Variant report

Variant	nsv518746
Chromosome Location	chr12:49870964-49924637
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:792)
CpG islands
(count:184)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:7)

(count:792 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:49907987-49908359	K562	blood:	n/a	n/a
2	ARID3A	chr12:49876184-49876519	HepG2	liver:	n/a	n/a
3	ATF1	chr12:49923328-49923532	K562	blood:	n/a	n/a
4	ATF3	chr12:49900645-49901369	A549	lung:	n/a	n/a
5	ATF3	chr12:49900841-49901438	A549	lung:	n/a	n/a
6	BACH1	chr12:49877568-49877605	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:49876035-49876213	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr12:49890272-49891278	A549	lung:	n/a	chr12:49890818-49890827
9	BCL3	chr12:49900449-49901476	A549	lung:	n/a	chr12:49901063-49901072 chr12:49901062-49901071
10	BCL3	chr12:49900858-49901378	A549	lung:	n/a	chr12:49901063-49901072 chr12:49901062-49901071
11	BCLAF1	chr12:49907852-49908277	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:49909105-49909338	A549	lung:	n/a	n/a
13	BHLHE40	chr12:49907986-49908149	K562	blood:	n/a	n/a
14	CBX3	chr12:49899964-49901335	HCT-116	colon:	n/a	n/a
15	CBX3	chr12:49912564-49913228	HCT-116	colon:	n/a	n/a
16	CBX3	chr12:49897374-49898184	HCT-116	colon:	n/a	n/a
17	CBX3	chr12:49900851-49901285	HCT-116	colon:	n/a	n/a
18	CBX3	chr12:49876423-49876933	HCT-116	colon:	n/a	n/a
19	CBX3	chr12:49883420-49884052	HCT-116	colon:	n/a	n/a
20	CEBPB	chr12:49901006-49901381	A549	lung:	n/a	n/a
21	CEBPB	chr12:49877293-49877318	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr12:49906471-49906671	A549	lung:	n/a	chr12:49906562-49906573
23	CEBPB	chr12:49900761-49901490	HCT-116	colon:	n/a	n/a
24	CEBPB	chr12:49877753-49878007	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr12:49885154-49885726	A549	lung:	n/a	chr12:49885458-49885469
26	CEBPB	chr12:49900603-49901398	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:49902046-49902077	K562	blood:	n/a	chr12:49902046-49902057
28	CEBPB	chr12:49901969-49902212	A549	lung:	n/a	chr12:49902046-49902057
29	CEBPB	chr12:49901933-49902068	HepG2	liver:	n/a	chr12:49902046-49902057
30	CEBPB	chr12:49909095-49909531	IMR90	lung:	n/a	chr12:49909375-49909388 chr12:49909375-49909388
31	CEBPB	chr12:49908913-49909464	A549	lung:	n/a	chr12:49909375-49909388 chr12:49909375-49909388
32	CEBPB	chr12:49900491-49901502	A549	lung:	n/a	n/a
33	CEBPB	chr12:49876177-49876897	HCT-116	colon:	n/a	n/a
34	CEBPB	chr12:49907917-49908226	IMR90	lung:	n/a	n/a
35	CEBPB	chr12:49907949-49908213	K562	blood:	n/a	n/a
36	CEBPB	chr12:49876254-49876727	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr12:49885369-49885529	HepG2	liver:	n/a	chr12:49885458-49885469
38	CEBPB	chr12:49907909-49908316	A549	lung:	n/a	n/a
39	CEBPB	chr12:49885114-49885907	IMR90	lung:	n/a	chr12:49885458-49885469
40	CEBPB	chr12:49908626-49909673	HCT-116	colon:	n/a	chr12:49909375-49909388 chr12:49909375-49909388
