Variant report

Variant	nsv559049
Chromosome Location	chr12:59359937-59436179
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:322)
CpG islands
(count:122)
Chromatin interactive
region (count:25)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:322 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:59382413-59382887	GM12878	blood:	n/a	n/a
2	ATF2	chr12:59382458-59382738	GM12878	blood:	n/a	n/a
3	BACH1	chr12:59360748-59360988	K562	blood:	n/a	chr12:59360900-59360914
4	BACH1	chr12:59360636-59361052	H1-hESC	embryonic stem cell:	n/a	chr12:59360900-59360914
5	BATF	chr12:59430873-59431101	GM12878	blood:	n/a	n/a
6	BATF	chr12:59430802-59431120	GM12878	blood:	n/a	n/a
7	BCL3	chr12:59434986-59435561	A549	lung:	n/a	chr12:59435377-59435386
8	BRCA1	chr12:59434681-59435914	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr12:59435033-59435560	MCF-7	breast:	n/a	chr12:59435298-59435309
10	CEBPB	chr12:59434995-59435853	Hela-S3	cervix:	n/a	chr12:59435298-59435309
11	CEBPB	chr12:59422466-59422666	A549	lung:	n/a	chr12:59422524-59422533 chr12:59422524-59422533 chr12:59422524-59422533 chr12:59422522-59422533 chr12:59422524-59422533 chr12:59422524-59422535
12	CEBPB	chr12:59435049-59435608	A549	lung:	n/a	chr12:59435298-59435309
13	CEBPB	chr12:59434922-59435638	MCF-7	breast:	n/a	chr12:59435298-59435309
14	CEBPB	chr12:59435143-59435629	A549	lung:	n/a	chr12:59435298-59435309
15	CEBPB	chr12:59420905-59421451	MCF-7	breast:	n/a	chr12:59421183-59421194
16	CEBPB	chr12:59434973-59435737	A549	lung:	n/a	chr12:59435298-59435309
17	CEBPB	chr12:59364978-59365248	IMR90	lung:	n/a	chr12:59365144-59365155
18	CEBPB	chr12:59409569-59409871	IMR90	lung:	n/a	n/a
19	CEBPB	chr12:59435251-59435408	HepG2	liver:	n/a	chr12:59435298-59435309
20	CEBPB	chr12:59409611-59409884	A549	lung:	n/a	n/a
21	CEBPB	chr12:59364996-59365299	HepG2	liver:	n/a	chr12:59365144-59365155
22	CEBPB	chr12:59405214-59405425	HepG2	liver:	n/a	n/a
23	CEBPB	chr12:59435025-59436355	IMR90	lung:	n/a	chr12:59435298-59435309 chr12:59436175-59436184 chr12:59436175-59436184
24	CEBPB	chr12:59422407-59422651	HepG2	liver:	n/a	chr12:59422524-59422533 chr12:59422524-59422533 chr12:59422524-59422533 chr12:59422522-59422533 chr12:59422524-59422533 chr12:59422524-59422535
25	CEBPB	chr12:59433863-59434076	Hela-S3	cervix:	n/a	chr12:59434009-59434020
26	CEBPB	chr12:59426520-59426780	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:59434994-59435728	HCT-116	colon:	n/a	chr12:59435298-59435309
28	CEBPB	chr12:59421021-59421369	MCF-7	breast:	n/a	chr12:59421183-59421194
29	CEBPB	chr12:59433789-59434137	MCF-7	breast:	n/a	chr12:59434009-59434020
30	CEBPB	chr12:59435012-59435604	HCT-116	colon:	n/a	chr12:59435298-59435309
31	CEBPB	chr12:59433853-59434152	IMR90	lung:	n/a	chr12:59434009-59434020
32	CEBPB	chr12:59430875-59431217	IMR90	lung:	n/a	n/a
33	CEBPB	chr12:59364992-59365215	A549	lung:	n/a	chr12:59365144-59365155
34	CHD2	chr12:59435069-59435766	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:59397466-59397502	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr12:59376478-59376522	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr12:59414340-59414490	AG10803	skin:	n/a	n/a
38	CTCF	chr12:59374384-59374420	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr12:59380717-59380757	LNCaP	prostate:	n/a	n/a
40	CTCF	chr12:59434680-59434830	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr12:59414340-59414490	AG04449	skin:	n/a	n/a
42	CTCF	chr12:59370100-59370250	HRE	kidney:	n/a	n/a
43	CTCF	chr12:59424260-59424410	HEEpiC	esophagus:	n/a	n/a
44	CTCF	chr12:59434480-59434630	GM12873	blood:	n/a	n/a
45	E2F4	chr12:59434080-59434485	MCF10A-Er-Src	breast:	n/a	chr12:59434293-59434302 chr12:59434294-59434301 chr12:59434294-59434301 chr12:59434290-59434302 chr12:59434294-59434301
46	E2F4	chr12:59413124-59413281	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr12:59374619-59374790	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr12:59395512-59395661	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr12:59417159-59417354	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr12:59419610-59419688	MCF10A-Er-Src	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:59426481-59426531	IMR90	lung:	fetal
