Variant report

Variant	nsv541039
Chromosome Location	chr11:48127618-48616507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2387)
CpG islands
(count:1527)
Chromatin interactive
region (count:62)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:2387 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48130883-48131832	K562	blood:	n/a	n/a
2	ARID3A	chr11:48194471-48194702	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:48600198-48600306	K562	blood:	n/a	n/a
4	ARID3A	chr11:48130891-48131217	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:48131445-48131835	HepG2	liver:	n/a	n/a
6	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
7	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
8	ATF2	chr11:48131303-48131862	GM12878	blood:	n/a	n/a
9	ATF2	chr11:48131384-48131873	GM12878	blood:	n/a	n/a
10	ATF2	chr11:48128530-48129047	GM12878	blood:	n/a	n/a
11	ATF2	chr11:48128499-48129217	GM12878	blood:	n/a	n/a
12	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
13	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
14	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
15	BATF	chr11:48131359-48131717	GM12878	blood:	n/a	n/a
16	BATF	chr11:48128651-48129130	GM12878	blood:	n/a	n/a
17	BATF	chr11:48128657-48129110	GM12878	blood:	n/a	n/a
18	BATF	chr11:48131437-48131740	GM12878	blood:	n/a	n/a
19	BCL11A	chr11:48128709-48129015	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
20	BCL11A	chr11:48128623-48129135	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
21	BCL11A	chr11:48131334-48131777	GM12878	blood:	n/a	n/a
22	BCL3	chr11:48128713-48129121	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
23	BCL3	chr11:48393835-48394182	GM12878	blood:	n/a	n/a
24	BCL3	chr11:48128638-48129194	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
25	BCLAF1	chr11:48131284-48131807	GM12878	blood:	n/a	n/a
26	BCLAF1	chr11:48128565-48129092	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
27	BCLAF1	chr11:48131240-48131877	GM12878	blood:	n/a	n/a
28	BCLAF1	chr11:48128578-48129221	GM12878	blood:	n/a	chr11:48128925-48128934 chr11:48128836-48128843 chr11:48128926-48128935
29	BHLHE40	chr11:48131324-48131977	GM12878	blood:	n/a	chr11:48131376-48131392
30	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:48131523-48131855	HepG2	liver:	n/a	n/a
32	BHLHE40	chr11:48130984-48131970	K562	blood:	n/a	chr11:48131376-48131392
33	BHLHE40	chr11:48128654-48129077	GM12878	blood:	n/a	n/a
34	BRCA1	chr11:48130922-48131812	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr11:48131531-48131726	HepG2	liver:	n/a	n/a
36	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr11:48361931-48361935	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
39	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
40	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr11:48175001-48175304	K562	blood:	n/a	n/a
42	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
43	CBX3	chr11:48136314-48136661	K562	blood:	n/a	n/a
44	CBX3	chr11:48136304-48136617	K562	blood:	n/a	n/a
45	CEBPB	chr11:48194408-48194759	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
47	CEBPB	chr11:48232368-48232629	A549	lung:	n/a	chr11:48232504-48232515
48	CEBPB	chr11:48131413-48131757	GM12878	blood:	n/a	n/a
49	CEBPB	chr11:48374701-48375094	Hela-S3	cervix:	n/a	chr11:48374900-48374913
50	CEBPB	chr11:48161501-48161776	Hela-S3	cervix:	n/a	chr11:48161642-48161653

