Variant report

Variant	nsv521717
Chromosome Location	chr2:64104132-64186582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:62)
Chromatin interactive
region (count:54)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:64115950-64116277	HepG2	liver:	n/a	n/a
2	ATF2	chr2:64130070-64130560	GM12878	blood:	n/a	n/a
3	ATF2	chr2:64120140-64120720	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr2:64108319-64109801	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:64113563-64114044	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:64120101-64121601	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:64115647-64116451	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr2:64115575-64116325	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:64107478-64108299	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr2:64111275-64111902	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr2:64130136-64130490	GM12878	blood:	n/a	n/a
12	BATF	chr2:64130168-64130435	GM12878	blood:	n/a	n/a
13	BATF	chr2:64109599-64109806	GM12878	blood:	n/a	n/a
14	BCLAF1	chr2:64130157-64130568	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:64130231-64130424	GM12878	blood:	n/a	n/a
16	CBX3	chr2:64130183-64130537	K562	blood:	n/a	n/a
17	CBX3	chr2:64130168-64130579	K562	blood:	n/a	n/a
18	CBX3	chr2:64130157-64130601	HCT-116	colon:	n/a	n/a
19	CBX3	chr2:64130202-64130550	HCT-116	colon:	n/a	n/a
20	CCNT2	chr2:64136049-64136232	K562	blood:	n/a	n/a
21	CEBPB	chr2:64175568-64175616	HepG2	liver:	n/a	n/a
22	CEBPB	chr2:64105390-64105581	HepG2	liver:	n/a	chr2:64105499-64105510
23	CEBPB	chr2:64114313-64114398	K562	blood:	n/a	n/a
24	CEBPB	chr2:64118499-64118815	HepG2	liver:	n/a	chr2:64118685-64118696
25	CEBPB	chr2:64143672-64143679	A549	lung:	n/a	n/a
26	CEBPB	chr2:64175534-64175643	IMR90	lung:	n/a	n/a
27	CEBPB	chr2:64114324-64114398	IMR90	lung:	n/a	n/a
28	CEBPB	chr2:64184694-64184781	K562	blood:	n/a	chr2:64184711-64184724 chr2:64184711-64184724 chr2:64184711-64184724 chr2:64184711-64184722 chr2:64184711-64184722
29	CEBPB	chr2:64118557-64118785	A549	lung:	n/a	chr2:64118685-64118696
30	CEBPB	chr2:64130707-64130907	HepG2	liver:	n/a	n/a
31	CEBPB	chr2:64145789-64145989	HepG2	liver:	n/a	chr2:64145918-64145929
32	CEBPZ	chr2:64116013-64116253	HepG2	liver:	n/a	n/a
33	CHD2	chr2:64115638-64116267	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr2:64107885-64107936	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr2:64115842-64116159	HepG2	liver:	n/a	n/a
36	CHD2	chr2:64120267-64120642	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr2:64115900-64116050	GM12867	blood:	n/a	n/a
38	CTCF	chr2:64116100-64116250	AG09319	gingival:	n/a	n/a
39	CTCF	chr2:64116060-64116210	HCT-116	colon:	n/a	n/a
40	CTCF	chr2:64116060-64116210	HAc	cerebellar:	n/a	n/a
41	CTCF	chr2:64116140-64116290	HFF	foreskin:	n/a	n/a
42	CTCF	chr2:64116040-64116190	GM12864	blood:	n/a	n/a
43	CTCF	chr2:64116400-64116550	HMEC	breast:	n/a	n/a
44	CTCF	chr2:64116009-64116279	HUVEC	blood vessel:	n/a	n/a
45	CTCF	chr2:64116009-64116212	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:64116060-64116210	GM12872	blood:	n/a	n/a
47	CTCF	chr2:64115145-64116698	A549	lung:	n/a	n/a
48	CTCF	chr2:64129246-64129305	LNCaP	prostate:	n/a	n/a
49	CTCF	chr2:64116080-64116230	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr2:64116002-64116263	GM13977	blood:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:64153811-64153861	AoSMC	blood vessel:	n/a
2	chr2:64153811-64153861	AoSMC	blood vessel:	n/a
3	chr2:64153811-64153861	PANC-1	pancreas:	n/a
4	chr2:64153811-64153861	HAEpiC	amniotic membrane:	n/a
5	chr2:64153811-64153861	Caco-2	colon:	n/a
6	chr2:64153811-64153861	HCT-116	colon:	n/a
7	chr2:64153811-64153861	GM12891	blood:	n/a
8	chr2:64153811-64153861	NHBE	bronchial:	n/a
9	chr2:64153811-64153861	HMEC	breast:	n/a
10	chr2:64153811-64153861	A549	lung:	n/a
11	chr2:64153811-64153861	HCPEpiC	choroid plexus:	n/a
12	chr2:64153811-64153861	AG09309	skin:	n/a
13	chr2:64153811-64153861	ovcar-3	ovarian:	n/a
14	chr2:64153811-64153861	HRPEpiC	eye:	n/a
15	chr2:64153811-64153861	AG04449	skin:	fetal
16	chr2:64153811-64153861	HRCEpiC	kidney:	n/a
17	chr2:64153811-64153861	AG04450	lung:	fetal
18	chr2:64153811-64153861	K562	blood:	n/a
19	chr2:64153811-64153861	SAEC	small airway:	n/a
20	chr2:64153811-64153861	HIPEpiC	eye:	n/a
21	chr2:64153811-64153861	GM19239	blood:	n/a
22	chr2:64153811-64153861	NHDF-neo	bronchial:	n/a
23	chr2:64153811-64153861	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:64153811-64153861	SK-N-SH	brain:	n/a
