Variant report

Variant	nsv1050895
Chromosome Location	chr12:1941618-1983445
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:275)
CpG islands
(count:1711)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:1947034-1947306	HepG2	liver:	n/a	n/a
2	ATF1	chr12:1950924-1951113	K562	blood:	n/a	n/a
3	BHLHE40	chr12:1979460-1979468	K562	blood:	n/a	n/a
4	BHLHE40	chr12:1974549-1974700	K562	blood:	n/a	n/a
5	CEBPB	chr12:1947056-1947318	HepG2	liver:	n/a	n/a
6	CEBPB	chr12:1944440-1944697	HepG2	liver:	n/a	chr12:1944546-1944557
7	CEBPB	chr12:1948985-1949607	MCF-7	breast:	n/a	n/a
8	CEBPB	chr12:1944453-1944613	H1-hESC	embryonic stem cell:	n/a	chr12:1944546-1944557
9	CEBPB	chr12:1960290-1960578	IMR90	lung:	n/a	n/a
10	CEBPB	chr12:1944447-1944650	K562	blood:	n/a	chr12:1944546-1944557
11	CEBPB	chr12:1949067-1949617	MCF-7	breast:	n/a	n/a
12	CTCF	chr12:1960540-1960690	AG10803	skin:	n/a	n/a
13	CTCF	chr12:1946360-1946510	HepG2	liver:	n/a	chr12:1946470-1946488
14	CTCF	chr12:1942460-1942610	HAc	cerebellar:	n/a	n/a
15	CTCF	chr12:1945340-1945490	NB4	blood:	n/a	n/a
16	CTCF	chr12:1945380-1945530	GM12873	blood:	n/a	n/a
17	CTCF	chr12:1966944-1966981	LNCaP	prostate:	n/a	n/a
18	CTCF	chr12:1945300-1945450	GM12878	blood:	n/a	n/a
19	CTCF	chr12:1945238-1945405	HepG2	liver:	n/a	n/a
20	CTCF	chr12:1945260-1945410	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr12:1980617-1980698	ProgFib	skin:	n/a	n/a
22	CTCF	chr12:1962700-1962850	GM12872	blood:	n/a	chr12:1962840-1962848
23	CTCF	chr12:1945332-1945388	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr12:1945301-1945414	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:1945313-1945406	MCF-7	breast:	n/a	n/a
26	CTCF	chr12:1945329-1945409	GM12891	blood:	n/a	n/a
27	CTCF	chr12:1945311-1945430	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:1945274-1945454	MCF-7	breast:	n/a	n/a
29	CTCF	chr12:1945260-1945410	Caco-2	colon:	n/a	n/a
30	CTCF	chr12:1945335-1945429	GM12892	blood:	n/a	n/a
31	CTCF	chr12:1980682-1980762	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr12:1980225-1980843	GM19239	blood:	n/a	n/a
33	CTCF	chr12:1949740-1949890	HepG2	liver:	n/a	n/a
34	CTCF	chr12:1946340-1946490	RPTEC	kidney:	n/a	chr12:1946470-1946488
35	CTCF	chr12:1945300-1945450	HepG2	liver:	n/a	n/a
36	CTCF	chr12:1942340-1942477	H1-hESC	embryonic stem cell:	n/a	chr12:1942405-1942423
37	CTCF	chr12:1942305-1942486	K562	blood:	n/a	chr12:1942405-1942423
38	CTCF	chr12:1947340-1947490	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr12:1942344-1942461	K562	blood:	n/a	chr12:1942405-1942423
40	CTCF	chr12:1945304-1945424	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:1942300-1942450	K562	blood:	n/a	chr12:1942405-1942423
42	CTCF	chr12:1945320-1945420	HepG2	liver:	n/a	n/a
43	CTCF	chr12:1942380-1942530	HPF	lung:	n/a	chr12:1942405-1942423
44	CTCF	chr12:1946360-1946510	HCPEpiC	choroid plexus:	n/a	chr12:1946470-1946488
45	CTCF	chr12:1945300-1945450	MCF-7	breast:	n/a	n/a
46	CTCF	chr12:1946340-1946490	NHEK	skin:	n/a	chr12:1946470-1946488
47	E2F4	chr12:1968881-1969065	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr12:1958924-1959064	MCF10A-Er-Src	breast:	n/a	n/a
49	EBF1	chr12:1951818-1952056	GM12878	blood:	n/a	chr12:1951932-1951941 chr12:1951931-1951942 chr12:1951932-1951942 chr12:1951932-1951941 chr12:1951907-1951918
50	EBF1	chr12:1951715-1952118	GM12878	blood:	n/a	chr12:1951932-1951941 chr12:1951931-1951942 chr12:1951932-1951942 chr12:1951932-1951941 chr12:1951907-1951918

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1945300-1945350	HUVEC	blood vessel:	n/a
2	chr12:1946957-1947007	Hela-S3	cervix:	n/a
3	chr12:1974122-1974172	HCPEpiC	choroid plexus:	n/a
4	chr12:1945300-1945350	HUVEC	blood vessel:	n/a
5	chr12:1946957-1947007	Hela-S3	cervix:	n/a
6	chr12:1974122-1974172	HCPEpiC	choroid plexus:	n/a
7	chr12:1945300-1945350	SK-N-SH_RA	brain:	n/a
8	chr12:1952798-1952848	T-47D	breast:	n/a
9	chr12:1973452-1973502	LNCaP	prostate:	n/a
10	chr12:1974122-1974172	NH-A	brain:	n/a
11	chr12:1973340-1973390	LNCaP	prostate:	n/a
12	chr12:1963310-1963360	SK-N-SH	brain:	n/a
13	chr12:1947479-1947529	GM12878	blood:	n/a
14	chr12:1947412-1947462	MCF-7	breast:	n/a
15	chr12:1948578-1948628	AG09319	gingival:	n/a
16	chr12:1970170-1970220	AG04450	lung:	fetal
17	chr12:1973367-1973417	ECC-1	luminal epithelium:	n/a
18	chr12:1974724-1974774	ProgFib	skin:	n/a
