Variant report

Variant	nsv555411
Chromosome Location	chr11:72647296-72800970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1125)
CpG islands
(count:428)
Chromatin interactive
region (count:54)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1125 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:72800018-72800022	K562	blood:	n/a	n/a
2	ARID3A	chr11:72680920-72681281	K562	blood:	n/a	n/a
3	ARID3A	chr11:72758637-72759056	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:72773312-72773313	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:72687003-72687104	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:72682391-72682571	K562	blood:	n/a	n/a
7	ARID3A	chr11:72769938-72770418	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:72770519-72770662	K562	blood:	n/a	n/a
9	ARID3A	chr11:72731093-72731355	HepG2	liver:	n/a	n/a
10	ATF1	chr11:72673207-72673482	K562	blood:	n/a	n/a
11	ATF1	chr11:72680973-72681264	K562	blood:	n/a	n/a
12	ATF1	chr11:72681855-72682055	K562	blood:	n/a	n/a
13	ATF2	chr11:72662878-72663450	GM12878	blood:	n/a	n/a
14	ATF2	chr11:72714056-72714505	GM12878	blood:	n/a	n/a
15	ATF2	chr11:72758728-72759536	GM12878	blood:	n/a	n/a
16	ATF2	chr11:72680738-72681511	GM12878	blood:	n/a	n/a
17	ATF2	chr11:72691975-72692488	GM12878	blood:	n/a	n/a
18	ATF2	chr11:72783904-72784579	GM12878	blood:	n/a	n/a
19	ATF2	chr11:72796235-72796697	GM12878	blood:	n/a	n/a
20	ATF2	chr11:72713971-72714544	GM12878	blood:	n/a	n/a
21	ATF2	chr11:72680732-72681425	GM12878	blood:	n/a	n/a
22	ATF3	chr11:72673077-72673548	HCT-116	colon:	n/a	n/a
23	ATF3	chr11:72673082-72673545	K562	blood:	n/a	n/a
24	ATF3	chr11:72673183-72673421	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr11:72686886-72687131	GM12878	blood:	n/a	n/a
26	BATF	chr11:72714096-72714331	GM12878	blood:	n/a	n/a
27	BATF	chr11:72680814-72681306	GM12878	blood:	n/a	n/a
28	BATF	chr11:72685600-72685849	GM12878	blood:	n/a	chr11:72685811-72685821
29	BATF	chr11:72665948-72666236	GM12878	blood:	n/a	n/a
30	BATF	chr11:72798778-72799097	GM12878	blood:	n/a	n/a
31	BATF	chr11:72783970-72784325	GM12878	blood:	n/a	n/a
32	BATF	chr11:72798820-72799079	GM12878	blood:	n/a	n/a
33	BATF	chr11:72680874-72681277	GM12878	blood:	n/a	n/a
34	BATF	chr11:72783947-72784355	GM12878	blood:	n/a	n/a
35	BATF	chr11:72759071-72759436	GM12878	blood:	n/a	n/a
36	BATF	chr11:72796274-72796612	GM12878	blood:	n/a	chr11:72796399-72796410
37	BCL11A	chr11:72714118-72714378	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:72665901-72666277	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:72783979-72784372	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:72783939-72784412	GM12878	blood:	n/a	n/a
41	BCL11A	chr11:72680788-72681282	GM12878	blood:	n/a	n/a
42	BCL3	chr11:72686828-72687182	GM12878	blood:	n/a	n/a
43	BCL3	chr11:72680888-72681333	GM12878	blood:	n/a	n/a
44	BCL3	chr11:72665892-72666240	GM12878	blood:	n/a	n/a
45	BCLAF1	chr11:72758805-72759555	GM12878	blood:	n/a	n/a
46	BCLAF1	chr11:72680675-72681471	GM12878	blood:	n/a	n/a
47	BCLAF1	chr11:72796231-72796645	GM12878	blood:	n/a	n/a
48	BCLAF1	chr11:72783787-72784642	GM12878	blood:	n/a	chr11:72784413-72784422
49	BCLAF1	chr11:72714009-72714452	GM12878	blood:	n/a	n/a
50	BCLAF1	chr11:72796165-72796736	GM12878	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:72662461-72662511	IMR90	lung:	fetal
2	chr11:72662461-72662511	IMR90	lung:	fetal
3	chr11:72724062-72724112	U87	brain:	n/a
4	chr11:72741250-72741300	NHDF-neo	bronchial:	n/a
5	chr11:72770858-72770908	RPTEC	kidney:	n/a
6	chr11:72724062-72724112	CMK	blood:	n/a
7	chr11:72682460-72682510	Caco-2	colon:	n/a
8	chr11:72682460-72682510	BE2_C	brain:	n/a
9	chr11:72682460-72682510	SKMC	muscle:	n/a
10	chr11:72662461-72662511	HUVEC	blood vessel:	n/a
11	chr11:72662461-72662511	GM12878	blood:	n/a
12	chr11:72724062-72724112	NHBE	bronchial:	n/a
13	chr11:72682460-72682510	HMEC	breast:	n/a
14	chr11:72759293-72759343	Caco-2	colon:	n/a
15	chr11:72662461-72662511	ovcar-3	ovarian:	n/a
16	chr11:72770858-72770908	MCF-7	breast:	n/a
17	chr11:72724062-72724112	IMR90	lung:	fetal
18	chr11:72770858-72770908	HCF	heart:	n/a
19	chr11:72759293-72759343	HRE	kidney:	n/a
20	chr11:72770858-72770908	LNCaP	prostate:	n/a
21	chr11:72682460-72682510	GM19239	blood:	n/a
22	chr11:72724062-72724112	GM12892	blood:	n/a
23	chr11:72750477-72750527	GM19239	blood:	n/a
24	chr11:72741250-72741300	HCM	heart:	n/a
25	chr11:72682460-72682510	A549	lung:	n/a
26	chr11:72682460-72682510	SK-N-MC	brain:	n/a
27	chr11:72750477-72750527	SAEC	small airway:	n/a
