048115-43048301	K562	blood:	n/a	n/a
14	CEBPB	chr10:43048102-43048620	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr10:43048285-43048642	K562	blood:	n/a	n/a
16	CEBPB	chr10:43051301-43051501	HepG2	liver:	n/a	n/a
17	CHD1	chr10:43048059-43048065	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr10:43047816-43048584	GM12878	blood:	n/a	n/a
19	CHD2	chr10:43048048-43048559	HepG2	liver:	n/a	n/a
20	CHD2	chr10:43048177-43048668	K562	blood:	n/a	n/a
21	CHD2	chr10:43047404-43047977	K562	blood:	n/a	n/a
22	CHD2	chr10:43047762-43048589	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr10:43047615-43048758	GM12878	blood:	n/a	n/a
24	CHD2	chr10:43048100-43048606	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr10:43048113-43048587	K562	blood:	n/a	n/a
26	CREB1	chr10:43048200-43048493	A549	lung:	n/a	n/a
27	CREB1	chr10:43048064-43048645	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr10:43048035-43048504	A549	lung:	n/a	n/a
29	CREB1	chr10:43048132-43048533	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr10:43047571-43048651	GM12878	blood:	n/a	n/a
31	CREB1	chr10:43047708-43048669	HepG2	liver:	n/a	n/a
32	CREB1	chr10:43048131-43048530	ECC-1	luminal epithelium:	n/a	n/a
33	CREB1	chr10:43047972-43048719	K562	blood:	n/a	n/a
34	CREB1	chr10:43047953-43048714	HepG2	liver:	n/a	n/a
35	CTCF	chr10:43047700-43047850	GM12869	blood:	n/a	n/a
36	CTCF	chr10:43048650-43048737	MCF-7	breast:	n/a	n/a
37	CTCF	chr10:43048171-43048445	GM12878	blood:	n/a	n/a
38	CTCF	chr10:43048540-43048690	HEEpiC	esophagus:	n/a	n/a
39	CTCF	chr10:43048580-43048730	Caco-2	colon:	n/a	n/a
40	CTCF	chr10:43048505-43048507	Lung_OC	lung:	n/a	n/a
41	CTCF	chr10:43047980-43048130	Caco-2	colon:	n/a	n/a
42	CTCF	chr10:43048645-43048705	Fibrobl	skin:	n/a	n/a
43	CTCF	chr10:43048364-43048512	Spleen_OC	spleen:	n/a	n/a
44	CTCF	chr10:43048403-43048501	Lung_OC	lung:	n/a	n/a
45	CTCF	chr10:43048296-43048606	K562	blood:	n/a	n/a
46	CTCF	chr10:43048669-43048705	MCF-7	breast:	n/a	n/a
47	CUX1	chr10:43048025-43048438	K562	blood:	n/a	n/a
48	CUX1	chr10:43048917-43049063	GM12878	blood:	n/a	n/a
49	E2F4	chr10:43047689-43048450	GM12878	blood:	n/a	chr10:43047814-43047825
50	E2F4	chr10:43047674-43048477	K562	blood:	n/a	chr10:43047814-43047825

(count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:43048342-43048392	NB4	blood:	n/a
2	chr10:43048206-43048256	GM06990	blood:	n/a
3	chr10:43048342-43048392	NB4	blood:	n/a
4	chr10:43048206-43048256	GM06990	blood:	n/a
5	chr10:43047784-43047834	HCM	heart:	n/a
6	chr10:43048609-43048659	U87	brain:	n/a
7	chr10:43047180-43047230	MCF-7	breast:	n/a
8	chr10:43050941-43050991	AG09319	gingival:	n/a
9	chr10:43048650-43048700	AG09309	skin:	n/a
10	chr10:43048609-43048659	NH-A	brain:	n/a
11	chr10:43048206-43048256	LNCaP	prostate:	n/a
12	chr10:43048342-43048392	ProgFib	skin:	n/a
13	chr10:43050881-43050931	Hepatocyte	liver:	n/a
14	chr10:43048696-43048746	SK-N-SH	brain:	n/a
15	chr10:43048298-43048348	HNPCEpiC	eye:	n/a
16	chr10:43048342-43048392	K562	blood:	n/a
17	chr10:43050881-43050931	MCF-7	breast:	n/a
18	chr10:43048342-43048392	CMK	blood:	n/a
19	chr10:43050881-43050931	PFSK-1	brain:	n/a
20	chr10:43048206-43048256	H1-hESC	embryonic stem cell:	embryo
21	chr10:43048298-43048348	BJ	skin:	n/a
22	chr10:43048734-43048784	GM12891	blood:	n/a
23	chr10:43047784-43047834	A549	lung:	n/a
24	chr10:43047893-43047943	SK-N-SH_RA	brain:	n/a
25	chr10:43048696-43048746	HRE	kidney:	n/a
26	chr10:43048206-43048256	NB4	blood:	n/a
27	chr10:43048650-43048700	BE2_C	brain:	n/a
28	chr10:43048696-43048746	HEK293	kidney:	embryo
29	chr10:43047784-43047834	Jurkat	blood:	n/a
30	chr10:43047784-43047834	NB4	blood:	n/a
31	chr10:43048696-43048746	Hepatocyte	liver:	n/a
32	chr10:43048646-43048696	HCF	heart:	n/a
33	chr10:43047784-43047834	AG09309	skin:	n/a
34	chr10:43048294-43048344	SKMC	muscle:	n/a
35	chr10:43047371-43047421	CMK	blood:	n/a
36	chr10:43048609-43048659	BJ	skin:	n/a
37	chr10:43048696-43048746	HRPEpiC	eye:	n/a
38	chr10:43048471-43048521	SKMC	muscle:	n/a
39	chr10:43048696-43048746	HCPEpiC	choroid plexus:	n/a
40	chr10:43048298-43048348	IMR90	lung:	fetal
41	chr10:43048298-43048348	GM19239	blood:	n/a
42	chr10:43047893-43047943	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:43048298-43048348	HRPEpiC	eye:	n/a
44	chr10:43047784-43047834	ECC-1	luminal epithelium:	n/a
45	chr10:43048471-43048521	MCF-7	breast:	n/a
46	chr10:43048665-43048715	GM06990	blood:	n/a
47	chr10:43050941-43050991	Hela-S3	cervix:	n/a
48	chr10:43047371-43047421	AG04450	lung:	fetal
49	chr10:43047134-43047184	K562	blood:	n/a
50	chr10:43048471-43048521	HCM	heart:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43043951..43049889-chr10:43132519..43135803,5	K562	blood:
2	chr10:43048254..43049868-chr10:43050241..43052640,2	K562	blood:
3	chr10:43046301..43049301-chr10:43278095..43279962,3	K562	blood:
4	chr10:43046145..43048386-chr10:43132522..43135382,4	MCF-7	breast:
5	chr10:43048254..43049868-chr10:43050241..43052640,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF33B-4	chr10:43048040-43048250	NONHSAT012899
