Variant report

Variant	esv3376719
Chromosome Location	chr3:52263462-52266260
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	BHLHE40	chr3:52265565-52265893	GM12878	blood:	n/a	chr3:52265692-52265708
2	BHLHE40	chr3:52265649-52265847	K562	blood:	n/a	chr3:52265692-52265708
3	CHD2	chr3:52265598-52265860	K562	blood:	n/a	n/a
4	CREB1	chr3:52265566-52265858	A549	lung:	n/a	n/a
5	CTCF	chr3:52264940-52265090	BJ	skin:	n/a	n/a
6	CTCF	chr3:52265362-52265879	GM19240	blood:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
7	CTCF	chr3:52265417-52265461	LNCaP	prostate:	n/a	n/a
8	CTCF	chr3:52265620-52265770	GM12801	blood:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
9	CTCF	chr3:52265390-52265435	MCF-7	breast:	n/a	n/a
10	CTCF	chr3:52265574-52265856	GM13977	blood:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
11	CTCF	chr3:52265360-52265510	GM12864	blood:	n/a	n/a
12	CTCF	chr3:52265560-52265710	GM12868	blood:	n/a	chr3:52265691-52265704
13	CTCF	chr3:52265640-52265790	HCFaa	heart:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
14	CTCF	chr3:52264388-52264422	Lung_OC	lung:	n/a	n/a
15	CTCF	chr3:52265594-52265805	SK-N-SH_RA	brain:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
16	CTCF	chr3:52265640-52265790	GM06990	blood:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
17	CTCF	chr3:52265541-52265893	MCF-7	breast:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
18	CTCF	chr3:52265574-52265873	ECC-1	luminal epithelium:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
19	CTCF	chr3:52265519-52265785	T-47D	breast:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
20	CTCF	chr3:52265961-52266027	GM12891	blood:	n/a	n/a
21	CTCF	chr3:52265620-52265770	AoAF	blood vessel:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
22	CTCF	chr3:52265509-52265902	K562	blood:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
23	CTCF	chr3:52265620-52265770	WERI-Rb-1	eye:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
24	CTCF	chr3:52265615-52265826	HepG2	liver:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
25	CTCF	chr3:52264369-52264372	Lung_OC	lung:	n/a	n/a
26	CTCF	chr3:52265200-52265350	GM12869	blood:	n/a	n/a
27	CTCF	chr3:52265640-52265790	HEK293	kidney:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
28	CTCF	chr3:52264901-52266096	SK-N-SH	brain:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
29	CTCF	chr3:52265383-52265479	GM10248	blood:	n/a	n/a
30	CTCF	chr3:52265640-52265790	HEEpiC	esophagus:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
31	CTCF	chr3:52265544-52265834	HepG2	liver:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
32	CTCF	chr3:52265354-52265898	GM12892	blood:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
33	CTCF	chr3:52265591-52265830	MCF-7	breast:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
34	CTCF	chr3:52265640-52265790	WERI-Rb-1	eye:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
35	CTCF	chr3:52265640-52265790	HCPEpiC	choroid plexus:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
36	CTCF	chr3:52265575-52265847	K562	blood:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
37	CTCF	chr3:52265580-52265730	WI-38	lung:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
38	CTCF	chr3:52265559-52265849	Medullo	brain:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
39	CTCF	chr3:52265378-52265479	GM13977	blood:	n/a	n/a
40	CTCF	chr3:52265640-52265790	HRPEpiC	eye:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
41	CTCF	chr3:52265494-52265920	MCF-7	breast:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
42	CTCF	chr3:52265555-52265826	Kidney_OC	kidney:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
43	CTCF	chr3:52265498-52266021	K562	blood:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
44	CTCF	chr3:52265640-52265790	HMF	breast:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
45	CTCF	chr3:52265527-52265810	A549	lung:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
46	CTCF	chr3:52265475-52265939	H1-hESC	embryonic stem cell:	n/a	chr3:52265854-52265863 chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
47	CTCF	chr3:52265400-52265465	GM10266	blood:	n/a	n/a
48	CTCF	chr3:52265980-52266130	GM12865	blood:	n/a	n/a
49	CTCF	chr3:52265640-52265790	RPTEC	kidney:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721
50	CTCF	chr3:52265620-52265770	GM12867	blood:	n/a	chr3:52265691-52265704 chr3:52265708-52265717 chr3:52265705-52265718 chr3:52265707-52265728 chr3:52265706-52265722 chr3:52265705-52265723 chr3:52265708-52265721

No.	Distal block	Cell Line	Cell type
1	chr3:52262375..52268246-chr3:52270366..52274345,8	K562	blood:
2	chr3:52263321..52268061-chr3:52310039..52314728,5	K562	blood:
3	chr3:52262890..52265555-chr3:52320474..52321976,2	MCF-7	breast:
4	chr3:52264055..52267306-chr3:52309351..52312799,8	MCF-7	breast:
5	chr3:52265291..52266190-chr3:52418948..52419840,4	K562	blood:
6	chr3:52264729..52268939-chr3:52269297..52274565,7	K562	blood:
7	chr3:52265330..52266149-chr3:52419100..52419914,3	MCF-7	breast:
8	chr3:52263787..52265921-chr3:52311180..52314270,4	MCF-7	breast:
9	chr3:52254174..52254866-chr3:52265283..52266177,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173366	TF binding region
TWF2	TF binding region
TLR9	TF binding region
ENSG00000247596	chromatin interactions
ENSG00000239732	chromatin interactions
ENSG00000168237	chromatin interactions
ENSG00000164091	chromatin interactions
ENSG00000243224	chromatin interactions

