Variant report

Variant	nsv911262
Chromosome Location	chr19:18288947-18312453
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:983)
CpG islands
(count:1161)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:983 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:18302779-18303107	K562	blood:	n/a	n/a
2	ARID3A	chr19:18302864-18303025	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:18303448-18303993	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:18303457-18304022	K562	blood:	n/a	n/a
5	ATF1	chr19:18303476-18304169	K562	blood:	n/a	n/a
6	ATF2	chr19:18303392-18304210	GM12878	blood:	n/a	n/a
7	ATF2	chr19:18302561-18303045	GM12878	blood:	n/a	n/a
8	ATF2	chr19:18291674-18292047	GM12878	blood:	n/a	n/a
9	ATF3	chr19:18303606-18304326	K562	blood:	n/a	chr19:18304042-18304051
10	BACH1	chr19:18304971-18305171	K562	blood:	n/a	n/a
11	BACH1	chr19:18304092-18304538	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr19:18305543-18305590	K562	blood:	n/a	n/a
13	BCLAF1	chr19:18302700-18303326	GM12878	blood:	n/a	n/a
14	BCLAF1	chr19:18291701-18292074	GM12878	blood:	n/a	n/a
15	BCLAF1	chr19:18303951-18304238	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:18291846-18291878	GM12878	blood:	n/a	n/a
17	BHLHE40	chr19:18304892-18304985	K562	blood:	n/a	n/a
18	BHLHE40	chr19:18305271-18305996	K562	blood:	n/a	n/a
19	BHLHE40	chr19:18303177-18303849	K562	blood:	n/a	n/a
20	BHLHE40	chr19:18303608-18304071	GM12878	blood:	n/a	n/a
21	BHLHE40	chr19:18304134-18304178	K562	blood:	n/a	n/a
22	BHLHE40	chr19:18305755-18305938	GM12878	blood:	n/a	n/a
23	BRCA1	chr19:18303551-18304145	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr19:18303639-18303791	HepG2	liver:	n/a	n/a
25	BRCA1	chr19:18303608-18303907	GM12878	blood:	n/a	n/a
26	CBX3	chr19:18296624-18296933	K562	blood:	n/a	n/a
27	CBX3	chr19:18303184-18304081	K562	blood:	n/a	n/a
28	CCNT2	chr19:18303541-18304385	K562	blood:	n/a	chr19:18303746-18303755
29	CEBPB	chr19:18300533-18300794	K562	blood:	n/a	chr19:18300705-18300716
30	CEBPB	chr19:18303437-18304023	IMR90	lung:	n/a	n/a
31	CEBPB	chr19:18303486-18303697	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:18302718-18303795	GM12878	blood:	n/a	n/a
33	CEBPB	chr19:18303448-18304059	HepG2	liver:	n/a	n/a
34	CEBPB	chr19:18300589-18300789	K562	blood:	n/a	chr19:18300705-18300716
35	CEBPB	chr19:18302743-18303043	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:18303443-18304044	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:18300587-18300793	HepG2	liver:	n/a	chr19:18300705-18300716
38	CEBPB	chr19:18303341-18304027	K562	blood:	n/a	n/a
39	CEBPB	chr19:18303706-18303874	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:18303406-18304021	K562	blood:	n/a	n/a
41	CEBPB	chr19:18302870-18302888	IMR90	lung:	n/a	n/a
42	CEBPB	chr19:18303407-18304070	MCF-7	breast:	n/a	n/a
43	CEBPB	chr19:18303454-18304009	A549	lung:	n/a	n/a
44	CEBPB	chr19:18303421-18304068	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr19:18303511-18303886	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPD	chr19:18303920-18304272	HepG2	liver:	n/a	n/a
47	CEBPD	chr19:18303449-18303778	HepG2	liver:	n/a	n/a
48	CEBPD	chr19:18300629-18300890	HepG2	liver:	n/a	n/a
49	CEBPZ	chr19:18303565-18304087	HepG2	liver:	n/a	n/a
50	CHD1	chr19:18304111-18304306	GM12878	blood:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:18311216-18311266	HepG2	liver:	n/a
2	chr19:18303626-18303676	GM06990	blood:	n/a
3	chr19:18311216-18311266	HepG2	liver:	n/a
4	chr19:18303626-18303676	GM06990	blood:	n/a
5	chr19:18304045-18304095	GM12878	blood:	n/a
6	chr19:18307048-18307098	T-47D	breast:	n/a
7	chr19:18304032-18304082	HCF	heart:	n/a
8	chr19:18303893-18303943	A549	lung:	n/a
9	chr19:18303865-18303915	HCF	heart:	n/a
10	chr19:18304286-18304336	HUVEC	blood vessel:	n/a
11	chr19:18303124-18303174	SK-N-MC	brain:	n/a
12	chr19:18304398-18304448	HIPEpiC	eye:	n/a
13	chr19:18304398-18304448	HL-60	blood:	n/a
14	chr19:18311216-18311266	HAEpiC	amniotic membrane:	n/a
15	chr19:18304045-18304095	Caco-2	colon:	n/a
16	chr19:18303124-18303174	HAEpiC	amniotic membrane:	n/a
17	chr19:18304032-18304082	PFSK-1	brain:	n/a
18	chr19:18304042-18304092	PrEC	prostate:	n/a
19	chr19:18311216-18311266	Hela-S3	cervix:	n/a
20	chr19:18303893-18303943	ovcar-3	ovarian:	n/a
21	chr19:18303124-18303174	HRCEpiC	kidney:	n/a
22	chr19:18304398-18304448	HCT-116	colon:	n/a
23	chr19:18303865-18303915	BJ	skin:	n/a
24	chr19:18304530-18304580	PFSK-1	brain:	n/a
25	chr19:18304045-18304095	GM12892	blood:	n/a
26	chr19:18303626-18303676	BJ	skin:	n/a
27	chr19:18304530-18304580	SK-N-MC	brain:	n/a
28	chr19:18303893-18303943	HL-60	blood:	n/a
29	chr19:18308021-18308071	HUVEC	blood vessel:	n/a
30	chr19:18307048-18307098	HCPEpiC	choroid plexus:	n/a
