Variant report

Variant	nsv523022
Chromosome Location	chr12:12673551-12688181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:173)
CpG islands
(count:122)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:173 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr12:12687145-12687343	K562	blood:	n/a	n/a
2	CEBPB	chr12:12674060-12674368	HepG2	liver:	n/a	chr12:12674334-12674351
3	CTCF	chr12:12685566-12685668	GM20000	blood:	n/a	n/a
4	CTCF	chr12:12687160-12687310	HRPEpiC	eye:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
5	CTCF	chr12:12687140-12687290	SK-N-SH_RA	brain:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
6	CTCF	chr12:12687195-12687262	K562	blood:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
7	CTCF	chr12:12687214-12687225	Pancreas_OC	pancreas:	n/a	n/a
8	CTCF	chr12:12687140-12687290	HCM	heart:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
9	CTCF	chr12:12687180-12687330	SK-N-SH_RA	brain:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
10	CTCF	chr12:12687160-12687310	HEK293	kidney:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
11	CTCF	chr12:12687140-12687290	BE2_C	brain:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
12	CTCF	chr12:12687160-12687310	Caco-2	colon:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
13	CTCF	chr12:12687220-12687370	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr12:12687194-12687413	K562	blood:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
15	CTCF	chr12:12687060-12687210	HRPEpiC	eye:	n/a	n/a
16	CTCF	chr12:12676375-12676409	Lung_OC	lung:	n/a	n/a
17	CTCF	chr12:12687263-12687269	K562	blood:	n/a	n/a
18	CTCF	chr12:12687200-12687350	K562	blood:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
19	CTCF	chr12:12687120-12687270	Caco-2	colon:	n/a	chr12:12687219-12687228 chr12:12687213-12687231
20	E2F4	chr12:12678787-12678814	MCF10A-Er-Src	breast:	n/a	n/a
21	EGR1	chr12:12681684-12681897	K562	blood:	n/a	n/a
22	EP300	chr12:12686110-12686789	ECC-1	luminal epithelium:	n/a	n/a
23	EP300	chr12:12681297-12681680	SK-N-SH_RA	brain:	n/a	chr12:12681320-12681329
24	EP300	chr12:12686991-12687479	SK-N-SH_RA	brain:	n/a	chr12:12687099-12687113
25	EP300	chr12:12687051-12687490	SK-N-SH_RA	brain:	n/a	chr12:12687099-12687113
26	FOS	chr12:12684218-12684516	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr12:12684278-12684436	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr12:12684227-12684513	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr12:12686226-12686427	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr12:12684211-12684529	MCF10A-Er-Src	breast:	n/a	n/a
31	FOSL2	chr12:12680720-12681244	HepG2	liver:	n/a	chr12:12680801-12680810
32	FOSL2	chr12:12684085-12684530	SK-N-SH	brain:	n/a	n/a
33	FOXA1	chr12:12683834-12684183	HepG2	liver:	n/a	n/a
34	FOXA1	chr12:12680656-12681033	HepG2	liver:	n/a	n/a
35	FOXA1	chr12:12688053-12688207	T-47D	breast:	n/a	n/a
36	FOXA1	chr12:12680609-12680949	HepG2	liver:	n/a	n/a
37	FOXA2	chr12:12680680-12680946	HepG2	liver:	n/a	n/a
38	GATA2	chr12:12687073-12687436	SH-SY5Y	brain:	n/a	n/a
39	GATA3	chr12:12686987-12687459	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr12:12675714-12676244	MCF-7	breast:	n/a	n/a
41	GATA3	chr12:12684027-12684679	SK-N-SH	brain:	n/a	n/a
42	GATA3	chr12:12684031-12684563	SK-N-SH	brain:	n/a	n/a
43	GATA3	chr12:12687020-12687550	SK-N-SH	brain:	n/a	n/a
44	GATA3	chr12:12676173-12676326	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr12:12686996-12687625	SK-N-SH	brain:	n/a	chr12:12687575-12687596
46	HDAC2	chr12:12686215-12686535	MCF-7	breast:	n/a	n/a
47	JUN	chr12:12674034-12674216	HepG2	liver:	n/a	chr12:12674076-12674089
48	JUND	chr12:12684062-12684669	SK-N-SH	brain:	n/a	chr12:12684364-12684375
49	JUND	chr12:12684259-12684531	HepG2	liver:	n/a	chr12:12684364-12684375
50	JUND	chr12:12683886-12684639	SK-N-SH	brain:	n/a	chr12:12684364-12684375

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:12680897-12680947	MCF-7	breast:	n/a
2	chr12:12686957-12687007	GM06990	blood:	n/a
3	chr12:12680897-12680947	PANC-1	pancreas:	n/a
4	chr12:12680897-12680947	BJ	skin:	n/a
5	chr12:12680897-12680947	MCF10A-Er-Src	breast:	n/a
6	chr12:12680897-12680947	ovcar-3	ovarian:	n/a
7	chr12:12680897-12680947	NB4	blood:	n/a