2	lnc-ZNF33B-4	chr10:43047021-43048044	NONHSAT012901
3	lnc-ZNF33B-4	chr10:43047836-43047990	NONHSAT012887
4	lnc-ZNF33B-4	chr10:43047021-43047262	NONHSAT012899
5	lnc-ZNF33B-4	chr10:43047025-43047739	NONHSAT012893
6	lnc-ZNF33B-4	chr10:43048247-43048270	NONHSAT012891
7	lnc-ZNF33B-4	chr10:43047836-43048236	NONHSAT012896
8	lnc-ZNF33B-4	chr10:43047025-43047306	NONHSAT012896
9	lnc-ZNF33B-4	chr10:43047025-43047262	NONHSAT012895
10	lnc-ZNF33B-4	chr10:43048222-43048280	NONHSAT012887
11	lnc-ZNF33B-4	chr10:43047438-43047899	NONHSAT012895
12	lnc-ZNF33B-4	chr10:43047438-43047728	NONHSAT012887
13	lnc-ZNF33B-4	chr10:43047025-43048044	NONHSAT012891
14	lnc-ZNF33B-4	chr10:43047438-43047739	NONHSAT012892
15	lnc-ZNF33B-4	chr10:43047438-43047550	NONHSAT012902
16	lnc-ZNF33B-4	chr10:43048018-43048236	NONHSAT012895
17	lnc-ZNF33B-4	chr10:43047025-43047262	NONHSAT012892
18	lnc-ZNF33B-4	chr10:43047021-43047262	NONHSAT012887
19	lnc-ZNF33B-4	chr10:43048247-43048263	NONHSAT012901
20	lnc-ZNF33B-4	chr10:43046966-43047262	NONHSAT012902
21	lnc-ZNF33B-4	chr10:43047025-43048236	NONHSAT012894
22	lnc-ZNF33B-4	chr10:43047438-43047728	NONHSAT012896

No data

Variant related genes	Relation type
ZNF37BP	TF binding region
FXYD6P1	TF binding region
ZNF37BP	CpG island
FXYD6P1	CpG island
ENSG00000272373	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000234420	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000270762	chromatin interactions

Extended variants
information (count: 262 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:262 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141995699	chr10:43046833-43046834	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs375822518	chr10:43046874-43046875	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs567062596	chr10:43046938-43046939	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs370127718	chr10:43046946-43046947	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs573941276	chr10:43046981-43046982	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
6	rs534966005	chr10:43047005-43047006	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
7	rs183214513	chr10:43047034-43047035	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
8	rs549733042	chr10:43047065-43047066	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
9	rs371422097	chr10:43047069-43047070	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
10	rs571675692	chr10:43047074-43047075	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
11	rs145759320	chr10:43047075-43047076	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
12	rs148232805	chr10:43047092-43047093	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
13	rs373619502	chr10:43047105-43047106	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
14	rs111607778	chr10:43047146-43047147	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs1831911	chr10:43047181-43047182	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
16	rs1831912	chr10:43047182-43047183	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
17	rs576065689	chr10:43047218-43047219	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
18	rs4112196	chr10:43047249-43047250	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs4112197	chr10:43047256-43047257	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs3740324	chr10:43047310-43047311	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs116171606	chr10:43047315-43047316	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs75462285	chr10:43047327-43047328	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs575230388	chr10:43047355-43047356	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
24	rs537458873	chr10:43047372-43047373	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs547432808	chr10:43047374-43047375	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
26	rs141181278	chr10:43047399-43047400	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs559705112	chr10:43047404-43047405	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs557707270	chr10:43047414-43047415	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs533311202	chr10:43047418-43047419	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs375234427	chr10:43047424-43047425	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs73262626	chr10:43047469-43047470	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187906985	chr10:43047478-43047479	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
33	rs530904739	chr10:43047483-43047484	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
34	rs549482726	chr10:43047521-43047522	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
35	rs12244913	chr10:43047544-43047545	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
36	rs567507585	chr10:43047546-43047547	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
37	rs534905952	chr10:43047547-43047548	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
