Variant report

Variant	nsv469358
Chromosome Location	chr12:38919524-38989405
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 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	BATF	chr12:38978987-38979244	GM12878	blood:	n/a	chr12:38979090-38979101
2	BATF	chr12:38978937-38979254	GM12878	blood:	n/a	chr12:38978975-38978984 chr12:38979090-38979101
3	BRCA1	chr12:38980636-38980915	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:38950379-38950387	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:38949928-38950461	Hela-S3	cervix:	n/a	chr12:38950417-38950428
6	CEBPB	chr12:38982893-38983133	MCF-7	breast:	n/a	chr12:38982971-38982982
7	CEBPB	chr12:38980443-38981124	Hela-S3	cervix:	n/a	chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980917-38980930 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980712
8	CEBPB	chr12:38950329-38950425	A549	lung:	n/a	n/a
9	CEBPB	chr12:38982562-38983243	Hela-S3	cervix:	n/a	chr12:38982971-38982982
10	CEBPB	chr12:38982837-38983151	H1-hESC	embryonic stem cell:	n/a	chr12:38982971-38982982
11	CEBPB	chr12:38951490-38951690	A549	lung:	n/a	chr12:38951566-38951577
12	CEBPB	chr12:38982717-38983202	ECC-1	luminal epithelium:	n/a	chr12:38982971-38982982
13	CEBPB	chr12:38982828-38983122	HepG2	liver:	n/a	chr12:38982971-38982982
14	CEBPB	chr12:38982762-38983190	ECC-1	luminal epithelium:	n/a	chr12:38982971-38982982
15	CEBPB	chr12:38981442-38981823	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr12:38980570-38980873	A549	lung:	n/a	chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980710 chr12:38980701-38980712
17	CEBPB	chr12:38933170-38933247	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr12:38951466-38951741	HepG2	liver:	n/a	chr12:38951566-38951577
19	CEBPB	chr12:38951464-38951704	IMR90	lung:	n/a	chr12:38951566-38951577
20	CHD2	chr12:38980670-38980954	Hela-S3	cervix:	n/a	n/a
21	CTCF	chr12:38938500-38938650	GM12878	blood:	n/a	n/a
22	CTCF	chr12:38938680-38938830	GM12866	blood:	n/a	n/a
23	CTCF	chr12:38988476-38988548	GM19239	blood:	n/a	n/a
24	CTCF	chr12:38938320-38938470	HCT-116	colon:	n/a	n/a
25	CTCF	chr12:38938600-38938750	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr12:38938620-38938770	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr12:38938400-38938550	A549	lung:	n/a	n/a
28	CTCF	chr12:38938600-38938750	HepG2	liver:	n/a	n/a
29	CTCF	chr12:38938588-38938731	HepG2	liver:	n/a	n/a
30	CTCF	chr12:38938593-38938737	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr12:38938658-38938737	GM13976	blood:	n/a	n/a
32	CTCF	chr12:38938600-38938750	GM12873	blood:	n/a	n/a
33	CTCF	chr12:38957486-38957542	GM20000	blood:	n/a	n/a
34	CTCF	chr12:38938636-38938729	GM13977	blood:	n/a	n/a
35	CTCF	chr12:38938580-38938730	GM12874	blood:	n/a	n/a
36	CTCF	chr12:38938527-38938841	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr12:38938660-38938810	BE2_C	brain:	n/a	n/a
38	CTCF	chr12:38938600-38938750	HMF	breast:	n/a	n/a
39	CTCF	chr12:38938580-38938730	GM06990	blood:	n/a	n/a
40	CTCF	chr12:38938620-38938770	HCT-116	colon:	n/a	n/a
41	CTCF	chr12:38949551-38949727	LNCaP	prostate:	n/a	n/a
42	CTCF	chr12:38938520-38938670	GM06990	blood:	n/a	n/a
43	CTCF	chr12:38938640-38938790	GM12872	blood:	n/a	n/a
44	CTCF	chr12:38938580-38938730	GM12873	blood:	n/a	n/a
45	CTCF	chr12:38938626-38938738	LNCaP	prostate:	n/a	n/a
46	CTCF	chr12:38938560-38938710	NB4	blood:	n/a	n/a
47	CTCF	chr12:38938622-38938739	GM19238	blood:	n/a	n/a
48	CTCF	chr12:38938580-38938730	GM12869	blood:	n/a	n/a
49	CTCF	chr12:38938634-38938708	GM12892	blood:	n/a	n/a
50	CTCF	chr12:38949562-38949736	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:38984007-38984057	HCF	heart:	n/a
2	chr12:38938054-38938104	Hela-S3	cervix:	n/a
3	chr12:38984007-38984057	HepG2	liver:	n/a
4	chr12:38938054-38938104	NHBE	bronchial:	n/a
5	chr12:38938054-38938104	AG04450	lung:	fetal
6	chr12:38984007-38984057	IMR90	lung:	fetal
7	chr12:38984007-38984057	RPTEC	kidney:	n/a
8	chr12:38984007-38984057	HIPEpiC	eye:	n/a
9	chr12:38938054-38938104	Jurkat	blood:	n/a
10	chr12:38984007-38984057	HEK293	kidney:	embryo
11	chr12:38984007-38984057	GM06990	blood:	n/a
12	chr12:38938054-38938104	LNCaP	prostate:	n/a
13	chr12:38984007-38984057	HUVEC	blood vessel:	n/a
14	chr12:38938054-38938104	MCF-7	breast:	n/a
15	chr12:38938054-38938104	H1-hESC	embryonic stem cell:	embryo
16	chr12:38938054-38938104	NH-A	brain:	n/a
17	chr12:38984007-38984057	NHDF-neo	bronchial:	n/a
18	chr12:38938054-38938104	HCT-116	colon:	n/a
19	chr12:38984007-38984057	ProgFib	skin:	n/a
20	chr12:38938054-38938104	SKMC	muscle:	n/a
21	chr12:38938054-38938104	HRE	kidney:	n/a
22	chr12:38984007-38984057	Hepatocyte	liver:	n/a
23	chr12:38938054-38938104	GM12891	blood:	n/a
24	chr12:38938054-38938104	T-47D	breast:	n/a
25	chr12:38984007-38984057	NH-A	brain:	n/a
26	chr12:38938054-38938104	AG09319	gingival:	n/a
27	chr12:38984007-38984057	HCPEpiC	choroid plexus:	n/a
28	chr12:38938054-38938104	GM12892	blood:	n/a
29	chr12:38938054-38938104	HL-60	blood:	n/a
30	chr12:38938054-38938104	Caco-2	colon:	n/a
31	chr12:38984007-38984057	HCM	heart:	n/a
32	chr12:38984007-38984057	SK-N-MC	brain:	n/a