28	chr11:72724062-72724112	HRPEpiC	eye:	n/a
29	chr11:72682460-72682510	HNPCEpiC	eye:	n/a
30	chr11:72770858-72770908	CMK	blood:	n/a
31	chr11:72724062-72724112	T-47D	breast:	n/a
32	chr11:72750477-72750527	HCM	heart:	n/a
33	chr11:72682460-72682510	AG10803	skin:	n/a
34	chr11:72750477-72750527	HNPCEpiC	eye:	n/a
35	chr11:72662461-72662511	CMK	blood:	n/a
36	chr11:72741250-72741300	IMR90	lung:	fetal
37	chr11:72741250-72741300	CMK	blood:	n/a
38	chr11:72662461-72662511	HCT-116	colon:	n/a
39	chr11:72750477-72750527	GM12891	blood:	n/a
40	chr11:72759293-72759343	HEEpiC	esophagus:	n/a
41	chr11:72759293-72759343	HL-60	blood:	n/a
42	chr11:72741250-72741300	NH-A	brain:	n/a
43	chr11:72759293-72759343	H1-hESC	embryonic stem cell:	embryo
44	chr11:72759293-72759343	GM19239	blood:	n/a
45	chr11:72682460-72682510	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:72724062-72724112	ProgFib	skin:	n/a
47	chr11:72724062-72724112	A549	lung:	n/a
48	chr11:72682460-72682510	GM12878	blood:	n/a
49	chr11:72770858-72770908	HIPEpiC	eye:	n/a
50	chr11:72750477-72750527	SK-N-MC	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:72781352..72782941-chr11:72784676..72786662,2	MCF-7	breast:
2	chr11:72682058..72684979-chr11:72694471..72696981,2	MCF-7	breast:
3	chr11:72664177..72665992-chr11:72667609..72669662,2	K562	blood:
4	chr11:72694533..72697472-chr11:72703924..72706266,2	K562	blood:
5	chr11:72687090..72688837-chr11:72693209..72695483,2	MCF-7	breast:
6	chr11:72679416..72681431-chr11:72682250..72684865,2	K562	blood:
7	chr11:72681582..72683189-chr11:72684693..72686760,2	K562	blood:
8	chr11:72502299..72505277-chr11:72732916..72736864,3	MCF-7	breast:
9	chr11:72783683..72785788-chr11:72789075..72790894,2	MCF-7	breast:
10	chr11:72686975..72688834-chr11:72691101..72692704,2	MCF-7	breast:
11	chr11:72782635..72785353-chr11:72791682..72794185,2	MCF-7	breast:
12	chr11:72682058..72684979-chr11:72694471..72696981,2	MCF-7	breast:
13	chr11:72656692..72659445-chr11:72660931..72662895,2	MCF-7	breast:
14	chr11:72784638..72786554-chr11:72789101..72790627,2	MCF-7	breast:
15	chr11:72681582..72683189-chr11:72684693..72686760,2	K562	blood:
16	chr11:72670744..72672393-chr11:72782076..72784290,2	MCF-7	breast:
17	chr11:72770414..72772587-chr11:72778481..72781095,2	MCF-7	breast:
18	chr11:72795559..72797402-chr11:72798255..72800366,2	K562	blood:
19	chr11:72670744..72672393-chr11:72782076..72784290,2	MCF-7	breast:
20	chr11:72784638..72786554-chr11:72789101..72790627,2	MCF-7	breast:
21	chr11:72679416..72681431-chr11:72682250..72684865,2	K562	blood:
22	chr11:72664177..72665992-chr11:72667609..72669662,2	K562	blood:
23	chr11:72740332..72742221-chr11:72743270..72746059,2	K562	blood:
24	chr11:72662616..72664158-chr11:72667252..72669595,2	K562	blood:
25	chr11:72642359..72644585-chr11:72662494..72664932,2	MCF-7	breast:
26	chr11:72740332..72742221-chr11:72743270..72746059,2	K562	blood:
27	chr11:72692583..72696422-chr11:72698620..72700256,3	MCF-7	breast:
28	chr11:72783683..72785788-chr11:72789075..72790894,2	MCF-7	breast:
29	chr11:72676776..72678415-chr11:72679843..72681427,2	MCF-7	breast:
30	chr11:72689559..72692269-chr11:72695713..72698108,2	K562	blood:
31	chr11:72693768..72696510-chr11:72699239..72701764,2	K562	blood:
32	chr11:72770414..72772587-chr11:72778481..72781095,2	MCF-7	breast:
33	chr11:72662616..72664158-chr11:72667252..72669595,2	K562	blood:
34	chr11:72795559..72797402-chr11:72798255..72800366,2	K562	blood:
35	chr11:72662658..72664172-chr11:72667529..72669595,2	K562	blood:
36	chr11:72782635..72785353-chr11:72791682..72794185,2	MCF-7	breast:
37	chr11:72794791..72796457-chr11:72847518..72849670,2	MCF-7	breast:
38	chr11:72676395..72677930-chr11:72681229..72683225,2	K562	blood:
39	chr11:72741325..72744798-chr11:72852592..72854519,3	K562	blood:
40	chr11:72713297..72718110-chr11:72852062..72855076,4	K562	blood:
41	chr11:72533161..72535862-chr11:72680892..72683128,2	K562	blood:
42	chr11:72686975..72688834-chr11:72691101..72692704,2	MCF-7	breast:
43	chr11:72656692..72659445-chr11:72660931..72662895,2	MCF-7	breast:
44	chr11:72694533..72697472-chr11:72703924..72706266,2	K562	blood:
45	chr11:72724109..72726917-chr11:72853072..72855247,2	MCF-7	breast:
46	chr11:72687090..72688837-chr11:72693209..72695483,2	MCF-7	breast:
47	chr1:167522606..167523250-chr11:72697395..72698131,2	HCT-116	colon:
48	chr11:72743552..72745923-chr11:72752498..72755495,2	MCF-7	breast:
49	chr11:72662658..72664172-chr11:72667529..72669595,2	K562	blood:
50	chr11:72743552..72745923-chr11:72752498..72755495,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-P2RY2-6	chr11:72775149-72775473	expReg_chr11_7599_+
2	lnc-STARD10-4	chr11:72793405-72793680	expReg_chr11_7223_-
3	lnc-P2RY2-5	chr11:72776077-72776433	expReg_chr11_7601_+
4	lnc-STARD10-3	chr11:72792116-72793219	expReg_chr11_7220_-
5	lnc-ATG16L2-9	chr11:72651543-72652157	NONHSAT022807
6	lnc-STARD10-2	chr11:72789997-72790571	expReg_chr11_7217_-

No data

Variant related genes	Relation type
ENSG00000234751	TF binding region
FCHSD2	TF binding region
ENSG00000234751	CpG island
FCHSD2	CpG island
ENSG00000214530	chromatin interactions
ENSG00000137478	chromatin interactions
ENSG00000168010	chromatin interactions
ENSG00000143162	chromatin interactions
ENSG00000186635	chromatin interactions

Extended variants
information (count: 5146 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:5146 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7926133	chr11:72647296-72647297	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566438305	chr11:72647358-72647359	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs184536470	chr11:72647380-72647381	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs553592776	chr11:72647508-72647509	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs561270621	chr11:72647538-72647539	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs76404487	chr11:72647548-72647549	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs545581545	chr11:72647578-72647579	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs72979433	chr11:72647596-72647597	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs568847706	chr11:72647652-72647653	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs575320038	chr11:72647786-72647787	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181380863	chr11:72647795-72647796	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76641528	chr11:72647796-72647797	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538121894	chr11:72647831-72647832	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540167154	chr11:72647845-72647846	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370191845	chr11:72647923-72647924	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565175823	chr11:72647933-72647934	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs532252822	chr11:72647964-72647965	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141804665	chr11:72647966-72647967	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186337358	chr11:72647967-72647968	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529827925	chr11:72647968-72647969	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548276498	chr11:72647978-72647979	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6592498	chr11:72648005-72648006	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs77041803	chr11:72648019-72648020	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6592499	chr11:72648044-72648045	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs374694171	chr11:72648083-72648084	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11607217	chr11:72648085-72648086	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs566654419	chr11:72648119-72648120	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557546958	chr11:72648130-72648131	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575405114	chr11:72648177-72648178	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs539955833	chr11:72648188-72648189	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542715395	chr11:72648211-72648212	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554602939	chr11:72648218-72648219	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572942649	chr11:72648332-72648333	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190665296	chr11:72648401-72648402	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs369363765	chr11:72648433-72648434	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs181490623	chr11:72648456-72648457	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533992897	chr11:72648464-72648465	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs114772218	chr11:72648469-72648470	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs143563717	chr11:72648491-72648492	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs117279208	chr11:72648511-72648512	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529865650	chr11:72648558-72648559	