Variant report

Variant	esv2760888
Chromosome Location	chr12:31232970-31417391
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2154)
CpG islands
(count:1586)
Chromatin interactive
region (count:32)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2154 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31391820-31391981	K562	blood:	n/a	n/a
2	ARID3A	chr12:31399086-31399282	HepG2	liver:	n/a	n/a
3	ATF1	chr12:31365662-31365782	K562	blood:	n/a	n/a
4	ATF1	chr12:31267437-31267611	K562	blood:	n/a	n/a
5	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
6	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
9	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr12:31358978-31359188	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr12:31390681-31390963	GM12878	blood:	n/a	n/a
13	BATF	chr12:31233393-31233591	GM12878	blood:	n/a	n/a
14	BATF	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
15	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
16	BATF	chr12:31233397-31233563	GM12878	blood:	n/a	n/a
17	BCL3	chr12:31357958-31358220	GM12878	blood:	n/a	chr12:31358098-31358107
18	BCL3	chr12:31236203-31236417	GM12878	blood:	n/a	n/a
19	BCL3	chr12:31236196-31236433	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:31391786-31392031	K562	blood:	n/a	n/a
25	BHLHE40	chr12:31390183-31390447	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
28	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
29	BRCA1	chr12:31390019-31390036	GM12878	blood:	n/a	n/a
30	BRCA1	chr12:31391842-31392078	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr12:31358885-31359398	HCT-116	colon:	n/a	n/a
32	CEBPB	chr12:31391866-31392108	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
34	CEBPB	chr12:31401755-31402127	A549	lung:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
35	CEBPB	chr12:31401823-31402021	Hela-S3	cervix:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
36	CEBPB	chr12:31355347-31355432	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:31268138-31268370	H1-hESC	embryonic stem cell:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
38	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
39	CEBPB	chr12:31401830-31402026	HepG2	liver:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
40	CEBPB	chr12:31414835-31414948	K562	blood:	n/a	n/a
41	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
42	CEBPB	chr12:31395234-31395493	IMR90	lung:	n/a	n/a
43	CEBPB	chr12:31395273-31395514	HepG2	liver:	n/a	n/a
44	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
45	CEBPB	chr12:31391806-31392080	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
48	CHD2	chr12:31271851-31272155	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr12:31253424-31253892	GM12878	blood:	n/a	n/a
50	CHD2	chr12:31271857-31272216	K562	blood:	n/a	n/a

