Variant report

Variant	nsv976471
Chromosome Location	chr11:76435262-76459660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:76446949-76447230	K562	blood:	n/a	n/a
2	ARID3A	chr11:76458629-76458856	K562	blood:	n/a	n/a
3	ARID3A	chr11:76456593-76457227	K562	blood:	n/a	n/a
4	ATF1	chr11:76456584-76457197	K562	blood:	n/a	n/a
5	ATF1	chr11:76446898-76447251	K562	blood:	n/a	n/a
6	ATF3	chr11:76446942-76447222	K562	blood:	n/a	n/a
7	BACH1	chr11:76451851-76452356	K562	blood:	n/a	n/a
8	BACH1	chr11:76447086-76447173	K562	blood:	n/a	n/a
9	BHLHE40	chr11:76441976-76442310	K562	blood:	n/a	n/a
10	BHLHE40	chr11:76458709-76458978	K562	blood:	n/a	n/a
11	BHLHE40	chr11:76456529-76457209	K562	blood:	n/a	n/a
12	BHLHE40	chr11:76446913-76447288	K562	blood:	n/a	n/a
13	BRCA1	chr11:76445047-76445260	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr11:76458407-76458807	K562	blood:	n/a	n/a
15	CBX3	chr11:76456485-76457599	K562	blood:	n/a	n/a
16	CBX3	chr11:76446869-76447346	K562	blood:	n/a	n/a
17	CCNT2	chr11:76447005-76447310	K562	blood:	n/a	n/a
18	CCNT2	chr11:76456576-76457268	K562	blood:	n/a	n/a
19	CEBPB	chr11:76456891-76457115	K562	blood:	n/a	n/a
20	CEBPB	chr11:76450822-76451197	A549	lung:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
21	CEBPB	chr11:76448262-76448463	IMR90	lung:	n/a	chr11:76448404-76448415
22	CEBPB	chr11:76450860-76451141	K562	blood:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
23	CEBPB	chr11:76450825-76451197	HepG2	liver:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
24	CEBPB	chr11:76446972-76447270	K562	blood:	n/a	n/a
25	CEBPB	chr11:76448325-76448546	HepG2	liver:	n/a	chr11:76448404-76448415
26	CEBPB	chr11:76450790-76451352	K562	blood:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
27	CEBPB	chr11:76450746-76451263	MCF-7	breast:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
28	CEBPB	chr11:76450779-76451287	MCF-7	breast:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
29	CEBPB	chr11:76448240-76448555	K562	blood:	n/a	chr11:76448404-76448415
30	CEBPB	chr11:76456553-76457191	K562	blood:	n/a	n/a
31	CEBPB	chr11:76442082-76442147	K562	blood:	n/a	n/a
32	CEBPB	chr11:76456656-76457268	K562	blood:	n/a	n/a
33	CEBPB	chr11:76450824-76451192	Hela-S3	cervix:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
34	CEBPB	chr11:76450834-76451221	ECC-1	luminal epithelium:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
35	CEBPB	chr11:76450823-76451191	H1-hESC	embryonic stem cell:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
36	CEBPB	chr11:76450803-76451378	A549	lung:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
37	CEBPB	chr11:76444993-76445279	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr11:76450789-76451225	ECC-1	luminal epithelium:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
39	CEBPB	chr11:76450833-76451240	A549	lung:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
40	CEBPB	chr11:76450788-76451224	K562	blood:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
41	CEBPB	chr11:76450813-76451205	IMR90	lung:	n/a	chr11:76451002-76451011 chr11:76451001-76451012 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451002-76451011 chr11:76451000-76451013
42	CEBPB	chr11:76448277-76448545	Hela-S3	cervix:	n/a	chr11:76448404-76448415
43	CEBPD	chr11:76446936-76447340	K562	blood:	n/a	n/a
44	CEBPD	chr11:76456461-76457283	K562	blood:	n/a	n/a
45	CEBPD	chr11:76456564-76457247	K562	blood:	n/a	n/a
46	CEBPD	chr11:76446519-76447373	K562	blood:	n/a	n/a
47	CHD1	chr11:76445011-76445343	IMR90	lung:	n/a	n/a
48	CHD2	chr11:76446935-76447090	K562	blood:	n/a	n/a
49	CHD2	chr11:76445094-76445266	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr11:76456736-76456990	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:76446769-76446819	H1-hESC	embryonic stem cell:	embryo
2	chr11:76455541-76455591	HRE	kidney:	n/a
3	chr11:76455541-76455591	NH-A	brain:	n/a
4	chr11:76446769-76446819	HCF	heart:	n/a
5	chr11:76446769-76446819	A549	lung:	n/a
6	chr11:76446769-76446819	SKMC	muscle:	n/a
7	chr11:76455541-76455591	H1-hESC	embryonic stem cell:	embryo
8	chr11:76455541-76455591	ProgFib	skin:	n/a
9	chr11:76446769-76446819	HUVEC	blood vessel:	n/a
10	chr11:76446769-76446819	AG04449	skin:	fetal
11	chr11:76446769-76446819	Hela-S3	cervix:	n/a
12	chr11:76446769-76446819	GM19239	blood:	n/a
13	chr11:76455541-76455591	NB4	blood:	n/a
14	chr11:76455541-76455591	NT2-D1	testis:	n/a
15	chr11:76455541-76455591	HMEC	breast:	n/a
16	chr11:76455541-76455591	RPTEC	kidney:	n/a
