Variant report

Variant	nsv1045312
Chromosome Location	chr12:1805856-1843202
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:450)
CpG islands
(count:122)
Chromatin interactive
region (count:44)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:1838167-1838407	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:1813364-1813804	K562	blood:	n/a	n/a
3	ARID3A	chr12:1842030-1842391	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:1820147-1820260	K562	blood:	n/a	n/a
5	ARID3A	chr12:1807816-1808131	K562	blood:	n/a	n/a
6	ATF1	chr12:1820930-1821300	K562	blood:	n/a	n/a
7	ATF1	chr12:1823340-1823526	K562	blood:	n/a	n/a
8	ATF1	chr12:1806570-1806724	K562	blood:	n/a	n/a
9	ATF3	chr12:1820877-1821253	K562	blood:	n/a	n/a
10	CBX3	chr12:1824583-1825011	K562	blood:	n/a	n/a
11	CBX3	chr12:1824624-1824909	K562	blood:	n/a	n/a
12	CCNT2	chr12:1823011-1823191	K562	blood:	n/a	n/a
13	CEBPB	chr12:1805997-1806329	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr12:1811209-1811516	A549	lung:	n/a	chr12:1811339-1811350
15	CEBPB	chr12:1825484-1825737	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:1811244-1811509	HepG2	liver:	n/a	chr12:1811339-1811350
17	CEBPB	chr12:1820965-1821184	K562	blood:	n/a	n/a
18	CEBPB	chr12:1814064-1814165	A549	lung:	n/a	n/a
19	CEBPB	chr12:1832956-1833145	K562	blood:	n/a	n/a
20	CEBPB	chr12:1820876-1821280	K562	blood:	n/a	n/a
21	CEBPB	chr12:1811201-1811478	IMR90	lung:	n/a	chr12:1811339-1811350
22	CEBPB	chr12:1813951-1814224	K562	blood:	n/a	chr12:1814059-1814072 chr12:1814059-1814072 chr12:1814059-1814072 chr12:1814059-1814070
23	CEBPB	chr12:1811189-1811592	A549	lung:	n/a	chr12:1811339-1811350
24	CEBPB	chr12:1820905-1821386	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:1815230-1816127	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr12:1820897-1821283	K562	blood:	n/a	n/a
27	CEBPB	chr12:1820927-1821265	A549	lung:	n/a	n/a
28	CEBPB	chr12:1806086-1806248	IMR90	lung:	n/a	n/a
29	CEBPB	chr12:1829781-1829954	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:1820922-1821327	IMR90	lung:	n/a	n/a
31	CEBPB	chr12:1806006-1806316	MCF-7	breast:	n/a	n/a
32	CEBPB	chr12:1815528-1815859	IMR90	lung:	n/a	n/a
33	CEBPB	chr12:1805989-1806314	HepG2	liver:	n/a	n/a
34	CEBPB	chr12:1820904-1821293	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr12:1811202-1811513	Hela-S3	cervix:	n/a	chr12:1811339-1811350
36	CEBPB	chr12:1820914-1821387	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:1811186-1811430	K562	blood:	n/a	chr12:1811339-1811350
38	CEBPD	chr12:1815678-1816109	K562	blood:	n/a	n/a
39	CTCF	chr12:1820000-1820150	A549	lung:	n/a	n/a
40	CTCF	chr12:1808080-1808230	BE2_C	brain:	n/a	n/a
41	CTCF	chr12:1808080-1808230	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr12:1820103-1820401	K562	blood:	n/a	n/a
43	CTCF	chr12:1808080-1808230	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr12:1820126-1820329	HepG2	liver:	n/a	n/a
45	CTCF	chr12:1820120-1820270	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr12:1820180-1820330	A549	lung:	n/a	n/a
47	CTCF	chr12:1820960-1821110	HCM	heart:	n/a	n/a
48	CTCF	chr12:1808100-1808250	Caco-2	colon:	n/a	n/a
49	CTCF	chr12:1808060-1808210	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr12:1808060-1808210	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1815334-1815384	HCM	heart:	n/a
2	chr12:1807305-1807355	HMEC	breast:	n/a
3	chr12:1815334-1815384	GM12892	blood:	n/a
4	chr12:1815334-1815384	ECC-1	luminal epithelium:	n/a
5	chr12:1807305-1807355	HCT-116	colon:	n/a
6	chr12:1807305-1807355	GM12878	blood:	n/a
7	chr12:1807305-1807355	HAEpiC	amniotic membrane:	n/a
8	chr12:1815334-1815384	AG10803	skin:	n/a
9	chr12:1815334-1815384	ovcar-3	ovarian:	n/a
10	chr12:1807305-1807355	GM06990	blood:	n/a
11	chr12:1807305-1807355	ProgFib	skin:	n/a
12	chr12:1807305-1807355	NHBE	bronchial:	n/a
13	chr12:1815334-1815384	CMK	blood:	n/a
14	chr12:1815334-1815384	PrEC	prostate:	n/a
15	chr12:1815334-1815384	AG04449	skin:	fetal
16	chr12:1807305-1807355	HCPEpiC	choroid plexus:	n/a
17	chr12:1807305-1807355	HRE	kidney:	n/a
18	chr12:1815334-1815384	SK-N-SH_RA	brain:	n/a
19	chr12:1807305-1807355	GM12892	blood:	n/a
20	chr12:1807305-1807355	SKMC	muscle:	n/a
21	chr12:1807305-1807355	Caco-2	colon:	n/a
22	chr12:1807305-1807355	RPTEC	kidney:	n/a
23	chr12:1815334-1815384	PANC-1	pancreas:	n/a