2	chr12:59434386-59434436	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:59434386-59434436	MCF10A-Er-Src	breast:	n/a
4	chr12:59426481-59426531	AG09319	gingival:	n/a
5	chr12:59434386-59434436	HIPEpiC	eye:	n/a
6	chr12:59426481-59426531	HL-60	blood:	n/a
7	chr12:59434386-59434436	Jurkat	blood:	n/a
8	chr12:59434386-59434436	Hela-S3	cervix:	n/a
9	chr12:59434386-59434436	HMEC	breast:	n/a
10	chr12:59434386-59434436	GM19239	blood:	n/a
11	chr12:59426481-59426531	HCM	heart:	n/a
12	chr12:59426481-59426531	HEEpiC	esophagus:	n/a
13	chr12:59434386-59434436	AoSMC	blood vessel:	n/a
14	chr12:59434386-59434436	SK-N-MC	brain:	n/a
15	chr12:59434386-59434436	SAEC	small airway:	n/a
16	chr12:59426481-59426531	ovcar-3	ovarian:	n/a
17	chr12:59434386-59434436	HEK293	kidney:	embryo
18	chr12:59426481-59426531	K562	blood:	n/a
19	chr12:59434386-59434436	SK-N-SH_RA	brain:	n/a
20	chr12:59426481-59426531	HEK293	kidney:	embryo
21	chr12:59426481-59426531	AoSMC	blood vessel:	n/a
22	chr12:59434386-59434436	HRCEpiC	kidney:	n/a
23	chr12:59434386-59434436	CMK	blood:	n/a
24	chr12:59434386-59434436	U87	brain:	n/a
25	chr12:59434386-59434436	A549	lung:	n/a
26	chr12:59434386-59434436	NHBE	bronchial:	n/a
27	chr12:59434386-59434436	HNPCEpiC	eye:	n/a
28	chr12:59426481-59426531	AG04449	skin:	fetal
29	chr12:59434386-59434436	HEEpiC	esophagus:	n/a
30	chr12:59434386-59434436	BJ	skin:	n/a
31	chr12:59434386-59434436	NB4	blood:	n/a
32	chr12:59434386-59434436	H1-hESC	embryonic stem cell:	embryo
33	chr12:59426481-59426531	U87	brain:	n/a
34	chr12:59426481-59426531	GM12891	blood:	n/a
35	chr12:59426481-59426531	SAEC	small airway:	n/a
36	chr12:59434386-59434436	Hepatocyte	liver:	n/a
37	chr12:59426481-59426531	HepG2	liver:	n/a
38	chr12:59426481-59426531	SKMC	muscle:	n/a
39	chr12:59434386-59434436	HCF	heart:	n/a
40	chr12:59434386-59434436	K562	blood:	n/a
41	chr12:59426481-59426531	H1-hESC	embryonic stem cell:	embryo
42	chr12:59426481-59426531	GM19239	blood:	n/a
43	chr12:59434386-59434436	NT2-D1	testis:	n/a
44	chr12:59434386-59434436	HCT-116	colon:	n/a
45	chr12:59434386-59434436	NHDF-neo	bronchial:	n/a
46	chr12:59434386-59434436	AG09319	gingival:	n/a
47	chr12:59426481-59426531	BJ	skin:	n/a
48	chr12:59426481-59426531	NHBE	bronchial:	n/a
49	chr12:59426481-59426531	HUVEC	blood vessel:	n/a
50	chr12:59426481-59426531	HCT-116	colon:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:59424176..59425822-chr12:59427744..59429676,2	MCF-7	breast:
2	chr12:59312784..59315143-chr12:59433489..59436442,3	MCF-7	breast:
3	chr12:59433661..59435709-chr12:59436125..59437780,2	MCF-7	breast:
4	chr12:59374063..59376075-chr12:59376225..59377871,2	MCF-7	breast:
5	chr12:59379293..59381113-chr12:59382068..59383913,2	MCF-7	breast:
6	chr12:59379293..59381113-chr12:59382068..59383913,2	MCF-7	breast:
7	chr12:59374063..59376075-chr12:59376225..59377871,2	MCF-7	breast:
8	chr12:59431224..59433433-chr12:59436117..59438900,2	MCF-7	breast:
9	chr12:59427199..59431136-chr12:59432633..59435371,3	MCF-7	breast:
10	chr12:59423710..59426596-chr12:59433286..59435504,3	MCF-7	breast:
11	chr12:59311843..59315228-chr12:59434167..59436634,3	MCF-7	breast:
12	chr12:59434389..59437372-chr12:59438954..59440734,2	MCF-7	breast:
13	chr12:59424515..59427009-chr12:59427477..59429305,2	MCF-7	breast:
14	chr12:58926114..58928462-chr12:59432345..59434886,2	MCF-7	breast:
15	chr12:59424515..59427009-chr12:59427477..59429305,2	MCF-7	breast:
16	chr12:59316988..59319843-chr12:59408494..59410579,2	MCF-7	breast:
17	chr12:59411769..59412269-chr7:158497029..158497610,2	Hela-S3	cervix:
18	chr12:59433661..59435709-chr12:59436125..59437780,2	MCF-7	breast:
19	chr12:59237601..59239530-chr12:59433065..59435700,2	MCF-7	breast:
20	chr12:59424176..59425822-chr12:59427744..59429676,2	MCF-7	breast:
21	chr12:59427199..59431136-chr12:59432633..59435371,3	MCF-7	breast:
22	chr12:59312321..59314665-chr12:59372859..59375029,2	MCF-7	breast:
23	chr12:59423710..59426596-chr12:59433286..59435504,3	MCF-7	breast:
24	chr12:59413167..59414727-chr12:59431190..59432775,2	MCF-7	breast:
25	chr12:59431224..59433433-chr12:59436117..59438900,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-362K2.2.1-3	chr12:59413950-59414675	NONHSAT029040

No data

Variant related genes	Relation type
