Variant report

Variant	esv3407307
Chromosome Location	chr11:46142401-46144949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:759)
CpG islands
(count:367)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:759 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46142914-46143059	K562	blood:	n/a	n/a
2	ARID3A	chr11:46144371-46144871	K562	blood:	n/a	n/a
3	ARID3A	chr11:46143322-46143585	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:46143897-46144099	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:46144336-46144766	HepG2	liver:	n/a	n/a
6	ATF3	chr11:46142430-46143127	A549	lung:	n/a	n/a
7	BCL3	chr11:46142399-46143143	A549	lung:	n/a	chr11:46143007-46143016
8	BCL3	chr11:46142338-46142949	A549	lung:	n/a	n/a
9	BCLAF1	chr11:46142792-46143216	GM12878	blood:	n/a	chr11:46143007-46143016
10	BHLHE40	chr11:46143380-46143851	K562	blood:	n/a	chr11:46143696-46143712 chr11:46143642-46143658
11	BHLHE40	chr11:46142573-46143793	GM12878	blood:	n/a	chr11:46143696-46143712 chr11:46142991-46143007 chr11:46143642-46143658
12	BHLHE40	chr11:46142369-46143089	K562	blood:	n/a	chr11:46142991-46143007
13	BRCA1	chr11:46142905-46143053	HepG2	liver:	n/a	n/a
14	BRCA1	chr11:46143369-46143533	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr11:46142870-46143067	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr11:46142320-46142919	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr11:46142854-46143074	GM12878	blood:	n/a	n/a
18	BRCA1	chr11:46143978-46144218	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr11:46142793-46143064	K562	blood:	n/a	n/a
20	CCNT2	chr11:46142347-46143802	K562	blood:	n/a	chr11:46142804-46142813 chr11:46142789-46142798
21	CEBPB	chr11:46143283-46144052	A549	lung:	n/a	chr11:46143931-46143943
22	CEBPB	chr11:46142890-46143074	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:46144633-46144718	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:46143770-46143889	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:46143768-46143876	HepG2	liver:	n/a	n/a
26	CEBPB	chr11:46142319-46144272	Hela-S3	cervix:	n/a	chr11:46143931-46143943
27	CEBPB	chr11:46142895-46143034	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPD	chr11:46142675-46143079	HepG2	liver:	n/a	n/a
29	CEBPD	chr11:46142274-46142549	HepG2	liver:	n/a	n/a
30	CEBPD	chr11:46143080-46143825	HepG2	liver:	n/a	n/a
31	CHD1	chr11:46143400-46143543	GM12878	blood:	n/a	n/a
32	CHD1	chr11:46142810-46143163	GM12878	blood:	n/a	n/a
33	CHD2	chr11:46142219-46144110	GM12878	blood:	n/a	chr11:46143922-46143932 chr11:46143897-46143907
34	CHD2	chr11:46142339-46143602	K562	blood:	n/a	n/a
35	CHD2	chr11:46143826-46143996	HepG2	liver:	n/a	chr11:46143922-46143932 chr11:46143897-46143907
36	CHD2	chr11:46142817-46143616	HepG2	liver:	n/a	n/a
37	CHD2	chr11:46142297-46144249	H1-hESC	embryonic stem cell:	n/a	chr11:46143922-46143932 chr11:46143897-46143907
38	CHD2	chr11:46142047-46144237	Hela-S3	cervix:	n/a	chr11:46143922-46143932 chr11:46143897-46143907
39	CREB1	chr11:46143248-46143573	H1-hESC	embryonic stem cell:	n/a	n/a
40	CREB1	chr11:46142805-46143903	A549	lung:	n/a	n/a
41	CREB1	chr11:46143266-46143653	GM12878	blood:	n/a	n/a
42	CREB1	chr11:46142790-46143581	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTBP2	chr11:46142280-46142726	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTBP2	chr11:46143608-46144034	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr11:46144340-46144490	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr11:46142668-46142762	ProgFib	skin:	n/a	n/a
47	CTCF	chr11:46144400-46144550	AG04450	lung:	n/a	n/a
48	CTCF	chr11:46144240-46144390	HMF	breast:	n/a	n/a
49	CTCF	chr11:46142760-46142910	AG04449	skin:	n/a	n/a
50	CTCF	chr11:46144220-46144370	AG04450	lung:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46143434-46143484	SK-N-SH_RA	brain:	n/a
2	chr11:46143434-46143484	SK-N-SH_RA	brain:	n/a
3	chr11:46143014-46143064	HIPEpiC	eye:	n/a
4	chr11:46143014-46143064	SKMC	muscle:	n/a
5	chr11:46143993-46144043	SK-N-SH	brain:	n/a
6	chr11:46143011-46143061	SK-N-SH_RA	brain:	n/a
7	chr11:46143993-46144043	GM06990	blood:	n/a
8	chr11:46143014-46143064	HAEpiC	amniotic membrane:	n/a
9	chr11:46143461-46143511	BE2_C	brain:	n/a
