Variant report

Variant	nsv833825
Chromosome Location	chr2:37808169-37985917
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4033)
CpG islands
(count:2261)
Chromatin interactive
region (count:94)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:4033 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:37940290-37940750	K562	blood:	n/a	n/a
2	ARID3A	chr2:37813485-37813599	K562	blood:	n/a	n/a
3	ARID3A	chr2:37843852-37844052	K562	blood:	n/a	n/a
4	ARID3A	chr2:37945884-37946232	K562	blood:	n/a	n/a
5	ARID3A	chr2:37899378-37899397	K562	blood:	n/a	n/a
6	ARID3A	chr2:37899629-37899649	K562	blood:	n/a	n/a
7	ARID3A	chr2:37860715-37860729	K562	blood:	n/a	n/a
8	ARID3A	chr2:37911892-37911895	K562	blood:	n/a	n/a
9	ATF1	chr2:37843821-37844106	K562	blood:	n/a	n/a
10	ATF1	chr2:37945872-37946265	K562	blood:	n/a	n/a
11	ATF1	chr2:37910388-37910830	K562	blood:	n/a	n/a
12	ATF1	chr2:37938545-37938858	K562	blood:	n/a	n/a
13	ATF1	chr2:37858521-37859005	K562	blood:	n/a	n/a
14	ATF1	chr2:37813344-37813675	K562	blood:	n/a	n/a
15	ATF1	chr2:37940479-37940807	K562	blood:	n/a	n/a
16	ATF1	chr2:37909689-37909972	K562	blood:	n/a	n/a
17	ATF2	chr2:37850936-37852115	GM12878	blood:	n/a	n/a
18	ATF2	chr2:37856482-37857126	GM12878	blood:	n/a	n/a
19	ATF2	chr2:37884146-37884546	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr2:37862323-37863607	GM12878	blood:	n/a	n/a
21	ATF2	chr2:37827809-37828379	GM12878	blood:	n/a	n/a
22	ATF2	chr2:37880684-37882566	GM12878	blood:	n/a	n/a
23	ATF2	chr2:37879245-37879775	GM12878	blood:	n/a	n/a
24	ATF2	chr2:37862185-37863679	GM12878	blood:	n/a	n/a
25	ATF2	chr2:37813152-37813759	GM12878	blood:	n/a	n/a
26	ATF2	chr2:37880078-37882602	GM12878	blood:	n/a	n/a
27	ATF2	chr2:37899676-37900188	GM12878	blood:	n/a	n/a
28	ATF2	chr2:37857759-37858362	GM12878	blood:	n/a	n/a
29	ATF2	chr2:37850974-37852084	GM12878	blood:	n/a	n/a
30	ATF2	chr2:37852754-37853735	GM12878	blood:	n/a	n/a
31	ATF2	chr2:37857844-37858344	GM12878	blood:	n/a	n/a
32	ATF2	chr2:37856610-37857037	GM12878	blood:	n/a	n/a
33	ATF3	chr2:37899123-37899611	A549	lung:	n/a	n/a
34	ATF3	chr2:37862785-37862993	GM12878	blood:	n/a	n/a
35	ATF3	chr2:37843784-37844144	K562	blood:	n/a	n/a
36	ATF3	chr2:37899215-37900104	A549	lung:	n/a	n/a
37	BACH1	chr2:37898413-37898823	H1-hESC	embryonic stem cell:	n/a	n/a
38	BATF	chr2:37827908-37828305	GM12878	blood:	n/a	chr2:37828080-37828091 chr2:37828085-37828095
39	BATF	chr2:37827898-37828213	GM12878	blood:	n/a	chr2:37828080-37828091 chr2:37828085-37828095
40	BATF	chr2:37856660-37856960	GM12878	blood:	n/a	n/a
41	BATF	chr2:37851096-37851582	GM12878	blood:	n/a	n/a
42	BATF	chr2:37850556-37851920	GM12878	blood:	n/a	n/a
43	BATF	chr2:37829881-37830169	GM12878	blood:	n/a	n/a
44	BATF	chr2:37829221-37829480	GM12878	blood:	n/a	n/a
45	BATF	chr2:37829880-37830187	GM12878	blood:	n/a	n/a
46	BATF	chr2:37862299-37863295	GM12878	blood:	n/a	chr2:37862792-37862803
47	BATF	chr2:37862598-37863169	GM12878	blood:	n/a	chr2:37862792-37862803
48	BATF	chr2:37880923-37881321	GM12878	blood:	n/a	n/a
49	BATF	chr2:37813371-37813678	GM12878	blood:	n/a	n/a
50	BATF	chr2:37880915-37881386	GM12878	blood:	n/a	n/a

(count:2261 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:37899776-37899826	HRPEpiC	eye:	n/a
2	chr2:37869895-37869945	NHDF-neo	bronchial:	n/a
3	chr2:37813553-37813603	SK-N-SH	brain:	n/a
4	chr2:37917061-37917111	MCF10A-Er-Src	breast:	n/a
5	chr2:37899776-37899826	HRPEpiC	eye:	n/a
6	chr2:37869895-37869945	NHDF-neo	bronchial:	n/a
7	chr2:37813553-37813603	SK-N-SH	brain:	n/a
8	chr2:37917061-37917111	MCF10A-Er-Src	breast:	n/a
9	chr2:37887034-37887084	SK-N-MC	brain:	n/a
10	chr2:37813553-37813603	PFSK-1	brain:	n/a
11	chr2:37883934-37883984	SAEC	small airway:	n/a
12	chr2:37841934-37841984	HMEC	breast:	n/a
13	chr2:37897716-37897766	HPAEpiC	pulmonary alveolar:	n/a
14	chr2:37909996-37910046	PFSK-1	brain:	n/a
15	chr2:37862761-37862811	GM19239	blood:	n/a
