Variant report

Variant	nsv1014394
Chromosome Location	chr3:119360506-119412275
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1358)
CpG islands
(count:1405)
Chromatin interactive
region (count:71)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:119364618-119364967	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:119396340-119396590	HepG2	liver:	n/a	n/a
3	ATF1	chr3:119383818-119384285	K562	blood:	n/a	n/a
4	ATF2	chr3:119381367-119382130	GM12878	blood:	n/a	n/a
5	ATF2	chr3:119396010-119396847	GM12878	blood:	n/a	n/a
6	ATF2	chr3:119395877-119396708	GM12878	blood:	n/a	n/a
7	ATF2	chr3:119396199-119396619	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr3:119396345-119396712	GM12878	blood:	n/a	n/a
9	BATF	chr3:119395983-119396296	GM12878	blood:	n/a	chr3:119396132-119396143
10	BCL3	chr3:119396088-119396722	A549	lung:	n/a	chr3:119396235-119396244
11	BCL3	chr3:119396033-119396688	A549	lung:	n/a	chr3:119396235-119396244
12	BCLAF1	chr3:119395929-119396740	GM12878	blood:	n/a	chr3:119396235-119396244
13	BCLAF1	chr3:119396285-119396736	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:119362024-119362252	K562	blood:	n/a	n/a
15	BHLHE40	chr3:119383660-119383917	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:119395933-119396517	K562	blood:	n/a	n/a
17	BHLHE40	chr3:119386084-119386321	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:119376901-119377016	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:119396120-119396932	GM12878	blood:	n/a	n/a
20	BRCA1	chr3:119393784-119393787	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr3:119368797-119368851	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr3:119395772-119396625	Hela-S3	cervix:	n/a	n/a
23	CBX3	chr3:119396090-119396510	K562	blood:	n/a	n/a
24	CBX3	chr3:119395842-119396684	K562	blood:	n/a	n/a
25	CBX3	chr3:119383903-119384211	K562	blood:	n/a	n/a
26	CCNT2	chr3:119395892-119396167	K562	blood:	n/a	n/a
27	CEBPB	chr3:119362507-119362745	A549	lung:	n/a	n/a
28	CEBPB	chr3:119362423-119362815	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:119396480-119396689	K562	blood:	n/a	n/a
30	CEBPB	chr3:119396355-119396643	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:119408747-119409002	K562	blood:	n/a	n/a
32	CEBPB	chr3:119396168-119396772	GM12878	blood:	n/a	n/a
33	CEBPB	chr3:119396362-119396652	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr3:119368694-119369032	IMR90	lung:	n/a	n/a
35	CEBPB	chr3:119395973-119396124	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:119408860-119409068	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr3:119408865-119409057	A549	lung:	n/a	n/a
38	CEBPB	chr3:119396367-119396677	A549	lung:	n/a	n/a
39	CEBPB	chr3:119368660-119368998	Hela-S3	cervix:	n/a	n/a
40	CEBPZ	chr3:119404012-119404021	HepG2	liver:	n/a	n/a
41	CHD1	chr3:119395527-119396899	GM12878	blood:	n/a	n/a
42	CHD2	chr3:119395638-119396153	K562	blood:	n/a	n/a
43	CHD2	chr3:119396423-119396604	K562	blood:	n/a	n/a
44	CHD2	chr3:119395783-119396500	HepG2	liver:	n/a	n/a
45	CHD2	chr3:119400279-119400353	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr3:119395780-119396613	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr3:119395654-119396561	Hela-S3	cervix:	n/a	n/a
48	CHD2	chr3:119395797-119396649	GM12878	blood:	n/a	n/a
49	CHD2	chr3:119386075-119386365	GM12878	blood:	n/a	n/a
50	CREB1	chr3:119395666-119396760	HepG2	liver:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:119395580-119395630	GM06990	blood:	n/a
2	chr3:119396868-119396918	K562	blood:	n/a
3	chr3:119395580-119395630	GM06990	blood:	n/a
4	chr3:119396868-119396918	K562	blood:	n/a
5	chr3:119396868-119396918	HCM	heart:	n/a
6	chr3:119393058-119393108	MCF-7	breast:	n/a
7	chr3:119396027-119396077	Jurkat	blood:	n/a
8	chr3:119396868-119396918	BJ	skin:	n/a
9	chr3:119379792-119379842	H1-hESC	embryonic stem cell:	embryo
10	chr3:119399324-119399374	A549	lung:	n/a
11	chr3:119361670-119361720	RPTEC	kidney:	n/a
12	chr3:119395580-119395630	HCT-116	colon:	n/a
13	chr3:119395842-119395892	GM12892	blood:	n/a
14	chr3:119396640-119396690	BE2_C	brain:	n/a
15	chr3:119379530-119379580	ProgFib	skin:	n/a
16	chr3:119361179-119361229	PrEC	prostate:	n/a
17	chr3:119396640-119396690	AG10803	skin:	n/a
18	chr3:119379220-119379270	SK-N-SH	brain:	n/a
19	chr3:119396386-119396436	AG04450	lung:	fetal
20	chr3:119379414-119379464	NHBE	bronchial:	n/a
21	chr3:119399324-119399374	U87	brain:	n/a
22	chr3:119367048-119367098	AG09319	gingival:	n/a
23	chr3:119379414-119379464	HPAEpiC	pulmonary alveolar:	n/a
24	chr3:119379414-119379464	HL-60	blood:	n/a
25	chr3:119395580-119395630	AG09309	skin:	n/a
26	chr3:119367048-119367098	NB4	blood:	n/a
27	chr3:119396386-119396436	SK-N-SH_RA	brain:	n/a
28	chr3:119399324-119399374	CMK	blood:	n/a
29	chr3:119396640-119396690	HRE	kidney:	n/a
