Variant report

Variant	nsv933450
Chromosome Location	chr12:1949712-1984604
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:131)
CpG islands
(count:977)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:131 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:1950924-1951113	K562	blood:	n/a	n/a
2	BHLHE40	chr12:1979460-1979468	K562	blood:	n/a	n/a
3	BHLHE40	chr12:1974549-1974700	K562	blood:	n/a	n/a
4	CEBPB	chr12:1960290-1960578	IMR90	lung:	n/a	n/a
5	CTCF	chr12:1960540-1960690	AG10803	skin:	n/a	n/a
6	CTCF	chr12:1962700-1962850	GM12872	blood:	n/a	chr12:1962840-1962848
7	CTCF	chr12:1980682-1980762	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr12:1966944-1966981	LNCaP	prostate:	n/a	n/a
9	CTCF	chr12:1980617-1980698	ProgFib	skin:	n/a	n/a
10	CTCF	chr12:1980225-1980843	GM19239	blood:	n/a	n/a
11	CTCF	chr12:1949740-1949890	HepG2	liver:	n/a	n/a
12	E2F4	chr12:1968881-1969065	MCF10A-Er-Src	breast:	n/a	n/a
13	E2F4	chr12:1958924-1959064	MCF10A-Er-Src	breast:	n/a	n/a
14	EBF1	chr12:1951715-1952118	GM12878	blood:	n/a	chr12:1951932-1951941 chr12:1951931-1951942 chr12:1951932-1951942 chr12:1951932-1951941 chr12:1951907-1951918
15	EBF1	chr12:1951818-1952056	GM12878	blood:	n/a	chr12:1951932-1951941 chr12:1951931-1951942 chr12:1951932-1951942 chr12:1951932-1951941 chr12:1951907-1951918
16	ELF1	chr12:1974521-1974807	HepG2	liver:	n/a	chr12:1974668-1974679 chr12:1974667-1974680 chr12:1974668-1974679
17	ELF1	chr12:1974459-1974841	K562	blood:	n/a	chr12:1974668-1974679 chr12:1974667-1974680 chr12:1974668-1974679
18	ELF1	chr12:1974497-1974834	HepG2	liver:	n/a	chr12:1974668-1974679 chr12:1974667-1974680 chr12:1974668-1974679
19	EP300	chr12:1979216-1979485	T-47D	breast:	n/a	n/a
20	FOS	chr12:1960240-1960731	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
21	FOS	chr12:1968778-1969070	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr12:1968777-1969073	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr12:1961505-1961544	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr12:1968763-1969077	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr12:1960260-1960690	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
26	FOS	chr12:1960227-1960683	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
27	FOS	chr12:1971920-1971943	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr12:1960364-1960660	HUVEC	blood vessel:	n/a	chr12:1960508-1960519
29	FOS	chr12:1960240-1960701	MCF10A-Er-Src	breast:	n/a	chr12:1960508-1960519
30	FOS	chr12:1968778-1969078	MCF10A-Er-Src	breast:	n/a	n/a
31	FOSL2	chr12:1960283-1960747	SK-N-SH	brain:	n/a	n/a
32	FOXA1	chr12:1971298-1971541	T-47D	breast:	n/a	n/a
33	FOXA1	chr12:1971224-1971579	T-47D	breast:	n/a	n/a
34	FOXA1	chr12:1968871-1969216	T-47D	breast:	n/a	n/a
35	FOXA1	chr12:1979174-1979614	T-47D	breast:	n/a	n/a
36	GATA2	chr12:1972860-1973198	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr12:1979187-1979630	T-47D	breast:	n/a	n/a
38	GATA3	chr12:1968697-1969101	MCF-7	breast:	n/a	chr12:1969041-1969049
39	GATA3	chr12:1948692-1949735	MCF-7	breast:	n/a	n/a
40	GATA3	chr12:1972819-1973121	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr12:1979269-1979600	T-47D	breast:	n/a	n/a
42	GATA3	chr12:1960335-1960780	SK-N-SH	brain:	n/a	n/a
43	JUN	chr12:1980723-1980931	H1-hESC	embryonic stem cell:	n/a	n/a
44	KAP1	chr12:1968804-1969161	U2OS	brain:	n/a	n/a
45	KAP1	chr12:1964381-1964816	HEK293	kidney:	n/a	n/a
46	MAX	chr12:1980261-1981013	NB4	blood:	n/a	chr12:1980846-1980856
47	MAX	chr12:1949655-1949994	NB4	blood:	n/a	chr12:1949810-1949820
48	MAX	chr12:1957941-1958303	NB4	blood:	n/a	n/a
49	MAX	chr12:1955748-1956842	NB4	blood:	n/a	n/a
50	MAX	chr12:1949638-1950124	HepG2	liver:	n/a	chr12:1949810-1949820

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1978889-1978939	AoSMC	blood vessel:	n/a
2	chr12:1978889-1978939	AoSMC	blood vessel:	n/a
3	chr12:1973237-1973287	PANC-1	pancreas:	n/a
4	chr12:1973340-1973390	HCT-116	colon:	n/a
5	chr12:1974168-1974218	AG10803	skin:	n/a
6	chr12:1973237-1973287	A549	lung:	n/a
7	chr12:1973208-1973258	LNCaP	prostate:	n/a
8	chr12:1974724-1974774	HCF	heart:	n/a
9	chr12:1973452-1973502	NB4	blood:	n/a
10	chr12:1952798-1952848	HAEpiC	amniotic membrane:	n/a