10	chr11:46143014-46143064	HCM	heart:	n/a
11	chr11:46143434-46143484	NB4	blood:	n/a
12	chr11:46143461-46143511	AoSMC	blood vessel:	n/a
13	chr11:46143461-46143511	SKMC	muscle:	n/a
14	chr11:46143993-46144043	HEK293	kidney:	embryo
15	chr11:46143011-46143061	NB4	blood:	n/a
16	chr11:46143461-46143511	HRCEpiC	kidney:	n/a
17	chr11:46143993-46144043	AG04449	skin:	fetal
18	chr11:46143434-46143484	GM12891	blood:	n/a
19	chr11:46143434-46143484	AG04449	skin:	fetal
20	chr11:46143461-46143511	GM12892	blood:	n/a
21	chr11:46143434-46143484	H1-hESC	embryonic stem cell:	embryo
22	chr11:46143011-46143061	HCM	heart:	n/a
23	chr11:46143993-46144043	GM12892	blood:	n/a
24	chr11:46143000-46143050	IMR90	lung:	fetal
25	chr11:46143014-46143064	BE2_C	brain:	n/a
26	chr11:46143461-46143511	MCF10A-Er-Src	breast:	n/a
27	chr11:46143434-46143484	GM12892	blood:	n/a
28	chr11:46143014-46143064	T-47D	breast:	n/a
29	chr11:46143011-46143061	HCPEpiC	choroid plexus:	n/a
30	chr11:46143000-46143050	NH-A	brain:	n/a
31	chr11:46143993-46144043	AG04450	lung:	fetal
32	chr11:46143000-46143050	SK-N-MC	brain:	n/a
33	chr11:46143014-46143064	HEK293	kidney:	embryo
34	chr11:46143014-46143064	AG09319	gingival:	n/a
35	chr11:46143014-46143064	HL-60	blood:	n/a
36	chr11:46143993-46144043	AG10803	skin:	n/a
37	chr11:46143000-46143050	GM12878	blood:	n/a
38	chr11:46143014-46143064	HRCEpiC	kidney:	n/a
39	chr11:46143993-46144043	CMK	blood:	n/a
40	chr11:46143461-46143511	HIPEpiC	eye:	n/a
41	chr11:46143000-46143050	HL-60	blood:	n/a
42	chr11:46143993-46144043	NB4	blood:	n/a
43	chr11:46143434-46143484	HMEC	breast:	n/a
44	chr11:46143993-46144043	HRE	kidney:	n/a
45	chr11:46143461-46143511	SK-N-SH	brain:	n/a
46	chr11:46143434-46143484	A549	lung:	n/a
47	chr11:46143461-46143511	ProgFib	skin:	n/a
48	chr11:46143434-46143484	Hepatocyte	liver:	n/a
49	chr11:46143011-46143061	Hela-S3	cervix:	n/a
50	chr11:46143000-46143050	SK-N-SH_RA	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:46142486..46143034-chr5:64064158..64064978,2	Hela-S3	cervix:
2	chr11:46141504..46142447-chr19:8386292..8386834,2	NB4	blood:
3	chr11:46141914..46143962-chr11:46401995..46404790,2	K562	blood:
4	chr11:45986176..45988319-chr11:46143475..46145056,2	MCF-7	breast:
5	chr11:45942020..45943576-chr11:46141975..46144467,2	MCF-7	breast:
6	chr11:45867179..45868974-chr11:46142893..46144558,2	K562	blood:
7	chr11:45920093..45922965-chr11:46143378..46145105,2	K562	blood:
8	chr11:46143507..46145451-chr11:46333298..46335406,2	K562	blood:
9	chr11:46141272..46145852-chr11:46256882..46262702,15	MCF-7	breast:
10	chr11:46143580..46145236-chr11:46369479..46372129,2	MCF-7	breast:
11	chr11:46143224..46145220-chr11:46317344..46319023,2	K562	blood:
12	chr11:46136566..46145134-chr11:46256772..46268048,26	K562	blood:
13	chr11:46140376..46142887-chr11:46639092..46640615,2	MCF-7	breast:
14	chr1:28286209..28286793-chr11:46142913..46143431,2	Hela-S3	cervix:
15	chr11:46141950..46143787-chr11:46718847..46721759,2	K562	blood:
16	chr11:46028036..46029889-chr11:46143429..46146254,2	K562	blood:
17	chr11:46125754..46127349-chr11:46143825..46145810,2	MCF-7	breast:
18	chr11:46092605..46094562-chr11:46143473..46145813,3	K562	blood:
19	chr11:45939411..45941074-chr11:46142423..46143961,2	MCF-7	breast:
20	chr11:46140775..46145022-chr11:46256711..46262008,9	MCF-7	breast:
21	chr11:46139740..46148810-chr11:46253862..46264263,27	K562	blood:
22	chr11:45942684..45944705-chr11:46141351..46143147,2	K562	blood:
23	chr11:46141780..46143612-chr11:46331038..46333172,2	MCF-7	breast:
24	chr11:46142872..46144744-chr11:46382813..46385236,2	MCF-7	breast:
25	chr11:46141379..46143279-chr11:46237350..46239276,2	MCF-7	breast:
26	chr11:46143681..46146343-chr11:46159365..46161019,2	K562	blood:

No data

Variant related genes	Relation type
PHF21A	TF binding region
PHF21A	CpG island
ENSG00000110492	chromatin interactions
ENSG00000153006	chromatin interactions
ENSG00000255269	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000175224	chromatin interactions
ENSG00000254639	chromatin interactions
ENSG00000227050	chromatin interactions
ENSG00000135365	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000180423	chromatin interactions
ENSG00000153015	chromatin interactions