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48345815-48345865	SK-N-SH_RA	brain:	n/a
2	chr11:48238724-48238774	HEK293	kidney:	embryo
3	chr11:48345815-48345865	SK-N-SH_RA	brain:	n/a
4	chr11:48238724-48238774	HEK293	kidney:	embryo
5	chr11:48161380-48161430	CMK	blood:	n/a
6	chr11:48346680-48346730	GM12878	blood:	n/a
7	chr11:48238296-48238346	MCF10A-Er-Src	breast:	n/a
8	chr11:48161380-48161430	LNCaP	prostate:	n/a
9	chr11:48346680-48346730	HEEpiC	esophagus:	n/a
10	chr11:48327164-48327214	NHBE	bronchial:	n/a
11	chr11:48346680-48346730	NHBE	bronchial:	n/a
12	chr11:48345361-48345411	HRE	kidney:	n/a
13	chr11:48238296-48238346	HEK293	kidney:	embryo
14	chr11:48285200-48285250	NHDF-neo	bronchial:	n/a
15	chr11:48284249-48284299	MCF10A-Er-Src	breast:	n/a
16	chr11:48367974-48368024	Hepatocyte	liver:	n/a
17	chr11:48509488-48509538	HCT-116	colon:	n/a
18	chr11:48129067-48129117	HEK293	kidney:	embryo
19	chr11:48285821-48285871	HCPEpiC	choroid plexus:	n/a
20	chr11:48237353-48237403	NT2-D1	testis:	n/a
21	chr11:48345361-48345411	HEK293	kidney:	embryo
22	chr11:48346680-48346730	PFSK-1	brain:	n/a
23	chr11:48285821-48285871	PFSK-1	brain:	n/a
24	chr11:48284249-48284299	HMEC	breast:	n/a
25	chr11:48328132-48328182	GM19239	blood:	n/a
26	chr11:48510647-48510697	HRPEpiC	eye:	n/a
27	chr11:48237358-48237408	LNCaP	prostate:	n/a
28	chr11:48238296-48238346	HNPCEpiC	eye:	n/a
29	chr11:48327164-48327214	IMR90	lung:	fetal
30	chr11:48510647-48510697	NH-A	brain:	n/a
31	chr11:48510647-48510697	AG04450	lung:	fetal
32	chr11:48185069-48185119	HRCEpiC	kidney:	n/a
33	chr11:48327164-48327214	SAEC	small airway:	n/a
34	chr11:48327164-48327214	PrEC	prostate:	n/a
35	chr11:48374446-48374496	IMR90	lung:	fetal
36	chr11:48367974-48368024	MCF-7	breast:	n/a
37	chr11:48266856-48266906	HEK293	kidney:	embryo
38	chr11:48326388-48326438	HepG2	liver:	n/a
39	chr11:48509488-48509538	MCF10A-Er-Src	breast:	n/a
40	chr11:48161861-48161911	K562	blood:	n/a
41	chr11:48238296-48238346	GM12892	blood:	n/a
42	chr11:48266856-48266906	RPTEC	kidney:	n/a
43	chr11:48129067-48129117	HCM	heart:	n/a
44	chr11:48161861-48161911	PANC-1	pancreas:	n/a
45	chr11:48509778-48509828	MCF-7	breast:	n/a
46	chr11:48185069-48185119	Jurkat	blood:	n/a
47	chr11:48238724-48238774	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:48285821-48285871	HUVEC	blood vessel:	n/a
49	chr11:48374446-48374496	HPAEpiC	pulmonary alveolar:	n/a
50	chr11:48328132-48328182	IMR90	lung:	fetal

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:47985574..47986089-chr11:48131663..48132191,2	K562	blood:
2	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
3	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
4	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
5	chr11:48147029..48148645-chr11:48154007..48155529,2	MCF-7	breast:
6	chr11:47985506..47986348-chr11:48130588..48131464,3	MCF-7	breast:
7	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
8	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:
9	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
10	chr11:48001502..48002444-chr11:48131229..48132098,2	MCF-7	breast:
11	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
12	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
13	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
14	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
15	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
16	chr11:47999992..48004999-chr11:48128626..48133853,5	MCF-7	breast:
17	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
18	chr11:48131666..48133452-chr11:48135727..48137956,2	MCF-7	breast:
19	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
20	chr11:48147029..48148645-chr11:48154007..48155529,2	MCF-7	breast:
21	chr11:47955553..47956701-chr11:48130593..48132313,16	K562	blood:
22	chr11:47868317..47870983-chr11:48125503..48128104,3	K562	blood:
23	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
24	chr11:47879130..47879931-chr11:48131064..48131706,2	MCF-7	breast:
25	chr11:48000640..48001500-chr11:48131020..48132149,3	MCF-7	breast:
26	chr11:48119543..48121197-chr11:48126844..48128670,2	K562	blood:
27	chr1:153895897..153896422-chr11:48153597..48154395,2	Hela-S3	cervix:
28	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
29	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
30	chr11:47955523..47956710-chr11:48130209..48132188,17	MCF-7	breast:
31	chr11:47967425..47969925-chr11:48129768..48132712,2	MCF-7	breast:
32	chr11:47956073..47956643-chr11:48155973..48156490,2	MCF-7	breast:
33	chr11:48131666..48133452-chr11:48135727..48137956,2	MCF-7	breast:
34	chr11:48125100..48126917-chr11:48129444..48131504,2	MCF-7	breast:
35	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
36	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
37	chr11:48046572..48047306-chr11:48130972..48131586,2	MCF-7	breast:
38	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
39	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
40	chr11:48036717..48039459-chr11:48129718..48132138,2	MCF-7	breast:
41	chr11:48120614..48123449-chr11:48129423..48131714,2	MCF-7	breast:
42	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
43	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
44	chr11:48068073..48069888-chr11:48129032..48131534,2	MCF-7	breast:
45	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
46	chr11:47955472..47956729-chr11:48130954..48132546,8	MCF-7	breast:
47	chr11:47985562..47986062-chr11:48130641..48131468,2	K562	blood:
48	chr11:48071477..48072173-chr11:48130347..48131089,2	MCF-7	breast:
49	chr11:48129232..48130878-chr11:48134176..48136053,2	K562	blood:
50	chr11:47968790..47969517-chr11:48130956..48131704,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C5-1	chr11:48507915-48508377	NONHSAT021297

