Variant report

Variant	esv2761503
Chromosome Location	chr9:14960217-15049343
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:478)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:478 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14967513-14968337	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14960946-14962339	HepG2	liver:	n/a	n/a
3	ATF1	chr9:14992118-14992479	K562	blood:	n/a	n/a
4	ATF1	chr9:14993152-14993450	K562	blood:	n/a	n/a
5	BATF	chr9:14992095-14992275	GM12878	blood:	n/a	n/a
6	BCL3	chr9:14974056-14974338	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:14993063-14993414	K562	blood:	n/a	n/a
8	BHLHE40	chr9:14961666-14961683	K562	blood:	n/a	n/a
9	CBX3	chr9:14993086-14993431	K562	blood:	n/a	n/a
10	CCNT2	chr9:14993093-14993468	K562	blood:	n/a	chr9:14993195-14993204
11	CEBPB	chr9:14978581-14978815	HepG2	liver:	n/a	chr9:14978687-14978698
12	CEBPB	chr9:14974036-14974356	A549	lung:	n/a	chr9:14974218-14974229
13	CEBPB	chr9:14993420-14993444	K562	blood:	n/a	n/a
14	CEBPB	chr9:15045687-15045972	HepG2	liver:	n/a	chr9:15045833-15045844
15	CEBPB	chr9:14978650-14978695	A549	lung:	n/a	n/a
16	CEBPB	chr9:15044267-15044502	HepG2	liver:	n/a	chr9:15044351-15044362
17	CEBPB	chr9:15045847-15046039	K562	blood:	n/a	n/a
18	CEBPB	chr9:14978624-14978819	IMR90	lung:	n/a	chr9:14978687-14978698
19	CEBPB	chr9:14974108-14974375	HepG2	liver:	n/a	chr9:14974218-14974229
20	CEBPB	chr9:15010647-15010868	HepG2	liver:	n/a	chr9:15010746-15010757 chr9:15010745-15010758
21	CEBPB	chr9:15044264-15044450	A549	lung:	n/a	chr9:15044351-15044362
22	CEBPB	chr9:14975880-14976085	HepG2	liver:	n/a	n/a
23	CEBPB	chr9:15045696-15046018	IMR90	lung:	n/a	chr9:15045833-15045844
24	CEBPB	chr9:15044258-15044401	H1-hESC	embryonic stem cell:	n/a	chr9:15044351-15044362
25	CEBPB	chr9:14992111-14992396	K562	blood:	n/a	n/a
26	CEBPB	chr9:15044270-15044442	HepG2	liver:	n/a	chr9:15044351-15044362
27	CEBPB	chr9:15045815-15045862	H1-hESC	embryonic stem cell:	n/a	chr9:15045833-15045844
28	CEBPB	chr9:14960939-14961821	HepG2	liver:	n/a	n/a
29	CEBPB	chr9:15044309-15044494	Hela-S3	cervix:	n/a	chr9:15044351-15044362
30	CEBPB	chr9:15044258-15044505	IMR90	lung:	n/a	chr9:15044351-15044362
31	CHD2	chr9:14961345-14962017	HepG2	liver:	n/a	n/a
32	CHD2	chr9:14993152-14993465	K562	blood:	n/a	n/a
33	CHD2	chr9:14993084-14993550	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr9:14993066-14993633	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr9:14961190-14962077	HepG2	liver:	n/a	n/a
36	CREB1	chr9:14993147-14993530	A549	lung:	n/a	n/a
37	CREB1	chr9:14993016-14993607	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:15013015-15013047	Pancreas_OC	pancreas:	n/a	n/a
39	CTCF	chr9:14996176-14996206	LNCaP	prostate:	n/a	n/a
40	CTCF	chr9:15018300-15018450	Caco-2	colon:	n/a	n/a
41	CTCF	chr9:15034677-15034700	GM13976	blood:	n/a	n/a
42	CTCF	chr9:15042046-15042166	GM12878	blood:	n/a	n/a
43	CTCF	chr9:14961350-14961409	Lung_OC	lung:	n/a	n/a
44	CTCF	chr9:14982580-14982730	Caco-2	colon:	n/a	n/a
45	CTCF	chr9:15018293-15018526	MCF-7	breast:	n/a	n/a
46	CTCF	chr9:14967602-14967684	HepG2	liver:	n/a	n/a
47	CTCF	chr9:14968079-14968215	HepG2	liver:	n/a	n/a
48	CTCF	chr9:15043860-15044010	WI-38	lung:	n/a	n/a
49	CTCF	chr9:14967502-14967791	K562	blood:	n/a	n/a
50	CTCF	chr9:14961715-14962010	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:14978400-14978450	K562	blood:	n/a
2	chr9:14992172-14992222	HUVEC	blood vessel:	n/a
3	chr9:14978400-14978450	HEK293	kidney:	embryo
4	chr9:14993584-14993634	HCT-116	colon:	n/a
5	chr9:14992172-14992222	SAEC	small airway:	n/a
6	chr9:14993466-14993516	HNPCEpiC	eye:	n/a
7	chr9:14992172-14992222	ProgFib	skin:	n/a
8	chr9:14978400-14978450	CMK	blood:	n/a
9	chr9:14978400-14978450	Hepatocyte	liver:	n/a
10	chr9:14993584-14993634	T-47D	breast:	n/a
11	chr9:14993584-14993634	AG04449	skin:	fetal
12	chr9:14993584-14993634	ProgFib	skin:	n/a
13	chr9:14993584-14993634	ovcar-3	ovarian:	n/a
14	chr9:14992172-14992222	Jurkat	blood:	n/a
15	chr9:14978400-14978450	GM12878	blood:	n/a
16	chr9:14978400-14978450	HUVEC	blood vessel:	n/a
17	chr9:14993584-14993634	BE2_C	brain:	n/a
18	chr9:14978400-14978450	RPTEC	kidney:	n/a
19	chr9:14993584-14993634	AG09319	gingival:	n/a
20	chr9:14992172-14992222	BE2_C	brain:	n/a
21	chr9:14993584-14993634	HNPCEpiC	eye:	n/a
22	chr9:14992172-14992222	GM12892	blood:	n/a
23	chr9:14992172-14992222	HepG2	liver:	n/a
24	chr9:14993466-14993516	Caco-2	colon:	n/a
25	chr9:14992172-14992222	PANC-1	pancreas:	n/a
26	chr9:14992172-14992222	K562	blood:	n/a
27	chr9:14993584-14993634	HepG2	liver:	n/a
28	chr9:14993466-14993516	GM12878	blood:	n/a
29	chr9:14993466-14993516	ProgFib	skin:	n/a
30	chr9:14993466-14993516	ovcar-3	ovarian:	n/a
31	chr9:14978400-14978450	A549	lung:	n/a
32	chr9:14992172-14992222	GM19239	blood:	n/a
33	chr9:14993466-14993516	BE2_C	brain:	n/a
34	chr9:14992172-14992222	HCM	heart:	n/a
35	chr9:14978400-14978450	NH-A	brain:	n/a
36	chr9:14978400-14978450	BJ	skin:	n/a
37	chr9:14993584-14993634	SK-N-SH_RA	brain:	n/a
38	chr9:14993466-14993516	T-47D	breast:	n/a
39	chr9:14978400-14978450	ovcar-3	ovarian:	n/a
40	chr9:14978400-14978450	LNCaP	prostate:	n/a
41	chr9:14993466-14993516	HRCEpiC	kidney:	n/a
42	chr9:14992172-14992222	IMR90	lung:	fetal
43	chr9:14992172-14992222	SKMC	muscle:	n/a
44	chr9:14993466-14993516	NH-A	brain:	n/a
45	chr9:14978400-14978450	U87	brain:	n/a
46	chr9:14978400-14978450	NHBE	bronchial:	n/a
47	chr9:14978400-14978450	GM19239	blood:	n/a
48	chr9:14978400-14978450	SAEC	small airway:	n/a
49	chr9:14978400-14978450	GM12892	blood:	n/a
50	chr9:14978400-14978450	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:
2	chr9:15036109..15038088-chr9:15043149..15044736,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FREM1-1	chr9:14983147-14983179	l_3739_chr9:14977433-14983179_testes
2	lnc-FREM1-1	chr9:14977434-14977699	l_3739_chr9:14977433-14983179_testes
3	lnc-FREM1-1	chr9:14980226-14980343	l_3739_chr9:14977433-14983179_testes
4	lnc-FREM1-1	chr9:14979298-14979338	l_3739_chr9:14977433-14983179_testes
5	lnc-FREM1-1	chr9:14977891-14977954	l_3739_chr9:14977433-14983179_testes

