Variant report

Variant	nsv1038425
Chromosome Location	chr12:1857052-1902302
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:906)
CpG islands
(count:244)
Chromatin interactive
region (count:83)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:906 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:1876897-1877213	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:1900339-1900587	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:1869596-1870519	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:1875286-1875672	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:1870054-1870261	K562	blood:	n/a	n/a
6	ARID3A	chr12:1879255-1879642	HepG2	liver:	n/a	n/a
7	ATF1	chr12:1869962-1870502	K562	blood:	n/a	n/a
8	ATF3	chr12:1856816-1857148	K562	blood:	n/a	n/a
9	BCL3	chr12:1879331-1879595	GM12878	blood:	n/a	n/a
10	BCL3	chr12:1879287-1879580	GM12878	blood:	n/a	n/a
11	BHLHE40	chr12:1899791-1900022	K562	blood:	n/a	chr12:1899838-1899847 chr12:1899832-1899853 chr12:1899836-1899849 chr12:1899838-1899847 chr12:1899837-1899846
12	BRCA1	chr12:1869802-1870204	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr12:1856699-1857264	K562	blood:	n/a	n/a
14	CBX3	chr12:1856692-1857139	HCT-116	colon:	n/a	n/a
15	CBX3	chr12:1869574-1870361	HCT-116	colon:	n/a	n/a
16	CBX3	chr12:1856668-1857180	HCT-116	colon:	n/a	n/a
17	CBX3	chr12:1856768-1857170	K562	blood:	n/a	n/a
18	CCNT2	chr12:1899920-1900205	K562	blood:	n/a	n/a
19	CEBPB	chr12:1869659-1870236	A549	lung:	n/a	chr12:1870000-1870011
20	CEBPB	chr12:1876343-1876522	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr12:1869890-1870174	HepG2	liver:	n/a	chr12:1870000-1870011
22	CEBPB	chr12:1869966-1870095	K562	blood:	n/a	chr12:1870000-1870011
23	CEBPB	chr12:1869834-1870205	A549	lung:	n/a	chr12:1870000-1870011
24	CEBPB	chr12:1886996-1887380	IMR90	lung:	n/a	n/a
25	CEBPB	chr12:1869873-1870195	IMR90	lung:	n/a	chr12:1870000-1870011
26	CEBPB	chr12:1869611-1870386	HCT-116	colon:	n/a	chr12:1870000-1870011
27	CEBPB	chr12:1887094-1887279	A549	lung:	n/a	n/a
28	CEBPB	chr12:1869917-1870195	HepG2	liver:	n/a	chr12:1870000-1870011
29	CEBPB	chr12:1879173-1879639	A549	lung:	n/a	n/a
30	CEBPB	chr12:1876776-1877325	MCF-7	breast:	n/a	chr12:1877042-1877053
31	CEBPB	chr12:1870595-1870851	HepG2	liver:	n/a	chr12:1870734-1870745
32	CEBPB	chr12:1876894-1877225	HepG2	liver:	n/a	chr12:1877042-1877053
33	CEBPB	chr12:1893249-1893427	K562	blood:	n/a	chr12:1893302-1893313
34	CEBPB	chr12:1876293-1876440	A549	lung:	n/a	n/a
35	CEBPB	chr12:1893136-1893471	IMR90	lung:	n/a	chr12:1893302-1893313
36	CEBPB	chr12:1869888-1870202	HepG2	liver:	n/a	chr12:1870000-1870011
37	CEBPB	chr12:1879296-1879577	MCF-7	breast:	n/a	n/a
38	CEBPB	chr12:1870593-1870918	A549	lung:	n/a	chr12:1870734-1870745
39	CEBPB	chr12:1876281-1876490	K562	blood:	n/a	n/a
40	CEBPB	chr12:1893137-1893443	HepG2	liver:	n/a	chr12:1893302-1893313
41	CEBPB	chr12:1876783-1877289	MCF-7	breast:	n/a	chr12:1877042-1877053
42	CEBPB	chr12:1869813-1870297	HepG2	liver:	n/a	chr12:1870000-1870011
43	CEBPB	chr12:1869850-1870184	A549	lung:	n/a	chr12:1870000-1870011
44	CEBPB	chr12:1859609-1859775	HepG2	liver:	n/a	n/a
45	CEBPB	chr12:1879271-1879594	IMR90	lung:	n/a	n/a
46	CEBPB	chr12:1869811-1870266	Hela-S3	cervix:	n/a	chr12:1870000-1870011
47	CEBPB	chr12:1869695-1870374	HCT-116	colon:	n/a	chr12:1870000-1870011
48	CEBPB	chr12:1869862-1870201	MCF-7	breast:	n/a	chr12:1870000-1870011
49	CEBPB	chr12:1869855-1870156	K562	blood:	n/a	chr12:1870000-1870011
50	CHD2	chr12:1895881-1895889	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1890922-1890972	NHBE	bronchial:	n/a
2	chr12:1896394-1896444	NH-A	brain:	n/a
3	chr12:1885861-1885911	BE2_C	brain:	n/a
4	chr12:1885861-1885911	AG04450	lung:	fetal
5	chr12:1885861-1885911	MCF-7	breast:	n/a
6	chr12:1890922-1890972	Caco-2	colon:	n/a
7	chr12:1896394-1896444	RPTEC	kidney:	n/a
8	chr12:1890922-1890972	K562	blood:	n/a
9	chr12:1901788-1901838	AG10803	skin:	n/a
10	chr12:1896394-1896444	BJ	skin:	n/a
11	chr12:1896394-1896444	HCT-116	colon:	n/a
12	chr12:1896394-1896444	AG10803	skin:	n/a
13	chr12:1890922-1890972	HUVEC	blood vessel:	n/a
14	chr12:1901788-1901838	GM19239	blood:	n/a
15	chr12:1885861-1885911	SAEC	small airway:	n/a
16	chr12:1896394-1896444	MCF-7	breast:	n/a
17	chr12:1896394-1896444	HPAEpiC	pulmonary alveolar:	n/a
18	chr12:1890922-1890972	SKMC	muscle:	n/a
19	chr12:1885861-1885911	HCM	heart:	n/a
20	chr12:1901788-1901838	GM12892	blood:	n/a
21	chr12:1901788-1901838	H1-hESC	embryonic stem cell:	embryo