RPS6P22	TF binding region
RPS6P22	CpG island
ENSG00000139263	chromatin interactions
ENSG00000146918	chromatin interactions
ENSG00000257443	chromatin interactions
ENSG00000244390	chromatin interactions

Extended variants
information (count: 2252 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2252 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10877195	chr12:59359937-59359938	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564148330	chr12:59360049-59360050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532674981	chr12:59360149-59360150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs548043435	chr12:59360222-59360223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559814054	chr12:59360225-59360226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533763431	chr12:59360255-59360256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181206708	chr12:59360270-59360271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548376792	chr12:59360446-59360447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs67446558	chr12:59360450-59360451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs77597743	chr12:59360507-59360508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs61919514	chr12:59360525-59360526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569812073	chr12:59360592-59360593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1148527	chr12:59360601-59360602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145107769	chr12:59360676-59360677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552273661	chr12:59360703-59360704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138868414	chr12:59360706-59360707	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534730084	chr12:59360707-59360708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578102115	chr12:59360753-59360754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553198115	chr12:59360789-59360790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574792920	chr12:59360793-59360794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535596237	chr12:59360815-59360816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371425608	chr12:59360829-59360830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553830998	chr12:59360851-59360852	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186520875	chr12:59360915-59360916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs142000362	chr12:59360930-59360931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190290312	chr12:59360947-59360948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7957374	chr12:59360952-59360953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542250064	chr12:59361001-59361002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572765996	chr12:59361074-59361075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs539859336	chr12:59361081-59361082	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs61224379	chr12:59361082-59361083	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs148080311	chr12:59361089-59361090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73118596	chr12:59361098-59361099	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs59693178	chr12:59361167-59361168	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs530892954	chr12:59361211-59361212	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576634841	chr12:59361256-59361257	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545368847	chr12:59361271-59361272	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562162994	chr12:59361300-59361301	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552610696	chr12:59361309-59361310	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570872074	chr12:59361396-59361397	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528445149	chr12:59361397-59361398	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141827587	chr12:59361425-59361426	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527823856	chr12:59361447-59361448	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78067201	chr12:59361450-59361451	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1823337	chr12:59361467-59361468	