Variant report

Variant	esv2762359
Chromosome Location	chr3:162961220-163350596
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1328)
CpG islands
(count:244)
Chromatin interactive
region (count:100)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1328 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:163005669-163005678	K562	blood:	n/a	n/a
2	ATF1	chr3:163194056-163194256	K562	blood:	n/a	n/a
3	ATF1	chr3:163267915-163268115	K562	blood:	n/a	n/a
4	BACH1	chr3:163332402-163332473	K562	blood:	n/a	n/a
5	BATF	chr3:163262663-163262812	GM12878	blood:	n/a	chr3:163262754-163262765
6	BCL11A	chr3:163035507-163035684	GM12878	blood:	n/a	n/a
7	BCL3	chr3:163247171-163247356	K562	blood:	n/a	n/a
8	BCLAF1	chr3:163217558-163219570	K562	blood:	n/a	n/a
9	BCLAF1	chr3:163220154-163220822	K562	blood:	n/a	n/a
10	BRCA1	chr3:163340493-163340554	GM12878	blood:	n/a	n/a
11	BRCA1	chr3:163239302-163239458	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr3:163261385-163261850	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr3:163207996-163208446	HCT-116	colon:	n/a	n/a
14	CBX3	chr3:163053313-163053625	K562	blood:	n/a	n/a
15	CBX3	chr3:163053325-163053544	K562	blood:	n/a	n/a
16	CBX3	chr3:163207943-163208459	HCT-116	colon:	n/a	n/a
17	CBX3	chr3:163024140-163024571	HCT-116	colon:	n/a	n/a
18	CCNT2	chr3:163231805-163232070	K562	blood:	n/a	n/a
19	CCNT2	chr3:163216821-163217005	K562	blood:	n/a	n/a
20	CCNT2	chr3:163113728-163113917	K562	blood:	n/a	n/a
21	CEBPB	chr3:162995031-162995257	A549	lung:	n/a	chr3:162995163-162995176
22	CEBPB	chr3:163221456-163221672	K562	blood:	n/a	n/a
23	CEBPB	chr3:163324771-163325088	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:163244526-163244636	H1-hESC	embryonic stem cell:	n/a	chr3:163244583-163244596
25	CEBPB	chr3:163340283-163340503	K562	blood:	n/a	n/a
26	CEBPB	chr3:163156621-163156876	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:163097193-163097391	A549	lung:	n/a	chr3:163097277-163097288
28	CEBPB	chr3:163263802-163263923	K562	blood:	n/a	chr3:163263862-163263875
29	CEBPB	chr3:163244151-163244872	Hela-S3	cervix:	n/a	chr3:163244583-163244596
30	CEBPB	chr3:163163503-163163772	A549	lung:	n/a	n/a
31	CEBPB	chr3:163156603-163156994	MCF-7	breast:	n/a	n/a
32	CEBPB	chr3:163156613-163156901	A549	lung:	n/a	n/a
33	CEBPB	chr3:163324840-163325091	A549	lung:	n/a	n/a
34	CEBPB	chr3:163135827-163136125	HepG2	liver:	n/a	chr3:163135991-163136002 chr3:163135992-163136001 chr3:163135992-163136001
35	CEBPB	chr3:163340325-163340525	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:163342743-163342808	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:163261340-163262144	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:163156609-163156913	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:163221525-163221686	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:163214208-163214544	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:163324781-163325109	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:163241318-163241709	Hela-S3	cervix:	n/a	chr3:163241521-163241532
43	CEBPB	chr3:163171743-163171942	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr3:163097121-163097403	K562	blood:	n/a	chr3:163097277-163097288
45	CEBPB	chr3:163340132-163340617	MCF-7	breast:	n/a	n/a
46	CEBPB	chr3:163077613-163077856	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:163277868-163279533	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr3:163293198-163293407	HepG2	liver:	n/a	chr3:163293253-163293264 chr3:163293253-163293266 chr3:163293280-163293291
49	CEBPB	chr3:163004717-163004994	IMR90	lung:	n/a	chr3:163004841-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004841-163004850 chr3:163004841-163004850 chr3:163004839-163004852 chr3:163004839-163004852 chr3:163004839-163004850
50	CEBPB	chr3:163308305-163308535	K562	blood:	n/a	chr3:163308420-163308432