31	chr19:18304042-18304092	NHBE	bronchial:	n/a
32	chr19:18304398-18304448	HCF	heart:	n/a
33	chr19:18304398-18304448	A549	lung:	n/a
34	chr19:18307048-18307098	SK-N-SH	brain:	n/a
35	chr19:18303124-18303174	HEEpiC	esophagus:	n/a
36	chr19:18307048-18307098	HUVEC	blood vessel:	n/a
37	chr19:18307048-18307098	Caco-2	colon:	n/a
38	chr19:18308021-18308071	NHBE	bronchial:	n/a
39	chr19:18304398-18304448	HCPEpiC	choroid plexus:	n/a
40	chr19:18303624-18303674	Caco-2	colon:	n/a
41	chr19:18303893-18303943	PrEC	prostate:	n/a
42	chr19:18304286-18304336	ECC-1	luminal epithelium:	n/a
43	chr19:18304398-18304448	SK-N-SH	brain:	n/a
44	chr19:18304286-18304336	GM06990	blood:	n/a
45	chr19:18303849-18303899	SK-N-SH	brain:	n/a
46	chr19:18303626-18303676	U87	brain:	n/a
47	chr19:18303626-18303676	GM12891	blood:	n/a
48	chr19:18304530-18304580	PrEC	prostate:	n/a
49	chr19:18304042-18304092	HRPEpiC	eye:	n/a
50	chr19:18300773-18300823	GM12878	blood:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:18302080..18305763-chr19:18333769..18336252,4	K562	blood:
2	chr19:18275085..18277218-chr19:18301566..18304039,2	K562	blood:
3	chr19:18303589..18305920-chr19:18390305..18393671,4	K562	blood:
4	chr19:18272224..18273796-chr19:18288060..18290729,2	K562	blood:
5	chr19:18295110..18297534-chr19:18303888..18305642,2	K562	blood:
6	chr19:18301148..18305001-chr19:18389528..18394862,10	MCF-7	breast:
7	chr19:18301435..18303273-chr19:18392277..18393876,2	K562	blood:
8	chr19:18304348..18305156-chr19:18313206..18314123,2	K562	blood:
9	chr19:18302642..18303148-chr19:18362353..18362883,2	MCF-7	breast:
10	chr19:18283035..18288338-chr19:18301660..18307351,8	K562	blood:
11	chr19:18262556..18266763-chr19:18301801..18307197,7	K562	blood:
12	chr19:18110949..18114806-chr19:18305445..18308231,3	MCF-7	breast:
13	chr19:18302057..18307216-chr19:18311605..18315914,14	MCF-7	breast:
14	chr19:18261707..18265058-chr19:18302365..18306548,5	K562	blood:
15	chr19:18304435..18306025-chr19:18527889..18530586,2	K562	blood:
16	chr19:18282590..18284654-chr19:18287591..18290357,2	K562	blood:
17	chr19:18301872..18305883-chr19:18307026..18310830,7	K562	blood:
18	chr19:18301873..18308921-chr19:18309874..18315133,13	MCF-7	breast:
19	chr19:18302931..18304464-chr19:18547111..18549483,2	K562	blood:
20	chr19:18301633..18303907-chr19:18432550..18435095,2	MCF-7	breast:
21	chr19:18263401..18266218-chr19:18302169..18305024,2	MCF-7	breast:
22	chr19:18302575..18305285-chr19:18390568..18392250,2	MCF-7	breast:
23	chr19:18287723..18291034-chr19:18291646..18293887,3	K562	blood:
24	chr19:18278665..18280705-chr19:18302559..18305155,2	K562	blood:
25	chr19:18268586..18275019-chr19:18302013..18308723,7	MCF-7	breast:
26	chr19:18303831..18304563-chr7:117823865..117824765,2	Hela-S3	cervix:
27	chr19:18302289..18309850-chr19:18311214..18320810,23	K562	blood:
28	chr19:18300044..18302631-chr19:18389476..18391618,2	K562	blood:
29	chr19:18304140..18306823-chr19:18518548..18520720,2	K562	blood:
30	chr19:18296099..18298993-chr19:18315054..18317073,2	MCF-7	breast:
31	chr19:18282952..18288338-chr19:18301660..18306832,7	K562	blood:
32	chr19:18303217..18304201-chrX:153626030..153626916,2	Hela-S3	cervix:
33	chr19:18311216..18316508-chr19:18389022..18394678,9	MCF-7	breast:
34	chr19:18302787..18307396-chr19:18383842..18390051,8	K562	blood:
35	chr19:18302942..18305811-chr19:18331893..18333423,2	MCF-7	breast:
36	chr19:18223936..18224487-chr19:18302381..18303176,2	K562	blood:
37	chr19:18311642..18316628-chr19:18388957..18392513,10	K562	blood:
38	chr19:18294511..18296251-chr19:18303064..18304696,2	MCF-7	breast:
39	chr19:18302289..18309850-chr19:18311214..18320810,23	K562	blood:
40	chr19:18302057..18307216-chr19:18311605..18315914,14	MCF-7	breast:
41	chr19:18287723..18291034-chr19:18291646..18293887,3	K562	blood:
42	chr19:18303093..18307365-chr19:18386584..18393500,10	K562	blood:
43	chr19:18302376..18304166-chr19:18432954..18434966,2	K562	blood:
44	chr19:18307764..18309976-chr19:18313429..18315883,3	MCF-7	breast:
45	chr19:18301873..18308921-chr19:18309874..18315133,13	MCF-7	breast:
46	chr19:18303468..18305230-chr19:18519611..18522345,2	MCF-7	breast:
47	chr19:18308165..18311046-chr19:18390577..18392563,2	MCF-7	breast:
48	chr19:18311250..18312881-chr19:18314295..18315974,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000268650	TF binding region
MPV17L2	TF binding region
ENSG00000268650	CpG island
MPV17L2	CpG island
ENSG00000130518	chromatin interactions
ENSG00000128534	chromatin interactions
ENSG00000254858	chromatin interactions
ENSG00000221167	chromatin interactions
ENSG00000105649	chromatin interactions
ENSG00000105647	chromatin interactions
ENSG00000130511	chromatin interactions
ENSG00000105650	chromatin interactions
