Variant report

Variant	nsv895909
Chromosome Location	chr10:98354924-98382165
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:448)
CpG islands
(count:122)
Chromatin interactive
region (count:38)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:448 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:98378896-98379223	K562	blood:	n/a	n/a
2	ARID3A	chr10:98356379-98356808	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:98372105-98372473	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:98382063-98382477	K562	blood:	n/a	n/a
5	ATF1	chr10:98378820-98379344	K562	blood:	n/a	n/a
6	ATF1	chr10:98382162-98382468	K562	blood:	n/a	n/a
7	BACH1	chr10:98362013-98362118	K562	blood:	n/a	n/a
8	BHLHE40	chr10:98356268-98356429	K562	blood:	n/a	n/a
9	BHLHE40	chr10:98368041-98368356	K562	blood:	n/a	chr10:98368214-98368223 chr10:98368213-98368222 chr10:98368214-98368223 chr10:98368212-98368225
10	BHLHE40	chr10:98356410-98356727	HepG2	liver:	n/a	n/a
11	BHLHE40	chr10:98378738-98379314	K562	blood:	n/a	n/a
12	CBX3	chr10:98382112-98382490	K562	blood:	n/a	n/a
13	CBX3	chr10:98378778-98379283	K562	blood:	n/a	n/a
14	CBX3	chr10:98378874-98379243	K562	blood:	n/a	n/a
15	CCNT2	chr10:98378763-98379350	K562	blood:	n/a	n/a
16	CCNT2	chr10:98382037-98382499	K562	blood:	n/a	n/a
17	CCNT2	chr10:98373842-98374042	K562	blood:	n/a	n/a
18	CCNT2	chr10:98356212-98356556	K562	blood:	n/a	n/a
19	CEBPB	chr10:98367279-98367417	A549	lung:	n/a	n/a
20	CEBPB	chr10:98382106-98382479	K562	blood:	n/a	n/a
21	CEBPB	chr10:98378382-98379184	K562	blood:	n/a	chr10:98378557-98378568 chr10:98378557-98378570 chr10:98378559-98378570 chr10:98378559-98378568
22	CEBPB	chr10:98357216-98357344	HepG2	liver:	n/a	chr10:98357235-98357246 chr10:98357296-98357308
23	CEBPB	chr10:98378371-98378763	ECC-1	luminal epithelium:	n/a	chr10:98378557-98378568 chr10:98378557-98378570 chr10:98378559-98378570 chr10:98378559-98378568
24	CEBPB	chr10:98367215-98367504	K562	blood:	n/a	n/a
25	CEBPB	chr10:98367223-98367461	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr10:98378814-98379320	K562	blood:	n/a	n/a
27	CEBPB	chr10:98373338-98373649	IMR90	lung:	n/a	chr10:98373472-98373485 chr10:98373472-98373485
28	CEBPB	chr10:98378414-98378662	IMR90	lung:	n/a	chr10:98378557-98378568 chr10:98378557-98378570 chr10:98378559-98378570 chr10:98378559-98378568
29	CEBPB	chr10:98378370-98378839	ECC-1	luminal epithelium:	n/a	chr10:98378557-98378568 chr10:98378557-98378570 chr10:98378559-98378570 chr10:98378559-98378568
30	CEBPB	chr10:98357822-98358012	HepG2	liver:	n/a	chr10:98357856-98357867
31	CEBPB	chr10:98356550-98356750	HepG2	liver:	n/a	n/a
32	CEBPB	chr10:98357762-98357878	A549	lung:	n/a	chr10:98357856-98357867
33	CEBPB	chr10:98378386-98378733	HepG2	liver:	n/a	chr10:98378557-98378568 chr10:98378557-98378570 chr10:98378559-98378570 chr10:98378559-98378568
34	CEBPB	chr10:98357686-98357886	H1-hESC	embryonic stem cell:	n/a	chr10:98357856-98357867
35	CEBPB	chr10:98357780-98358054	MCF-7	breast:	n/a	chr10:98357856-98357867
36	CEBPB	chr10:98378423-98378662	H1-hESC	embryonic stem cell:	n/a	chr10:98378557-98378568 chr10:98378557-98378570 chr10:98378559-98378570 chr10:98378559-98378568
37	CEBPB	chr10:98357682-98358051	IMR90	lung:	n/a	chr10:98357856-98357867
38	CEBPB	chr10:98378451-98378683	A549	lung:	n/a	chr10:98378557-98378568 chr10:98378557-98378570 chr10:98378559-98378570 chr10:98378559-98378568
39	CEBPD	chr10:98382047-98382525	K562	blood:	n/a	n/a
40	CEBPD	chr10:98356180-98356602	K562	blood:	n/a	n/a
41	CEBPD	chr10:98378799-98379309	K562	blood:	n/a	n/a
42	CEBPD	chr10:98378763-98379421	K562	blood:	n/a	n/a
43	CEBPD	chr10:98382056-98382593	K562	blood:	n/a	n/a
44	CEBPD	chr10:98356252-98356644	K562	blood:	n/a	n/a
45	CHD2	chr10:98378847-98379207	K562	blood:	n/a	n/a
46	CREB1	chr10:98378733-98379408	K562	blood:	n/a	n/a
47	CREB1	chr10:98378865-98379320	K562	blood:	n/a	n/a
48	CTCF	chr10:98378560-98378710	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr10:98378851-98379219	K562	blood:	n/a	n/a
50	CTCF	chr10:98374460-98374610	HMEC	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:98367715-98367765	NB4	blood:	n/a
2	chr10:98367715-98367765	HRPEpiC	eye:	n/a
3	chr10:98367715-98367765	BE2_C	brain:	n/a
4	chr10:98367715-98367765	Caco-2	colon:	n/a
5	chr10:98367715-98367765	SK-N-SH_RA	brain:	n/a
6	chr10:98367715-98367765	HMEC	breast:	n/a
7	chr10:98366681-98366731	HNPCEpiC	eye:	n/a
