Variant report

Variant	nsv482136
Chromosome Location	chr1:161185087-161189038
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:305)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:161188006-161189463	HepG2	liver:	n/a	n/a
2	ATF2	chr1:161187053-161187590	GM12878	blood:	n/a	n/a
3	ATF2	chr1:161187029-161187678	GM12878	blood:	n/a	n/a
4	BCL11A	chr1:161187155-161187530	GM12878	blood:	n/a	n/a
5	BCL11A	chr1:161187198-161187554	GM12878	blood:	n/a	n/a
6	BCLAF1	chr1:161187207-161187683	GM12878	blood:	n/a	n/a
7	BHLHE40	chr1:161187120-161187601	GM12878	blood:	n/a	n/a
8	CEBPB	chr1:161186717-161186970	A549	lung:	n/a	n/a
9	CEBPB	chr1:161186662-161187233	IMR90	lung:	n/a	n/a
10	CEBPB	chr1:161186823-161186942	K562	blood:	n/a	n/a
11	CEBPB	chr1:161186722-161187082	HepG2	liver:	n/a	n/a
12	CEBPD	chr1:161188259-161188683	HepG2	liver:	n/a	n/a
13	CHD2	chr1:161186892-161187746	GM12878	blood:	n/a	n/a
14	CHD2	chr1:161187769-161187775	HepG2	liver:	n/a	n/a
15	CHD2	chr1:161188356-161188735	HepG2	liver:	n/a	chr1:161188590-161188600
16	CHD2	chr1:161188993-161189433	HepG2	liver:	n/a	n/a
17	E2F4	chr1:161186630-161187180	MCF10A-Er-Src	breast:	n/a	n/a
18	EBF1	chr1:161187238-161187613	GM12878	blood:	n/a	chr1:161187445-161187454 chr1:161187444-161187455 chr1:161187444-161187454
19	EBF1	chr1:161187159-161187607	GM12878	blood:	n/a	chr1:161187445-161187454 chr1:161187444-161187455 chr1:161187444-161187454
20	EBF1	chr1:161186908-161187696	GM12878	blood:	n/a	chr1:161187445-161187454 chr1:161187444-161187455 chr1:161187444-161187454
21	EGR1	chr1:161187327-161187453	GM12878	blood:	n/a	chr1:161187378-161187392
22	EGR1	chr1:161187289-161187438	GM12878	blood:	n/a	chr1:161187378-161187392
23	ELF1	chr1:161188442-161188597	K562	blood:	n/a	n/a
24	ELF1	chr1:161188244-161188755	HepG2	liver:	n/a	n/a
25	ELF1	chr1:161187115-161187572	GM12878	blood:	n/a	n/a
26	ELF1	chr1:161188313-161188830	HepG2	liver:	n/a	n/a
27	EP300	chr1:161187194-161187566	GM12878	blood:	n/a	n/a
28	EP300	chr1:161188368-161188699	HepG2	liver:	n/a	chr1:161188584-161188600
29	EP300	chr1:161187158-161187767	GM12878	blood:	n/a	chr1:161187637-161187651
30	EP300	chr1:161187250-161187399	K562	blood:	n/a	n/a
31	EP300	chr1:161188201-161188732	HepG2	liver:	n/a	chr1:161188584-161188600
32	EP300	chr1:161188142-161188868	HepG2	liver:	n/a	chr1:161188584-161188600
33	FOS	chr1:161186780-161187010	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr1:161186683-161187219	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr1:161186741-161187120	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:161186699-161187176	MCF10A-Er-Src	breast:	n/a	n/a
37	FOXA1	chr1:161187973-161188773	HepG2	liver:	n/a	n/a
38	FOXA1	chr1:161188068-161188805	HepG2	liver:	n/a	n/a
39	FOXA1	chr1:161188218-161188760	HepG2	liver:	n/a	n/a
40	FOXA1	chr1:161188147-161188787	HepG2	liver:	n/a	n/a
41	FOXA2	chr1:161188191-161188667	HepG2	liver:	n/a	n/a
42	FOXM1	chr1:161187105-161187650	GM12878	blood:	n/a	n/a
43	HDAC2	chr1:161188308-161188779	HepG2	liver:	n/a	chr1:161188468-161188482
44	HDAC2	chr1:161188285-161188800	HepG2	liver:	n/a	chr1:161188468-161188482
45	HEY1	chr1:161187665-161190931	HepG2	liver:	n/a	n/a
46	HEY1	chr1:161187172-161187596	HepG2	liver:	n/a	n/a
47	HEY1	chr1:161187602-161194631	HepG2	liver:	n/a	n/a
48	HNF4A	chr1:161188287-161188770	HepG2	liver:	n/a	n/a
49	HNF4A	chr1:161189038-161189352	HepG2	liver:	n/a	chr1:161189191-161189205
50	HNF4A	chr1:161188286-161188725	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:161185061-161185111	SKMC	muscle:	n/a
2	chr1:161187776-161187826	HRCEpiC	kidney:	n/a
3	chr1:161185061-161185111	HPAEpiC	pulmonary alveolar:	n/a
4	chr1:161186839-161186889	AG04450	lung:	fetal
5	chr1:161186839-161186889	HNPCEpiC	eye:	n/a
6	chr1:161188921-161188971	A549	lung:	n/a
7	chr1:161187776-161187826	NH-A	brain:	n/a
8	chr1:161188921-161188971	HAEpiC	amniotic membrane:	n/a
9	chr1:161185092-161185142	NT2-D1	testis:	n/a
10	chr1:161188921-161188971	GM12892	blood:	n/a
11	chr1:161187776-161187826	Jurkat	blood:	n/a
12	chr1:161187776-161187826	BJ	skin:	n/a
13	chr1:161187776-161187826	ProgFib	skin:	n/a
