Variant report

Variant	nsv1051661
Chromosome Location	chr11:48149295-48616507
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1494)
CpG islands
(count:1468)
Chromatin interactive
region (count:32)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1494 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48194471-48194702	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48600198-48600306	K562	blood:	n/a	n/a
3	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
4	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
5	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
6	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
7	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
8	BCL3	chr11:48393835-48394182	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
10	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
12	BRCA1	chr11:48361931-48361935	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
15	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
16	CBX3	chr11:48175001-48175304	K562	blood:	n/a	n/a
17	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
18	CEBPB	chr11:48497081-48497188	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:48367044-48367318	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:48477483-48477823	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:48194408-48194759	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:48232368-48232629	A549	lung:	n/a	chr11:48232504-48232515
23	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
24	CEBPB	chr11:48477613-48477707	K562	blood:	n/a	n/a
25	CEBPB	chr11:48232376-48232660	HepG2	liver:	n/a	chr11:48232504-48232515
26	CEBPB	chr11:48170213-48170393	A549	lung:	n/a	n/a
27	CEBPB	chr11:48367001-48367415	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr11:48477500-48477793	IMR90	lung:	n/a	n/a
29	CEBPB	chr11:48186415-48186684	A549	lung:	n/a	n/a
30	CEBPB	chr11:48155839-48155929	HepG2	liver:	n/a	chr11:48155883-48155894
31	CEBPB	chr11:48477590-48477827	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr11:48186361-48186787	MCF-7	breast:	n/a	n/a
33	CEBPB	chr11:48376639-48376671	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr11:48151304-48151612	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr11:48171812-48172128	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr11:48151484-48151532	K562	blood:	n/a	n/a
37	CEBPB	chr11:48477506-48477722	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:48186338-48186812	MCF-7	breast:	n/a	n/a
39	CEBPB	chr11:48232372-48232647	Hela-S3	cervix:	n/a	chr11:48232504-48232515
40	CEBPB	chr11:48161558-48161771	H1-hESC	embryonic stem cell:	n/a	chr11:48161642-48161653
41	CEBPB	chr11:48161501-48161776	Hela-S3	cervix:	n/a	chr11:48161642-48161653
42	CEBPB	chr11:48171761-48172146	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
44	CEBPB	chr11:48161546-48161713	K562	blood:	n/a	chr11:48161642-48161653
45	CEBPB	chr11:48161560-48161749	HepG2	liver:	n/a	chr11:48161642-48161653
46	CEBPB	chr11:48161530-48161773	A549	lung:	n/a	chr11:48161642-48161653
47	CEBPB	chr11:48171833-48172148	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr11:48232351-48232666	K562	blood:	n/a	chr11:48232504-48232515
49	CEBPB	chr11:48161481-48161783	IMR90	lung:	n/a	chr11:48161642-48161653
50	CEBPB	chr11:48477489-48477840	A549	lung:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48374446-48374496	NB4	blood:	n/a
2	chr11:48238296-48238346	HEK293	kidney:	embryo
3	chr11:48509488-48509538	HRCEpiC	kidney:	n/a
4	chr11:48509488-48509538	AG04449	skin:	fetal
5	chr11:48374446-48374496	NB4	blood:	n/a
6	chr11:48238296-48238346	HEK293	kidney:	embryo
7	chr11:48509488-48509538	HRCEpiC	kidney:	n/a
8	chr11:48509488-48509538	AG04449	skin:	fetal
9	chr11:48509488-48509538	T-47D	breast:	n/a
10	chr11:48509488-48509538	MCF-7	breast:	n/a
11	chr11:48285200-48285250	SK-N-SH_RA	brain:	n/a
12	chr11:48509488-48509538	SKMC	muscle:	n/a
13	chr11:48509488-48509538	GM06990	blood:	n/a
14	chr11:48374446-48374496	GM12892	blood:	n/a
15	chr11:48327164-48327214	HMEC	breast:	n/a
16	chr11:48285821-48285871	HepG2	liver:	n/a
17	chr11:48328132-48328182	SK-N-SH_RA	brain:	n/a
18	chr11:48328132-48328182	HRPEpiC	eye:	n/a
19	chr11:48328132-48328182	HEEpiC	esophagus:	n/a
20	chr11:48238724-48238774	HCM	heart:	n/a
21	chr11:48509488-48509538	NH-A	brain:	n/a
22	chr11:48161380-48161430	Jurkat	blood:	n/a
23	chr11:48509488-48509538	GM12892	blood:	n/a
24	chr11:48327164-48327214	HRCEpiC	kidney:	n/a
25	chr11:48285821-48285871	ProgFib	skin:	n/a
26	chr11:48238724-48238774	HUVEC	blood vessel:	n/a
27	chr11:48284249-48284299	Caco-2	colon:	n/a
28	chr11:48161380-48161430	K562	blood:	n/a
29	chr11:48326388-48326438	Hela-S3	cervix:	n/a
30	chr11:48374446-48374496	PANC-1	pancreas:	n/a
31	chr11:48374446-48374496	NHDF-neo	bronchial:	n/a
32	chr11:48153832-48153882	K562	blood:	n/a
33	chr11:48161861-48161911	BJ	skin:	n/a
34	chr11:48161380-48161430	IMR90	lung:	fetal
35	chr11:48374446-48374496	HCPEpiC	choroid plexus:	n/a
36	chr11:48238724-48238774	AG09309	skin:	n/a
37	chr11:48237358-48237408	T-47D	breast:	n/a
38	chr11:48238296-48238346	GM06990	blood:	n/a
39	chr11:48191068-48191118	RPTEC	kidney:	n/a
40	chr11:48345361-48345411	HRPEpiC	eye:	n/a
41	chr11:48237353-48237403	HEK293	kidney:	embryo
42	chr11:48509778-48509828	PFSK-1	brain:	n/a
43	chr11:48326388-48326438	AG04450	lung:	fetal
44	chr11:48285821-48285871	AG09319	gingival:	n/a
45	chr11:48185069-48185119	SAEC	small airway:	n/a
46	chr11:48285200-48285250	IMR90	lung:	fetal
47	chr11:48374446-48374496	HRE	kidney:	n/a
