Variant report

Variant	esv3370587
Chromosome Location	chr12:57577235-57580033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:55)
CpG islands
(count:672)
Chromatin interactive
region (count:27)
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	BCL3	chr12:57576609-57577464	A549	lung:	n/a	n/a
2	CTCF	chr12:57577220-57577370	WERI-Rb-1	eye:	n/a	n/a
3	CTCF	chr12:57577222-57577301	GM19238	blood:	n/a	n/a
4	CTCF	chr12:57576518-57577325	A549	lung:	n/a	chr12:57576921-57576939 chr12:57576948-57576956 chr12:57576916-57576937
5	CTCF	chr12:57577204-57577282	GM13976	blood:	n/a	n/a
6	CTCF	chr12:57576635-57577243	MCF-7	breast:	n/a	chr12:57576921-57576939 chr12:57576948-57576956 chr12:57576916-57576937
7	CTCF	chr12:57577616-57577677	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr12:57576473-57577374	HCT-116	colon:	n/a	chr12:57576921-57576939 chr12:57576948-57576956 chr12:57576916-57576937
9	CTCF	chr12:57577240-57577390	GM12866	blood:	n/a	n/a
10	CTCF	chr12:57577249-57577282	GM12891	blood:	n/a	n/a
11	CTCF	chr12:57577680-57577830	AG04449	skin:	n/a	n/a
12	CTCF	chr12:57577320-57577470	GM12872	blood:	n/a	n/a
13	CTCF	chr12:57577280-57577430	GM12864	blood:	n/a	n/a
14	CTCF	chr12:57576503-57577467	SK-N-SH	brain:	n/a	chr12:57576921-57576939 chr12:57576948-57576956 chr12:57576916-57576937
15	CTCF	chr12:57577589-57577659	GM12891	blood:	n/a	n/a
16	EGR1	chr12:57579635-57579948	K562	blood:	n/a	chr12:57579715-57579724
17	EGR1	chr12:57579700-57579926	K562	blood:	n/a	chr12:57579715-57579724
18	HMGN3	chr12:57577332-57577380	K562	blood:	n/a	n/a
19	MAX	chr12:57576694-57577272	MCF-7	breast:	n/a	n/a
20	MYC	chr12:57577973-57578074	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr12:57578573-57578580	HepG2	liver:	n/a	n/a
22	POLR2A	chr12:57578761-57579306	U87	brain:	n/a	n/a
23	POLR2A	chr12:57576482-57577290	U87	brain:	n/a	n/a
24	POLR2A	chr12:57579389-57579593	HepG2	liver:	n/a	n/a
25	POLR2A	chr12:57577543-57578576	U87	brain:	n/a	n/a
26	POLR2A	chr12:57578707-57579350	U87	brain:	n/a	n/a
27	POLR2A	chr12:57578260-57578747	HepG2	liver:	n/a	n/a
28	POLR2A	chr12:57577570-57577719	MCF-7	breast:	n/a	n/a
29	POLR2A	chr12:57576482-57577322	U87	brain:	n/a	n/a
30	POLR2A	chr12:57579955-57580004	HepG2	liver:	n/a	n/a
31	POLR2A	chr12:57577528-57577534	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr12:57577829-57577970	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr12:57579744-57581826	U87	brain:	n/a	n/a
34	POLR2A	chr12:57577344-57577359	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr12:57577543-57578636	U87	brain:	n/a	n/a
36	POLR2A	chr12:57576641-57577329	HepG2	liver:	n/a	n/a
37	POLR2A	chr12:57578204-57578258	HepG2	liver:	n/a	n/a
38	POLR2A	chr12:57579365-57579385	HepG2	liver:	n/a	n/a
39	POLR2A	chr12:57577423-57577591	HepG2	liver:	n/a	n/a
40	POLR2A	chr12:57576687-57578009	HepG2	liver:	n/a	n/a
41	POLR2A	chr12:57579804-57581774	U87	brain:	n/a	n/a
42	POLR2A	chr12:57578008-57578045	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr12:57577579-57577771	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr12:57579340-57579364	HepG2	liver:	n/a	n/a
45	RAD21	chr12:57576488-57577345	HCT-116	colon:	n/a	chr12:57576919-57576938
46	RAD21	chr12:57576468-57577399	SK-N-SH	brain:	n/a	chr12:57576919-57576938
47	RAD21	chr12:57576664-57577290	MCF-7	breast:	n/a	chr12:57576919-57576938
48	RAD21	chr12:57576567-57577250	A549	lung:	n/a	chr12:57576919-57576938
49	RAD21	chr12:57576536-57577242	ECC-1	luminal epithelium:	n/a	chr12:57576919-57576938
50	RELA	chr12:57576756-57577235	GM18951	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57579466-57579516	HCM	heart:	n/a
2	chr12:57579466-57579516	HCM	heart:	n/a
3	chr12:57579466-57579516	NB4	blood:	n/a
4	chr12:57578667-57578717	SKMC	muscle:	n/a
5	chr12:57577597-57577647	PFSK-1	brain:	n/a
6	chr12:57579596-57579646	PANC-1	pancreas:	n/a
7	chr12:57578649-57578699	Hepatocyte	liver:	n/a
8	chr12:57578642-57578692	NHBE	bronchial:	n/a
9	chr12:57578694-57578744	HNPCEpiC	eye:	n/a
