Variant report

Variant	esv2757842
Chromosome Location	chr2:183437700-183835084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4208)
CpG islands
(count:2624)
Chromatin interactive
region (count:229)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:4208 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:183649459-183649762	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:183777917-183777921	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:183817079-183817215	K562	blood:	n/a	n/a
4	ARID3A	chr2:183515581-183515755	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:183679569-183679767	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:183804408-183804539	K562	blood:	n/a	n/a
7	ARID3A	chr2:183648439-183648583	K562	blood:	n/a	n/a
8	ARID3A	chr2:183483411-183483533	K562	blood:	n/a	n/a
9	ARID3A	chr2:183593463-183593469	K562	blood:	n/a	n/a
10	ARID3A	chr2:183764997-183765224	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:183649467-183649783	K562	blood:	n/a	n/a
12	ARID3A	chr2:183755294-183756486	HepG2	liver:	n/a	n/a
13	ARID3A	chr2:183580474-183581183	HepG2	liver:	n/a	n/a
14	ARID3A	chr2:183772253-183772399	K562	blood:	n/a	n/a
15	ARID3A	chr2:183460601-183460670	K562	blood:	n/a	n/a
16	ARID3A	chr2:183668859-183669300	HepG2	liver:	n/a	n/a
17	ARID3A	chr2:183514101-183514302	HepG2	liver:	n/a	n/a
18	ARID3A	chr2:183481518-183482276	HepG2	liver:	n/a	n/a
19	ARID3A	chr2:183731010-183731021	HepG2	liver:	n/a	n/a
20	ARID3A	chr2:183806683-183807362	K562	blood:	n/a	n/a
21	ARID3A	chr2:183814330-183814953	K562	blood:	n/a	n/a
22	ATF1	chr2:183507090-183507423	K562	blood:	n/a	n/a
23	ATF1	chr2:183806793-183807002	K562	blood:	n/a	n/a
24	ATF1	chr2:183725934-183726010	K562	blood:	n/a	n/a
25	ATF1	chr2:183813973-183814881	K562	blood:	n/a	n/a
26	ATF1	chr2:183647473-183647647	K562	blood:	n/a	n/a
27	ATF2	chr2:183580338-183581152	GM12878	blood:	n/a	n/a
28	ATF2	chr2:183785387-183785939	GM12878	blood:	n/a	n/a
29	ATF2	chr2:183785311-183785714	GM12878	blood:	n/a	n/a
30	ATF2	chr2:183580660-183581148	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr2:183580660-183581085	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF3	chr2:183580790-183581114	K562	blood:	n/a	chr2:183580978-183580987
33	ATF3	chr2:183814349-183814528	K562	blood:	n/a	n/a
34	ATF3	chr2:183814286-183814639	K562	blood:	n/a	n/a
35	BACH1	chr2:183814525-183814793	K562	blood:	n/a	n/a
36	BACH1	chr2:183732098-183732408	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr2:183581406-183581577	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr2:183802778-183802790	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr2:183490541-183490891	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr2:183771914-183772348	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr2:183730971-183731063	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr2:183515561-183515598	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr2:183581032-183581106	K562	blood:	n/a	n/a
44	BACH1	chr2:183580525-183581202	H1-hESC	embryonic stem cell:	n/a	n/a
45	BATF	chr2:183460356-183460628	GM12878	blood:	n/a	n/a
46	BATF	chr2:183471691-183471996	GM12878	blood:	n/a	chr2:183471798-183471809
47	BATF	chr2:183591303-183591561	GM12878	blood:	n/a	n/a
48	BATF	chr2:183591221-183591595	GM12878	blood:	n/a	n/a
49	BATF	chr2:183769640-183769883	GM12878	blood:	n/a	chr2:183769744-183769755 chr2:183769745-183769755
50	BCL11A	chr2:183471755-183471955	GM12878	blood:	n/a	n/a

(count:2624 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:183580910-183580960	A549	lung:	n/a
2	chr2:183580910-183580960	A549	lung:	n/a
3	chr2:183729189-183729239	AG10803	skin:	n/a
4	chr2:183723096-183723146	SK-N-MC	brain:	n/a
5	chr2:183580818-183580868	MCF10A-Er-Src	breast:	n/a
6	chr2:183683268-183683318	HCM	heart:	n/a
7	chr2:183731944-183731994	HL-60	blood:	n/a
8	chr2:183731599-183731649	PFSK-1	brain:	n/a
9	chr2:183458286-183458336	NB4	blood:	n/a
10	chr2:183731824-183731874	HRCEpiC	kidney:	n/a
11	chr2:183730940-183730990	GM12892	blood:	n/a
12	chr2:183732062-183732112	HRE	kidney:	n/a
13	chr2:183731407-183731457	GM06990	blood:	n/a
14	chr2:183473088-183473138	GM06990	blood:	n/a
