Variant report

Variant	nsv2840
Chromosome Location	chr2:99116934-99162190
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:659)
CpG islands
(count:427)
Chromatin interactive
region (count:51)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:659 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:99124847-99125621	K562	blood:	n/a	n/a
2	ATF1	chr2:99126282-99126638	K562	blood:	n/a	n/a
3	ATF1	chr2:99124761-99125489	K562	blood:	n/a	n/a
4	BACH1	chr2:99122213-99122279	K562	blood:	n/a	n/a
5	BATF	chr2:99131603-99131873	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:99120905-99120993	K562	blood:	n/a	n/a
7	BHLHE40	chr2:99125930-99125943	K562	blood:	n/a	n/a
8	BHLHE40	chr2:99124732-99125650	K562	blood:	n/a	n/a
9	BHLHE40	chr2:99125122-99125426	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:99126347-99126567	K562	blood:	n/a	n/a
11	BHLHE40	chr2:99134739-99134886	K562	blood:	n/a	n/a
12	BHLHE40	chr2:99129110-99129128	K562	blood:	n/a	n/a
13	BRCA1	chr2:99130331-99130402	GM12878	blood:	n/a	n/a
14	CBX3	chr2:99124714-99125532	K562	blood:	n/a	n/a
15	CCNT2	chr2:99124507-99125578	K562	blood:	n/a	n/a
16	CEBPB	chr2:99125150-99125486	K562	blood:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
17	CEBPB	chr2:99145832-99145924	A549	lung:	n/a	chr2:99145876-99145887
18	CEBPB	chr2:99134464-99134766	H1-hESC	embryonic stem cell:	n/a	chr2:99134640-99134653
19	CEBPB	chr2:99130590-99130917	A549	lung:	n/a	chr2:99130754-99130765
20	CEBPB	chr2:99155396-99155458	A549	lung:	n/a	n/a
21	CEBPB	chr2:99145697-99146044	IMR90	lung:	n/a	chr2:99145876-99145887
22	CEBPB	chr2:99130609-99130909	H1-hESC	embryonic stem cell:	n/a	chr2:99130754-99130765
23	CEBPB	chr2:99130584-99130937	IMR90	lung:	n/a	chr2:99130754-99130765
24	CEBPB	chr2:99155376-99155502	K562	blood:	n/a	n/a
25	CEBPB	chr2:99154962-99155567	IMR90	lung:	n/a	n/a
26	CEBPB	chr2:99130586-99130940	HepG2	liver:	n/a	chr2:99130754-99130765
27	CEBPB	chr2:99143232-99143452	MCF-7	breast:	n/a	n/a
28	CEBPB	chr2:99130507-99131004	ECC-1	luminal epithelium:	n/a	chr2:99130754-99130765
29	CEBPB	chr2:99134413-99134928	MCF-7	breast:	n/a	chr2:99134640-99134653
30	CEBPB	chr2:99145767-99146047	HepG2	liver:	n/a	chr2:99145876-99145887
31	CEBPB	chr2:99134469-99134797	K562	blood:	n/a	chr2:99134640-99134653
32	CEBPB	chr2:99125174-99125506	A549	lung:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
33	CEBPB	chr2:99134493-99134828	HepG2	liver:	n/a	chr2:99134640-99134653
34	CEBPB	chr2:99125128-99125526	IMR90	lung:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
35	CEBPB	chr2:99121398-99121498	HepG2	liver:	n/a	chr2:99121443-99121454
36	CEBPB	chr2:99130540-99130924	ECC-1	luminal epithelium:	n/a	chr2:99130754-99130765
37	CEBPB	chr2:99124721-99125568	K562	blood:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
38	CEBPB	chr2:99125220-99125430	Hela-S3	cervix:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
39	CEBPB	chr2:99145742-99146034	Hela-S3	cervix:	n/a	chr2:99145876-99145887
40	CEBPB	chr2:99130590-99130915	K562	blood:	n/a	chr2:99130754-99130765
41	CEBPB	chr2:99126066-99126613	K562	blood:	n/a	n/a
42	CEBPB	chr2:99125124-99125477	MCF-7	breast:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
43	CEBPB	chr2:99155321-99155492	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:99143284-99143449	HepG2	liver:	n/a	n/a
45	CEBPB	chr2:99145810-99146003	K562	blood:	n/a	chr2:99145876-99145887
46	CEBPB	chr2:99125171-99125509	HepG2	liver:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
47	CEBPB	chr2:99124699-99125576	K562	blood:	n/a	chr2:99125328-99125339 chr2:99125327-99125340
48	CEBPB	chr2:99143299-99143468	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPD	chr2:99124684-99125555	K562	blood:	n/a	chr2:99125327-99125338
50	CEBPD	chr2:99124683-99125533	K562	blood:	n/a	chr2:99125327-99125338

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:99124870-99124920	HMEC	breast:	n/a
2	chr2:99119499-99119549	MCF10A-Er-Src	breast:	n/a
3	chr2:99135471-99135521	GM06990	blood:	n/a
4	chr2:99134857-99134907	HCF	heart:	n/a
5	chr2:99132041-99132091	K562	blood:	n/a
6	chr2:99119499-99119549	GM12891	blood:	n/a
7	chr2:99135014-99135064	SK-N-SH	brain:	n/a
8	chr2:99119499-99119549	GM19239	blood:	n/a
9	chr2:99120630-99120680	AG09319	gingival:	n/a
10	chr2:99132041-99132091	HRPEpiC	eye:	n/a
11	chr2:99120630-99120680	LNCaP	prostate:	n/a
12	chr2:99134857-99134907	RPTEC	kidney:	n/a
13	chr2:99120630-99120680	SK-N-SH	brain:	n/a
14	chr2:99120630-99120680	ovcar-3	ovarian:	n/a