41	CEBPB	chr12:49900455-49901490	HCT-116	colon:	n/a	n/a
42	CEBPB	chr12:49897364-49898038	HCT-116	colon:	n/a	n/a
43	CEBPB	chr12:49877747-49878005	IMR90	lung:	n/a	n/a
44	CEBPB	chr12:49900871-49901416	A549	lung:	n/a	n/a
45	CEBPB	chr12:49885337-49885596	K562	blood:	n/a	chr12:49885458-49885469
46	CEBPB	chr12:49897384-49898199	HCT-116	colon:	n/a	n/a
47	CEBPB	chr12:49876233-49876453	HepG2	liver:	n/a	n/a
48	CEBPB	chr12:49907888-49908224	A549	lung:	n/a	n/a
49	CEBPB	chr12:49907910-49908228	Hela-S3	cervix:	n/a	n/a
50	CHD1	chr12:49907779-49908373	IMR90	lung:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:49877875-49877925	PANC-1	pancreas:	n/a
2	chr12:49877875-49877925	PANC-1	pancreas:	n/a
3	chr12:49877875-49877925	MCF10A-Er-Src	breast:	n/a
4	chr12:49877875-49877925	T-47D	breast:	n/a
5	chr12:49920480-49920530	CMK	blood:	n/a
6	chr12:49877875-49877925	K562	blood:	n/a
7	chr12:49920480-49920530	T-47D	breast:	n/a
8	chr12:49877875-49877925	ProgFib	skin:	n/a
9	chr12:49883750-49883800	HCF	heart:	n/a
10	chr12:49920480-49920530	GM06990	blood:	n/a
11	chr12:49920480-49920530	AG10803	skin:	n/a
12	chr12:49920480-49920530	GM12878	blood:	n/a
13	chr12:49877875-49877925	H1-hESC	embryonic stem cell:	embryo
14	chr12:49877875-49877925	U87	brain:	n/a
15	chr12:49883750-49883800	HEK293	kidney:	embryo
16	chr12:49877875-49877925	LNCaP	prostate:	n/a
17	chr12:49920480-49920530	ProgFib	skin:	n/a
18	chr12:49920480-49920530	NHBE	bronchial:	n/a
19	chr12:49920480-49920530	NB4	blood:	n/a
20	chr12:49883750-49883800	Hela-S3	cervix:	n/a
21	chr12:49883750-49883800	MCF-7	breast:	n/a
22	chr12:49920480-49920530	PANC-1	pancreas:	n/a
23	chr12:49877875-49877925	PrEC	prostate:	n/a
24	chr12:49920480-49920530	HEK293	kidney:	embryo
25	chr12:49883750-49883800	AG04449	skin:	fetal
26	chr12:49883750-49883800	HRE	kidney:	n/a
27	chr12:49877875-49877925	NHBE	bronchial:	n/a
28	chr12:49883750-49883800	LNCaP	prostate:	n/a
29	chr12:49883750-49883800	Caco-2	colon:	n/a
30	chr12:49920480-49920530	AG04449	skin:	fetal
31	chr12:49877875-49877925	HEEpiC	esophagus:	n/a
32	chr12:49877875-49877925	IMR90	lung:	fetal
33	chr12:49883750-49883800	AG09309	skin:	n/a
34	chr12:49920480-49920530	NHDF-neo	bronchial:	n/a
35	chr12:49920480-49920530	HNPCEpiC	eye:	n/a
36	chr12:49920480-49920530	GM12891	blood:	n/a
37	chr12:49877875-49877925	SAEC	small airway:	n/a
38	chr12:49877875-49877925	HCF	heart:	n/a
39	chr12:49883750-49883800	Jurkat	blood:	n/a
40	chr12:49883750-49883800	ovcar-3	ovarian:	n/a
41	chr12:49883750-49883800	SK-N-SH	brain:	n/a
42	chr12:49883750-49883800	HepG2	liver:	n/a
43	chr12:49883750-49883800	A549	lung:	n/a
44	chr12:49883750-49883800	ECC-1	luminal epithelium:	n/a
45	chr12:49883750-49883800	U87	brain:	n/a
46	chr12:49920480-49920530	SK-N-SH	brain:	n/a
47	chr12:49883750-49883800	HUVEC	blood vessel:	n/a
48	chr12:49920480-49920530	HepG2	liver:	n/a
49	chr12:49883750-49883800	AG09319	gingival:	n/a
50	chr12:49920480-49920530	Jurkat	blood:	n/a

