Variant report

Variant	nsv898389
Chromosome Location	chr11:108724639-108891986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1403)
CpG islands
(count:1098)
Chromatin interactive
region (count:55)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:108741853-108742177	HepG2	liver:	n/a	n/a
2	ATF1	chr11:108804468-108804677	K562	blood:	n/a	n/a
3	ATF1	chr11:108829565-108829796	K562	blood:	n/a	n/a
4	ATF1	chr11:108818568-108818767	K562	blood:	n/a	n/a
5	ATF2	chr11:108725040-108725608	GM12878	blood:	n/a	n/a
6	ATF2	chr11:108724956-108725543	GM12878	blood:	n/a	n/a
7	ATF3	chr11:108799841-108800458	A549	lung:	n/a	n/a
8	BATF	chr11:108844208-108844473	GM12878	blood:	n/a	chr11:108844343-108844354 chr11:108844344-108844354 chr11:108844358-108844369
9	BCL3	chr11:108799714-108800505	A549	lung:	n/a	chr11:108800109-108800118
10	BHLHE40	chr11:108844105-108844309	K562	blood:	n/a	n/a
11	BHLHE40	chr11:108783360-108783637	K562	blood:	n/a	n/a
12	BHLHE40	chr11:108784105-108784304	K562	blood:	n/a	n/a
13	BRCA1	chr11:108777106-108778080	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr11:108757248-108757888	HCT-116	colon:	n/a	chr11:108757273-108757284
15	CBX3	chr11:108767630-108768538	HCT-116	colon:	n/a	n/a
16	CBX3	chr11:108766352-108767099	HCT-116	colon:	n/a	chr11:108767047-108767058
17	CBX3	chr11:108766421-108767011	HCT-116	colon:	n/a	n/a
18	CBX3	chr11:108776904-108777978	HCT-116	colon:	n/a	n/a
19	CBX3	chr11:108828230-108828784	HCT-116	colon:	n/a	n/a
20	CBX3	chr11:108757377-108757867	HCT-116	colon:	n/a	n/a
21	CBX3	chr11:108767617-108768605	HCT-116	colon:	n/a	n/a
22	CEBPB	chr11:108836415-108836729	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:108818405-108818897	A549	lung:	n/a	n/a
24	CEBPB	chr11:108742648-108742972	K562	blood:	n/a	n/a
25	CEBPB	chr11:108767677-108768571	HCT-116	colon:	n/a	n/a
26	CEBPB	chr11:108843852-108844148	HepG2	liver:	n/a	chr11:108843979-108843988 chr11:108843977-108843988
27	CEBPB	chr11:108725718-108726003	K562	blood:	n/a	chr11:108725841-108725850 chr11:108725841-108725850 chr11:108725841-108725850 chr11:108725839-108725850 chr11:108725841-108725850
28	CEBPB	chr11:108766455-108767097	HCT-116	colon:	n/a	n/a
29	CEBPB	chr11:108777038-108777524	HCT-116	colon:	n/a	n/a
30	CEBPB	chr11:108771305-108771343	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr11:108819397-108819574	K562	blood:	n/a	chr11:108819484-108819495
32	CEBPB	chr11:108831857-108832087	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:108819302-108819650	A549	lung:	n/a	chr11:108819484-108819495
34	CEBPB	chr11:108819293-108819677	A549	lung:	n/a	chr11:108819484-108819495
35	CEBPB	chr11:108819332-108819651	HepG2	liver:	n/a	chr11:108819484-108819495
36	CEBPB	chr11:108783257-108783754	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:108738867-108739051	HepG2	liver:	n/a	chr11:108738932-108738943
38	CEBPB	chr11:108742639-108742970	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:108844047-108844503	A549	lung:	n/a	n/a
40	CEBPB	chr11:108818430-108818886	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr11:108766582-108766934	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:108799811-108800387	HCT-116	colon:	n/a	n/a
43	CEBPB	chr11:108783378-108783684	K562	blood:	n/a	n/a
44	CEBPB	chr11:108819368-108819547	MCF-7	breast:	n/a	chr11:108819484-108819495
45	CEBPB	chr11:108819305-108819675	HepG2	liver:	n/a	chr11:108819484-108819495
46	CEBPB	chr11:108843957-108844526	Hela-S3	cervix:	n/a	chr11:108843979-108843988 chr11:108843977-108843988
47	CEBPB	chr11:108799832-108800405	A549	lung:	n/a	n/a
48	CEBPB	chr11:108776975-108778050	Hela-S3	cervix:	n/a	chr11:108777939-108777950
49	CEBPB	chr11:108836442-108836720	A549	lung:	n/a	n/a
50	CEBPB	chr11:108819298-108819677	IMR90	lung:	n/a	chr11:108819484-108819495

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:108777990-108778040	LNCaP	prostate:	n/a
2	chr11:108844084-108844134	SK-N-SH	brain:	n/a
3	chr11:108837640-108837690	NHBE	bronchial:	n/a
4	chr11:108811287-108811337	HRE	kidney:	n/a
5	chr11:108831036-108831086	AG04449	skin:	fetal
6	chr11:108786955-108787005	HCT-116	colon:	n/a
7	chr11:108765859-108765909	GM12892	blood:	n/a
8	chr11:108831036-108831086	NB4	blood:	n/a
9	chr11:108765859-108765909	GM06990	blood:	n/a
10	chr11:108829471-108829521	AG04449	skin:	fetal
11	chr11:108728931-108728981	HEEpiC	esophagus:	n/a
12	chr11:108742393-108742443	CMK	blood:	n/a
13	chr11:108855882-108855932	GM06990	blood:	n/a
14	chr11:108767893-108767943	GM12892	blood:	n/a
15	chr11:108765859-108765909	HPAEpiC	pulmonary alveolar:	n/a
16	chr11:108831036-108831086	NHBE	bronchial:	n/a
17	chr11:108767893-108767943	AoSMC	blood vessel:	n/a
18	chr11:108829918-108829968	GM06990	blood:	n/a
19	chr11:108829471-108829521	BE2_C	brain:	n/a