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:163216910-163216960	K562	blood:	n/a
2	chr3:163021378-163021428	SK-N-SH_RA	brain:	n/a
3	chr3:163216910-163216960	HUVEC	blood vessel:	n/a
4	chr3:163216910-163216960	GM19239	blood:	n/a
5	chr3:163269462-163269512	Caco-2	colon:	n/a
6	chr3:163269462-163269512	Hepatocyte	liver:	n/a
7	chr3:163021378-163021428	SK-N-SH	brain:	n/a
8	chr3:163270483-163270533	SK-N-SH_RA	brain:	n/a
9	chr3:163216910-163216960	HL-60	blood:	n/a
10	chr3:163021378-163021428	AG04450	lung:	fetal
11	chr3:163270483-163270533	HUVEC	blood vessel:	n/a
12	chr3:163269462-163269512	HRPEpiC	eye:	n/a
13	chr3:163021378-163021428	PrEC	prostate:	n/a
14	chr3:163270483-163270533	H1-hESC	embryonic stem cell:	embryo
15	chr3:163216910-163216960	HRCEpiC	kidney:	n/a
16	chr3:163021378-163021428	NH-A	brain:	n/a
17	chr3:163216910-163216960	Jurkat	blood:	n/a
18	chr3:163216910-163216960	ProgFib	skin:	n/a
19	chr3:163021378-163021428	SKMC	muscle:	n/a
20	chr3:163021378-163021428	AG09319	gingival:	n/a
21	chr3:163021378-163021428	AG10803	skin:	n/a
22	chr3:163269462-163269512	Jurkat	blood:	n/a
23	chr3:163270483-163270533	GM12891	blood:	n/a
24	chr3:163270483-163270533	PrEC	prostate:	n/a
25	chr3:163216910-163216960	SK-N-MC	brain:	n/a
26	chr3:163216910-163216960	HCT-116	colon:	n/a
27	chr3:163270483-163270533	GM19239	blood:	n/a
28	chr3:163021378-163021428	HIPEpiC	eye:	n/a
29	chr3:163270483-163270533	NH-A	brain:	n/a
30	chr3:163021378-163021428	ProgFib	skin:	n/a
31	chr3:163270483-163270533	HPAEpiC	pulmonary alveolar:	n/a
32	chr3:163216910-163216960	AG04450	lung:	fetal
33	chr3:163216910-163216960	RPTEC	kidney:	n/a
34	chr3:163021378-163021428	Hepatocyte	liver:	n/a
35	chr3:163270483-163270533	RPTEC	kidney:	n/a
36	chr3:163216910-163216960	HEK293	kidney:	embryo
37	chr3:163021378-163021428	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:163270483-163270533	PFSK-1	brain:	n/a
39	chr3:163021378-163021428	HCT-116	colon:	n/a
40	chr3:163216910-163216960	H1-hESC	embryonic stem cell:	embryo
41	chr3:163270483-163270533	HIPEpiC	eye:	n/a
42	chr3:163269462-163269512	HIPEpiC	eye:	n/a
43	chr3:163269462-163269512	HCM	heart:	n/a
44	chr3:163216910-163216960	IMR90	lung:	fetal
45	chr3:163021378-163021428	HCPEpiC	choroid plexus:	n/a
46	chr3:163269462-163269512	BE2_C	brain:	n/a
47	chr3:163269462-163269512	ProgFib	skin:	n/a
48	chr3:163216910-163216960	NB4	blood:	n/a
49	chr3:163270483-163270533	SK-N-MC	brain:	n/a
50	chr3:163216910-163216960	HRPEpiC	eye:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:163272392..163273925-chr3:163274947..163276664,2	K562	blood:
2	chr3:163093927..163096694-chr3:163097446..163100303,3	K562	blood:
3	chr3:163204667..163207682-chr3:163209349..163211725,3	K562	blood:
4	chr3:163056333..163058966-chr3:163059531..163061180,3	K562	blood:
5	chr3:163098893..163101155-chr3:163335067..163337245,2	K562	blood:
6	chr3:163056333..163058966-chr3:163059531..163061180,3	K562	blood:
7	chr3:163193836..163194683-chr3:163339947..163340824,6	MCF-7	breast:
8	chr3:163213538..163215501-chr3:163219578..163221117,2	K562	blood:
9	chr3:163250811..163253608-chr3:163262373..163264339,2	K562	blood:
10	chr3:163216437..163219618-chr3:163219745..163223215,4	K562	blood:
11	chr3:163090274..163091850-chr3:163098856..163100455,2	K562	blood:
12	chr3:163193915..163194594-chr3:163339922..163340818,3	MCF-7	breast:
13	chr3:163230380..163232923-chr3:163236002..163238220,2	K562	blood:
14	chr3:163244079..163246070-chr3:163322398..163324984,2	MCF-7	breast:
15	chr3:162774415..162775478-chr3:163207241..163208645,5	MCF-7	breast:
16	chr3:163208497..163210817-chr3:163211089..163213660,2	K562	blood:
17	chr16:17545591..17546532-chr3:163096602..163097414,2	MCF-7	breast:
18	chr3:163217040..163218685-chr3:163234333..163236869,2	K562	blood:
19	chr3:163267923..163271361-chr3:163273489..163277862,5	K562	blood:
20	chr3:163227245..163228768-chr3:163230069..163232558,2	MCF-7	breast:
21	chr3:163267923..163271361-chr3:163273489..163277862,5	K562	blood:
22	chr3:163213538..163215501-chr3:163219578..163221117,2	K562	blood:
23	chr3:163098893..163101155-chr3:163335067..163337245,2	K562	blood:
24	chr3:162973215..162973789-chr3:163207913..163208691,2	MCF-7	breast:
25	chr3:163207821..163208574-chr3:163340096..163340824,2	MCF-7	breast:
26	chr3:163261473..163265718-chr3:163265860..163268345,3	K562	blood:
27	chr3:163193915..163194594-chr3:163339922..163340818,3	MCF-7	breast:
28	chr3:163272392..163273925-chr3:163274947..163276664,2	K562	blood:
29	chr3:163235931..163238963-chr3:163240600..163242314,3	K562	blood:
30	chr3:163271731..163274404-chr3:163278013..163279806,2	K562	blood:
31	chr3:162965564..162967593-chr3:162971986..162973917,2	K562	blood:
32	chr3:163266767..163268587-chr3:163269344..163271343,2	K562	blood:
33	chr3:163271731..163274404-chr3:163278013..163279806,2	K562	blood:
34	chr3:163153075..163155845-chr3:163158514..163160684,2	K562	blood:
35	chr3:163236766..163238963-chr3:163240046..163242119,2	K562	blood:
36	chr3:163208497..163210817-chr3:163211089..163213660,2	K562	blood:
37	chr3:163259280..163261541-chr3:163262492..163264749,2	K562	blood:
38	chr3:163099881..163101461-chr3:163102597..163105467,2	K562	blood:
39	chr3:163296408..163298794-chr3:163316972..163318704,2	K562	blood:
40	chr3:163266767..163268587-chr3:163269344..163271343,2	K562	blood:
41	chr3:163228792..163232819-chr3:163240810..163244604,3	K562	blood:
42	chr3:163216437..163219618-chr3:163219745..163223215,4	K562	blood:
43	chr3:163259280..163261541-chr3:163262492..163264749,2	K562	blood:
44	chr3:163105916..163108059-chr3:163125965..163128652,2	K562	blood:
45	chr3:163230237..163233801-chr3:163239062..163243391,4	K562	blood:
46	chr3:163267923..163270791-chr3:163274503..163276060,2	K562	blood:
47	chr3:163193836..163194683-chr3:163339947..163340824,6	MCF-7	breast:
48	chr10:69265595..69266499-chr3:162973315..162973821,2	MCF-7	breast:
49	chr3:163252335..163254174-chr3:163256755..163258981,2	MCF-7	breast:
50	chr3:163099881..163101461-chr3:163102597..163105467,2	K562	blood:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOL1-10	chr3:163031456-163031501	NONHSAT093040
2	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
3	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
4	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
5	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
6	lnc-OTOL1-3	chr3:163192855-163192939	XLOC_002898
7	lnc-SI-4	chr3:163021026-163021105	ENSG00000241369
8	lnc-SI-4	chr3:163020984-163021076	ENSG00000241369
9	lnc-SI-4	chr3:163021026-163021089	ENSG00000241369
10	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
11	lnc-SI-4	chr3:163021026-163021110	ENSG00000241369
12	lnc-SI-4	chr3:162967053-162967162	ENSG00000241369
13	lnc-OTOL1-10	chr3:163021583-163022065	NONHSAT093040
14	lnc-SI-4	chr3:163079232-163079351	ENSG00000241369
15	lnc-OTOL1-3	chr3:163196490-163197153	XLOC_002898
16	lnc-SI-4	chr3:163054933-163055024	ENSG00000241369
17	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
18	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
19	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
20	lnc-SI-4	chr3:162992984-162993107	ENSG00000241369
21	lnc-SI-4	chr3:162996298-162996391	ENSG00000241369
22	lnc-SI-4	chr3:162996298-162996361	ENSG00000241369
23	lnc-SI-4	chr3:163021026-163021103	ENSG00000241369

No data

Variant related genes	Relation type
ENSG00000265090	TF binding region
CT64	TF binding region
ENSG00000240792	TF binding region
ENSG00000265090	CpG island
CT64	CpG island
ENSG00000240792	CpG island
ENSG00000265090	chromatin interactions
ENSG00000241369	chromatin interactions
MEOX2	miRNA target sites

Extended variants