16	chr2:37899561-37899611	NHBE	bronchial:	n/a
17	chr2:37813553-37813603	U87	brain:	n/a
18	chr2:37899464-37899514	MCF10A-Er-Src	breast:	n/a
19	chr2:37909996-37910046	U87	brain:	n/a
20	chr2:37899355-37899405	PFSK-1	brain:	n/a
21	chr2:37882358-37882408	HAEpiC	amniotic membrane:	n/a
22	chr2:37899355-37899405	AG09309	skin:	n/a
23	chr2:37909996-37910046	ovcar-3	ovarian:	n/a
24	chr2:37898101-37898151	BJ	skin:	n/a
25	chr2:37985316-37985366	BJ	skin:	n/a
26	chr2:37899561-37899611	H1-hESC	embryonic stem cell:	embryo
27	chr2:37899023-37899073	Hela-S3	cervix:	n/a
28	chr2:37962248-37962298	K562	blood:	n/a
29	chr2:37841934-37841984	HRPEpiC	eye:	n/a
30	chr2:37841934-37841984	HCF	heart:	n/a
31	chr2:37899357-37899407	HNPCEpiC	eye:	n/a
32	chr2:37899464-37899514	HNPCEpiC	eye:	n/a
33	chr2:37841934-37841984	PFSK-1	brain:	n/a
34	chr2:37917061-37917111	MCF-7	breast:	n/a
35	chr2:37985316-37985366	T-47D	breast:	n/a
36	chr2:37899953-37900003	ProgFib	skin:	n/a
37	chr2:37899023-37899073	BE2_C	brain:	n/a
38	chr2:37873474-37873524	T-47D	breast:	n/a
39	chr2:37875836-37875886	AG04450	lung:	fetal
40	chr2:37909996-37910046	BJ	skin:	n/a
41	chr2:37903481-37903531	GM19239	blood:	n/a
42	chr2:37862761-37862811	Jurkat	blood:	n/a
43	chr2:37883934-37883984	NH-A	brain:	n/a
44	chr2:37896583-37896633	HRPEpiC	eye:	n/a
45	chr2:37899357-37899407	NB4	blood:	n/a
46	chr2:37917061-37917111	T-47D	breast:	n/a
47	chr2:37927157-37927207	GM12878	blood:	n/a
48	chr2:37903481-37903531	AG04449	skin:	fetal
49	chr2:37899464-37899514	GM12878	blood:	n/a
50	chr2:37813553-37813603	AG09319	gingival:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:37810708..37813206-chr2:37814020..37815979,2	K562	blood:
2	chr2:37839740..37841439-chr2:37842697..37845685,2	K562	blood:
3	chr2:37877216..37879655-chr2:37884753..37886765,2	MCF-7	breast:
4	chr2:37871133..37873297-chr2:37883736..37885444,2	K562	blood:
5	chr2:37810708..37813206-chr2:37814020..37815979,2	K562	blood:
6	chr2:37872963..37873673-chr2:38059260..38059938,2	MCF-7	breast:
7	chr2:37810267..37812004-chr2:37812621..37814787,2	MCF-7	breast:
8	chr2:37839740..37841439-chr2:37842697..37845685,2	K562	blood:
9	chr2:37841368..37843390-chr2:37884441..37885959,2	K562	blood:
10	chr2:37944151..37947328-chr2:37948654..37951437,3	K562	blood:
11	chr2:37900528..37902254-chr2:37903447..37906132,2	MCF-7	breast:
12	chr2:37958368..37961444-chr2:37963169..37965814,4	K562	blood:
13	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
14	chr2:37888261..37891302-chr2:37893460..37895154,3	K562	blood:
15	chr2:37881322..37883473-chr2:37897027..37898680,2	MCF-7	breast:
16	chr2:37961835..37963512-chr2:37971098..37973001,2	MCF-7	breast:
17	chr2:37901542..37903159-chr2:37919185..37920897,2	K562	blood:
18	chr2:37877539..37880523-chr2:37887000..37889009,2	K562	blood:
19	chr2:37888739..37890489-chr2:37897152..37899856,2	MCF-7	breast:
20	chr2:37807890..37810236-chr2:37813003..37815246,2	K562	blood:
21	chr2:37869759..37872018-chr2:37878989..37880854,2	MCF-7	breast:
22	chr2:37859378..37862018-chr2:37863759..37867582,3	K562	blood:
23	chr2:37853940..37855732-chr2:37858093..37860839,2	K562	blood:
24	chr2:37813986..37816982-chr2:37818783..37822459,3	K562	blood:
25	chr2:37858708..37861309-chr2:37897496..37899960,2	MCF-7	breast:
26	chr2:37892381..37894768-chr2:37914084..37916577,2	MCF-7	breast:
27	chr2:37853880..37855440-chr2:37859339..37862241,2	K562	blood:
28	chr2:37860354..37862423-chr2:37867033..37868574,2	MCF-7	breast:
29	chr2:37887881..37890513-chr2:37893460..37895028,2	K562	blood:
30	chr2:37884189..37885698-chr2:37890544..37892731,2	K562	blood:
31	chr2:37853940..37855732-chr2:37858093..37860839,2	K562	blood:
32	chr2:37877539..37880523-chr2:37887000..37889009,2	K562	blood:
33	chr2:37871133..37873297-chr2:37883736..37885444,2	K562	blood:
34	chr2:37886213..37888801-chr2:37890844..37893237,2	MCF-7	breast:
35	chr2:37887881..37890513-chr2:37893460..37895028,2	K562	blood:
36	chr2:37888781..37890355-chr2:37896503..37898938,2	MCF-7	breast:
37	chr2:37887391..37889613-chr2:38000617..38003018,2	K562	blood:
38	chr2:37860354..37862423-chr2:37867033..37868574,2	MCF-7	breast:
39	chr2:37841338..37843499-chr2:37914010..37916606,2	K562	blood:
40	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
41	chr2:37931880..37933672-chr2:37934871..37936423,2	MCF-7	breast:
42	chr2:37965210..37967124-chr2:37973295..37975217,2	MCF-7	breast:
43	chr2:37860309..37862165-chr2:37866082..37868468,2	K562	blood:
44	chr2:37886940..37888699-chr2:37890365..37892218,2	K562	blood:
45	chr2:37919594..37922588-chr2:37925498..37927589,2	K562	blood:
46	chr2:37897976..37899851-chr2:37913464..37916015,2	MCF-7	breast:
47	chr19:39109060..39109842-chr2:37898536..37899149,2	HCT-116	colon:
48	chr2:37901542..37903159-chr2:37919185..37920897,2	K562	blood:
49	chr2:37877216..37879655-chr2:37884753..37886765,2	MCF-7	breast:
50	chr2:37906138..37908983-chr2:37910229..37911986,2	MCF-7	breast:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-QPCT-3	chr2:37827065-37827505	XLOC_001430
2	lnc-QPCT-3	chr2:37831452-37831572	NONHSAT070127
3	lnc-FAM82A1-3	chr2:37971476-37971786	XLOC_001431
4	lnc-PRKD3-1	chr2:37906894-37908525	ucscGeneNc_uc002rqj_1
5	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070138
6	lnc-PRKD3-1	chr2:37956390-37956510	NONHSAT070138
7	lnc-PRKD3-1	chr2:37908256-37908525	NONHSAT070138
8	lnc-PRKD3-1	chr2:37945761-37945925	NONHSAT070140
9	lnc-QPCT-4	chr2:37827621-37827693	NONHSAT070126
10	lnc-PRKD3-1	chr2:37909580-37909685	ucscGeneNc_uc002rqj_1
11	lnc-PRKD3-1	chr2:37909580-37909685	NONHSAT070138
12	lnc-QPCT-3	chr2:37839316-37839401	ENSG00000236213.1
13	lnc-PRKD3-1	chr2:37909895-37910079	NONHSAT070137
14	lnc-QPCT-3	chr2:37827279-37827505	ENSG00000236213.1
15	lnc-QPCT-3	chr2:37832379-37870742	NONHSAT070127
16	lnc-QPCT-4	chr2:37824980-37825290	NONHSAT070126
17	lnc-PRKD3-1	chr2:37909895-37910045	ucscGeneNc_uc002rqj_1
18	lnc-PRKD3-1	chr2:37909580-37909685	NONHSAT070137
19	lnc-FAM82A1-11	chr2:37898911-37899815	NONHSAT070135
20	lnc-PRKD3-1	chr2:37906894-37908525	NONHSAT070137
21	lnc-QPCT-3	chr2:37826300-37827505	NONHSAT070127
22	lnc-PRKD3-1	chr2:37920685-37920906	NONHSAT070140
23	lnc-QPCT-3	chr2:37864557-37865599	NONHSAT070132
24	lnc-QPCT-3	chr2:37871560-37871584	ENSG00000236213.1
25	lnc-FAM82A1-11	chr2:37899328-37900292	NONHSAT070136
26	lnc-PRKD3-2	chr2:37915960-37915992	NONHSAT070139
27	lnc-PRKD3-2	chr2:37911626-37915318	NONHSAT070139
28	lnc-QPCT-3	chr2:37831452-37831877	XLOC_001430
29	lnc-QPCT-3	chr2:37869884-37870070	ENSG00000236213.1
30	lnc-QPCT-3	chr2:37827040-37827505	XLOC_001430
31	lnc-PRKD3-1	chr2:37956758-37956921	NONHSAT070140
32	lnc-QPCT-3	chr2:37839316-37839573	XLOC_001430
33	lnc-QPCT-3	chr2:37873819-37873841	ENSG00000236213.1
34	lnc-FAM82A1-3	chr2:37974117-37974189	XLOC_001431

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CDC42EP3	hsa-miR-124-3p	chr2:37872312-37872306
2	CDC42EP3	hsa-miR-124-3p	chr2:37872306-37872324

Variant related genes	Relation type
ENSG00000236213	TF binding region
ENSG00000236572	TF binding region
CDC42EP3	TF binding region
ENSG00000236213	CpG island
ENSG00000236572	CpG island
CDC42EP3	CpG island
ENSG00000151458	chromatin interactions
ENSG00000178982	chromatin interactions
ENSG00000236572	chromatin interactions
ENSG00000163171	chromatin interactions
ENSG00000104814	chromatin interactions
ACVR2B	miRNA target sites

Extended variants
information (count: 8552 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:8552 , 50 per page) page: 1 2 3 4 5 6 7 ... 172

