Variant report

Variant	nsv1052261
Chromosome Location	chr12:31251314-31410284
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1982)
CpG islands
(count:1406)
Chromatin interactive
region (count:29)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1982 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

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	chr12:31357881-31358323	GM12878	blood:	n/a	n/a
6	ATF2	chr12:31357817-31358350	GM12878	blood:	n/a	n/a
7	ATF2	chr12:31391675-31392058	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr12:31391648-31392128	H1-hESC	embryonic stem cell:	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	chr12:31345648-31345920	GM12878	blood:	n/a	n/a
14	BATF	chr12:31253312-31253563	GM12878	blood:	n/a	n/a
15	BCL3	chr12:31357958-31358220	GM12878	blood:	n/a	chr12:31358098-31358107
16	BHLHE40	chr12:31253434-31253625	GM12878	blood:	n/a	n/a
17	BHLHE40	chr12:31391786-31392031	K562	blood:	n/a	n/a
18	BHLHE40	chr12:31252507-31252676	GM12878	blood:	n/a	n/a
19	BHLHE40	chr12:31270127-31270331	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:31270186-31270438	K562	blood:	n/a	n/a
21	BHLHE40	chr12:31333006-31333037	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:31390183-31390447	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:31253866-31254071	GM12878	blood:	n/a	n/a
24	BRCA1	chr12:31390019-31390036	GM12878	blood:	n/a	n/a
25	BRCA1	chr12:31391842-31392078	Hela-S3	cervix:	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	chr12:31268034-31268387	A549	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
29	CEBPB	chr12:31391806-31392080	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:31391866-31392108	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr12:31268038-31268391	IMR90	lung:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
32	CEBPB	chr12:31268200-31268216	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr12:31401755-31402127	A549	lung:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
34	CEBPB	chr12:31268131-31268303	K562	blood:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
35	CEBPB	chr12:31355347-31355432	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr12:31268032-31268392	HepG2	liver:	n/a	chr12:31268208-31268217 chr12:31268206-31268219 chr12:31268208-31268217 chr12:31268208-31268217
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	chr12:31395234-31395493	IMR90	lung:	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	chr12:31401830-31402026	HepG2	liver:	n/a	chr12:31401914-31401925 chr12:31401931-31401942 chr12:31401890-31401901
42	CEBPB	chr12:31395273-31395514	HepG2	liver:	n/a	n/a
43	CHD2	chr12:31253424-31253892	GM12878	blood:	n/a	n/a
44	CHD2	chr12:31271974-31272145	GM12878	blood:	n/a	n/a
45	CHD2	chr12:31271851-31272155	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr12:31270114-31270314	GM12878	blood:	n/a	n/a
47	CHD2	chr12:31358885-31359207	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr12:31271857-31272216	K562	blood:	n/a	n/a
49	CHD2	chr12:31270194-31270459	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr12:31371770-31371778	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:31276852-31276902	HRE	kidney:	n/a
2	chr12:31255279-31255329	HepG2	liver:	n/a
3	chr12:31405359-31405409	AG09319	gingival:	n/a
4	chr12:31276852-31276902	HRE	kidney:	n/a
5	chr12:31255279-31255329	HepG2	liver:	n/a
6	chr12:31405359-31405409	AG09319	gingival:	n/a
7	chr12:31370930-31370980	NHBE	bronchial:	n/a
8	chr12:31272112-31272162	AG09319	gingival:	n/a
9	chr12:31256838-31256888	NT2-D1	testis:	n/a
10	chr12:31255279-31255329	IMR90	lung:	fetal
11	chr12:31257362-31257412	HMEC	breast:	n/a
12	chr12:31378024-31378074	PFSK-1	brain:	n/a
13	chr12:31254007-31254057	T-47D	breast:	n/a
14	chr12:31271429-31271479	Hepatocyte	liver:	n/a
15	chr12:31272119-31272169	CMK	blood:	n/a
16	chr12:31272114-31272164	ovcar-3	ovarian:	n/a
17	chr12:31272114-31272164	T-47D	breast:	n/a
18	chr12:31255279-31255329	SAEC	small airway:	n/a
19	chr12:31370930-31370980	GM12891	blood:	n/a
20	chr12:31402470-31402520	HCM	heart:	n/a
21	chr12:31270326-31270376	HCF	heart:	n/a
22	chr12:31256838-31256888	SK-N-SH	brain:	n/a
23	chr12:31370930-31370980	HRE	kidney:	n/a
24	chr12:31256838-31256888	IMR90	lung:	fetal
25	chr12:31272112-31272162	H1-hESC	embryonic stem cell:	embryo
26	chr12:31272119-31272169	GM19239	blood:	n/a
27	chr12:31272865-31272915	HMEC	breast:	n/a
28	chr12:31316348-31316398	HNPCEpiC	eye:	n/a
29	chr12:31272865-31272915	AG09319	gingival:	n/a
30	chr12:31255279-31255329	ProgFib	skin:	n/a
31	chr12:31360362-31360412	CMK	blood:	n/a
32	chr12:31405359-31405409	NHDF-neo	bronchial:	n/a
33	chr12:31360362-31360412	HRE	kidney:	n/a
34	chr12:31272114-31272164	Hela-S3	cervix:	n/a
35	chr12:31272114-31272164	AG04449	skin:	fetal
36	chr12:31378024-31378074	HIPEpiC	eye:	n/a
37	chr12:31254007-31254057	HPAEpiC	pulmonary alveolar:	n/a
38	chr12:31405499-31405549	H1-hESC	embryonic stem cell:	embryo
39	chr12:31255279-31255329	HRE	kidney:	n/a
40	chr12:31316348-31316398	HCF	heart:	n/a
41	chr12:31254007-31254057	AoSMC	blood vessel:	n/a
42	chr12:31276852-31276902	HRCEpiC	kidney:	n/a
43	chr12:31272865-31272915	SK-N-SH	brain:	n/a
44	chr12:31257362-31257412	GM19239	blood:	n/a
45	chr12:31316348-31316398	SKMC	muscle:	n/a
46	chr12:31316348-31316398	HRE	kidney:	n/a
47	chr12:31360362-31360412	SAEC	small airway:	n/a
48	chr12:31256838-31256888	PANC-1	pancreas:	n/a
49	chr12:31255279-31255329	Hela-S3	cervix:	n/a
50	chr12:31255279-31255329	HL-60	blood:	n/a

