Variant report

Variant	nsv428253
Chromosome Location	chr11:48133996-48524981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1638)
CpG islands
(count:1467)
Chromatin interactive
region (count:37)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

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	ATF1	chr11:48356437-48356637	K562	blood:	n/a	n/a
3	ATF1	chr11:48292484-48292679	K562	blood:	n/a	n/a
4	ATF3	chr11:48194364-48194613	K562	blood:	n/a	n/a
5	ATF3	chr11:48194480-48194676	K562	blood:	n/a	n/a
6	BACH1	chr11:48356973-48356986	K562	blood:	n/a	n/a
7	BCL3	chr11:48393835-48394182	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:48194470-48194703	GM12878	blood:	n/a	n/a
9	BRCA1	chr11:48194475-48194742	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr11:48235490-48235559	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr11:48329323-48329679	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr11:48361931-48361935	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr11:48194532-48194633	GM12878	blood:	n/a	n/a
14	CBX3	chr11:48136314-48136661	K562	blood:	n/a	n/a
15	CBX3	chr11:48136304-48136617	K562	blood:	n/a	n/a
16	CBX3	chr11:48175001-48175304	K562	blood:	n/a	n/a
17	CBX3	chr11:48329320-48329744	HCT-116	colon:	n/a	n/a
18	CEBPB	chr11:48186361-48186787	MCF-7	breast:	n/a	n/a
19	CEBPB	chr11:48332469-48332671	HepG2	liver:	n/a	chr11:48332598-48332609
20	CEBPB	chr11:48477489-48477840	A549	lung:	n/a	n/a
21	CEBPB	chr11:48497081-48497188	IMR90	lung:	n/a	n/a
22	CEBPB	chr11:48367001-48367415	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr11:48477483-48477823	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:48367044-48367318	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:48186415-48186684	A549	lung:	n/a	n/a
26	CEBPB	chr11:48367027-48367324	HCT-116	colon:	n/a	n/a
27	CEBPB	chr11:48171823-48172149	IMR90	lung:	n/a	n/a
28	CEBPB	chr11:48161501-48161776	Hela-S3	cervix:	n/a	chr11:48161642-48161653
29	CEBPB	chr11:48340990-48341301	A549	lung:	n/a	n/a
30	CEBPB	chr11:48161546-48161713	K562	blood:	n/a	chr11:48161642-48161653
31	CEBPB	chr11:48151484-48151532	K562	blood:	n/a	n/a
32	CEBPB	chr11:48374701-48375094	Hela-S3	cervix:	n/a	chr11:48374900-48374913
33	CEBPB	chr11:48477613-48477707	K562	blood:	n/a	n/a
34	CEBPB	chr11:48151304-48151612	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr11:48161558-48161771	H1-hESC	embryonic stem cell:	n/a	chr11:48161642-48161653
36	CEBPB	chr11:48477500-48477793	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:48138237-48138548	A549	lung:	n/a	n/a
38	CEBPB	chr11:48477506-48477722	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:48155839-48155929	HepG2	liver:	n/a	chr11:48155883-48155894
40	CEBPB	chr11:48477590-48477827	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr11:48232376-48232660	HepG2	liver:	n/a	chr11:48232504-48232515
42	CEBPB	chr11:48161530-48161773	A549	lung:	n/a	chr11:48161642-48161653
43	CEBPB	chr11:48161560-48161749	HepG2	liver:	n/a	chr11:48161642-48161653
44	CEBPB	chr11:48148221-48148469	A549	lung:	n/a	n/a
45	CEBPB	chr11:48186338-48186812	MCF-7	breast:	n/a	n/a
46	CEBPB	chr11:48376639-48376671	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr11:48148135-48148517	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr11:48232346-48232660	IMR90	lung:	n/a	chr11:48232504-48232515
49	CEBPB	chr11:48148713-48148726	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:48161481-48161783	IMR90	lung:	n/a	chr11:48161642-48161653

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48191068-48191118	SKMC	muscle:	n/a
2	chr11:48185069-48185119	HCT-116	colon:	n/a
3	chr11:48374446-48374496	MCF10A-Er-Src	breast:	n/a
4	chr11:48191068-48191118	SKMC	muscle:	n/a
5	chr11:48185069-48185119	HCT-116	colon:	n/a
6	chr11:48374446-48374496	MCF10A-Er-Src	breast:	n/a
7	chr11:48345815-48345865	HMEC	breast:	n/a
8	chr11:48161380-48161430	Hela-S3	cervix:	n/a
9	chr11:48266856-48266906	BJ	skin:	n/a
10	chr11:48161380-48161430	GM12892	blood:	n/a
11	chr11:48161380-48161430	HEEpiC	esophagus:	n/a
12	chr11:48237353-48237403	NHDF-neo	bronchial:	n/a
13	chr11:48237358-48237408	PANC-1	pancreas:	n/a
14	chr11:48509778-48509828	GM12892	blood:	n/a
15	chr11:48285200-48285250	PFSK-1	brain:	n/a
16	chr11:48238724-48238774	U87	brain:	n/a