14	chr1:161185061-161185111	IMR90	lung:	fetal
15	chr1:161185092-161185142	AG09309	skin:	n/a
16	chr1:161186839-161186889	HEEpiC	esophagus:	n/a
17	chr1:161187776-161187826	PFSK-1	brain:	n/a
18	chr1:161185092-161185142	Hepatocyte	liver:	n/a
19	chr1:161186839-161186889	NT2-D1	testis:	n/a
20	chr1:161185061-161185111	NB4	blood:	n/a
21	chr1:161185061-161185111	AG09309	skin:	n/a
22	chr1:161188921-161188971	SK-N-MC	brain:	n/a
23	chr1:161185061-161185111	HMEC	breast:	n/a
24	chr1:161186839-161186889	SK-N-SH_RA	brain:	n/a
25	chr1:161187776-161187826	HAEpiC	amniotic membrane:	n/a
26	chr1:161185092-161185142	ovcar-3	ovarian:	n/a
27	chr1:161187776-161187826	SKMC	muscle:	n/a
28	chr1:161188921-161188971	GM19239	blood:	n/a
29	chr1:161187776-161187826	HIPEpiC	eye:	n/a
30	chr1:161185061-161185111	HepG2	liver:	n/a
31	chr1:161185061-161185111	ProgFib	skin:	n/a
32	chr1:161186839-161186889	NHDF-neo	bronchial:	n/a
33	chr1:161185061-161185111	HL-60	blood:	n/a
34	chr1:161186839-161186889	NH-A	brain:	n/a
35	chr1:161188921-161188971	HepG2	liver:	n/a
36	chr1:161186839-161186889	PANC-1	pancreas:	n/a
37	chr1:161185092-161185142	GM12891	blood:	n/a
38	chr1:161187776-161187826	PrEC	prostate:	n/a
39	chr1:161187776-161187826	SK-N-SH_RA	brain:	n/a
40	chr1:161185092-161185142	NH-A	brain:	n/a
41	chr1:161185092-161185142	AG04450	lung:	fetal
42	chr1:161185092-161185142	GM12878	blood:	n/a
43	chr1:161185061-161185111	AG04450	lung:	fetal
44	chr1:161188921-161188971	PANC-1	pancreas:	n/a
45	chr1:161185092-161185142	CMK	blood:	n/a
46	chr1:161186839-161186889	BE2_C	brain:	n/a
47	chr1:161185092-161185142	SKMC	muscle:	n/a
48	chr1:161186839-161186889	RPTEC	kidney:	n/a
49	chr1:161186839-161186889	Hela-S3	cervix:	n/a
50	chr1:161188921-161188971	AG10803	skin:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:161168408..161172447-chr1:161188045..161190714,3	K562	blood:
2	chr1:161172161..161173838-chr1:161184406..161186813,2	MCF-7	breast:
3	chr1:161173901..161175436-chr1:161186742..161188476,2	MCF-7	breast:
4	chr1:161167824..161171271-chr1:161185300..161189545,6	K562	blood:
5	chr1:161175566..161178282-chr1:161184177..161186435,3	K562	blood:
6	chr1:161174340..161177261-chr1:161184177..161187109,2	K562	blood:
7	chr1:161180679..161184131-chr1:161186023..161188339,4	MCF-7	breast:
8	chr1:161184335..161187137-chr1:161197763..161199815,2	MCF-7	breast:
9	chr1:161179856..161181957-chr1:161183468..161185300,2	MCF-7	breast:
10	chr1:161187686..161190489-chr1:161204186..161207080,2	K562	blood:
11	chr1:161187330..161192033-chr1:161197583..161201870,4	K562	blood:
12	chr1:161178470..161182189-chr1:161183792..161185908,3	K562	blood:
13	chr1:161185902..161187747-chr1:161348758..161351326,2	K562	blood:
14	chr1:161171283..161173285-chr1:161186307..161187899,2	K562	blood:
15	chr1:161183575..161186410-chr1:161283060..161284793,2	K562	blood:
16	chr1:161185948..161188924-chr1:161331742..161333361,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000268387	TF binding region
FCER1G	TF binding region
ENSG00000268387	CpG island
FCER1G	CpG island
ENSG00000158864	chromatin interactions
ENSG00000158859	chromatin interactions
ENSG00000143252	chromatin interactions
ENSG00000236484	chromatin interactions
ENSG00000158882	chromatin interactions
ENSG00000143257	chromatin interactions

Extended variants
information (count: 161 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:161 , 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	rs543677403	chr1:161185092-161185093	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs113220867	chr1:161185096-161185097	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs112839285	chr1:161185097-161185098	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs188955540	chr1:161185117-161185118	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs144682477	chr1:161185124-161185125	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs369286776	chr1:161185135-161185136	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs559837665	chr1:161185165-161185166	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs201271754	