Variant report

Variant	nsv1049949
Chromosome Location	chr12:9008609-9049198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:649)
CpG islands
(count:122)
Chromatin interactive
region (count:26)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:649 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9008598-9008962	K562	blood:	n/a	n/a
2	ARID3A	chr12:9039783-9040356	K562	blood:	n/a	n/a
3	ARID3A	chr12:9038564-9038669	K562	blood:	n/a	n/a
4	ARID3A	chr12:9013071-9013271	K562	blood:	n/a	n/a
5	ATF1	chr12:9019650-9019855	K562	blood:	n/a	n/a
6	ATF1	chr12:9039858-9040231	K562	blood:	n/a	n/a
7	BACH1	chr12:9013088-9013325	K562	blood:	n/a	n/a
8	BACH1	chr12:9043216-9043548	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr12:9038477-9038523	K562	blood:	n/a	n/a
10	BACH1	chr12:9012962-9013388	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr12:9013063-9013340	K562	blood:	n/a	n/a
12	BHLHE40	chr12:9043308-9043675	K562	blood:	n/a	n/a
13	BHLHE40	chr12:9039830-9040257	K562	blood:	n/a	n/a
14	BRCA1	chr12:9033574-9033581	GM12878	blood:	n/a	n/a
15	CBX3	chr12:9039812-9040396	K562	blood:	n/a	n/a
16	CBX3	chr12:9039842-9040320	K562	blood:	n/a	n/a
17	CCNT2	chr12:9039867-9040265	K562	blood:	n/a	n/a
18	CEBPB	chr12:9012041-9012521	A549	lung:	n/a	chr12:9012224-9012235
19	CEBPB	chr12:9011980-9012477	MCF-7	breast:	n/a	chr12:9012224-9012235
20	CEBPB	chr12:9043182-9043726	K562	blood:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
21	CEBPB	chr12:9043187-9043679	A549	lung:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
22	CEBPB	chr12:9011961-9012311	ECC-1	luminal epithelium:	n/a	chr12:9012224-9012235
23	CEBPB	chr12:9012043-9012420	Hela-S3	cervix:	n/a	chr12:9012224-9012235
24	CEBPB	chr12:9043211-9043444	ECC-1	luminal epithelium:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
25	CEBPB	chr12:9025600-9025824	K562	blood:	n/a	n/a
26	CEBPB	chr12:9043175-9043656	Hela-S3	cervix:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
27	CEBPB	chr12:9043280-9043454	K562	blood:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
28	CEBPB	chr12:9012036-9012419	H1-hESC	embryonic stem cell:	n/a	chr12:9012224-9012235
29	CEBPB	chr12:9043167-9043540	K562	blood:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
30	CEBPB	chr12:9011987-9012488	A549	lung:	n/a	chr12:9012224-9012235
31	CEBPB	chr12:9012056-9012327	MCF-7	breast:	n/a	chr12:9012224-9012235
32	CEBPB	chr12:9012947-9013286	K562	blood:	n/a	n/a
33	CEBPB	chr12:9043174-9043658	H1-hESC	embryonic stem cell:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
34	CEBPB	chr12:9039796-9040271	K562	blood:	n/a	n/a
35	CEBPB	chr12:9039833-9040608	K562	blood:	n/a	n/a
36	CEBPB	chr12:9043184-9043552	IMR90	lung:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
37	CEBPB	chr12:9011994-9012338	A549	lung:	n/a	chr12:9012224-9012235
38	CEBPB	chr12:9012016-9012470	ECC-1	luminal epithelium:	n/a	chr12:9012224-9012235
39	CEBPB	chr12:9043161-9043593	MCF-7	breast:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
40	CEBPB	chr12:9043221-9043418	HepG2	liver:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
41	CEBPB	chr12:9013207-9013523	Hela-S3	cervix:	n/a	chr12:9013401-9013414
42	CEBPB	chr12:9012040-9012415	HepG2	liver:	n/a	chr12:9012224-9012235
43	CEBPB	chr12:9024789-9024841	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr12:9012046-9012417	IMR90	lung:	n/a	chr12:9012224-9012235
45	CEBPB	chr12:9043178-9043532	HepG2	liver:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
46	CEBPB	chr12:9012177-9012274	HepG2	liver:	n/a	chr12:9012224-9012235
47	CEBPB	chr12:9012087-9012279	K562	blood:	n/a	chr12:9012224-9012235
48	CEBPB	chr12:9043118-9043584	A549	lung:	n/a	chr12:9043358-9043369 chr12:9043360-9043369
49	CEBPB	chr12:9012030-9012488	K562	blood:	n/a	chr12:9012224-9012235
50	CEBPB	chr12:9012022-9012365	K562	blood:	n/a	chr12:9012224-9012235