15	chr2:183732062-183732112	HEK293	kidney:	embryo
16	chr2:183699153-183699203	SK-N-SH_RA	brain:	n/a
17	chr2:183473411-183473461	NHDF-neo	bronchial:	n/a
18	chr2:183667124-183667174	K562	blood:	n/a
19	chr2:183580906-183580956	CMK	blood:	n/a
20	chr2:183580829-183580879	NB4	blood:	n/a
21	chr2:183580694-183580744	HCF	heart:	n/a
22	chr2:183580906-183580956	SK-N-SH_RA	brain:	n/a
23	chr2:183642235-183642285	GM12891	blood:	n/a
24	chr2:183580574-183580624	NHDF-neo	bronchial:	n/a
25	chr2:183584043-183584093	A549	lung:	n/a
26	chr2:183667124-183667174	BJ	skin:	n/a
27	chr2:183580463-183580513	AG10803	skin:	n/a
28	chr2:183580910-183580960	PrEC	prostate:	n/a
29	chr2:183584043-183584093	IMR90	lung:	fetal
30	chr2:183731676-183731726	MCF-7	breast:	n/a
31	chr2:183580906-183580956	Hela-S3	cervix:	n/a
32	chr2:183580574-183580624	NH-A	brain:	n/a
33	chr2:183498282-183498332	HUVEC	blood vessel:	n/a
34	chr2:183658977-183659027	LNCaP	prostate:	n/a
35	chr2:183473411-183473461	AoSMC	blood vessel:	n/a
36	chr2:183580829-183580879	AG09319	gingival:	n/a
37	chr2:183580818-183580868	HIPEpiC	eye:	n/a
38	chr2:183580818-183580868	IMR90	lung:	fetal
39	chr2:183731407-183731457	HEEpiC	esophagus:	n/a
40	chr2:183580463-183580513	Hepatocyte	liver:	n/a
41	chr2:183584043-183584093	GM12892	blood:	n/a
42	chr2:183580694-183580744	HL-60	blood:	n/a
43	chr2:183658977-183659027	ovcar-3	ovarian:	n/a
44	chr2:183699153-183699203	AG04450	lung:	fetal
45	chr2:183731832-183731882	NB4	blood:	n/a
46	chr2:183719355-183719405	T-47D	breast:	n/a
47	chr2:183731563-183731613	BJ	skin:	n/a
48	chr2:183731599-183731649	GM12891	blood:	n/a
49	chr2:183658977-183659027	RPTEC	kidney:	n/a
50	chr2:183580523-183580573	AG09309	skin:	n/a

(count:229 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr2:183816568..183818121-chr2:183820543..183822285,2	K562	blood:
2	chr2:183561976..183564805-chr2:183566522..183568031,2	K562	blood:
3	chr2:183658306..183660291-chr2:183661982..183664789,2	K562	blood:
4	chr2:183786363..183790600-chr2:183794242..183796759,3	K562	blood:
5	chr2:183050662..183051405-chr2:183513747..183514396,3	MCF-7	breast:
6	chr2:183580461..183581050-chr9:132388456..132389164,2	Hela-S3	cervix:
7	chr2:183676835..183678660-chr2:183680847..183683198,2	K562	blood:
8	chr2:183808744..183810851-chr2:183812471..183814250,2	K562	blood:
9	chr2:183781828..183783867-chr2:183783906..183785691,2	MCF-7	breast:
10	chr2:183557913..183559489-chr2:183567582..183569465,2	K562	blood:
11	chr2:183587075..183588639-chr2:183597814..183600510,2	MCF-7	breast:
12	chr2:183484463..183486734-chr2:183489147..183491693,3	K562	blood:
13	chr2:183497857..183499568-chr2:183500564..183503369,2	K562	blood:
14	chr2:183648162..183650730-chr2:183663988..183666770,2	K562	blood:
15	chr2:183585145..183587372-chr2:183598804..183601047,2	K562	blood:
16	chr2:183706094..183709034-chr2:183715040..183717717,2	K562	blood:
17	chr2:183564408..183567308-chr2:183580527..183582877,2	K562	blood:
18	chr2:183561976..183564805-chr2:183566522..183568031,2	K562	blood:
19	chr2:183808744..183810851-chr2:183812471..183814250,2	K562	blood:
20	chr2:183546308..183548876-chr2:183579294..183581951,2	MCF-7	breast:
21	chr2:183691013..183692579-chr2:183710091..183711908,2	MCF-7	breast:
22	chr2:183783194..183785818-chr2:183787179..183789437,2	MCF-7	breast:
23	chr2:183758074..183761061-chr2:183762442..183764748,3	MCF-7	breast:
24	chr2:183765609..183768304-chr2:183794647..183796212,2	K562	blood:
25	chr2:183695751..183697908-chr2:183701079..183703543,2	K562	blood:
26	chr2:183485234..183486908-chr2:183488749..183490647,2	K562	blood:
27	chr2:183105157..183107059-chr2:183513716..183516271,10	MCF-7	breast:
28	chr2:183050932..183051609-chr2:183514883..183516080,4	MCF-7	breast:
29	chr2:183462276..183465034-chr2:183470042..183471619,2	K562	blood:
30	chr2:183816933..183819427-chr2:183831655..183834604,2	K562	blood:
31	chr2:183598562..183601239-chr2:183604490..183606088,2	K562	blood:
32	chr2:183775532..183777640-chr2:183990491..183993127,2	K562	blood:
33	chr2:183615250..183618246-chr2:183622533..183624342,2	K562	blood:
34	chr2:183659213..183661128-chr2:183664377..183666463,2	MCF-7	breast:
35	chr2:183598869..183601540-chr2:183602374..183605129,3	MCF-7	breast:
36	chr2:183600490..183602060-chr2:183603873..183605839,2	K562	blood:
37	chr2:183579526..183582519-chr2:183598356..183600848,2	K562	blood:
38	chr2:183826876..183828751-chr2:183831035..183834010,2	K562	blood:
39	chr2:183051017..183051535-chr2:183513719..183514634,2	K562	blood:
40	chr2:183666474..183669367-chr2:183675559..183677309,2	K562	blood:
41	chr2:183700483..183702944-chr2:183767110..183769629,2	K562	blood:
42	chr2:183568340..183570140-chr2:183571899..183573989,2	K562	blood:
43	chr2:183462276..183465034-chr2:183470042..183471619,2	K562	blood:
44	chr2:183664890..183667245-chr2:183673485..183675403,2	K562	blood:
45	chr2:183600490..183602060-chr2:183603873..183605839,2	K562	blood:
46	chr2:183706383..183709007-chr2:183718084..183719976,2	K562	blood:
47	chr2:183615854..183617746-chr2:183618708..183621163,2	K562	blood:
48	chr2:183628146..183628821-chr2:183844437..183845367,4	K562	blood:
49	chr2:183516388..183518623-chr2:183519704..183522732,3	K562	blood:
50	chr2:183666474..183669367-chr2:183675559..183677309,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDE1A-1	chr2:183536804-183536945	XLOC_002420
2	lnc-DNAJC10-2	chr2:183654087-183659706	NONHSAT075921
3	lnc-PDE1A-1	chr2:183536803-183536945	NONHSAT075909
4	lnc-PDE1A-1	chr2:183537302-183537749	NONHSAT075911
5	lnc-NCKAP1-2	chr2:183774745-183774992	NONHSAT075924
6	lnc-DNAJC10-3	chr2:183513193-183513418	NONHSAT075908
7	lnc-PDE1A-1	chr2:183537628-183537875	XLOC_002420
8	lnc-NCKAP1-2	chr2:183786808-183787397	NONHSAT075924
9	lnc-NCKAP1-2	chr2:183778648-183779176	NONHSAT075924
10	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
11	lnc-DUSP19-3	chr2:183652825-183653162	NONHSAT075920
12	lnc-NCKAP1-2	chr2:183786673-183786706	NONHSAT075924
13	lnc-NCKAP1-2	chr2:183780848-183780918	NONHSAT075924
14	lnc-FRZB-3	chr2:183821190-183821772	NONHSAT075930
15	lnc-DNAJC10-4	chr2:183783951-183784252	NONHSAT075925
16	lnc-DNAJC10-3	chr2:183510878-183510968	NONHSAT075908
17	lnc-PDE1A-1	chr2:183539150-183539242	NONHSAT075911
18	lnc-DNAJC10-5	chr2:183788072-183788310	NONHSAT075926
19	lnc-PDE1A-1	chr2:183537627-183537875	NONHSAT075909
20	lnc-DNAJC10-5	chr2:183784638-183787512	NONHSAT075926
21	lnc-NCKAP1-2	chr2:183780604-183780782	NONHSAT075924
22	lnc-PDE1A-1	chr2:183538117-183538135	XLOC_002420
23	lnc-FRZB-2	chr2:183800021-183800231	NONHSAT075929
24	lnc-FRZB-3	chr2:183818028-183818059	NONHSAT075930
25	lnc-FRZB-2	chr2:183799130-183799560	NONHSAT075929
26	lnc-PDE1A-1	chr2:183537303-183537749	XLOC_002420
27	lnc-PDE1A-1	chr2:183539151-183539242	XLOC_002420
28	lnc-DUSP19-4	chr2:183650679-183652638	NONHSAT075919
29	lnc-DNAJC10-4	chr2:183778179-183778332	NONHSAT075925
30	lnc-NCKAP1-2	chr2:183785780-183786620	NONHSAT075924

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NCKAP1	hsa-miR-142-3p	chr2:183789764-183789786
2	FRZB	hsa-miR-30b-5p	chr2:183699467-183699488
3	NCKAP1	hsa-miR-30a-5p	chr2:183790122-183790143
4	NCKAP1	hsa-miR-132-3p	chr2:183789619-183789640
5	FRZB	hsa-miR-30b-5p	chr2:183699473-183699467
6	NCKAP1	hsa-miR-132-3p	chr2:183790366-183790387
7	FRZB	hsa-miR-30b-5p	chr2:183699080-183699101
8	NCKAP1	hsa-miR-142-3p	chr2:183789625-183789644
9	NCKAP1	hsa-miR-132-3p	chr2:183789715-183789736

Variant related genes	Relation type
RPL31P15	TF binding region
ENSG00000212404	TF binding region
NCKAP1	TF binding region
DNAJC10	TF binding region
RNU6-1122P	TF binding region
FRZB	TF binding region
RPL31P15	CpG island
ENSG00000212404	CpG island
NCKAP1	CpG island
DNAJC10	CpG island
RNU6-1122P	CpG island
FRZB	CpG island
ENSG00000122545	chromatin interactions
ENSG00000221498	chromatin interactions
ENSG00000061676	chromatin interactions
ENSG00000142230	chromatin interactions
ENSG00000212404	chromatin interactions
ENSG00000232430	chromatin interactions
ENSG00000260742	chromatin interactions
ENSG00000077232	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000230658	chromatin interactions
ENSG00000181218	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000122550	chromatin interactions
ENSG00000138434	chromatin interactions
