Variant report

Variant	esv3361030
Chromosome Location	chr12:57583385-57587783
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:671)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:55 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:57587218-57587332	K562	blood:	n/a	n/a
2	CBX3	chr12:57585567-57585774	K562	blood:	n/a	n/a
3	CTCF	chr12:57585523-57585907	GM19239	blood:	n/a	n/a
4	CTCF	chr12:57585334-57585507	GM19239	blood:	n/a	n/a
5	EGR1	chr12:57586816-57586991	K562	blood:	n/a	n/a
6	EGR1	chr12:57586806-57587057	K562	blood:	n/a	n/a
7	HMGN3	chr12:57587016-57587095	K562	blood:	n/a	n/a
8	JUND	chr12:57586622-57586760	H1-hESC	embryonic stem cell:	n/a	n/a
9	MYC	chr12:57585320-57585363	GM12878	blood:	n/a	n/a
10	MYC	chr12:57585306-57585414	MCF-7	breast:	n/a	n/a
11	NFIC	chr12:57583739-57584677	ECC-1	luminal epithelium:	n/a	n/a
12	NR2C2	chr12:57585317-57585939	GM12878	blood:	n/a	n/a
13	POLR2A	chr12:57582883-57585896	U87	brain:	n/a	n/a
14	POLR2A	chr12:57586688-57587080	U87	brain:	n/a	n/a
15	POLR2A	chr12:57585278-57585350	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr12:57587758-57587900	HepG2	liver:	n/a	n/a
17	POLR2A	chr12:57583608-57583855	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr12:57583264-57583517	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr12:57586328-57586400	HepG2	liver:	n/a	n/a
20	POLR2A	chr12:57584848-57585070	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr12:57583280-57584377	HepG2	liver:	n/a	n/a
22	POLR2A	chr12:57585309-57585739	HepG2	liver:	n/a	n/a
23	POLR2A	chr12:57583202-57583397	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr12:57585396-57585401	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr12:57585085-57586265	HepG2	liver:	n/a	n/a
26	POLR2A	chr12:57585212-57585831	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr12:57586667-57587080	U87	brain:	n/a	n/a
28	POLR2A	chr12:57586454-57586698	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr12:57585545-57585586	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr12:57587011-57587147	HepG2	liver:	n/a	n/a
31	POLR2A	chr12:57584101-57584332	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr12:57584510-57584694	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr12:57585371-57585394	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr12:57586149-57587494	U87	brain:	n/a	n/a
35	POLR2A	chr12:57583338-57583742	HepG2	liver:	n/a	n/a
36	POLR2A	chr12:57584357-57585330	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr12:57586405-57586785	HepG2	liver:	n/a	n/a
38	POLR2A	chr12:57587159-57587460	HepG2	liver:	n/a	n/a
39	POLR2A	chr12:57585197-57586098	U87	brain:	n/a	n/a
40	POLR2A	chr12:57585403-57585534	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr12:57582803-57586073	U87	brain:	n/a	n/a
42	POLR2A	chr12:57583993-57584581	HepG2	liver:	n/a	n/a
43	POLR2A	chr12:57586435-57586729	HepG2	liver:	n/a	n/a
44	POLR2A	chr12:57585266-57586555	HepG2	liver:	n/a	n/a
45	POLR2A	chr12:57584028-57584126	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr12:57587091-57587102	HepG2	liver:	n/a	n/a
47	POLR2A	chr12:57586149-57587574	U87	brain:	n/a	n/a
48	POLR2A	chr12:57585157-57586098	U87	brain:	n/a	n/a
49	POLR2A	chr12:57584674-57584690	HepG2	liver:	n/a	n/a
50	POLR2A	chr12:57583419-57583478	H1-hESC	embryonic stem cell:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57584720-57584770	NHDF-neo	bronchial:	n/a
