Variant report

Variant	nsv1038015
Chromosome Location	chr11:18435855-18558211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1217)
CpG islands
(count:1831)
Chromatin interactive
region (count:94)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1217 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:18547537-18549440	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:18555956-18556078	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:18548406-18548804	K562	blood:	n/a	n/a
4	ARID3A	chr11:18545752-18546166	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:18479092-18479320	HepG2	liver:	n/a	n/a
6	ATF1	chr11:18548160-18548970	K562	blood:	n/a	n/a
7	ATF1	chr11:18512610-18512972	K562	blood:	n/a	n/a
8	ATF2	chr11:18548230-18548811	GM12878	blood:	n/a	n/a
9	ATF2	chr11:18548106-18548710	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr11:18547861-18548881	GM12878	blood:	n/a	n/a
11	ATF2	chr11:18547962-18548740	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr11:18517243-18517546	K562	blood:	n/a	n/a
13	ATF3	chr11:18548122-18548801	A549	lung:	n/a	chr11:18548453-18548461 chr11:18548505-18548525 chr11:18548173-18548182 chr11:18548591-18548599
14	ATF3	chr11:18548287-18548758	K562	blood:	n/a	chr11:18548453-18548461 chr11:18548505-18548525 chr11:18548591-18548599
15	ATF3	chr11:18548242-18548894	A549	lung:	n/a	chr11:18548453-18548461 chr11:18548505-18548525 chr11:18548591-18548599
16	BACH1	chr11:18542792-18542918	K562	blood:	n/a	n/a
17	BACH1	chr11:18441872-18441909	K562	blood:	n/a	n/a
18	BACH1	chr11:18533463-18533474	K562	blood:	n/a	n/a
19	BACH1	chr11:18548580-18548740	K562	blood:	n/a	n/a
20	BACH1	chr11:18548195-18548751	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:18477287-18477564	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr11:18542195-18542267	K562	blood:	n/a	n/a
23	BATF	chr11:18548313-18548641	GM12878	blood:	n/a	n/a
24	BATF	chr11:18490527-18490838	GM12878	blood:	n/a	chr11:18490690-18490701 chr11:18490691-18490701
25	BATF	chr11:18490570-18490770	GM12878	blood:	n/a	chr11:18490690-18490701 chr11:18490691-18490701
26	BCL11A	chr11:18548304-18548589	GM12878	blood:	n/a	chr11:18548512-18548521 chr11:18548492-18548501
27	BCL3	chr11:18547993-18548668	GM12878	blood:	n/a	chr11:18548512-18548521 chr11:18548492-18548501 chr11:18548086-18548095
28	BCL3	chr11:18507479-18507913	GM12878	blood:	n/a	n/a
29	BCL3	chr11:18547901-18548733	A549	lung:	n/a	chr11:18548512-18548521 chr11:18548492-18548501 chr11:18548086-18548095
30	BCL3	chr11:18547927-18549021	A549	lung:	n/a	chr11:18548512-18548521 chr11:18548492-18548501 chr11:18548086-18548095
31	BCLAF1	chr11:18547917-18548872	GM12878	blood:	n/a	chr11:18548512-18548521 chr11:18548492-18548501 chr11:18548086-18548095
32	BCLAF1	chr11:18547778-18548789	GM12878	blood:	n/a	chr11:18548512-18548521 chr11:18548492-18548501 chr11:18548086-18548095
33	BHLHE40	chr11:18548135-18548907	K562	blood:	n/a	n/a
34	BHLHE40	chr11:18474554-18474624	K562	blood:	n/a	n/a
35	BHLHE40	chr11:18479101-18479289	A549	lung:	n/a	n/a
36	BHLHE40	chr11:18479046-18479396	HepG2	liver:	n/a	n/a
37	BHLHE40	chr11:18479063-18479387	K562	blood:	n/a	n/a
38	BHLHE40	chr11:18548028-18548708	GM12878	blood:	n/a	n/a
39	BRCA1	chr11:18548071-18548701	HepG2	liver:	n/a	n/a
40	BRCA1	chr11:18547785-18548695	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr11:18478869-18479367	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr11:18554886-18555238	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr11:18548483-18548667	H1-hESC	embryonic stem cell:	n/a	n/a
44	CBX3	chr11:18547799-18548986	K562	blood:	n/a	n/a
45	CCNT2	chr11:18548046-18548906	K562	blood:	n/a	n/a
46	CCNT2	chr11:18512616-18513161	K562	blood:	n/a	n/a
47	CEBPB	chr11:18452469-18452615	HepG2	liver:	n/a	chr11:18452577-18452588
48	CEBPB	chr11:18495235-18495455	K562	blood:	n/a	chr11:18495281-18495292
49	CEBPB	chr11:18444389-18444575	K562	blood:	n/a	n/a
50	CEBPB	chr11:18547812-18548144	HepG2	liver:	n/a	n/a

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:18548210-18548260	HCT-116	colon:	n/a
2	chr11:18548210-18548260	HCT-116	colon:	n/a