17	chr11:48326388-48326438	MCF-7	breast:	n/a
18	chr11:48345361-48345411	PFSK-1	brain:	n/a
19	chr11:48367974-48368024	H1-hESC	embryonic stem cell:	embryo
20	chr11:48345815-48345865	HUVEC	blood vessel:	n/a
21	chr11:48237358-48237408	HRCEpiC	kidney:	n/a
22	chr11:48367974-48368024	HRPEpiC	eye:	n/a
23	chr11:48185069-48185119	SK-N-MC	brain:	n/a
24	chr11:48161380-48161430	SK-N-SH	brain:	n/a
25	chr11:48191068-48191118	AG04450	lung:	fetal
26	chr11:48185069-48185119	HCPEpiC	choroid plexus:	n/a
27	chr11:48285200-48285250	HEEpiC	esophagus:	n/a
28	chr11:48185069-48185119	PFSK-1	brain:	n/a
29	chr11:48285200-48285250	MCF-7	breast:	n/a
30	chr11:48345361-48345411	CMK	blood:	n/a
31	chr11:48161861-48161911	Hepatocyte	liver:	n/a
32	chr11:48284249-48284299	AoSMC	blood vessel:	n/a
33	chr11:48374446-48374496	BE2_C	brain:	n/a
34	chr11:48346680-48346730	PrEC	prostate:	n/a
35	chr11:48328132-48328182	NB4	blood:	n/a
36	chr11:48346680-48346730	AG09309	skin:	n/a
37	chr11:48161861-48161911	K562	blood:	n/a
38	chr11:48345361-48345411	SAEC	small airway:	n/a
39	chr11:48161861-48161911	HCPEpiC	choroid plexus:	n/a
40	chr11:48153832-48153882	AG10803	skin:	n/a
41	chr11:48328132-48328182	LNCaP	prostate:	n/a
42	chr11:48191068-48191118	HAEpiC	amniotic membrane:	n/a
43	chr11:48284249-48284299	SAEC	small airway:	n/a
44	chr11:48346680-48346730	PFSK-1	brain:	n/a
45	chr11:48161380-48161430	H1-hESC	embryonic stem cell:	embryo
46	chr11:48326388-48326438	SAEC	small airway:	n/a
47	chr11:48266856-48266906	ovcar-3	ovarian:	n/a
48	chr11:48266856-48266906	AG04449	skin:	fetal
49	chr11:48509778-48509828	HRE	kidney:	n/a
50	chr11:48374446-48374496	NB4	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
2	chr11:48194206..48195039-chr11:49190936..49191807,2	MCF-7	breast:
3	chr11:48000629..48003536-chr11:48164616..48166215,2	K562	blood:
4	chr1:153895897..153896422-chr11:48153597..48154395,2	Hela-S3	cervix:
5	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
6	chr11:48478071..48478587-chr11:49191267..49191777,2	MCF-7	breast:
7	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
8	chr11:48162891..48165104-chr11:48166215..48167785,2	K562	blood:
9	chr11:48205861..48206473-chr11:48233802..48234494,2	MCF-7	breast:
10	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
11	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
12	chr11:48167809..48169447-chr6:82621853..82624317,2	MCF-7	breast:
13	chr11:47857319..47859657-chr11:48158646..48160993,2	K562	blood:
14	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
15	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
16	chr11:48147718..48152937-chr11:48156132..48159658,5	MCF-7	breast:
17	chr11:48129232..48130878-chr11:48134176..48136053,2	K562	blood:
18	chr11:48142980..48145287-chr11:48148448..48150580,3	MCF-7	breast:
19	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:
20	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
21	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
22	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
23	chr11:48366878..48368914-chr11:48372533..48375413,2	MCF-7	breast:
24	chr11:48131666..48133452-chr11:48135727..48137956,2	MCF-7	breast:
25	chr11:48361908..48364233-chr11:48365831..48368223,2	MCF-7	breast:
26	chr11:48234220..48234962-chr11:48329425..48329937,2	MCF-7	breast:
27	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
28	chr11:48194137..48195015-chr11:48231499..48232341,4	MCF-7	breast:
29	chr11:48144846..48146446-chr11:48150418..48153152,2	K562	blood:
30	chr11:48147029..48148645-chr11:48154007..48155529,2	MCF-7	breast:
31	chr11:48147718..48150018-chr11:48150075..48152129,2	K562	blood:
32	chr11:48147029..48148645-chr11:48154007..48155529,2	MCF-7	breast:
33	chr11:48175475..48177463-chr11:48181716..48184556,2	MCF-7	breast:
34	chr11:48205381..48206618-chr11:48231139..48232409,4	MCF-7	breast:
35	chr11:47956073..47956643-chr11:48155973..48156490,2	MCF-7	breast:
36	chr11:48193798..48195313-chr11:48231364..48232253,10	MCF-7	breast:
37	chr11:48292794..48294613-chr11:48297509..48299435,2	K562	blood:

(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-26b-5p	chr11:48190233-48190256
2	PTPRJ	hsa-miR-124-3p	chr11:48189418-48189438
3	PTPRJ	hsa-miR-155-5p	chr11:48190351-48190373
4	PTPRJ	hsa-miR-16-5p	chr11:48190225-48190243