19	chr12:1948435-1948485	GM12892	blood:	n/a
20	chr12:1952798-1952848	HRPEpiC	eye:	n/a
21	chr12:1974168-1974218	CMK	blood:	n/a
22	chr12:1947479-1947529	GM12892	blood:	n/a
23	chr12:1973872-1973922	ovcar-3	ovarian:	n/a
24	chr12:1952798-1952848	AG09309	skin:	n/a
25	chr12:1976671-1976721	HNPCEpiC	eye:	n/a
26	chr12:1952798-1952848	HAEpiC	amniotic membrane:	n/a
27	chr12:1974724-1974774	HCPEpiC	choroid plexus:	n/a
28	chr12:1943722-1943772	HCF	heart:	n/a
29	chr12:1973340-1973390	Caco-2	colon:	n/a
30	chr12:1946957-1947007	HUVEC	blood vessel:	n/a
31	chr12:1952798-1952848	SAEC	small airway:	n/a
32	chr12:1947479-1947529	T-47D	breast:	n/a
33	chr12:1949586-1949636	HRPEpiC	eye:	n/a
34	chr12:1974724-1974774	HCM	heart:	n/a
35	chr12:1974122-1974172	RPTEC	kidney:	n/a
36	chr12:1973872-1973922	IMR90	lung:	fetal
37	chr12:1963310-1963360	HRPEpiC	eye:	n/a
38	chr12:1974122-1974172	AG10803	skin:	n/a
39	chr12:1948578-1948628	AG10803	skin:	n/a
40	chr12:1947479-1947529	HL-60	blood:	n/a
41	chr12:1943758-1943808	AG04449	skin:	fetal
42	chr12:1976671-1976721	NB4	blood:	n/a
43	chr12:1948435-1948485	HCPEpiC	choroid plexus:	n/a
44	chr12:1943758-1943808	PrEC	prostate:	n/a
45	chr12:1970170-1970220	SK-N-SH_RA	brain:	n/a
46	chr12:1973367-1973417	HNPCEpiC	eye:	n/a
47	chr12:1974168-1974218	GM12892	blood:	n/a
48	chr12:1948435-1948485	Hepatocyte	liver:	n/a
49	chr12:1973340-1973390	NB4	blood:	n/a
50	chr12:1970170-1970220	RPTEC	kidney:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:1945750..1946705-chr12:2048995..2049750,2	MCF-7	breast:
2	chr12:1876884..1877711-chr12:1950746..1951257,2	MCF-7	breast:
3	chr12:1905054..1907716-chr12:1943766..1946105,3	MCF-7	breast:
4	chr12:1947643..1951345-chr12:1957413..1959557,3	MCF-7	breast:
5	chr12:1910081..1912246-chr12:1949040..1950547,2	K562	blood:
6	chr12:1950335..1952773-chr12:1969860..1971374,2	MCF-7	breast:
7	chr12:1946363..1947932-chr12:2045137..2046691,2	MCF-7	breast:
8	chr12:1877224..1880546-chr12:1949279..1951143,3	MCF-7	breast:
9	chr12:1918012..1920353-chr12:1939627..1941633,2	MCF-7	breast:
10	chr12:1901985..1907754-chr12:1946580..1951659,8	MCF-7	breast:
11	chr12:1944160..1952960-chr12:2039965..2049915,22	MCF-7	breast:
12	chr12:1956703..1959604-chr12:1963408..1966102,2	MCF-7	breast:
13	chr12:1910843..1912522-chr12:1945003..1947651,2	MCF-7	breast:
14	chr12:1968515..1969082-chr12:2040995..2041606,2	MCF-7	breast:
15	chr12:1952274..1954241-chr12:1954730..1957718,2	K562	blood:
16	chr12:1953795..1956547-chr12:1969421..1971021,2	MCF-7	breast:
17	chr12:1976877..1978383-chr12:1995618..1998420,2	MCF-7	breast:
18	chr12:1945038..1946828-chr12:1971867..1974133,2	K562	blood:
19	chr12:1945477..1946181-chr12:2041443..2042003,2	MCF-7	breast:
20	chr12:1956703..1959604-chr12:1963408..1966102,2	MCF-7	breast:
21	chr12:1947284..1949728-chr12:2036486..2038838,2	MCF-7	breast:
22	chr12:1968515..1969333-chr12:2041106..2041850,2	MCF-7	breast:
23	chr12:1905374..1907142-chr12:1951674..1953593,2	MCF-7	breast:
24	chr12:1933541..1935951-chr12:1940567..1942424,2	K562	blood:
25	chr12:1950359..1950994-chr12:2041053..2041904,2	MCF-7	breast:
26	chr12:1978767..1980595-chr12:2025590..2028373,2	MCF-7	breast:
27	chr12:1959456..1961016-chr12:1962388..1965205,2	MCF-7	breast:
28	chr12:1952274..1954241-chr12:1954730..1957718,2	K562	blood:
29	chr12:1947445..1949197-chr12:2016726..2018832,2	MCF-7	breast:
30	chr12:1920587..1924096-chr12:1946145..1949569,4	MCF-7	breast:
31	chr12:1950359..1950994-chr12:2041053..2041904,3	MCF-7	breast:
32	chr12:1929539..1932583-chr12:1944891..1948429,3	MCF-7	breast:
33	chr12:1741511..1744510-chr12:1943871..1945697,2	K562	blood:
34	chr12:1949995..1951546-chr12:1955088..1956789,2	MCF-7	breast:
35	chr12:1949995..1951546-chr12:1955088..1956789,2	MCF-7	breast:
36	chr12:1936574..1939225-chr12:1940094..1944386,3	K562	blood:
37	chr12:1909603..1910441-chr12:1945244..1945817,2	MCF-7	breast:
38	chr12:1947774..1950374-chr12:1986873..1988503,2	MCF-7	breast:
39	chr12:1982062..1983660-chr12:1991935..1993547,2	MCF-7	breast:
40	chr12:1954206..1956342-chr12:2043639..2046868,3	MCF-7	breast:
41	chr12:1947643..1951345-chr12:1957413..1959557,3	MCF-7	breast:
42	chr12:1962397..1965390-chr12:1965944..1968413,2	K562	blood:
43	chr12:1950335..1952773-chr12:1969860..1971374,2	MCF-7	breast:
44	chr12:1951607..1953524-chr12:2057455..2059714,2	MCF-7	breast:
45	chr12:1799987..1802012-chr12:1946925..1950411,3	MCF-7	breast:
46	chr12:1737994..1740960-chr12:1947307..1949303,2	MCF-7	breast:
47	chr12:1945038..1946828-chr12:1971867..1974133,2	K562	blood:
48	chr12:1932447..1935067-chr12:1939828..1942115,3	MCF-7	breast:
49	chr12:1905042..1905969-chr12:1944742..1945885,3	MCF-7	breast:
50	chr12:1925102..1928805-chr12:1946979..1949915,3	MCF-7	breast:

No data

Variant related genes	Relation type
CACNA2D4	TF binding region
CACNA2D4	CpG island
ENSG00000111186	chromatin interactions
ENSG00000256706	chromatin interactions
ENSG00000235049	chromatin interactions
ENSG00000166159	chromatin interactions
ENSG00000151062	chromatin interactions
ENSG00000006831	chromatin interactions

Extended variants
information (count: 1669 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1669 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190873042	chr12:1941623-1941624	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs76587253	chr12:1941643-1941644	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs552262991	chr12:1941644-1941645	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs576734420	chr12:1941777-1941778	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs138194232	chr12:1941814-1941815	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs570842415	chr12:1941844-1941845	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs35397964	chr12:1941892-1941893	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs7961753	chr12:1941932-1941933	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs142785954	chr12:1942003-1942004	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7961866	chr12:1942018-1942019	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs182422590	chr12:1942059-1942060	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs115013245	chr12:1942070-1942071	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs144265452	chr12:1942090-1942091	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547450373	chr12:1942131-1942132	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs554384394	chr12:1942166-1942167	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs371907087	chr12:1942170-1942171	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs187053381	chr12:1942180-1942181	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs148325983	chr12:1942191-1942192	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112289389	chr12:1942196-1942197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576787147	chr12:1942231-1942232	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191895644	chr12:1942266-1942267	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182878439	chr12:1942315-1942316	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs559276898	chr12:1942371-1942372	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528024317	chr12:1942377-1942378	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543331066	chr12:1942378-1942379	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs141493742	chr12:1942388-1942389	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs531902662	chr12:1942390-1942391	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550266746	chr12:1942398-1942399	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565208798	chr12:1942399-1942400	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs77934635	chr12:1942408-1942409	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs74786746	chr12:1942445-1942446	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566056253	chr12:1942509-1942510	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs536193641	chr12:1942531-1942532	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs78592391	chr12:1942557-1942558	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs569524531	chr12:1942579-1942580	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs375996802	chr12:1942584-1942585	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs150875761	chr12:1942601-1942602	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs558639579	chr12:1942661-1942662	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs575996724	chr12:1942690-1942691	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544531109	chr12:1942696-1942697	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs140122267	chr12:1942713-1942714	