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9028945-9028995	HNPCEpiC	eye:	n/a
2	chr12:9019044-9019094	RPTEC	kidney:	n/a
3	chr12:9028945-9028995	PANC-1	pancreas:	n/a
4	chr12:9019044-9019094	NH-A	brain:	n/a
5	chr12:9019044-9019094	Hepatocyte	liver:	n/a
6	chr12:9019044-9019094	A549	lung:	n/a
7	chr12:9028945-9028995	HRCEpiC	kidney:	n/a
8	chr12:9028945-9028995	HMEC	breast:	n/a
9	chr12:9019044-9019094	AG09319	gingival:	n/a
10	chr12:9019044-9019094	AG04450	lung:	fetal
11	chr12:9019044-9019094	IMR90	lung:	fetal
12	chr12:9028945-9028995	AG09319	gingival:	n/a
13	chr12:9028945-9028995	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:9019044-9019094	HCPEpiC	choroid plexus:	n/a
15	chr12:9028945-9028995	GM12891	blood:	n/a
16	chr12:9019044-9019094	BE2_C	brain:	n/a
17	chr12:9019044-9019094	HCF	heart:	n/a
18	chr12:9028945-9028995	HepG2	liver:	n/a
19	chr12:9019044-9019094	MCF-7	breast:	n/a
20	chr12:9019044-9019094	GM06990	blood:	n/a
21	chr12:9028945-9028995	Hela-S3	cervix:	n/a
22	chr12:9028945-9028995	BJ	skin:	n/a
23	chr12:9019044-9019094	T-47D	breast:	n/a
24	chr12:9028945-9028995	GM12892	blood:	n/a
25	chr12:9019044-9019094	MCF10A-Er-Src	breast:	n/a
26	chr12:9019044-9019094	SKMC	muscle:	n/a
27	chr12:9028945-9028995	MCF10A-Er-Src	breast:	n/a
28	chr12:9019044-9019094	K562	blood:	n/a
29	chr12:9019044-9019094	CMK	blood:	n/a
30	chr12:9019044-9019094	HAEpiC	amniotic membrane:	n/a
31	chr12:9019044-9019094	AG09309	skin:	n/a
32	chr12:9028945-9028995	A549	lung:	n/a
33	chr12:9028945-9028995	HUVEC	blood vessel:	n/a
34	chr12:9028945-9028995	PrEC	prostate:	n/a
35	chr12:9028945-9028995	AG10803	skin:	n/a
36	chr12:9028945-9028995	AG09309	skin:	n/a
37	chr12:9019044-9019094	U87	brain:	n/a
38	chr12:9019044-9019094	GM19239	blood:	n/a
39	chr12:9019044-9019094	GM12891	blood:	n/a
40	chr12:9028945-9028995	SK-N-SH_RA	brain:	n/a
41	chr12:9028945-9028995	SKMC	muscle:	n/a
42	chr12:9019044-9019094	HRPEpiC	eye:	n/a
43	chr12:9028945-9028995	HAEpiC	amniotic membrane:	n/a
44	chr12:9019044-9019094	NT2-D1	testis:	n/a
45	chr12:9028945-9028995	T-47D	breast:	n/a
46	chr12:9028945-9028995	HEK293	kidney:	embryo
47	chr12:9028945-9028995	U87	brain:	n/a
48	chr12:9019044-9019094	HepG2	liver:	n/a
49	chr12:9028945-9028995	Jurkat	blood:	n/a
50	chr12:9019044-9019094	Caco-2	colon:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9011608..9013932-chr12:9031539..9033182,2	MCF-7	breast:
2	chr12:9043152..9045198-chr12:9065013..9067722,3	MCF-7	breast:
3	chr12:8833699..8835263-chr12:9042738..9043900,4	MCF-7	breast:
4	chr12:9043166..9043816-chr6:144262954..144263503,2	MCF-7	breast:
5	chr12:9040198..9041798-chr12:9041859..9043625,2	K562	blood:
6	chr12:9043294..9043953-chr7:82352710..82353230,2	MCF-7	breast:
7	chr12:8832360..8833354-chr12:9043185..9043776,2	MCF-7	breast:
8	chr12:8932743..8934022-chr12:9012782..9013946,5	MCF-7	breast:
9	chr12:8932208..8933632-chr12:9042892..9044093,10	MCF-7	breast:
10	chr12:9040198..9041798-chr12:9041859..9043625,2	K562	blood:
11	chr12:9022965..9025697-chr12:9025731..9027490,2	K562	blood:
12	chr12:8834370..8834975-chr12:9013092..9013685,2	MCF-7	breast:
13	chr12:9011608..9013932-chr12:9031539..9033182,2	MCF-7	breast:
14	chr12:8834350..8835349-chr12:9042854..9043829,4	K562	blood:
15	chr12:9018817..9020521-chr12:9023671..9026255,2	K562	blood:
16	chr12:9034468..9037230-chr12:9037942..9040529,2	K562	blood:
17	chr12:9022965..9025697-chr12:9025731..9027490,2	K562	blood:
18	chr12:9013967..9016629-chr12:9021892..9024498,2	K562	blood:
19	chr12:9018817..9020521-chr12:9023671..9026255,2	K562	blood:
20	chr12:9040138..9041843-chr12:9048318..9050318,2	K562	blood:
21	chr12:8932764..8933606-chr12:9042861..9043830,2	MCF-7	breast:
22	chr12:9013967..9016629-chr12:9021892..9024498,2	K562	blood:
23	chr12:9034468..9037230-chr12:9037942..9040529,2	K562	blood:
24	chr12:9040138..9041843-chr12:9048318..9050318,2	K562	blood:
25	chr12:8849598..8851653-chr12:9040944..9042624,2	MCF-7	breast:
26	chr12:9008234..9009916-chr12:9010931..9013875,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-M6PR-5	chr12:9010526-9010872	NONHSAT026375