8	chr10:98367715-98367765	Hepatocyte	liver:	n/a
9	chr10:98367715-98367765	AG09319	gingival:	n/a
10	chr10:98367715-98367765	IMR90	lung:	fetal
11	chr10:98367715-98367765	K562	blood:	n/a
12	chr10:98366681-98366731	NT2-D1	testis:	n/a
13	chr10:98366681-98366731	PFSK-1	brain:	n/a
14	chr10:98366681-98366731	NB4	blood:	n/a
15	chr10:98367715-98367765	Hela-S3	cervix:	n/a
16	chr10:98367715-98367765	BJ	skin:	n/a
17	chr10:98366681-98366731	Caco-2	colon:	n/a
18	chr10:98367715-98367765	AG04450	lung:	fetal
19	chr10:98366681-98366731	HAEpiC	amniotic membrane:	n/a
20	chr10:98366681-98366731	ProgFib	skin:	n/a
21	chr10:98367715-98367765	HIPEpiC	eye:	n/a
22	chr10:98366681-98366731	GM12891	blood:	n/a
23	chr10:98366681-98366731	PANC-1	pancreas:	n/a
24	chr10:98367715-98367765	HPAEpiC	pulmonary alveolar:	n/a
25	chr10:98367715-98367765	A549	lung:	n/a
26	chr10:98366681-98366731	ECC-1	luminal epithelium:	n/a
27	chr10:98366681-98366731	HEK293	kidney:	embryo
28	chr10:98366681-98366731	A549	lung:	n/a
29	chr10:98366681-98366731	AG10803	skin:	n/a
30	chr10:98367715-98367765	HCT-116	colon:	n/a
31	chr10:98366681-98366731	AG04449	skin:	fetal
32	chr10:98366681-98366731	T-47D	breast:	n/a
33	chr10:98366681-98366731	SAEC	small airway:	n/a
34	chr10:98366681-98366731	SK-N-MC	brain:	n/a
35	chr10:98367715-98367765	HEEpiC	esophagus:	n/a
36	chr10:98366681-98366731	SK-N-SH	brain:	n/a
37	chr10:98366681-98366731	HCT-116	colon:	n/a
38	chr10:98367715-98367765	NT2-D1	testis:	n/a
39	chr10:98366681-98366731	Hepatocyte	liver:	n/a
40	chr10:98367715-98367765	NH-A	brain:	n/a
41	chr10:98367715-98367765	U87	brain:	n/a
42	chr10:98366681-98366731	NH-A	brain:	n/a
43	chr10:98366681-98366731	CMK	blood:	n/a
44	chr10:98367715-98367765	AG09309	skin:	n/a
45	chr10:98366681-98366731	BE2_C	brain:	n/a
46	chr10:98366681-98366731	BJ	skin:	n/a
47	chr10:98367715-98367765	SK-N-MC	brain:	n/a
48	chr10:98366681-98366731	HCPEpiC	choroid plexus:	n/a
49	chr10:98367715-98367765	SAEC	small airway:	n/a
50	chr10:98367715-98367765	HNPCEpiC	eye:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:98344369..98347860-chr10:98359714..98362869,3	MCF-7	breast:
2	chr10:98346216..98350490-chr10:98369688..98376085,7	K562	blood:
3	chr10:98360613..98362809-chr10:98373002..98374950,2	K562	blood:
4	chr10:98376679..98380080-chr10:98381155..98385346,4	MCF-7	breast:
5	chr10:98354342..98356014-chr10:98357344..98358952,2	MCF-7	breast:
6	chr10:98360613..98362809-chr10:98373002..98374950,2	K562	blood:
7	chr10:98352916..98354492-chr10:98357583..98359914,2	K562	blood:
8	chr10:98344788..98348353-chr10:98381480..98384091,4	K562	blood:
9	chr10:98344272..98346550-chr10:98357968..98360744,2	K562	blood:
10	chr10:98372394..98374938-chr10:98530168..98532928,2	MCF-7	breast:
11	chr10:98359371..98362187-chr10:98366935..98369063,2	K562	blood:
12	chr10:98349885..98352079-chr10:98354867..98358726,5	MCF-7	breast:
13	chr10:98345353..98347090-chr10:98380383..98383295,2	K562	blood:
14	chr10:98344931..98348193-chr10:98359191..98361698,3	K562	blood:
15	chr10:98345226..98348138-chr10:98356435..98359434,3	MCF-7	breast:
16	chr10:98345541..98351057-chr10:98372487..98376675,6	K562	blood:
17	chr10:98367008..98370019-chr10:98371148..98375452,4	K562	blood:
18	chr10:98346219..98349334-chr10:98373001..98374910,3	MCF-7	breast:
19	chr10:98376151..98378929-chr10:98479647..98482597,2	K562	blood:
20	chr10:98366804..98369956-chr10:98370785..98374405,6	K562	blood:
21	chr10:98359371..98362187-chr10:98366935..98369063,2	K562	blood:
22	chr10:98347309..98348851-chr10:98354166..98356679,2	K562	blood:
23	chr10:98344232..98346275-chr10:98354019..98356301,2	K562	blood:
24	chr10:98345341..98350021-chr10:98351580..98356203,7	MCF-7	breast:
25	chr10:98354342..98356014-chr10:98357344..98358952,2	MCF-7	breast:
26	chr10:98373312..98375091-chr10:98382282..98385347,3	K562	blood:
27	chr10:98345273..98348471-chr10:98351958..98358343,11	MCF-7	breast:
28	chr10:98345342..98348493-chr10:98363756..98366724,3	K562	blood:
29	chr10:98357043..98359893-chr10:98362984..98364964,2	K562	blood:
30	chr10:98366804..98369956-chr10:98370785..98374405,6	K562	blood:
31	chr10:98376679..98380080-chr10:98381155..98385346,4	MCF-7	breast:
32	chr10:98357043..98359893-chr10:98362984..98364964,2	K562	blood:
33	chr10:98349121..98351177-chr10:98359782..98361320,2	K562	blood:
34	chr10:98367008..98370019-chr10:98371148..98375452,4	K562	blood:
35	chr10:98345726..98350448-chr10:98373759..98376409,5	MCF-7	breast:
36	chr10:98341817..98344367-chr10:98373392..98375014,2	K562	blood:
37	chr10:98346216..98348806-chr10:98369688..98372310,2	K562	blood:
38	chr10:98372033..98373765-chr10:98376062..98378595,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LCOR-3	chr10:98374647-98374849	NONHSAT015825
2	lnc-LCOR-3	chr10:98376776-98377011	NONHSAT015825
3	lnc-TM9SF3-2	chr10:98380634-98381464	NONHSAT015826

No data

Variant related genes	Relation type
ENSG00000227032	TF binding region
PIK3AP1	TF binding region
RNA5SP324	TF binding region
ENSG00000227032	CpG island
PIK3AP1	CpG island
RNA5SP324	CpG island
ENSG00000227032	chromatin interactions
ENSG00000155629	chromatin interactions
ENSG00000077147	chromatin interactions
ENSG00000202047	chromatin interactions

Extended variants
information (count: 1015 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7074516	chr10:98354924-98354925	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187143764	chr10:98354926-98354927	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs569668667	chr10:98354976-98354977	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537056755	chr10:98355059-98355060	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs549030276	chr10:98355114-98355115	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs567441488	chr10:98355138-98355139	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534834321	chr10:98355156-98355157	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553514914	chr10:98355219-98355220	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577943758	chr10:98355225-98355226	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs372080759	chr10:98355292-98355293	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs200758067	chr10:98355297-98355298	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374409007	chr10:98355311-98355312	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201824606	chr10:98355373-98355374	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140404891	chr10:98355374-98355375	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs539312620	chr10:98355440-98355441	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371510754	chr10:98355441-98355442	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs111577025	chr10:98355489-98355490	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375031647	chr10:98355499-98355500	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs557311534	chr10:98355516-98355517	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs192326231	chr10:98355540-98355541	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs574184093	chr10:98355559-98355560	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542804150	chr10:98355561-98355562	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs576068805	chr10:98355596-98355597	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs183483873	chr10:98355627-98355628	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561739883	chr10:98355628-98355629	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188483179	chr10:98355644-98355645	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs540803251	chr10:98355645-98355646	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs559489980	chr10:98355743-98355744	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533026133	chr10:98355751-98355752	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551610889	chr10:98355774-98355775	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs7097291	chr10:98355870-98355871	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs530784896	chr10:98355871-98355872	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142609807	chr10:98355872-98355873	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs193123510	chr10:98355907-98355908	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs75439767	chr10:98355971-98355972	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185543685	chr10:98355983-98355984	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372902935	chr10:98356052-98356053	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs188281000	chr10:98356063-98356064	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191185006	chr10:98356068-98356069	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143382090	chr10:98356074-98356075	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs114526585	chr10:98356098-98356099	