ENSG00000233927	chromatin interactions
ENSG00000157613	chromatin interactions
ENSG00000121671	chromatin interactions
ENSG00000165905	chromatin interactions
ENSG00000175220	chromatin interactions

Extended variants
information (count: 69 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:69 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185025534	chr11:46142499-46142500	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs372848607	chr11:46142661-46142662	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs549316344	chr11:46142721-46142722	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs77717223	chr11:46142724-46142725	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs142787547	chr11:46142728-46142729	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs368044954	chr11:46142732-46142733	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs61884081	chr11:46142742-46142743	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs61884082	chr11:46142743-46142744	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs60788619	chr11:46142754-46142755	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs569678009	chr11:46142789-46142790	Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
11	rs535373611	chr11:46142821-46142822	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
12	rs555664938	chr11:46142946-46142947	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
13	rs565858503	chr11:46142964-46142965	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
14	rs7117810	chr11:46143414-46143415	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
15	rs534783979	chr11:46143442-46143443	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs557994083	chr11:46143535-46143536	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
17	rs189882449	chr11:46143539-46143540	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
18	rs543981439	chr11:46143550-46143551	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
19	rs557382046	chr11:46143636-46143637	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs11397119	chr11:46143658-46143659	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs398015942	chr11:46143665-46143666	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs574013371	chr11:46143705-46143706	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs542928761	chr11:46143742-46143743	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs565062088	chr11:46143764-46143765	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs559967589	chr11:46143767-46143768	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs528796372	chr11:46143768-46143769	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs11038772	chr11:46143769-46143770	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs78452453	chr11:46143774-46143775	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs528079895	chr11:46143778-46143779	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs551008579	chr11:46143809-46143810	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs565138264	chr11:46143811-46143812	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs73457874	chr11:46143856-46143857	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs532858778	chr11:46143888-46143889	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs370718662	chr11:46143904-46143905	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs549501868	chr11:46143917-46143918	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs569531843	chr11:46143936-46143937	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs528854865	chr11:46143938-46143939	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs548720099	chr11:46143962-46143963	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs565926444	chr11:46144024-46144025	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs201036024	chr11:46144090-46144091	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs534921221	chr11:46144113-46144114	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs551599345	chr11:46144133-46144134	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs571508471	chr11:46144190-46144191	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs537526074	