30	chr3:119381682-119381732	GM12891	blood:	n/a
31	chr3:119361670-119361720	AG09309	skin:	n/a
32	chr3:119361179-119361229	Jurkat	blood:	n/a
33	chr3:119396465-119396515	AG04449	skin:	fetal
34	chr3:119393058-119393108	ECC-1	luminal epithelium:	n/a
35	chr3:119379792-119379842	Hela-S3	cervix:	n/a
36	chr3:119361670-119361720	HCM	heart:	n/a
37	chr3:119367048-119367098	HEEpiC	esophagus:	n/a
38	chr3:119381682-119381732	BJ	skin:	n/a
39	chr3:119396313-119396363	NHDF-neo	bronchial:	n/a
40	chr3:119395842-119395892	HCM	heart:	n/a
41	chr3:119396640-119396690	HL-60	blood:	n/a
42	chr3:119379220-119379270	K562	blood:	n/a
43	chr3:119396309-119396359	NHBE	bronchial:	n/a
44	chr3:119379414-119379464	AG10803	skin:	n/a
45	chr3:119395580-119395630	Jurkat	blood:	n/a
46	chr3:119396640-119396690	AoSMC	blood vessel:	n/a
47	chr3:119395580-119395630	CMK	blood:	n/a
48	chr3:119379220-119379270	Hela-S3	cervix:	n/a
49	chr3:119379530-119379580	MCF-7	breast:	n/a
50	chr3:119361179-119361229	LNCaP	prostate:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:119356916..119358623-chr3:119366628..119369264,2	K562	blood:
2	chr3:119276867..119278435-chr3:119399645..119402371,2	MCF-7	breast:
3	chr3:119040381..119043387-chr3:119393976..119396207,3	K562	blood:
4	chr3:119297880..119300098-chr3:119394986..119397161,3	MCF-7	breast:
5	chr3:119384220..119388638-chr3:119390311..119393902,4	K562	blood:
6	chr3:119371437..119373754-chr3:119392688..119396112,3	K562	blood:
7	chr3:119408612..119410162-chr3:119814493..119816849,2	K562	blood:
8	chr3:118959788..118961472-chr3:119396304..119398038,2	MCF-7	breast:
9	chr3:119396379..119398214-chr3:119398308..119400262,2	MCF-7	breast:
10	chr3:119181316..119183992-chr3:119395288..119397711,2	MCF-7	breast:
11	chr3:119387339..119389333-chr3:119392737..119395674,3	K562	blood:
12	chr3:119375861..119378454-chr3:119387094..119389806,2	K562	blood:
13	chr3:119365198..119367042-chr3:119394724..119396860,2	MCF-7	breast:
14	chr3:119389471..119391263-chr3:119394151..119396440,3	K562	blood:
15	chr3:119383202..119386543-chr3:119393770..119396267,3	MCF-7	breast:
16	chr3:119138626..119139712-chr3:119399725..119401267,5	MCF-7	breast:
17	chr3:119215767..119217677-chr3:119394561..119396315,2	MCF-7	breast:
18	chr3:119396379..119398214-chr3:119398308..119400262,2	MCF-7	breast:
19	chr3:119363598..119365543-chr3:119365969..119367975,2	MCF-7	breast:
20	chr3:119377372..119379623-chr3:119387851..119390487,2	K562	blood:
21	chr3:119375924..119378034-chr3:119380150..119381686,2	K562	blood:
22	chr3:119367081..119370215-chr3:119370341..119373711,3	MCF-7	breast:
23	chr3:119367190..119369718-chr3:119370796..119372691,2	MCF-7	breast:
24	chr3:119366599..119368508-chr3:119385647..119388287,2	MCF-7	breast:
25	chr3:119394727..119396286-chr3:119814089..119815777,2	K562	blood:
26	chr3:119380060..119382164-chr3:119384940..119387375,2	K562	blood:
27	chr3:119374497..119376158-chr3:119382205..119383830,2	K562	blood:
28	chr3:119297190..119298785-chr3:119385064..119387274,2	MCF-7	breast:
29	chr3:119381330..119383043-chr3:119394436..119396057,2	MCF-7	breast:
30	chr3:119391312..119393236-chr3:119393602..119396027,2	K562	blood:
31	chr3:119393569..119396281-chr3:119421855..119424087,2	MCF-7	breast:
32	chr3:119367190..119369718-chr3:119370796..119372691,2	MCF-7	breast:
33	chr3:119383202..119386543-chr3:119393770..119396267,3	MCF-7	breast:
34	chr3:119217361..119219124-chr3:119394788..119396855,3	MCF-7	breast:
35	chr3:119382052..119384819-chr3:119387419..119389641,2	K562	blood:
36	chr3:119380060..119382164-chr3:119384940..119387375,2	K562	blood:
37	chr3:119383319..119384856-chr3:119387419..119389947,2	K562	blood:
38	chr3:119181523..119183291-chr3:119394912..119396579,2	MCF-7	breast:
39	chr3:119371913..119374680-chr3:119377229..119379559,2	MCF-7	breast:
40	chr3:119383346..119386464-chr3:119395342..119399056,3	K562	blood:
41	chr3:119384409..119387165-chr3:119391759..119393266,2	K562	blood:
42	chr3:119374497..119376158-chr3:119382205..119383830,2	K562	blood:
43	chr3:119389108..119393521-chr3:119393632..119397776,6	MCF-7	breast:
44	chr3:119397978..119400630-chr3:119401218..119403216,2	MCF-7	breast:
45	chr3:119328437..119330333-chr3:119390205..119392685,2	K562	blood:
46	chr3:119380893..119382995-chr3:119385609..119387430,2	MCF-7	breast:
47	chr3:119363598..119365543-chr3:119365969..119367975,2	MCF-7	breast:
48	chr3:119243377..119244472-chr3:119399849..119400744,3	MCF-7	breast:
49	chr3:118876250..118878600-chr3:119400821..119403241,2	MCF-7	breast:
50	chr3:119383346..119386464-chr3:119395342..119399056,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf15-1	chr3:119384932-119385285	NONHSAT091400
2	lnc-POPDC2-1	chr3:119384098-119384170	NONHSAT091399
3	lnc-POPDC2-1	chr3:119383296-119383529	NONHSAT091399