8	chr12:12686957-12687007	PFSK-1	brain:	n/a
9	chr12:12686957-12687007	IMR90	lung:	fetal
10	chr12:12686957-12687007	HIPEpiC	eye:	n/a
11	chr12:12686957-12687007	HUVEC	blood vessel:	n/a
12	chr12:12686957-12687007	SAEC	small airway:	n/a
13	chr12:12680897-12680947	HCF	heart:	n/a
14	chr12:12680897-12680947	HEEpiC	esophagus:	n/a
15	chr12:12680897-12680947	GM19239	blood:	n/a
16	chr12:12680897-12680947	AG10803	skin:	n/a
17	chr12:12686957-12687007	Caco-2	colon:	n/a
18	chr12:12686957-12687007	HAEpiC	amniotic membrane:	n/a
19	chr12:12686957-12687007	CMK	blood:	n/a
20	chr12:12680897-12680947	SK-N-MC	brain:	n/a
21	chr12:12680897-12680947	HUVEC	blood vessel:	n/a
22	chr12:12680897-12680947	AoSMC	blood vessel:	n/a
23	chr12:12680897-12680947	HAEpiC	amniotic membrane:	n/a
24	chr12:12680897-12680947	H1-hESC	embryonic stem cell:	embryo
25	chr12:12686957-12687007	ProgFib	skin:	n/a
26	chr12:12680897-12680947	HCPEpiC	choroid plexus:	n/a
27	chr12:12680897-12680947	T-47D	breast:	n/a
28	chr12:12680897-12680947	CMK	blood:	n/a
29	chr12:12686957-12687007	ovcar-3	ovarian:	n/a
30	chr12:12686957-12687007	BE2_C	brain:	n/a
31	chr12:12686957-12687007	H1-hESC	embryonic stem cell:	embryo
32	chr12:12680897-12680947	Jurkat	blood:	n/a
33	chr12:12686957-12687007	Hela-S3	cervix:	n/a
34	chr12:12680897-12680947	NH-A	brain:	n/a
35	chr12:12680897-12680947	NHBE	bronchial:	n/a
36	chr12:12680897-12680947	HMEC	breast:	n/a
37	chr12:12680897-12680947	ProgFib	skin:	n/a
38	chr12:12680897-12680947	HCM	heart:	n/a
39	chr12:12686957-12687007	AG04450	lung:	fetal
40	chr12:12686957-12687007	SKMC	muscle:	n/a
41	chr12:12680897-12680947	GM06990	blood:	n/a
42	chr12:12680897-12680947	BE2_C	brain:	n/a
43	chr12:12680897-12680947	U87	brain:	n/a
44	chr12:12686957-12687007	HCF	heart:	n/a
45	chr12:12680897-12680947	HepG2	liver:	n/a
46	chr12:12686957-12687007	HMEC	breast:	n/a
47	chr12:12680897-12680947	SKMC	muscle:	n/a
48	chr12:12680897-12680947	NT2-D1	testis:	n/a
49	chr12:12686957-12687007	A549	lung:	n/a
50	chr12:12686957-12687007	Hepatocyte	liver:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:12676702..12679662-chr12:12711991..12714895,3	MCF-7	breast:
2	chr12:12676154..12677988-chr12:12685954..12688802,2	MCF-7	breast:
3	chr12:12679007..12681498-chr12:12683733..12686607,2	K562	blood:
4	chr12:12686997..12688577-chr12:12699822..12702095,2	K562	blood:
5	chr12:12677909..12679570-chr12:12685352..12687736,2	MCF-7	breast:
6	chr12:12663586..12666811-chr12:12669278..12673958,4	MCF-7	breast:
7	chr12:12673839..12677511-chr12:12678935..12682743,3	MCF-7	breast:
8	chr12:12673672..12675472-chr12:12680343..12682514,2	MCF-7	breast:
9	chr12:12672602..12674761-chr12:12714230..12715790,2	MCF-7	breast:
10	chr12:12679007..12681498-chr12:12683733..12686607,2	K562	blood:
11	chr12:12675003..12677370-chr12:12678643..12681429,2	K562	blood:
12	chr12:12682433..12684454-chr12:12714001..12716465,2	MCF-7	breast:
13	chr12:12672595..12674438-chr12:12675513..12677632,2	MCF-7	breast:
14	chr12:12673127..12675193-chr12:12712366..12713939,3	MCF-7	breast:
15	chr12:12672692..12674511-chr12:12674724..12676812,2	MCF-7	breast:
16	chr12:12602118..12604673-chr12:12687247..12689420,2	MCF-7	breast:
17	chr12:12676963..12678914-chr12:12679102..12682035,2	MCF-7	breast:
18	chr12:12672853..12675163-chr12:12712393..12714277,2	K562	blood:
19	chr12:12677909..12679570-chr12:12685352..12687736,2	MCF-7	breast:
20	chr12:12676963..12678914-chr12:12679102..12682035,2	MCF-7	breast:
21	chr12:12681668..12683344-chr12:12686468..12688798,2	MCF-7	breast:
22	chr12:12551031..12553032-chr12:12674320..12676066,2	MCF-7	breast:
23	chr12:12681668..12683344-chr12:12686468..12688798,2	MCF-7	breast:
24	chr12:12675003..12677370-chr12:12678643..12681429,2	K562	blood:
25	chr12:12657662..12660778-chr12:12669355..12673750,5	MCF-7	breast:
26	chr12:12685312..12688917-chr12:12690468..12693651,8	MCF-7	breast:
27	chr12:12676154..12677988-chr12:12685954..12688802,2	MCF-7	breast:
28	chr12:12684001..12705444-chr12:12707828..12718639,50	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR19-3	chr12:12674261-12674397	NONHSAT026985

No data

Variant related genes	Relation type
DUSP16	TF binding region
DUSP16	CpG island
ENSG00000111266	chromatin interactions

Extended variants
