Variant report

Variant	nsv591822
Chromosome Location	chr3:133292102-133293489
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:133293326-133293655	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:133292569-133292724	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:133291592-133292278	HepG2	liver:	n/a	n/a
4	ATF1	chr3:133291290-133292586	K562	blood:	n/a	n/a
5	ATF2	chr3:133293160-133294099	GM12878	blood:	n/a	n/a
6	ATF2	chr3:133291149-133292254	GM12878	blood:	n/a	n/a
7	ATF2	chr3:133290917-133292593	GM12878	blood:	n/a	n/a
8	ATF2	chr3:133291659-133292286	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:133293175-133293723	GM12878	blood:	n/a	n/a
10	ATF3	chr3:133293098-133293392	K562	blood:	n/a	n/a
11	ATF3	chr3:133293083-133293387	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr3:133293118-133293400	HepG2	liver:	n/a	n/a
13	ATF3	chr3:133293112-133293707	GM12878	blood:	n/a	chr3:133293434-133293445
14	ATF3	chr3:133293088-133293348	GM12878	blood:	n/a	n/a
15	BACH1	chr3:133291718-133292900	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr3:133293198-133293700	GM12878	blood:	n/a	n/a
17	BATF	chr3:133291188-133292141	GM12878	blood:	n/a	chr3:133291397-133291407
18	BATF	chr3:133293281-133293612	GM12878	blood:	n/a	n/a
19	BCL11A	chr3:133293317-133293597	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:133293259-133293647	GM12878	blood:	n/a	n/a
21	BCL3	chr3:133293060-133293605	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:133291137-133292200	GM12878	blood:	n/a	chr3:133291906-133291915 chr3:133291421-133291429 chr3:133291396-133291405 chr3:133291503-133291512
23	BCLAF1	chr3:133292364-133293853	GM12878	blood:	n/a	chr3:133292366-133292379 chr3:133292672-133292681 chr3:133292720-133292733 chr3:133292540-133292553 chr3:133293658-133293666 chr3:133292639-133292652 chr3:133292648-133292661
24	BCLAF1	chr3:133293192-133293868	GM12878	blood:	n/a	chr3:133293658-133293666
25	BCLAF1	chr3:133291095-133292241	GM12878	blood:	n/a	chr3:133291906-133291915 chr3:133291421-133291429 chr3:133291396-133291405 chr3:133291503-133291512
26	BHLHE40	chr3:133291925-133292220	A549	lung:	n/a	n/a
27	BHLHE40	chr3:133291569-133293601	HepG2	liver:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
28	BHLHE40	chr3:133291893-133292162	HepG2	liver:	n/a	n/a
29	BHLHE40	chr3:133291327-133293834	K562	blood:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
30	BHLHE40	chr3:133291182-133293907	GM12878	blood:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
31	BHLHE40	chr3:133292540-133292786	A549	lung:	n/a	chr3:133292670-133292686 chr3:133292636-133292652 chr3:133292628-133292644
32	BRCA1	chr3:133292574-133292752	HepG2	liver:	n/a	n/a
33	BRCA1	chr3:133293279-133293853	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr3:133291829-133292903	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr3:133292578-133292699	GM12878	blood:	n/a	n/a
36	CBX3	chr3:133291268-133292248	K562	blood:	n/a	n/a
37	CCNT2	chr3:133291928-133293606	K562	blood:	n/a	chr3:133292264-133292273
38	CEBPB	chr3:133291481-133292169	A549	lung:	n/a	chr3:133291668-133291681 chr3:133291668-133291681
39	CEBPB	chr3:133293224-133293808	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:133291321-133292258	IMR90	lung:	n/a	chr3:133291668-133291681 chr3:133291668-133291681
41	CEBPB	chr3:133291393-133292718	Hela-S3	cervix:	n/a	chr3:133292335-133292343 chr3:133291668-133291681 chr3:133291668-133291681
42	CEBPB	chr3:133291332-133292110	K562	blood:	n/a	chr3:133291668-133291681 chr3:133291668-133291681
43	CEBPB	chr3:133290857-133292235	GM12878	blood:	n/a	chr3:133291668-133291681 chr3:133291668-133291681
44	CEBPD	chr3:133292326-133293281	HepG2	liver:	n/a	n/a
45	CHD1	chr3:133292466-133295357	GM12878	blood:	n/a	n/a
46	CHD1	chr3:133293203-133293597	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr3:133292529-133292915	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD1	chr3:133291159-133295702	IMR90	lung:	n/a	chr3:133292262-133292272 chr3:133292366-133292376
49	CHD2	chr3:133291191-133292830	GM12878	blood:	n/a	chr3:133292262-133292272 chr3:133292366-133292376
50	CHD2	chr3:133291691-133292718	K562	blood:	n/a	chr3:133292262-133292272 chr3:133292366-133292376

