Variant report

Variant	nsv1037113
Chromosome Location	chr12:11512480-11589497
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:125)
CpG islands
(count:244)
Chromatin interactive
region (count:1)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:125 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr12:11569521-11569734	K562	blood:	n/a	n/a
2	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
4	CEBPB	chr12:11584855-11585296	MCF-7	breast:	n/a	chr12:11585039-11585052
5	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
6	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
7	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr12:11584903-11585301	MCF-7	breast:	n/a	chr12:11585039-11585052
9	CTCF	chr12:11568873-11568951	LNCaP	prostate:	n/a	n/a
10	CTCF	chr12:11552280-11552316	GM13977	blood:	n/a	n/a
11	CTCF	chr12:11549867-11549930	GM13976	blood:	n/a	n/a
12	CTCF	chr12:11527332-11527390	GM13976	blood:	n/a	n/a
13	CTCF	chr12:11545750-11545873	GM13977	blood:	n/a	n/a
14	CTCF	chr12:11548407-11548506	Lung_OC	lung:	n/a	n/a
15	CTCF	chr12:11557375-11557427	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr12:11548021-11548061	LNCaP	prostate:	n/a	n/a
17	CTCF	chr12:11545778-11545816	GM12891	blood:	n/a	n/a
18	CTCF	chr12:11545775-11545832	MCF-7	breast:	n/a	n/a
19	CTCF	chr12:11584613-11584674	MCF-7	breast:	n/a	chr12:11584636-11584649 chr12:11584634-11584652
20	CTCF	chr12:11584604-11584702	MCF-7	breast:	n/a	chr12:11584636-11584649 chr12:11584634-11584652
21	CTCF	chr12:11545806-11545841	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:11544846-11544963	GM13976	blood:	n/a	n/a
23	CTCF	chr12:11584599-11584672	HUVEC	blood vessel:	n/a	chr12:11584636-11584649 chr12:11584634-11584652
24	CTCF	chr12:11584583-11584674	H1-hESC	embryonic stem cell:	n/a	chr12:11584636-11584649 chr12:11584634-11584652
25	CTCF	chr12:11584620-11584770	HEK293	kidney:	n/a	chr12:11584636-11584649 chr12:11584634-11584652
26	CTCF	chr12:11524600-11524750	GM12865	blood:	n/a	n/a
27	CTCF	chr12:11545746-11545856	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:11531414-11531456	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr12:11556054-11556104	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr12:11557353-11557374	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr12:11584626-11584660	MCF-7	breast:	n/a	chr12:11584636-11584649 chr12:11584634-11584652
32	CTCF	chr12:11569479-11569545	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:11529002-11529034	GM10266	blood:	n/a	n/a
34	CTCF	chr12:11545730-11545872	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr12:11566785-11566861	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chr12:11581499-11581557	Fibrobl	skin:	n/a	n/a
37	CTCF	chr12:11584540-11584690	Caco-2	colon:	n/a	chr12:11584636-11584649 chr12:11584634-11584652
38	CTCF	chr12:11545671-11545700	GM10266	blood:	n/a	n/a
39	CTCF	chr12:11528342-11528385	LNCaP	prostate:	n/a	n/a
40	E2F4	chr12:11588912-11588970	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr12:11542959-11542990	MCF10A-Er-Src	breast:	n/a	n/a
42	EP300	chr12:11584901-11585476	MCF-7	breast:	n/a	n/a
43	EP300	chr12:11584874-11585411	MCF-7	breast:	n/a	n/a
44	FOS	chr12:11538676-11538692	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr12:11513152-11513541	MCF10A-Er-Src	breast:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
46	FOS	chr12:11544405-11544693	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr12:11544409-11544699	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr12:11513116-11513579	MCF10A-Er-Src	breast:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
49	FOS	chr12:11513175-11513539	HUVEC	blood vessel:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
