Variant report

Variant	nsv899384
Chromosome Location	chr12:85233731-85345154
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1100)
CpG islands
(count:1587)
Chromatin interactive
region (count:22)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:85268279-85268603	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:85236213-85236485	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:85268354-85268642	K562	blood:	n/a	n/a
4	ATF2	chr12:85304987-85305439	H1-hESC	embryonic stem cell:	n/a	chr12:85305196-85305207
5	ATF2	chr12:85304904-85305500	H1-hESC	embryonic stem cell:	n/a	chr12:85305196-85305207
6	BACH1	chr12:85318786-85319125	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:85251635-85251968	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:85306376-85307360	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr12:85305066-85305337	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr12:85307093-85307218	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr12:85236243-85236478	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr12:85306516-85306552	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr12:85314034-85314408	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr12:85267940-85268140	K562	blood:	n/a	n/a
15	CEBPB	chr12:85273382-85273621	IMR90	lung:	n/a	chr12:85273466-85273477 chr12:85273465-85273478
16	CEBPB	chr12:85306502-85307327	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr12:85268297-85268666	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr12:85305055-85305369	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:85268104-85268751	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr12:85273326-85273578	Hela-S3	cervix:	n/a	chr12:85273466-85273477 chr12:85273465-85273478
21	CEBPB	chr12:85306919-85307191	HepG2	liver:	n/a	n/a
22	CEBPB	chr12:85283076-85283339	H1-hESC	embryonic stem cell:	n/a	chr12:85283223-85283234
23	CEBPB	chr12:85268226-85268674	HCT-116	colon:	n/a	n/a
24	CEBPB	chr12:85312245-85312403	H1-hESC	embryonic stem cell:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
25	CEBPB	chr12:85273336-85273604	HepG2	liver:	n/a	chr12:85273466-85273477 chr12:85273465-85273478
26	CEBPB	chr12:85268226-85268641	HepG2	liver:	n/a	n/a
27	CEBPB	chr12:85293930-85294083	A549	lung:	n/a	chr12:85293967-85293978
28	CEBPB	chr12:85268353-85268653	MCF-7	breast:	n/a	n/a
29	CEBPB	chr12:85261428-85261650	HepG2	liver:	n/a	chr12:85261574-85261587 chr12:85261574-85261587 chr12:85261575-85261586
30	CEBPB	chr12:85306754-85307282	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr12:85312319-85312504	K562	blood:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
32	CEBPB	chr12:85312228-85312506	A549	lung:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
33	CEBPB	chr12:85283148-85283255	HepG2	liver:	n/a	chr12:85283223-85283234
34	CEBPB	chr12:85306923-85307295	A549	lung:	n/a	n/a
35	CEBPB	chr12:85283044-85283335	HepG2	liver:	n/a	chr12:85283223-85283234
36	CEBPB	chr12:85285233-85285419	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr12:85332468-85332718	HepG2	liver:	n/a	n/a
38	CEBPB	chr12:85268168-85268658	A549	lung:	n/a	n/a
39	CEBPB	chr12:85312217-85312538	IMR90	lung:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
40	CEBPB	chr12:85316431-85316947	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr12:85305037-85305389	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr12:85260209-85260382	A549	lung:	n/a	n/a
43	CEBPB	chr12:85306902-85307256	A549	lung:	n/a	n/a
44	CEBPB	chr12:85268313-85268684	IMR90	lung:	n/a	n/a
45	CEBPB	chr12:85293832-85294105	HepG2	liver:	n/a	chr12:85293967-85293978
46	CEBPB	chr12:85306847-85307357	A549	lung:	n/a	n/a
47	CEBPB	chr12:85273318-85273635	A549	lung:	n/a	chr12:85273466-85273477 chr12:85273465-85273478
48	CEBPB	chr12:85312197-85312540	HepG2	liver:	n/a	chr12:85312380-85312391 chr12:85312378-85312391 chr12:85312378-85312391 chr12:85312378-85312389 chr12:85312378-85312391
49	CEBPB	chr12:85313948-85314603	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:85268323-85268623	K562	blood:	n/a	n/a