38	rs191210916	chr10:43047548-43047549	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
39	rs367943626	chr10:43047550-43047551	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
40	rs571612464	chr10:43047592-43047593	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
41	rs539379633	chr10:43047605-43047606	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
42	rs557459924	chr10:43047610-43047611	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
43	rs540281161	chr10:43047631-43047632	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
44	rs370001416	chr10:43047706-43047707	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
45	rs369458816	chr10:43047756-43047757	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
46	rs61742438	chr10:43047758-43047759	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
47	rs184452934	chr10:43047762-43047763	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
48	rs189525801	chr10:43047797-43047798	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
49	rs111280507	chr10:43047841-43047842	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
50	rs573851342	chr10:43047857-43047858	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Lung cancer	21569311	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
Autism	20531469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43020400-43047000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr10:43020600-43047000	Weak transcription	HSMM	muscle
3	chr10:43021600-43047000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr10:43035000-43047400	Weak transcription	Stomach Mucosa	stomach
5	chr10:43035600-43047000	Weak transcription	Fetal Thymus	thymus
6	chr10:43035600-43047000	Weak transcription	Gastric	stomach
7	chr10:43035600-43047000	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:43035600-43047000	Weak transcription	Right Ventricle	heart
9	chr10:43035600-43047200	Weak transcription	Colonic Mucosa	Colon
10	chr10:43035800-43047000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr10:43035800-43047000	Weak transcription	NHDF-Ad	bronchial
12	chr10:43038200-43047000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr10:43039400-43047000	Weak transcription	Placenta	Placenta
14	chr10:43039400-43047000	Weak transcription	HMEC	breast
15	chr10:43039600-43047000	Weak transcription	Thymus	Thymus
16	chr10:43039800-43047000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr10:43039800-43047000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr10:43039800-43047000	Weak transcription	Brain Substantia Nigra	brain
19	chr10:43039800-43047000	Weak transcription	Left Ventricle	heart
20	chr10:43039800-43047000	Weak transcription	Pancreas	Pancrea
21	chr10:43039800-43047200	Weak transcription	Psoas Muscle	Psoas
22	chr10:43041400-43047000	Weak transcription	Liver	Liver
23	chr10:43041800-43047200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr10:43042800-43047000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr10:43043200-43047400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr10:43043400-43047000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr10:43043400-43047000	Weak transcription	Lung	lung
28	chr10:43043400-43047200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr10:43043800-43047000	Weak transcription	Fetal Stomach	stomach
30	chr10:43044000-43047000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr10:43044000-43047000	Weak transcription	Fetal Intestine Large	intestine
32	chr10:43044200-43047000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr10:43044200-43047200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr10:43044600-43047000	Weak transcription	NHLF	lung
35	chr10:43044800-43047400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr10:43045200-43047000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr10:43045400-43047000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr10:43045400-43047200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr10:43045400-43047200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr10:43045600-43047000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr10:43045800-43047000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr10:43045800-43047000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
43	chr10:43045800-43047000	Weak transcription	Fetal Kidney	kidney
44	chr10:43045800-43047200	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr10:43046000-43047000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:43046000-43047000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr10:43046000-43047000	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr10:43046000-43047000	Enhancers	Colon Smooth Muscle	Colon
49	chr10:43046000-43047000	Weak transcription	Monocytes-CD14+_RO01746	blood
50	chr10:43046200-43047000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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