50	FOS	chr12:11513145-11513524	MCF10A-Er-Src	breast:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11548867-11548917	Jurkat	blood:	n/a
2	chr12:11549555-11549605	SK-N-SH_RA	brain:	n/a
3	chr12:11549192-11549242	PANC-1	pancreas:	n/a
4	chr12:11549555-11549605	HL-60	blood:	n/a
5	chr12:11548867-11548917	HEEpiC	esophagus:	n/a
6	chr12:11548867-11548917	AoSMC	blood vessel:	n/a
7	chr12:11548867-11548917	HEK293	kidney:	embryo
8	chr12:11548867-11548917	HRE	kidney:	n/a
9	chr12:11548019-11548069	PFSK-1	brain:	n/a
10	chr12:11548019-11548069	NB4	blood:	n/a
11	chr12:11549555-11549605	U87	brain:	n/a
12	chr12:11549555-11549605	NT2-D1	testis:	n/a
13	chr12:11549192-11549242	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:11548867-11548917	PFSK-1	brain:	n/a
15	chr12:11548019-11548069	HCPEpiC	choroid plexus:	n/a
16	chr12:11548019-11548069	AG09319	gingival:	n/a
17	chr12:11548867-11548917	HUVEC	blood vessel:	n/a
18	chr12:11549192-11549242	NT2-D1	testis:	n/a
19	chr12:11548867-11548917	K562	blood:	n/a
20	chr12:11549555-11549605	AoSMC	blood vessel:	n/a
21	chr12:11549555-11549605	HRE	kidney:	n/a
22	chr12:11549555-11549605	HRPEpiC	eye:	n/a
23	chr12:11549192-11549242	U87	brain:	n/a
24	chr12:11549192-11549242	HRCEpiC	kidney:	n/a
25	chr12:11548019-11548069	AoSMC	blood vessel:	n/a
26	chr12:11549192-11549242	GM06990	blood:	n/a
27	chr12:11548019-11548069	SK-N-SH	brain:	n/a
28	chr12:11548867-11548917	BE2_C	brain:	n/a
29	chr12:11548019-11548069	GM06990	blood:	n/a
30	chr12:11548019-11548069	AG09309	skin:	n/a
31	chr12:11549555-11549605	AG04450	lung:	fetal
32	chr12:11549555-11549605	H1-hESC	embryonic stem cell:	embryo
33	chr12:11549192-11549242	NH-A	brain:	n/a
34	chr12:11549192-11549242	A549	lung:	n/a
35	chr12:11549192-11549242	GM19239	blood:	n/a
36	chr12:11548867-11548917	GM12878	blood:	n/a
37	chr12:11549192-11549242	BJ	skin:	n/a
38	chr12:11549192-11549242	Hela-S3	cervix:	n/a
39	chr12:11549555-11549605	HAEpiC	amniotic membrane:	n/a
40	chr12:11548867-11548917	HMEC	breast:	n/a
41	chr12:11548019-11548069	SKMC	muscle:	n/a
42	chr12:11548867-11548917	LNCaP	prostate:	n/a
43	chr12:11548019-11548069	AG04449	skin:	fetal
44	chr12:11548867-11548917	IMR90	lung:	fetal
45	chr12:11549192-11549242	SKMC	muscle:	n/a
46	chr12:11548019-11548069	MCF-7	breast:	n/a
47	chr12:11548867-11548917	BJ	skin:	n/a
48	chr12:11549555-11549605	SK-N-MC	brain:	n/a
49	chr12:11549555-11549605	K562	blood:	n/a
50	chr12:11548867-11548917	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:11380961..11381600-chr12:11584509..11585267,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRB1-1	chr12:11552315-11552411	ENSG00000255790.1
2	lnc-PRB1-1	chr12:11583172-11583398	XLOC_010018
3	lnc-PRB1-1	chr12:11583144-11583398	ENSG00000255790.1
4	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
5	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
6	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
7	lnc-PRB1-1	chr12:11587926-11588092	ENSG00000255790.1
8	lnc-PRB1-1	chr12:11589237-11589254	ENSG00000255790.1
9	lnc-PRB1-1	chr12:11583186-11583398	XLOC_010018
10	lnc-PRB1-1	chr12:11559632-11559826	ENSG00000255790.1
11	lnc-PRB1-1	chr12:11584416-11584496	XLOC_010018
12	lnc-PRB1-1	chr12:11588060-11588076	XLOC_010018
13	lnc-PRB1-1	chr12:11554419-11554457	ENSG00000255790.1
14	lnc-PRB1-1	chr12:11584416-11584496	ENSG00000255790.1
15	lnc-PRB1-1	chr12:11552784-11552937	ENSG00000255790.1
16	lnc-PRB1-1	chr12:11588060-11588092	ENSG00000255790.1
17	lnc-PRB1-1	chr12:11588060-11588092	ENSG00000255790.1
18	lnc-PRB1-1	chr12:11583296-11583398	ENSG00000255790.1
19	lnc-PRB1-1	chr12:11584416-11584496	XLOC_010018
20	lnc-PRB1-1	chr12:11587926-11588092	XLOC_010018

