Variant report

Variant	nsv898769
Chromosome Location	chr12:10565453-10600368
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:403)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:403 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:10592356-10592503	HepG2	liver:	n/a	n/a
2	BATF	chr12:10598779-10599011	GM12878	blood:	n/a	chr12:10598893-10598904
3	BATF	chr12:10583308-10583579	GM12878	blood:	n/a	chr12:10583461-10583472
4	BCL11A	chr12:10583293-10583483	GM12878	blood:	n/a	n/a
5	BCL11A	chr12:10598783-10598965	GM12878	blood:	n/a	n/a
6	BCL3	chr12:10592167-10592607	A549	lung:	n/a	n/a
7	BRCA1	chr12:10574950-10575149	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:10574938-10575152	A549	lung:	n/a	n/a
9	CEBPB	chr12:10574839-10575068	K562	blood:	n/a	n/a
10	CEBPB	chr12:10574947-10575139	K562	blood:	n/a	n/a
11	CEBPB	chr12:10588520-10588745	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr12:10577271-10577431	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:10574940-10575149	HepG2	liver:	n/a	n/a
14	CEBPB	chr12:10592348-10592508	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:10574805-10575159	K562	blood:	n/a	n/a
16	CEBPB	chr12:10600201-10600212	A549	lung:	n/a	n/a
17	CEBPB	chr12:10590205-10590581	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:10592194-10592559	A549	lung:	n/a	n/a
19	CEBPB	chr12:10590386-10590401	HepG2	liver:	n/a	n/a
20	CEBPB	chr12:10574775-10575160	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr12:10592190-10592807	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr12:10590272-10590510	K562	blood:	n/a	n/a
23	CEBPB	chr12:10573229-10573321	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr12:10585773-10585908	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr12:10590372-10590413	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr12:10574937-10575144	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr12:10592724-10592809	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr12:10577654-10577777	A549	lung:	n/a	n/a
29	CTCF	chr12:10593932-10594014	A549	lung:	n/a	n/a
30	CTCF	chr12:10593072-10593203	GM19239	blood:	n/a	n/a
31	CTCF	chr12:10577678-10577792	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr12:10585469-10585543	Kidney_OC	kidney:	n/a	n/a
33	CTCF	chr12:10593047-10593172	Fibrobl	skin:	n/a	n/a
34	CTCF	chr12:10577713-10577786	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:10577681-10577775	NHEK	skin:	n/a	n/a
36	CTCF	chr12:10577729-10577796	LNCaP	prostate:	n/a	n/a
37	CTCF	chr12:10577689-10577783	GM19238	blood:	n/a	n/a
38	CTCF	chr12:10569292-10569341	GM10248	blood:	n/a	n/a
39	CTCF	chr12:10593095-10593127	MCF-7	breast:	n/a	n/a
40	CTCF	chr12:10582121-10582214	MCF-7	breast:	n/a	n/a
41	CTCF	chr12:10577339-10577398	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr12:10593080-10593174	MCF-7	breast:	n/a	n/a
43	CTCF	chr12:10582117-10582206	MCF-7	breast:	n/a	n/a
44	CTCF	chr12:10583540-10583606	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr12:10600167-10600223	LNCaP	prostate:	n/a	n/a