48	chr11:48326388-48326438	H1-hESC	embryonic stem cell:	embryo
49	chr11:48285200-48285250	U87	brain:	n/a
50	chr11:48284249-48284299	ProgFib	skin:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
2	chr1:153895897..153896422-chr11:48153597..48154395,2	Hela-S3	cervix:
3	chr11:48147029..48148645-chr11:48154007..48155529,2	MCF-7	breast:
4	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
5	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
6	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
7	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
8	chr11:48000629..48003536-chr11:48164616..48166215,2	K562	blood:
9	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
10	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
11	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
12	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
13	chr11:48167809..48169447-chr6:82621853..82624317,2	MCF-7	breast:
14	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
15	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
16	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
17	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
18	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
19	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
20	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
21	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
22	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
23	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
24	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:
25	chr11:48162891..48165104-chr11:48166215..48167785,2	K562	blood:
26	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
27	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
28	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
29	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
30	chr11:47857319..47859657-chr11:48158646..48160993,2	K562	blood:
31	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
32	chr11:47956073..47956643-chr11:48155973..48156490,2	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-155-5p	chr11:48190367-48190373
2	PTPRJ	hsa-miR-16-5p	chr11:48190236-48190242
3	PTPRJ	hsa-miR-26b-5p	chr11:48190233-48190256
4	PTPRJ	hsa-miR-16-5p	chr11:48190225-48190243
5	PTPRJ	hsa-miR-124-3p	chr11:48189431-48189437
6	PTPRJ	hsa-miR-124-3p	chr11:48189418-48189438
7	PTPRJ	hsa-miR-155-5p	chr11:48190351-48190373
8	PTPRJ	hsa-miR-328-3p	chr11:48191725-48191748

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
ENSG00000149177	chromatin interactions

Extended variants
information (count: 7386 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:7386 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538154652	chr11:48149300-48149301	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375923513	chr11:48149319-48149320	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147814465	chr11:48149337-48149338	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2229703	chr11:48149352-48149353	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs145270865	chr11:48149384-48149385	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs147639990	chr11:48149411-48149412	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs368884395	chr11:48149416-48149417	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs373034804	chr11:48149449-48149450	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs140746006	chr11:48149478-48149479	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs201275741	chr11:48149482-48149483	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs377560733	chr11:48149490-48149491	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs61739179	chr11:48149491-48149492	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs145529081	chr11:48149504-48149505	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs201570482	chr11:48149505-48149506	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs373741778	chr11:48149511-48149512	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs151256577	chr11:48149512-48149513	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs561061051	chr11:48149530-48149531	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs529943730	chr11:48149540-48149541	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs201089282	chr11:48149561-48149562	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs35331651	chr11:48149566-48149567	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs78258670	chr11:48149572-48149573	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs140439773	chr11:48149575-48149576	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs138926177	chr11:48149585-48149586	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs61739249	chr11:48149590-48149591	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs373367979	chr11:48149627-48149628	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs11039536	chr11:48149636-48149637	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs113929359	chr11:48149642-48149643	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs538142343	chr11:48149707-48149708	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs548497527	chr11:48149711-48149712	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs568297289	chr11:48149715-48149716	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs184903629	chr11:48149719-48149720	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs371209097	chr11:48149745-48149746	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs905475	