Variant report

Variant	nsv468964
Chromosome Location	chr12:1749905-1769930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:473)
CpG islands
(count:1039)
Chromatin interactive
region (count:40)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:2)

(count:473 , 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	chr12:1762133-1762250	K562	blood:	n/a	n/a
2	ARID3A	chr12:1761998-1762255	HepG2	liver:	n/a	n/a
3	BHLHE40	chr12:1769432-1769793	HepG2	liver:	n/a	n/a
4	BHLHE40	chr12:1766107-1766279	K562	blood:	n/a	n/a
5	BHLHE40	chr12:1755884-1756045	K562	blood:	n/a	n/a
6	BHLHE40	chr12:1769422-1769770	K562	blood:	n/a	n/a
7	BHLHE40	chr12:1762087-1762183	K562	blood:	n/a	n/a
8	BHLHE40	chr12:1751637-1752006	K562	blood:	n/a	chr12:1751802-1751811
9	BRCA1	chr12:1769221-1769902	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr12:1769416-1769767	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:1769438-1769826	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:1769454-1769750	A549	lung:	n/a	n/a
13	CEBPB	chr12:1769470-1769812	K562	blood:	n/a	n/a
14	CEBPB	chr12:1769449-1769802	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:1769531-1769672	HepG2	liver:	n/a	n/a
16	CEBPB	chr12:1754325-1754418	HepG2	liver:	n/a	n/a
17	CEBPB	chr12:1769299-1770103	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:1754187-1754499	IMR90	lung:	n/a	n/a
19	CEBPB	chr12:1769263-1770021	HCT-116	colon:	n/a	n/a
20	CEBPB	chr12:1769279-1769956	HCT-116	colon:	n/a	n/a
21	CHD2	chr12:1769382-1769692	HepG2	liver:	n/a	n/a
22	CHD2	chr12:1769322-1770028	Hela-S3	cervix:	n/a	n/a
23	CREB1	chr12:1769386-1769887	HepG2	liver:	n/a	n/a
24	CREB1	chr12:1769340-1769688	A549	lung:	n/a	n/a
25	CREB1	chr12:1769301-1769936	HepG2	liver:	n/a	n/a
26	CTCF	chr12:1762080-1762230	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr12:1762060-1762210	HVMF	connective:	n/a	n/a
28	CTCF	chr12:1762042-1762280	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:1762020-1762283	A549	lung:	n/a	n/a
30	CTCF	chr12:1762060-1762210	GM12872	blood:	n/a	n/a
31	CTCF	chr12:1766234-1766290	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:1762000-1762150	NHLF	lung:	n/a	n/a
33	CTCF	chr12:1756100-1756250	GM12867	blood:	n/a	n/a
34	CTCF	chr12:1762037-1762277	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:1761950-1762357	K562	blood:	n/a	n/a
36	CTCF	chr12:1762080-1762230	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr12:1762053-1762221	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr12:1762021-1762293	LNCaP	prostate:	n/a	n/a
39	CTCF	chr12:1762026-1762373	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr12:1762100-1762250	GM12868	blood:	n/a	n/a
41	CTCF	chr12:1761789-1762519	A549	lung:	n/a	n/a
42	CTCF	chr12:1762100-1762250	RPTEC	kidney:	n/a	n/a