3	chr11:18477753-18477803	HAEpiC	amniotic membrane:	n/a
4	chr11:18477534-18477584	SK-N-SH_RA	brain:	n/a
5	chr11:18477280-18477330	ProgFib	skin:	n/a
6	chr11:18478135-18478185	AG09309	skin:	n/a
7	chr11:18477753-18477803	SKMC	muscle:	n/a
8	chr11:18481032-18481082	HL-60	blood:	n/a
9	chr11:18548665-18548715	MCF-7	breast:	n/a
10	chr11:18548595-18548645	AoSMC	blood vessel:	n/a
11	chr11:18548609-18548659	BE2_C	brain:	n/a
12	chr11:18477280-18477330	GM12892	blood:	n/a
13	chr11:18548609-18548659	HAEpiC	amniotic membrane:	n/a
14	chr11:18548302-18548352	IMR90	lung:	fetal
15	chr11:18548595-18548645	NB4	blood:	n/a
16	chr11:18476081-18476131	HCPEpiC	choroid plexus:	n/a
17	chr11:18548302-18548352	BE2_C	brain:	n/a
18	chr11:18477299-18477349	ProgFib	skin:	n/a
19	chr11:18548806-18548856	GM06990	blood:	n/a
20	chr11:18476131-18476181	LNCaP	prostate:	n/a
21	chr11:18548709-18548759	NHDF-neo	bronchial:	n/a
22	chr11:18477299-18477349	HPAEpiC	pulmonary alveolar:	n/a
23	chr11:18548665-18548715	NH-A	brain:	n/a
24	chr11:18548408-18548458	AoSMC	blood vessel:	n/a
25	chr11:18548595-18548645	RPTEC	kidney:	n/a
26	chr11:18500649-18500699	MCF-7	breast:	n/a
27	chr11:18477153-18477203	HAEpiC	amniotic membrane:	n/a
28	chr11:18476131-18476181	AoSMC	blood vessel:	n/a
29	chr11:18548308-18548358	K562	blood:	n/a
30	chr11:18477303-18477353	GM06990	blood:	n/a
31	chr11:18549053-18549103	AG04450	lung:	fetal
32	chr11:18481032-18481082	SK-N-MC	brain:	n/a
33	chr11:18548308-18548358	A549	lung:	n/a
34	chr11:18548609-18548659	SK-N-SH_RA	brain:	n/a
35	chr11:18477254-18477304	HPAEpiC	pulmonary alveolar:	n/a
36	chr11:18476131-18476181	SKMC	muscle:	n/a
37	chr11:18548210-18548260	HL-60	blood:	n/a
38	chr11:18473775-18473825	SK-N-SH	brain:	n/a
39	chr11:18477280-18477330	HNPCEpiC	eye:	n/a
40	chr11:18476081-18476131	GM12892	blood:	n/a
41	chr11:18481032-18481082	ECC-1	luminal epithelium:	n/a
42	chr11:18477753-18477803	HRE	kidney:	n/a
43	chr11:18548609-18548659	Caco-2	colon:	n/a
44	chr11:18548609-18548659	HepG2	liver:	n/a
45	chr11:18473775-18473825	PFSK-1	brain:	n/a
46	chr11:18477280-18477330	Hepatocyte	liver:	n/a
47	chr11:18547893-18547943	PANC-1	pancreas:	n/a
48	chr11:18500649-18500699	HAEpiC	amniotic membrane:	n/a
49	chr11:18548609-18548659	HUVEC	blood vessel:	n/a
50	chr11:18548302-18548352	MCF-7	breast:	n/a

(count:94 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:18341846..18344494-chr11:18547115..18549354,2	MCF-7	breast:
2	chr11:18489055..18490593-chr11:18496337..18497953,2	K562	blood:
3	chr11:18467637..18469491-chr11:18477590..18480318,2	K562	blood:
4	chr11:18467637..18469491-chr11:18477590..18480318,2	K562	blood:
5	chr11:18533507..18535848-chr11:18546408..18548301,3	K562	blood:
6	chr11:18462496..18464309-chr11:18472211..18474246,2	MCF-7	breast:
7	chr11:18551088..18554076-chr11:18654231..18656218,2	K562	blood:
8	chr11:18533757..18535476-chr11:18537479..18539659,2	MCF-7	breast:
9	chr11:18489055..18490593-chr11:18496337..18497953,2	K562	blood:
10	chr11:18511993..18514415-chr11:18543719..18545830,2	K562	blood:
11	chr11:18547881..18548707-chr21:44313013..44313598,2	Hela-S3	cervix:
12	chr11:18548430..18549296-chr17:72199825..72200786,2	Hela-S3	cervix:
13	chr11:18555936..18558894-chr11:18654308..18656138,2	K562	blood:
14	chr11:18527234..18530120-chr11:18547134..18549808,2	MCF-7	breast:
15	chr11:18531181..18534158-chr11:18547173..18549352,2	MCF-7	breast:
16	chr11:18415718..18417839-chr11:18444013..18446628,2	K562	blood:
17	chr11:18470144..18471841-chr11:18477720..18480127,2	MCF-7	breast:
18	chr11:18415520..18417740-chr11:18457174..18459027,2	K562	blood:
19	chr11:18548142..18548670-chr11:18609940..18610633,2	MCF-7	breast:
20	chr11:18552647..18555345-chr20:55842668..55844786,2	MCF-7	breast:
21	chr11:18342189..18343915-chr11:18546820..18548379,2	MCF-7	breast:
22	chr1:1334202..1334912-chr11:18547765..18548751,2	Hela-S3	cervix:
23	chr11:18546581..18551368-chr11:18654825..18657467,6	K562	blood:
24	chr11:18433811..18435344-chr11:18439087..18441090,2	K562	blood:
25	chr11:18546489..18551340-chr11:18552893..18563258,14	MCF-7	breast:
26	chr11:18538359..18545865-chr11:18546460..18550640,13	MCF-7	breast:
27	chr11:18479966..18482806-chr11:18549124..18551467,2	K562	blood:
28	chr11:18430626..18432747-chr11:18545645..18547445,2	K562	blood:
29	chr11:18414619..18417567-chr11:18475840..18478644,2	K562	blood:
30	chr11:18464968..18467411-chr11:18470062..18474152,3	K562	blood:
31	chr11:18474174..18475881-chr11:18477733..18480422,2	MCF-7	breast:
32	chr11:18415765..18417941-chr11:18547561..18549649,2	K562	blood:
33	chr11:18535996..18538848-chr11:18539751..18543150,4	MCF-7	breast:
34	chr11:18546489..18551340-chr11:18552893..18563258,14	MCF-7	breast:
35	chr11:18414985..18417480-chr11:18436029..18437614,2	K562	blood:
36	chr11:18530933..18533061-chr11:18534871..18536748,2	MCF-7	breast:
37	chr11:18556808..18558328-chr11:18600770..18602452,2	MCF-7	breast:
38	chr11:18479966..18482806-chr11:18549124..18551467,2	K562	blood:
39	chr10:70091815..70092544-chr11:18548061..18548917,2	Hela-S3	cervix:
40	chr1:225117317..225117947-chr11:18547900..18548603,2	NB4	blood:
41	chr11:18432193..18433875-chr11:18547475..18550164,2	MCF-7	breast:
42	chr11:18430457..18432481-chr11:18456231..18458824,2	K562	blood:
43	chr1:36396047..36396934-chr11:18547924..18549049,4	Hela-S3	cervix:
44	chr11:18548392..18548985-chr16:58231117..58232045,2	Hela-S3	cervix:
45	chr11:18544251..18545770-chr11:18654653..18657542,2	K562	blood:
46	chr11:18548007..18548707-chr15:89877506..89878449,2	Hela-S3	cervix:
47	chr11:18429708..18432011-chr11:18438993..18440849,2	MCF-7	breast:
48	chr11:18548066..18548848-chr20:48789021..48789605,2	Hela-S3	cervix:
49	chr11:18415628..18417423-chr11:18491063..18493599,2	MCF-7	breast:
50	chr11:18531181..18534158-chr11:18547173..18549352,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UEVLD-2	chr11:18529155-18529447	ENSG00000256588.1
2	lnc-UEVLD-2	chr11:18530031-18530367	ENSG00000256588.1
3	lnc-LDHAL6A-1	chr11:18548579-18550760	NONHSAT018294
4	lnc-UEVLD-5	chr11:18511790-18512502	NONHSAT018288
5	lnc-UEVLD-4	chr11:18532590-18533022	NONHSAT018293
6	lnc-TSG101-2	chr11:18471659-18472415	NONHSAT018286

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TSG101	hsa-miR-130b-3p	chr11:18501920-18501941
2	TSG101	hsa-miR-93-5p	chr11:18501918-18501939
3	TSG101	hsa-miR-20a-5p	chr11:18501918-18501939
4	UEVLD	hsa-miR-20a-5p	chr11:18553306-18553328
5	TSG101	hsa-miR-130b-3p	chr11:18502003-18502024
6	UEVLD	hsa-miR-20a-5p	chr11:18553312-18553305
7	TSG101	hsa-miR-20a-5p	chr11:18501924-18501918
8	TSG101	hsa-miR-33a-5p	chr11:18501922-18501943
9	TSG101	hsa-miR-93-5p	chr11:18501924-18501918

Variant related genes	Relation type
ENSG00000256361	TF binding region
TSG101	TF binding region
LDHAL6A	TF binding region
ENSG00000256464	TF binding region
ENSG00000256588	TF binding region
ENSG00000256734	TF binding region
ENSG00000256361	CpG island
TSG101	CpG island
LDHAL6A	CpG island
ENSG00000256464	CpG island
ENSG00000256588	CpG island
ENSG00000256734	CpG island
ENSG00000110768	chromatin interactions
ENSG00000006831	chromatin interactions
ENSG00000110756	chromatin interactions
ENSG00000231742	chromatin interactions
ENSG00000113460	chromatin interactions
ENSG00000070770	chromatin interactions
ENSG00000151116	chromatin interactions
ENSG00000256361	chromatin interactions
ENSG00000256588	chromatin interactions
ENSG00000113456	chromatin interactions
ENSG00000172809	chromatin interactions
ENSG00000160194	chromatin interactions
ENSG00000126070	chromatin interactions
ENSG00000074319	chromatin interactions
ENSG00000128789	chromatin interactions
ENSG00000224870	chromatin interactions
ENSG00000096746	chromatin interactions
ENSG00000158710	chromatin interactions
ENSG00000148337	chromatin interactions
ENSG00000164296	chromatin interactions
ENSG00000140521	chromatin interactions
ENSG00000166796	chromatin interactions
ENSG00000256464	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000179119	chromatin interactions
ENSG00000101624	chromatin interactions
ENSG00000241990	chromatin interactions
ENSG00000113716	chromatin interactions
ENSG00000185842	chromatin interactions
ENSG00000188002	chromatin interactions
ENSG00000221978	chromatin interactions
ENSG00000256734	chromatin interactions
