Variant report

Variant	nsv555617
Chromosome Location	chr11:84394622-84493877
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	chr11:84425391-84425616	HepG2	liver:	n/a	n/a
2	ATF2	chr11:84425281-84425625	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr11:84402769-84403192	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:84453284-84453645	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr11:84402840-84403053	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr11:84402863-84403040	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr11:84465652-84465923	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:84423471-84423495	GM12878	blood:	n/a	n/a
9	CBX3	chr11:84425239-84425761	HCT-116	colon:	n/a	n/a
10	CBX3	chr11:84425346-84425608	K562	blood:	n/a	n/a
11	CEBPB	chr11:84483215-84483418	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:84455324-84455488	K562	blood:	n/a	chr11:84455338-84455349
13	CEBPB	chr11:84398455-84398885	MCF-7	breast:	n/a	n/a
14	CEBPB	chr11:84398496-84398985	MCF-7	breast:	n/a	n/a
15	CEBPB	chr11:84441215-84441415	HepG2	liver:	n/a	n/a
16	CEBPB	chr11:84441166-84441336	A549	lung:	n/a	n/a
17	CEBPB	chr11:84455217-84455511	A549	lung:	n/a	chr11:84455338-84455349
18	CEBPB	chr11:84396442-84396583	HepG2	liver:	n/a	chr11:84396450-84396461
19	CEBPB	chr11:84455235-84455534	IMR90	lung:	n/a	chr11:84455338-84455349
20	CHD1	chr11:84394677-84394716	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr11:84402822-84403169	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr11:84430898-84432454	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr11:84491840-84491990	HBMEC	blood vessel:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
24	CTCF	chr11:84425416-84425619	GM12892	blood:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
25	CTCF	chr11:84491820-84491970	GM12867	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
26	CTCF	chr11:84425380-84425530	HVMF	connective:	n/a	n/a
27	CTCF	chr11:84425371-84425593	SK-N-SH_RA	brain:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
28	CTCF	chr11:84425440-84425590	GM12875	blood:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
29	CTCF	chr11:84433752-84433903	LNCaP	prostate:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
30	CTCF	chr11:84433700-84433850	HMF	breast:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
31	CTCF	chr11:84491840-84491990	AG09309	skin:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
32	CTCF	chr11:84433740-84433890	MCF-7	breast:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
33	CTCF	chr11:84433621-84434095	MCF-7	breast:	n/a	chr11:84433816-84433837 chr11:84433814-84433832
34	CTCF	chr11:84425680-84425830	SAEC	small airway:	n/a	n/a
35	CTCF	chr11:84425440-84425590	HEK293	kidney:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
36	CTCF	chr11:84491840-84491990	Hela-S3	cervix:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
37	CTCF	chr11:84425386-84425649	A549	lung:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
38	CTCF	chr11:84491840-84491990	GM12878	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
39	CTCF	chr11:84491860-84492010	GM12873	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
40	CTCF	chr11:84425440-84425590	HPF	lung:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
41	CTCF	chr11:84491800-84491950	WERI-Rb-1	eye:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
42	CTCF	chr11:84425420-84425570	HPAF	blood vessel:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
43	CTCF	chr11:84491900-84492050	GM06990	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
44	CTCF	chr11:84491815-84492123	H1-hESC	embryonic stem cell:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
45	CTCF	chr11:84425480-84425630	NHEK	skin:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
46	CTCF	chr11:84491747-84492131	GM12878	blood:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
47	CTCF	chr11:84425460-84425610	HRPEpiC	eye:	n/a	chr11:84425532-84425550 chr11:84425527-84425548
48	CTCF	chr11:84491860-84492010	NHDF-neo	bronchial:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949
49	CTCF	chr11:84433640-84433790	GM12873	blood:	n/a	n/a
50	CTCF	chr11:84491793-84492000	A549	lung:	n/a	chr11:84491931-84491939 chr11:84491926-84491944 chr11:84491928-84491949

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:84431970-84432020	HCM	heart:	n/a
2	chr11:84431535-84431585	AG10803	skin:	n/a
3	chr11:84431970-84432020	HCM	heart:	n/a
4	chr11:84431535-84431585	AG10803	skin:	n/a
5	chr11:84432312-84432362	AG09309	skin:	n/a