5	PTPRJ	hsa-miR-124-3p	chr11:48189431-48189437
6	PTPRJ	hsa-miR-16-5p	chr11:48190236-48190242
7	PTPRJ	hsa-miR-155-5p	chr11:48190367-48190373
8	PTPRJ	hsa-miR-328-3p	chr11:48191725-48191748

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

Extended variants
information (count: 7805 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:7805 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536905304	chr11:48134023-48134024	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs192084133	chr11:48134055-48134056	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs557012769	chr11:48134094-48134095	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs567448596	chr11:48134147-48134148	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs185408412	chr11:48134186-48134187	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs148660345	chr11:48134228-48134229	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs142242039	chr11:48134240-48134241	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs190335565	chr11:48134253-48134254	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs375895000	chr11:48134254-48134255	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs77238727	chr11:48134261-48134262	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs374375816	chr11:48134264-48134265	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs575321600	chr11:48134299-48134300	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs143621466	chr11:48134316-48134317	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs544880649	chr11:48134336-48134337	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs561474801	chr11:48134359-48134360	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs146294071	chr11:48134360-48134361	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs369591621	chr11:48134414-48134415	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139633857	chr11:48134456-48134457	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142849806	chr11:48134465-48134466	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs559628758	chr11:48134520-48134521	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150984827	chr11:48134527-48134528	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560334491	chr11:48134646-48134647	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532423080	chr11:48134647-48134648	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374553685	chr11:48134650-48134651	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117679206	chr11:48134682-48134683	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs111831922	chr11:48134710-48134711	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531652128	chr11:48134755-48134756	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550827938	chr11:48134779-48134780	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs114888235	chr11:48134832-48134833	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577801518	chr11:48134885-48134886	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536565335	chr11:48134928-48134929	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546790929	chr11:48134935-48134936	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566678704	chr11:48134942-48134943	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538699796	chr11:48134980-48134981	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550622448	chr11:48135014-48135015	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs151221874	chr11:48135032-48135033	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575309155	chr11:48135090-48135091	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537473337	chr11:48135266-48135267	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs11039522	chr11:48135271-48135272	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs1566735	chr11:48135286-48135287	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs564490066	chr11:48135336-48135337	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs560272634	chr11:48135391-48135392	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs577062650	chr11:48135393-48135394	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs55746858	chr11:48135442-48135443	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs545887418	