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372808884	chr11:72648566-72648567	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148042453	chr11:72648572-72648573	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186386691	chr11:72648578-72648579	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527319341	chr11:72648583-72648584	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552137553	chr11:72648606-72648607	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371403865	chr11:72648615-72648616	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs570318515	chr11:72648661-72648662	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539341086	chr11:72648679-72648680	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs550816570	chr11:72648685-72648686	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	19153074	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2822 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:72577200-72651600	Weak transcription	Gastric	stomach
2	chr11:72600800-72653200	Weak transcription	Lung	lung
3	chr11:72612400-72649000	Weak transcription	Aorta	Aorta
4	chr11:72621000-72651000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:72624200-72654400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr11:72624400-72652000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr11:72628800-72649000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:72630800-72662400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr11:72633000-72648600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr11:72633000-72654400	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr11:72633000-72680000	Weak transcription	Dnd41	blood
12	chr11:72633000-72684000	Weak transcription	Primary T cells from cord blood	blood
13	chr11:72633200-72651600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr11:72633200-72668400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr11:72633400-72679400	Weak transcription	Fetal Thymus	thymus
16	chr11:72634000-72648600	Weak transcription	HepG2	liver
17	chr11:72636200-72694800	Weak transcription	Adipose Nuclei	Adipose
18	chr11:72636400-72680200	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr11:72636400-72712600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr11:72637000-72721600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr11:72637200-72653200	Weak transcription	Psoas Muscle	Psoas
22	chr11:72637400-72666000	Weak transcription	Ovary	ovary
23	chr11:72637400-72666400	Weak transcription	Right Ventricle	heart
24	chr11:72637600-72651600	Weak transcription	Left Ventricle	heart
25	chr11:72640400-72649400	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr11:72640400-72652400	Strong transcription	GM12878-XiMat	blood
27	chr11:72641000-72649600	Weak transcription	Brain Anterior Caudate	brain
28	chr11:72641200-72650800	Weak transcription	Brain Angular Gyrus	brain
29	chr11:72641200-72654400	Weak transcription	Fetal Kidney	kidney
30	chr11:72641400-72651000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr11:72641800-72653200	Weak transcription	Pancreas	Pancrea
32	chr11:72641800-72680200	Weak transcription	HSMMtube	muscle
33	chr11:72643600-72676400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr11:72643800-72653000	Weak transcription	HSMM	muscle
35	chr11:72643800-72668400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr11:72643800-72673000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr11:72644000-72662000	Weak transcription	Osteobl	bone
38	chr11:72644600-72662000	Weak transcription	Liver	Liver
39	chr11:72645400-72652000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr11:72645800-72648800	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr11:72646000-72647400	Enhancers	Fetal Lung	lung
42	chr11:72646200-72648400	Genic enhancers	Primary B cells from cord blood	blood
43	chr11:72646400-72647400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr11:72646400-72647600	Enhancers	Small Intestine	intestine
45	chr11:72646600-72651600	Weak transcription	Fetal Intestine Small	intestine
46	chr11:72646800-72647600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr11:72646800-72647600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr11:72646800-72647800	Genic enhancers	Primary B cells from peripheral blood	blood
49	chr11:72647200-72647400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr11:72647200-72648200	Enhancers	HUVEC	blood vessel

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