ENSG00000130520	chromatin interactions
ENSG00000267959	chromatin interactions
ENSG00000147403	chromatin interactions
ENSG00000105643	chromatin interactions
ENSG00000216490	chromatin interactions
ENSG00000268173	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000105655	chromatin interactions
ENSG00000268650	chromatin interactions
ENSG00000269145	chromatin interactions

Extended variants
information (count: 1054 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1054 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4808118	chr19:18288947-18288948	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs560390079	chr19:18288994-18288995	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs4808757	chr19:18289028-18289029	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs368726091	chr19:18289029-18289030	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs201974407	chr19:18289033-18289034	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs543195170	chr19:18289034-18289035	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs540243268	chr19:18289038-18289039	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs375461212	chr19:18289091-18289092	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551551195	chr19:18289107-18289108	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565301824	chr19:18289115-18289116	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs527666137	chr19:18289120-18289121	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs546950563	chr19:18289122-18289123	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373828370	chr19:18289123-18289124	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs112504981	chr19:18289130-18289131	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs182095156	chr19:18289170-18289171	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs112973145	chr19:18289174-18289175	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs374971772	chr19:18289196-18289197	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537960085	chr19:18289210-18289211	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs557537721	chr19:18289286-18289287	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs577245776	chr19:18289317-18289318	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs533527028	chr19:18289341-18289342	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147448477	chr19:18289351-18289352	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573989604	chr19:18289355-18289356	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528413791	chr19:18289367-18289368	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs187137893	chr19:18289369-18289370	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs188878807	chr19:18289386-18289387	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs199673242	chr19:18289398-18289399	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs576533073	chr19:18289411-18289412	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs545512078	chr19:18289427-18289428	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs548466877	chr19:18289431-18289432	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs62120360	chr19:18289471-18289472	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs71164377	chr19:18289503-18289504	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs139369343	chr19:18289509-18289510	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs565365018	chr19:18289517-18289518	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs181291827	chr19:18289519-18289520	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs540250031	chr19:18289538-18289539	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs547811772	chr19:18289544-18289545	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561222030	chr19:18289545-18289546	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77496786	chr19:18289561-18289562	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs200378	chr19:18289634-18289635	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs372064288	chr19:18289642-18289643	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs111614217	chr19:18289660-18289661	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569052193	chr19:18289674-18289675	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs537620080	chr19:18289677-18289678	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs550683972	chr19:18289682-18289683	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs565369830	chr19:18289704-18289705	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs116893986	chr19:18289720-18289721	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs553354368	chr19:18289735-18289736	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs7249773	chr19:18289760-18289761	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs78946197	chr19:18289837-18289838	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Follicular lymphoma	20505157	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	20179077	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Lung cancer	17297452	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Chordoma	18071362	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Basal cell lymphoma	21115979	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21364760	CNVD