chr11:46144202-46144203	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs373246171	chr11:46144207-46144208	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs75220124	chr11:46144297-46144298	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs7122062	chr11:46144300-46144301	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs7946524	chr11:46144455-46144456	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs150727247	chr11:46144521-46144522	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs188465813	chr11:46144571-46144572	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	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
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46138200-46144200	Active TSS	Ovary	ovary
2	chr11:46138800-46144600	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr11:46138800-46144800	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr11:46139000-46144400	Active TSS	GM12878-XiMat	blood
5	chr11:46139200-46144200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr11:46139400-46144600	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr11:46139600-46144000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr11:46139600-46144400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:46139600-46145000	Active TSS	H1 Cell Line	embryonic stem cell
10	chr11:46139800-46144600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:46139800-46144600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:46139800-46144600	Active TSS	K562	blood
13	chr11:46140200-46143800	Active TSS	Primary T cells fromperipheralblood	blood
14	chr11:46140200-46144400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:46140200-46144400	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr11:46140200-46144400	Active TSS	NHLF	lung
17	chr11:46140200-46144600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr11:46140200-46144600	Active TSS	HUES6 Cell Line	embryonic stem cell
19	chr11:46140200-46144600	Active TSS	Brain Germinal Matrix	brain
20	chr11:46140400-46144200	Active TSS	Colonic Mucosa	Colon
21	chr11:46140400-46144400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr11:46140400-46144400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:46140400-46144400	Active TSS	Brain Angular Gyrus	brain
24	chr11:46140400-46144400	Active TSS	Fetal Kidney	kidney
25	chr11:46140400-46144400	Active TSS	Psoas Muscle	Psoas
26	chr11:46140400-46144400	Active TSS	Stomach Smooth Muscle	stomach
27	chr11:46140400-46144400	Active TSS	HSMMtube	muscle
28	chr11:46140400-46144600	Active TSS	H9 Cell Line	embryonic stem cell
29	chr11:46140400-46144600	Active TSS	A549	lung
30	chr11:46140400-46144800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:46140400-46144800	Active TSS	Right Ventricle	heart
32	chr11:46140600-46144000	Active TSS	Fetal Stomach	stomach
33	chr11:46140600-46144000	Active TSS	Skeletal Muscle Male	skeletal muscle
34	chr11:46140600-46144200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr11:46140600-46144200	Active TSS	Left Ventricle	heart
36	chr11:46140600-46144200	Active TSS	Small Intestine	intestine
37	chr11:46140600-46144400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr11:46140600-46144400	Active TSS	Brain Inferior Temporal Lobe	brain
39	chr11:46140600-46144400	Active TSS	Brain Substantia Nigra	brain
40	chr11:46140600-46144400	Active TSS	Colon Smooth Muscle	Colon
41	chr11:46140600-46144400	Active TSS	Pancreatic Islets	Pancreatic Islet
42	chr11:46140600-46144600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr11:46140600-46144600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr11:46140600-46144600	Active TSS	Breast Myoepithelial Primary Cells	Breast
45	chr11:46140600-46144600	Active TSS	NHDF-Ad	bronchial
46	chr11:46140600-46144800	Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr11:46140600-46144800	Active TSS	Fetal Brain Female	brain
48	chr11:46140600-46145000	Active TSS	iPS-15b Cell Line	embryonic stem cell
49	chr11:46140800-46142600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
50	chr11:46140800-46142600	Active TSS	Placenta Amnion	Placenta Amnion

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