ENSG00000182257	chromatin interactions
ENSG00000261441	chromatin interactions
ENSG00000116560	chromatin interactions

Extended variants
information (count: 4324 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4324 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373800566	chr11:18435889-18435890	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs368845044	chr11:18435945-18435946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs539257574	chr11:18435981-18435982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557905820	chr11:18436025-18436026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs75762326	chr11:18436028-18436029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs543733562	chr11:18436035-18436036	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561625749	chr11:18436081-18436082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs112667328	chr11:18436096-18436097	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs141187582	chr11:18436100-18436101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs183428965	chr11:18436117-18436118	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs187969196	chr11:18436145-18436146	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs533000960	chr11:18436200-18436201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs552521241	chr11:18436201-18436202	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs11024648	chr11:18436204-18436205	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs550539770	chr11:18436208-18436209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs137886935	chr11:18436232-18436233	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149468315	chr11:18436260-18436261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs374780731	chr11:18436264-18436265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547764282	chr11:18436268-18436269	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs113822754	chr11:18436295-18436296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
21	rs112883073	chr11:18436322-18436323	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561502168	chr11:18436332-18436333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs144140402	chr11:18436352-18436353	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs569859426	chr11:18436353-18436354	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112382681	chr11:18436373-18436374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536851155	chr11:18436424-18436425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191248232	chr11:18436445-18436446	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75305886	chr11:18436448-18436449	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
29	rs540628689	chr11:18436470-18436471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs139150798	chr11:18436474-18436475	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs552526077	chr11:18436568-18436569	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139946387	chr11:18436578-18436579	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368062664	chr11:18436622-18436623	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs373305670	chr11:18436680-18436681	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370080971	chr11:18436682-18436683	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563217843	chr11:18436736-18436737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs11558332	chr11:18436759-18436760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs376543708	chr11:18436767-18436768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370079739	chr11:18436790-18436791	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs551119181	chr11:18436794-18436795	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146233108	chr11:18436799-18436800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs151274027	chr11:18436805-18436806	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs373834035	chr11:18436828-18436829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs367772851	chr11:18436858-18436859	