information (count: 570 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:570 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7309730	chr12:12673551-12673552	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs200384576	chr12:12673559-12673560	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs73293611	chr12:12673617-12673618	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs3815591	chr12:12673637-12673638	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs78599844	chr12:12673640-12673641	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372032722	chr12:12673762-12673763	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375022019	chr12:12673817-12673818	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs369034520	chr12:12673850-12673851	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs372330415	chr12:12673866-12673867	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs150551431	chr12:12673878-12673879	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs537793872	chr12:12673882-12673883	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151208994	chr12:12673910-12673911	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs79481328	chr12:12673922-12673923	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs199904637	chr12:12673941-12673942	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535245321	chr12:12673952-12673953	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs140424552	chr12:12673957-12673958	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs36049447	chr12:12673965-12673966	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs147374839	chr12:12673967-12673968	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546181616	chr12:12674000-12674001	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs373253988	chr12:12674016-12674017	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs139487616	chr12:12674026-12674027	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201928459	chr12:12674033-12674034	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs376185234	chr12:12674040-12674041	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs543790502	chr12:12674045-12674046	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371763478	chr12:12674079-12674080	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs186720750	chr12:12674107-12674108	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529531363	chr12:12674157-12674158	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs541602232	chr12:12674229-12674230	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs191501155	chr12:12674232-12674233	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184031085	chr12:12674236-12674237	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs527444761	chr12:12674250-12674251	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566064932	chr12:12674292-12674293	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs140396576	chr12:12674334-12674335	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs558280733	chr12:12674357-12674358	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs188713606	chr12:12674366-12674367	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs150288888	chr12:12674401-12674402	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs559943408	chr12:12674402-12674403	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs61913552	chr12:12674425-12674426	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs147568810	chr12:12674469-12674470	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs193153798	chr12:12674474-12674475	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537230159	chr12:12674514-12674515	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs7313936	chr12:12674520-12674521	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs373564185	chr12:12674533-12674534	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553503271	chr12:12674602-12674603	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs565535206	chr12:12674668-12674669	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs556992623	chr12:12674813-12674814	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570702204	chr12:12674827-12674828	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs77421746	chr12:12674838-12674839	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs80070391	chr12:12674839-12674840	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200108328	chr12:12674882-12674883	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	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