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:49759630..49760473-chr12:49907526..49908336,2	MCF-7	breast:
2	chr12:49760603..49763130-chr12:49876900..49878678,2	MCF-7	breast:
3	chr12:49657840..49660330-chr12:49922519..49924856,2	K562	blood:
4	chr12:49760922..49762570-chr12:49885897..49888563,2	MCF-7	breast:
5	chr12:49875150..49877752-chr12:49892252..49894698,2	MCF-7	breast:
6	chr12:49888728..49890695-chr12:49907270..49908908,2	MCF-7	breast:
7	chr12:49657014..49659216-chr12:49904463..49906074,2	MCF-7	breast:
8	chr12:49909845..49911821-chr12:49917345..49920112,2	K562	blood:
9	chr12:49892298..49894551-chr12:49905722..49908567,2	MCF-7	breast:
10	chr12:49875150..49877752-chr12:49892252..49894698,2	MCF-7	breast:
11	chr12:49889623..49891962-chr12:49960007..49961809,2	MCF-7	breast:
12	chr12:49920492..49922115-chr12:49926233..49928971,2	MCF-7	breast:
13	chr12:49759340..49761846-chr12:49889579..49891546,2	MCF-7	breast:
14	chr12:49759543..49761872-chr12:49900750..49903722,2	K562	blood:
15	chr12:49760336..49762548-chr12:49871449..49873344,2	K562	blood:
16	chr12:49888436..49891158-chr12:49893639..49895369,2	K562	blood:
17	chr12:49759096..49761213-chr12:49881834..49884299,3	K562	blood:
18	chr12:49755189..49756815-chr12:49905367..49908024,2	K562	blood:
19	chr12:49867597..49869734-chr12:49873325..49875572,2	MCF-7	breast:
20	chr12:49759716..49761843-chr12:49896903..49899179,2	MCF-7	breast:
21	chr12:49760673..49762332-chr12:49904037..49906456,2	MCF-7	breast:
22	chr12:49888436..49891158-chr12:49893639..49895369,2	K562	blood:
23	chr12:49725159..49725975-chr12:49907593..49908174,2	MCF-7	breast:
24	chr12:49872294..49876193-chr12:49879137..49882751,3	K562	blood:
25	chr12:49890275..49892320-chr12:49896364..49899114,2	MCF-7	breast:
26	chr12:49724272..49727239-chr12:49903612..49905113,2	MCF-7	breast:
27	chr12:49759750..49761525-chr12:49890654..49893195,2	K562	blood:
28	chr12:49892592..49895117-chr12:49904211..49906790,2	MCF-7	breast:
29	chr12:49739423..49741666-chr12:49907974..49910735,2	MCF-7	breast:
30	chr12:49909845..49911821-chr12:49916454..49920112,3	K562	blood:
31	chr12:49759409..49762538-chr12:49903673..49906483,5	MCF-7	breast:
32	chr12:49897809..49900904-chr12:49903027..49905509,4	MCF-7	breast:
33	chr12:49757995..49761023-chr12:49883452..49885795,3	MCF-7	breast:
34	chr12:49915417..49918018-chr12:49960149..49961960,3	MCF-7	breast:
35	chr12:49759014..49760653-chr12:49904638..49907185,2	K562	blood:
36	chr12:49872294..49876193-chr12:49879137..49882751,3	K562	blood:
37	chr12:49689762..49691903-chr12:49905234..49907428,2	MCF-7	breast:
38	chr12:49923572..49927432-chr12:49929998..49933415,4	K562	blood:
39	chr12:49905164..49907122-chr12:49909196..49912005,2	K562	blood:
40	chr12:49909845..49911821-chr12:49917345..49920112,2	K562	blood:
41	chr12:49743272..49745246-chr12:49919993..49922237,2	MCF-7	breast:
42	chr12:49867080..49869633-chr12:49872021..49873614,2	MCF-7	breast:
43	chr12:49892592..49895117-chr12:49904211..49906790,2	MCF-7	breast:
44	chr12:49750854..49751500-chr12:49907554..49908179,2	MCF-7	breast:
45	chr12:49921630..49924042-chr12:49926070..49928576,2	K562	blood:
46	chr12:49890275..49892320-chr12:49896364..49899114,2	MCF-7	breast:
47	chr12:49912988..49915445-chr12:49916293..49919057,4	K562	blood:
48	chr12:49752289..49753081-chr12:49906577..49907444,2	MCF-7	breast:
49	chr12:49758876..49762155-chr12:49906533..49909731,5	MCF-7	breast:
50	chr12:49921712..49923511-chr12:49960745..49963724,3	MCF-7	breast:

No data

(count:7 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SPATS2	hsa-miR-103a-3p	chr12:49890616-49890628
2	SPATS2	hsa-miR-103a-3p	chr12:49890687-49890707
3	SPATS2	hsa-miR-103a-3p	chr12:49888775-49888785
4	SPATS2	hsa-miR-103a-3p	chr12:49893980-49893988
5	SPATS2	hsa-miR-296-3p	chr12:49921066-49921087
6	SPATS2	hsa-miR-103a-3p	chr12:49921141-49921163
7	SPATS2	hsa-miR-103a-3p	chr12:49906645-49906660

Variant related genes	Relation type
SPATS2	TF binding region
SPATS2	CpG island
ENSG00000110844	chromatin interactions
ENSG00000258101	chromatin interactions
ENSG00000187778	chromatin interactions
ENSG00000135519	chromatin interactions
ENSG00000135406	chromatin interactions
ENSG00000123352	chromatin interactions
ENSG00000178401	chromatin interactions
ENSG00000167553	chromatin interactions

Extended variants
information (count: 1889 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1889 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11169042	chr12:49870964-49870965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs142971021	chr12:49870967-49870968	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs111256003	chr12:49871011-49871012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368920994	chr12:49871092-49871093	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs74089520	chr12:49871113-49871114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs184498037	chr12:49871171-49871172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139887867	chr12:49871351-49871352	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs188751032	chr12:49871400-49871401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs144796868	chr12:49871479-49871480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112894677	chr12:49871524-49871525	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192535211	chr12:49871555-49871556	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs550204711	chr12:49871562-49871563	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs117872391	chr12:49871670-49871671	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs370638950	chr12:49871735-49871736	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536914740	chr12:49871736-49871737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs374884866	chr12:49871745-49871746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs537690099	chr12:49871808-49871809	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs11169043	chr12:49871812-49871813	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs542782624	chr12:49871826-49871827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs184576389	chr12:49871860-49871861	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs12819350	chr12:49871862-49871863	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs553022240	chr12:49871898-49871899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs576656282	chr12:49871921-49871922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572948194	chr12:49871933-49871934	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs545105916	chr12:49871971-49871972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558653940	chr12:49871977-49871978	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs575338711	chr12:49871999-49872000	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544441933	chr12:49872008-49872009	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs560978980	chr12:49872012-49872013	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs529953722	chr12:49872039-49872040	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs77208473	chr12:49872045-49872046	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542584174	chr12:49872053-49872054	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189545054	chr12:49872093-49872094	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554886023	chr12:49872140-49872141	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373543337	chr12:49872145-49872146	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376762367	chr12:49872216-49872217	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530958866	chr12:49872220-49872221	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs370489445	chr12:49872243-49872244	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567831030	chr12:49872262-49872263	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147592860	chr12:49872317-49872318	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553733803	chr12:49872329-49872330	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566460829	chr12:49872371-49872372	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs180986308	chr12:49872385-49872386	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs558367641	chr12:49872430-49872431	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7294973	chr12:49872443-49872444	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs377599302	chr12:49872495-49872496	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554769285	chr12:49872524-49872525	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574320047	chr12:49872552-49872553	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540119473	chr12:49872564-49872565	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534925060	chr12:49872636-49872637	Enhancers Genic enhancers Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Cancer	17160897	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:1584 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49823000-49915800	Weak transcription	Primary B cells from cord blood	blood
2	chr12:49823400-49876000	Weak transcription	Osteobl	bone
3	chr12:49839200-49876000	Weak transcription	Fetal Thymus	thymus
4	chr12:49840200-49900600	Weak transcription	Pancreas	Pancrea
5	chr12:49840600-49875800	Weak transcription	Hela-S3	cervix
6	chr12:49846000-49879800	Weak transcription	Fetal Lung	lung
7	chr12:49846400-49878400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr12:49849400-49875800	Weak transcription	HepG2	liver
9	chr12:49850400-49876000	Weak transcription	Fetal Intestine Large	intestine
10	chr12:49850400-49876000	Weak transcription	Small Intestine	intestine
11	chr12:49850400-49878800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr12:49850400-49911000	Weak transcription	K562	blood
13	chr12:49850600-49876200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr12:49853200-49876000	Weak transcription	HSMMtube	muscle
15	chr12:49853200-49913400	Weak transcription	Thymus	Thymus
16	chr12:49854400-49878400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr12:49855200-49872600	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr12:49856400-49872600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr12:49856400-49883400	Weak transcription	Brain Anterior Caudate	brain
20	chr12:49856600-49872800	Weak transcription	Fetal Muscle Leg	muscle
21	chr12:49856600-49874400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:49856600-49875800	Weak transcription	Adipose Nuclei	Adipose
23	chr12:49856600-49890200	Weak transcription	Primary T cells from cord blood	blood
24	chr12:49856600-49890200	Weak transcription	Ovary	ovary
25	chr12:49856800-49872600	Weak transcription	NHEK	skin
26	chr12:49856800-49876000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr12:49856800-49876000	Weak transcription	Duodenum Mucosa	Duodenum
28	chr12:49856800-49876000	Weak transcription	HSMM	muscle
29	chr12:49856800-49876200	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr12:49856800-49883600	Weak transcription	Dnd41	blood
31	chr12:49856800-49898400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr12:49857000-49876000	Weak transcription	NH-A	brain
33	chr12:49858200-49875800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr12:49859200-49876000	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr12:49859400-49883400	Weak transcription	Primary hematopoietic stem cells	blood
36	chr12:49859400-49888600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr12:49865000-49872800	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr12:49865200-49876000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:49865600-49872600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr12:49865600-49875600	Weak transcription	A549	lung
41	chr12:49865800-49875800	Weak transcription	HMEC	breast
42	chr12:49867200-49876000	Weak transcription	Psoas Muscle	Psoas
43	chr12:49867800-49872800	Weak transcription	Right Ventricle	heart
44	chr12:49867800-49875400	Weak transcription	HUVEC	blood vessel
45	chr12:49868000-49872400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:49869000-49872800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:49869400-49876200	Weak transcription	Brain Germinal Matrix	brain
48	chr12:49869600-49890000	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr12:49869600-49918400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr12:49870000-49877600	Weak transcription	GM12878-XiMat	blood

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