15	chr2:99124870-99124920	Hela-S3	cervix:	n/a
16	chr2:99124870-99124920	NHDF-neo	bronchial:	n/a
17	chr2:99119499-99119549	AG04450	lung:	fetal
18	chr2:99134857-99134907	SK-N-SH_RA	brain:	n/a
19	chr2:99124870-99124920	HAEpiC	amniotic membrane:	n/a
20	chr2:99124870-99124920	A549	lung:	n/a
21	chr2:99134857-99134907	SK-N-MC	brain:	n/a
22	chr2:99135014-99135064	HCT-116	colon:	n/a
23	chr2:99124870-99124920	HNPCEpiC	eye:	n/a
24	chr2:99135471-99135521	U87	brain:	n/a
25	chr2:99135014-99135064	HCM	heart:	n/a
26	chr2:99124870-99124920	HepG2	liver:	n/a
27	chr2:99124870-99124920	NH-A	brain:	n/a
28	chr2:99120630-99120680	Hepatocyte	liver:	n/a
29	chr2:99135014-99135064	AG09309	skin:	n/a
30	chr2:99132041-99132091	PANC-1	pancreas:	n/a
31	chr2:99119499-99119549	Hepatocyte	liver:	n/a
32	chr2:99124870-99124920	NB4	blood:	n/a
33	chr2:99135471-99135521	Jurkat	blood:	n/a
34	chr2:99132041-99132091	Jurkat	blood:	n/a
35	chr2:99135014-99135064	ovcar-3	ovarian:	n/a
36	chr2:99134857-99134907	HMEC	breast:	n/a
37	chr2:99120630-99120680	ProgFib	skin:	n/a
38	chr2:99132041-99132091	HCF	heart:	n/a
39	chr2:99120630-99120680	MCF-7	breast:	n/a
40	chr2:99120630-99120680	CMK	blood:	n/a
41	chr2:99134857-99134907	HCPEpiC	choroid plexus:	n/a
42	chr2:99134857-99134907	GM19239	blood:	n/a
43	chr2:99134857-99134907	GM06990	blood:	n/a
44	chr2:99134857-99134907	K562	blood:	n/a
45	chr2:99119499-99119549	HRE	kidney:	n/a
46	chr2:99135471-99135521	NH-A	brain:	n/a
47	chr2:99119499-99119549	Jurkat	blood:	n/a
48	chr2:99132041-99132091	HL-60	blood:	n/a
49	chr2:99119499-99119549	HCPEpiC	choroid plexus:	n/a
50	chr2:99119499-99119549	Caco-2	colon:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:99108653..99110260-chr2:99120805..99122639,2	K562	blood:
2	chr2:99124298..99126771-chr2:99127183..99129014,2	K562	blood:
3	chr2:99121252..99123677-chr2:99147089..99148766,2	K562	blood:
4	chr2:99155790..99159181-chr2:99223448..99226329,4	MCF-7	breast:
5	chr2:99151217..99153111-chr2:99155244..99157121,2	K562	blood:
6	chr2:99028796..99031072-chr2:99132217..99134716,3	MCF-7	breast:
7	chr2:99089938..99092200-chr2:99129449..99131064,2	K562	blood:
8	chr2:99119306..99122236-chr2:99124547..99127818,4	MCF-7	breast:
9	chr2:99118086..99120077-chr2:99123851..99125912,3	K562	blood:
10	chr2:99136443..99139324-chr2:99146701..99148652,2	K562	blood:
11	chr2:99161541..99164254-chr2:99172596..99174510,2	K562	blood:
12	chr2:99042444..99044574-chr2:99162010..99163835,2	MCF-7	breast:
13	chr2:99160013..99163753-chr2:99164839..99167282,4	K562	blood:
14	chr2:99124187..99127172-chr2:99129019..99132025,3	K562	blood:
15	chr2:99160013..99162321-chr2:99164839..99166505,3	K562	blood:
16	chr2:99096047..99098588-chr2:99150160..99153117,3	K562	blood:
17	chr2:99060131..99062941-chr2:99132482..99135840,4	MCF-7	breast:
18	chr2:99140535..99142504-chr2:99146739..99149511,3	K562	blood:
19	chr2:99119880..99121608-chr2:99124862..99126749,2	MCF-7	breast:
20	chr2:99062866..99063818-chr2:99134237..99134814,3	MCF-7	breast:
21	chr2:99116277..99118383-chr2:99120002..99123147,3	K562	blood:
22	chr2:99104757..99106560-chr2:99122762..99124646,2	K562	blood:
23	chr2:99028450..99030099-chr2:99134152..99135233,24	MCF-7	breast:
24	chr2:99119306..99122236-chr2:99124547..99127818,4	MCF-7	breast:
25	chr2:99119880..99121608-chr2:99124862..99126749,2	MCF-7	breast:
26	chr2:99121740..99124378-chr2:99222432..99225473,3	K562	blood:
27	chr2:99029070..99029723-chr2:99131863..99132507,2	MCF-7	breast:
28	chr2:99061003..99063481-chr2:99139125..99141607,2	MCF-7	breast:
29	chr2:99114971..99120077-chr2:99122258..99125912,6	K562	blood:
30	chr2:99124310..99124811-chr2:128568506..128569006,2	NB4	blood:
31	chr2:99060996..99061880-chr2:99134281..99135202,3	MCF-7	breast:
32	chr2:99129963..99131558-chr2:99133211..99134846,2	MCF-7	breast:
33	chr2:99103835..99106316-chr2:99117856..99120129,2	MCF-7	breast:
34	chr2:99131738..99134767-chr2:99148666..99151301,3	K562	blood:
35	chr2:99060766..99062706-chr2:99117889..99120341,3	MCF-7	breast:
36	chr2:99124187..99127172-chr2:99129019..99132025,3	K562	blood:
37	chr2:99079622..99082074-chr2:99124173..99125944,2	K562	blood:
38	chr2:99104123..99104970-chr2:99134286..99134811,2	MCF-7	breast:
39	chr2:99131738..99134767-chr2:99148666..99151301,3	K562	blood:
40	chr2:99114971..99120077-chr2:99122258..99125912,6	K562	blood:
41	chr2:99157396..99159729-chr2:99164659..99167537,2	MCF-7	breast:
42	chr2:99121252..99123677-chr2:99147089..99148766,2	K562	blood:
43	chr2:99029016..99029537-chr2:99134305..99135036,2	K562	blood:
44	chr2:99116277..99118383-chr2:99120002..99123147,3	K562	blood:
45	chr2:99140535..99142504-chr2:99146739..99149511,3	K562	blood:
46	chr2:99151217..99153111-chr2:99155244..99157121,2	K562	blood:
47	chr2:99097127..99101392-chr2:99116860..99119795,3	MCF-7	breast:
48	chr2:99124298..99126771-chr2:99127183..99129014,2	K562	blood:
49	chr2:99029335..99029944-chr2:99134222..99135159,5	MCF-7	breast:
50	chr2:99118086..99120077-chr2:99123851..99125912,3	K562	blood:

No data

Variant related genes	Relation type
INPP4A	TF binding region
INPP4A	CpG island
ENSG00000136709	chromatin interactions
ENSG00000183513	chromatin interactions
ENSG00000040933	chromatin interactions
ENSG00000115446	chromatin interactions

Extended variants
information (count: 1628 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193198374	chr2:99116940-99116941	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371780318	chr2:99116941-99116942	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs544968537	chr2:99116959-99116960	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535639598	chr2:99117009-99117010	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565210398	chr2:99117015-99117016	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77931525	chr2:99117048-99117049	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs550714931	chr2:99117049-99117050	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561086502	chr2:99117052-99117053	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185122168	chr2:99117057-99117058	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372203719	chr2:99117087-99117088	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs546726018	chr2:99117088-99117089	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs566466778	chr2:99117108-99117109	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3835898	chr2:99117112-99117113	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs532181207	chr2:99117160-99117161	Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs138898289	chr2:99117284-99117285	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569570162	chr2:99117395-99117396	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs375272268	chr2:99117487-99117488	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538172871	chr2:99117498-99117499	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554717424	chr2:99117505-99117506	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568320503	chr2:99117519-99117520	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs9308809	chr2:99117526-99117527	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553891671	chr2:99117528-99117529	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576801942	chr2:99117534-99117535	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs546210376	chr2:99117545-99117546	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376843183	chr2:99117546-99117547	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs141949665	chr2:99117555-99117556	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544181602	chr2:99117639-99117640	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561022487	chr2:99117673-99117674	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557755383	chr2:99117721-99117722	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372948135	chr2:99117745-99117746	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559021179	chr2:99117762-99117763	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113596202	chr2:99117796-99117797	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75437600	chr2:99117797-99117798	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs367971561	chr2:99117834-99117835	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529956359	chr2:99117867-99117868	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs78466244	chr2:99117873-99117874	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189973603	chr2:99117895-99117896	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531996627	chr2:99117939-99117940	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs533307400	chr2:99117992-99117993	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs201126376	chr2:99117998-99117999	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs568783643	chr2:99118003-99118004	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs76362434	chr2:99118005-99118006	