Variant report

Variant	nsv875486
Chromosome Location	chr2:184016627-184095979
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:455)
CpG islands
(count:122)
Chromatin interactive
region (count:41)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:184060870-184061220	K562	blood:	n/a	n/a
2	ARID3A	chr2:184089745-184089757	K562	blood:	n/a	n/a
3	ARID3A	chr2:184091759-184091794	K562	blood:	n/a	n/a
4	ARID3A	chr2:184021991-184022497	K562	blood:	n/a	n/a
5	ARID3A	chr2:184054026-184054043	K562	blood:	n/a	n/a
6	ARID3A	chr2:184055323-184055341	K562	blood:	n/a	n/a
7	ATF1	chr2:184060724-184061238	K562	blood:	n/a	n/a
8	ATF1	chr2:184058453-184058776	K562	blood:	n/a	n/a
9	ATF1	chr2:184019613-184019907	K562	blood:	n/a	n/a
10	ATF1	chr2:184080692-184081046	K562	blood:	n/a	n/a
11	BACH1	chr2:184092795-184092808	K562	blood:	n/a	n/a
12	BATF	chr2:184079498-184079825	GM12878	blood:	n/a	chr2:184079644-184079654 chr2:184079648-184079658 chr2:184079571-184079580
13	BATF	chr2:184079355-184079781	GM12878	blood:	n/a	chr2:184079644-184079654 chr2:184079648-184079658 chr2:184079571-184079580
14	BCL11A	chr2:184078568-184078977	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:184079428-184079857	GM12878	blood:	n/a	chr2:184079647-184079656 chr2:184079646-184079655
16	BHLHE40	chr2:184078784-184079243	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:184079511-184079801	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:184022092-184022187	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:184060834-184061270	K562	blood:	n/a	n/a
20	BHLHE40	chr2:184080582-184080992	K562	blood:	n/a	n/a
21	CBX3	chr2:184060664-184061237	K562	blood:	n/a	n/a
22	CCNT2	chr2:184060821-184061212	K562	blood:	n/a	n/a
23	CEBPB	chr2:184033954-184034306	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:184033996-184034254	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:184050338-184050394	HepG2	liver:	n/a	n/a
26	CEBPB	chr2:184033942-184034289	A549	lung:	n/a	n/a
27	CEBPB	chr2:184033979-184034281	K562	blood:	n/a	n/a
28	CEBPB	chr2:184089521-184089724	HepG2	liver:	n/a	chr2:184089656-184089667 chr2:184089579-184089590 chr2:184089656-184089669 chr2:184089578-184089589
29	CEBPB	chr2:184033934-184034249	K562	blood:	n/a	n/a
30	CEBPB	chr2:184081441-184081635	HepG2	liver:	n/a	chr2:184081507-184081518
31	CEBPB	chr2:184028965-184029346	K562	blood:	n/a	n/a
32	CEBPB	chr2:184033982-184034275	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:184029048-184029311	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr2:184033959-184034330	MCF-7	breast:	n/a	n/a
35	CEBPB	chr2:184074194-184074490	H1-hESC	embryonic stem cell:	n/a	chr2:184074360-184074371
36	CEBPB	chr2:184017127-184017340	HepG2	liver:	n/a	chr2:184017193-184017204
37	CEBPB	chr2:184061790-184062158	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:184028991-184029389	K562	blood:	n/a	n/a
39	CEBPB	chr2:184027122-184027416	IMR90	lung:	n/a	n/a
40	CEBPB	chr2:184089472-184089640	H1-hESC	embryonic stem cell:	n/a	chr2:184089579-184089590 chr2:184089578-184089589
41	CEBPB	chr2:184074301-184074801	HepG2	liver:	n/a	chr2:184074652-184074665 chr2:184074360-184074371 chr2:184074654-184074665 chr2:184074721-184074734 chr2:184074654-184074665 chr2:184074721-184074732 chr2:184074721-184074734 chr2:184074721-184074732 chr2:184074652-184074665