46	CTCF	chr12:10574917-10574984	GM19239	blood:	n/a	n/a
47	CTCF	chr12:10593138-10593151	NHEK	skin:	n/a	n/a
48	CTCF	chr12:10577702-10577734	LNCaP	prostate:	n/a	n/a
49	CTCF	chr12:10569977-10570074	GM10266	blood:	n/a	n/a
50	CTCF	chr12:10591453-10591491	A549	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:10588483-10588533	RPTEC	kidney:	n/a
2	chr12:10588483-10588533	A549	lung:	n/a
3	chr12:10570179-10570229	BJ	skin:	n/a
4	chr12:10599740-10599790	HCT-116	colon:	n/a
5	chr12:10599740-10599790	HEK293	kidney:	embryo
6	chr12:10588483-10588533	HCF	heart:	n/a
7	chr12:10586130-10586180	K562	blood:	n/a
8	chr12:10586130-10586180	HRCEpiC	kidney:	n/a
9	chr12:10599740-10599790	RPTEC	kidney:	n/a
10	chr12:10570179-10570229	K562	blood:	n/a
11	chr12:10588483-10588533	PrEC	prostate:	n/a
12	chr12:10588483-10588533	Hepatocyte	liver:	n/a
13	chr12:10588483-10588533	HUVEC	blood vessel:	n/a
14	chr12:10599740-10599790	AG10803	skin:	n/a
15	chr12:10570179-10570229	HCM	heart:	n/a
16	chr12:10588483-10588533	AG04449	skin:	fetal
17	chr12:10570179-10570229	HEK293	kidney:	embryo
18	chr12:10599740-10599790	U87	brain:	n/a
19	chr12:10586130-10586180	H1-hESC	embryonic stem cell:	embryo
20	chr12:10586130-10586180	AG04449	skin:	fetal
21	chr12:10586130-10586180	ProgFib	skin:	n/a
22	chr12:10599740-10599790	Hela-S3	cervix:	n/a
23	chr12:10599740-10599790	GM19239	blood:	n/a
24	chr12:10570179-10570229	MCF-7	breast:	n/a
25	chr12:10570179-10570229	CMK	blood:	n/a
26	chr12:10570179-10570229	NB4	blood:	n/a
27	chr12:10599740-10599790	GM12892	blood:	n/a
28	chr12:10588483-10588533	HNPCEpiC	eye:	n/a
29	chr12:10583355-10583405	SKMC	muscle:	n/a
30	chr12:10570179-10570229	MCF10A-Er-Src	breast:	n/a
31	chr12:10570179-10570229	A549	lung:	n/a
32	chr12:10599740-10599790	HCPEpiC	choroid plexus:	n/a
33	chr12:10586130-10586180	HNPCEpiC	eye:	n/a
34	chr12:10588483-10588533	AG04450	lung:	fetal
35	chr12:10588483-10588533	ECC-1	luminal epithelium:	n/a
36	chr12:10586130-10586180	HCM	heart:	n/a
37	chr12:10583355-10583405	HL-60	blood:	n/a
38	chr12:10599740-10599790	GM12891	blood:	n/a
39	chr12:10570179-10570229	AoSMC	blood vessel:	n/a
40	chr12:10599740-10599790	SK-N-SH	brain:	n/a
41	chr12:10570179-10570229	HRPEpiC	eye:	n/a
42	chr12:10599740-10599790	LNCaP	prostate:	n/a
43	chr12:10599740-10599790	ECC-1	luminal epithelium:	n/a
44	chr12:10570179-10570229	HAEpiC	amniotic membrane:	n/a
45	chr12:10588483-10588533	HRE	kidney:	n/a
46	chr12:10599740-10599790	NHDF-neo	bronchial:	n/a
47	chr12:10570179-10570229	IMR90	lung:	fetal
48	chr12:10599740-10599790	HCF	heart:	n/a
49	chr12:10599740-10599790	HRCEpiC	kidney:	n/a
50	chr12:10588483-10588533	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:
2	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:
3	chr12:10572017..10574193-chr12:10588542..10590731,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EIF2S3L.1-6	chr12:10597246-10597382	l_610_chr12:10597245-10602083_whiteBloodCell