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs199626810	chr2:99118006-99118007	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548483728	chr2:99118126-99118127	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568309937	chr2:99118241-99118242	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534172596	chr2:99118244-99118245	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146302255	chr2:99118296-99118297	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139736537	chr2:99118318-99118319	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556030023	chr2:99118342-99118343	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539569188	chr2:99118353-99118354	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Glioblastoma multiforme	21138945	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1550 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99072600-99119600	Weak transcription	Aorta	Aorta
2	chr2:99100400-99121600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:99101600-99121200	Weak transcription	Gastric	stomach
4	chr2:99101600-99131400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:99102200-99122200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:99103600-99118400	Weak transcription	HSMMtube	muscle
7	chr2:99104000-99118400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:99105200-99120400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr2:99106800-99119600	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr2:99106800-99119800	Weak transcription	Pancreas	Pancrea
11	chr2:99108000-99120200	Weak transcription	Esophagus	oesophagus
12	chr2:99108200-99118400	Weak transcription	Brain Angular Gyrus	brain
13	chr2:99111000-99118800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:99111600-99118400	Weak transcription	Right Atrium	heart
15	chr2:99111600-99118400	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr2:99111800-99118200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:99111800-99121200	Weak transcription	K562	blood
18	chr2:99112000-99118400	Weak transcription	Rectal Smooth Muscle	rectum
19	chr2:99112200-99130600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr2:99112400-99118600	Weak transcription	Colon Smooth Muscle	Colon
21	chr2:99112800-99117200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:99112800-99118400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr2:99113400-99118800	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr2:99113600-99117800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr2:99113600-99118600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr2:99113600-99123600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr2:99114000-99117400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr2:99114000-99118000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:99114000-99119400	Weak transcription	Fetal Muscle Leg	muscle
30	chr2:99114000-99119600	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr2:99114000-99120000	Weak transcription	Dnd41	blood
32	chr2:99114000-99124200	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr2:99114000-99137600	Weak transcription	Fetal Intestine Large	intestine
34	chr2:99114200-99118200	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr2:99114200-99118600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr2:99114400-99121200	Weak transcription	Fetal Intestine Small	intestine
37	chr2:99114400-99123400	Weak transcription	Brain Germinal Matrix	brain
38	chr2:99114400-99131200	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:99114400-99154000	Weak transcription	HepG2	liver
40	chr2:99114600-99118600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr2:99114600-99120000	Weak transcription	Liver	Liver
42	chr2:99114800-99117000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr2:99114800-99117000	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr2:99114800-99117200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
45	chr2:99114800-99120000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:99115000-99117200	Enhancers	Fetal Kidney	kidney
47	chr2:99115000-99117400	Genic enhancers	Primary T cells from cord blood	blood
48	chr2:99115000-99118000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr2:99115000-99119600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:99115000-99135000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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