11	chr12:1974168-1974218	AG04450	lung:	fetal
12	chr12:1970170-1970220	HRPEpiC	eye:	n/a
13	chr12:1970170-1970220	GM19239	blood:	n/a
14	chr12:1974122-1974172	SKMC	muscle:	n/a
15	chr12:1970170-1970220	HMEC	breast:	n/a
16	chr12:1976671-1976721	BE2_C	brain:	n/a
17	chr12:1973340-1973390	Jurkat	blood:	n/a
18	chr12:1974814-1974864	HRCEpiC	kidney:	n/a
19	chr12:1952798-1952848	ProgFib	skin:	n/a
20	chr12:1974724-1974774	Hepatocyte	liver:	n/a
21	chr12:1963310-1963360	AG04450	lung:	fetal
22	chr12:1973367-1973417	NT2-D1	testis:	n/a
23	chr12:1978889-1978939	AG04449	skin:	fetal
24	chr12:1973237-1973287	BJ	skin:	n/a
25	chr12:1963310-1963360	SK-N-SH_RA	brain:	n/a
26	chr12:1964603-1964653	BJ	skin:	n/a
27	chr12:1963310-1963360	SK-N-MC	brain:	n/a
28	chr12:1976671-1976721	NT2-D1	testis:	n/a
29	chr12:1973452-1973502	SK-N-SH	brain:	n/a
30	chr12:1952798-1952848	PrEC	prostate:	n/a
31	chr12:1964603-1964653	MCF10A-Er-Src	breast:	n/a
32	chr12:1964603-1964653	NB4	blood:	n/a
33	chr12:1970170-1970220	ovcar-3	ovarian:	n/a
34	chr12:1973367-1973417	AG04449	skin:	fetal
35	chr12:1973340-1973390	SK-N-MC	brain:	n/a
36	chr12:1976671-1976721	SK-N-SH_RA	brain:	n/a
37	chr12:1963310-1963360	NHBE	bronchial:	n/a
38	chr12:1973452-1973502	Hela-S3	cervix:	n/a
39	chr12:1974724-1974774	AG10803	skin:	n/a
40	chr12:1973367-1973417	HEEpiC	esophagus:	n/a
41	chr12:1974122-1974172	SK-N-SH_RA	brain:	n/a
42	chr12:1973872-1973922	HepG2	liver:	n/a
43	chr12:1973237-1973287	AG09319	gingival:	n/a
44	chr12:1952798-1952848	AG04450	lung:	fetal
45	chr12:1973872-1973922	ovcar-3	ovarian:	n/a
46	chr12:1976671-1976721	T-47D	breast:	n/a
47	chr12:1964603-1964653	Hela-S3	cervix:	n/a
48	chr12:1964603-1964653	HMEC	breast:	n/a
49	chr12:1973340-1973390	HRPEpiC	eye:	n/a
50	chr12:1974168-1974218	SKMC	muscle:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:1951607..1953524-chr12:2057455..2059714,2	MCF-7	breast:
2	chr12:1952274..1954241-chr12:1954730..1957718,2	K562	blood:
3	chr12:1950359..1950994-chr12:2041053..2041904,3	MCF-7	breast:
4	chr12:1944160..1952960-chr12:2039965..2049915,22	MCF-7	breast:
5	chr12:1949517..1951136-chr12:2022065..2024789,2	MCF-7	breast:
6	chr12:1968515..1969333-chr12:2041106..2041850,2	MCF-7	breast:
7	chr12:1982062..1983660-chr12:1991935..1993547,2	MCF-7	breast:
8	chr12:1949995..1951546-chr12:1955088..1956789,2	MCF-7	breast:
9	chr12:1950335..1952773-chr12:1969860..1971374,2	MCF-7	breast:
10	chr12:1947643..1951345-chr12:1957413..1959557,3	MCF-7	breast:
11	chr12:1956703..1959604-chr12:1963408..1966102,2	MCF-7	breast:
12	chr12:1976877..1978383-chr12:1995618..1998420,2	MCF-7	breast:
13	chr12:1954206..1956342-chr12:2043639..2046868,3	MCF-7	breast:
14	chr12:1876884..1877711-chr12:1950746..1951257,2	MCF-7	breast:
15	chr12:1959456..1961016-chr12:1962388..1965205,2	MCF-7	breast:
16	chr12:1939207..1940397-chr12:1950388..1951271,5	MCF-7	breast:
17	chr12:1978767..1980595-chr12:2025590..2028373,2	MCF-7	breast:
18	chr12:1956703..1959604-chr12:1963408..1966102,2	MCF-7	breast:
19	chr12:1947774..1950374-chr12:1986873..1988503,2	MCF-7	breast:
20	chr12:1950359..1950994-chr12:2041053..2041904,2	MCF-7	breast:
21	chr12:1952274..1954241-chr12:1954730..1957718,2	K562	blood:
22	chr12:1962397..1965390-chr12:1965944..1968413,2	K562	blood:
23	chr12:1799987..1802012-chr12:1946925..1950411,3	MCF-7	breast:
24	chr12:1968515..1969082-chr12:2040995..2041606,2	MCF-7	breast:
25	chr12:1905374..1907142-chr12:1951674..1953593,2	MCF-7	breast:
26	chr12:1901985..1907754-chr12:1946580..1951659,8	MCF-7	breast:
27	chr12:1877224..1880546-chr12:1949279..1951143,3	MCF-7	breast:
28	chr12:1947643..1951345-chr12:1957413..1959557,3	MCF-7	breast:
29	chr12:1925102..1928805-chr12:1946979..1949915,3	MCF-7	breast:
30	chr12:1953795..1956547-chr12:1969421..1971021,2	MCF-7	breast:
31	chr12:1945038..1946828-chr12:1971867..1974133,2	K562	blood:
32	chr12:1910081..1912246-chr12:1949040..1950547,2	K562	blood:
33	chr12:1949995..1951546-chr12:1955088..1956789,2	MCF-7	breast:
34	chr12:1947284..1949728-chr12:2036486..2038838,2	MCF-7	breast:
35	chr12:1953795..1956547-chr12:1969421..1971021,2	MCF-7	breast:
36	chr12:1950335..1952773-chr12:1969860..1971374,2	MCF-7	breast:

No data

Variant related genes	Relation type