25	chr2:64153811-64153861	Jurkat	blood:	n/a
26	chr2:64153811-64153861	HUVEC	blood vessel:	n/a
27	chr2:64153811-64153861	SK-N-MC	brain:	n/a
28	chr2:64153811-64153861	LNCaP	prostate:	n/a
29	chr2:64153811-64153861	PFSK-1	brain:	n/a
30	chr2:64153811-64153861	HNPCEpiC	eye:	n/a
31	chr2:64153811-64153861	IMR90	lung:	fetal
32	chr2:64153811-64153861	ECC-1	luminal epithelium:	n/a
33	chr2:64153811-64153861	NT2-D1	testis:	n/a
34	chr2:64153811-64153861	MCF10A-Er-Src	breast:	n/a
35	chr2:64153811-64153861	HEEpiC	esophagus:	n/a
36	chr2:64153811-64153861	H1-hESC	embryonic stem cell:	embryo
37	chr2:64153811-64153861	GM12878	blood:	n/a
38	chr2:64153811-64153861	HL-60	blood:	n/a
39	chr2:64153811-64153861	MCF-7	breast:	n/a
40	chr2:64153811-64153861	RPTEC	kidney:	n/a
41	chr2:64153811-64153861	Hela-S3	cervix:	n/a
42	chr2:64153811-64153861	SK-N-SH_RA	brain:	n/a
43	chr2:64153811-64153861	AG09319	gingival:	n/a
44	chr2:64153811-64153861	ProgFib	skin:	n/a
45	chr2:64153811-64153861	HCM	heart:	n/a
46	chr2:64153811-64153861	BE2_C	brain:	n/a
47	chr2:64153811-64153861	CMK	blood:	n/a
48	chr2:64153811-64153861	AG10803	skin:	n/a
49	chr2:64153811-64153861	T-47D	breast:	n/a
50	chr2:64153811-64153861	BJ	skin:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:64110163..64112527-chr2:64113887..64115612,2	K562	blood:
2	chr2:64170689..64173594-chr2:64176755..64179622,2	K562	blood:
3	chr2:64067276..64069517-chr2:64115717..64120116,4	K562	blood:
4	chr2:64174430..64176440-chr2:64194001..64195513,2	K562	blood:
5	chr2:64126493..64128913-chr2:64128922..64131491,2	K562	blood:
6	chr2:64141121..64142770-chr2:64145680..64147722,3	MCF-7	breast:
7	chr2:64162645..64165591-chr2:64171046..64173038,2	MCF-7	breast:
8	chr2:64137390..64139134-chr2:64141328..64143487,2	MCF-7	breast:
9	chr2:64137390..64139134-chr2:64141328..64143487,2	MCF-7	breast:
10	chr2:64108206..64110150-chr2:64110899..64112601,2	MCF-7	breast:
11	chr2:62930818..62932949-chr2:64183956..64185514,2	K562	blood:
12	chr2:64116985..64119241-chr2:64121510..64125671,3	K562	blood:
13	chr2:64121804..64124503-chr2:64129282..64132356,3	K562	blood:
14	chr2:64183197..64185119-chr2:64186153..64188187,2	MCF-7	breast:
15	chr2:64108363..64110268-chr2:64112506..64114878,2	K562	blood:
16	chr2:64160279..64161972-chr2:64164608..64167275,2	K562	blood:
17	chr2:64116985..64119241-chr2:64121510..64125671,3	K562	blood:
18	chr2:64183197..64185119-chr2:64186153..64188187,2	MCF-7	breast:
19	chr2:64115192..64117886-chr2:64118727..64121614,2	MCF-7	breast:
20	chr2:64115956..64116564-chr2:64250969..64251483,2	MCF-7	breast:
21	chr2:64124663..64126805-chr2:64129629..64131901,2	MCF-7	breast:
22	chr2:64178266..64179991-chr2:64182528..64185252,2	K562	blood:
23	chr2:63814363..63816642-chr2:64115803..64118315,3	MCF-7	breast:
24	chr2:64122001..64123547-chr2:64129156..64130782,2	K562	blood:
25	chr2:64070153..64071712-chr2:64106669..64108533,2	K562	blood:
26	chr2:64104526..64107169-chr2:64109891..64112515,3	K562	blood:
27	chr2:64160279..64161972-chr2:64164608..64167275,2	K562	blood:
28	chr2:64101796..64104187-chr2:64117437..64118984,2	MCF-7	breast:
29	chr2:64101527..64104952-chr2:64106115..64108831,3	MCF-7	breast:
30	chr2:64121804..64124503-chr2:64129282..64132356,3	K562	blood:
31	chr2:64108363..64110268-chr2:64112506..64114878,2	K562	blood:
32	chr2:64170689..64173594-chr2:64176755..64179622,2	K562	blood:
33	chr2:64108472..64110999-chr2:64116518..64118075,2	K562	blood:
34	chr2:64118955..64120810-chr2:64121223..64123718,2	K562	blood:
35	chr2:64115192..64117886-chr2:64118727..64121614,2	MCF-7	breast:
36	chr2:63918845..63919758-chr2:64115634..64116545,4	MCF-7	breast:
37	chr2:64126493..64128913-chr2:64128922..64131491,2	K562	blood:
38	chr2:64108206..64110150-chr2:64110899..64112601,2	MCF-7	breast:
39	chr2:64110843..64112629-chr2:64128824..64132161,3	MCF-7	breast:
40	chr2:64101796..64104187-chr2:64117437..64118984,2	MCF-7	breast:
41	chr2:64124663..64126805-chr2:64129629..64131901,2	MCF-7	breast:
42	chr2:63821933..63822875-chr2:64115658..64116471,2	MCF-7	breast:
43	chr2:64100029..64102701-chr2:64113484..64115928,2	K562	blood:
44	chr2:63918999..63919566-chr2:64115735..64116240,2	K562	blood:
45	chr2:64101527..64104952-chr2:64106115..64108831,3	MCF-7	breast:
46	chr2:63905199..63906853-chr2:64102018..64104600,2	MCF-7	breast:
47	chr2:64098930..64100745-chr2:64106674..64109185,2	MCF-7	breast:
48	chr2:64110843..64112629-chr2:64128824..64132161,3	MCF-7	breast:
49	chr2:64162645..64165591-chr2:64171046..64173038,2	MCF-7	breast:
