Variant report

Variant	esv3355709
Chromosome Location	chr3:52088937-52091485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:931)
CpG islands
(count:549)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:931 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:52091171-52091620	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:52091304-52091460	K562	blood:	n/a	n/a
3	ATF3	chr3:52091179-52091464	K562	blood:	n/a	n/a
4	ATF3	chr3:52091223-52091370	GM12878	blood:	n/a	n/a
5	BACH1	chr3:52090669-52092031	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr3:52089565-52090065	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr3:52089325-52089338	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:52090568-52091738	K562	blood:	n/a	chr3:52091498-52091514 chr3:52090590-52090606
9	BHLHE40	chr3:52089955-52090163	K562	blood:	n/a	n/a
10	BHLHE40	chr3:52091060-52091780	GM12878	blood:	n/a	chr3:52091498-52091514
11	BHLHE40	chr3:52091071-52091368	A549	lung:	n/a	n/a
12	BHLHE40	chr3:52090014-52090259	GM12878	blood:	n/a	n/a
13	BHLHE40	chr3:52091031-52091599	HepG2	liver:	n/a	chr3:52091498-52091514
14	BHLHE40	chr3:52090492-52090850	GM12878	blood:	n/a	chr3:52090590-52090606
15	BHLHE40	chr3:52089631-52089671	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:52090153-52090187	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr3:52091286-52091629	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr3:52090881-52091344	K562	blood:	n/a	n/a
19	CCNT2	chr3:52090536-52091099	K562	blood:	n/a	chr3:52090909-52090918
20	CCNT2	chr3:52091319-52091762	K562	blood:	n/a	n/a
21	CCNT2	chr3:52089689-52090249	K562	blood:	n/a	n/a
22	CEBPB	chr3:52090025-52090132	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr3:52091112-52091711	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:52091057-52091843	Hela-S3	cervix:	n/a	n/a
25	CEBPD	chr3:52091363-52091723	HepG2	liver:	n/a	n/a
26	CEBPD	chr3:52090478-52090797	HepG2	liver:	n/a	n/a
27	CHD1	chr3:52089299-52089518	GM12878	blood:	n/a	n/a
28	CHD2	chr3:52091286-52091446	HepG2	liver:	n/a	n/a
29	CHD2	chr3:52090566-52091794	Hela-S3	cervix:	n/a	chr3:52090988-52090998 chr3:52090658-52090665
30	CHD2	chr3:52090621-52091791	GM12878	blood:	n/a	chr3:52090988-52090998 chr3:52090658-52090665
31	CHD2	chr3:52090025-52090207	GM12878	blood:	n/a	n/a
32	CHD2	chr3:52088970-52089132	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr3:52091241-52091652	K562	blood:	n/a	n/a
34	CHD2	chr3:52090894-52091692	H1-hESC	embryonic stem cell:	n/a	chr3:52090988-52090998
35	CHD2	chr3:52090664-52090890	K562	blood:	n/a	n/a
36	CHD2	chr3:52089502-52090307	Hela-S3	cervix:	n/a	n/a
37	CREB1	chr3:52090810-52091839	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr3:52091101-52091718	A549	lung:	n/a	n/a
39	CREB1	chr3:52091014-52091831	GM12878	blood:	n/a	n/a
40	CREB1	chr3:52090713-52091930	H1-hESC	embryonic stem cell:	n/a	n/a
41	CREB1	chr3:52090526-52090768	A549	lung:	n/a	n/a
42	CREB1	chr3:52089895-52090385	A549	lung:	n/a	n/a
43	CTCF	chr3:52091460-52091610	HepG2	liver:	n/a	n/a
44	CTCF	chr3:52089310-52089451	A549	lung:	n/a	chr3:52089350-52089368 chr3:52089351-52089367
45	CTCF	chr3:52090040-52090190	SAEC	small airway:	n/a	n/a
46	CTCF	chr3:52090047-52090280	HepG2	liver:	n/a	n/a
47	CTCF	chr3:52090091-52090250	K562	blood:	n/a	n/a
48	CTCF	chr3:52089220-52089370	RPTEC	kidney:	n/a	chr3:52089239-52089249 chr3:52089350-52089368 chr3:52089351-52089367
49	CTCF	chr3:52089320-52089470	GM12864	blood:	n/a	chr3:52089350-52089368 chr3:52089351-52089367
50	CTCF	chr3:52089260-52089410	AoAF	blood vessel:	n/a	chr3:52089350-52089368 chr3:52089351-52089367