Acute lymphoblastic leukemia	17690704	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
Acute lymphoblastic leukemia	21248843	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
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Myelofibrosis	22110671	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:694 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12630800-12681000	Weak transcription	Colonic Mucosa	Colon
2	chr12:12634400-12685200	Weak transcription	Hela-S3	cervix
3	chr12:12639400-12679600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:12641600-12686200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr12:12659800-12674200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:12659800-12678600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr12:12660000-12681800	Weak transcription	Fetal Kidney	kidney
8	chr12:12660400-12686200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr12:12660800-12676600	Weak transcription	Pancreas	Pancrea
10	chr12:12660800-12679800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr12:12664000-12690400	Weak transcription	NHLF	lung
12	chr12:12664800-12673600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr12:12665000-12684400	Weak transcription	NHDF-Ad	bronchial
14	chr12:12665000-12685600	Weak transcription	HMEC	breast
15	chr12:12665000-12686200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr12:12665800-12678800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr12:12666800-12681200	Weak transcription	Colon Smooth Muscle	Colon
18	chr12:12667000-12674400	Strong transcription	Fetal Thymus	thymus
19	chr12:12667000-12675000	Weak transcription	Spleen	Spleen
20	chr12:12667400-12686400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:12667600-12680800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr12:12668000-12680800	Weak transcription	Right Atrium	heart
23	chr12:12668800-12674200	Strong transcription	Placenta	Placenta
24	chr12:12668800-12674600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr12:12669200-12674200	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr12:12669200-12674400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:12669200-12674400	Strong transcription	Adipose Nuclei	Adipose
28	chr12:12670000-12674200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
29	chr12:12670000-12674400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:12670000-12674400	Genic enhancers	Fetal Intestine Large	intestine
31	chr12:12670000-12677400	Enhancers	Stomach Mucosa	stomach
32	chr12:12671000-12674400	Strong transcription	GM12878-XiMat	blood
33	chr12:12671200-12674400	Active TSS	Brain Substantia Nigra	brain
34	chr12:12671200-12674600	Active TSS	Brain Hippocampus Middle	brain
35	chr12:12671200-12676200	Weak transcription	Gastric	stomach
36	chr12:12671200-12677000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr12:12671200-12681200	Weak transcription	HUVEC	blood vessel
38	chr12:12671400-12674200	Genic enhancers	HUES48 Cell Line	embryonic stem cell
39	chr12:12671400-12686200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:12671400-12686200	Weak transcription	Fetal Stomach	stomach
41	chr12:12671600-12674200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
42	chr12:12671600-12674200	Genic enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr12:12671600-12674200	Active TSS	Brain Angular Gyrus	brain
44	chr12:12671600-12675000	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr12:12671600-12678600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
46	chr12:12671600-12680800	Weak transcription	Lung	lung
47	chr12:12671800-12674400	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr12:12672000-12678000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr12:12672400-12674400	Genic enhancers	H1 Cell Line	embryonic stem cell
50	chr12:12672400-12680600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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