Variant report

Variant	esv1808272
Chromosome Location	chr12:122208492-122216042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:914)
CpG islands
(count:122)
Chromatin interactive
region (count:47)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:122211141-122211434	HepG2	liver:	n/a	n/a
2	ATF2	chr12:122214016-122214438	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr12:122211053-122211498	GM12878	blood:	n/a	n/a
4	ATF2	chr12:122213989-122214733	GM12878	blood:	n/a	n/a
5	ATF2	chr12:122214054-122214360	GM12878	blood:	n/a	n/a
6	ATF3	chr12:122213789-122214494	A549	lung:	n/a	n/a
7	ATF3	chr12:122210884-122211520	A549	lung:	n/a	n/a
8	BACH1	chr12:122214086-122214384	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:122212877-122212906	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr12:122213445-122214964	A549	lung:	n/a	n/a
11	BCL3	chr12:122215169-122216141	A549	lung:	n/a	n/a
12	BCL3	chr12:122215038-122216206	A549	lung:	n/a	n/a
13	BCL3	chr12:122213219-122213789	A549	lung:	n/a	n/a
14	BCL3	chr12:122215277-122216031	GM12878	blood:	n/a	n/a
15	BCL3	chr12:122213877-122214828	A549	lung:	n/a	n/a
16	BCLAF1	chr12:122213976-122214438	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:122214086-122214376	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:122214165-122214310	K562	blood:	n/a	n/a
19	BHLHE40	chr12:122211138-122211452	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:122211114-122211433	K562	blood:	n/a	n/a
21	BRCA1	chr12:122211161-122211513	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr12:122211217-122211396	GM12878	blood:	n/a	n/a
23	CBX3	chr12:122214040-122214436	K562	blood:	n/a	n/a
24	CEBPB	chr12:122211206-122211451	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr12:122209206-122209644	MCF-7	breast:	n/a	n/a
26	CEBPB	chr12:122209207-122209672	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr12:122209330-122209604	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr12:122209270-122209596	IMR90	lung:	n/a	n/a
29	CEBPB	chr12:122209249-122209629	A549	lung:	n/a	n/a
30	CEBPB	chr12:122211277-122211366	K562	blood:	n/a	n/a
31	CEBPB	chr12:122209231-122209606	K562	blood:	n/a	n/a
32	CEBPB	chr12:122209192-122209612	K562	blood:	n/a	n/a
33	CEBPB	chr12:122209305-122209536	K562	blood:	n/a	n/a
34	CEBPB	chr12:122209272-122209598	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr12:122209250-122209602	A549	lung:	n/a	n/a
36	CEBPB	chr12:122209173-122209750	A549	lung:	n/a	n/a
37	CEBPB	chr12:122209239-122209598	HepG2	liver:	n/a	n/a
38	CHD2	chr12:122213913-122214611	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr12:122211161-122211630	Hela-S3	cervix:	n/a	n/a
40	CHD2	chr12:122214123-122214402	HepG2	liver:	n/a	n/a
41	CHD2	chr12:122214082-122214577	GM12878	blood:	n/a	n/a
42	CHD2	chr12:122211263-122211472	GM12878	blood:	n/a	n/a
43	CHD2	chr12:122215339-122216067	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr12:122213009-122213040	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr12:122212987-122213481	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr12:122209484-122209730	A549	lung:	n/a	n/a
47	CREB1	chr12:122211114-122211505	A549	lung:	n/a	n/a
48	CREB1	chr12:122214011-122214402	A549	lung:	n/a	n/a
49	CTCF	chr12:122211220-122211370	GM12872	blood:	n/a	n/a
50	CTCF	chr12:122211240-122211390	GM12867	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:122211282-122211332	AG04449	skin:	fetal
2	chr12:122212949-122212999	AG04449	skin:	fetal
3	chr12:122212949-122212999	AG09319	gingival:	n/a
4	chr12:122211282-122211332	SKMC	muscle:	n/a
5	chr12:122211282-122211332	NB4	blood:	n/a
6	chr12:122211282-122211332	H1-hESC	embryonic stem cell:	embryo
7	chr12:122211282-122211332	CMK	blood:	n/a
8	chr12:122212949-122212999	ovcar-3	ovarian:	n/a
9	chr12:122212949-122212999	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:122212949-122212999	HL-60	blood:	n/a
11	chr12:122212949-122212999	SK-N-SH_RA	brain:	n/a
12	chr12:122211282-122211332	NT2-D1	testis:	n/a
13	chr12:122212949-122212999	HUVEC	blood vessel:	n/a
14	chr12:122211282-122211332	HEK293	kidney:	embryo
15	chr12:122212949-122212999	AoSMC	blood vessel:	n/a
16	chr12:122211282-122211332	MCF-7	breast:	n/a
17	chr12:122212949-122212999	HCF	heart:	n/a
18	chr12:122212949-122212999	GM12891	blood:	n/a
19	chr12:122212949-122212999	GM06990	blood:	n/a
20	chr12:122212949-122212999	ECC-1	luminal epithelium:	n/a
21	chr12:122212949-122212999	NT2-D1	testis:	n/a
22	chr12:122212949-122212999	NH-A	brain:	n/a
23	chr12:122211282-122211332	HepG2	liver:	n/a
24	chr12:122211282-122211332	AG10803	skin:	n/a
25	chr12:122211282-122211332	GM06990	blood:	n/a