20	chr11:108811287-108811337	SKMC	muscle:	n/a
21	chr11:108767893-108767943	LNCaP	prostate:	n/a
22	chr11:108761383-108761433	AG09309	skin:	n/a
23	chr11:108761383-108761433	PANC-1	pancreas:	n/a
24	chr11:108765859-108765909	BJ	skin:	n/a
25	chr11:108831036-108831086	BJ	skin:	n/a
26	chr11:108798655-108798705	HNPCEpiC	eye:	n/a
27	chr11:108844084-108844134	HCPEpiC	choroid plexus:	n/a
28	chr11:108844084-108844134	MCF-7	breast:	n/a
29	chr11:108765859-108765909	AoSMC	blood vessel:	n/a
30	chr11:108767893-108767943	HCPEpiC	choroid plexus:	n/a
31	chr11:108797471-108797521	MCF10A-Er-Src	breast:	n/a
32	chr11:108844084-108844134	IMR90	lung:	fetal
33	chr11:108829918-108829968	HIPEpiC	eye:	n/a
34	chr11:108786955-108787005	Jurkat	blood:	n/a
35	chr11:108844084-108844134	AG04450	lung:	fetal
36	chr11:108786955-108787005	Caco-2	colon:	n/a
37	chr11:108765859-108765909	HAEpiC	amniotic membrane:	n/a
38	chr11:108837640-108837690	K562	blood:	n/a
39	chr11:108829471-108829521	LNCaP	prostate:	n/a
40	chr11:108797471-108797521	AG04450	lung:	fetal
41	chr11:108829918-108829968	HEK293	kidney:	embryo
42	chr11:108761383-108761433	GM12878	blood:	n/a
43	chr11:108756966-108757016	T-47D	breast:	n/a
44	chr11:108811287-108811337	GM12878	blood:	n/a
45	chr11:108831036-108831086	Caco-2	colon:	n/a
46	chr11:108829471-108829521	HAEpiC	amniotic membrane:	n/a
47	chr11:108855882-108855932	HRE	kidney:	n/a
48	chr11:108811287-108811337	PFSK-1	brain:	n/a
49	chr11:108767893-108767943	U87	brain:	n/a
50	chr11:108811287-108811337	NHBE	bronchial:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:108823089..108826152-chr11:108827854..108830831,3	K562	blood:
2	chr11:108757832..108759632-chr11:108760933..108762823,2	K562	blood:
3	chr11:108745387..108747861-chr11:108753103..108755912,2	K562	blood:
4	chr11:108723598..108725944-chr11:108749030..108751490,2	K562	blood:
5	chr11:108735096..108738037-chr11:108740814..108742369,2	K562	blood:
6	chr11:108745387..108747861-chr11:108753103..108755912,2	K562	blood:
7	chr11:108754142..108756715-chr11:108759942..108762833,2	K562	blood:
8	chr11:108728605..108731193-chr11:108732068..108735115,3	K562	blood:
9	chr11:108769970..108771676-chr11:108772383..108774669,2	K562	blood:
10	chr11:108743296..108746092-chr11:108747045..108750308,3	K562	blood:
11	chr11:108791030..108793676-chr11:108795093..108797855,3	K562	blood:
12	chr11:108568251..108569546-chr11:108741508..108742629,6	MCF-7	breast:
13	chr11:108757832..108759632-chr11:108760933..108762823,2	K562	blood:
14	chr11:108658928..108659997-chr11:108741741..108742558,3	MCF-7	breast:
15	chr11:108568310..108568880-chr11:108741623..108742180,2	K562	blood:
16	chr11:108754015..108756864-chr11:108777755..108780371,2	K562	blood:
17	chr11:108727866..108730452-chr11:108738042..108739776,2	K562	blood:
18	chr11:108791917..108793676-chr11:108795093..108797181,2	K562	blood:
19	chr11:108743296..108746092-chr11:108747045..108750308,3	K562	blood:
20	chr11:108808750..108811658-chr11:108812114..108813943,2	K562	blood:
21	chr11:108873859..108875938-chr11:108935111..108937056,2	K562	blood:
22	chr11:108846642..108848456-chr11:108853031..108855206,2	MCF-7	breast:
23	chr11:108846642..108848456-chr11:108853031..108855206,2	MCF-7	breast:
24	chr11:108754015..108756864-chr11:108777755..108780371,2	K562	blood:
25	chr11:108836021..108838767-chr11:108843306..108845536,2	K562	blood:
26	chr11:108742339..108744507-chr11:108746363..108748537,2	K562	blood:
27	chr11:108757820..108759522-chr11:108793976..108796483,2	K562	blood:
28	chr11:108835137..108837080-chr11:108838395..108840634,2	K562	blood:
29	chr11:108724551..108728039-chr11:108729309..108732263,3	K562	blood:
30	chr11:108773142..108775690-chr11:108777634..108779166,2	K562	blood:
31	chr11:108722445..108725318-chr11:108725821..108728693,2	MCF-7	breast:
32	chr11:108722445..108725318-chr11:108725821..108728693,2	MCF-7	breast:
33	chr11:108824459..108826637-chr11:108828282..108831060,3	K562	blood:
34	chr11:108773142..108775690-chr11:108777634..108779166,2	K562	blood:
35	chr11:108746537..108749328-chr11:108750101..108751983,2	K562	blood:
36	chr11:108796329..108798320-chr11:108799460..108801702,2	K562	blood:
37	chr11:108799365..108802197-chr11:108803040..108805563,2	K562	blood:
38	chr11:108722635..108725308-chr11:108736229..108737984,2	K562	blood:
39	chr11:108794799..108797753-chr11:108810221..108812207,2	K562	blood:
40	chr11:108717216..108720020-chr11:108723886..108726081,2	K562	blood:
41	chr11:108746537..108749328-chr11:108750101..108751983,2	K562	blood:
42	chr11:108754142..108756715-chr11:108759942..108762833,2	K562	blood:
43	chr11:108742339..108744507-chr11:108746363..108748537,2	K562	blood:
44	chr11:108722635..108725308-chr11:108736229..108737984,2	K562	blood:
45	chr11:108723598..108725944-chr11:108749030..108751490,2	K562	blood:
46	chr11:108835137..108837080-chr11:108838395..108840634,2	K562	blood:
47	chr11:108769970..108771676-chr11:108772383..108774669,2	K562	blood:
48	chr11:108735096..108738037-chr11:108740814..108742369,2	K562	blood:
49	chr11:108728605..108731193-chr11:108732068..108735115,3	K562	blood:
50	chr11:108791030..108793676-chr11:108795093..108797855,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXPH5-1	chr11:108873192-108873299	ENSG00000255528
2	lnc-ATM-4	chr11:108788600-108788651	NONHSAT024042
3	lnc-ATM-4	chr11:108731302-108731684	NONHSAT024042
4	lnc-DDX10-1	chr11:108828445-108830523	NONHSAT024045

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	DDX10	hsa-miR-155-5p	chr11:108791003-108791025
2	DDX10	hsa-let-7b-5p	chr11:108790698-108790721
3	DDX10	hsa-miR-34a-5p	chr11:108811424-108811445

Variant related genes	Relation type
DDX10	TF binding region
ENSG00000203334	TF binding region
RNU6-654P	TF binding region
DDX10	CpG island
ENSG00000203334	CpG island
RNU6-654P	CpG island
ENSG00000178105	chromatin interactions
ENSG00000203334	chromatin interactions

Extended variants
information (count: 5432 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5432 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2726923	chr11:108724639-108724640	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs190110776	chr11:108724640-108724641	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs564283840	chr11:108724693-108724694	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528490847	chr11:108724745-108724746	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs182323342	chr11:108724746-108724747	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs112538186	chr11:108724752-108724753	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs578052042	chr11:108724774-108724775	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529424828	chr11:108724810-108724811	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142854389	chr11:108724846-108724847	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs377595005	chr11:108724898-108724899	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs2726921	chr11:108724899-108724900	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552051184	chr11:108725029-108725030	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145407233	chr11:108725101-108725102	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs187385654	chr11:108725170-108725171	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555484211	chr11:108725189-108725190	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528293995	chr11:108725220-108725221	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs369334755	chr11:108725222-108725223	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76903796	chr11:108725228-108725229	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs574215910	chr11:108725256-108725257	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs537963731	chr11:108725318-108725319	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536335528	chr11:108725385-108725386	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs79837188	chr11:108725426-108725427	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191020423	chr11:108725428-108725429	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182365191	chr11:108725433-108725434	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs5794608	chr11:108725455-108725456	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs397716025	chr11:108725465-108725466	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs199780846	chr11:108725466-108725467	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200420611	chr11:108725468-108725469	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs573147206	chr11:108725474-108725475	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185344026	chr11:108725546-108725547	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561767680	chr11:108725553-108725554	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576358381	chr11:108725554-108725555	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190104042	chr11:108725565-108725566	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs142635472	chr11:108725577-108725578	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544309293	chr11:108725627-108725628	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182751460	chr11:108725635-108725636	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs5794609	chr11:108725701-108725702	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs113727648	chr11:108725702-108725703	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs113282641	chr11:108725703-108725704	