24	chr12:1815334-1815384	LNCaP	prostate:	n/a
25	chr12:1815334-1815384	ProgFib	skin:	n/a
26	chr12:1815334-1815384	Caco-2	colon:	n/a
27	chr12:1807305-1807355	NB4	blood:	n/a
28	chr12:1807305-1807355	HIPEpiC	eye:	n/a
29	chr12:1815334-1815384	HAEpiC	amniotic membrane:	n/a
30	chr12:1815334-1815384	HMEC	breast:	n/a
31	chr12:1815334-1815384	SK-N-MC	brain:	n/a
32	chr12:1807305-1807355	HCF	heart:	n/a
33	chr12:1815334-1815384	HRPEpiC	eye:	n/a
34	chr12:1807305-1807355	HEK293	kidney:	embryo
35	chr12:1807305-1807355	AoSMC	blood vessel:	n/a
36	chr12:1815334-1815384	NH-A	brain:	n/a
37	chr12:1807305-1807355	NH-A	brain:	n/a
38	chr12:1815334-1815384	RPTEC	kidney:	n/a
39	chr12:1807305-1807355	PrEC	prostate:	n/a
40	chr12:1815334-1815384	HRCEpiC	kidney:	n/a
41	chr12:1815334-1815384	SK-N-SH	brain:	n/a
42	chr12:1807305-1807355	BJ	skin:	n/a
43	chr12:1815334-1815384	AG09319	gingival:	n/a
44	chr12:1815334-1815384	HPAEpiC	pulmonary alveolar:	n/a
45	chr12:1807305-1807355	HEEpiC	esophagus:	n/a
46	chr12:1815334-1815384	HCF	heart:	n/a
47	chr12:1815334-1815384	Hepatocyte	liver:	n/a
48	chr12:1815334-1815384	AG09309	skin:	n/a
49	chr12:1815334-1815384	BE2_C	brain:	n/a
50	chr12:1807305-1807355	AG09319	gingival:	n/a

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1824311..1826936-chr12:1833466..1835089,2	K562	blood:
2	chr12:1805184..1807328-chr12:1869608..1872383,2	K562	blood:
3	chr12:1797812..1801808-chr12:1810068..1813967,7	MCF-7	breast:
4	chr12:1770854..1772922-chr12:1803554..1806296,3	MCF-7	breast:
5	chr12:1797706..1801661-chr12:1812450..1816186,4	MCF-7	breast:
6	chr12:1799601..1802514-chr12:1838626..1842574,3	K562	blood:
7	chr12:1798875..1801741-chr12:1813995..1816503,2	MCF-7	breast:
8	chr12:1798636..1800286-chr12:1827290..1830049,2	K562	blood:
9	chr12:1807973..1810676-chr12:1846571..1848723,2	K562	blood:
10	chr12:1814191..1816713-chr12:1818333..1820469,2	K562	blood:
11	chr12:1817233..1819242-chr12:1821456..1823051,3	K562	blood:
12	chr12:1817233..1819242-chr12:1821456..1823051,3	K562	blood:
13	chr12:1815063..1817215-chr12:1824872..1827970,3	K562	blood:
14	chr12:1769488..1776078-chr12:1798561..1806450,20	K562	blood:
15	chr12:1833771..1836345-chr12:1836866..1838536,2	K562	blood:
16	chr12:1815656..1816160-chr12:1876746..1877565,2	MCF-7	breast:
17	chr1:45986260..45988935-chr12:1830161..1832459,2	MCF-7	breast:
18	chr12:1798783..1800757-chr12:1820278..1821875,2	K562	blood:
19	chr12:1838787..1840977-chr12:1852855..1855148,3	K562	blood:
20	chr12:1800172..1801733-chr12:1832908..1834964,2	K562	blood:
21	chr12:1812993..1815717-chr12:1847079..1848811,2	K562	blood:
22	chr12:1807864..1808637-chr12:1900082..1900831,4	MCF-7	breast:
23	chr12:1801036..1802914-chr12:1804421..1806179,3	MCF-7	breast:
24	chr12:1807832..1811641-chr12:1812567..1815374,5	K562	blood:
25	chr12:1769759..1773174-chr12:1808605..1811319,4	K562	blood:
26	chr12:1805534..1808436-chr12:1826572..1828951,2	K562	blood:
27	chr12:1800176..1802514-chr12:1841146..1842876,2	MCF-7	breast:
28	chr12:1807832..1811641-chr12:1812567..1815374,5	K562	blood:
29	chr12:1817051..1819015-chr12:1820770..1822956,2	K562	blood:
30	chr12:1825414..1827008-chr12:1830876..1832417,2	K562	blood:
31	chr12:1771225..1773425-chr12:1825793..1828213,2	K562	blood:
32	chr12:1824311..1826936-chr12:1833466..1835089,2	K562	blood:
33	chr12:1815063..1817215-chr12:1824872..1827970,3	K562	blood:
34	chr12:1827102..1828667-chr12:1833731..1835866,2	K562	blood:
35	chr12:1815296..1817227-chr12:1871744..1873347,2	MCF-7	breast:
36	chr12:1827102..1828667-chr12:1833731..1835866,2	K562	blood:
37	chr12:1814191..1816713-chr12:1818333..1820469,2	K562	blood:
38	chr12:1814200..1816471-chr12:1849026..1851387,2	MCF-7	breast:
39	chr12:1833771..1836345-chr12:1836866..1838536,2	K562	blood:
40	chr12:1805073..1809008-chr12:1822212..1826429,4	K562	blood:
41	chr12:1817051..1819015-chr12:1820770..1822956,2	K562	blood:
42	chr12:1799438..1802227-chr12:1816513..1818304,2	MCF-7	breast:
43	chr12:1808402..1809980-chr12:1899022..1901826,2	MCF-7	breast:
44	chr12:1825414..1827008-chr12:1830876..1832417,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WNT5B-1	chr12:1812052-1812148	NONHSAT025412
2	lnc-CACNA2D4-2	chr12:1805791-1807210	NONHSAT025413
3	lnc-WNT5B-1	chr12:1839891-1840222	NONHSAT025412

No data

Variant related genes	Relation type
ENSG00000271500	TF binding region