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145921231	chr2:37808185-37808186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138423761	chr2:37808186-37808187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561399381	chr2:37808386-37808387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs184093516	chr2:37808472-37808473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547324439	chr2:37808483-37808484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs557477506	chr2:37808521-37808522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532944847	chr2:37808565-37808566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551279140	chr2:37808598-37808599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10208172	chr2:37808611-37808612	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs548554510	chr2:37808621-37808622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs567295386	chr2:37808624-37808625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35401546	chr2:37808632-37808633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113683343	chr2:37808641-37808642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552751653	chr2:37808656-37808657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs578134950	chr2:37808671-37808672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546217302	chr2:37808679-37808680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558898231	chr2:37808682-37808683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs372377228	chr2:37808691-37808692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539205164	chr2:37808719-37808720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557712244	chr2:37808725-37808726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575989651	chr2:37808726-37808727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs10184610	chr2:37808745-37808746	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs573110621	chr2:37808760-37808761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540731169	chr2:37808773-37808774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs565202604	chr2:37808786-37808787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs143907924	chr2:37808837-37808838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs371546516	chr2:37808857-37808858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10173816	chr2:37808868-37808869	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs563278051	chr2:37808877-37808878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530711707	chr2:37808881-37808882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10184801	chr2:37808882-37808883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs542294160	chr2:37808885-37808886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567262061	chr2:37808900-37808901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528039451	chr2:37808925-37808926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs115810952	chr2:37808939-37808940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372835467	chr2:37808951-37808952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs571231023	chr2:37808956-37808957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs539267169	chr2:37808973-37808974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs147257741	chr2:37809006-37809007	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569620329	chr2:37809053-37809054	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75782418	chr2:37809056-37809057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554925244	chr2:37809075-37809076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573207564	chr2:37809115-37809116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76291298	chr2:37809116-37809117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs112307176	chr2:37809166-37809167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188595815	chr2:37809175-37809176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576911325	chr2:37809201-37809202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs6707072	chr2:37809230-37809231	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs541564515	chr2:37809250-37809251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116246669	chr2:37809341-37809342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:4957 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37796400-37809600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr2:37796600-37810200	Weak transcription	Pancreas	Pancrea