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs552731510	chr12:1942723-1942724	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs188542233	chr12:1942731-1942732	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs543355064	chr12:1942751-1942752	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs7303599	chr12:1942752-1942753	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs576733699	chr12:1942765-1942766	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs193239383	chr12:1942778-1942779	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs185635747	chr12:1942837-1942838	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs7303742	chr12:1942840-1942841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs368763707	chr12:1942843-1942844	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:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1935200-1946000	Weak transcription	Brain Angular Gyrus	brain
2	chr12:1940200-1949400	Weak transcription	Right Atrium	heart
3	chr12:1940400-1945800	Weak transcription	Brain Germinal Matrix	brain
4	chr12:1940600-1942000	Weak transcription	Fetal Brain Male	brain
5	chr12:1940600-1942400	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr12:1940600-1944400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr12:1940600-1946000	Weak transcription	Spleen	Spleen
8	chr12:1940800-1942600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:1940800-1944000	Weak transcription	Gastric	stomach
10	chr12:1940800-1944400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:1940800-1946200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr12:1940800-1953400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr12:1941400-1942400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:1941400-1942600	Weak transcription	Brain Anterior Caudate	brain
15	chr12:1942000-1942600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr12:1942000-1943200	Enhancers	Fetal Brain Female	brain
17	chr12:1942000-1943400	Enhancers	Fetal Brain Male	brain
18	chr12:1942200-1942400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
19	chr12:1942400-1942600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:1942400-1942600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
21	chr12:1942400-1942800	Enhancers	Brain Inferior Temporal Lobe	brain
22	chr12:1942600-1942800	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr12:1942600-1943200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr12:1942600-1943200	Enhancers	Brain Anterior Caudate	brain
25	chr12:1942800-1945000	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr12:1943200-1944800	Weak transcription	Fetal Brain Female	brain
27	chr12:1943200-1945600	Weak transcription	Brain Anterior Caudate	brain
28	chr12:1943200-1948600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:1943400-1944600	Weak transcription	Fetal Brain Male	brain
30	chr12:1944200-1944400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr12:1944400-1945000	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr12:1944400-1948400	Enhancers	Brain Cingulate Gyrus	brain
33	chr12:1944600-1945000	Weak transcription	Brain Hippocampus Middle	brain
34	chr12:1944600-1949200	Enhancers	Fetal Brain Male	brain
35	chr12:1944800-1945000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr12:1944800-1945000	Enhancers	Fetal Brain Female	brain
37	chr12:1944800-1945000	Bivalent Enhancer	HepG2	liver
38	chr12:1944800-1949200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr12:1945000-1945400	Weak transcription	Fetal Brain Female	brain
40	chr12:1945000-1945800	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr12:1945000-1946000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr12:1945000-1946200	Enhancers	HepG2	liver
43	chr12:1945000-1948200	Enhancers	Brain Hippocampus Middle	brain
44	chr12:1945200-1950600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr12:1945400-1947400	Enhancers	Fetal Brain Female	brain
46	chr12:1945600-1946000	Enhancers	Brain Anterior Caudate	brain
47	chr12:1945800-1946400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
48	chr12:1945800-1948400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr12:1945800-1950000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr12:1945800-1950600	Enhancers	Brain Germinal Matrix	brain

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