33	chr12:38984007-38984057	AG04450	lung:	fetal
34	chr12:38938054-38938104	HPAEpiC	pulmonary alveolar:	n/a
35	chr12:38984007-38984057	HRE	kidney:	n/a
36	chr12:38938054-38938104	K562	blood:	n/a
37	chr12:38984007-38984057	Caco-2	colon:	n/a
38	chr12:38938054-38938104	HEK293	kidney:	embryo
39	chr12:38938054-38938104	HNPCEpiC	eye:	n/a
40	chr12:38984007-38984057	HMEC	breast:	n/a
41	chr12:38984007-38984057	PANC-1	pancreas:	n/a
42	chr12:38984007-38984057	ECC-1	luminal epithelium:	n/a
43	chr12:38938054-38938104	A549	lung:	n/a
44	chr12:38984007-38984057	Jurkat	blood:	n/a
45	chr12:38984007-38984057	SAEC	small airway:	n/a
46	chr12:38984007-38984057	AG10803	skin:	n/a
47	chr12:38984007-38984057	HNPCEpiC	eye:	n/a
48	chr12:38984007-38984057	PFSK-1	brain:	n/a
49	chr12:38984007-38984057	BJ	skin:	n/a
50	chr12:38984007-38984057	GM19239	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:38954957..38957532-chr12:38958850..38960983,2	K562	blood:
2	chr12:38917479..38920369-chr12:38920412..38922084,2	K562	blood:
3	chr12:38954957..38957532-chr12:38958850..38960983,2	K562	blood:
4	chr12:38917479..38920369-chr12:38920412..38922084,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPNE8-1	chr12:38983517-38983614	XLOC_010050
2	lnc-CPNE8-1	chr12:38937979-38938333	ENSG00000258119
3	lnc-CPNE8-1	chr12:38937980-38938333	XLOC_010050
4	lnc-CPNE8-1	chr12:38983132-38983232	ENSG00000258119
5	lnc-CPNE8-1	chr12:38940187-38940279	ENSG00000258119
6	lnc-CPNE8-1	chr12:38940187-38940310	ENSG00000258119
7	lnc-CPNE8-1	chr12:38938130-38938378	ENSG00000258119
8	lnc-CPNE8-1	chr12:38983517-38983614	ENSG00000258119
9	lnc-CPNE8-1	chr12:38983132-38983232	XLOC_010050
10	lnc-CPNE8-1	chr12:38940187-38940310	XLOC_010050

No data

Variant related genes	Relation type
ENSG00000258119	TF binding region
ENSG00000257645	TF binding region
ENSG00000258119	CpG island
ENSG00000257645	CpG island
C1D	miRNA target sites
ZFP1	miRNA target sites
SLC39A14	miRNA target sites
NSF	miRNA target sites
SLC39A10	miRNA target sites
GREB1	miRNA target sites
HECTD3	miRNA target sites
SLC39A11	miRNA target sites

Extended variants
information (count: 653 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:653 , 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	rs562960441	chr12:38919831-38919832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2730907	chr12:38919869-38919870	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs562180109	chr12:38919885-38919886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551565379	chr12:38919902-38919903	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147984482	chr12:38919912-38919913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs74087079	chr12:38919934-38919935	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs141612546	chr12:38919983-38919984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374560988	chr12:38920006-38920007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188122253	chr12:38920020-38920021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181347128	chr12:38920137-38920138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569735890	chr12:38920141-38920142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185276498	chr12:38920173-38920174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113653600	chr12:38920197-38920198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs570004484	chr12:38920204-38920205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181661012	chr12:38920218-38920219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2730908	chr12:38920247-38920248	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs375743515	chr12:38920256-38920257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574358320	chr12:38920266-38920267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs7976704	chr12:38920327-38920328	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563228698	chr12:38920355-38920356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs12580227	chr12:38920421-38920422	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs545626504	chr12:38920447-38920448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565194825	chr12:38920449-38920450	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138341293	chr12:38920489-38920490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs559129969	chr12:38920491-38920492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547358823	chr12:38920567-38920568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144076055	chr12:38920639-38920640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530070778	chr12:38920645-38920646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549786674	chr12:38920655-38920656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs187294756	chr12:38920657-38920658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538446237	chr12:38920673-38920674	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552813285	chr12:38920711-38920712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192405956	chr12:38920762-38920763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377365395	