Extended variants
information (count: 171 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:171 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144582432	chr3:52263470-52263471	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs534218240	chr3:52263495-52263496	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs547889055	chr3:52263515-52263516	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs573646225	chr3:52263527-52263528	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs567780316	chr3:52263546-52263547	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs187770966	chr3:52263571-52263572	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs535377297	chr3:52263572-52263573	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs556801891	chr3:52263596-52263597	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs377409810	chr3:52263616-52263617	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs147881772	chr3:52263622-52263623	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs375292646	chr3:52263630-52263631	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs577552085	chr3:52263644-52263645	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs377341844	chr3:52263657-52263658	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs575309854	chr3:52263664-52263665	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs370941749	chr3:52263671-52263672	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs539872493	chr3:52263673-52263674	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs578235922	chr3:52263679-52263680	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs55836915	chr3:52263686-52263687	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs147578749	chr3:52263696-52263697	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs559788903	chr3:52263719-52263720	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs377753240	chr3:52263726-52263727	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs370212205	chr3:52263804-52263805	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs374922294	chr3:52263834-52263835	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs201505921	chr3:52263851-52263852	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs563863286	chr3:52263853-52263854	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs141598715	chr3:52263859-52263860	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs542373367	chr3:52263883-52263884	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs199663186	chr3:52263896-52263897	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs374109549	chr3:52263902-52263903	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs377621507	chr3:52263903-52263904	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs201549689	chr3:52263920-52263921	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs367943989	chr3:52263929-52263930	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs565212275	chr3:52263943-52263944	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs114956852	chr3:52263948-52263949	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs547826086	chr3:52263954-52263955	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs34038856	chr3:52263967-52263968	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs370783502	chr3:52264005-52264006	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs374151672	chr3:52264028-52264029	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs536744957	chr3:52264047-52264048	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs550294256	chr3:52264070-52264071	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs141989183	chr3:52264075-52264076	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs370171952	chr3:52264084-52264085	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs199985752	chr3:52264103-52264104	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs375689345	chr3:52264109-52264110	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs541342629	chr3:52264125-52264126	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs35042785	chr3:52264128-52264129	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs572721219	chr3:52264192-52264193	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs533512463	chr3:52264197-52264198	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs553360547	chr3:52264218-52264219	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs573354469	chr3:52264219-52264220	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:249 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52247800-52272200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr3:52251000-52266600	Weak transcription	Fetal Brain Male	brain
3	chr3:52251600-52263600	Weak transcription	HSMM	muscle
4	chr3:52251600-52264200	Weak transcription	HSMMtube	muscle
5	chr3:52251600-52266600	Weak transcription	Psoas Muscle	Psoas
6	chr3:52253200-52269600	Weak transcription	Fetal Kidney	kidney
7	chr3:52253400-52264400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr3:52255000-52263800	Weak transcription	HUVEC	blood vessel
9	chr3:52255000-52263800	Weak transcription	K562	blood
10	chr3:52255000-52268600	Weak transcription	Right Atrium	heart
11	chr3:52255200-52263600	Weak transcription	Stomach Mucosa	stomach
12	chr3:52255200-52270400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr3:52255400-52264200	Weak transcription	Hela-S3	cervix
14	chr3:52259600-52268200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr3:52260600-52265600	Strong transcription	Esophagus	oesophagus
16	chr3:52261000-52264200	Strong transcription	Skeletal Muscle Male	skeletal muscle
17	chr3:52261000-52265400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr3:52261000-52265800	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr3:52261000-52266600	Strong transcription	Placenta Amnion	Placenta Amnion
20	chr3:52261000-52269400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:52261200-52264200	Weak transcription	Primary hematopoietic stem cells	blood
22	chr3:52261200-52264200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr3:52261200-52264600	Strong transcription	Right Ventricle	heart
24	chr3:52261200-52265000	Strong transcription	Fetal Intestine Small	intestine
25	chr3:52261200-52265600	Strong transcription	Primary neutrophils fromperipheralblood	blood
26	chr3:52261200-52265800	Strong transcription	Primary T cells from cord blood	blood
27	chr3:52261200-52265800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr3:52261200-52266400	Strong transcription	Lung	lung
29	chr3:52261200-52267000	Strong transcription	Fetal Muscle Trunk	muscle
30	chr3:52261200-52270800	Strong transcription	Fetal Stomach	stomach
31	chr3:52261400-52264400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr3:52261400-52265200	Strong transcription	Primary T helper cells PMA-I stimulated	--
33	chr3:52261400-52265600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:52261400-52265600	Strong transcription	Liver	Liver
35	chr3:52261400-52269000	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr3:52261400-52269600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr3:52261600-52264600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr3:52261600-52264600	Strong transcription	Skeletal Muscle Female	skeletal muscle
39	chr3:52261600-52265400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr3:52261600-52265400	Strong transcription	Spleen	Spleen
41	chr3:52261600-52265800	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr3:52261600-52266000	Strong transcription	Brain Anterior Caudate	brain
43	chr3:52261600-52266800	Strong transcription	Placenta	Placenta
44	chr3:52261600-52267000	Strong transcription	Gastric	stomach
45	chr3:52261600-52267200	Strong transcription	Fetal Muscle Leg	muscle
46	chr3:52261600-52269800	Strong transcription	Rectal Mucosa Donor 29	rectum
47	chr3:52261600-52270000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:52261600-52270000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr3:52261600-52270600	Strong transcription	NHEK	skin
50	chr3:52261800-52264200	Strong transcription	Primary T cells fromperipheralblood	blood

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