Variant report

Variant	esv1823607
Chromosome Location	chr12:104506318-104549541
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:940)
CpG islands
(count:795)
Chromatin interactive
region (count:84)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:940 , 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	chr12:104531844-104532097	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:104525456-104525662	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:104549428-104549945	K562	blood:	n/a	n/a
4	ATF1	chr12:104548203-104548427	K562	blood:	n/a	n/a
5	ATF2	chr12:104531677-104532104	GM12878	blood:	n/a	n/a
6	ATF2	chr12:104531766-104532062	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr12:104531777-104532351	A549	lung:	n/a	n/a
8	BACH1	chr12:104531077-104531218	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:104531839-104532100	GM12878	blood:	n/a	n/a
10	BCL3	chr12:104531716-104532463	A549	lung:	n/a	chr12:104532036-104532045 chr12:104532401-104532410 chr12:104532174-104532183
11	BCL3	chr12:104514668-104515387	A549	lung:	n/a	chr12:104514969-104514978 chr12:104514891-104514898
12	BCLAF1	chr12:104531764-104532118	GM12878	blood:	n/a	chr12:104532036-104532045
13	BCLAF1	chr12:104531731-104532209	GM12878	blood:	n/a	chr12:104532036-104532045 chr12:104532174-104532183
14	BCLAF1	chr12:104530703-104531373	GM12878	blood:	n/a	n/a
15	BHLHE40	chr12:104531797-104532337	K562	blood:	n/a	n/a
16	BHLHE40	chr12:104531679-104532329	HepG2	liver:	n/a	n/a
17	BHLHE40	chr12:104531812-104532099	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:104531274-104531321	GM12878	blood:	n/a	n/a
19	BRCA1	chr12:104531864-104532064	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr12:104531880-104532070	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr12:104532366-104532463	HepG2	liver:	n/a	n/a
22	BRCA1	chr12:104532027-104532072	GM12878	blood:	n/a	n/a
23	BRCA1	chr12:104532312-104532329	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr12:104531739-104532735	K562	blood:	n/a	n/a
25	CBX3	chr12:104531726-104532544	HCT-116	colon:	n/a	n/a
26	CBX3	chr12:104532099-104532313	K562	blood:	n/a	n/a
27	CCNT2	chr12:104531162-104532555	K562	blood:	n/a	chr12:104531268-104531277
28	CCNT2	chr12:104548815-104549179	K562	blood:	n/a	n/a
29	CEBPB	chr12:104531877-104532046	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr12:104535283-104535476	HepG2	liver:	n/a	chr12:104535316-104535327
31	CEBPB	chr12:104548375-104548376	HepG2	liver:	n/a	n/a
32	CEBPB	chr12:104525427-104525762	HepG2	liver:	n/a	n/a
33	CEBPB	chr12:104514763-104515233	A549	lung:	n/a	n/a
34	CEBPB	chr12:104548315-104548507	K562	blood:	n/a	n/a
35	CEBPB	chr12:104531828-104532155	Hela-S3	cervix:	n/a	n/a
36	CEBPD	chr12:104531596-104531953	HepG2	liver:	n/a	n/a
37	CEBPD	chr12:104531053-104531540	HepG2	liver:	n/a	n/a
38	CEBPD	chr12:104531997-104532367	HepG2	liver:	n/a	n/a
39	CHD1	chr12:104530515-104531269	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr12:104531530-104531992	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr12:104530868-104532056	GM12878	blood:	n/a	n/a
42	CHD2	chr12:104531768-104532683	K562	blood:	n/a	n/a
43	CHD2	chr12:104531722-104532380	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr12:104531776-104532367	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr12:104531081-104531332	GM12878	blood:	n/a	n/a
46	CHD2	chr12:104531781-104532351	GM12878	blood:	n/a	n/a
47	CHD2	chr12:104531788-104532527	HepG2	liver:	n/a	n/a
48	CREB1	chr12:104531728-104532290	HepG2	liver:	n/a	n/a
49	CREB1	chr12:104531759-104532301	GM12878	blood:	n/a	n/a
50	CREB1	chr12:104531546-104532447	HepG2	liver:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:104530941-104530991	Hela-S3	cervix:	n/a
2	chr12:104532339-104532389	AG09309	skin:	n/a
3	chr12:104530941-104530991	Hela-S3	cervix:	n/a
4	chr12:104532339-104532389	AG09309	skin:	n/a
5	chr12:104532011-104532061	HUVEC	blood vessel:	n/a
6	chr12:104513155-104513205	SK-N-SH	brain:	n/a
7	chr12:104526470-104526520	NHDF-neo	bronchial:	n/a
8	chr12:104530941-104530991	LNCaP	prostate:	n/a
9	chr12:104531175-104531225	PANC-1	pancreas:	n/a
10	chr12:104536393-104536443	HCT-116	colon:	n/a
11	chr12:104530941-104530991	GM12878	blood:	n/a
12	chr12:104532907-104532957	HNPCEpiC	eye:	n/a
13	chr12:104532339-104532389	HEEpiC	esophagus:	n/a
14	chr12:104532011-104532061	HepG2	liver:	n/a
15	chr12:104532524-104532574	AG10803	skin:	n/a
16	chr12:104532907-104532957	SKMC	muscle:	n/a
17	chr12:104513155-104513205	NB4	blood:	n/a
18	chr12:104530941-104530991	HRPEpiC	eye:	n/a
19	chr12:104528079-104528129	AG10803	skin:	n/a
20	chr12:104531891-104531941	NH-A	brain:	n/a
21	chr12:104532377-104532427	Caco-2	colon:	n/a
22	chr12:104532524-104532574	U87	brain:	n/a
23	chr12:104532377-104532427	AG04450	lung:	fetal
24	chr12:104528079-104528129	SK-N-SH_RA	brain:	n/a
25	chr12:104530941-104530991	U87	brain:	n/a
26	chr12:104528079-104528129	MCF-7	breast:	n/a
27	chr12:104532907-104532957	HAEpiC	amniotic membrane:	n/a
28	chr12:104532907-104532957	K562	blood:	n/a