22	chr12:1890922-1890972	NB4	blood:	n/a
23	chr12:1901788-1901838	SAEC	small airway:	n/a
24	chr12:1901788-1901838	HPAEpiC	pulmonary alveolar:	n/a
25	chr12:1896394-1896444	LNCaP	prostate:	n/a
26	chr12:1896394-1896444	PFSK-1	brain:	n/a
27	chr12:1885861-1885911	NT2-D1	testis:	n/a
28	chr12:1890922-1890972	AG04450	lung:	fetal
29	chr12:1890922-1890972	ProgFib	skin:	n/a
30	chr12:1890922-1890972	MCF10A-Er-Src	breast:	n/a
31	chr12:1901788-1901838	PANC-1	pancreas:	n/a
32	chr12:1885861-1885911	ovcar-3	ovarian:	n/a
33	chr12:1896394-1896444	GM12891	blood:	n/a
34	chr12:1885861-1885911	GM12892	blood:	n/a
35	chr12:1901788-1901838	SK-N-SH	brain:	n/a
36	chr12:1890922-1890972	Hela-S3	cervix:	n/a
37	chr12:1901788-1901838	SK-N-MC	brain:	n/a
38	chr12:1890922-1890972	Jurkat	blood:	n/a
39	chr12:1896394-1896444	SK-N-MC	brain:	n/a
40	chr12:1896394-1896444	HRE	kidney:	n/a
41	chr12:1901788-1901838	BE2_C	brain:	n/a
42	chr12:1885861-1885911	SK-N-SH	brain:	n/a
43	chr12:1885861-1885911	SKMC	muscle:	n/a
44	chr12:1885861-1885911	HepG2	liver:	n/a
45	chr12:1890922-1890972	NH-A	brain:	n/a
46	chr12:1896394-1896444	NT2-D1	testis:	n/a
47	chr12:1896394-1896444	SK-N-SH	brain:	n/a
48	chr12:1890922-1890972	NT2-D1	testis:	n/a
49	chr12:1896394-1896444	AG09309	skin:	n/a
50	chr12:1901788-1901838	PFSK-1	brain:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:1743763..1744406-chr12:1900002..1900715,3	K562	blood:
2	chr12:1867589..1870103-chr12:1873330..1875021,2	K562	blood:
3	chr12:1798163..1800510-chr12:1865299..1867613,2	K562	blood:
4	chr12:1799303..1801733-chr12:1901384..1903711,2	MCF-7	breast:
5	chr12:1806785..1809377-chr12:1875667..1878614,2	K562	blood:
6	chr12:1869685..1874044-chr12:1876530..1880194,4	K562	blood:
7	chr12:1867305..1870150-chr12:1874080..1875881,2	K562	blood:
8	chr12:1859249..1861989-chr12:1877875..1880136,2	MCF-7	breast:
9	chr12:1808402..1809980-chr12:1899022..1901826,2	MCF-7	breast:
10	chr12:1801029..1803898-chr12:1875286..1877234,3	MCF-7	breast:
11	chr12:1895293..1898168-chr12:1899496..1904929,5	MCF-7	breast:
12	chr12:1769289..1772614-chr12:1889825..1893235,5	K562	blood:
13	chr12:1890411..1894703-chr12:1895509..1898196,4	K562	blood:
14	chr12:1885828..1887529-chr12:1888844..1891201,2	K562	blood:
15	chr12:1884779..1887439-chr12:1888065..1890449,2	K562	blood:
16	chr12:1884663..1886181-chr12:1889838..1891641,2	MCF-7	breast:
17	chr12:1760029..1761750-chr12:1899014..1900987,2	K562	blood:
18	chr12:1856721..1858693-chr12:1863172..1864680,2	MCF-7	breast:
19	chr12:1805184..1807328-chr12:1869608..1872383,2	K562	blood:
20	chr12:1848455..1851151-chr12:1856944..1859382,3	K562	blood:
21	chr12:1807035..1807582-chr12:1899570..1900524,2	MCF-7	breast:
22	chr12:1892244..1894703-chr12:1895509..1898196,2	K562	blood:
23	chr12:1762065..1762643-chr12:1900057..1900968,4	MCF-7	breast:
24	chr12:1859249..1861989-chr12:1877875..1880136,2	MCF-7	breast:
25	chr12:1799392..1801611-chr12:1889513..1892415,2	MCF-7	breast:
26	chr12:1872563..1875477-chr12:1898217..1901063,2	MCF-7	breast:
27	chr12:1869879..1872809-chr12:1873786..1877350,6	MCF-7	breast:
28	chr12:1894451..1896976-chr12:1899245..1901715,2	K562	blood:
29	chr12:1875581..1877544-chr12:1893631..1897459,3	MCF-7	breast:
30	chr12:1856328..1858670-chr12:1861251..1864008,2	K562	blood:
31	chr12:1806568..1808285-chr12:1875506..1878614,3	K562	blood:
32	chr12:1877747..1879413-chr12:1888732..1890364,2	MCF-7	breast:
33	chr12:1892244..1894703-chr12:1895509..1898196,2	K562	blood:
34	chr12:1799342..1802388-chr12:1883886..1887202,3	MCF-7	breast:
35	chr12:1883679..1886349-chr12:1898971..1901942,2	MCF-7	breast:
36	chr12:1800200..1801967-chr12:1874547..1878145,4	MCF-7	breast:
37	chr12:1881087..1883067-chr12:1886344..1888819,2	K562	blood:
38	chr12:1799462..1802204-chr12:1898001..1899846,2	MCF-7	breast:
39	chr12:1896710..1899686-chr6:3019390..3022643,4	K562	blood:
40	chr12:1875185..1877560-chr12:1885723..1887474,2	MCF-7	breast:
41	chr12:1805846..1808126-chr12:1899606..1902092,2	MCF-7	breast:
42	chr12:1853793..1856029-chr12:1861433..1863477,2	MCF-7	breast:
43	chr12:1815656..1816160-chr12:1876746..1877565,2	MCF-7	breast:
44	chr12:1874559..1877368-chr12:12662625..12665193,2	MCF-7	breast:
45	chr12:1741431..1743986-chr12:1900425..1902270,2	MCF-7	breast:
46	chr12:1856721..1858693-chr12:1863172..1864680,2	MCF-7	breast:
47	chr12:1894451..1896976-chr12:1899245..1901715,2	K562	blood:
48	chr12:1889254..1891602-chr12:1898742..1901715,2	MCF-7	breast:
49	chr12:1800061..1801858-chr12:1877724..1879510,3	MCF-7	breast:
50	chr12:1725835..1728588-chr12:1894437..1896352,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CACNA2D4-1	chr12:1866397-1867177	NONHSAT025414
2	lnc-ADIPOR2-1	chr12:1863424-1863680	NONHSAT025411
3	lnc-ADIPOR2-1	chr12:1882008-1882090	NONHSAT025411

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	ADIPOR2	hsa-miR-124-3p	chr12:1897550-1897556
2	ADIPOR2	hsa-let-7b-5p	chr12:1895421-1895427
3	ADIPOR2	hsa-miR-124-3p	chr12:1895888-1895908

Variant related genes	Relation type
ADIPOR2	TF binding region
RPS4XP14	TF binding region
ADIPOR2	CpG island
RPS4XP14	CpG island
ENSG00000111186	chromatin interactions
ENSG00000266043	chromatin interactions
ENSG00000203593	chromatin interactions
ENSG00000151065	chromatin interactions
ENSG00000270346	chromatin interactions
ENSG00000271500	chromatin interactions
ENSG00000006831	chromatin interactions

Extended variants
information (count: 1777 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1777 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536923696	chr12:1857168-1857169	ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530173277	chr12:1857191-1857192	ZNF genes & repeats Weak transcription Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183780435	chr12:1857222-1857223	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145598098	chr12:1857233-1857234	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs377013052	chr12:1857258-1857259	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568811644	chr12:1857265-1857266	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558592729	chr12:1857274-1857275	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570694182	chr12:1857275-1857276	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs536055603	chr12:1857371-1857372	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534517443	chr12:1857375-1857376	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553175799	chr12:1857384-1857385	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12828599	chr12:1857387-1857388	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs10744551	chr12:1857421-1857422	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs6489327	chr12:1857432-1857433	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6489328	chr12:1857438-1857439	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs575327898	chr12:1857445-1857446	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138289316	chr12:1857446-1857447	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577427740	chr12:1857450-1857451	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373090709	chr12:1857453-1857454	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs12372053	chr12:1857454-1857455	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111738359	chr12:1857458-1857459	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576367431	chr12:1857461-1857462	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532351275	chr12:1857466-1857467	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs555237274	chr12:1857475-1857476	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148331003	chr12:1857476-1857477	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540785230	chr12:1857477-1857478	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376010884	chr12:1857478-1857479	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559138134	chr12:1857484-1857485	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11061964	chr12:1857488-1857489	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs11061965	chr12:1857496-1857497	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs534966418	chr12:1857498-1857499	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190643710	chr12:1857500-1857501	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182887932	chr12:1857501-1857502	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186821542	chr12:1857507-1857508	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557115965	chr12:1857508-1857509	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs386759486	chr12:1857513-1857514	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201751720	chr12:1857514-1857515	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4765841	chr12:1857515-1857516	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372886074	chr12:1857524-1857525	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184115648	