42	CEBPB	chr2:184089438-184089726	K562	blood:	n/a	chr2:184089656-184089667 chr2:184089579-184089590 chr2:184089656-184089669 chr2:184089578-184089589
43	CEBPB	chr2:184060657-184061284	K562	blood:	n/a	n/a
44	CEBPB	chr2:184033955-184034276	A549	lung:	n/a	n/a
45	CHD1	chr2:184079334-184079566	GM12878	blood:	n/a	n/a
46	CHD2	chr2:184037242-184037331	K562	blood:	n/a	n/a
47	CHD2	chr2:184019622-184019875	K562	blood:	n/a	n/a
48	CTCF	chr2:184057826-184058023	K562	blood:	n/a	n/a
49	CTCF	chr2:184038900-184039050	AG04450	lung:	n/a	chr2:184038970-184038988 chr2:184038965-184038986 chr2:184038972-184038985
50	CTCF	chr2:184037341-184037511	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:184069151-184069201	NHDF-neo	bronchial:	n/a
2	chr2:184069151-184069201	PrEC	prostate:	n/a
3	chr2:184069151-184069201	A549	lung:	n/a
4	chr2:184069151-184069201	HCF	heart:	n/a
5	chr2:184050946-184050996	HCF	heart:	n/a
6	chr2:184050946-184050996	NT2-D1	testis:	n/a
7	chr2:184069151-184069201	LNCaP	prostate:	n/a
8	chr2:184050946-184050996	IMR90	lung:	fetal
9	chr2:184069151-184069201	ECC-1	luminal epithelium:	n/a
10	chr2:184050946-184050996	SKMC	muscle:	n/a
11	chr2:184069151-184069201	RPTEC	kidney:	n/a
12	chr2:184050946-184050996	BJ	skin:	n/a
13	chr2:184050946-184050996	A549	lung:	n/a
14	chr2:184069151-184069201	MCF10A-Er-Src	breast:	n/a
15	chr2:184050946-184050996	BE2_C	brain:	n/a
16	chr2:184050946-184050996	AG10803	skin:	n/a
17	chr2:184069151-184069201	HL-60	blood:	n/a
18	chr2:184050946-184050996	GM06990	blood:	n/a
19	chr2:184050946-184050996	T-47D	breast:	n/a
20	chr2:184050946-184050996	HCT-116	colon:	n/a
21	chr2:184069151-184069201	PANC-1	pancreas:	n/a
22	chr2:184069151-184069201	K562	blood:	n/a
23	chr2:184050946-184050996	HEEpiC	esophagus:	n/a
24	chr2:184050946-184050996	RPTEC	kidney:	n/a
25	chr2:184050946-184050996	HRE	kidney:	n/a
26	chr2:184069151-184069201	HEEpiC	esophagus:	n/a
27	chr2:184069151-184069201	H1-hESC	embryonic stem cell:	embryo
28	chr2:184069151-184069201	NHBE	bronchial:	n/a
29	chr2:184050946-184050996	PFSK-1	brain:	n/a
30	chr2:184069151-184069201	GM12878	blood:	n/a
31	chr2:184069151-184069201	Caco-2	colon:	n/a
32	chr2:184069151-184069201	HRCEpiC	kidney:	n/a
33	chr2:184050946-184050996	K562	blood:	n/a
34	chr2:184069151-184069201	Hela-S3	cervix:	n/a
35	chr2:184069151-184069201	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:184069151-184069201	HEK293	kidney:	embryo
37	chr2:184069151-184069201	SK-N-MC	brain:	n/a
38	chr2:184069151-184069201	SKMC	muscle:	n/a
39	chr2:184050946-184050996	GM12891	blood:	n/a
40	chr2:184069151-184069201	AG10803	skin:	n/a
41	chr2:184069151-184069201	AG09309	skin:	n/a
42	chr2:184050946-184050996	LNCaP	prostate:	n/a
43	chr2:184050946-184050996	SK-N-MC	brain:	n/a
44	chr2:184069151-184069201	ovcar-3	ovarian:	n/a
45	chr2:184069151-184069201	Jurkat	blood:	n/a
46	chr2:184050946-184050996	NHDF-neo	bronchial:	n/a
47	chr2:184050946-184050996	NHBE	bronchial:	n/a
48	chr2:184050946-184050996	U87	brain:	n/a
49	chr2:184050946-184050996	CMK	blood:	n/a
50	chr2:184069151-184069201	NT2-D1	testis:	n/a