10	chr12:57578642-57578692	A549	lung:	n/a
11	chr12:57579382-57579432	PFSK-1	brain:	n/a
12	chr12:57578667-57578717	H1-hESC	embryonic stem cell:	embryo
13	chr12:57578696-57578746	PFSK-1	brain:	n/a
14	chr12:57577597-57577647	GM06990	blood:	n/a
15	chr12:57578642-57578692	T-47D	breast:	n/a
16	chr12:57579466-57579516	GM12892	blood:	n/a
17	chr12:57579466-57579516	HEEpiC	esophagus:	n/a
18	chr12:57578642-57578692	SKMC	muscle:	n/a
19	chr12:57579444-57579494	ovcar-3	ovarian:	n/a
20	chr12:57579444-57579494	NHDF-neo	bronchial:	n/a
21	chr12:57577597-57577647	AG04449	skin:	fetal
22	chr12:57578667-57578717	HRE	kidney:	n/a
23	chr12:57578667-57578717	HEEpiC	esophagus:	n/a
24	chr12:57578642-57578692	NH-A	brain:	n/a
25	chr12:57578696-57578746	Caco-2	colon:	n/a
26	chr12:57577597-57577647	NH-A	brain:	n/a
27	chr12:57579466-57579516	SK-N-SH_RA	brain:	n/a
28	chr12:57579382-57579432	CMK	blood:	n/a
29	chr12:57579596-57579646	NHDF-neo	bronchial:	n/a
30	chr12:57579382-57579432	ProgFib	skin:	n/a
31	chr12:57579382-57579432	MCF10A-Er-Src	breast:	n/a
32	chr12:57578696-57578746	HL-60	blood:	n/a
33	chr12:57578649-57578699	SK-N-SH	brain:	n/a
34	chr12:57579466-57579516	K562	blood:	n/a
35	chr12:57578649-57578699	LNCaP	prostate:	n/a
36	chr12:57578649-57578699	IMR90	lung:	fetal
37	chr12:57578694-57578744	PANC-1	pancreas:	n/a
38	chr12:57578667-57578717	AG10803	skin:	n/a
39	chr12:57578672-57578722	PANC-1	pancreas:	n/a
40	chr12:57579466-57579516	Hela-S3	cervix:	n/a
41	chr12:57578694-57578744	RPTEC	kidney:	n/a
42	chr12:57579382-57579432	HEK293	kidney:	embryo
43	chr12:57579466-57579516	PANC-1	pancreas:	n/a
44	chr12:57578642-57578692	SAEC	small airway:	n/a
45	chr12:57578649-57578699	HL-60	blood:	n/a
46	chr12:57578696-57578746	PANC-1	pancreas:	n/a
47	chr12:57578649-57578699	PFSK-1	brain:	n/a
48	chr12:57579596-57579646	SK-N-SH	brain:	n/a
49	chr12:57578696-57578746	GM12891	blood:	n/a
50	chr12:57578672-57578722	Hela-S3	cervix:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:57579991..57582969-chr12:57586992..57588793,2	K562	blood:
2	chr12:57480529..57483357-chr12:57577907..57579973,2	K562	blood:
3	chr12:57516722..57519853-chr12:57574836..57577747,5	MCF-7	breast:
4	chr12:57485447..57487110-chr12:57577683..57580330,2	MCF-7	breast:
5	chr12:57480163..57483856-chr12:57574484..57579428,5	K562	blood:
6	chr12:57517952..57518717-chr12:57576444..57577434,3	K562	blood:
7	chr12:57401359..57402312-chr12:57576362..57577409,4	K562	blood:
8	chr12:57504591..57506895-chr12:57575667..57579338,3	MCF-7	breast:
9	chr12:57504145..57507554-chr12:57578690..57582057,3	MCF-7	breast:
10	chr12:57566443..57567143-chr12:57576444..57577432,3	MCF-7	breast:
11	chr12:57578786..57581016-chr12:57606054..57608817,2	MCF-7	breast:
12	chr12:57492932..57495251-chr12:57576530..57578969,2	MCF-7	breast:
13	chr12:57576952..57579593-chr12:57580712..57583251,3	K562	blood:
14	chr12:57577559..57581276-chr12:57585770..57588469,3	MCF-7	breast:
15	chr12:57505585..57506379-chr12:57576444..57577269,2	MCF-7	breast:
16	chr12:57569226..57571527-chr12:57578285..57580181,2	K562	blood:
17	chr12:57565032..57567264-chr12:57576993..57578694,2	MCF-7	breast:
18	chr12:57576825..57577375-chr12:57636951..57637488,2	MCF-7	breast:
19	chr12:57482136..57484560-chr12:57577498..57579207,2	MCF-7	breast:
20	chr12:57568118..57572450-chr12:57574080..57578347,5	MCF-7	breast:
21	chr12:57479937..57482573-chr12:57575541..57577379,3	MCF-7	breast:
22	chr12:57520642..57521644-chr12:57576487..57577362,6	MCF-7	breast:
23	chr12:57517714..57518858-chr12:57576416..57577659,16	MCF-7	breast:
24	chr12:57574962..57576998-chr12:57578959..57581082,2	K562	blood:
25	chr12:57576887..57577443-chr12:57589478..57590363,2	K562	blood:
26	chr12:57476897..57479666-chr12:57576067..57577675,2	MCF-7	breast:
27	chr12:57463328..57464070-chr12:57576781..57577340,2	MCF-7	breast:

No data

Variant related genes	Relation type
LRP1	TF binding region
LRP1	CpG island
ENSG00000166888	chromatin interactions
ENSG00000123384	chromatin interactions
ENSG00000166881	chromatin interactions