chr11:48149755-48149756	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs34073149	chr11:48149817-48149818	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs114249990	chr11:48149843-48149844	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138321285	chr11:48149891-48149892	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs142824784	chr11:48149892-48149893	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs370345453	chr11:48149940-48149941	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190984694	chr11:48149955-48149956	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182743767	chr11:48150001-48150002	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs560094477	chr11:48150023-48150024	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs144793866	chr11:48150103-48150104	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs77074615	chr11:48150104-48150105	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs562119039	chr11:48150164-48150165	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs138571698	chr11:48150244-48150245	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs547498093	chr11:48150247-48150248	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs547796486	chr11:48150266-48150267	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs149333337	chr11:48150270-48150271	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs186419531	chr11:48150285-48150286	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs375466361	chr11:48150353-48150354	Weak transcription Strong transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Breast cancer	21990379	CNVD
Acute myeloid leukemia	20729466	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	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:1944 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48131600-48153200	Weak transcription	HSMM	muscle
2	chr11:48131600-48155800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:48131600-48191600	Weak transcription	Small Intestine	intestine
4	chr11:48137000-48149400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr11:48137000-48150600	Weak transcription	Fetal Kidney	kidney
6	chr11:48137000-48172000	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr11:48137000-48175200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr11:48137200-48161000	Weak transcription	NHDF-Ad	bronchial
9	chr11:48137600-48151600	Weak transcription	Fetal Lung	lung
10	chr11:48137600-48156600	Strong transcription	A549	lung
11	chr11:48138200-48192600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr11:48139600-48153600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:48139600-48172200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr11:48139800-48150800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:48139800-48151000	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr11:48140000-48155400	Strong transcription	Liver	Liver
17	chr11:48140200-48155600	Strong transcription	Primary B cells from cord blood	blood
18	chr11:48140400-48149400	Weak transcription	Left Ventricle	heart
19	chr11:48140600-48155600	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr11:48141200-48151200	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr11:48141200-48162800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr11:48141200-48163200	Strong transcription	Fetal Intestine Large	intestine
23	chr11:48141400-48152200	Strong transcription	Rectal Mucosa Donor 31	rectum
24	chr11:48141400-48155200	Strong transcription	Primary T helper cells PMA-I stimulated	--
25	chr11:48141800-48152200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:48142600-48152200	Strong transcription	Duodenum Mucosa	Duodenum
27	chr11:48142600-48155000	Strong transcription	Primary T cells from cord blood	blood
28	chr11:48143200-48164200	Weak transcription	Ovary	ovary
29	chr11:48143400-48151800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr11:48143400-48152400	Strong transcription	Fetal Intestine Small	intestine
31	chr11:48143800-48152400	Strong transcription	Lung	lung
32	chr11:48144000-48175200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr11:48144400-48153600	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr11:48145000-48152400	Strong transcription	Osteobl	bone
35	chr11:48145000-48153200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr11:48145000-48153400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr11:48145200-48153400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr11:48145200-48153600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:48145400-48149600	Strong transcription	Hela-S3	cervix
40	chr11:48145400-48152200	Strong transcription	Cortex derived primary cultured neurospheres	brain
41	chr11:48145400-48152400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:48145400-48153400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr11:48145400-48154800	Weak transcription	HUVEC	blood vessel
44	chr11:48145400-48155000	Strong transcription	Adipose Nuclei	Adipose
45	chr11:48145600-48152200	Strong transcription	Fetal Brain Female	brain
46	chr11:48145600-48155000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr11:48145600-48175600	Weak transcription	Fetal Brain Male	brain
48	chr11:48145800-48153400	Strong transcription	Rectal Mucosa Donor 29	rectum
49	chr11:48145800-48184200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:48146000-48149800	Strong transcription	Skeletal Muscle Male	skeletal muscle

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