3	chr2:37799200-37812400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr2:37801600-37809600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:37802000-37812400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:37804400-37809400	Weak transcription	Primary T cells from cord blood	blood
7	chr2:37804600-37809800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:37804600-37810000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:37804600-37810200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:37804600-37810200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr2:37804800-37808800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr2:37804800-37809400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr2:37804800-37809600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr2:37804800-37809600	Weak transcription	NH-A	brain
15	chr2:37806400-37810200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:37806600-37809000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr2:37806600-37809000	Weak transcription	NHDF-Ad	bronchial
18	chr2:37806600-37810400	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr2:37806800-37810000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr2:37807800-37808400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr2:37807800-37808800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr2:37807800-37808800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr2:37807800-37809400	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr2:37807800-37809600	Weak transcription	K562	blood
25	chr2:37807800-37809800	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr2:37808200-37809800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr2:37808400-37809600	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr2:37808400-37809800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
29	chr2:37808600-37808800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr2:37808800-37809000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:37808800-37809400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr2:37808800-37809600	Enhancers	Primary T helper naive cells from peripheral blood	blood
33	chr2:37808800-37809600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr2:37808800-37809800	Enhancers	Primary T cells fromperipheralblood	blood
35	chr2:37808800-37809800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
36	chr2:37808800-37818000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr2:37809000-37809200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:37809000-37809400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:37809000-37809600	Enhancers	NHDF-Ad	bronchial
40	chr2:37809000-37809800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr2:37809200-37810200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr2:37809400-37809600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr2:37809400-37809600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
44	chr2:37809400-37809600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr2:37809400-37809600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr2:37809400-37809600	Enhancers	HSMM	muscle
47	chr2:37809400-37809800	Enhancers	Primary T cells from cord blood	blood
48	chr2:37809400-37809800	Enhancers	Primary T helper cells fromperipheralblood	blood
49	chr2:37809400-37809800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
50	chr2:37809400-37809800	Enhancers	Fetal Muscle Leg	muscle

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