ENSG00000115252	chromatin interactions
ENSG00000148335	chromatin interactions
ENSG00000130749	chromatin interactions

Extended variants
information (count: 13244 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:13244 , 50 per page) page: 1 2 3 4 5 6 7 ... 265

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372494684	chr2:183442078-183442079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569633200	chr2:183442151-183442152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72892780	chr2:183442160-183442161	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs549049084	chr2:183442169-183442170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565655912	chr2:183442206-183442207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189473829	chr2:183442213-183442214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553949590	chr2:183442240-183442241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs570770459	chr2:183442312-183442313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73048367	chr2:183442361-183442362	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs532139930	chr2:183442393-183442394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191204373	chr2:183442396-183442397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6758080	chr2:183442443-183442444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs13423096	chr2:183442449-183442450	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs555794409	chr2:183442482-183442483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372793224	chr2:183442487-183442488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs184213982	chr2:183442518-183442519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs189525891	chr2:183442584-183442585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181134472	chr2:183442645-183442646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs533212497	chr2:183442658-183442659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528767393	chr2:183442659-183442660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543722140	chr2:183442687-183442688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186572146	chr2:183442713-183442714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6433980	chr2:183442717-183442718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112912141	chr2:183442719-183442720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71008231	chr2:183442720-183442721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs189065575	chr2:183442822-183442823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs146408010	chr2:183442892-183442893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181730041	chr2:183442931-183442932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373200096	chr2:183442945-183442946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534407046	chr2:183443013-183443014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139754462	chr2:183443030-183443031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143179207	chr2:183443061-183443062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186391027	chr2:183443133-183443134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7570144	chr2:183443136-183443137	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs369003085	chr2:183443153-183443154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs558493221	chr2:183443170-183443171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191145535	chr2:183443264-183443265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs184126029	chr2:183443321-183443322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76761827	chr2:183443342-183443343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572529112	chr2:183443375-183443376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541526372	chr2:183443377-183443378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558315326	chr2:183443424-183443425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs59060920	chr2:183443443-183443444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs112356951	chr2:183443507-183443508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs543270134	