4	lnc-POPDC2-1	chr3:119385766-119386938	NONHSAT091399
5	lnc-POPDC2-3	chr3:119390786-119391185	NONHSAT091402
6	lnc-POPDC2-1	chr3:119382857-119383529	NONHSAT091398
7	lnc-POPDC2-3	chr3:119389611-119390692	NONHSAT091402
8	lnc-POPDC2-4	chr3:119388381-119388512	NONHSAT091401
9	lnc-POPDC2-1	chr3:119384336-119384615	NONHSAT091398
10	lnc-POPDC2-4	chr3:119393992-119394424	NONHSAT091401
11	lnc-POPDC2-1	chr3:119384098-119384323	NONHSAT091398
12	lnc-C3orf15-1	chr3:119387108-119387283	NONHSAT091400

No data

Variant related genes	Relation type
COX17	TF binding region
POPDC2	TF binding region
COX17	CpG island
POPDC2	CpG island
ENSG00000121577	chromatin interactions
ENSG00000241155	chromatin interactions
ENSG00000138495	chromatin interactions
ENSG00000121594	chromatin interactions
ENSG00000113845	chromatin interactions
ENSG00000144843	chromatin interactions
ENSG00000183833	chromatin interactions
ENSG00000272967	chromatin interactions
ENSG00000176142	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000121578	chromatin interactions
ENSG00000272662	chromatin interactions

Extended variants
information (count: 1992 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1992 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557021255	chr3:119360507-119360508	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs373379229	chr3:119360513-119360514	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75985224	chr3:119360534-119360535	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552605564	chr3:119360596-119360597	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4687869	chr3:119360621-119360622	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs545639215	chr3:119360624-119360625	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs34787881	chr3:119360651-119360652	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs145590180	chr3:119360710-119360711	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200520738	chr3:119360750-119360751	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568242528	chr3:119360751-119360752	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6792223	chr3:119360867-119360868	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs74660570	chr3:119360890-119360891	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565440482	chr3:119360924-119360925	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539106889	chr3:119360929-119360930	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188973697	chr3:119360942-119360943	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs8422	chr3:119360944-119360945	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs142454286	chr3:119360945-119360946	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556852538	chr3:119360953-119360954	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575024887	chr3:119360970-119360971	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs146467467	chr3:119360974-119360975	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563344022	chr3:119360988-119360989	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560619006	chr3:119361032-119361033	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs151250557	chr3:119361061-119361062	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1728	chr3:119361062-119361063	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564492816	chr3:119361112-119361113	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531765980	chr3:119361179-119361180	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs549891030	chr3:119361244-119361245	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs8007	chr3:119361250-119361251	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs544195649	chr3:119361254-119361255	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs76321131	chr3:119361255-119361256	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs367653448	chr3:119361264-119361265	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547077659	chr3:119361283-119361284	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200006707	chr3:119361287-119361288	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539169025	chr3:119361291-119361292	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143015321	chr3:119361333-119361334	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs201733949	chr3:119361335-119361336	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs151178767	chr3:119361336-119361337	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569398858	chr3:119361409-119361410	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs77900383	chr3:119361412-119361413	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs1985724	chr3:119361415-119361416	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs372475108	