No data

Variant related genes	Relation type
PRB2	TF binding region
ENSG00000255790	TF binding region
PRB1	TF binding region
PRB2	CpG island
ENSG00000255790	CpG island
PRB1	CpG island

Extended variants
information (count: 2774 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2774 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115700772	chr12:11512493-11512494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559547691	chr12:11512503-11512504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs149642389	chr12:11512505-11512506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370836079	chr12:11512506-11512507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144949863	chr12:11512528-11512529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs574800594	chr12:11512542-11512543	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs568212866	chr12:11512565-11512566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543520787	chr12:11512567-11512568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567039686	chr12:11512633-11512634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12296615	chr12:11512647-11512648	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs552808520	chr12:11512662-11512663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs570793683	chr12:11512708-11512709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370157820	chr12:11512753-11512754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553285462	chr12:11512807-11512808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138823875	chr12:11512810-11512811	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs535639655	chr12:11512827-11512828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555552826	chr12:11512831-11512832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374390288	chr12:11512849-11512850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141981836	chr12:11512850-11512851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs376027592	chr12:11512860-11512861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563946175	chr12:11512866-11512867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs181607616	chr12:11512884-11512885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146328528	chr12:11512906-11512907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559610623	chr12:11512929-11512930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148544590	chr12:11512944-11512945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184373606	chr12:11512948-11512949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561907902	chr12:11512951-11512952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141256361	chr12:11512968-11512969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188832509	chr12:11512972-11512973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150772255	chr12:11512982-11512983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs55954825	chr12:11512997-11512998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181340834	chr12:11513013-11513014	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149963481	chr12:11513015-11513016	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4114021	chr12:11513067-11513068	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs112875869	chr12:11513069-11513070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555614568	chr12:11513096-11513097	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs186071926	chr12:11513157-11513158	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs140281128	chr12:11513160-11513161	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs61930112	chr12:11513179-11513180	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs368308323	chr12:11513203-11513204	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs534017220	chr12:11513265-11513266	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs577608132	chr12:11513283-11513284	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs539839674	chr12:11513290-11513291	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs7969988	chr12:11513312-11513313	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs572969906	chr12:11513314-11513315	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs544995178	chr12:11513320-11513321	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs573210806	chr12:11513326-11513327	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs190969641	chr12:11513337-11513338	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs542086026	chr12:11513338-11513339	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs374051022	chr12:11513350-11513351	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11511200-11519600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr12:11512400-11514000	Enhancers	HUVEC	blood vessel
3	chr12:11513000-11513800	Enhancers	HMEC	breast
4	chr12:11513000-11514000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr12:11513000-11514000	Enhancers	NHEK	skin
6	chr12:11513400-11513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr12:11513600-11514200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr12:11513600-11521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:11516600-11517000	Enhancers	HepG2	liver
10	chr12:11519600-11520200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr12:11520000-11520600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr12:11520200-11521200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr12:11521200-11521800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr12:11521400-11521600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:11529600-11529800	Weak transcription	Primary hematopoietic stem cells	blood
16	chr12:11530200-11531200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:11539200-11539400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:11539400-11539800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr12:11544000-11544800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr12:11544000-11544800	Enhancers	HUVEC	blood vessel
21	chr12:11544800-11550000	Weak transcription	HUVEC	blood vessel
22	chr12:11544800-11550200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr12:11550000-11550600	Enhancers	HUVEC	blood vessel
24	chr12:11550000-11550800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:11550000-11551000	Enhancers	Primary neutrophils fromperipheralblood	blood
26	chr12:11550200-11550800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr12:11550200-11550800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr12:11550200-11551000	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr12:11550800-11551600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr12:11550800-11568400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:11551600-11551800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr12:11560600-11561800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr12:11561000-11561600	Enhancers	HMEC	breast
34	chr12:11561000-11561800	Enhancers	NHEK	skin
35	chr12:11561800-11563000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:11568800-11569200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr12:11569200-11569600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr12:11569200-11570000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr12:11570000-11579000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr12:11575800-11576200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr12:11584400-11584800	Enhancers	Fetal Thymus	thymus
42	chr12:11584600-11586200	Enhancers	GM12878-XiMat	blood
43	chr12:11585000-11586000	Enhancers	Stomach Mucosa	stomach
44	chr12:11585200-11586800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr12:11585800-11586800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr12:11585800-11587000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr12:11586000-11587200	Weak transcription	Stomach Mucosa	stomach
48	chr12:11586400-11587000	Enhancers	H9 Cell Line	embryonic stem cell
49	chr12:11587400-11587600	Enhancers	Stomach Mucosa	stomach

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