CACNA2D4	TF binding region
CACNA2D4	CpG island
ENSG00000235049	chromatin interactions
ENSG00000006831	chromatin interactions
ENSG00000256706	chromatin interactions
ENSG00000151062	chromatin interactions

Extended variants
information (count: 1347 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557370329	chr12:1949717-1949718	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs191637534	chr12:1949776-1949777	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs112913129	chr12:1949783-1949784	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs546096128	chr12:1949794-1949795	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs564347831	chr12:1949826-1949827	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs573156722	chr12:1949858-1949859	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs183421147	chr12:1949896-1949897	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs376597005	chr12:1949897-1949898	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs533220267	chr12:1949904-1949905	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs540468160	chr12:1949915-1949916	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs369000289	chr12:1949924-1949925	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs79821996	chr12:1949927-1949928	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs200977656	chr12:1949932-1949933	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs377756881	chr12:1949933-1949934	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs33972365	chr12:1949939-1949940	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs146752598	chr12:1949940-1949941	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs199688605	chr12:1949957-1949958	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs532757608	chr12:1949958-1949959	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs576179739	chr12:1949966-1949967	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs376350677	chr12:1949978-1949979	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs552472772	chr12:1949979-1949980	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs570838032	chr12:1950007-1950008	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs58188909	chr12:1950011-1950012	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs140208475	chr12:1950012-1950013	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs528741800	chr12:1950015-1950016	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs546829030	chr12:1950027-1950028	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs568555086	chr12:1950096-1950097	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs187641962	chr12:1950102-1950103	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs557143147	chr12:1950111-1950112	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs569257651	chr12:1950114-1950115	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs539872775	chr12:1950170-1950171	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs139284422	chr12:1950225-1950226	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs56764283	chr12:1950240-1950241	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs368690086	chr12:1950245-1950246	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs117572973	chr12:1950255-1950256	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs555604359	chr12:1950266-1950267	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs149426291	chr12:1950269-1950270	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs544310296	chr12:1950290-1950291	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs190957506	chr12:1950303-1950304	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs144854032	chr12:1950311-1950312	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs117856415	chr12:1950395-1950396	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs148185988	chr12:1950409-1950410	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs528805004	chr12:1950446-1950447	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs375671444	chr12:1950449-1950450	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs11835900	chr12:1950457-1950458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs568655685	chr12:1950490-1950491	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs141158706	chr12:1950500-1950501	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs117113203	chr12:1950537-1950538	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs569289762	chr12:1950539-1950540	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs11061998	chr12:1950551-1950552	Weak transcription Enhancers	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