chr3:119361452-119361453	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145319889	chr3:119361493-119361494	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567321940	chr3:119361503-119361504	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs78903440	chr3:119361513-119361514	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs535730532	chr3:119361518-119361519	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs554420010	chr3:119361523-119361524	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs572646935	chr3:119361544-119361545	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546395135	chr3:119361556-119361557	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs564603637	chr3:119361562-119361563	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs112071257	chr3:119361567-119361568	Strong transcription Weak transcription Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Glioblastoma multiforme	22286061	CNVD
Neurodevelopmental disorder	22521361	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD

Chromatin state (count:1644 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:119341400-119364600	Weak transcription	Liver	Liver
2	chr3:119349800-119378800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:119352000-119378600	Weak transcription	Thymus	Thymus
4	chr3:119352600-119367000	Weak transcription	Ovary	ovary
5	chr3:119354000-119387600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr3:119355400-119361000	Weak transcription	Pancreas	Pancrea
7	chr3:119356200-119360800	Weak transcription	Brain Hippocampus Middle	brain
8	chr3:119356200-119389000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr3:119356800-119360800	Weak transcription	Aorta	Aorta
10	chr3:119356800-119361400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr3:119356800-119364800	Weak transcription	Stomach Mucosa	stomach
12	chr3:119356800-119390000	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr3:119356800-119391800	Weak transcription	Brain Substantia Nigra	brain
14	chr3:119356800-119391800	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr3:119357200-119361800	Weak transcription	A549	lung
16	chr3:119357200-119383800	Weak transcription	Primary B cells from cord blood	blood
17	chr3:119357800-119360600	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr3:119357800-119360800	Weak transcription	Fetal Muscle Trunk	muscle
19	chr3:119357800-119360800	Weak transcription	Rectal Smooth Muscle	rectum
20	chr3:119357800-119361800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr3:119357800-119366600	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr3:119357800-119367000	Weak transcription	Fetal Intestine Large	intestine
23	chr3:119357800-119386400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr3:119358000-119360800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:119358000-119360800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr3:119358000-119361000	Weak transcription	Right Ventricle	heart
27	chr3:119358000-119361000	Weak transcription	Spleen	Spleen
28	chr3:119358000-119361800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr3:119358000-119361800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr3:119358000-119361800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr3:119358000-119361800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr3:119358000-119361800	Weak transcription	NH-A	brain
33	chr3:119358000-119362000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr3:119358000-119362000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr3:119358000-119371200	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr3:119358000-119390600	Weak transcription	Brain Anterior Caudate	brain
37	chr3:119358000-119391800	Weak transcription	Colonic Mucosa	Colon
38	chr3:119358200-119361200	Weak transcription	NHLF	lung
39	chr3:119358200-119361400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr3:119358200-119361400	Weak transcription	HSMMtube	muscle
41	chr3:119358200-119361600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr3:119358200-119362000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:119358200-119362800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr3:119358200-119366200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr3:119358200-119372600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:119358400-119361000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr3:119358400-119361000	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr3:119358400-119361000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
49	chr3:119358400-119361000	Weak transcription	Right Atrium	heart
50	chr3:119358400-119361200	Weak transcription	HSMM	muscle

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