50	chr2:64100029..64102648-chr2:64113034..64115092,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDPCP-6	chr2:64168495-64168884	NONHSAT071081
2	lnc-WDPCP-6	chr2:64166988-64167160	NONHSAT071081

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	UGP2	hsa-miR-32-5p	chr2:64118582-64118589
2	UGP2	hsa-miR-106b-5p	chr2:64118637-64118657
3	VPS54	hsa-miR-26b-5p	chr2:64120228-64120247
4	UGP2	hsa-miR-32-5p	chr2:64118571-64118589

Variant related genes	Relation type
ENSG00000251775	TF binding region
VPS54	TF binding region
ENSG00000251775	CpG island
VPS54	CpG island
ENSG00000143952	chromatin interactions
ENSG00000143951	chromatin interactions
ENSG00000115504	chromatin interactions
ENSG00000014641	chromatin interactions
ENSG00000251775	chromatin interactions
ENSG00000169764	chromatin interactions

Extended variants
information (count: 3266 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3266 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4616468	chr2:64104132-64104133	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543419326	chr2:64104167-64104168	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562147641	chr2:64104182-64104183	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs35358659	chr2:64104199-64104200	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529130013	chr2:64104223-64104224	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547333884	chr2:64104272-64104273	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565529281	chr2:64104291-64104292	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs149204171	chr2:64104331-64104332	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs35266126	chr2:64104332-64104333	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532921301	chr2:64104334-64104335	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185805070	chr2:64104349-64104350	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569619773	chr2:64104468-64104469	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138272111	chr2:64104472-64104473	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149193373	chr2:64104529-64104530	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs567319014	chr2:64104541-64104542	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs190381862	chr2:64104582-64104583	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114268555	chr2:64104583-64104584	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572782872	chr2:64104600-64104601	Genic enhancers Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181998822	chr2:64104617-64104618	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558346258	chr2:64104631-64104632	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs576681487	chr2:64104654-64104655	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs186541240	chr2:64104697-64104698	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs576445702	chr2:64104790-64104791	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs528769488	chr2:64104849-64104850	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs543922711	chr2:64104850-64104851	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561743064	chr2:64104882-64104883	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529288979	chr2:64104890-64104891	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541036358	chr2:64104951-64104952	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs62136387	chr2:64104990-64104991	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559172977	chr2:64105044-64105045	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533275610	chr2:64105051-64105052	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7599448	chr2:64105059-64105060	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs563530710	chr2:64105083-64105084	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs562270280	chr2:64105112-64105113	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190179466	chr2:64105128-64105129	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548286544	chr2:64105134-64105135	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560060441	chr2:64105155-64105156	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61669991	chr2:64105156-64105157	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549104548	chr2:64105196-64105197	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs567381602	chr2:64105214-64105215	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs139162330	chr2:64105215-64105216	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142961141	chr2:64105216-64105217	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs147452857	