Variant report

Variant	nsv558038
Chromosome Location	chr12:31247098-31410821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2019)
CpG islands
(count:1405)
Chromatin interactive
region (count:29)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2019 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:31399086-31399282	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:31391820-31391981	K562	blood:	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	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr12:31270089-31270375	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
8	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
10	BACH1	chr12:31270094-31270475	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr12:31358978-31359188	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
13	BATF	chr12:31390681-31390963	GM12878	blood:	n/a	n/a
14	BATF	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
15	BCL3	chr12:31357958-31358220	GM12878	blood:	n/a	chr12:31358098-31358107
16	BHLHE40	chr12:31390183-31390447	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
19	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
21	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:31391786-31392031	K562	blood:	n/a	n/a
23	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
24	BRCA1	chr12:31391842-31392078	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr12:31390019-31390036	GM12878	blood:	n/a	n/a
26	BRCA1	chr12:31270178-31270208	GM12878	blood:	n/a	n/a
27	CBX3	chr12:31358885-31359398	HCT-116	colon:	n/a	n/a
28	CEBPB	chr12:31395234-31395493	IMR90	lung:	n/a	n/a
29	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
30	CEBPB	chr12:31268138-31268370	H1-hESC	embryonic stem cell:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
31	CEBPB	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
32	CEBPB	chr12:31355347-31355432	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr12:31391866-31392108	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
35	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr12:31395273-31395514	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
38	CEBPB	chr12:31391806-31392080	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr12:31268025-31268366	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
40	CEBPB	chr12:31401823-31402021	Hela-S3	cervix:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
41	CEBPB	chr12:31401755-31402127	A549	lung:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
42	CEBPB	chr12:31401830-31402026	HepG2	liver:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
43	CHD2	chr12:31270114-31270314	GM12878	blood:	n/a	n/a
44	CHD2	chr12:31271857-31272216	K562	blood:	n/a	n/a
45	CHD2	chr12:31358885-31359207	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr12:31253424-31253892	GM12878	blood:	n/a	n/a
47	CHD2	chr12:31270194-31270459	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr12:31271974-31272145	GM12878	blood:	n/a	n/a
49	CHD2	chr12:31371770-31371778	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr12:31271851-31272155	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31272114-31272164	HRE	kidney:	n/a
2	chr12:31360362-31360412	AG04449	skin:	fetal
3	chr12:31272114-31272164	HRE	kidney:	n/a
4	chr12:31360362-31360412	AG04449	skin:	fetal
5	chr12:31274424-31274474	GM12878	blood:	n/a
6	chr12:31406441-31406491	RPTEC	kidney:	n/a
7	chr12:31405499-31405549	HAEpiC	amniotic membrane:	n/a
8	chr12:31255279-31255329	NHBE	bronchial:	n/a
9	chr12:31254007-31254057	SK-N-SH	brain:	n/a
10	chr12:31272865-31272915	AoSMC	blood vessel:	n/a
11	chr12:31270326-31270376	IMR90	lung:	fetal
12	chr12:31405359-31405409	LNCaP	prostate:	n/a
13	chr12:31360362-31360412	HepG2	liver:	n/a
14	chr12:31254036-31254086	SKMC	muscle:	n/a
15	chr12:31316348-31316398	HNPCEpiC	eye:	n/a
16	chr12:31271783-31271833	HCPEpiC	choroid plexus:	n/a
17	chr12:31272119-31272169	HRPEpiC	eye:	n/a
18	chr12:31370930-31370980	ProgFib	skin:	n/a
19	chr12:31272119-31272169	U87	brain:	n/a
20	chr12:31254007-31254057	NT2-D1	testis:	n/a
21	chr12:31270326-31270376	Jurkat	blood:	n/a
22	chr12:31270326-31270376	HCPEpiC	choroid plexus:	n/a
23	chr12:31405499-31405549	SK-N-MC	brain:	n/a
24	chr12:31276852-31276902	PANC-1	pancreas:	n/a
25	chr12:31257362-31257412	SK-N-MC	brain:	n/a
26	chr12:31272114-31272164	PANC-1	pancreas:	n/a
27	chr12:31254007-31254057	BE2_C	brain:	n/a
28	chr12:31270326-31270376	HAEpiC	amniotic membrane:	n/a
29	chr12:31254036-31254086	PFSK-1	brain:	n/a
30	chr12:31254036-31254086	HNPCEpiC	eye:	n/a
31	chr12:31272119-31272169	RPTEC	kidney:	n/a
32	chr12:31272114-31272164	HepG2	liver:	n/a
33	chr12:31272114-31272164	AG09309	skin:	n/a
34	chr12:31272865-31272915	NHBE	bronchial:	n/a
35	chr12:31256838-31256888	PANC-1	pancreas:	n/a
36	chr12:31272114-31272164	RPTEC	kidney:	n/a
37	chr12:31272114-31272164	SAEC	small airway:	n/a
38	chr12:31405499-31405549	IMR90	lung:	fetal
39	chr12:31272119-31272169	A549	lung:	n/a
40	chr12:31271429-31271479	T-47D	breast:	n/a
41	chr12:31378024-31378074	MCF-7	breast:	n/a
42	chr12:31272114-31272164	SK-N-SH_RA	brain:	n/a
43	chr12:31272114-31272164	HCPEpiC	choroid plexus:	n/a
44	chr12:31272112-31272162	ProgFib	skin:	n/a
45	chr12:31402470-31402520	GM06990	blood:	n/a
46	chr12:31405499-31405549	BE2_C	brain:	n/a
47	chr12:31257362-31257412	CMK	blood:	n/a
48	chr12:31405359-31405409	GM12892	blood:	n/a
49	chr12:31256838-31256888	A549	lung:	n/a
50	chr12:31276852-31276902	HCPEpiC	choroid plexus:	n/a