(count:1586 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31271429-31271479	HCT-116	colon:	n/a
2	chr12:31405359-31405409	NB4	blood:	n/a
3	chr12:31272865-31272915	HNPCEpiC	eye:	n/a
4	chr12:31271429-31271479	BE2_C	brain:	n/a
5	chr12:31254007-31254057	AG09319	gingival:	n/a
6	chr12:31405359-31405409	GM12891	blood:	n/a
7	chr12:31360362-31360412	Hela-S3	cervix:	n/a
8	chr12:31360362-31360412	T-47D	breast:	n/a
9	chr12:31257362-31257412	HMEC	breast:	n/a
10	chr12:31271429-31271479	HEK293	kidney:	embryo
11	chr12:31360362-31360412	HCPEpiC	choroid plexus:	n/a
12	chr12:31370930-31370980	NHDF-neo	bronchial:	n/a
13	chr12:31257362-31257412	MCF-7	breast:	n/a
14	chr12:31272114-31272164	NH-A	brain:	n/a
15	chr12:31412980-31413030	BE2_C	brain:	n/a
16	chr12:31405369-31405419	NB4	blood:	n/a
17	chr12:31272114-31272164	SK-N-SH	brain:	n/a
18	chr12:31271783-31271833	MCF-7	breast:	n/a
19	chr12:31272865-31272915	K562	blood:	n/a
20	chr12:31402470-31402520	ovcar-3	ovarian:	n/a
21	chr12:31402470-31402520	HCPEpiC	choroid plexus:	n/a
22	chr12:31233201-31233251	PANC-1	pancreas:	n/a
23	chr12:31271429-31271479	HIPEpiC	eye:	n/a
24	chr12:31316348-31316398	K562	blood:	n/a
25	chr12:31274424-31274474	HEEpiC	esophagus:	n/a
26	chr12:31241496-31241546	SKMC	muscle:	n/a
27	chr12:31378024-31378074	GM12892	blood:	n/a
28	chr12:31271783-31271833	ProgFib	skin:	n/a
29	chr12:31378024-31378074	PrEC	prostate:	n/a
30	chr12:31257362-31257412	PrEC	prostate:	n/a
31	chr12:31405499-31405549	HCT-116	colon:	n/a
32	chr12:31276852-31276902	ProgFib	skin:	n/a
33	chr12:31271429-31271479	NHDF-neo	bronchial:	n/a
34	chr12:31241496-31241546	NHBE	bronchial:	n/a
35	chr12:31256838-31256888	SKMC	muscle:	n/a
36	chr12:31370930-31370980	GM12878	blood:	n/a
37	chr12:31412980-31413030	GM12891	blood:	n/a
38	chr12:31272114-31272164	HCPEpiC	choroid plexus:	n/a
39	chr12:31272865-31272915	MCF-7	breast:	n/a
40	chr12:31272112-31272162	T-47D	breast:	n/a
41	chr12:31405369-31405419	MCF-7	breast:	n/a
42	chr12:31256838-31256888	Caco-2	colon:	n/a
43	chr12:31241496-31241546	HCM	heart:	n/a
44	chr12:31274424-31274474	IMR90	lung:	fetal
45	chr12:31272865-31272915	SAEC	small airway:	n/a
46	chr12:31378024-31378074	GM12891	blood:	n/a
47	chr12:31276852-31276902	HRE	kidney:	n/a
48	chr12:31256838-31256888	LNCaP	prostate:	n/a
49	chr12:31256838-31256888	H1-hESC	embryonic stem cell:	embryo
50	chr12:31405499-31405549	GM19239	blood:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
2	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
3	chr12:31358059..31360304-chr12:31368898..31371452,2	MCF-7	breast:
4	chr12:31406545..31409230-chr12:31409522..31411986,2	MCF-7	breast:
5	chr12:31354080..31355986-chr12:31357943..31360954,3	K562	blood:
6	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
7	chr12:31403415..31403922-chr12:31424976..31425527,2	MCF-7	breast:
8	chr12:31269781..31270824-chr12:31398705..31400061,4	MCF-7	breast:
9	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
10	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
11	chr12:31388279..31391169-chr12:31396495..31398764,2	K562	blood:
12	chr12:31226022..31227620-chr12:31260408..31262678,2	MCF-7	breast:
13	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
14	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
15	chr12:31354464..31355986-chr12:31358238..31360954,2	K562	blood:
16	chr12:31379295..31381181-chr12:31382279..31384326,2	MCF-7	breast:
17	chr12:31362737..31365081-chr12:31371772..31373605,2	MCF-7	breast:
18	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
19	chr12:31412613..31414977-chr12:31423446..31425840,2	K562	blood:
20	chr12:31399094..31400618-chr12:31401527..31404209,2	K562	blood:
21	chr12:31269688..31270486-chr12:31404974..31405959,2	K562	blood:
22	chr12:31399111..31400912-chr12:31476871..31479529,2	MCF-7	breast:
23	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
24	chr12:31367559..31369470-chr12:31371193..31372754,2	MCF-7	breast:
25	chr12:30999874..31000492-chr12:31398859..31399728,2	K562	blood:
26	chr12:31269943..31270748-chr12:31391487..31392373,2	K562	blood:
27	chr12:31402332..31404405-chr12:31413108..31415272,2	MCF-7	breast:
28	chr12:31269317..31270662-chr12:31391620..31392355,3	MCF-7	breast:
29	chr12:31402402..31404809-chr12:31411238..31413851,2	K562	blood:
30	chr12:31375655..31377165-chr12:31378438..31380681,2	K562	blood:
31	chr12:31379791..31381896-chr12:31385949..31387933,2	MCF-7	breast:
32	chr12:31391273..31391961-chr12:31404788..31405659,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM60A-7	chr12:31267330-31267397	NONHSAT027538
2	lnc-AC024940.1-3	chr12:31397374-31397619	NONHSAT027541
3	lnc-FAM60A-6	chr12:31270354-31270558	NONHSAT140066
4	lnc-FAM60A-4	chr12:31367135-31367371	expReg_chr12_2391_-
5	lnc-FAM60A-2	chr12:31412950-31413502	ucscGeneNc_uc001rkg_2
6	lnc-FAM60A-7	chr12:31264627-31264743	NONHSAT027538
7	lnc-FAM60A-2	chr12:31407684-31407996	ucscGeneNc_uc001rkg_2
8	lnc-FAM60A-7	chr12:31265915-31266017	NONHSAT027538
9	lnc-FAM60A-6	chr12:31269291-31269403	NONHSAT140066

No data

Variant related genes	Relation type
ENSG00000270926	TF binding region
ENSG00000212533	TF binding region
ENSG00000270766	TF binding region
ENSG00000270395	TF binding region
ENSG00000243517	TF binding region
ENSG00000177359	TF binding region
DDX11	TF binding region
ENSG00000270926	CpG island
ENSG00000212533	CpG island
ENSG00000270766	CpG island
ENSG00000270395	CpG island
ENSG00000243517	CpG island
ENSG00000177359	CpG island
DDX11	CpG island
ENSG00000270766	chromatin interactions
ENSG00000013573	chromatin interactions
ENSG00000245614	chromatin interactions
ENSG00000270395	chromatin interactions
ENSG00000177340	chromatin interactions
ENSG00000177359	chromatin interactions
ENSG00000139146	chromatin interactions
ENSG00000243517	chromatin interactions

Extended variants
information (count: 5641 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:5641 , 50 per page) page: 1 2 3 4 5 6 7 ... 113