Mycobacterial infection	18421352	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute monocytic leukemia	16498392	CNVD
Lung cancer	18438408	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Liver carcinoma	19366792	CNVD
Colorectal cancer	19455253	CNVD
Lujan-Fryns syndrom	21521776	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Cancer	17440070	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1070 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:18285000-18290200	Transcr. at gene 5' and 3'	Monocytes-CD14+_RO01746	blood
2	chr19:18285200-18289600	Weak transcription	Small Intestine	intestine
3	chr19:18285400-18296200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr19:18285600-18289000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr19:18285600-18291800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr19:18286000-18290200	Weak transcription	Osteobl	bone
7	chr19:18286000-18291200	Weak transcription	Brain Hippocampus Middle	brain
8	chr19:18286200-18290600	Weak transcription	Pancreas	Pancrea
9	chr19:18286200-18290800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr19:18286200-18292200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr19:18286200-18292400	Weak transcription	Colon Smooth Muscle	Colon
12	chr19:18286200-18294200	Weak transcription	Stomach Mucosa	stomach
13	chr19:18286400-18290400	Genic enhancers	Primary B cells from peripheral blood	blood
14	chr19:18286400-18296200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr19:18286600-18289000	Genic enhancers	Primary B cells from cord blood	blood
16	chr19:18286600-18289400	Weak transcription	Esophagus	oesophagus
17	chr19:18286600-18289400	Strong transcription	Gastric	stomach
18	chr19:18286600-18290400	Strong transcription	Fetal Intestine Small	intestine
19	chr19:18286600-18290800	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr19:18286600-18294200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr19:18286600-18296200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr19:18286600-18296200	Weak transcription	K562	blood
23	chr19:18286600-18296400	Weak transcription	HepG2	liver
24	chr19:18286600-18302600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr19:18287200-18289400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr19:18287400-18289200	Strong transcription	Duodenum Mucosa	Duodenum
27	chr19:18287400-18289400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr19:18287600-18289200	Weak transcription	Primary hematopoietic stem cells	blood
29	chr19:18287800-18289200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr19:18287800-18290000	Strong transcription	Fetal Intestine Large	intestine
31	chr19:18287800-18290200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr19:18287800-18293000	Weak transcription	Hela-S3	cervix
33	chr19:18287800-18295000	Weak transcription	Colonic Mucosa	Colon
34	chr19:18288000-18290000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr19:18288000-18296400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr19:18288200-18294800	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr19:18288400-18302600	Weak transcription	Liver	Liver
38	chr19:18288600-18290200	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr19:18288800-18290000	Strong transcription	Placenta	Placenta
40	chr19:18288800-18290000	Strong transcription	GM12878-XiMat	blood
41	chr19:18288800-18290200	Strong transcription	Spleen	Spleen
42	chr19:18288800-18290400	Genic enhancers	Primary monocytes fromperipheralblood	blood
43	chr19:18288800-18291200	Weak transcription	Lung	lung
44	chr19:18288800-18292200	Weak transcription	Adipose Nuclei	Adipose
45	chr19:18289000-18289600	Strong transcription	Primary B cells from cord blood	blood
46	chr19:18289200-18293400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr19:18289200-18294200	Weak transcription	Duodenum Mucosa	Duodenum
48	chr19:18289400-18290800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr19:18289400-18291000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
50	chr19:18289400-18294200	Weak transcription	Gastric	stomach

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