ENSG00000221365	chromatin interactions
ENSG00000166886	chromatin interactions

Extended variants
information (count: 145 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:145 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142834460	chr12:57577239-57577240	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs186945792	chr12:57577256-57577257	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs191768462	chr12:57577265-57577266	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs560161034	chr12:57577289-57577290	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs540804622	chr12:57577315-57577316	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs370287263	chr12:57577325-57577326	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs556022723	chr12:57577345-57577346	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs574305343	chr12:57577348-57577349	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs544288781	chr12:57577382-57577383	Strong transcription Weak transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs146150281	chr12:57577409-57577410	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs573982184	chr12:57577450-57577451	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs545602154	chr12:57577463-57577464	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs544723463	chr12:57577494-57577495	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs373938784	chr12:57577524-57577525	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs560383704	chr12:57577533-57577534	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs34183166	chr12:57577540-57577541	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs151062304	chr12:57577590-57577591	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs200139006	chr12:57577598-57577599	Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs200133275	chr12:57577625-57577626	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs200890734	chr12:57577630-57577631	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs138993371	chr12:57577637-57577638	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs144804370	chr12:57577638-57577639	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs182778466	chr12:57577659-57577660	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs375074699	chr12:57577682-57577683	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs368721493	chr12:57577688-57577689	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs371605852	chr12:57577716-57577717	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs374491273	chr12:57577719-57577720	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs34423990	chr12:57577722-57577723	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs201373554	chr12:57577726-57577727	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs374971952	chr12:57577743-57577744	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs34548137	chr12:57577756-57577757	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs35161844	chr12:57577840-57577841	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs34398639	chr12:57577872-57577873	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs141826184	chr12:57577915-57577916	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs372035479	chr12:57577977-57577978	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs150485916	chr12:57577981-57577982	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs369518216	chr12:57578018-57578019	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs539793305	chr12:57578019-57578020	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs201830166	chr12:57578036-57578037	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs377223131	chr12:57578037-57578038	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs77492261	chr12:57578048-57578049	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs559868698	chr12:57578055-57578056	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs369233341	