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557175476	chr12:59361484-59361485	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576144246	chr12:59361490-59361491	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147812393	chr12:59361504-59361505	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569046962	chr12:59361505-59361506	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs539274159	chr12:59361528-59361529	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Glioblastoma	17090523	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	16773561	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Breast cancer	21364760	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59356000-59364000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr12:59356600-59360600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr12:59360600-59361000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr12:59360600-59361000	Enhancers	A549	lung
5	chr12:59360600-59361000	Enhancers	HSMMtube	muscle
6	chr12:59360600-59361200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:59360600-59361600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr12:59360600-59361800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr12:59360600-59361800	Enhancers	NHDF-Ad	bronchial
10	chr12:59360800-59361000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr12:59360800-59361200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:59360800-59361800	Enhancers	Muscle Satellite Cultured Cells	--
13	chr12:59361200-59361400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr12:59361200-59361600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:59361200-59361600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:59361200-59361600	Enhancers	Fetal Brain Male	brain
17	chr12:59361200-59361800	Enhancers	Fetal Brain Female	brain
18	chr12:59361200-59361800	Enhancers	NHEK	skin
19	chr12:59361400-59361600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:59361400-59362000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:59361600-59362000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:59361600-59362600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:59361800-59362800	Weak transcription	NHDF-Ad	bronchial
24	chr12:59362600-59363400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr12:59362800-59363000	Enhancers	NHDF-Ad	bronchial
26	chr12:59362800-59363800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:59363400-59364200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr12:59364000-59364800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:59364200-59365400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr12:59369600-59370200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:59369800-59370200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:59369800-59370200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr12:59370200-59373400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr12:59373400-59373600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr12:59375800-59377800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:59377600-59378200	Enhancers	Brain Germinal Matrix	brain
37	chr12:59377800-59381200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr12:59378000-59378400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr12:59379400-59379600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr12:59379600-59381400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:59381200-59382200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr12:59381400-59382600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr12:59382200-59383200	Enhancers	HUVEC	blood vessel
44	chr12:59382600-59391000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:59396400-59396600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:59397800-59398000	Enhancers	NHDF-Ad	bronchial
47	chr12:59398000-59398200	Flanking Active TSS	NHDF-Ad	bronchial
48	chr12:59398000-59398600	Active TSS	Pancreatic Islets	Pancreatic Islet
49	chr12:59398200-59398400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:59398200-59398400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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