chr2:183443527-183443528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs556547588	chr2:183443543-183443544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563571883	chr2:183443600-183443601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573857972	chr2:183443683-183443684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72892790	chr2:183443743-183443744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs376352381	chr2:183443747-183443748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:5587 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183442000-183442400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:183442000-183442400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:183442400-183447000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:183443800-183444200	Enhancers	Fetal Intestine Small	intestine
5	chr2:183445400-183447000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr2:183445600-183446400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr2:183445600-183446800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr2:183445600-183447000	Enhancers	Osteobl	bone
9	chr2:183445800-183447000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:183446200-183446400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:183446400-183451000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr2:183446800-183451200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr2:183446800-183451800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr2:183447000-183447200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr2:183447000-183447400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr2:183447000-183451400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr2:183447000-183451800	Weak transcription	Osteobl	bone
18	chr2:183449200-183449400	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr2:183449200-183449600	Enhancers	Fetal Muscle Leg	muscle
20	chr2:183449200-183449600	Enhancers	Left Ventricle	heart
21	chr2:183449200-183449600	Enhancers	NHLF	lung
22	chr2:183449200-183449800	Enhancers	Fetal Heart	heart
23	chr2:183449600-183451600	Weak transcription	NHLF	lung
24	chr2:183449800-183452600	Weak transcription	Fetal Heart	heart
25	chr2:183451000-183451200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr2:183451000-183451400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:183451000-183451400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr2:183451000-183451400	Enhancers	Brain Angular Gyrus	brain
29	chr2:183451000-183451400	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr2:183451000-183452000	Enhancers	Brain Cingulate Gyrus	brain
31	chr2:183451000-183453000	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:183451000-183453200	Enhancers	HSMMtube	muscle
33	chr2:183451000-183453400	Enhancers	NHDF-Ad	bronchial
34	chr2:183451200-183451800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr2:183451200-183452200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:183451200-183453000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:183451200-183453000	Enhancers	HSMM	muscle
38	chr2:183451200-183453400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr2:183451400-183451600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:183451400-183451800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:183451400-183452000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:183451400-183452200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr2:183451400-183452400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr2:183451600-183452200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:183451600-183453200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr2:183451600-183453400	Enhancers	NHLF	lung
47	chr2:183451800-183452000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr2:183451800-183452000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr2:183451800-183452200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:183451800-183452400	Enhancers	Muscle Satellite Cultured Cells	--

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