chr12:57578094-57578095	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs200384133	chr12:57578100-57578101	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs368827914	chr12:57578105-57578106	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs34890517	chr12:57578142-57578143	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs193167795	chr12:57578158-57578159	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs145430854	chr12:57578159-57578160	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs61734594	chr12:57578164-57578165	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs148823753	chr12:57578171-57578172	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	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:128 , 50 per page) page: 1 2 3

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	chr12:57555400-57583200	Weak transcription	Fetal Heart	heart
8	chr12:57557400-57606800	Strong transcription	Primary monocytes fromperipheralblood	blood
9	chr12:57560800-57606200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:57560800-57606600	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr12:57565800-57606600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr12:57566000-57604200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr12:57566400-57583600	Strong transcription	Colon Smooth Muscle	Colon
14	chr12:57566600-57606200	Strong transcription	HUES48 Cell Line	embryonic stem cell
15	chr12:57567200-57583600	Weak transcription	Right Atrium	heart
16	chr12:57567400-57584200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr12:57569400-57584000	Strong transcription	Rectal Smooth Muscle	rectum
18	chr12:57569800-57600800	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr12:57570000-57581200	Strong transcription	Fetal Muscle Trunk	muscle
20	chr12:57570000-57582000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr12:57570000-57583200	Strong transcription	Fetal Muscle Leg	muscle
22	chr12:57570200-57606800	Strong transcription	Fetal Stomach	stomach
23	chr12:57570400-57581200	Strong transcription	HSMM	muscle
24	chr12:57570600-57606800	Strong transcription	Osteobl	bone
25	chr12:57570800-57605400	Strong transcription	Muscle Satellite Cultured Cells	--
26	chr12:57571000-57585200	Weak transcription	Fetal Brain Male	brain
27	chr12:57571400-57580000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr12:57573800-57577600	Weak transcription	Pancreas	Pancrea
29	chr12:57574400-57586400	Weak transcription	Small Intestine	intestine
30	chr12:57574600-57584400	Genic enhancers	Placenta	Placenta
31	chr12:57574800-57578200	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr12:57575200-57577400	Weak transcription	Left Ventricle	heart
33	chr12:57575600-57577400	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr12:57575600-57577600	Weak transcription	Lung	lung
35	chr12:57575600-57578000	Weak transcription	NH-A	brain
36	chr12:57575600-57585400	Strong transcription	NHLF	lung
37	chr12:57575800-57577600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr12:57575800-57583800	Strong transcription	Fetal Lung	lung
39	chr12:57576000-57577400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:57576000-57586400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr12:57576200-57583800	Strong transcription	Adipose Nuclei	Adipose
42	chr12:57576200-57605600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr12:57576200-57606400	Strong transcription	NHDF-Ad	bronchial
44	chr12:57576600-57577400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:57576600-57577600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:57576600-57577600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr12:57576600-57577600	Enhancers	HMEC	breast
48	chr12:57576600-57577600	Enhancers	NHEK	skin
49	chr12:57576600-57578800	Strong transcription	Fetal Kidney	kidney
50	chr12:57576600-57583800	Strong transcription	Duodenum Smooth Muscle	Duodenum

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