26	chr12:122211282-122211332	HRE	kidney:	n/a
27	chr12:122212949-122212999	HRE	kidney:	n/a
28	chr12:122211282-122211332	HPAEpiC	pulmonary alveolar:	n/a
29	chr12:122211282-122211332	GM12891	blood:	n/a
30	chr12:122212949-122212999	NHDF-neo	bronchial:	n/a
31	chr12:122211282-122211332	Hepatocyte	liver:	n/a
32	chr12:122211282-122211332	NHBE	bronchial:	n/a
33	chr12:122211282-122211332	SK-N-SH	brain:	n/a
34	chr12:122212949-122212999	AG10803	skin:	n/a
35	chr12:122212949-122212999	SK-N-SH	brain:	n/a
36	chr12:122211282-122211332	PrEC	prostate:	n/a
37	chr12:122211282-122211332	AG09309	skin:	n/a
38	chr12:122212949-122212999	A549	lung:	n/a
39	chr12:122211282-122211332	MCF10A-Er-Src	breast:	n/a
40	chr12:122212949-122212999	HRCEpiC	kidney:	n/a
41	chr12:122212949-122212999	PrEC	prostate:	n/a
42	chr12:122211282-122211332	HCT-116	colon:	n/a
43	chr12:122211282-122211332	T-47D	breast:	n/a
44	chr12:122212949-122212999	HCM	heart:	n/a
45	chr12:122212949-122212999	HRPEpiC	eye:	n/a
46	chr12:122212949-122212999	SK-N-MC	brain:	n/a
47	chr12:122211282-122211332	Hela-S3	cervix:	n/a
48	chr12:122211282-122211332	Jurkat	blood:	n/a
49	chr12:122211282-122211332	HNPCEpiC	eye:	n/a
50	chr12:122212949-122212999	Hela-S3	cervix:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:122186493..122188379-chr12:122211134..122213755,2	K562	blood:
2	chr12:122134662..122135654-chr12:122210878..122211737,2	MCF-7	breast:
3	chr12:122149338..122152297-chr12:122207626..122210986,3	MCF-7	breast:
4	chr12:122207172..122208678-chr12:122212545..122214339,2	MCF-7	breast:
5	chr12:122203003..122205744-chr12:122206968..122208544,2	K562	blood:
6	chr12:122212415..122216174-chr12:122326415..122328726,3	K562	blood:
7	chr12:122189168..122192098-chr12:122209448..122211416,2	K562	blood:
8	chr12:122181449..122183305-chr12:122208481..122211230,2	MCF-7	breast:
9	chr12:122214898..122215746-chr12:122231761..122232743,2	K562	blood:
10	chr12:122203162..122205076-chr12:122211295..122213283,2	K562	blood:
11	chr12:122204123..122206945-chr12:122208235..122211295,4	MCF-7	breast:
12	chr12:122134674..122135744-chr12:122210813..122211800,14	K562	blood:
13	chr12:122154851..122156894-chr12:122210970..122213688,2	MCF-7	breast:
14	chr12:122139766..122142322-chr12:122210806..122212590,2	MCF-7	breast:
15	chr12:122213395..122216201-chr12:122325531..122328146,2	MCF-7	breast:
16	chr12:122134190..122135735-chr12:122208204..122211190,2	K562	blood:
17	chr12:122214138..122216054-chr12:122231373..122233377,2	K562	blood:
18	chr12:122134607..122135427-chr12:122208084..122208877,2	K562	blood:
19	chr12:121990627..121991186-chr12:122210896..122211757,2	K562	blood:
20	chr12:122212254..122213915-chr12:122326858..122328726,2	K562	blood:
21	chr12:122210394..122211915-chr8:144681811..144685202,3	MCF-7	breast:
22	chr12:122191495..122194594-chr12:122209584..122212747,5	MCF-7	breast:
23	chr12:122213296..122215371-chr12:122231546..122233202,23	MCF-7	breast:
24	chr12:122214221..122214729-chr12:122234661..122235608,2	K562	blood:
25	chr12:122196785..122199427-chr12:122208494..122211480,2	MCF-7	breast:
26	chr12:122214559..122216075-chr12:122238255..122240656,2	K562	blood:
27	chr12:122211057..122211772-chr12:122231743..122232368,2	MCF-7	breast:
28	chr12:122207619..122210268-chr12:122236043..122238040,2	K562	blood:
29	chr12:122148985..122154094-chr12:122210649..122217008,11	MCF-7	breast:
30	chr12:121916472..121917415-chr12:122210813..122211489,2	K562	blood:
31	chr12:122209736..122211434-chr12:122241509..122244035,2	K562	blood:
32	chr12:122211020..122211736-chr3:125852890..125853780,2	MCF-7	breast:
33	chr12:122214406..122216955-chr12:122229851..122233377,3	K562	blood:
34	chr12:122209251..122211627-chr12:122216844..122219191,2	K562	blood:
35	chr12:122207127..122210356-chr12:122210673..122214780,4	K562	blood:
36	chr12:122202494..122205546-chr12:122209395..122213283,3	K562	blood:
37	chr12:122134705..122135736-chr12:122210853..122211809,10	MCF-7	breast:
38	chr12:122213768..122214693-chr12:122231771..122233483,12	K562	blood:
39	chr12:122209495..122213691-chr12:122231244..122236279,5	K562	blood:
40	chr12:122165981..122168764-chr12:122207099..122209426,2	K562	blood:
41	chr12:122199720..122201840-chr12:122206766..122209575,2	K562	blood:
42	chr12:122213751..122214258-chr12:122326222..122327055,2	MCF-7	breast:
43	chr12:121935059..121936948-chr12:122215760..122217685,2	MCF-7	breast:
44	chr12:122213783..122214655-chr12:122231473..122233403,7	MCF-7	breast:
45	chr12:122214229..122218603-chr12:122325636..122328202,4	MCF-7	breast:
46	chr12:122215351..122218115-chr12:122220558..122222536,3	K562	blood:
47	chr12:122127171..122128973-chr12:122208402..122210704,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SETD1B-4	chr12:122215983-122216033	NONHSAT031438
2	lnc-SETD1B-4	chr12:122214728-122215803	NONHSAT031441
3	lnc-SETD1B-4	chr12:122215983-122216033	NONHSAT031441
4	lnc-SETD1B-4	chr12:122215983-122216262	NONHSAT031440
5	lnc-SETD1B-4	chr12:122214169-122214350	NONHSAT031438
6	lnc-SETD1B-4	chr12:122214190-122214350	NONHSAT031440
7	lnc-SETD1B-4	chr12:122214281-122214350	NONHSAT031441
8	lnc-SETD1B-4	chr12:122214171-122214350	NONHSAT031439

No data

Variant related genes	Relation type
TMEM120B	TF binding region
TMEM120B	CpG island
ENSG00000139725	chromatin interactions
ENSG00000272849	chromatin interactions
ENSG00000188735	chromatin interactions
ENSG00000110801	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000271912	chromatin interactions
ENSG00000256950	chromatin interactions
ENSG00000139718	chromatin interactions

Extended variants
information (count: 403 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3893308	chr12:122208492-122208493	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs185169118	chr12:122208493-122208494	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548536009	chr12:122208495-122208496	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs567057616	chr12:122208512-122208513	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534398995	chr12:122208516-122208517	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs80320137	chr12:122208522-122208523	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577752304	chr12:122208527-122208528	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538783548	chr12:122208528-122208529	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556976367	chr12:122208538-122208539	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs563280055	chr12:122208631-122208632	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs73411793	chr12:122208638-122208639	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140146628	chr12:122208649-122208650	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7955827	chr12:122208661-122208662	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs190067763	chr12:122208666-122208667	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548300681	chr12:122208668-122208669	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs143776029	chr12:122208670-122208671	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs192732523	chr12:122208678-122208679	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs565342144	chr12:122208700-122208701	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs532601420	chr12:122208705-122208706	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs151285935	chr12:122208706-122208707	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs562858278	chr12:122208717-122208718	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs530314301	chr12:122208727-122208728	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs79944789	chr12:122208767-122208768	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566919388	chr12:122208794-122208795	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs534755619	chr12:122208804-122208805	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184767447	chr12:122208809-122208810	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs139299980	chr12:122208810-122208811	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs375249240	chr12:122208837-122208838	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs200861818	chr12:122208843-122208844	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs368861780	chr12:122208844-122208845	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376403880	chr12:122208848-122208849	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370439191	chr12:122208863-122208864	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs575641179	chr12:122208892-122208893	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536549611	chr12:122208893-122208894	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs372468519	chr12:122208925-122208926	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs573285737	chr12:122208935-122208936	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs540576216	chr12:122208964-122208965	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs558806929	chr12:122208965-122208966	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs28685863	chr12:122208966-122208967	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs11608693	chr12:122208968-122208969	