ENSG00000271500	CpG island
ENSG00000006831	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000266043	chromatin interactions
ENSG00000271500	chromatin interactions

Extended variants
information (count: 1532 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1532 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552670312	chr12:1805859-1805860	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs570767924	chr12:1805964-1805965	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs117759791	chr12:1806008-1806009	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs553089058	chr12:1806024-1806025	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs568382402	chr12:1806041-1806042	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs16928652	chr12:1806056-1806057	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs75261770	chr12:1806063-1806064	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs575066915	chr12:1806077-1806078	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs189604780	chr12:1806079-1806080	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs7132033	chr12:1806096-1806097	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs572851791	chr12:1806102-1806103	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs140012958	chr12:1806164-1806165	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs563370737	chr12:1806186-1806187	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs530445708	chr12:1806238-1806239	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs542513961	chr12:1806274-1806275	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs563888371	chr12:1806285-1806286	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs531087283	chr12:1806287-1806288	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs143518644	chr12:1806340-1806341	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs146269978	chr12:1806432-1806433	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs139354049	chr12:1806448-1806449	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs539488432	chr12:1806452-1806453	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs373195914	chr12:1806475-1806476	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs547005486	chr12:1806496-1806497	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs568340091	chr12:1806501-1806502	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs530811552	chr12:1806519-1806520	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs557408401	chr12:1806544-1806545	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs568718883	chr12:1806589-1806590	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs539297140	chr12:1806645-1806646	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs557660042	chr12:1806646-1806647	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs549074986	chr12:1806666-1806667	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs572931114	chr12:1806684-1806685	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs78166310	chr12:1806685-1806686	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs149932151	chr12:1806706-1806707	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs573645852	chr12:1806712-1806713	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs144980060	chr12:1806720-1806721	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs563925436	chr12:1806749-1806750	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs536642542	chr12:1806769-1806770	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs149063998	chr12:1806791-1806792	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs554992557	chr12:1806793-1806794	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs546416367	chr12:1806857-1806858	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs564506683	chr12:1806869-1806870	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs575033349	chr12:1806916-1806917	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs142101018	chr12:1806936-1806937	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs554645140	chr12:1806963-1806964	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs573915687	chr12:1807005-1807006	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs151151398	chr12:1807042-1807043	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs535786352	