6	chr11:84432312-84432362	NT2-D1	testis:	n/a
7	chr11:84403466-84403516	Hela-S3	cervix:	n/a
8	chr11:84431918-84431968	K562	blood:	n/a
9	chr11:84403466-84403516	U87	brain:	n/a
10	chr11:84403466-84403516	BE2_C	brain:	n/a
11	chr11:84431535-84431585	BJ	skin:	n/a
12	chr11:84431535-84431585	HRCEpiC	kidney:	n/a
13	chr11:84431850-84431900	HNPCEpiC	eye:	n/a
14	chr11:84431970-84432020	AG10803	skin:	n/a
15	chr11:84431535-84431585	CMK	blood:	n/a
16	chr11:84432312-84432362	NHDF-neo	bronchial:	n/a
17	chr11:84431850-84431900	HepG2	liver:	n/a
18	chr11:84431535-84431585	NH-A	brain:	n/a
19	chr11:84431535-84431585	HPAEpiC	pulmonary alveolar:	n/a
20	chr11:84431535-84431585	Hela-S3	cervix:	n/a
21	chr11:84431850-84431900	Hepatocyte	liver:	n/a
22	chr11:84431850-84431900	ovcar-3	ovarian:	n/a
23	chr11:84403466-84403516	IMR90	lung:	fetal
24	chr11:84431850-84431900	HCF	heart:	n/a
25	chr11:84431535-84431585	HRE	kidney:	n/a
26	chr11:84431535-84431585	AoSMC	blood vessel:	n/a
27	chr11:84431850-84431900	HEK293	kidney:	embryo
28	chr11:84403466-84403516	Caco-2	colon:	n/a
29	chr11:84431850-84431900	ECC-1	luminal epithelium:	n/a
30	chr11:84431918-84431968	GM12891	blood:	n/a
31	chr11:84431918-84431968	AG09309	skin:	n/a
32	chr11:84431970-84432020	HIPEpiC	eye:	n/a
33	chr11:84431850-84431900	IMR90	lung:	fetal
34	chr11:84432312-84432362	HCT-116	colon:	n/a
35	chr11:84431918-84431968	HRCEpiC	kidney:	n/a
36	chr11:84432312-84432362	Jurkat	blood:	n/a
37	chr11:84431918-84431968	AG10803	skin:	n/a
38	chr11:84403466-84403516	PFSK-1	brain:	n/a
39	chr11:84403466-84403516	SAEC	small airway:	n/a
40	chr11:84432312-84432362	SAEC	small airway:	n/a
41	chr11:84403466-84403516	AG09319	gingival:	n/a
42	chr11:84431970-84432020	U87	brain:	n/a
43	chr11:84403466-84403516	HCPEpiC	choroid plexus:	n/a
44	chr11:84431918-84431968	HEK293	kidney:	embryo
45	chr11:84432312-84432362	HRPEpiC	eye:	n/a
46	chr11:84431850-84431900	AG04449	skin:	fetal
47	chr11:84432312-84432362	GM12878	blood:	n/a
48	chr11:84431970-84432020	IMR90	lung:	fetal
49	chr11:84431970-84432020	HEEpiC	esophagus:	n/a
50	chr11:84403466-84403516	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:84470491..84472543-chr11:84477634..84479392,2	MCF-7	breast:
2	chr11:84398696..84400791-chr11:84407010..84409416,2	MCF-7	breast:
3	chr11:84491891..84492728-chr11:84673979..84674886,2	MCF-7	breast:
4	chr11:84399428..84402012-chr11:84409062..84411909,2	MCF-7	breast:
5	chr11:84353205..84353720-chr11:84425398..84425994,2	MCF-7	breast:
6	chr11:84405567..84407918-chr11:84410069..84411733,2	MCF-7	breast:
7	chr11:84280312..84283130-chr11:84397090..84398747,2	MCF-7	breast:
8	chr11:84269079..84271717-chr11:84447544..84450102,2	MCF-7	breast:
9	chr11:84268829..84269798-chr11:84425022..84425965,7	MCF-7	breast:
10	chr11:84398979..84400532-chr11:84402254..84404090,2	MCF-7	breast:
11	chr11:84269134..84270255-chr11:84430304..84431248,5	MCF-7	breast:
12	chr11:84380382..84385547-chr11:84394508..84399622,6	MCF-7	breast:
13	chr11:84492333..84495051-chr11:84901283..84903076,2	MCF-7	breast:
14	chr11:84433336..84434202-chr11:85301668..85302606,6	MCF-7	breast:
15	chr11:84382646..84384164-chr11:84421223..84423854,2	MCF-7	breast:
16	chr11:84274871..84276645-chr11:84399735..84401764,2	MCF-7	breast:
17	chr11:84398979..84400532-chr11:84402254..84404090,2	MCF-7	breast:
18	chr11:84360777..84362282-chr11:84396654..84399433,2	MCF-7	breast:
19	chr11:84398696..84400791-chr11:84407010..84409416,2	MCF-7	breast:
20	chr11:84491944..84492445-chr11:85301546..85302502,2	MCF-7	breast:
21	chr11:84415255..84417235-chr11:84419666..84422634,2	MCF-7	breast:
22	chr11:84394938..84395530-chr22:33505824..33506512,2	MCF-7	breast:
23	chr11:84470491..84472543-chr11:84477634..84479392,2	MCF-7	breast:
24	chr11:84353266..84354226-chr11:84425005..84426301,12	MCF-7	breast:
25	chr11:84390374..84393326-chr11:84393925..84396078,2	MCF-7	breast:
26	chr11:84269617..84270472-chr11:84425387..84425965,2	MCF-7	breast:
27	chr11:84405567..84407918-chr11:84410069..84411733,2	MCF-7	breast:
28	chr11:84397361..84400181-chr11:84400344..84403864,3	MCF-7	breast:
29	chr11:84415255..84417235-chr11:84419666..84422634,2	MCF-7	breast:
30	chr11:84398248..84399038-chr20:52811668..52812485,2	MCF-7	breast:
31	chr11:84435745..84436679-chr11:85301971..85302607,2	MCF-7	breast:
32	chr11:84268928..84269579-chr11:84425061..84426012,3	MCF-7	breast:
33	chr11:84397898..84400132-chr11:84429987..84432965,2	MCF-7	breast:
34	chr11:84101140..84101859-chr11:84425077..84425854,3	MCF-7	breast:
35	chr11:84397361..84400181-chr11:84400344..84403864,3	MCF-7	breast:
36	chr11:84491046..84493285-chr11:84497010..84499873,2	MCF-7	breast:
37	chr11:84381891..84384378-chr11:84414753..84417179,2	K562	blood:
38	chr11:84268874..84269428-chr11:84491493..84492369,2	MCF-7	breast:
39	chr11:84364746..84366334-chr11:84397631..84400045,2	MCF-7	breast:
40	chr11:84399428..84402012-chr11:84409062..84411909,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CREBZF-5	chr11:84397843-84398320	NONHSAT023427
2	lnc-TMEM126B-2	chr11:84431869-84431924	ENSG00000254787.1
3	lnc-TMEM126B-2	chr11:84473154-84473211	ENSG00000254787.1
4	lnc-TMEM126B-2	chr11:84474333-84474398	ENSG00000254787.1

Variant related genes	Relation type
ENSG00000254787	TF binding region
ENSG00000254787	CpG island
ENSG00000254787	chromatin interactions

Extended variants
information (count: 3012 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3012 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11234125	chr11:84394622-84394623	Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140765777	chr11:84394721-84394722	Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181245082	chr11:84394746-84394747	Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs11828437	chr11:84394755-84394756	Flanking Bivalent TSS/Enh Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530583681	chr11:84394817-84394818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369436917	chr11:84394827-84394828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552001629	chr11:84394840-84394841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571479700	chr11:84394918-84394919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538824660	chr11:84394982-84394983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150176637	chr11:84395090-84395091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs60049596	chr11:84395106-84395107	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs184964656	chr11:84395172-84395173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554909649	chr11:84395181-84395182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576374777	chr11:84395207-84395208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537527125	chr11:84395251-84395252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559075294	chr11:84395290-84395291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188057366	chr11:84395292-84395293	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181006071	chr11:84395312-84395313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs559631776	chr11:84395333-84395334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542933507	chr11:84395340-84395341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574626529	chr11:84395358-84395359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138633786	chr11:84395363-84395364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs563258439	chr11:84395372-84395373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs373487251	chr11:84395495-84395496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs17147499	chr11:84395554-84395555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs118128180	chr11:84395708-84395709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539751210	chr11:84395712-84395713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563821612	chr11:84395759-84395760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576284386	chr11:84395778-84395779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200540716	chr11:84395780-84395781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373948803	chr11:84395781-84395782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149310792	chr11:84395820-84395821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10437749	chr11:84395839-84395840	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs201273442	chr11:84395848-84395849	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565942801	chr11:84395863-84395864	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376443938	chr11:84395892-84395893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187339058	chr11:84395893-84395894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533238816	chr11:84395899-84395900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548626756	chr11:84395913-84395914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570358621	chr11:84395931-84395932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs537037829	chr11:84395981-84395982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192133867	chr11:84396048-84396049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570953025	