Variant report

Variant	nsv976031
Chromosome Location	chr12:48594968-48610975
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:52)
CpG islands
(count:368)
Chromatin interactive
region (count:9)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:52 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:48606538-48606570	K562	blood:	n/a	n/a
2	BHLHE40	chr12:48607870-48607924	K562	blood:	n/a	n/a
3	CEBPB	chr12:48610729-48610872	K562	blood:	n/a	n/a
4	CEBPB	chr12:48610672-48610942	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr12:48604423-48604451	GM10266	blood:	n/a	n/a
6	EP300	chr12:48606381-48606467	K562	blood:	n/a	n/a
7	GATA3	chr12:48607913-48608113	SH-SY5Y	brain:	n/a	n/a
8	JUN	chr12:48606044-48606142	H1-hESC	embryonic stem cell:	n/a	chr12:48606063-48606073 chr12:48606063-48606073
9	JUND	chr12:48606439-48606575	K562	blood:	n/a	chr12:48606445-48606454
10	MAX	chr12:48606470-48606573	NB4	blood:	n/a	n/a
11	MAX	chr12:48606182-48606496	K562	blood:	n/a	n/a
12	MAX	chr12:48606377-48606471	K562	blood:	n/a	n/a
13	MAZ	chr12:48606361-48606709	K562	blood:	n/a	n/a
14	MYC	chr12:48605557-48605692	K562	blood:	n/a	n/a
15	MYC	chr12:48606382-48606478	NB4	blood:	n/a	n/a
16	MYC	chr12:48606378-48606577	K562	blood:	n/a	n/a
17	POLR2A	chr12:48598586-48598898	K562	blood:	n/a	n/a
18	POLR2A	chr12:48595998-48596070	K562	blood:	n/a	n/a
19	POLR2A	chr12:48596146-48596789	K562	blood:	n/a	n/a
20	POLR2A	chr12:48606510-48606533	K562	blood:	n/a	n/a
21	POLR2A	chr12:48606284-48606338	GM12878	blood:	n/a	n/a
22	POLR2A	chr12:48596316-48596500	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr12:48595801-48598103	K562	blood:	n/a	n/a
24	POLR2A	chr12:48594682-48595168	K562	blood:	n/a	n/a
25	POLR2A	chr12:48601330-48601432	K562	blood:	n/a	n/a
26	POLR2A	chr12:48595997-48596313	K562	blood:	n/a	n/a
27	POLR2A	chr12:48596382-48596615	GM12878	blood:	n/a	n/a
28	POLR2A	chr12:48600651-48600701	K562	blood:	n/a	n/a
29	POLR2A	chr12:48599021-48599116	GM12878	blood:	n/a	n/a
30	POLR2A	chr12:48596640-48596663	K562	blood:	n/a	n/a
31	POLR2A	chr12:48606871-48606898	A549	lung:	n/a	n/a
32	POLR2A	chr12:48599110-48599208	K562	blood:	n/a	n/a
33	POLR2A	chr12:48597210-48597410	GM12878	blood:	n/a	n/a
34	POLR2A	chr12:48597771-48597794	MCF-7	breast:	n/a	n/a
35	POLR2A	chr12:48595376-48595525	K562	blood:	n/a	n/a
36	POLR2A	chr12:48595888-48597149	K562	blood:	n/a	n/a
37	POLR2A	chr12:48601845-48602040	K562	blood:	n/a	n/a
38	POLR2A	chr12:48596445-48596456	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr12:48606542-48606618	K562	blood:	n/a	n/a
40	POLR2A	chr12:48605003-48605098	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr12:48596682-48597212	K562	blood:	n/a	n/a
42	RAD21	chr12:48597685-48597698	HepG2	liver:	n/a	n/a
43	RCOR1	chr12:48606390-48606598	K562	blood:	n/a	n/a
44	RXRA	chr12:48606896-48607193	H1-hESC	embryonic stem cell:	n/a	n/a
45	SETDB1	chr12:48600186-48601125	U2OS	brain:	n/a	n/a
46	SPI1	chr12:48610466-48610975	HL-60	blood:	n/a	n/a
47	SPI1	chr12:48610542-48610876	HL-60	blood:	n/a	n/a
48	SPI1	chr12:48606343-48607160	HL-60	blood:	n/a	chr12:48606912-48606919
49	STAT3	chr12:48610751-48610852	MCF10A-Er-Src	breast:	n/a	n/a
50	TBP	chr12:48606547-48606643	K562	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:48596817-48596867	GM19239	blood:	n/a
2	chr12:48596817-48596867	GM12892	blood:	n/a
3	chr12:48596817-48596867	GM19239	blood:	n/a
4	chr12:48596817-48596867	GM12892	blood:	n/a
5	chr12:48598048-48598098	HCF	heart:	n/a
6	chr12:48596195-48596245	SAEC	small airway:	n/a
7	chr12:48598048-48598098	HRPEpiC	eye:	n/a
8	chr12:48596195-48596245	Jurkat	blood:	n/a
9	chr12:48596195-48596245	GM12878	blood:	n/a
10	chr12:48596195-48596245	SKMC	muscle:	n/a
11	chr12:48598048-48598098	SK-N-SH	brain:	n/a
12	chr12:48598048-48598098	PFSK-1	brain:	n/a
13	chr12:48596195-48596245	HCF	heart:	n/a
14	chr12:48596195-48596245	HMEC	breast:	n/a
15	chr12:48596195-48596245	HL-60	blood:	n/a
16	chr12:48597239-48597289	SK-N-MC	brain:	n/a
17	chr12:48597881-48597931	HRCEpiC	kidney:	n/a
18	chr12:48596195-48596245	A549	lung:	n/a
19	chr12:48597758-48597808	AG04450	lung:	fetal
20	chr12:48596817-48596867	HMEC	breast:	n/a
21	chr12:48596817-48596867	GM06990	blood:	n/a
22	chr12:48597239-48597289	HRPEpiC	eye:	n/a
23	chr12:48596817-48596867	SK-N-SH	brain:	n/a
24	chr12:48597758-48597808	Hepatocyte	liver:	n/a
25	chr12:48597881-48597931	HCM	heart:	n/a
26	chr12:48596195-48596245	HIPEpiC	eye:	n/a
27	chr12:48597881-48597931	PANC-1	pancreas:	n/a
28	chr12:48598048-48598098	A549	lung:	n/a
29	chr12:48596195-48596245	GM12892	blood:	n/a
30	chr12:48596817-48596867	SAEC	small airway:	n/a
31	chr12:48598048-48598098	MCF-7	breast:	n/a
32	chr12:48596817-48596867	AG09309	skin:	n/a
33	chr12:48598048-48598098	HCT-116	colon:	n/a
34	chr12:48596195-48596245	NT2-D1	testis:	n/a
35	chr12:48597239-48597289	HCF	heart:	n/a
36	chr12:48596817-48596867	BJ	skin:	n/a
37	chr12:48597881-48597931	AG04450	lung:	fetal
38	chr12:48596817-48596867	HCM	heart:	n/a
39	chr12:48596195-48596245	AG09319	gingival:	n/a
40	chr12:48597758-48597808	SK-N-SH	brain:	n/a
41	chr12:48597239-48597289	BJ	skin:	n/a
42	chr12:48597881-48597931	GM12891	blood:	n/a
43	chr12:48597758-48597808	HCPEpiC	choroid plexus:	n/a
44	chr12:48597758-48597808	SK-N-SH_RA	brain:	n/a
45	chr12:48597239-48597289	IMR90	lung:	fetal
46	chr12:48597881-48597931	HIPEpiC	eye:	n/a
47	chr12:48598048-48598098	U87	brain:	n/a
48	chr12:48597881-48597931	AG09319	gingival:	n/a
49	chr12:48597239-48597289	NHBE	bronchial:	n/a
50	chr12:48596817-48596867	AG04450	lung:	fetal