chr12:1857526-1857527	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs572746910	chr12:1857532-1857533	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs541737056	chr12:1857539-1857540	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559602749	chr12:1857540-1857541	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562323401	chr12:1857550-1857551	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs187299071	chr12:1857557-1857558	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138301043	chr12:1857559-1857560	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530992767	chr12:1857560-1857561	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs12319781	chr12:1857564-1857565	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs185427801	chr12:1857571-1857572	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149639586	chr12:1857575-1857576	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1828 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1816200-1857800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr12:1816200-1866400	Weak transcription	Esophagus	oesophagus
3	chr12:1816200-1897400	Weak transcription	Aorta	Aorta
4	chr12:1823000-1866600	Weak transcription	Gastric	stomach
5	chr12:1824000-1866600	Weak transcription	HSMM	muscle
6	chr12:1826000-1885400	Weak transcription	NH-A	brain
7	chr12:1831400-1857800	Weak transcription	Lung	lung
8	chr12:1837000-1861600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr12:1845600-1885200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr12:1847600-1857800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr12:1847600-1863800	Weak transcription	Ovary	ovary
12	chr12:1847600-1885200	Weak transcription	Right Atrium	heart
13	chr12:1849800-1868400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr12:1849800-1868800	Weak transcription	Pancreas	Pancrea
15	chr12:1849800-1905600	Weak transcription	Small Intestine	intestine
16	chr12:1850000-1866600	Weak transcription	Fetal Lung	lung
17	chr12:1850200-1865800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr12:1850200-1885200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr12:1850400-1863400	Weak transcription	Fetal Stomach	stomach
20	chr12:1850400-1870400	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr12:1850400-1904800	Weak transcription	Fetal Kidney	kidney
22	chr12:1850800-1863400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr12:1850800-1863400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr12:1850800-1885200	Weak transcription	Right Ventricle	heart
25	chr12:1851000-1863400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:1851000-1866400	Weak transcription	NHLF	lung
27	chr12:1851200-1858000	Weak transcription	Osteobl	bone
28	chr12:1851400-1866600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr12:1851600-1858000	Weak transcription	Psoas Muscle	Psoas
30	chr12:1851600-1863400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:1851600-1866400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:1851800-1863400	Weak transcription	Thymus	Thymus
33	chr12:1851800-1863600	Weak transcription	Skeletal Muscle Female	skeletal muscle
34	chr12:1851800-1876600	Weak transcription	Stomach Mucosa	stomach
35	chr12:1854000-1858800	ZNF genes & repeats	GM12878-XiMat	blood
36	chr12:1854400-1864400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:1854600-1859200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr12:1854600-1863400	Weak transcription	Adipose Nuclei	Adipose
39	chr12:1854600-1863400	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr12:1854600-1870400	Weak transcription	HSMMtube	muscle
41	chr12:1854800-1858200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr12:1855200-1858200	Weak transcription	Brain Substantia Nigra	brain
43	chr12:1855200-1861800	Weak transcription	Brain Anterior Caudate	brain
44	chr12:1855600-1857400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
45	chr12:1855600-1858000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:1855600-1858600	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:1855600-1858600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr12:1855600-1863400	Weak transcription	Left Ventricle	heart
49	chr12:1855800-1857400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
50	chr12:1855800-1857400	ZNF genes & repeats	Primary T cells fromperipheralblood	blood

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