chr1:161185179-161185180	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs372924282	chr1:161185186-161185187	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs377123904	chr1:161185191-161185192	Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs146654137	chr1:161185224-161185225	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs140245883	chr1:161185225-161185226	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs565258595	chr1:161185246-161185247	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs530844219	chr1:161185286-161185287	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs150370338	chr1:161185295-161185296	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs567913219	chr1:161185310-161185311	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs74124668	chr1:161185311-161185312	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs546800846	chr1:161185371-161185372	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs565405455	chr1:161185380-161185381	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs200113251	chr1:161185388-161185389	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs534431005	chr1:161185406-161185407	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs138104808	chr1:161185440-161185441	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs570892144	chr1:161185447-161185448	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs536686649	chr1:161185496-161185497	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs557217497	chr1:161185508-161185509	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs118038066	chr1:161185555-161185556	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs562436749	chr1:161185579-161185580	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs553218414	chr1:161185604-161185605	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs573102963	chr1:161185634-161185635	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs542454981	chr1:161185703-161185704	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs545505008	chr1:161185726-161185727	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs114495062	chr1:161185729-161185730	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs530930711	chr1:161185763-161185764	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs544285595	chr1:161185824-161185825	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs181636561	chr1:161185943-161185944	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs561589100	chr1:161185960-161185961	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs530344375	chr1:161185983-161185984	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs546759948	chr1:161186056-161186057	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs566700883	chr1:161186096-161186097	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs187407187	chr1:161186097-161186098	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs112447263	chr1:161186099-161186100	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs530290249	chr1:161186133-161186134	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs528324367	chr1:161186147-161186148	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs190542717	chr1:161186148-161186149	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs564689915	chr1:161186152-161186153	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs531374322	chr1:161186153-161186154	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs199510387	chr1:161186167-161186168	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs548854070	chr1:161186168-161186169	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs571301814	chr1:161186185-161186186	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs199604831	chr1:161186196-161186197	Weak transcription Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Systemic lupus erythematosus	19220326	CNVD
Systemic lupus erythematosus	19287148	CNVD
Glomerulonephritis	19341492	CNVD
Systemic lupus erythematosus	18559452	CNVD
Systemic autoimmune disease	17597778	CNVD