chr2:64105232-64105233	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540161295	chr2:64105270-64105271	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570484727	chr2:64105278-64105279	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs558048675	chr2:64105281-64105282	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576622922	chr2:64105286-64105287	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537139530	chr2:64105398-64105399	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34363455	chr2:64105454-64105455	Genic enhancers Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555401106	chr2:64105460-64105461	Genic enhancers Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
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
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Pancreatic cancer	17952125	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2313 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:64078000-64108000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr2:64082200-64110000	Weak transcription	Colon Smooth Muscle	Colon
3	chr2:64083000-64123000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:64083000-64129200	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr2:64083200-64110200	Weak transcription	Small Intestine	intestine
6	chr2:64083200-64110600	Weak transcription	Pancreas	Pancrea
7	chr2:64086600-64110000	Weak transcription	Esophagus	oesophagus
8	chr2:64088000-64107800	Weak transcription	Colonic Mucosa	Colon
9	chr2:64091400-64110000	Weak transcription	Rectal Smooth Muscle	rectum
10	chr2:64091800-64107800	Weak transcription	Brain Germinal Matrix	brain
11	chr2:64093000-64106400	Strong transcription	Fetal Thymus	thymus
12	chr2:64093800-64107600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr2:64093800-64109200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr2:64093800-64110000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr2:64094000-64107800	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr2:64094000-64109400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr2:64094000-64110800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr2:64098600-64106000	Strong transcription	Primary T cells from cord blood	blood
19	chr2:64099000-64105800	Strong transcription	Primary B cells from peripheral blood	blood
20	chr2:64099400-64106200	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr2:64099600-64105400	Strong transcription	Muscle Satellite Cultured Cells	--
22	chr2:64100000-64106400	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr2:64101200-64105400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr2:64101200-64105600	Strong transcription	HSMM	muscle
25	chr2:64101200-64107600	Weak transcription	NH-A	brain
26	chr2:64101200-64113600	Weak transcription	Fetal Stomach	stomach
27	chr2:64101400-64104200	Weak transcription	Placenta	Placenta
28	chr2:64101400-64104800	Genic enhancers	Fetal Heart	heart
29	chr2:64101400-64110000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr2:64101400-64110600	Weak transcription	HUVEC	blood vessel
31	chr2:64101600-64104400	Enhancers	HMEC	breast
32	chr2:64101600-64104600	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr2:64101600-64106000	Strong transcription	Primary B cells from cord blood	blood
34	chr2:64101600-64106000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
35	chr2:64101600-64106200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr2:64101600-64108800	Genic enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:64101600-64109400	Weak transcription	Fetal Intestine Large	intestine
38	chr2:64101600-64110000	Weak transcription	NHLF	lung
39	chr2:64101800-64104200	Strong transcription	Liver	Liver
40	chr2:64101800-64105000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:64101800-64106600	Strong transcription	Dnd41	blood
42	chr2:64101800-64110000	Weak transcription	Fetal Lung	lung
43	chr2:64101800-64110400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:64101800-64110400	Weak transcription	Aorta	Aorta
45	chr2:64101800-64112800	Weak transcription	Fetal Kidney	kidney
46	chr2:64102000-64104200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr2:64102000-64104200	Strong transcription	GM12878-XiMat	blood
48	chr2:64102000-64105400	Strong transcription	Primary hematopoietic stem cells	blood
49	chr2:64102000-64107400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:64102000-64107800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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