2	chr12:57587701-57587751	HAEpiC	amniotic membrane:	n/a
3	chr12:57584802-57584852	Jurkat	blood:	n/a
4	chr12:57587773-57587823	HRPEpiC	eye:	n/a
5	chr12:57587714-57587764	H1-hESC	embryonic stem cell:	embryo
6	chr12:57585184-57585234	SAEC	small airway:	n/a
7	chr12:57584971-57585021	HRCEpiC	kidney:	n/a
8	chr12:57585135-57585185	AG09309	skin:	n/a
9	chr12:57584929-57584979	NH-A	brain:	n/a
10	chr12:57586714-57586764	Caco-2	colon:	n/a
11	chr12:57587773-57587823	HCM	heart:	n/a
12	chr12:57584802-57584852	LNCaP	prostate:	n/a
13	chr12:57584929-57584979	BE2_C	brain:	n/a
14	chr12:57586714-57586764	PFSK-1	brain:	n/a
15	chr12:57584971-57585021	GM12891	blood:	n/a
16	chr12:57587701-57587751	PFSK-1	brain:	n/a
17	chr12:57585184-57585234	PANC-1	pancreas:	n/a
18	chr12:57584971-57585021	MCF-7	breast:	n/a
19	chr12:57584929-57584979	HNPCEpiC	eye:	n/a
20	chr12:57584720-57584770	AG09309	skin:	n/a
21	chr12:57586714-57586764	SK-N-SH	brain:	n/a
22	chr12:57584971-57585021	GM06990	blood:	n/a
23	chr12:57585135-57585185	HRCEpiC	kidney:	n/a
24	chr12:57584720-57584770	AG10803	skin:	n/a
25	chr12:57584802-57584852	AG09319	gingival:	n/a
26	chr12:57587773-57587823	MCF-7	breast:	n/a
27	chr12:57584971-57585021	HepG2	liver:	n/a
28	chr12:57586714-57586764	GM06990	blood:	n/a
29	chr12:57587701-57587751	AG04450	lung:	fetal
30	chr12:57584929-57584979	CMK	blood:	n/a
31	chr12:57584802-57584852	HEEpiC	esophagus:	n/a
32	chr12:57584802-57584852	GM12878	blood:	n/a
33	chr12:57585184-57585234	NB4	blood:	n/a
34	chr12:57584720-57584770	HRPEpiC	eye:	n/a
35	chr12:57584720-57584770	HCPEpiC	choroid plexus:	n/a
36	chr12:57587714-57587764	HCPEpiC	choroid plexus:	n/a
37	chr12:57584802-57584852	HCT-116	colon:	n/a
38	chr12:57585184-57585234	HIPEpiC	eye:	n/a
39	chr12:57587714-57587764	Caco-2	colon:	n/a
40	chr12:57585184-57585234	AG09309	skin:	n/a
41	chr12:57587714-57587764	BE2_C	brain:	n/a
42	chr12:57584971-57585021	BE2_C	brain:	n/a
43	chr12:57585184-57585234	PrEC	prostate:	n/a
44	chr12:57587422-57587472	BE2_C	brain:	n/a
45	chr12:57584971-57585021	HL-60	blood:	n/a
46	chr12:57587714-57587764	LNCaP	prostate:	n/a
47	chr12:57587773-57587823	Jurkat	blood:	n/a
48	chr12:57585135-57585185	HCM	heart:	n/a
49	chr12:57587422-57587472	A549	lung:	n/a
50	chr12:57587701-57587751	HPAEpiC	pulmonary alveolar:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57583820..57586424-chr12:57618362..57620239,2	K562	blood:
2	chr12:57502051..57503963-chr12:57583125..57585468,2	K562	blood:
3	chr12:57580575..57582415-chr12:57582574..57584680,3	MCF-7	breast:
4	chr12:57577559..57581276-chr12:57585770..57588469,3	MCF-7	breast:
5	chr12:57584008..57585901-chr12:57591267..57593221,2	MCF-7	breast:
6	chr12:57585683..57586259-chr12:57632623..57633497,2	MCF-7	breast:
7	chr12:57586062..57588945-chr12:57630038..57631841,2	K562	blood:
8	chr12:57585370..57589160-chr12:57594423..57597879,4	K562	blood:
9	chr12:57585543..57587547-chr12:57591115..57593361,2	MCF-7	breast:
10	chr12:57575198..57577019-chr12:57585311..57587590,2	K562	blood:
11	chr12:57579991..57582969-chr12:57586992..57588793,2	K562	blood:
12	chr12:57587383..57589092-chr12:57594725..57596825,2	MCF-7	breast:
13	chr12:57582255..57585186-chr12:57590822..57593487,2	MCF-7	breast:
14	chr12:57581983..57583861-chr12:57587969..57590424,2	K562	blood:
15	chr12:57586668..57589157-chr12:57592385..57594069,2	MCF-7	breast:

No data

Variant related genes	Relation type
MIR1228	TF binding region
MIR1228	CpG island
ENSG00000185633	chromatin interactions
ENSG00000166888	chromatin interactions
ENSG00000221365	chromatin interactions
ENSG00000123384	chromatin interactions

Extended variants
information (count: 229 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:229 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113334092	chr12:57583469-57583470	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs140769128	chr12:57583481-57583482	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs7312323	chr12:57583486-57583487	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs544170799	chr12:57583539-57583540	Strong transcription Weak transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs562316659	chr12:57583613-57583614	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs188571756	chr12:57583630-57583631	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs544933752	chr12:57583651-57583652	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs6581128	chr12:57583672-57583673	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs550433095	chr12:57583710-57583711	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs193234197	chr12:57583711-57583712	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs548800655	chr12:57583712-57583713	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs144745898	chr12:57583745-57583746	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs529340966	chr12:57583762-57583763	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs551072965	chr12:57583833-57583834	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs79434392	chr12:57583853-57583854	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs6581129	chr12:57583880-57583881	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs552098967	chr12:57583892-57583893	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs567210364	chr12:57583902-57583903	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs184830262	chr12:57583911-57583912	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs556022407	chr12:57583924-57583925	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs111990274	chr12:57583987-57583988	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs76892406	chr12:57584108-57584109	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs530101601	chr12:57584144-57584145	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs537508317	chr12:57584147-57584148	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs556232584	chr12:57584156-57584157	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs571784575	chr12:57584166-57584167	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs577518065	chr12:57584174-57584175	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs545030067	chr12:57584192-57584193	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs546478160	chr12:57584193-57584194	Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs35118304	chr12:57584227-57584228	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs551065713	chr12:57584280-57584281	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs553636525	chr12:57584291-57584292	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs572037390	chr12:57584309-57584310	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs531347748	chr12:57584318-57584319	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs115777808	chr12:57584337-57584338	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs376139868	chr12:57584375-57584376	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs570969820	chr12:57584395-57584396	Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs544335062	chr12:57584402-57584403	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs533634053	chr12:57584423-57584424	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs563047718	chr12:57584468-57584469	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs1800183	chr12:57584498-57584499	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs551832690	chr12:57584519-57584520	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs540760613	chr12:57584520-57584521	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs368247394	chr12:57584537-57584538	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs369869344	chr12:57584575-57584576	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs201043786	chr12:57584605-57584606	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs372880658	chr12:57584632-57584633	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs375847370	chr12:57584639-57584640	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs111471605	chr12:57584642-57584643	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs35484999	chr12:57584648-57584649	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57541600-57606600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:57541800-57607400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:57547000-57606400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
4	chr12:57552800-57606800	Strong transcription	Fetal Intestine Large	intestine
5	chr12:57552800-57607000	Strong transcription	Liver	Liver
6	chr12:57553200-57607400	Strong transcription	Fetal Intestine Small	intestine
7	chr12:57557400-57606800	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr12:57560800-57606200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:57560800-57606600	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr12:57565800-57606600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr12:57566000-57604200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr12:57566400-57583600	Strong transcription	Colon Smooth Muscle	Colon
13	chr12:57566600-57606200	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr12:57567200-57583600	Weak transcription	Right Atrium	heart
15	chr12:57567400-57584200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr12:57569400-57584000	Strong transcription	Rectal Smooth Muscle	rectum
17	chr12:57569800-57600800	Strong transcription	Brain Inferior Temporal Lobe	brain
18	chr12:57570200-57606800	Strong transcription	Fetal Stomach	stomach
19	chr12:57570600-57606800	Strong transcription	Osteobl	bone
20	chr12:57570800-57605400	Strong transcription	Muscle Satellite Cultured Cells	--
21	chr12:57571000-57585200	Weak transcription	Fetal Brain Male	brain
22	chr12:57574400-57586400	Weak transcription	Small Intestine	intestine
23	chr12:57574600-57584400	Genic enhancers	Placenta	Placenta
24	chr12:57575600-57585400	Strong transcription	NHLF	lung
25	chr12:57575800-57583800	Strong transcription	Fetal Lung	lung
26	chr12:57576000-57586400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:57576200-57583800	Strong transcription	Adipose Nuclei	Adipose
28	chr12:57576200-57605600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr12:57576200-57606400	Strong transcription	NHDF-Ad	bronchial
30	chr12:57576600-57583800	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr12:57576800-57583400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr12:57576800-57583600	Strong transcription	Brain Angular Gyrus	brain
33	chr12:57576800-57583800	Strong transcription	Fetal Brain Female	brain
34	chr12:57576800-57583800	Strong transcription	Right Ventricle	heart
35	chr12:57576800-57584000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:57576800-57604800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr12:57576800-57605000	Strong transcription	HSMMtube	muscle
38	chr12:57576800-57606600	Strong transcription	HepG2	liver
39	chr12:57576800-57607000	Strong transcription	Brain Germinal Matrix	brain
40	chr12:57577000-57583800	Strong transcription	Brain Hippocampus Middle	brain
41	chr12:57577000-57585200	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr12:57577000-57585400	Strong transcription	Gastric	stomach
43	chr12:57577000-57585800	Strong transcription	Spleen	Spleen
44	chr12:57577000-57591600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr12:57577000-57600600	Strong transcription	Brain Cingulate Gyrus	brain
46	chr12:57577000-57600600	Strong transcription	Brain Substantia Nigra	brain
47	chr12:57577000-57606000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:57577000-57606400	Strong transcription	H1 Cell Line	embryonic stem cell
49	chr12:57577000-57606400	Strong transcription	HUES64 Cell Line	embryonic stem cell
50	chr12:57577000-57606400	Strong transcription	Rectal Mucosa Donor 31	rectum

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