43	CTCF	chr12:1762005-1762305	Medullo	brain:	n/a	n/a
44	CTCF	chr12:1769750-1769817	Lung_OC	lung:	n/a	n/a
45	CTCF	chr12:1762013-1762240	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr12:1762028-1762261	A549	lung:	n/a	n/a
47	CTCF	chr12:1762080-1762230	GM12867	blood:	n/a	n/a
48	CTCF	chr12:1762080-1762230	GM06990	blood:	n/a	n/a
49	CTCF	chr12:1754100-1754250	HAc	cerebellar:	n/a	n/a
50	CTCF	chr12:1761949-1762452	MCF-7	breast:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1752104-1752154	BE2_C	brain:	n/a
2	chr12:1754980-1755030	HRCEpiC	kidney:	n/a
3	chr12:1752104-1752154	BE2_C	brain:	n/a
4	chr12:1754980-1755030	HRCEpiC	kidney:	n/a
5	chr12:1759064-1759114	HRPEpiC	eye:	n/a
6	chr12:1753440-1753490	MCF10A-Er-Src	breast:	n/a
7	chr12:1754980-1755030	GM06990	blood:	n/a
8	chr12:1755322-1755372	GM12892	blood:	n/a
9	chr12:1751357-1751407	PFSK-1	brain:	n/a
10	chr12:1755322-1755372	GM19239	blood:	n/a
11	chr12:1755068-1755118	NHBE	bronchial:	n/a
12	chr12:1754980-1755030	SK-N-MC	brain:	n/a
13	chr12:1751897-1751947	U87	brain:	n/a
14	chr12:1753866-1753916	HL-60	blood:	n/a
15	chr12:1756074-1756124	K562	blood:	n/a
16	chr12:1755322-1755372	NHDF-neo	bronchial:	n/a
17	chr12:1759721-1759771	AG04450	lung:	fetal
18	chr12:1759721-1759771	NHDF-neo	bronchial:	n/a
19	chr12:1754156-1754206	CMK	blood:	n/a
20	chr12:1751357-1751407	U87	brain:	n/a
21	chr12:1755162-1755212	IMR90	lung:	fetal
22	chr12:1754156-1754206	U87	brain:	n/a
23	chr12:1754750-1754800	GM12892	blood:	n/a
24	chr12:1755322-1755372	BJ	skin:	n/a
25	chr12:1754980-1755030	HCPEpiC	choroid plexus:	n/a
26	chr12:1769824-1769874	Hela-S3	cervix:	n/a
27	chr12:1752104-1752154	HCPEpiC	choroid plexus:	n/a
28	chr12:1755162-1755212	SK-N-MC	brain:	n/a
29	chr12:1754750-1754800	SK-N-SH	brain:	n/a
30	chr12:1751357-1751407	NB4	blood:	n/a
31	chr12:1755162-1755212	HCT-116	colon:	n/a
32	chr12:1755162-1755212	ProgFib	skin:	n/a
33	chr12:1755162-1755212	NT2-D1	testis:	n/a
34	chr12:1755322-1755372	Jurkat	blood:	n/a
35	chr12:1751897-1751947	HPAEpiC	pulmonary alveolar:	n/a
36	chr12:1754750-1754800	ovcar-3	ovarian:	n/a
37	chr12:1754156-1754206	ovcar-3	ovarian:	n/a
38	chr12:1768513-1768563	AG10803	skin:	n/a
39	chr12:1751357-1751407	SK-N-MC	brain:	n/a
40	chr12:1754750-1754800	AG09309	skin:	n/a
41	chr12:1756074-1756124	HMEC	breast:	n/a
42	chr12:1753440-1753490	GM19239	blood:	n/a
43	chr12:1755322-1755372	GM12891	blood:	n/a
44	chr12:1755068-1755118	NHDF-neo	bronchial:	n/a
45	chr12:1759064-1759114	H1-hESC	embryonic stem cell:	embryo
46	chr12:1754980-1755030	GM12891	blood:	n/a
47	chr12:1754156-1754206	HCM	heart:	n/a
48	chr12:1759721-1759771	GM19239	blood:	n/a
49	chr12:1752104-1752154	HRPEpiC	eye:	n/a
50	chr12:1754156-1754206	AG10803	skin:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1768367..1774746-chr12:1797764..1801789,11	MCF-7	breast:
2	chr12:1760533..1762632-chr12:1798960..1801485,2	MCF-7	breast:
3	chr12:1758373..1760405-chr12:1760521..1762073,2	K562	blood:
4	chr12:1761202..1763486-chr14:90976670..90979042,2	MCF-7	breast:
5	chr12:1764396..1766319-chr12:1799382..1802362,3	MCF-7	breast:
6	chr12:1761722..1762668-chr12:1899936..1901006,8	MCF-7	breast:
7	chr12:1769374..1771394-chr12:1903241..1905339,2	K562	blood:
8	chr12:1769818..1772528-chr12:1789216..1791447,2	MCF-7	breast:
9	chr12:1760516..1766942-chr12:1799167..1803711,7	MCF-7	breast:
10	chr12:1769759..1773174-chr12:1808605..1811319,4	K562	blood:
11	chr12:1761434..1762152-chr12:1902846..1903644,2	K562	blood:
12	chr12:1762065..1762643-chr12:1900057..1900968,4	MCF-7	breast:
13	chr12:1761185..1762659-chr12:1899957..1901020,13	K562	blood:
14	chr12:1764971..1767607-chr12:1903787..1905417,2	MCF-7	breast:
15	chr12:1761655..1762203-chr12:1904881..1905529,2	MCF-7	breast:
16	chr12:1769631..1770598-chr12:130611123..130611927,2	Hela-S3	cervix:
17	chr12:1758373..1760405-chr12:1760521..1762073,2	K562	blood:
18	chr12:1757039..1760239-chr12:1798333..1801306,3	K562	blood:
19	chr12:1748743..1751681-chr12:1751691..1754305,2	MCF-7	breast:
20	chr12:1758528..1761484-chr12:1903323..1905403,2	K562	blood:
21	chr12:1713956..1716010-chr12:1769729..1772627,2	K562	blood:
22	chr12:1769849..1773599-chr12:1775643..1780093,7	K562	blood:
23	chr12:1760029..1761750-chr12:1899014..1900987,2	K562	blood:
24	chr12:1763598..1768100-chr12:1769091..1773201,7	K562	blood:
25	chr12:1769575..1772464-chr12:1879364..1881156,2	MCF-7	breast:
26	chr12:1714073..1716320-chr12:1769729..1772377,3	K562	blood:
27	chr12:1764668..1766758-chr12:1769528..1771633,2	K562	blood:
28	chr12:1750618..1752879-chr12:1756177..1759095,2	K562	blood:
29	chr12:1758821..1762858-chr12:1765486..1772233,6	K562	blood:
30	chr12:1762971..1767394-chr12:1768101..1772798,5	MCF-7	breast:
31	chr12:1769387..1773191-chr12:1797591..1801415,7	K562	blood:
32	chr12:1751543..1753813-chr12:1771357..1773090,2	K562	blood:
33	chr12:1753397..1755607-chr12:1757750..1759353,2	K562	blood:
34	chr12:1769488..1776078-chr12:1798561..1806450,20	K562	blood:
35	chr12:1727058..1729024-chr12:1769642..1771498,2	K562	blood:
36	chr12:1762177..1762977-chr12:2048944..2049844,2	K562	blood:
37	chr12:1745580..1751053-chr12:1752530..1755627,4	K562	blood:
38	chr12:1750618..1752879-chr12:1756177..1759095,2	K562	blood:
39	chr12:1764519..1766471-chr12:1793295..1795076,2	MCF-7	breast:
40	chr12:1758821..1761926-chr12:1767018..1769867,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXL14-2	chr12:1764009-1764268	XLOC_009974
2	lnc-FBXL14-2	chr12:1762424-1764268	XLOC_009974
3	lnc-FBXL14-2	chr12:1769127-1769166	XLOC_009974