29	chr12:104516317-104516367	ECC-1	luminal epithelium:	n/a
30	chr12:104526470-104526520	PFSK-1	brain:	n/a
31	chr12:104536393-104536443	HRE	kidney:	n/a
32	chr12:104531891-104531941	HNPCEpiC	eye:	n/a
33	chr12:104530941-104530991	Caco-2	colon:	n/a
34	chr12:104528079-104528129	HMEC	breast:	n/a
35	chr12:104516317-104516367	GM12878	blood:	n/a
36	chr12:104530941-104530991	RPTEC	kidney:	n/a
37	chr12:104532524-104532574	NHDF-neo	bronchial:	n/a
38	chr12:104536393-104536443	PANC-1	pancreas:	n/a
39	chr12:104532524-104532574	Hepatocyte	liver:	n/a
40	chr12:104526470-104526520	HAEpiC	amniotic membrane:	n/a
41	chr12:104532524-104532574	HRE	kidney:	n/a
42	chr12:104526470-104526520	NB4	blood:	n/a
43	chr12:104532377-104532427	NHDF-neo	bronchial:	n/a
44	chr12:104530941-104530991	SKMC	muscle:	n/a
45	chr12:104536393-104536443	GM12878	blood:	n/a
46	chr12:104516317-104516367	PrEC	prostate:	n/a
47	chr12:104528079-104528129	Hela-S3	cervix:	n/a
48	chr12:104531175-104531225	HCM	heart:	n/a
49	chr12:104528079-104528129	CMK	blood:	n/a
50	chr12:104532377-104532427	IMR90	lung:	fetal

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:104503448..104507553-chr12:104508039..104511568,3	MCF-7	breast:
2	chr12:104530429..104534144-chr12:104679811..104684673,6	MCF-7	breast:
3	chr12:104234047..104236214-chr12:104531313..104532962,2	MCF-7	breast:
4	chr12:104322442..104325161-chr12:104524149..104527737,3	K562	blood:
5	chr12:104481200..104483346-chr12:104529918..104531545,2	K562	blood:
6	chr12:104515519..104518229-chr12:104522556..104526007,3	MCF-7	breast:
7	chr12:104513301..104516062-chr12:104519027..104521801,2	MCF-7	breast:
8	chr12:104531440..104533678-chr17:57914653..57916695,2	MCF-7	breast:
9	chr12:104545972..104549947-chr12:104555023..104560302,4	K562	blood:
10	chr12:104530782..104534411-chr12:104679881..104682289,3	K562	blood:
11	chr12:104513301..104516062-chr12:104519027..104521801,2	MCF-7	breast:
12	chr1:154946283..154947051-chr12:104531811..104532400,2	Hela-S3	cervix:
13	chr12:104531360..104532346-chr4:185395679..185396224,2	Hela-S3	cervix:
14	chr12:104529986..104533486-chr12:104678703..104682517,5	MCF-7	breast:
15	chr12:104456193..104459744-chr12:104529847..104533076,6	K562	blood:
16	chr12:104356409..104362053-chr12:104528975..104533138,7	MCF-7	breast:
17	chr12:104534094..104536721-chr12:104557947..104560428,2	MCF-7	breast:
18	chr12:104532395..104534218-chr12:104535636..104537137,2	K562	blood:
19	chr12:104457763..104459399-chr12:104511021..104513721,2	K562	blood:
20	chr12:104534231..104536425-chr12:104537537..104539299,2	K562	blood:
21	chr12:104521574..104524477-chr12:105501454..105503015,2	MCF-7	breast:
22	chr12:104536331..104537899-chr12:104541231..104543008,2	K562	blood:
23	chr12:104508030..104510211-chr12:104530373..104532165,2	MCF-7	breast:
24	chr12:104528832..104532197-chr12:105351511..105353407,3	MCF-7	breast:
25	chr12:104500985..104502634-chr12:104512619..104514999,2	MCF-7	breast:
26	chr12:104529888..104531745-chr12:104641591..104644080,2	MCF-7	breast:
27	chr12:104531343..104532062-chr14:24036745..24037302,2	HCT-116	colon:
28	chr12:104513649..104515856-chr12:104516374..104518763,2	MCF-7	breast:
29	chr12:104501111..104503090-chr12:104506610..104509450,2	K562	blood:
30	chr12:104531573..104532274-chr3:49058505..49059412,2	Hela-S3	cervix:
31	chr12:104513649..104515856-chr12:104516374..104518763,2	MCF-7	breast:
32	chr12:104531173..104532708-chr12:104546943..104548666,2	MCF-7	breast:
33	chr12:104348297..104351124-chr12:104530392..104533056,3	MCF-7	breast:
34	chr12:104530438..104533662-chr12:104564030..104567253,5	K562	blood:
35	chr12:104528672..104531458-chr12:104545242..104548166,3	K562	blood:
36	chr12:104529255..104533674-chr12:104537632..104543794,8	K562	blood:
37	chr12:104530514..104533012-chr12:104679009..104681675,2	K562	blood:
38	chr12:104263974..104266600-chr12:104512244..104514894,2	MCF-7	breast:
39	chr12:104512826..104514662-chr12:104519104..104521337,2	K562	blood:
40	chr12:104322684..104325586-chr12:104530441..104532019,2	K562	blood:
41	chr12:104512826..104514662-chr12:104519104..104521337,2	K562	blood:
42	chr12:104515373..104518868-chr12:104529903..104532012,3	K562	blood:
43	chr12:104358049..104359986-chr12:104530882..104532737,3	K562	blood:
44	chr12:104528011..104530810-chr12:104621683..104623795,2	K562	blood:
45	chr12:104526354..104529452-chr12:104565610..104568678,3	MCF-7	breast:
46	chr12:104455182..104458865-chr12:104529769..104532559,3	MCF-7	breast:
47	chr12:104510515..104519727-chr12:104525085..104533754,15	MCF-7	breast:
48	chr12:104499633..104501724-chr12:104506063..104508976,2	MCF-7	breast:
49	chr12:104542011..104544016-chr12:104556575..104558622,2	MCF-7	breast:
50	chr12:104531363..104532174-chr20:25228138..25229130,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLT8D2-1	chr12:104529226-104529310	NONHSAT030410
2	lnc-GLT8D2-1	chr12:104524910-104525616	NONHSAT030410
3	lnc-GLT8D2-1	chr12:104531919-104532040	NONHSAT030410