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:133293427-133293477	GM12878	blood:	n/a
2	chr3:133293427-133293477	GM12878	blood:	n/a
3	chr3:133293165-133293215	MCF-7	breast:	n/a
4	chr3:133293153-133293203	Jurkat	blood:	n/a
5	chr3:133292540-133292590	GM12891	blood:	n/a
6	chr3:133293427-133293477	PANC-1	pancreas:	n/a
7	chr3:133293427-133293477	HRPEpiC	eye:	n/a
8	chr3:133292540-133292590	SKMC	muscle:	n/a
9	chr3:133293153-133293203	NHDF-neo	bronchial:	n/a
10	chr3:133292291-133292341	HCM	heart:	n/a
11	chr3:133293460-133293510	HEK293	kidney:	embryo
12	chr3:133292323-133292373	HRPEpiC	eye:	n/a
13	chr3:133292432-133292482	HepG2	liver:	n/a
14	chr3:133292323-133292373	BJ	skin:	n/a
15	chr3:133293153-133293203	AG10803	skin:	n/a
16	chr3:133292376-133292426	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:133292212-133292262	CMK	blood:	n/a
18	chr3:133292432-133292482	Hepatocyte	liver:	n/a
19	chr3:133293165-133293215	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:133292291-133292341	HCF	heart:	n/a
21	chr3:133292540-133292590	H1-hESC	embryonic stem cell:	embryo
22	chr3:133292432-133292482	AG04450	lung:	fetal
23	chr3:133293460-133293510	HRE	kidney:	n/a
24	chr3:133292291-133292341	IMR90	lung:	fetal
25	chr3:133292540-133292590	HCPEpiC	choroid plexus:	n/a
26	chr3:133293165-133293215	PANC-1	pancreas:	n/a
27	chr3:133293146-133293196	GM12878	blood:	n/a
28	chr3:133292373-133292423	Caco-2	colon:	n/a
29	chr3:133292095-133292145	A549	lung:	n/a
30	chr3:133293460-133293510	HepG2	liver:	n/a
31	chr3:133292212-133292262	SK-N-MC	brain:	n/a
32	chr3:133292212-133292262	HIPEpiC	eye:	n/a
33	chr3:133292432-133292482	BE2_C	brain:	n/a
34	chr3:133293146-133293196	ovcar-3	ovarian:	n/a
35	chr3:133292373-133292423	NHBE	bronchial:	n/a
36	chr3:133293153-133293203	HEEpiC	esophagus:	n/a
37	chr3:133292540-133292590	AG10803	skin:	n/a
38	chr3:133292212-133292262	HEEpiC	esophagus:	n/a
39	chr3:133292291-133292341	NHBE	bronchial:	n/a
40	chr3:133292373-133292423	ovcar-3	ovarian:	n/a
41	chr3:133293427-133293477	HMEC	breast:	n/a
42	chr3:133293427-133293477	AG10803	skin:	n/a
43	chr3:133293165-133293215	SKMC	muscle:	n/a
44	chr3:133292373-133292423	H1-hESC	embryonic stem cell:	embryo
45	chr3:133292899-133292949	CMK	blood:	n/a
46	chr3:133292540-133292590	PrEC	prostate:	n/a
47	chr3:133292323-133292373	HepG2	liver:	n/a
48	chr3:133292323-133292373	RPTEC	kidney:	n/a
49	chr3:133292540-133292590	A549	lung:	n/a
50	chr3:133292373-133292423	SAEC	small airway:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:123380262..123380795-chr3:133292200..133293035,2	Hela-S3	cervix:
2	chr3:133292322..133293201-chr3:142314859..142315610,2	HCT-116	colon:
3	chr1:144533945..144534883-chr3:133292589..133293471,2	Hela-S3	cervix:
4	chr20:57467067..57467853-chr3:133292915..133293441,2	Hela-S3	cervix:
5	chr3:133287190..133289166-chr3:133290175..133292220,2	K562	blood:
6	chr15:65596825..65597694-chr3:133292711..133293433,2	Hela-S3	cervix:
7	chr3:133164640..133168534-chr3:133291750..133294077,5	MCF-7	breast:
8	chr3:133207094..133210649-chr3:133290648..133294454,4	MCF-7	breast:
9	chr21:38737416..38739692-chr3:133291408..133294289,2	MCF-7	breast:
10	chr19:47291403..47292001-chr3:133293045..133294029,2	NB4	blood:
11	chr3:132439752..132442432-chr3:133291591..133294160,3	K562	blood:
12	chr3:133169398..133190840-chr3:133288286..133298861,41	MCF-7	breast:
13	chr3:132440102..132442906-chr3:133291126..133294877,5	K562	blood:
14	chr16:30006617..30007124-chr3:133292657..133293213,2	Hela-S3	cervix:
15	chr10:71930068..71930946-chr3:133292953..133293844,2	Hela-S3	cervix:
16	chr3:133207179..133209818-chr3:133291516..133294111,3	MCF-7	breast:

Variant related genes	Relation type
CDV3	TF binding region
CDV3	CpG island
ENSG00000113971	chromatin interactions
ENSG00000249993	chromatin interactions
ENSG00000273210	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000120756	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000149929	chromatin interactions
ENSG00000170819	chromatin interactions
ENSG00000214301	chromatin interactions
ENSG00000248724	chromatin interactions
ENSG00000157540	chromatin interactions
ENSG00000169592	chromatin interactions
ENSG00000105281	chromatin interactions
ENSG00000087460	chromatin interactions