No data

Variant related genes	Relation type
A2ML1	TF binding region
A2ML1	CpG island
ENSG00000166535	chromatin interactions
ENSG00000166532	chromatin interactions
ENSG00000111752	chromatin interactions

Extended variants
information (count: 1185 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2110079	chr12:9008609-9008610	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189538025	chr12:9008862-9008863	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs181551712	chr12:9008875-9008876	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs137916692	chr12:9008901-9008902	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs186210609	chr12:9008920-9008921	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs73234353	chr12:9008924-9008925	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs191162349	chr12:9008926-9008927	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs143372440	chr12:9008942-9008943	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs141144326	chr12:9008964-9008965	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs11047617	chr12:9009042-9009043	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs146207656	chr12:9009086-9009087	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs370758133	chr12:9009091-9009092	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs11047620	chr12:9009111-9009112	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs11047622	chr12:9009234-9009235	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs11047623	chr12:9009257-9009258	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs538485813	chr12:9009330-9009331	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs138893751	chr12:9009343-9009344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs207472645	chr12:9009364-9009365	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs142875870	chr12:9009464-9009465	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs71891886	chr12:9009495-9009496	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368233975	chr12:9009514-9009515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12423748	chr12:9009515-9009516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551912753	chr12:9009542-9009543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144563064	chr12:9009562-9009563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34670177	chr12:9009589-9009590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183422479	chr12:9009598-9009599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs117033574	chr12:9009607-9009608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs186373929	chr12:9009622-9009623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79279876	chr12:9009637-9009638	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190836514	chr12:9009645-9009646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs117701006	chr12:9009675-9009676	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375355896	chr12:9009687-9009688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78452682	chr12:9009731-9009732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs267603716	chr12:9009760-9009761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535988756	chr12:9009773-9009774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs56179521	chr12:9009779-9009780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11047625	chr12:9009785-9009786	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs11047626	chr12:9009806-9009807	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs202194008	chr12:9009811-9009812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1558526	chr12:9009820-9009821	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs74378424	chr12:9009821-9009822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs202179061	chr12:9009835-9009836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201725377	chr12:9009912-9009913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200269317	chr12:9009914-9009915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547891207	chr12:9009939-9009940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371525262	chr12:9009987-9009988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200249816	chr12:9009997-9009998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs386375554	chr12:9009998-9009999	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs3079157	chr12:9009999-9010000	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74472917	chr12:9010000-9010001	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	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
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:261 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8982200-9022000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:8983400-9017600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr12:8987600-9040000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr12:8987800-9012800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr12:8988200-9012800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr12:8994800-9016600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:8996000-9040000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:8998800-9014600	Weak transcription	Right Atrium	heart
9	chr12:8999000-9016400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr12:9000800-9012400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr12:9001200-9010200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr12:9001200-9011600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr12:9005000-9013400	Weak transcription	Brain Anterior Caudate	brain
14	chr12:9005200-9017800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr12:9007000-9029600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr12:9007200-9027600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr12:9007400-9009600	Weak transcription	Esophagus	oesophagus
18	chr12:9008000-9009200	Enhancers	K562	blood
19	chr12:9008000-9011400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:9008200-9009400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr12:9008400-9009200	Enhancers	Primary hematopoietic stem cells	blood
22	chr12:9008400-9009200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr12:9008400-9009200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:9008400-9009200	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr12:9008600-9008800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr12:9008600-9009000	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr12:9008800-9009000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr12:9009000-9011200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr12:9009200-9012800	Weak transcription	K562	blood
30	chr12:9009600-9012600	Strong transcription	Esophagus	oesophagus
31	chr12:9010200-9011400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
32	chr12:9011400-9011800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:9011400-9012800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr12:9011600-9011800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr12:9011800-9021600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:9011800-9029800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr12:9012600-9020400	Weak transcription	Esophagus	oesophagus
38	chr12:9012800-9013600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr12:9012800-9013600	Enhancers	K562	blood
40	chr12:9012800-9013800	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr12:9013000-9013400	Enhancers	Placenta	Placenta
42	chr12:9013000-9013800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:9013400-9013600	Enhancers	Brain Anterior Caudate	brain
44	chr12:9013400-9013600	Enhancers	Spleen	Spleen
45	chr12:9013600-9019200	Weak transcription	K562	blood
46	chr12:9013600-9029400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr12:9013800-9033800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr12:9016400-9016600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr12:9016400-9016600	Enhancers	Gastric	stomach
50	chr12:9019200-9019800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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