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:48418539..48420191-chr12:48595608..48598283,2	K562	blood:
2	chr12:48591422..48593721-chr12:48594349..48596928,3	MCF-7	breast:
3	chr12:48604281..48606360-chr12:48747019..48749419,2	K562	blood:
4	chr12:48597340..48600068-chr12:48604806..48607585,2	MCF-7	breast:
5	chr12:48604805..48606809-chr12:48611988..48614761,2	K562	blood:
6	chr12:48590967..48599544-chr12:48603415..48609675,11	K562	blood:
7	chr12:48593487..48595723-chr12:48689162..48691231,3	K562	blood:
8	chr12:48597340..48600068-chr12:48604806..48607585,2	MCF-7	breast:
9	chr12:48592235..48597569-chr12:48604278..48609203,8	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C12orf68-3	chr12:48603675-48603731	l_639_chr12:48591967-48607174_testes
2	lnc-C12orf68-1	chr12:48606567-48606681	XLOC_009734
3	lnc-C12orf68-3	chr12:48604986-48605137	l_639_chr12:48591967-48607174_testes
4	lnc-C12orf68-3	chr12:48609426-48609593	l_639_chr12:48591967-48607174_testes
5	lnc-C12orf68-3	chr12:48606131-48606195	l_639_chr12:48591967-48607174_testes
6	lnc-C12orf68-3	chr12:48603832-48604439	l_639_chr12:48591967-48607174_testes
7	lnc-C12orf68-3	chr12:48604450-48604563	l_639_chr12:48591967-48607174_testes
8	lnc-C12orf68-3	chr12:48606998-48607174	l_639_chr12:48591967-48607174_testes
9	lnc-C12orf68-3	chr12:48600924-48601045	l_639_chr12:48591967-48607174_testes
10	lnc-C12orf68-3	chr12:48609730-48610374	l_639_chr12:48591967-48607174_testes
11	lnc-C12orf68-3	chr12:48601976-48602029	l_639_chr12:48591967-48607174_testes

No data

Variant related genes	Relation type
OR10AD1	TF binding region
OR10AD1	CpG island
ENSG00000269514	chromatin interactions
ENSG00000172640	chromatin interactions
ENSG00000257955	chromatin interactions
RHOA	miRNA target sites