No data

Variant related genes	Relation type
KLRC3	TF binding region
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000255641	TF binding region
KLRC2	TF binding region
KLRC3	CpG island
KLRC4	CpG island
KLRC4-KLRK1	CpG island
ENSG00000255641	CpG island
KLRC2	CpG island
ENSG00000255641	chromatin interactions
ENSG00000245648	chromatin interactions
ENSG00000205810	chromatin interactions
ENSG00000205809	chromatin interactions

Extended variants
information (count: 1543 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1545750	chr12:10565453-10565454	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566043503	chr12:10565454-10565455	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs142189087	chr12:10565463-10565464	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs142825811	chr12:10565501-10565502	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs1971939	chr12:10565515-10565516	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs151195245	chr12:10565610-10565611	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs537184428	chr12:10565626-10565627	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs557444132	chr12:10565634-10565635	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs577237538	chr12:10565635-10565636	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs546023727	chr12:10565702-10565703	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs553162895	chr12:10565724-10565725	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs573214189	chr12:10565776-10565777	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs542140358	chr12:10565794-10565795	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs111830381	chr12:10565818-10565819	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs184888670	chr12:10565847-10565848	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs543825408	chr12:10565849-10565850	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs564215268	chr12:10565861-10565862	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs532826155	chr12:10565877-10565878	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs190970681	chr12:10565899-10565900	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs552396657	chr12:10565918-10565919	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs76879108	chr12:10565961-10565962	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs528788998	chr12:10565977-10565978	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs548458016	chr12:10565989-10565990	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs568627234	chr12:10565997-10565998	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs2617175	chr12:10566061-10566062	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs550798584	chr12:10566127-10566128	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs76170662	chr12:10566221-10566222	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs61919127	chr12:10566237-10566238	Strong transcription Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs2682505	chr12:10566302-10566303	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539929250	chr12:10566401-10566402	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553248953	chr12:10566448-10566449	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12297284	chr12:10566456-10566457	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs573049910	chr12:10566506-10566507	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs535779951	chr12:10566535-10566536	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555648353	chr12:10566553-10566554	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs575405307	chr12:10566560-10566561	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs2682504	chr12:10566573-10566574	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs569063847	chr12:10566579-10566580	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs577366235	chr12:10566598-10566599	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs539920261	chr12:10566601-10566602	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs191702369	chr12:10566608-10566609	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2682503	chr12:10566610-10566611	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs2682502	chr12:10566616-10566617	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs562407730	chr12:10566701-10566702	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs72475439	chr12:10566786-10566787	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550993143	chr12:10566792-10566793	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs76257986	chr12:10566847-10566848	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs545272388	chr12:10566866-10566867	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562368399	chr12:10566907-10566908	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539965438	chr12:10566966-10566967	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10562200-10566600	Weak transcription	Hela-S3	cervix
2	chr12:10562200-10572800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:10564400-10570200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr12:10565400-10567400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr12:10566600-10567800	Strong transcription	Hela-S3	cervix
6	chr12:10567400-10569200	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:10567800-10569200	Genic enhancers	Hela-S3	cervix
8	chr12:10569200-10570200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:10569200-10570200	Weak transcription	Hela-S3	cervix
10	chr12:10570200-10570400	Flanking Active TSS	Hela-S3	cervix
11	chr12:10570200-10570600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
12	chr12:10570200-10571600	Transcr. at gene 5' and 3'	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:10570400-10571400	Active TSS	Hela-S3	cervix
14	chr12:10570600-10572600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr12:10571400-10572600	Weak transcription	Hela-S3	cervix
16	chr12:10571600-10573800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
17	chr12:10572600-10573000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
18	chr12:10572600-10573200	Active TSS	Hela-S3	cervix
19	chr12:10572600-10573600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:10572800-10573000	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr12:10572800-10573600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr12:10572800-10573600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:10572800-10573600	Enhancers	Muscle Satellite Cultured Cells	--
24	chr12:10572800-10573600	Enhancers	A549	lung
25	chr12:10572800-10573600	Enhancers	Osteobl	bone
26	chr12:10572800-10573800	Enhancers	HUVEC	blood vessel
27	chr12:10573200-10573600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr12:10573200-10573600	Enhancers	Hela-S3	cervix
29	chr12:10573600-10575200	Weak transcription	Hela-S3	cervix
30	chr12:10573600-10578200	Weak transcription	A549	lung
31	chr12:10573800-10585600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr12:10575200-10575800	Enhancers	Hela-S3	cervix
33	chr12:10575800-10584400	Weak transcription	Hela-S3	cervix
34	chr12:10578000-10578800	Active TSS	Brain Hippocampus Middle	brain
35	chr12:10578000-10579000	Active TSS	Brain Anterior Caudate	brain
36	chr12:10578000-10579000	Active TSS	Brain Cingulate Gyrus	brain
37	chr12:10578000-10579000	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr12:10578000-10579000	Active TSS	Brain Substantia Nigra	brain
39	chr12:10578200-10578400	Enhancers	A549	lung
40	chr12:10578200-10578800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr12:10578200-10579000	Active TSS	Brain Angular Gyrus	brain
42	chr12:10582600-10584200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:10584200-10588000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr12:10584400-10584600	Strong transcription	Hela-S3	cervix
45	chr12:10584600-10585400	Weak transcription	Hela-S3	cervix
46	chr12:10585400-10585600	Genic enhancers	Hela-S3	cervix
47	chr12:10585600-10585800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr12:10585600-10586200	Transcr. at gene 5' and 3'	Hela-S3	cervix
49	chr12:10585800-10589000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
50	chr12:10586200-10587000	Active TSS	Hela-S3	cervix

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