17	chr11:76455541-76455591	BJ	skin:	n/a
18	chr11:76446769-76446819	RPTEC	kidney:	n/a
19	chr11:76446769-76446819	HEEpiC	esophagus:	n/a
20	chr11:76446769-76446819	HRE	kidney:	n/a
21	chr11:76455541-76455591	Hela-S3	cervix:	n/a
22	chr11:76446769-76446819	Hepatocyte	liver:	n/a
23	chr11:76455541-76455591	PrEC	prostate:	n/a
24	chr11:76446769-76446819	SK-N-MC	brain:	n/a
25	chr11:76455541-76455591	SK-N-MC	brain:	n/a
26	chr11:76455541-76455591	AG04450	lung:	fetal
27	chr11:76446769-76446819	U87	brain:	n/a
28	chr11:76446769-76446819	HAEpiC	amniotic membrane:	n/a
29	chr11:76455541-76455591	HCM	heart:	n/a
30	chr11:76446769-76446819	ovcar-3	ovarian:	n/a
31	chr11:76455541-76455591	HL-60	blood:	n/a
32	chr11:76446769-76446819	LNCaP	prostate:	n/a
33	chr11:76455541-76455591	BE2_C	brain:	n/a
34	chr11:76455541-76455591	NHDF-neo	bronchial:	n/a
35	chr11:76455541-76455591	GM12878	blood:	n/a
36	chr11:76455541-76455591	HCT-116	colon:	n/a
37	chr11:76446769-76446819	HRPEpiC	eye:	n/a
38	chr11:76455541-76455591	HepG2	liver:	n/a
39	chr11:76446769-76446819	SAEC	small airway:	n/a
40	chr11:76446769-76446819	HRCEpiC	kidney:	n/a
41	chr11:76446769-76446819	K562	blood:	n/a
42	chr11:76446769-76446819	BE2_C	brain:	n/a
43	chr11:76446769-76446819	Caco-2	colon:	n/a
44	chr11:76455541-76455591	T-47D	breast:	n/a
45	chr11:76446769-76446819	PrEC	prostate:	n/a
46	chr11:76455541-76455591	LNCaP	prostate:	n/a
47	chr11:76446769-76446819	NHDF-neo	bronchial:	n/a
48	chr11:76455541-76455591	HPAEpiC	pulmonary alveolar:	n/a
49	chr11:76446769-76446819	HepG2	liver:	n/a
50	chr11:76446769-76446819	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:76448672..76451202-chr11:76476087..76478426,2	MCF-7	breast:
2	chr11:76444817..76447367-chr11:76477489..76481018,3	MCF-7	breast:
3	chr11:76444941..76447137-chr11:76494986..76497317,3	K562	blood:
4	chr11:76433483..76435648-chr11:76441734..76444276,2	K562	blood:
5	chr11:76430934..76434920-chr11:76435609..76442633,7	MCF-7	breast:
6	chr11:76451295..76455303-chr11:76456358..76459104,3	K562	blood:
7	chr11:76444941..76446826-chr11:76495647..76497317,2	K562	blood:
8	chr11:76446515..76448277-chr11:76483918..76485534,2	MCF-7	breast:
9	chr11:76458389..76460958-chr11:76461404..76463823,3	K562	blood:
10	chr11:76457514..76460124-chr11:76468465..76470695,2	MCF-7	breast:
11	chr11:76454654..76458636-chr11:76475295..76479345,4	MCF-7	breast:
12	chr11:76444642..76445671-chr11:76509955..76510846,7	K562	blood:
13	chr11:76457361..76460008-chr11:76475009..76477808,2	MCF-7	breast:
14	chr11:76426123..76429227-chr11:76433055..76436273,3	K562	blood:
15	chr11:76443783..76447678-chr11:76493146..76497317,7	MCF-7	breast:
16	chr11:76432736..76434565-chr11:76442976..76445333,2	MCF-7	breast:
17	chr11:76446132..76447728-chr11:76448521..76450951,2	K562	blood:
18	chr11:76444616..76445153-chr11:76518177..76519095,2	MCF-7	breast:
19	chr11:76444583..76446069-chr11:76756756..76757887,9	MCF-7	breast:
20	chr11:76410635..76412831-chr11:76434613..76437612,2	K562	blood:
21	chr11:76455249..76457100-chr11:76493512..76497788,3	K562	blood:
22	chr11:76444797..76445605-chr11:76756797..76757751,2	K562	blood:
23	chr11:76445009..76450493-chr11:76452594..76458852,7	K562	blood:
24	chr11:76445248..76448071-chr11:76628717..76631883,4	MCF-7	breast:
25	chr11:76449564..76451543-chr11:76496131..76497754,2	MCF-7	breast:
26	chr11:76454033..76456801-chr11:76571027..76573144,2	K562	blood:
27	chr11:76433483..76435648-chr11:76441734..76444276,2	K562	blood:
28	chr11:76447864..76450852-chr11:76476429..76482016,6	MCF-7	breast:
29	chr11:76447052..76448597-chr11:76481342..76483373,2	K562	blood:
30	chr11:76445665..76448359-chr11:76459229..76461438,2	K562	blood:
31	chr11:76445987..76448531-chr11:76494334..76496063,4	MCF-7	breast:
32	chr11:76446441..76446993-chr11:76509968..76510808,2	K562	blood:
33	chr11:76446403..76452318-chr11:76452779..76457589,9	K562	blood:
34	chr11:76455720..76457823-chr11:76458498..76460199,2	MCF-7	breast:
35	chr11:76455720..76457823-chr11:76458498..76460199,2	MCF-7	breast:
36	chr11:76444321..76446462-chr11:76517342..76520030,2	K562	blood:
37	chr11:76459617..76462522-chr11:76481019..76482707,2	K562	blood:
38	chr11:76456730..76465168-chr11:76492668..76497012,7	K562	blood:
39	chr11:76448481..76450108-chr11:76494249..76496577,2	K562	blood:
40	chr11:76458614..76461290-chr11:76467564..76470157,3	K562	blood:
41	chr11:76450787..76452506-chr11:76497901..76500387,2	K562	blood:
42	chr11:76444677..76445621-chr11:76756756..76757566,3	MCF-7	breast:
43	chr11:76448469..76450791-chr11:76488926..76490777,2	K562	blood:
44	chr11:76444600..76445268-chr11:76549508..76550407,4	MCF-7	breast:
45	chr11:76445344..76446073-chr11:76801899..76802836,2	K562	blood:
46	chr11:76443601..76445826-chr11:76571953..76574772,2	K562	blood:
47	chr11:76445009..76450493-chr11:76452594..76458852,7	K562	blood:
48	chr11:76446132..76447728-chr11:76448521..76450951,2	K562	blood:
49	chr11:76448456..76450010-chr11:76482180..76484132,2	MCF-7	breast:
50	chr11:76444256..76445576-chr11:76630135..76631218,4	K562	blood:

Variant related genes	Relation type
ENSG00000254761	TF binding region
ENSG00000254761	CpG island
ENSG00000255100	chromatin interactions
ENSG00000182704	chromatin interactions
ENSG00000078124	chromatin interactions
ENSG00000254632	chromatin interactions

Extended variants
information (count: 1037 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143924139	chr11:76435263-76435264	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs184852793	chr11:76435280-76435281	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs548822908	chr11:76435341-76435342	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs555948587	chr11:76435346-76435347	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs576212153	chr11:76435352-76435353	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs542131417	chr11:76435365-76435366	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs375237338	chr11:76435429-76435430	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs574761464	chr11:76435435-76435436	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567236576	chr11:76435493-76435494	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs144312963	chr11:76435539-76435540	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs560567668	chr11:76435540-76435541	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs148772376	chr11:76435607-76435608	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs370450944	chr11:76435618-76435619	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs116551586	chr11:76435626-76435627	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142453561	chr11:76435627-76435628	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs531873407	chr11:76435659-76435660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189700130	chr11:76435668-76435669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs548846426	chr11:76435694-76435695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562272133	chr11:76435701-76435702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538726762	chr11:76435774-76435775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368038127	chr11:76435776-76435777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs180885377	chr11:76435796-76435797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185889908	chr11:76435839-76435840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539150565	chr11:76435882-76435883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371891876	chr11:76435916-76435917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs569849094	chr11:76435930-76435931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189684991	chr11:76435931-76435932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181996165	chr11:76435947-76435948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79426704	chr11:76435951-76435952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150917867	chr11:76436015-76436016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186182378	chr11:76436035-76436036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190597794	chr11:76436038-76436039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546333569	chr11:76436054-76436055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs79163849	chr11:76436080-76436081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61893547	chr11:76436201-76436202	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs201058665	chr11:76436223-76436224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150209788	chr11:76436262-76436263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183538704	chr11:76436263-76436264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188021569	chr11:76436277-76436278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75270588	chr11:76436300-76436301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs36009028	chr11:76436349-76436350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557698269	