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3649	chr12:1769482-1769500	MIMAT0018069

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	WNT5B	hsa-miR-185-5p	chr12:1755591-1755614
2	WNT5B	hsa-miR-185-5p	chr12:1755626-1755648

Variant related genes	Relation type
MIR3649	TF binding region
WNT5B	TF binding region
MIR3649	CpG island
WNT5B	CpG island
ENSG00000111186	chromatin interactions
ENSG00000006831	chromatin interactions
ENSG00000151062	chromatin interactions
ENSG00000266043	chromatin interactions
FAM120A	miRNA target sites

Extended variants
information (count: 875 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:875 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2270038	chr12:1749905-1749906	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74910030	chr12:1749909-1749910	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs11061890	chr12:1749912-1749913	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs530847859	chr12:1749945-1749946	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545663518	chr12:1749987-1749988	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564300821	chr12:1749995-1749996	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs71454834	chr12:1749998-1749999	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs2240507	chr12:1750047-1750048	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs374267489	chr12:1750061-1750062	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs546758249	chr12:1750062-1750063	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs11061891	chr12:1750069-1750070	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs528837596	chr12:1750093-1750094	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs550574747	chr12:1750095-1750096	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs570222125	chr12:1750185-1750186	Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs371438590	chr12:1750232-1750233	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192312772	chr12:1750252-1750253	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs557155977	chr12:1750270-1750271	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114787860	chr12:1750273-1750274	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs34250313	chr12:1750283-1750284	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377359545	chr12:1750285-1750286	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570748691	chr12:1750321-1750322	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534896145	chr12:1750322-1750323	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139516005	chr12:1750324-1750325	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs545545704	chr12:1750348-1750349	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs2240508	chr12:1750349-1750350	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs541822123	chr12:1750353-1750354	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563189727	chr12:1750396-1750397	Strong transcription Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557359675	chr12:1750429-1750430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs527334815	chr12:1750532-1750533	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs202211141	chr12:1750551-1750552	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs146187156	chr12:1750589-1750590	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs546166005	chr12:1750591-1750592	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564264104	chr12:1750596-1750597	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2240509	chr12:1750597-1750598	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs185494773	chr12:1750616-1750617	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542199498	chr12:1750679-1750680	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs111618399	chr12:1750690-1750691	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs561739871	chr12:1750697-1750698	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189167578	chr12:1750719-1750720	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550293669	chr12:1750732-1750733	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs562535107	chr12:1750739-1750740	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531110597	chr12:1750790-1750791	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs28969459	chr12:1750797-1750798	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs531266915	chr12:1750813-1750814	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs35381785	chr12:1750819-1750820	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192204106	chr12:1750826-1750827	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs184526422	chr12:1750886-1750887	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs546804616	chr12:1750925-1750926	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568445065	chr12:1750937-1750938	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs535971641	chr12:1750948-1750949	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	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
Pancreatic cancer	17952125	CNVD
Lung adenocarcinoma	21935476	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:784 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1739800-1753800	Weak transcription	Esophagus	oesophagus
2	chr12:1740600-1753400	Strong transcription	Osteobl	bone
3	chr12:1740600-1755000	Weak transcription	Spleen	Spleen
4	chr12:1740800-1751000	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr12:1740800-1753200	Weak transcription	NH-A	brain
6	chr12:1740800-1753600	Weak transcription	Placenta	Placenta
7	chr12:1740800-1757400	Weak transcription	GM12878-XiMat	blood
8	chr12:1741400-1752800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:1742000-1753400	Weak transcription	NHEK	skin
10	chr12:1743600-1759000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:1744000-1753000	Weak transcription	Colon Smooth Muscle	Colon
12	chr12:1744000-1753200	Weak transcription	Colonic Mucosa	Colon
13	chr12:1744200-1751600	Weak transcription	Duodenum Mucosa	Duodenum
14	chr12:1744200-1753400	Weak transcription	Adipose Nuclei	Adipose
15	chr12:1744400-1752000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr12:1744400-1753000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr12:1744400-1753200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr12:1744400-1753200	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr12:1744400-1759000	Weak transcription	Right Ventricle	heart
20	chr12:1744600-1753000	Weak transcription	Brain Cingulate Gyrus	brain
21	chr12:1744600-1753000	Weak transcription	Brain Substantia Nigra	brain
22	chr12:1744600-1758000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:1745000-1751400	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr12:1745000-1753200	Weak transcription	Brain Hippocampus Middle	brain
25	chr12:1745200-1750800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr12:1745200-1751400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:1745600-1753600	Weak transcription	Liver	Liver
28	chr12:1746200-1752000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr12:1746600-1758000	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr12:1747000-1750200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr12:1747400-1750400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:1747600-1752000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr12:1747800-1754600	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr12:1747800-1755800	Strong transcription	Primary neutrophils fromperipheralblood	blood
35	chr12:1747800-1756000	Weak transcription	K562	blood
36	chr12:1748000-1753400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:1748000-1753600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr12:1748200-1753400	Weak transcription	HSMM	muscle
39	chr12:1748400-1750000	Strong transcription	NHLF	lung
40	chr12:1748600-1750000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr12:1748600-1750400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr12:1748600-1750400	Enhancers	Brain Germinal Matrix	brain
43	chr12:1748600-1753000	Enhancers	Fetal Brain Male	brain
44	chr12:1748800-1750000	Enhancers	Pancreas	Pancrea
45	chr12:1748800-1753200	Weak transcription	Lung	lung
46	chr12:1749000-1750000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:1749000-1750200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr12:1749000-1750200	Strong transcription	Fetal Intestine Small	intestine
49	chr12:1749000-1750200	Strong transcription	Ovary	ovary
50	chr12:1749200-1750000	Strong transcription	Muscle Satellite Cultured Cells	--

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