chr12:38920810-38920811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147309437	chr12:38920841-38920842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183802126	chr12:38920881-38920882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185503279	chr12:38920924-38920925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574466671	chr12:38920930-38920931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs189672243	chr12:38920931-38920932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs568125027	chr12:38920955-38920956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1393536	chr12:38920956-38920957	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs558847147	chr12:38920958-38920959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1393537	chr12:38920961-38920962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs140916452	chr12:38920971-38920972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182719485	chr12:38920982-38920983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs75801959	chr12:38920996-38920997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2730909	chr12:38921000-38921001	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs530034715	chr12:38921034-38921035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550189035	chr12:38921043-38921044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577009067	chr12:38921063-38921064	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:76 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38919800-38922000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr12:38921400-38921800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:38936000-38936600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:38936000-38938000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr12:38936000-38938400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr12:38936200-38936400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr12:38936200-38936800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr12:38936200-38938400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr12:38936400-38937200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:38936400-38937600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr12:38936400-38938600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr12:38936400-38939000	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr12:38936400-38939000	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr12:38936600-38937200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:38936800-38937200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr12:38936800-38937400	Enhancers	Hela-S3	cervix
17	chr12:38936800-38939000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr12:38936800-38939000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr12:38937200-38937400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr12:38937200-38938000	Enhancers	Duodenum Smooth Muscle	Duodenum
21	chr12:38937200-38938600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr12:38937200-38938600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr12:38937200-38939000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:38937400-38939000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr12:38937400-38941000	Weak transcription	Hela-S3	cervix
26	chr12:38937600-38938200	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr12:38937800-38939000	Enhancers	Colon Smooth Muscle	Colon
28	chr12:38938000-38938200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr12:38938000-38938400	Active TSS	Duodenum Smooth Muscle	Duodenum
30	chr12:38938200-38938400	Enhancers	H1 Cell Line	embryonic stem cell
31	chr12:38938200-38938600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr12:38938200-38938600	Enhancers	Rectal Smooth Muscle	rectum
33	chr12:38938200-38938800	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr12:38938400-38938600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
35	chr12:38938400-38938800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr12:38938800-38939000	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr12:38938800-38939200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr12:38941000-38941800	Enhancers	Hela-S3	cervix
39	chr12:38941200-38942000	Enhancers	HMEC	breast
40	chr12:38941200-38942600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:38949600-38949800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr12:38949600-38950400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr12:38949600-38950400	Enhancers	Rectal Smooth Muscle	rectum
44	chr12:38949600-38950600	Enhancers	Hela-S3	cervix
45	chr12:38949600-38951000	Enhancers	Colon Smooth Muscle	Colon
46	chr12:38949800-38950000	Active TSS	Monocytes-CD14+_RO01746	blood
47	chr12:38949800-38950200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
48	chr12:38950000-38950400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr12:38950000-38950400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr12:38950000-38950800	Enhancers	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links