(count:41 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:184022891..184025672-chr2:184035459..184037994,2	K562	blood:
2	chr2:184090996..184094038-chr2:184094574..184096759,3	K562	blood:
3	chr2:184080700..184082212-chr2:184094955..184097317,2	K562	blood:
4	chr2:184081982..184083602-chr2:184085454..184088398,2	K562	blood:
5	chr2:184080634..184082480-chr2:184083427..184085243,2	K562	blood:
6	chr2:184095112..184100375-chr2:184102861..184106958,5	K562	blood:
7	chr2:184060293..184062928-chr2:184065628..184067485,2	K562	blood:
8	chr2:184045304..184046832-chr2:184050150..184052300,2	K562	blood:
9	chr2:184042932..184045706-chr2:184045938..184048137,2	K562	blood:
10	chr2:184064563..184067278-chr2:184068262..184071628,3	K562	blood:
11	chr2:183998810..184000982-chr2:184027517..184029612,2	K562	blood:
12	chr2:184064563..184067278-chr2:184068262..184071628,3	K562	blood:
13	chr2:183988386..183990737-chr2:184027696..184029728,3	K562	blood:
14	chr2:184015358..184018990-chr2:184020660..184023172,3	MCF-7	breast:
15	chr2:184042932..184045706-chr2:184045938..184048137,2	K562	blood:
16	chr2:184081982..184083602-chr2:184085454..184088398,2	K562	blood:
17	chr2:184095112..184100079-chr2:184103320..184106958,5	K562	blood:
18	chr2:184092172..184094879-chr2:184097017..184099581,2	K562	blood:
19	chr2:184012662..184015271-chr2:184018990..184021565,2	K562	blood:
20	chr2:184049106..184051291-chr2:184055965..184058710,2	MCF-7	breast:
21	chr2:183987752..183989755-chr2:184035957..184037928,2	MCF-7	breast:
22	chr2:184019137..184020799-chr2:184022946..184025022,2	K562	blood:
23	chr12:103034147..103036030-chr2:184031138..184032660,2	MCF-7	breast:
24	chr2:184020158..184022833-chr2:184025922..184028556,2	K562	blood:
25	chr2:184018781..184021679-chr2:184025666..184028556,3	K562	blood:
26	chr2:184070904..184072846-chr2:184078576..184081575,2	MCF-7	breast:
27	chr2:184091272..184093435-chr2:184098756..184100523,2	MCF-7	breast:
28	chr2:184015358..184018990-chr2:184020660..184023172,3	MCF-7	breast:
29	chr2:184018781..184021679-chr2:184025666..184028556,3	K562	blood:
30	chr2:183988386..183991369-chr2:184028228..184030386,3	K562	blood:
31	chr2:184020158..184022833-chr2:184025922..184028556,2	K562	blood:
32	chr2:184015191..184017995-chr2:184020754..184023549,2	K562	blood:
33	chr2:184015191..184017995-chr2:184020754..184023549,2	K562	blood:
34	chr2:184022891..184025672-chr2:184035459..184037994,2	K562	blood:
35	chr2:184060293..184062928-chr2:184065628..184067485,2	K562	blood:
36	chr2:184080700..184082212-chr2:184094955..184097317,2	K562	blood:
37	chr2:184019137..184020799-chr2:184022946..184025022,2	K562	blood:
38	chr2:184045304..184046832-chr2:184050150..184052300,2	K562	blood:
39	chr2:184090996..184094038-chr2:184094574..184096759,3	K562	blood:
40	chr2:184049106..184051291-chr2:184055965..184058710,2	MCF-7	breast:
41	chr2:184080634..184082480-chr2:184083427..184085243,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUP35-2	chr2:184077371-184078450	NONHSAT075940
2	lnc-NUP35-2	chr2:184043954-184044121	NONHSAT075940
3	lnc-NUP35-2	chr2:184073977-184075193	NONHSAT075944
4	lnc-NUP35-2	chr2:184075920-184076185	FPKM1_group_17816_transcript_3
5	lnc-NUP35-2	chr2:184060294-184061180	NONHSAT075940
6	lnc-NUP35-2	chr2:184059699-184060261	NONHSAT075940
7	lnc-NUP35-2	chr2:184079047-184080128	ENSG00000272800.1
8	lnc-NCKAP1-3	chr2:184044986-184046018	NONHSAT075943
9	lnc-NUP35-2	chr2:184079117-184080015	NONHSAT075940
10	lnc-NUP35-2	chr2:184073977-184075193	FPKM1_group_17816_transcript_3
11	lnc-NUP35-2	chr2:184075920-184078579	NONHSAT075944