Extended variants
information (count: 669 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562877192	chr12:48595010-48595011	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs17122802	chr12:48595012-48595013	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs75981470	chr12:48595032-48595033	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537816992	chr12:48595072-48595073	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs547988103	chr12:48595074-48595075	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs80004446	chr12:48595106-48595107	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
7	rs561991060	chr12:48595111-48595112	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77268213	chr12:48595173-48595174	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
9	rs55981608	chr12:48595195-48595196	Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558772459	chr12:48595214-48595215	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs76088235	chr12:48595215-48595216	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374131584	chr12:48595224-48595225	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs200814154	chr12:48595225-48595226	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs539720431	chr12:48595242-48595243	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374034417	chr12:48595244-48595245	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs11168458	chr12:48595245-48595246	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs74670151	chr12:48595249-48595250	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
18	rs374241951	chr12:48595292-48595293	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs569765716	chr12:48595307-48595308	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535178892	chr12:48595320-48595321	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548884961	chr12:48595325-48595326	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111992512	chr12:48595357-48595358	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
23	rs144733502	chr12:48595368-48595369	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs111890232	chr12:48595369-48595370	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560370221	chr12:48595397-48595398	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs533347413	chr12:48595406-48595407	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs75177996	chr12:48595417-48595418	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
28	rs552518569	chr12:48595421-48595422	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs566931050	chr12:48595425-48595426	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs139892830	chr12:48595444-48595445	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
31	rs61940962	chr12:48595477-48595478	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs145330499	chr12:48595532-48595533	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs567463298	chr12:48595547-48595548	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs187603017	chr12:48595605-48595606	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370587264	chr12:48595619-48595620	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs538076010	chr12:48595628-48595629	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs547611864	chr12:48595636-48595637	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs568768950	chr12:48595644-48595645	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs371486541	chr12:48595677-48595678	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs117413636	chr12:48595710-48595711	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs75038285	chr12:48595716-48595717	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
42	rs556582356	chr12:48595755-48595756	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs369287044	chr12:48595802-48595803	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570325221	chr12:48595813-48595814	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs535522021	chr12:48595829-48595830	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs140654091	chr12:48595858-48595859	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs372260792	chr12:48595863-48595864	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs555718443	chr12:48595886-48595887	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs192030592	chr12:48595897-48595898	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs541561439	chr12:48595898-48595899	Weak transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
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
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
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Intracranial ependymoma	16609018	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48592600-48595200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr12:48592800-48595200	Enhancers	Sigmoid Colon	Sigmoid Colon
3	chr12:48592800-48596000	Weak transcription	Gastric	stomach
4	chr12:48592800-48596000	Weak transcription	Ovary	ovary
5	chr12:48592800-48600400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:48593000-48595000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr12:48593000-48595600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr12:48593000-48595600	Enhancers	Placenta	Placenta
9	chr12:48593000-48596600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr12:48593200-48595000	Enhancers	Adipose Nuclei	Adipose
11	chr12:48593200-48595000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr12:48593200-48595200	Enhancers	Psoas Muscle	Psoas
13	chr12:48593200-48596800	Weak transcription	Brain Substantia Nigra	brain
14	chr12:48593200-48599000	Weak transcription	Brain Angular Gyrus	brain
15	chr12:48593200-48600200	Weak transcription	Right Ventricle	heart
16	chr12:48593400-48596000	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr12:48593400-48600800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:48593600-48595200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr12:48593600-48596600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr12:48593800-48595200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr12:48593800-48596000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr12:48593800-48596000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr12:48593800-48596000	Weak transcription	Fetal Stomach	stomach
24	chr12:48593800-48596400	Weak transcription	Stomach Smooth Muscle	stomach
25	chr12:48593800-48596600	Weak transcription	Left Ventricle	heart
26	chr12:48593800-48598400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr12:48593800-48598400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr12:48594000-48595000	Weak transcription	Small Intestine	intestine
29	chr12:48594000-48595200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr12:48594000-48595200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr12:48594000-48595200	Enhancers	Brain Anterior Caudate	brain
32	chr12:48594000-48595200	Enhancers	Fetal Lung	lung
33	chr12:48594000-48595600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chr12:48594000-48595800	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr12:48594000-48596800	Enhancers	Primary T cells fromperipheralblood	blood
36	chr12:48594000-48598400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr12:48594200-48595000	Weak transcription	K562	blood
38	chr12:48594200-48595200	Enhancers	Primary hematopoietic stem cells	blood
39	chr12:48594200-48595200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr12:48594200-48595200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr12:48594200-48595200	Enhancers	Thymus	Thymus
42	chr12:48594200-48595800	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr12:48594200-48595800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr12:48594200-48596400	Weak transcription	Fetal Kidney	kidney
45	chr12:48594200-48598600	Weak transcription	Colon Smooth Muscle	Colon
46	chr12:48594200-48598800	Weak transcription	Fetal Heart	heart
47	chr12:48594400-48595000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
48	chr12:48594400-48595200	Enhancers	Esophagus	oesophagus
49	chr12:48594400-48595200	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr12:48594400-48595200	Enhancers	Spleen	Spleen

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