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs558995377	chr11:108725739-108725740	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12293543	chr11:108725757-108725758	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs146038248	chr11:108725776-108725777	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs560873492	chr11:108725842-108725843	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527272685	chr11:108725862-108725863	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs372269274	chr11:108726068-108726069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs17108656	chr11:108726109-108726110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs567288297	chr11:108726194-108726195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs375689216	chr11:108726217-108726218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368273958	chr11:108726218-108726219	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549906323	chr11:108726228-108726229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Developmental delay	21147756	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2019 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108707600-108740800	Weak transcription	HMEC	breast
2	chr11:108708200-108729200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr11:108708600-108724800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr11:108709800-108724800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr11:108709800-108724800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr11:108710200-108729200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:108710200-108729400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr11:108710200-108735800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr11:108710200-108738200	Weak transcription	Gastric	stomach
10	chr11:108710600-108729800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:108712400-108725000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:108715400-108738200	Weak transcription	K562	blood
13	chr11:108715600-108725200	Weak transcription	Liver	Liver
14	chr11:108717400-108724800	Weak transcription	Primary B cells from cord blood	blood
15	chr11:108717600-108729600	Weak transcription	Dnd41	blood
16	chr11:108717800-108729400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr11:108721000-108725000	Enhancers	Fetal Lung	lung
18	chr11:108721400-108728200	Weak transcription	Lung	lung
19	chr11:108721600-108742200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:108722200-108724800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:108722600-108725000	Enhancers	NHDF-Ad	bronchial
22	chr11:108723200-108725000	Enhancers	Fetal Stomach	stomach
23	chr11:108723200-108725200	Enhancers	Psoas Muscle	Psoas
24	chr11:108723600-108724800	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr11:108723600-108733200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:108723800-108725000	Enhancers	Primary T killer memory cells from peripheral blood	blood
27	chr11:108723800-108725000	Enhancers	Adipose Nuclei	Adipose
28	chr11:108723800-108725000	Enhancers	Left Ventricle	heart
29	chr11:108723800-108725400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:108724000-108725000	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr11:108724000-108725400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr11:108724200-108724800	Enhancers	HUVEC	blood vessel
33	chr11:108724200-108725400	Flanking Active TSS	Fetal Heart	heart
34	chr11:108724200-108725400	Enhancers	NH-A	brain
35	chr11:108724400-108724800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr11:108724400-108724800	Enhancers	Primary B cells from peripheral blood	blood
37	chr11:108724400-108724800	Enhancers	Primary T cells fromperipheralblood	blood
38	chr11:108724400-108724800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr11:108724400-108724800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:108724400-108724800	Enhancers	Duodenum Mucosa	Duodenum
41	chr11:108724400-108724800	Flanking Active TSS	HSMMtube	muscle
42	chr11:108724400-108725000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:108724400-108725000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:108724400-108725000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:108724400-108725000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:108724400-108725000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr11:108724400-108725000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:108724400-108725000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr11:108724400-108725000	Enhancers	Brain Anterior Caudate	brain
50	chr11:108724400-108725000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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