chr11:48135446-48135447	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs182457291	chr11:48135479-48135480	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs185757783	chr11:48135483-48135484	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs188314865	chr11:48135510-48135511	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs566638991	chr11:48135592-48135593	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs56035718	chr11:48135672-48135673	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	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:2267 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48126400-48147400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:48126600-48136000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr11:48128200-48143400	Weak transcription	Gastric	stomach
4	chr11:48130600-48142600	Weak transcription	Lung	lung
5	chr11:48131600-48134200	Weak transcription	NH-A	brain
6	chr11:48131600-48134400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:48131600-48134800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:48131600-48135800	Weak transcription	Fetal Intestine Large	intestine
9	chr11:48131600-48135800	Weak transcription	Stomach Mucosa	stomach
10	chr11:48131600-48136000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:48131600-48136000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr11:48131600-48136000	Weak transcription	Primary T cells from cord blood	blood
13	chr11:48131600-48136000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr11:48131600-48136000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr11:48131600-48136000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:48131600-48136000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr11:48131600-48136200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr11:48131600-48136200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:48131600-48136200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr11:48131600-48136200	Weak transcription	Fetal Kidney	kidney
21	chr11:48131600-48136400	Weak transcription	Brain Substantia Nigra	brain
22	chr11:48131600-48138000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr11:48131600-48145200	Weak transcription	NHLF	lung
24	chr11:48131600-48146600	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:48131600-48148600	Weak transcription	Aorta	Aorta
26	chr11:48131600-48149000	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr11:48131600-48149000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr11:48131600-48149000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:48131600-48153200	Weak transcription	HSMM	muscle
30	chr11:48131600-48155800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr11:48131600-48191600	Weak transcription	Small Intestine	intestine
32	chr11:48131800-48136000	Weak transcription	Fetal Lung	lung
33	chr11:48131800-48136200	Weak transcription	Brain Hippocampus Middle	brain
34	chr11:48131800-48136400	Weak transcription	Brain Cingulate Gyrus	brain
35	chr11:48131800-48136600	Weak transcription	Osteobl	bone
36	chr11:48131800-48136800	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr11:48132000-48134200	Enhancers	Primary B cells from peripheral blood	blood
38	chr11:48132000-48134400	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:48132000-48135400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr11:48132000-48135600	Weak transcription	Fetal Intestine Small	intestine
41	chr11:48132000-48136000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr11:48132000-48136000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr11:48132000-48136000	Weak transcription	Brain Anterior Caudate	brain
44	chr11:48132000-48136200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
45	chr11:48132000-48136200	Weak transcription	Duodenum Mucosa	Duodenum
46	chr11:48132000-48136200	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr11:48132000-48136400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr11:48132000-48141400	Weak transcription	Placenta	Placenta
49	chr11:48132000-48142600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr11:48132000-48145000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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