No data

Variant related genes	Relation type
ENSG00000272800	TF binding region
ENSG00000272800	CpG island
ENSG00000272800	chromatin interactions
ENSG00000163002	chromatin interactions

Extended variants
information (count: 3221 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:3221 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3762477	chr2:184016627-184016628	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183218464	chr2:184016636-184016637	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs4666613	chr2:184016667-184016668	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs369630288	chr2:184016671-184016672	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs568480967	chr2:184016673-184016674	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs563002519	chr2:184016679-184016680	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs537004426	chr2:184016737-184016738	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs16824056	chr2:184016791-184016792	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs543008351	chr2:184016793-184016794	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs540628543	chr2:184016796-184016797	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs568142742	chr2:184016814-184016815	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs141396036	chr2:184016839-184016840	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs533914342	chr2:184016851-184016852	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs71008268	chr2:184016864-184016865	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs189161308	chr2:184016871-184016872	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs541044481	chr2:184016879-184016880	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs58605274	chr2:184016883-184016884	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs56941373	chr2:184016884-184016885	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs4666615	chr2:184016917-184016918	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs182661783	chr2:184016921-184016922	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs11904642	chr2:184016924-184016925	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs111380667	chr2:184016937-184016938	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs34186572	chr2:184016938-184016939	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs397697546	chr2:184016939-184016940	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs542119909	chr2:184016947-184016948	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs555681125	chr2:184016964-184016965	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs572106761	chr2:184016975-184016976	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs11894093	chr2:184017000-184017001	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs554649481	chr2:184017001-184017002	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs187668327	chr2:184017009-184017010	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs532842230	chr2:184017109-184017110	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs13420955	chr2:184017110-184017111	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs369913932	chr2:184017121-184017122	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs4666616	chr2:184017124-184017125	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs548503602	chr2:184017154-184017155	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs79741249	chr2:184017179-184017180	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs527724557	chr2:184017180-184017181	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs563187527	chr2:184017210-184017211	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs547425526	chr2:184017218-184017219	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs191624747	chr2:184017268-184017269	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs539515476	chr2:184017277-184017278	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs570769506	chr2:184017397-184017398	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs556347735	chr2:184017398-184017399	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs58965964	chr2:184017434-184017435	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569897090	chr2:184017442-184017443	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535629800	chr2:184017460-184017461	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555740357	chr2:184017466-184017467	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184203946	chr2:184017483-184017484	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs55764044	chr2:184017497-184017498	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs187486620	chr2:184017504-184017505	ZNF genes & repeats Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

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	22037309	CNVD

Chromatin state (count:1327 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183990000-184024400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr2:183990000-184050000	Weak transcription	Aorta	Aorta
3	chr2:183990200-184018800	Weak transcription	Placenta	Placenta
4	chr2:183990200-184036400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:183990600-184028600	Weak transcription	Colonic Mucosa	Colon
6	chr2:183990800-184025800	Weak transcription	Fetal Kidney	kidney
7	chr2:183990800-184031000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr2:183991000-184018400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:183991000-184018400	Weak transcription	Gastric	stomach
10	chr2:183991000-184028600	Weak transcription	Right Ventricle	heart
11	chr2:183991000-184030400	Weak transcription	Brain Hippocampus Middle	brain
12	chr2:183991000-184048400	Weak transcription	Brain Angular Gyrus	brain
13	chr2:183991000-184053400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr2:183991000-184055400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr2:183991200-184035400	Weak transcription	Fetal Brain Male	brain
16	chr2:183991400-184034000	Weak transcription	NHLF	lung
17	chr2:183991400-184049600	Weak transcription	NHDF-Ad	bronchial
18	chr2:183991600-184029600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr2:183992400-184047600	Weak transcription	Hela-S3	cervix
20	chr2:183995200-184026000	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr2:183996000-184026400	Weak transcription	Rectal Smooth Muscle	rectum
22	chr2:183996400-184018400	Weak transcription	Lung	lung
23	chr2:183996400-184025800	Weak transcription	Stomach Smooth Muscle	stomach
24	chr2:184002200-184017600	Weak transcription	Pancreas	Pancrea
25	chr2:184005000-184025200	Weak transcription	Left Ventricle	heart
26	chr2:184009000-184018200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr2:184009000-184018200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr2:184009000-184023000	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr2:184009000-184023600	Weak transcription	HMEC	breast
30	chr2:184009000-184028600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr2:184009000-184043800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:184009200-184017000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr2:184009200-184017000	Weak transcription	Fetal Intestine Large	intestine
34	chr2:184009200-184017000	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr2:184009200-184017000	Weak transcription	Thymus	Thymus
36	chr2:184009200-184017400	Weak transcription	Fetal Brain Female	brain
37	chr2:184009200-184017400	Weak transcription	Fetal Thymus	thymus
38	chr2:184009200-184018200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
39	chr2:184009200-184024200	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr2:184009200-184024200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr2:184009200-184025000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr2:184009200-184025200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr2:184009200-184025600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr2:184009200-184025800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
45	chr2:184009200-184028400	Weak transcription	Brain Anterior Caudate	brain
46	chr2:184009200-184034000	Weak transcription	Esophagus	oesophagus
47	chr2:184009200-184043600	Weak transcription	Psoas Muscle	Psoas
48	chr2:184009200-184048400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr2:184009400-184019600	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr2:184009400-184024200	Weak transcription	NH-A	brain

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