Urothelial carcinoma	21177765	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	22488967	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1940800-1953400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:1945200-1950600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:1945800-1950000	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr12:1945800-1950600	Enhancers	Brain Germinal Matrix	brain
5	chr12:1946000-1949800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr12:1946000-1950400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr12:1946200-1951000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:1946600-1949800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr12:1946800-1952600	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr12:1947200-1953400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr12:1947400-1950800	Enhancers	HepG2	liver
12	chr12:1948200-1950000	Enhancers	Fetal Brain Female	brain
13	chr12:1948600-1954000	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr12:1948800-1950200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr12:1948800-1950600	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr12:1949000-1949800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:1949000-1949800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr12:1949000-1949800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr12:1949000-1950000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr12:1949000-1952400	Enhancers	Primary B cells from cord blood	blood
21	chr12:1949000-1952800	Enhancers	Primary B cells from peripheral blood	blood
22	chr12:1949400-1951000	Weak transcription	Primary hematopoietic stem cells	blood
23	chr12:1949600-1950200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:1949600-1950600	Enhancers	Fetal Brain Male	brain
25	chr12:1949800-1950000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr12:1949800-1950000	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr12:1949800-1950000	Enhancers	Fetal Thymus	thymus
28	chr12:1949800-1950200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr12:1949800-1950400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr12:1949800-1950400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr12:1949800-1950400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr12:1949800-1950400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr12:1949800-1950400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:1950000-1950200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr12:1950000-1950200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
36	chr12:1950000-1952600	Weak transcription	Fetal Brain Female	brain
37	chr12:1950200-1950400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr12:1950200-1950400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr12:1950200-1951200	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr12:1950200-1951200	Weak transcription	Fetal Thymus	thymus
41	chr12:1950200-1953400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr12:1950400-1951400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:1950400-1951600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr12:1950400-1952600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr12:1950400-1953400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr12:1950400-1953600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr12:1950400-1953800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr12:1950600-1951000	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr12:1950600-1952000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:1950600-1953600	Weak transcription	Brain Germinal Matrix	brain

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