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

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

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

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

No data

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

Extended variants
information (count: 4350 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4350 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs78193575	chr12:31251318-31251319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77992808	chr12:31251319-31251320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570215093	chr12:31251322-31251323	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575977432	chr12:31251335-31251336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs61918664	chr12:31251404-31251405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs61918665	chr12:31251410-31251411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181704995	chr12:31251442-31251443	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs566342901	chr12:31251480-31251481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs72517779	chr12:31251483-31251484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374550728	chr12:31251535-31251536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150879386	chr12:31251538-31251539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs4931431	chr12:31251544-31251545	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs60746756	chr12:31251551-31251552	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573311426	chr12:31251621-31251622	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112052086	chr12:31251636-31251637	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12581764	chr12:31251694-31251695	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs555838301	chr12:31251719-31251720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576097850	chr12:31251734-31251735	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545172339	chr12:31251750-31251751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564959406	chr12:31251779-31251780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372808304	chr12:31251789-31251790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186720849	chr12:31251796-31251797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12581793	chr12:31251803-31251804	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs561224024	chr12:31251809-31251810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12579218	chr12:31251810-31251811	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs75461110	chr12:31251938-31251939	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs563791917	chr12:31251939-31251940	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs370009614	chr12:31252006-31252007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372805289	chr12:31252010-31252011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs377295435	chr12:31252014-31252015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs377253022	chr12:31252015-31252016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs77901987	chr12:31252018-31252019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
33	rs71052464	chr12:31252039-31252040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2352641	chr12:31252046-31252047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143639801	chr12:31252075-31252076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs2352642	chr12:31252084-31252085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7957732	chr12:31252091-31252092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146813314	chr12:31252108-31252109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs566160098	chr12:31252163-31252164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534947664	chr12:31252213-31252214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4012586	chr12:31252244-31252245	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542282746	chr12:31252293-31252294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548476323	chr12:31252304-31252305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111756006	chr12:31252307-31252308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4012588	chr12:31252338-31252339	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201302571	chr12:31252349-31252350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs60429105	chr12:31252351-31252352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4012589	chr12:31252370-31252371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563966176	chr12:31252466-31252467	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199993870	chr12:31252515-31252516	Weak transcription Strong transcription	TF binding region	1 gene(s)	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
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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1591 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:31227800-31266400	Weak transcription	HSMMtube	muscle
2	chr12:31228000-31255000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr12:31228000-31256400	Weak transcription	Liver	Liver
4	chr12:31228000-31258200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr12:31228000-31269800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr12:31228200-31261800	Weak transcription	Brain Substantia Nigra	brain
7	chr12:31228400-31259800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr12:31229000-31256200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:31230800-31258000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr12:31232000-31251800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:31233400-31257400	Weak transcription	NHEK	skin
12	chr12:31233400-31259000	Weak transcription	NH-A	brain
13	chr12:31233400-31259800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:31233800-31256400	Weak transcription	HUVEC	blood vessel
15	chr12:31233800-31256600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:31233800-31260800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr12:31234000-31252200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:31234000-31257600	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr12:31234400-31256400	Weak transcription	HMEC	breast
20	chr12:31234400-31256600	Weak transcription	Hela-S3	cervix
21	chr12:31234400-31257600	Strong transcription	HUES64 Cell Line	embryonic stem cell
22	chr12:31234800-31252600	Strong transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:31235200-31252000	Strong transcription	H9 Cell Line	embryonic stem cell
24	chr12:31235600-31251800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr12:31235600-31252000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr12:31236000-31251600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
27	chr12:31238000-31255000	Weak transcription	NHLF	lung
28	chr12:31238600-31261000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr12:31239800-31253800	Weak transcription	Placenta	Placenta
30	chr12:31242400-31256600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:31242600-31254000	Weak transcription	Aorta	Aorta
32	chr12:31242600-31257600	Weak transcription	K562	blood
33	chr12:31242600-31259000	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr12:31242600-31259200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:31242600-31259800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr12:31242600-31270200	Weak transcription	GM12878-XiMat	blood
37	chr12:31242800-31260000	Weak transcription	Left Ventricle	heart
38	chr12:31242800-31270200	Weak transcription	Primary B cells from cord blood	blood
39	chr12:31243000-31259800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:31244600-31251800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:31245000-31253800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:31245200-31256600	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr12:31245200-31259000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr12:31245200-31262200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr12:31245600-31259000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:31247400-31252000	Strong transcription	Fetal Brain Female	brain
47	chr12:31247800-31252200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:31248000-31252000	Strong transcription	Thymus	Thymus
49	chr12:31248200-31252000	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr12:31249400-31255400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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