ENSG00000139722	chromatin interactions
ENSG00000079332	chromatin interactions

Extended variants
information (count: 60 )
Associated
traits (count: 52 )

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35017405	chr3:133292102-133292103	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184882531	chr3:133292107-133292108	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs189739384	chr3:133292121-133292122	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs74950272	chr3:133292131-133292132	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs532379036	chr3:133292133-133292134	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs552386946	chr3:133292134-133292135	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs113022187	chr3:133292135-133292136	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs373484711	chr3:133292136-133292137	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs565854719	chr3:133292139-133292140	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs116092700	chr3:133292180-133292181	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs74796361	chr3:133292182-133292183	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs549735511	chr3:133292263-133292264	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs183107326	chr3:133292276-133292277	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs71317412	chr3:133292280-133292281	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370300187	chr3:133292302-133292303	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs539677486	chr3:133292308-133292309	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs553496974	chr3:133292321-133292322	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs188856134	chr3:133292374-133292375	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs542459749	chr3:133292376-133292377	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
20	rs71317413	chr3:133292385-133292386	Active TSS Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574523950	chr3:133292400-133292401	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs71317414	chr3:133292432-133292433	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs373449225	chr3:133292443-133292444	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs563408959	chr3:133292462-133292463	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs200294568	chr3:133292465-133292466	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs576980932	chr3:133292471-133292472	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs545704350	chr3:133292482-133292483	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs559452916	chr3:133292535-133292536	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
29	rs111722096	chr3:133292539-133292540	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs529595638	chr3:133292541-133292542	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
31	rs548505487	chr3:133292588-133292589	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs370687204	chr3:133292610-133292611	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs549361313	chr3:133292645-133292646	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs561646187	chr3:133292747-133292748	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs530840892	chr3:133292768-133292769	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs550544599	chr3:133292809-133292810	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs570627506	chr3:133292821-133292822	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs539518053	chr3:133292857-133292858	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
39	rs201192440	chr3:133292858-133292859	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
40	rs546879668	chr3:133292987-133292988	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
41	rs193280445	chr3:133293012-133293013	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
42	rs371742216	chr3:133293171-133293172	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
43	rs535661133	chr3:133293201-133293202	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	Overlapped CNVs	n/a