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:85305408-85305458	RPTEC	kidney:	n/a
2	chr12:85305408-85305458	RPTEC	kidney:	n/a
3	chr12:85306323-85306373	Hela-S3	cervix:	n/a
4	chr12:85305087-85305137	NB4	blood:	n/a
5	chr12:85305742-85305792	Caco-2	colon:	n/a
6	chr12:85306916-85306966	HCF	heart:	n/a
7	chr12:85306916-85306966	CMK	blood:	n/a
8	chr12:85306797-85306847	HPAEpiC	pulmonary alveolar:	n/a
9	chr12:85305219-85305269	NB4	blood:	n/a
10	chr12:85306854-85306904	HNPCEpiC	eye:	n/a
11	chr12:85306828-85306878	CMK	blood:	n/a
12	chr12:85305742-85305792	Hepatocyte	liver:	n/a
13	chr12:85307080-85307130	SAEC	small airway:	n/a
14	chr12:85282560-85282610	HEK293	kidney:	embryo
15	chr12:85306741-85306791	HNPCEpiC	eye:	n/a
16	chr12:85305829-85305879	HRCEpiC	kidney:	n/a
17	chr12:85305087-85305137	NHBE	bronchial:	n/a
18	chr12:85306548-85306598	CMK	blood:	n/a
19	chr12:85306741-85306791	AG09319	gingival:	n/a
20	chr12:85306648-85306698	HMEC	breast:	n/a
21	chr12:85304696-85304746	ovcar-3	ovarian:	n/a
22	chr12:85307080-85307130	SK-N-MC	brain:	n/a
23	chr12:85306854-85306904	AoSMC	blood vessel:	n/a
24	chr12:85282560-85282610	Hepatocyte	liver:	n/a
25	chr12:85307131-85307181	SK-N-MC	brain:	n/a
26	chr12:85306574-85306624	PrEC	prostate:	n/a
27	chr12:85306548-85306598	SK-N-SH_RA	brain:	n/a
28	chr12:85307080-85307130	HIPEpiC	eye:	n/a
29	chr12:85305829-85305879	HL-60	blood:	n/a
30	chr12:85307152-85307202	NH-A	brain:	n/a
31	chr12:85305742-85305792	SKMC	muscle:	n/a
32	chr12:85306828-85306878	HRPEpiC	eye:	n/a
33	chr12:85305408-85305458	MCF10A-Er-Src	breast:	n/a
34	chr12:85307152-85307202	NHDF-neo	bronchial:	n/a
35	chr12:85306574-85306624	HAEpiC	amniotic membrane:	n/a
36	chr12:85305087-85305137	PANC-1	pancreas:	n/a
37	chr12:85307080-85307130	K562	blood:	n/a
38	chr12:85304696-85304746	Hepatocyte	liver:	n/a
39	chr12:85306741-85306791	BE2_C	brain:	n/a
40	chr12:85306021-85306071	AoSMC	blood vessel:	n/a
41	chr12:85305742-85305792	H1-hESC	embryonic stem cell:	embryo
42	chr12:85305408-85305458	A549	lung:	n/a
43	chr12:85306828-85306878	U87	brain:	n/a
44	chr12:85306574-85306624	SAEC	small airway:	n/a
45	chr12:85305219-85305269	SKMC	muscle:	n/a
46	chr12:85306474-85306524	CMK	blood:	n/a
47	chr12:85305087-85305137	Jurkat	blood:	n/a
48	chr12:85306741-85306791	GM12878	blood:	n/a
49	chr12:85305087-85305137	HEEpiC	esophagus:	n/a
50	chr12:85306474-85306524	SAEC	small airway:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:85257218..85259275-chr12:85261171..85263278,2	K562	blood:
2	chr12:85232820..85235309-chr12:85237518..85239463,2	K562	blood:
3	chr11:10315577..10316374-chr12:85304790..85305756,2	Hela-S3	cervix:
4	chr12:85336200..85337142-chr21:42086859..42087753,2	MCF-7	breast:
5	chr12:85275674..85277179-chr12:85300709..85303261,2	K562	blood:
6	chr12:85287784..85288299-chr17:41465185..41465702,2	NB4	blood:
7	chr12:85275674..85277179-chr12:85300709..85303261,2	K562	blood:
8	chr12:85269198..85269791-chr12:85451134..85451813,2	MCF-7	breast:
9	chr12:85270876..85273150-chr12:85276094..85278154,2	MCF-7	breast:
10	chr12:85328199..85330648-chr17:56736325..56738042,2	MCF-7	breast:
11	chr12:85287797..85288304-chr3:73159863..73160610,2	Hela-S3	cervix:
12	chr11:62609070..62609626-chr12:85287765..85288304,2	NB4	blood:
13	chr1:47779341..47780185-chr12:85304853..85305718,2	Hela-S3	cervix:
14	chr12:85232820..85235309-chr12:85237518..85239463,2	K562	blood:
15	chr12:85270876..85273150-chr12:85276094..85278154,2	MCF-7	breast:
16	chr12:50222179..50223090-chr12:85304791..85305560,2	Hela-S3	cervix:
17	chr12:85031251..85032044-chr12:85236099..85236834,2	MCF-7	breast:
18	chr12:85305841..85306396-chr17:26988797..26989434,2	Hela-S3	cervix:
19	chr12:85287799..85288304-chr17:41465245..41465882,2	Hela-S3	cervix:
20	chr12:85268551..85271336-chr12:85421363..85424699,4	MCF-7	breast:
21	chr12:84896709..84897539-chr12:85236279..85236879,3	MCF-7	breast:
22	chr12:84901925..84902765-chr12:85235880..85236805,3	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRIQ1-1	chr12:85308536-85308641	XLOC_009819
2	lnc-TSPAN19-2	chr12:85258120-85259169	NONHSAT029740
3	lnc-LRRIQ1-1	chr12:85306655-85306683	XLOC_009819
4	lnc-LRRIQ1-1	chr12:85332117-85332243	XLOC_009819
5	lnc-LRRIQ1-1	chr12:85306659-85306683	XLOC_009819
6	lnc-LRRIQ1-1	chr12:85308536-85308641	XLOC_009819