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PTPRJ	hsa-miR-124-3p	chr11:48189431-48189437
2	PTPRJ	hsa-miR-124-3p	chr11:48189418-48189438
3	PTPRJ	hsa-miR-328-3p	chr11:48191725-48191748
4	PTPRJ	hsa-miR-26b-5p	chr11:48190233-48190256
5	PTPRJ	hsa-miR-155-5p	chr11:48190367-48190373
6	PTPRJ	hsa-miR-155-5p	chr11:48190351-48190373
7	PTPRJ	hsa-miR-16-5p	chr11:48190225-48190243
8	PTPRJ	hsa-miR-16-5p	chr11:48190236-48190242

Variant related genes	Relation type
OR4C9P	TF binding region
OR4C5	TF binding region
OR4C4P	TF binding region
OR4C10P	TF binding region
OR4A47	TF binding region
OR4C2P	TF binding region
OR4X2	TF binding region
OR4A41P	TF binding region
OR4A40P	TF binding region
OR4A46P	TF binding region
OR4B2P	TF binding region
OR4A45P	TF binding region
OR4A48P	TF binding region
OR4X1	TF binding region
PTPRJ	TF binding region
OR4R1P	TF binding region
OR4C3	TF binding region
OR4S1	TF binding region
OR4B1	TF binding region
OR4A43P	TF binding region
OR4C9P	CpG island
OR4C5	CpG island
OR4C4P	CpG island
OR4C10P	CpG island
OR4A47	CpG island
OR4C2P	CpG island
OR4X2	CpG island
OR4A41P	CpG island
OR4A40P	CpG island
OR4A46P	CpG island
OR4B2P	CpG island
OR4A45P	CpG island
OR4A48P	CpG island
OR4X1	CpG island
PTPRJ	CpG island
OR4R1P	CpG island
OR4C3	CpG island
OR4S1	CpG island
OR4B1	CpG island
OR4A43P	CpG island
ENSG00000197161	chromatin interactions
ENSG00000254879	chromatin interactions
ENSG00000030066	chromatin interactions
ENSG00000149177	chromatin interactions
ENSG00000165923	chromatin interactions