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:52090142-52090192	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:52089752-52089802	HAEpiC	amniotic membrane:	n/a
3	chr3:52090142-52090192	MCF10A-Er-Src	breast:	n/a
4	chr3:52091282-52091332	HCF	heart:	n/a
5	chr3:52091282-52091332	HMEC	breast:	n/a
6	chr3:52090647-52090697	NT2-D1	testis:	n/a
7	chr3:52090647-52090697	AG10803	skin:	n/a
8	chr3:52089752-52089802	PFSK-1	brain:	n/a
9	chr3:52091282-52091332	Caco-2	colon:	n/a
10	chr3:52090732-52090782	ovcar-3	ovarian:	n/a
11	chr3:52091282-52091332	NH-A	brain:	n/a
12	chr3:52091063-52091113	HRCEpiC	kidney:	n/a
13	chr3:52090142-52090192	GM12892	blood:	n/a
14	chr3:52091282-52091332	Jurkat	blood:	n/a
15	chr3:52091282-52091332	K562	blood:	n/a
16	chr3:52090125-52090175	A549	lung:	n/a
17	chr3:52091063-52091113	SK-N-MC	brain:	n/a
18	chr3:52089313-52089363	GM06990	blood:	n/a
19	chr3:52091282-52091332	Hepatocyte	liver:	n/a
20	chr3:52091063-52091113	HRE	kidney:	n/a
21	chr3:52089313-52089363	GM12891	blood:	n/a
22	chr3:52091484-52091534	HNPCEpiC	eye:	n/a
23	chr3:52090142-52090192	PANC-1	pancreas:	n/a
24	chr3:52090732-52090782	HIPEpiC	eye:	n/a
25	chr3:52090647-52090697	AG09309	skin:	n/a
26	chr3:52090732-52090782	NHBE	bronchial:	n/a
27	chr3:52090125-52090175	AG10803	skin:	n/a
28	chr3:52091484-52091534	CMK	blood:	n/a
29	chr3:52091282-52091332	GM12892	blood:	n/a
30	chr3:52089313-52089363	HEK293	kidney:	embryo
31	chr3:52090142-52090192	AG04450	lung:	fetal
32	chr3:52090142-52090192	NHDF-neo	bronchial:	n/a
33	chr3:52091484-52091534	GM12892	blood:	n/a
34	chr3:52090732-52090782	GM12892	blood:	n/a
35	chr3:52091063-52091113	SK-N-SH	brain:	n/a
36	chr3:52091063-52091113	HUVEC	blood vessel:	n/a
37	chr3:52090647-52090697	NHDF-neo	bronchial:	n/a
38	chr3:52090125-52090175	MCF-7	breast:	n/a
39	chr3:52090647-52090697	PFSK-1	brain:	n/a
40	chr3:52089313-52089363	HEEpiC	esophagus:	n/a
41	chr3:52090647-52090697	T-47D	breast:	n/a
42	chr3:52089313-52089363	BE2_C	brain:	n/a
43	chr3:52091282-52091332	NT2-D1	testis:	n/a
44	chr3:52089313-52089363	GM12878	blood:	n/a
45	chr3:52090125-52090175	Hepatocyte	liver:	n/a
46	chr3:52089313-52089363	Hela-S3	cervix:	n/a
47	chr3:52089313-52089363	RPTEC	kidney:	n/a
48	chr3:52090647-52090697	IMR90	lung:	fetal
49	chr3:52090732-52090782	HRCEpiC	kidney:	n/a
50	chr3:52090125-52090175	AG04449	skin:	fetal

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:52089534..52090129-chr5:139554580..139555447,2	Hela-S3	cervix:
2	chr1:149222699..149225112-chr3:52088904..52091700,2	MCF-7	breast:
3	chr3:52026823..52031380-chr3:52087204..52091486,4	K562	blood:
4	chr3:52088485..52093169-chr3:52093699..52100396,11	MCF-7	breast:
5	chr3:51974263..51977386-chr3:52088681..52091436,3	K562	blood:
6	chr3:52028061..52031321-chr3:52088873..52092735,5	MCF-7	breast:
7	chr3:52028475..52031255-chr3:52087467..52089239,2	MCF-7	breast:
8	chr3:52088419..52090155-chr3:52113932..52115849,2	K562	blood:
9	chr3:52087390..52089445-chr3:52228138..52231082,2	K562	blood:
10	chr3:52091359..52093112-chr3:52104568..52106950,2	K562	blood:
11	chr3:52015921..52019600-chr3:52088214..52092499,4	K562	blood:
12	chr19:12901888..12902868-chr3:52090426..52090997,2	Hela-S3	cervix:
13	chr3:52089814..52091351-chr3:52187528..52189873,2	K562	blood:
14	chr3:51975919..51976628-chr3:52090698..52091583,2	K562	blood:
15	chr3:52016320..52018909-chr3:52089400..52091632,2	MCF-7	breast:
16	chr3:52088633..52090447-chr3:52187469..52189147,2	MCF-7	breast:
17	chr3:51974895..51976742-chr3:52087202..52089493,2	K562	blood:
18	chr3:52088066..52089919-chr3:52114349..52115931,2	K562	blood:

No data

Variant related genes	Relation type
DUSP7	TF binding region
DUSP7	CpG island
ENSG00000162244	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000041880	chromatin interactions
ENSG00000114767	chromatin interactions
ENSG00000243989	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000256097	chromatin interactions
ENSG00000120306	chromatin interactions
ENSG00000164087	chromatin interactions
ENSG00000171223	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115221768	chr3:52088942-52088943	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs533890800	chr3:52088981-52088982	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs555616090	chr3:52089030-52089031	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs567384784	chr3:52089046-52089047	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs551697900	chr3:52089065-52089066	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs191561752	chr3:52089098-52089099	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs556367459	chr3:52089100-52089101	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs371264648	chr3:52089190-52089191	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs577816905	chr3:52089210-52089211	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs565813123	chr3:52089270-52089271	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs139046255	chr3:52089366-52089367	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs553528792	chr3:52089368-52089369	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs183820709	chr3:52089387-52089388	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs540604011	chr3:52089425-52089426	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs111549035	chr3:52089429-52089430	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs115842207	chr3:52089516-52089517	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs111787704	chr3:52089530-52089531	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs529513685	chr3:52089594-52089595	Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs368049025	chr3:52089601-52089602	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs117299655	chr3:52089606-52089607	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs562699468	chr3:52089636-52089637	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs113656369	chr3:52089637-52089638	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs571504091	chr3:52089639-52089640	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs373576554	chr3:52089644-52089645	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs566784260	chr3:52089696-52089697	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs368641924	chr3:52089721-52089722	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs527671886	chr3:52089739-52089740	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs372125431	chr3:52089754-52089755	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs188612381	chr3:52089794-52089795	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs549075665	chr3:52089797-52089798	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs372444938	chr3:52089803-52089804	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs372791699	chr3:52089822-52089823	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs375431632	chr3:52089840-52089841	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs567589496	chr3:52089851-52089852	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs569327849	chr3:52089869-52089870	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs538092289	chr3:52089927-52089928	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs371660097	chr3:52089939-52089940	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs571458726	chr3:52089997-52089998	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs374933715	chr3:52090053-52090054	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs148092517	chr3:52090158-52090159	Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs538765819	chr3:52090276-52090277	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs553815117	chr3:52090290-52090291	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs572009424	chr3:52090326-52090327	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs534175599	chr3:52090503-52090504	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs541808196	chr3:52090531-52090532	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs542627967	chr3:52090581-52090582	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs554218405	chr3:52090588-52090589	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs574001754	chr3:52090625-52090626	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs370131035	chr3:52090654-52090655	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs544491726	chr3:52090766-52090767	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52083200-52090200	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr3:52084800-52090000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr3:52085000-52089200	Enhancers	Primary B cells from peripheral blood	blood
4	chr3:52085000-52090200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr3:52085400-52089000	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
6	chr3:52085800-52089000	Flanking Active TSS	Primary T cells from cord blood	blood
7	chr3:52085800-52089000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
8	chr3:52085800-52089000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
9	chr3:52086000-52089000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
10	chr3:52086000-52089000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
11	chr3:52086000-52089400	Enhancers	Fetal Heart	heart
12	chr3:52086200-52089000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
13	chr3:52086200-52089000	Transcr. at gene 5' and 3'	Brain Inferior Temporal Lobe	brain
14	chr3:52086200-52090000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr3:52086400-52089000	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
16	chr3:52086400-52090200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
17	chr3:52086600-52089000	Transcr. at gene 5' and 3'	Fetal Adrenal Gland	Adrenal Gland
18	chr3:52086800-52089000	Flanking Active TSS	GM12878-XiMat	blood
19	chr3:52086800-52089400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr3:52086800-52090800	Active TSS	Rectal Smooth Muscle	rectum
21	chr3:52087000-52089200	Enhancers	Primary B cells from cord blood	blood
22	chr3:52087400-52089200	Enhancers	HepG2	liver
23	chr3:52087400-52091800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:52087600-52090800	Enhancers	Fetal Brain Male	brain
25	chr3:52087800-52089000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr3:52088000-52089000	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr3:52088000-52090200	Flanking Active TSS	Stomach Smooth Muscle	stomach
28	chr3:52088200-52089000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:52088200-52089000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
30	chr3:52088200-52089000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
31	chr3:52088200-52089200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
32	chr3:52088200-52090200	Flanking Active TSS	Adipose Nuclei	Adipose
33	chr3:52088400-52089000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
34	chr3:52088400-52089000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr3:52088400-52089000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr3:52088400-52089000	Flanking Active TSS	Duodenum Mucosa	Duodenum
37	chr3:52088400-52089000	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr3:52088400-52089000	Flanking Active TSS	Fetal Brain Female	brain
39	chr3:52088400-52089000	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
40	chr3:52088400-52089000	Flanking Active TSS	Left Ventricle	heart
41	chr3:52088400-52089000	Flanking Active TSS	Right Ventricle	heart
42	chr3:52088400-52089000	Flanking Active TSS	HUVEC	blood vessel
43	chr3:52088400-52089000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr3:52088400-52089000	Flanking Active TSS	NHLF	lung
45	chr3:52088400-52089200	Flanking Active TSS	NH-A	brain
46	chr3:52088400-52089400	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr3:52088400-52089800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr3:52088400-52089800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
49	chr3:52088400-52090000	Transcr. at gene 5' and 3'	Dnd41	blood
50	chr3:52088400-52090200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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