chr11:76436406-76436407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191243934	chr11:76436408-76436409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532830554	chr11:76436461-76436462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs34768666	chr11:76436475-76436476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549832420	chr11:76436498-76436499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569679669	chr11:76436502-76436503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114663696	chr11:76436521-76436522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs115233863	chr11:76436550-76436551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75458663	chr11:76436573-76436574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Melanoma	18172304	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
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	16620391	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21482786	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	16608533	CNVD
Usher syndrome	18421352	CNVD
Ovarian cancer	21240255	CNVD
Ovarian cancer	22355333	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76433400-76456400	Weak transcription	Right Atrium	heart
2	chr11:76433600-76440600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:76434400-76440000	Weak transcription	K562	blood
4	chr11:76439800-76440600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr11:76439800-76441200	Enhancers	Fetal Intestine Small	intestine
6	chr11:76440000-76441400	Enhancers	Liver	Liver
7	chr11:76440000-76442800	Enhancers	K562	blood
8	chr11:76440400-76443400	Enhancers	Placenta	Placenta
9	chr11:76440600-76441600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:76440600-76441600	Enhancers	Fetal Intestine Large	intestine
11	chr11:76441200-76445200	Weak transcription	Fetal Intestine Small	intestine
12	chr11:76441400-76450200	Weak transcription	Liver	Liver
13	chr11:76441600-76445200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr11:76441600-76445600	Weak transcription	Fetal Intestine Large	intestine
15	chr11:76442800-76445000	Weak transcription	K562	blood
16	chr11:76444000-76444200	Enhancers	Colonic Mucosa	Colon
17	chr11:76445000-76446800	Enhancers	K562	blood
18	chr11:76445200-76445400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr11:76445200-76445400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr11:76445200-76445400	Enhancers	Left Ventricle	heart
21	chr11:76445200-76445600	Enhancers	Fetal Thymus	thymus
22	chr11:76445200-76446200	Enhancers	Fetal Intestine Small	intestine
23	chr11:76445200-76446400	Enhancers	Fetal Muscle Trunk	muscle
24	chr11:76445200-76446600	Enhancers	Colon Smooth Muscle	Colon
25	chr11:76445200-76446800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr11:76445200-76446800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr11:76445200-76448000	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr11:76445200-76448800	Enhancers	A549	lung
29	chr11:76445400-76445800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:76445400-76448000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr11:76445600-76446000	Weak transcription	Fetal Thymus	thymus
32	chr11:76445600-76446200	Enhancers	Fetal Intestine Large	intestine
33	chr11:76445600-76446800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr11:76445600-76446800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:76445600-76447200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr11:76445600-76447200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr11:76445600-76447400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr11:76445600-76447800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr11:76445600-76448200	Enhancers	Placenta	Placenta
40	chr11:76445600-76450600	Enhancers	Fetal Heart	heart
41	chr11:76445800-76446400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr11:76445800-76446600	Enhancers	Fetal Stomach	stomach
43	chr11:76445800-76447200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr11:76445800-76448000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr11:76445800-76449200	Enhancers	Fetal Brain Male	brain
46	chr11:76446000-76446200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr11:76446000-76446200	Enhancers	Fetal Thymus	thymus
48	chr11:76446000-76446400	Enhancers	Brain Cingulate Gyrus	brain
49	chr11:76446000-76446400	Enhancers	Fetal Lung	lung
50	chr11:76446000-76446400	Enhancers	Stomach Smooth Muscle	stomach

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