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC6A15	hsa-miR-23a-3p	chr12:85277173-85277191
2	SLC6A15	hsa-miR-23b-3p	chr12:85277173-85277193

Variant related genes	Relation type
ENSG00000258073	TF binding region
SLC6A15	TF binding region
ENSG00000258073	CpG island
SLC6A15	CpG island
ENSG00000109111	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000258057	chromatin interactions
ENSG00000133812	chromatin interactions
ENSG00000132581	chromatin interactions
ENSG00000123473	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000167566	chromatin interactions
ENSG00000072041	chromatin interactions

Extended variants
information (count: 3723 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3723 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535974117	chr12:85234001-85234002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs554613804	chr12:85234022-85234023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575968726	chr12:85234070-85234071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182038674	chr12:85234076-85234077	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs145973496	chr12:85234102-85234103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115314815	chr12:85234162-85234163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541332428	chr12:85234190-85234191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148629419	chr12:85234203-85234204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs529858077	chr12:85234211-85234212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549227077	chr12:85234225-85234226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535540064	chr12:85234234-85234235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561458785	chr12:85234253-85234254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531694161	chr12:85234255-85234256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186019163	chr12:85234263-85234264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142178925	chr12:85234309-85234310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190536894	chr12:85234349-85234350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150779412	chr12:85234361-85234362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538949904	chr12:85234367-85234368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs143990999	chr12:85234423-85234424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs574122001	chr12:85234435-85234436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371266521	chr12:85234496-85234497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565946901	chr12:85234498-85234499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs536825576	chr12:85234528-85234529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs182042458	chr12:85234537-85234538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186194024	chr12:85234552-85234553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569767610	chr12:85234584-85234585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536738547	chr12:85234627-85234628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558632503	chr12:85234667-85234668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs576864576	chr12:85234736-85234737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541344923	chr12:85234752-85234753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530659002	chr12:85234757-85234758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553271482	chr12:85234790-85234791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200996649	chr12:85234801-85234802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35085699	chr12:85234805-85234806	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574570009	chr12:85234806-85234807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542039732	chr12:85234807-85234808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs139627548	chr12:85234813-85234814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548698976	chr12:85234819-85234820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs59695345	chr12:85234820-85234821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563328179	chr12:85234882-85234883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs12228652	chr12:85234883-85234884	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551808709	chr12:85234890-85234891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543462658	chr12:85234899-85234900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139139287	chr12:85234924-85234925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191436700	chr12:85235028-85235029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146973849	chr12:85235032-85235033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs386764875	chr12:85235035-85235036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374320000	chr12:85235036-85235037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs386764876	chr12:85235042-85235043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs61928633	chr12:85235044-85235045	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Breast cancer	17899364	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Renal cell carcinoma	18194544	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:645 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:85234000-85234400	Enhancers	NHDF-Ad	bronchial
2	chr12:85234000-85235800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr12:85234200-85236000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:85237400-85237600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr12:85238000-85238400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr12:85243000-85250200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:85249600-85251000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr12:85249600-85251000	Enhancers	NHEK	skin
9	chr12:85249800-85252200	Enhancers	HMEC	breast
10	chr12:85250000-85271400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:85250200-85250600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:85250200-85250600	Enhancers	Muscle Satellite Cultured Cells	--
13	chr12:85250200-85251000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr12:85250200-85251400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr12:85250400-85250600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr12:85250400-85250600	Enhancers	NHDF-Ad	bronchial
17	chr12:85250400-85251200	Enhancers	Esophagus	oesophagus
18	chr12:85250400-85251600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr12:85250600-85250800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr12:85250600-85251800	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:85250600-85264400	Weak transcription	NHDF-Ad	bronchial
22	chr12:85250800-85251400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr12:85251000-85251400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr12:85251000-85251600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:85251000-85303000	Weak transcription	NHEK	skin
26	chr12:85251200-85251400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr12:85251400-85251600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:85251400-85251600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr12:85251400-85252000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr12:85251400-85255400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:85251400-85256800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:85251600-85251800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr12:85251600-85255400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr12:85251600-85267200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:85251800-85257600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr12:85251800-85285400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr12:85252000-85255200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr12:85252000-85263400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr12:85252200-85254000	Weak transcription	HMEC	breast
40	chr12:85253800-85271200	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr12:85254000-85257200	Strong transcription	HMEC	breast
42	chr12:85254000-85276800	Weak transcription	Fetal Brain Male	brain
43	chr12:85254000-85289800	Weak transcription	Brain Angular Gyrus	brain
44	chr12:85254600-85270600	Weak transcription	Brain Substantia Nigra	brain
45	chr12:85254800-85271200	Weak transcription	Brain Hippocampus Middle	brain
46	chr12:85255000-85257600	Weak transcription	Brain Germinal Matrix	brain
47	chr12:85255200-85260400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr12:85255400-85257000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:85255400-85284200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr12:85256800-85257400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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