44	rs556070938	chr3:133293204-133293205	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs575995429	chr3:133293223-133293224	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
46	rs537061552	chr3:133293225-133293226	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
47	rs556971472	chr3:133293236-133293237	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
48	rs569973591	chr3:133293290-133293291	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
49	rs538540417	chr3:133293300-133293301	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
50	rs545843063	chr3:133293303-133293304	Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Hailey-hailey disease	17597066	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133288000-133292400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr3:133289400-133292600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:133289600-133292400	Weak transcription	Esophagus	oesophagus
4	chr3:133289600-133292400	Weak transcription	Lung	lung
5	chr3:133289800-133292400	Weak transcription	Small Intestine	intestine
6	chr3:133289800-133293200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr3:133290800-133292200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
8	chr3:133291000-133292200	Flanking Active TSS	Primary B cells from peripheral blood	blood
9	chr3:133291000-133292200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
10	chr3:133291000-133292200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr3:133291000-133292200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr3:133291200-133292200	Flanking Active TSS	Primary T cells from cord blood	blood
13	chr3:133291200-133292200	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr3:133291200-133292200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
15	chr3:133291200-133292400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr3:133291200-133294000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:133291400-133292200	Flanking Active TSS	Fetal Thymus	thymus
18	chr3:133291400-133292200	Flanking Active TSS	Dnd41	blood
19	chr3:133291400-133292200	Flanking Active TSS	K562	blood
20	chr3:133291400-133292400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr3:133291400-133293800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr3:133291600-133292200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr3:133291600-133292200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
24	chr3:133291600-133292200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
25	chr3:133291600-133292200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
26	chr3:133291600-133292200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:133291600-133292200	Flanking Active TSS	NHEK	skin
28	chr3:133291600-133292200	Flanking Active TSS	Osteobl	bone
29	chr3:133291600-133293600	Active TSS	Brain Cingulate Gyrus	brain
30	chr3:133291600-133293600	Active TSS	Brain Germinal Matrix	brain
31	chr3:133291600-133293600	Active TSS	Fetal Brain Female	brain
32	chr3:133291600-133293800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:133291600-133293800	Active TSS	Psoas Muscle	Psoas
34	chr3:133291600-133294000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr3:133291600-133294000	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr3:133291600-133294000	Active TSS	Right Ventricle	heart
37	chr3:133291600-133294400	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr3:133291600-133295000	Active TSS	Colonic Mucosa	Colon
39	chr3:133291600-133295000	Active TSS	Right Atrium	heart
40	chr3:133291800-133292200	Active TSS	Fetal Brain Male	brain
41	chr3:133291800-133292200	Flanking Active TSS	Fetal Muscle Leg	muscle
42	chr3:133291800-133292200	Flanking Active TSS	HMEC	breast
43	chr3:133291800-133293400	Active TSS	Brain Hippocampus Middle	brain
44	chr3:133291800-133293600	Active TSS	Liver	Liver
45	chr3:133291800-133293800	Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr3:133291800-133293800	Active TSS	Fetal Stomach	stomach
47	chr3:133291800-133293800	Active TSS	Thymus	Thymus
48	chr3:133291800-133293800	Active TSS	A549	lung
49	chr3:133291800-133294000	Active TSS	iPS-15b Cell Line	embryonic stem cell
50	chr3:133291800-133294000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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