Glomerulonephritis	17008540	CNVD
Glomerulonephritis	16482158	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Breast cancer	21045282	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Follicular lymphoma	18703704	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20409316	CNVD
Mental retardation	17847001	CNVD
Idiopathic thrombocytopenic purpura	17827395	CNVD

Chromatin state (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:161172800-161186800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:161172800-161193600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:161173400-161185200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:161173400-161185400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:161173800-161185400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:161173800-161185400	Strong transcription	Sigmoid Colon	Sigmoid Colon
7	chr1:161174200-161185200	Strong transcription	Brain Germinal Matrix	brain
8	chr1:161174200-161185400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:161175000-161185400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:161175000-161185800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:161175400-161185800	Strong transcription	Fetal Stomach	stomach
12	chr1:161176000-161185200	Strong transcription	Thymus	Thymus
13	chr1:161176000-161185400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:161176400-161185800	Strong transcription	Placenta Amnion	Placenta Amnion
15	chr1:161177200-161185600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:161177400-161186000	Weak transcription	Right Atrium	heart
17	chr1:161178200-161185400	Strong transcription	Gastric	stomach
18	chr1:161178200-161185400	Strong transcription	NH-A	brain
19	chr1:161178400-161185200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr1:161178600-161185600	Strong transcription	NHLF	lung
21	chr1:161178800-161185200	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr1:161178800-161185200	Strong transcription	HUVEC	blood vessel
23	chr1:161178800-161185400	Strong transcription	Fetal Brain Female	brain
24	chr1:161178800-161185400	Strong transcription	Pancreas	Pancrea
25	chr1:161178800-161185600	Strong transcription	HMEC	breast
26	chr1:161178800-161186000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:161179600-161185400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr1:161179800-161185400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr1:161180000-161185400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr1:161180000-161185400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr1:161180000-161185800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:161180200-161185200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr1:161180200-161185200	Strong transcription	Fetal Intestine Small	intestine
34	chr1:161180200-161185200	Strong transcription	A549	lung
35	chr1:161180200-161185400	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr1:161180200-161185400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
37	chr1:161180200-161185600	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chr1:161180400-161185200	Strong transcription	Brain Cingulate Gyrus	brain
39	chr1:161180600-161186200	Weak transcription	Fetal Heart	heart
40	chr1:161181200-161186400	Weak transcription	Stomach Mucosa	stomach
41	chr1:161182400-161193800	Weak transcription	Small Intestine	intestine
42	chr1:161183600-161185400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:161183800-161185200	Strong transcription	Lung	lung
44	chr1:161184000-161187000	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr1:161184000-161187200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr1:161184200-161185400	Genic enhancers	Primary T helper cells fromperipheralblood	blood
47	chr1:161184200-161185800	Weak transcription	K562	blood
48	chr1:161184200-161186200	Weak transcription	NHDF-Ad	bronchial
49	chr1:161184200-161186400	Weak transcription	Fetal Lung	lung
50	chr1:161184200-161186400	Weak transcription	HSMMtube	muscle

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