chr12:1807093-1807094	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs561759570	chr12:1807113-1807114	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs561385515	chr12:1807116-1807117	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs550560894	chr12:1807121-1807122	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glaucoma	21310917	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Squamous cell cancer	19607727	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Mental retardation	17847001	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ovarian cancer	20844748	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21509527	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	21720365	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:1117 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1801000-1815800	Weak transcription	Esophagus	oesophagus
2	chr12:1801000-1815800	Weak transcription	Gastric	stomach
3	chr12:1801200-1807200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr12:1801400-1806400	Weak transcription	Fetal Lung	lung
5	chr12:1801400-1806600	Weak transcription	Aorta	Aorta
6	chr12:1801600-1806000	Weak transcription	Colon Smooth Muscle	Colon
7	chr12:1801600-1806600	Weak transcription	Fetal Brain Male	brain
8	chr12:1801600-1807600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr12:1801600-1814200	Weak transcription	HSMM	muscle
10	chr12:1801600-1815200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:1801600-1823400	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr12:1801600-1827800	Weak transcription	Rectal Smooth Muscle	rectum
13	chr12:1801800-1806000	Weak transcription	Primary T cells from cord blood	blood
14	chr12:1801800-1807800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:1801800-1808200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr12:1801800-1811400	Weak transcription	NH-A	brain
17	chr12:1801800-1813400	Weak transcription	A549	lung
18	chr12:1801800-1823800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr12:1801800-1828200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr12:1801800-1830800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr12:1802200-1806000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr12:1802200-1806400	Weak transcription	Right Ventricle	heart
23	chr12:1802200-1806600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
24	chr12:1802200-1806600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr12:1802200-1806600	Weak transcription	Fetal Brain Female	brain
26	chr12:1802200-1807800	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr12:1802200-1815000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr12:1802200-1815000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr12:1802200-1815000	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr12:1802200-1815400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr12:1802200-1815800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr12:1802200-1822800	Weak transcription	Thymus	Thymus
33	chr12:1802400-1806000	Weak transcription	Fetal Stomach	stomach
34	chr12:1802400-1808800	Weak transcription	HUVEC	blood vessel
35	chr12:1802400-1811800	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr12:1802400-1815000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:1802400-1822800	Weak transcription	Fetal Thymus	thymus
38	chr12:1802400-1823000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr12:1802400-1824600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr12:1802400-1841200	Weak transcription	HMEC	breast
41	chr12:1802600-1806200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr12:1802600-1808000	Enhancers	Adipose Nuclei	Adipose
43	chr12:1802800-1807200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr12:1803000-1813400	Weak transcription	Primary B cells from cord blood	blood
45	chr12:1803200-1815800	Weak transcription	Primary B cells from peripheral blood	blood
46	chr12:1803600-1808400	Enhancers	Brain Hippocampus Middle	brain
47	chr12:1803600-1808400	Enhancers	HepG2	liver
48	chr12:1803800-1812400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr12:1804000-1806800	Enhancers	Primary hematopoietic stem cells	blood
50	chr12:1804200-1806000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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