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113463265	chr12:31233023-31233024	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
2	rs74087920	chr12:31233053-31233054	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs572680730	chr12:31233071-31233072	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs543204008	chr12:31233078-31233079	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs184960731	chr12:31233104-31233105	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs71440936	chr12:31233164-31233165	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs71455611	chr12:31233201-31233202	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs139732454	chr12:31233250-31233251	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region CpG island	2 gene(s)	Overlapped CNVs	n/a
9	rs532349850	chr12:31233257-31233258	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs184025336	chr12:31233316-31233317	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs547883497	chr12:31233342-31233343	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs188957546	chr12:31233358-31233359	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs143082531	chr12:31233379-31233380	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs192994348	chr12:31233401-31233402	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs530615174	chr12:31233408-31233409	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs551928182	chr12:31233409-31233410	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs555176462	chr12:31233431-31233432	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs534278678	chr12:31233448-31233449	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs4031360	chr12:31233519-31233520	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	mRNA abundance
20	rs5797398	chr12:31233538-31233539	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs569268209	chr12:31233572-31233573	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs368402573	chr12:31233602-31233603	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs148713756	chr12:31233623-31233624	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs536860223	chr12:31233646-31233647	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs555181338	chr12:31233704-31233705	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs576499114	chr12:31233728-31233729	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs142289055	chr12:31233804-31233805	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs4031361	chr12:31233828-31233829	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183004333	chr12:31233838-31233839	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150851196	chr12:31233842-31233843	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2432998	chr12:31233889-31233890	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs2432997	chr12:31233900-31233901	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs4031364	chr12:31233952-31233953	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7309520	chr12:31233957-31233958	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs2352619	chr12:31233959-31233960	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183856883	chr12:31233961-31233962	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139329335	chr12:31233962-31233963	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4031334	chr12:31233984-31233985	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs2432996	chr12:31234014-31234015	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs563135505	chr12:31234023-31234024	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530567661	chr12:31234036-31234037	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4031336	chr12:31234061-31234062	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4031337	chr12:31234067-31234068	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4031338	chr12:31234072-31234073	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563988915	chr12:31234116-31234117	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4031339	chr12:31234130-31234131	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528107288	chr12:31234161-31234162	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11051237	chr12:31234168-31234169	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566405776	chr12:31234217-31234218	Enhancers Genic enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536934375	chr12:31234224-31234225	Enhancers Genic enhancers Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	22522925	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2161 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31227600-31235600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:31227600-31235800	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr12:31227600-31236800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr12:31227600-31237000	Weak transcription	Aorta	Aorta
5	chr12:31227800-31233600	Weak transcription	Fetal Intestine Large	intestine
6	chr12:31227800-31234000	Weak transcription	Esophagus	oesophagus
7	chr12:31227800-31235600	Weak transcription	Primary B cells from cord blood	blood
8	chr12:31227800-31235600	Weak transcription	Fetal Intestine Small	intestine
9	chr12:31227800-31235800	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr12:31227800-31236000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr12:31227800-31236800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr12:31227800-31236800	Weak transcription	Brain Hippocampus Middle	brain
13	chr12:31227800-31237000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:31227800-31237000	Weak transcription	Gastric	stomach
15	chr12:31227800-31237000	Weak transcription	Lung	lung
16	chr12:31227800-31237000	Weak transcription	Right Ventricle	heart
17	chr12:31227800-31237400	Weak transcription	Ovary	ovary
18	chr12:31227800-31240200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr12:31227800-31242000	Weak transcription	Left Ventricle	heart
20	chr12:31227800-31242600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr12:31227800-31266400	Weak transcription	HSMMtube	muscle
22	chr12:31228000-31233000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:31228000-31233000	Weak transcription	NHEK	skin
24	chr12:31228000-31233600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr12:31228000-31233600	Weak transcription	Stomach Smooth Muscle	stomach
26	chr12:31228000-31233800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr12:31228000-31233800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr12:31228000-31234000	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr12:31228000-31234200	Weak transcription	Fetal Muscle Leg	muscle
30	chr12:31228000-31235200	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr12:31228000-31235600	Weak transcription	Thymus	Thymus
32	chr12:31228000-31235800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr12:31228000-31235800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:31228000-31235800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr12:31228000-31235800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr12:31228000-31235800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr12:31228000-31236000	Weak transcription	Fetal Muscle Trunk	muscle
38	chr12:31228000-31236200	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr12:31228000-31236600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr12:31228000-31236600	Weak transcription	Brain Germinal Matrix	brain
41	chr12:31228000-31236600	Weak transcription	Placenta	Placenta
42	chr12:31228000-31236800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr12:31228000-31236800	Weak transcription	Colonic Mucosa	Colon
44	chr12:31228000-31237000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:31228000-31237000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:31228000-31237000	Weak transcription	Adipose Nuclei	Adipose
47	chr12:31228000-31237000	Weak transcription	Brain Anterior Caudate	brain
48	chr12:31228000-31237000	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr12:31228000-31237000	Weak transcription	Pancreas	Pancrea
50	chr12:31228000-31237000	Weak transcription	Rectal Mucosa Donor 31	rectum

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