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NFYB	hsa-miR-30c-5p	chr12:104512867-104512889
2	NFYB	hsa-miR-30c-5p	chr12:104512873-104512866
3	NFYB	hsa-miR-181a-5p	chr12:104513090-104513112
4	NFYB	hsa-miR-181a-5p	chr12:104510936-104510958
5	NFYB	hsa-miR-181a-5p	chr12:104513330-104513352
6	NFYB	hsa-miR-181a-5p	chr12:104511019-104511040

Variant related genes	Relation type
NFYB	TF binding region
RNA5SP370	TF binding region
NFYB	CpG island
RNA5SP370	CpG island
ENSG00000160691	chromatin interactions
ENSG00000214198	chromatin interactions
ENSG00000204954	chromatin interactions
ENSG00000120820	chromatin interactions
ENSG00000136051	chromatin interactions
ENSG00000168310	chromatin interactions
ENSG00000139291	chromatin interactions
ENSG00000257999	chromatin interactions
ENSG00000265072	chromatin interactions
ENSG00000257193	chromatin interactions
ENSG00000166598	chromatin interactions
ENSG00000268364	chromatin interactions
ENSG00000143158	chromatin interactions
ENSG00000111727	chromatin interactions
ENSG00000153721	chromatin interactions
ENSG00000213983	chromatin interactions
ENSG00000257327	chromatin interactions
ENSG00000139372	chromatin interactions
ENSG00000198887	chromatin interactions
ENSG00000271646	chromatin interactions
ENSG00000173567	chromatin interactions
ENSG00000100994	chromatin interactions
ENSG00000199415	chromatin interactions
ENSG00000178149	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000111696	chromatin interactions
ENSG00000198431	chromatin interactions
ENSG00000136052	chromatin interactions
ENSG00000143164	chromatin interactions
ENSG00000178057	chromatin interactions
ENSG00000120837	chromatin interactions

Extended variants
information (count: 1479 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10861159	chr12:104506318-104506319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564218859	chr12:104506331-104506332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141559303	chr12:104506358-104506359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs373547365	chr12:104506383-104506384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142538562	chr12:104506389-104506390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150908310	chr12:104506414-104506415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563253535	chr12:104506438-104506439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529650127	chr12:104506474-104506475	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115522582	chr12:104506498-104506499	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115968528	chr12:104506537-104506538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528685208	chr12:104506549-104506550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551639856	chr12:104506564-104506565	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571420769	chr12:104506569-104506570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12580691	chr12:104506585-104506586	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs550587747	chr12:104506616-104506617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs11376222	chr12:104506666-104506667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553535340	chr12:104506667-104506668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs56675552	chr12:104506686-104506687	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567305844	chr12:104506708-104506709	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs535423611	chr12:104506753-104506754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549386310	chr12:104506907-104506908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs4964534	chr12:104506922-104506923	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs191925909	chr12:104506934-104506935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557641370	chr12:104506951-104506952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs111888426	chr12:104506961-104506962	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184854135	chr12:104506964-104506965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145057073	chr12:104507049-104507050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376606683	chr12:104507074-104507075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563315194	chr12:104507078-104507079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573678726	chr12:104507088-104507089	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542214880	chr12:104507093-104507094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187755565	chr12:104507112-104507113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528743343	chr12:104507185-104507186	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs58671692	chr12:104507199-104507200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59792967	chr12:104507211-104507212	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs59111719	chr12:104507216-104507217	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs60515547	chr12:104507240-104507241	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192772546	