information (count: 3878 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3878 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544729077	chr3:162967130-162967131	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs564520736	chr3:162967150-162967151	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs559771562	chr3:162975800-162975801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs115174184	chr3:162975821-162975822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542347142	chr3:162975830-162975831	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs843056	chr3:162975865-162975866	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs548080061	chr3:162975867-162975868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs190275384	chr3:162975889-162975890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549618281	chr3:162975924-162975925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139008831	chr3:162975965-162975966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373967755	chr3:162975993-162975994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565362745	chr3:162975997-162975998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7627386	chr3:162976011-162976012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552064695	chr3:162976012-162976013	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565899835	chr3:162976014-162976015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192747877	chr3:162976031-162976032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376857568	chr3:162976037-162976038	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145908124	chr3:162976055-162976056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537051026	chr3:162976124-162976125	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs843057	chr3:162976133-162976134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs184121076	chr3:162976178-162976179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6804797	chr3:162993012-162993013	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs140295187	chr3:162993040-162993041	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs545770618	chr3:162993080-162993081	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs535777135	chr3:162993103-162993104	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs1529366	chr3:162996318-162996319	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs367765403	chr3:162996386-162996387	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs145097998	chr3:163011622-163011623	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs199684730	chr3:163011629-163011630	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs569635358	chr3:163011632-163011633	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535152207	chr3:163011635-163011636	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs548951071	chr3:163011642-163011643	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs1688525	chr3:163011679-163011680	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs116412569	chr3:163011695-163011696	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs528550825	chr3:163011703-163011704	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548305459	chr3:163011743-163011744	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189445109	chr3:163011754-163011755	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537013891	chr3:163011755-163011756	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs34745202	chr3:163011757-163011758	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148928982	chr3:163011770-163011771	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs116121730	chr3:163011779-163011780	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145389648	chr3:163011829-163011830	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529415627	chr3:163011858-163011859	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558465196	chr3:163011859-163011860	