(count:29 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 4596 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4596 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11051241	chr12:31247098-31247099	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs563636109	chr12:31247159-31247160	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs200892366	chr12:31247214-31247215	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs71444376	chr12:31247220-31247221	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs71455619	chr12:31247243-31247244	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs552338746	chr12:31247259-31247260	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs566156369	chr12:31247262-31247263	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs528613687	chr12:31247275-31247276	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs547519762	chr12:31247290-31247291	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs186253513	chr12:31247333-31247334	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs537312938	chr12:31247368-31247369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs550871753	chr12:31247389-31247390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189891933	chr12:31247443-31247444	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs12816960	chr12:31247480-31247481	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs374521368	chr12:31247502-31247503	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs144908450	chr12:31247504-31247505	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs367562945	chr12:31247513-31247514	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs372263203	chr12:31247529-31247530	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs534444663	chr12:31247545-31247546	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs554718198	chr12:31247572-31247573	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs574695765	chr12:31247605-31247606	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs11051242	chr12:31247650-31247651	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs543697597	chr12:31247674-31247675	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201372033	chr12:31247681-31247682	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs61917225	chr12:31247682-31247683	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs563573274	chr12:31247684-31247685	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs577253047	chr12:31247693-31247694	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs546165283	chr12:31247704-31247705	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs142329572	chr12:31247713-31247714	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs146403928	chr12:31247722-31247723	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139754333	chr12:31247753-31247754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200316146	chr12:31247782-31247783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182165014	chr12:31247799-31247800	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548408664	chr12:31247807-31247808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61917226	chr12:31247863-31247864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115558646	chr12:31247885-31247886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs150413968	chr12:31247886-31247887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550808318	chr12:31247898-31247899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570799046	chr12:31247899-31247900	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11614855	chr12:31247922-31247923	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539777884	chr12:31247926-31247927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10771800	chr12:31247986-31247987	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs565558954	chr12:31248005-31248006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116757497	chr12:31248012-31248013	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554711017	chr12:31248038-31248039	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574634250	chr12:31248057-31248058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570282675	chr12:31248064-31248065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138059358	chr12:31248092-31248093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs187789376	chr12:31248093-31248094	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77174801	chr12:31248154-31248155	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	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:1723 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31227800-31266400	Weak transcription	HSMMtube	muscle
2	chr12:31228000-31249200	Weak transcription	Brain Angular Gyrus	brain
3	chr12:31228000-31255000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr12:31228000-31256400	Weak transcription	Liver	Liver
5	chr12:31228000-31258200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr12:31228000-31269800	Weak transcription	Rectal Smooth Muscle	rectum
7	chr12:31228200-31261800	Weak transcription	Brain Substantia Nigra	brain
8	chr12:31228400-31259800	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr12:31229000-31256200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:31230800-31258000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr12:31232000-31251800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr12:31232200-31249400	Weak transcription	Osteobl	bone
13	chr12:31232400-31247800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr12:31232800-31251000	Strong transcription	Duodenum Mucosa	Duodenum
15	chr12:31233400-31250400	Strong transcription	Dnd41	blood
16	chr12:31233400-31257400	Weak transcription	NHEK	skin
17	chr12:31233400-31259000	Weak transcription	NH-A	brain
18	chr12:31233400-31259800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:31233800-31256400	Weak transcription	HUVEC	blood vessel
20	chr12:31233800-31256600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:31233800-31260800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr12:31234000-31251200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr12:31234000-31252200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:31234000-31257600	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr12:31234400-31256400	Weak transcription	HMEC	breast
26	chr12:31234400-31256600	Weak transcription	Hela-S3	cervix
27	chr12:31234400-31257600	Strong transcription	HUES64 Cell Line	embryonic stem cell
28	chr12:31234800-31252600	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr12:31235200-31252000	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr12:31235600-31251800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr12:31235600-31252000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
32	chr12:31236000-31251600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
33	chr12:31237600-31249000	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr12:31238000-31255000	Weak transcription	NHLF	lung
35	chr12:31238600-31261000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr12:31239600-31247400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr12:31239800-31253800	Weak transcription	Placenta	Placenta
38	chr12:31240400-31251200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr12:31242400-31249000	Weak transcription	Fetal Lung	lung
40	chr12:31242400-31256600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:31242600-31247200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr12:31242600-31248200	Weak transcription	HepG2	liver
43	chr12:31242600-31249400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr12:31242600-31250600	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr12:31242600-31254000	Weak transcription	Aorta	Aorta
46	chr12:31242600-31257600	Weak transcription	K562	blood
47	chr12:31242600-31259000	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr12:31242600-31259200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:31242600-31259800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr12:31242600-31270200	Weak transcription	GM12878-XiMat	blood

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