chr12:104507242-104507243	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370401722	chr12:104507280-104507281	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184262442	chr12:104507303-104507304	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550650987	chr12:104507312-104507313	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377743581	chr12:104507353-104507354	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564234652	chr12:104507363-104507364	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189326507	chr12:104507375-104507376	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372604895	chr12:104507380-104507381	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs112686439	chr12:104507439-104507440	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73392505	chr12:104507480-104507481	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565988492	chr12:104507512-104507513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534594106	chr12:104507534-104507535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374237018	chr12:104507595-104507596	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	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
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:1612 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104460000-104511800	Weak transcription	Hela-S3	cervix
2	chr12:104460000-104526200	Weak transcription	Colonic Mucosa	Colon
3	chr12:104477200-104508400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr12:104480000-104508400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr12:104482800-104508200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr12:104491000-104508600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr12:104492000-104512400	Weak transcription	HMEC	breast
8	chr12:104493200-104512400	Weak transcription	Rectal Smooth Muscle	rectum
9	chr12:104493200-104514400	Weak transcription	NHEK	skin
10	chr12:104493400-104511800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr12:104493400-104513400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr12:104493400-104514400	Weak transcription	Brain Substantia Nigra	brain
13	chr12:104493400-104519200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr12:104493400-104519800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr12:104493600-104510800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:104493600-104517400	Weak transcription	Right Ventricle	heart
17	chr12:104493800-104515400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr12:104493800-104518400	Weak transcription	Gastric	stomach
19	chr12:104493800-104530600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr12:104494200-104509200	Weak transcription	Fetal Brain Male	brain
21	chr12:104494400-104508000	Weak transcription	GM12878-XiMat	blood
22	chr12:104494400-104513600	Weak transcription	Brain Germinal Matrix	brain
23	chr12:104494400-104514000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:104494400-104516200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:104494400-104516200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:104494400-104521000	Weak transcription	Lung	lung
27	chr12:104494400-104521200	Weak transcription	Aorta	Aorta
28	chr12:104494400-104522600	Weak transcription	Spleen	Spleen
29	chr12:104494600-104516000	Weak transcription	Fetal Stomach	stomach
30	chr12:104494800-104508400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr12:104494800-104509000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr12:104494800-104509200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr12:104495400-104506400	Weak transcription	Fetal Intestine Small	intestine
34	chr12:104495600-104508400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr12:104495600-104508400	Weak transcription	Fetal Intestine Large	intestine
36	chr12:104495600-104509000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr12:104495600-104510800	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr12:104495600-104514200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr12:104495600-104530800	Weak transcription	Esophagus	oesophagus
40	chr12:104495800-104508200	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr12:104496000-104508400	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr12:104497000-104506800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr12:104497000-104508200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr12:104497000-104508600	Weak transcription	HUVEC	blood vessel
45	chr12:104497000-104509600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr12:104497000-104514200	Weak transcription	NHLF	lung
47	chr12:104497000-104516000	Weak transcription	Ovary	ovary
48	chr12:104497000-104516200	Weak transcription	Left Ventricle	heart
49	chr12:104497000-104524600	Weak transcription	Pancreas	Pancrea
50	chr12:104497200-104508200	Weak transcription	Fetal Brain Female	brain

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