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572303060	chr3:163011896-163011897	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181327078	chr3:163011947-163011948	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534683202	chr3:163011968-163011969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs554674187	chr3:163012011-163012012	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375819466	chr3:163012025-163012026	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547849667	chr3:163012031-163012032	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Breast cancer	21364760	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioblastoma multiforme	21138945	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162975800-162976200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr3:163065600-163066400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr3:163065600-163066800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr3:163079000-163079600	Active TSS	Hela-S3	cervix
5	chr3:163085200-163085800	Enhancers	Aorta	Aorta
6	chr3:163086600-163086800	Enhancers	Adipose Nuclei	Adipose
7	chr3:163086800-163087400	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr3:163101600-163102800	Enhancers	Dnd41	blood
9	chr3:163103400-163104200	Active TSS	K562	blood
10	chr3:163108600-163109000	Enhancers	Adipose Nuclei	Adipose
11	chr3:163108800-163110400	Enhancers	Dnd41	blood
12	chr3:163136000-163144200	Weak transcription	Aorta	Aorta
13	chr3:163144200-163144400	ZNF genes & repeats	Aorta	Aorta
14	chr3:163156800-163157400	Enhancers	Adipose Nuclei	Adipose
15	chr3:163166400-163168600	Weak transcription	Aorta	Aorta
16	chr3:163168600-163169400	ZNF genes & repeats	Aorta	Aorta
17	chr3:163169400-163179400	Weak transcription	Aorta	Aorta
18	chr3:163171800-163172000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:163172800-163173200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr3:163172800-163173400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr3:163176600-163177000	Enhancers	Hela-S3	cervix
22	chr3:163177000-163177400	Active TSS	Hela-S3	cervix
23	chr3:163179200-163180000	Enhancers	Adipose Nuclei	Adipose
24	chr3:163179400-163180000	Enhancers	Aorta	Aorta
25	chr3:163210600-163211600	Enhancers	Hela-S3	cervix
26	chr3:163211600-163214200	Weak transcription	Hela-S3	cervix
27	chr3:163214200-163214600	Active TSS	Hela-S3	cervix
28	chr3:163214200-163220800	Active TSS	K562	blood
29	chr3:163216400-163216800	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr3:163216400-163217200	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr3:163220800-163235400	Weak transcription	K562	blood
32	chr3:163226200-163226600	Enhancers	Hela-S3	cervix
33	chr3:163226600-163229200	Weak transcription	Hela-S3	cervix
34	chr3:163227400-163227600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr3:163227800-163228000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr3:163229200-163229600	Enhancers	Hela-S3	cervix
37	chr3:163229600-163231000	Weak transcription	Hela-S3	cervix
38	chr3:163231000-163231200	Flanking Active TSS	Hela-S3	cervix
39	chr3:163231000-163231800	Enhancers	Dnd41	blood
40	chr3:163231200-163232400	Active TSS	Hela-S3	cervix
41	chr3:163232400-163234000	Weak transcription	Hela-S3	cervix
42	chr3:163234000-163235200	Active TSS	Hela-S3	cervix
43	chr3:163235200-163235400	Weak transcription	Hela-S3	cervix
44	chr3:163235400-163236600	Enhancers	Hela-S3	cervix
45	chr3:163236000-163236800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:163236600-163236800	Flanking Active TSS	Hela-S3	cervix
47	chr3:163236800-163237000	Genic enhancers	Hela-S3	cervix
48	chr3:163237000-163239200	Weak transcription	Hela-S3	cervix
49	chr3:163239200-163239400	Flanking Active TSS	Hela-S3	cervix
50	chr3:163239400-163239800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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