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368451212	chr11:18436888-18436889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs78252126	chr11:18436991-18436992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76915983	chr11:18436992-18436993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs551459153	chr11:18436999-18437000	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs386751167	chr11:18437003-18437004	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs116197547	chr11:18437004-18437005	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2381 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18430200-18440200	Weak transcription	K562	blood
2	chr11:18434200-18442200	Weak transcription	Pancreas	Pancrea
3	chr11:18434400-18438800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:18435000-18436000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:18436000-18442000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:18440200-18441800	Enhancers	K562	blood
7	chr11:18441800-18442400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr11:18442000-18442400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr11:18442000-18442600	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr11:18442000-18442600	Enhancers	HUVEC	blood vessel
11	chr11:18442000-18442800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:18442000-18442800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:18450800-18451200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr11:18451000-18451400	Enhancers	K562	blood
15	chr11:18457200-18479200	Weak transcription	Pancreas	Pancrea
16	chr11:18463200-18463800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:18463400-18463800	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr11:18463400-18463800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr11:18463400-18463800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr11:18463400-18464000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr11:18471000-18471400	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr11:18474200-18475000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr11:18474400-18474800	Enhancers	NHDF-Ad	bronchial
24	chr11:18474400-18475000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr11:18474400-18475000	Enhancers	Hela-S3	cervix
26	chr11:18475000-18476000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr11:18476000-18476200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:18476800-18477000	Active TSS	Spleen	Spleen
29	chr11:18477000-18477200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:18477000-18477600	Enhancers	Spleen	Spleen
31	chr11:18477200-18477400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr11:18477200-18477400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr11:18477200-18477600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr11:18477200-18477800	Active TSS	Brain Germinal Matrix	brain
35	chr11:18477200-18477800	Active TSS	Ovary	ovary
36	chr11:18477200-18478000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:18477400-18477600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
38	chr11:18477400-18477600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
39	chr11:18477400-18477600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:18477400-18477600	Bivalent Enhancer	Right Ventricle	heart
41	chr11:18477400-18477800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:18477400-18477800	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr11:18477400-18477800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr11:18477400-18477800	Active TSS	Fetal Brain Female	brain
45	chr11:18477400-18478000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:18477400-18478000	Active TSS	Primary neutrophils fromperipheralblood	blood
47	chr11:18477400-18478000	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
48	chr11:18477600-18477800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr11:18477600-18477800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr11:18477600-18478200	Enhancers	Right Ventricle	heart

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