Extended variants
information (count: 8172 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:8172 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76226314	chr11:48127620-48127621	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs560668483	chr11:48127653-48127654	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs75472696	chr11:48127702-48127703	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144756235	chr11:48127748-48127749	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs147900701	chr11:48127779-48127780	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs549320801	chr11:48127788-48127789	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs61915879	chr11:48127795-48127796	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs115883057	chr11:48127805-48127806	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs116501101	chr11:48127835-48127836	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs374586922	chr11:48127850-48127851	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191742631	chr11:48127898-48127899	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs551643196	chr11:48127949-48127950	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs571349497	chr11:48127973-48127974	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs367793530	chr11:48127974-48127975	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs139710567	chr11:48128079-48128080	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11039517	chr11:48128097-48128098	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538821510	chr11:48128154-48128155	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs558751041	chr11:48128164-48128165	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs10734562	chr11:48128189-48128190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs75539408	chr11:48128217-48128218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577655295	chr11:48128226-48128227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554745513	chr11:48128242-48128243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574370874	chr11:48128255-48128256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368948210	chr11:48128281-48128282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12576464	chr11:48128285-48128286	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs373615105	chr11:48128290-48128291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377600654	chr11:48128298-48128299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs370686960	chr11:48128303-48128304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs143042373	chr11:48128307-48128308	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs374144408	chr11:48128311-48128312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77579056	chr11:48128313-48128314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78485045	chr11:48128315-48128316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs145098040	chr11:48128316-48128317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs199633063	chr11:48128318-48128319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs36111682	chr11:48128319-48128320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34827149	chr11:48128322-48128323	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs35643138	chr11:48128337-48128338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554429726	chr11:48128373-48128374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188955563	chr11:48128376-48128377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542393460	chr11:48128382-48128383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562692245	chr11:48128383-48128384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576241833	chr11:48128389-48128390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541914268	chr11:48128407-48128408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371849369	chr11:48128521-48128522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181749102	chr11:48128523-48128524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544959652	chr11:48128620-48128621	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs527665760	chr11:48128652-48128653	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116262628	chr11:48128680-48128681	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373413205	chr11:48128699-48128700	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs564522070	chr11:48128733-48128734	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Glioblastoma multiforme	21390271	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:2727 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48114600-48131400	Weak transcription	Esophagus	oesophagus
2	chr11:48116400-48128600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr11:48116600-48131200	Weak transcription	Psoas Muscle	Psoas
4	chr11:48118800-48129800	Weak transcription	Lung	lung
5	chr11:48118800-48131200	Weak transcription	Ovary	ovary
6	chr11:48119600-48127800	Enhancers	Brain Substantia Nigra	brain
7	chr11:48119600-48131400	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:48119800-48128800	Weak transcription	Hela-S3	cervix
9	chr11:48121800-48128200	Enhancers	Fetal Intestine Small	intestine
10	chr11:48122200-48128200	Enhancers	Fetal Intestine Large	intestine
11	chr11:48122600-48127800	Enhancers	Brain Angular Gyrus	brain
12	chr11:48122600-48128200	Enhancers	Fetal Muscle Leg	muscle
13	chr11:48122600-48128400	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr11:48122800-48128200	Enhancers	Sigmoid Colon	Sigmoid Colon
15	chr11:48122800-48130600	Enhancers	Spleen	Spleen
16	chr11:48123200-48131200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr11:48123400-48128200	Enhancers	Skeletal Muscle Male	skeletal muscle
18	chr11:48123400-48129200	Weak transcription	Placenta	Placenta
19	chr11:48123400-48129200	Weak transcription	Fetal Thymus	thymus
20	chr11:48123400-48130400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr11:48123400-48131200	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr11:48123600-48131200	Enhancers	Liver	Liver
23	chr11:48123800-48128600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr11:48123800-48129000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:48124000-48128600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:48124000-48128600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:48124000-48131200	Weak transcription	Fetal Lung	lung
28	chr11:48124200-48131200	Enhancers	Primary B cells from peripheral blood	blood
29	chr11:48124600-48128000	Enhancers	Pancreas	Pancrea
30	chr11:48125200-48128400	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr11:48125400-48131200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr11:48125600-48132200	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr11:48125800-48129800	Weak transcription	Adipose Nuclei	Adipose
34	chr11:48125800-48130400	Weak transcription	Small Intestine	intestine
35	chr11:48125800-48130800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr11:48125800-48131200	Weak transcription	Aorta	Aorta
37	chr11:48125800-48131600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:48126000-48128200	Enhancers	Brain Anterior Caudate	brain
39	chr11:48126000-48129200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr11:48126000-48130200	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr11:48126000-48130800	Weak transcription	Fetal Brain Male	brain
42	chr11:48126000-48131000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr11:48126000-48131200	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr11:48126000-48131200	Weak transcription	NHEK	skin
45	chr11:48126200-48128600	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr11:48126200-48128800	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr11:48126200-48129000	Weak transcription	Fetal Kidney	kidney
48	chr11:48126200-48131200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr11:48126200-48132000	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr11:48126400-48128600	Weak transcription	Muscle Satellite Cultured Cells	--

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