chr11:84396088-84396089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183486200	chr11:84396097-84396098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186138831	chr11:84396203-84396204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs190118040	chr11:84396207-84396208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79699217	chr11:84396228-84396229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs556953674	chr11:84396297-84396298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116091205	chr11:84396303-84396304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116308255	chr11:84396338-84396339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Cancer	20164920	CNVD
Obesity	20622171	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21147756	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84386200-84394800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr11:84388000-84398400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr11:84393600-84395000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:84393600-84402800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:84393800-84396200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr11:84394600-84394800	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr11:84394800-84395000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:84395000-84398400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:84395000-84403000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr11:84396000-84398400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr11:84396200-84398000	Enhancers	Primary hematopoietic stem cells	blood
12	chr11:84396200-84399600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr11:84397200-84398000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr11:84397800-84398000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr11:84397800-84399400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr11:84398000-84398200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr11:84398000-84399800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr11:84398200-84401800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr11:84398400-84399800	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr11:84399400-84404400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr11:84399800-84400200	Active TSS	Pancreatic Islets	Pancreatic Islet
22	chr11:84399800-84400400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr11:84400200-84400400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr11:84400400-84402200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr11:84400400-84402800	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr11:84401800-84402000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr11:84401800-84402800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr11:84402000-84402400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr11:84402000-84404600	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr11:84402200-84402800	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr11:84402200-84403400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr11:84402200-84403400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:84402400-84402800	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr11:84402400-84403000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr11:84402600-84402800	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr11:84402600-84403000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:84402800-84403000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
38	chr11:84402800-84403000	Enhancers	Fetal Heart	heart
39	chr11:84402800-84403200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr11:84402800-84403200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr11:84402800-84403400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:84402800-84403400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr11:84402800-84403600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr11:84402800-84403600	Enhancers	Fetal Kidney	kidney
45	chr11:84402800-84403800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr11:84402800-84403800	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr11:84402800-84404200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr11:84402800-84404400	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr11:84403000-84403200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:84403000-84403400	Active TSS	ES-I3 Cell Line	embryonic stem cell

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