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs367663330	chr12:122208969-122208970	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562721388	chr12:122208970-122208971	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs528852180	chr12:122208971-122208972	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs34623055	chr12:122208989-122208990	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs562585896	chr12:122209016-122209017	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556688948	chr12:122209020-122209021	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs542106552	chr12:122209021-122209022	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188387103	chr12:122209024-122209025	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560372001	chr12:122209030-122209031	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs528075153	chr12:122209031-122209032	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122179800-122211000	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr12:122183800-122224400	Weak transcription	Small Intestine	intestine
3	chr12:122187400-122213800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:122187400-122213800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr12:122189200-122210800	Weak transcription	GM12878-XiMat	blood
6	chr12:122189200-122211000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr12:122190400-122217000	Weak transcription	Esophagus	oesophagus
8	chr12:122193000-122211000	Weak transcription	Pancreas	Pancrea
9	chr12:122193200-122211000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr12:122195000-122211000	Weak transcription	Fetal Thymus	thymus
11	chr12:122195000-122211200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:122195000-122211200	Weak transcription	Thymus	Thymus
13	chr12:122195000-122212600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr12:122195000-122213800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr12:122196200-122211000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr12:122200600-122211000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr12:122200800-122213800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr12:122203400-122208600	Weak transcription	Fetal Kidney	kidney
19	chr12:122203400-122209800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
20	chr12:122203600-122208800	Enhancers	Fetal Brain Male	brain
21	chr12:122203800-122211000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr12:122204000-122211000	Weak transcription	NHEK	skin
23	chr12:122204200-122210800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:122204200-122213400	Weak transcription	Lung	lung
25	chr12:122204600-122209000	Weak transcription	Hela-S3	cervix
26	chr12:122204600-122210800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:122204600-122215400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr12:122204800-122211000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr12:122205000-122211000	Weak transcription	Primary T cells from cord blood	blood
30	chr12:122205600-122209600	Enhancers	Left Ventricle	heart
31	chr12:122205800-122210000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr12:122205800-122210800	Weak transcription	HSMM	muscle
33	chr12:122206000-122216800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:122206200-122209000	Weak transcription	Placenta	Placenta
35	chr12:122206200-122209600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:122206200-122210800	Weak transcription	HSMMtube	muscle
37	chr12:122206200-122211000	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr12:122206200-122211200	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr12:122206400-122210800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr12:122206400-122211000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr12:122206400-122211000	Weak transcription	NH-A	brain
42	chr12:122206400-122211600	Enhancers	Fetal Intestine Large	intestine
43	chr12:122206400-122211800	Enhancers	Adipose Nuclei	Adipose
44	chr12:122206400-122214200	Weak transcription	Gastric	stomach
45	chr12:122206400-122214600	Enhancers	Fetal Heart	heart
46	chr12:122206400-122228200	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr12:122206400-122230600	Weak transcription	Brain Angular Gyrus	brain
48	chr12:122206600-122210600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr12:122206600-122210800	Weak transcription	Duodenum Smooth Muscle	Duodenum
50	chr12:122206600-122211000	Weak transcription	HUES48 Cell Line	embryonic stem cell

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