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs148307872	chr10:98356105-98356106	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536975278	chr10:98356108-98356109	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113094876	chr10:98356143-98356144	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573597733	chr10:98356145-98356146	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs58936355	chr10:98356315-98356316	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs141409333	chr10:98356328-98356329	Weak transcription Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577221549	chr10:98356432-98356433	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs184143124	chr10:98356449-98356450	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529922179	chr10:98356551-98356552	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:98347400-98358800	Weak transcription	Pancreas	Pancrea
2	chr10:98347800-98365800	Weak transcription	Ovary	ovary
3	chr10:98348000-98373600	Weak transcription	Left Ventricle	heart
4	chr10:98348200-98356200	Weak transcription	Adipose Nuclei	Adipose
5	chr10:98348200-98357800	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr10:98348200-98359000	Weak transcription	Brain Substantia Nigra	brain
7	chr10:98348800-98355200	Weak transcription	HSMMtube	muscle
8	chr10:98349600-98355600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr10:98349800-98355200	Weak transcription	K562	blood
10	chr10:98349800-98366400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr10:98349800-98367800	Weak transcription	Small Intestine	intestine
12	chr10:98350000-98355200	Weak transcription	Stomach Mucosa	stomach
13	chr10:98350800-98395600	Strong transcription	Primary neutrophils fromperipheralblood	blood
14	chr10:98351600-98363400	Weak transcription	Brain Hippocampus Middle	brain
15	chr10:98352400-98357200	Strong transcription	GM12878-XiMat	blood
16	chr10:98352400-98378600	Strong transcription	Liver	Liver
17	chr10:98352400-98399400	Strong transcription	Primary B cells from peripheral blood	blood
18	chr10:98352600-98369400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr10:98352600-98403000	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr10:98353000-98388400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr10:98353000-98403000	Strong transcription	Primary monocytes fromperipheralblood	blood
22	chr10:98353600-98362800	Strong transcription	Primary hematopoietic stem cells	blood
23	chr10:98353800-98355800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr10:98354200-98355200	Strong transcription	Placenta	Placenta
25	chr10:98354200-98360800	Enhancers	Fetal Intestine Large	intestine
26	chr10:98354400-98357000	Enhancers	Fetal Intestine Small	intestine
27	chr10:98354600-98357400	Strong transcription	Spleen	Spleen
28	chr10:98354600-98360800	Strong transcription	Primary B cells from cord blood	blood
29	chr10:98354600-98388600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr10:98354800-98355200	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr10:98354800-98357400	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr10:98354800-98370600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr10:98355200-98355400	Genic enhancers	Sigmoid Colon	Sigmoid Colon
34	chr10:98355200-98355800	Enhancers	K562	blood
35	chr10:98355200-98356000	Genic enhancers	Placenta	Placenta
36	chr10:98355200-98356800	Enhancers	HSMMtube	muscle
37	chr10:98355200-98357600	Enhancers	HepG2	liver
38	chr10:98355200-98360800	Enhancers	Stomach Mucosa	stomach
39	chr10:98355400-98355600	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr10:98355400-98356200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr10:98355600-98355800	Enhancers	Duodenum Mucosa	Duodenum
42	chr10:98355600-98356200	Enhancers	Colonic Mucosa	Colon
43	chr10:98355600-98357400	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr10:98355800-98356000	Enhancers	Gastric	stomach
45	chr10:98355800-98356200	Weak transcription	Duodenum Mucosa	Duodenum
46	chr10:98355800-98356400	Flanking Active TSS	K562	blood
47	chr10:98355800-98357400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr10:98356000-98356200	Enhancers	Placenta	Placenta
49	chr10:98356000-98357000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr10:98356000-98358000	Weak transcription	Gastric	stomach

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