No data

Variant related genes	Relation type
ENSG00000215237	TF binding region
ENSG00000232000	TF binding region
ENSG00000215237	CpG island
ENSG00000232000	CpG island

Extended variants
information (count: 2908 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2908 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1357474	chr9:14960217-14960218	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114949045	chr9:14960223-14960224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72715624	chr9:14960228-14960229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs143694997	chr9:14960230-14960231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs531200290	chr9:14960251-14960252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552603079	chr9:14960263-14960264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148035166	chr9:14960267-14960268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538300552	chr9:14960289-14960290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547504024	chr9:14960331-14960332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75734206	chr9:14960355-14960356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs7851480	chr9:14960401-14960402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs554778557	chr9:14960413-14960414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs114755737	chr9:14960451-14960452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537312052	chr9:14960471-14960472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558580106	chr9:14960478-14960479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs72715625	chr9:14960526-14960527	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs541067428	chr9:14960535-14960536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553027332	chr9:14960582-14960583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs59337468	chr9:14960590-14960591	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs374414429	chr9:14960591-14960592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35553221	chr9:14960592-14960593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138783289	chr9:14960605-14960606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189202040	chr9:14960606-14960607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141827114	chr9:14960614-14960615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192070470	chr9:14960619-14960620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs58796441	chr9:14960637-14960638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs7851938	chr9:14960674-14960675	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs146192679	chr9:14960682-14960683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs137865151	chr9:14960719-14960720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536482613	chr9:14960733-14960734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs548318052	chr9:14960735-14960736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs569787740	chr9:14960743-14960744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184256802	chr9:14960779-14960780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553008448	chr9:14960799-14960800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570688946	chr9:14960803-14960804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs534625569	chr9:14960812-14960813	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74928841	chr9:14960813-14960814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574500896	chr9:14960816-14960817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541873450	chr9:14960826-14960827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs188545624	chr9:14960853-14960854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs371620226	chr9:14960911-14960912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575783288	chr9:14960920-14960921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs77247737	chr9:14960981-14960982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs78928002	chr9:14960998-14960999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs548403880	chr9:14961019-14961020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs528769663	chr9:14961056-14961057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180895599	chr9:14961154-14961155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs368493469	chr9:14961187-14961188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs79420792	chr9:14961188-14961189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs543702434	chr9:14961192-14961193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:541 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14956200-14960800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:14957400-14961400	Weak transcription	Placenta	Placenta
3	chr9:14957400-14961600	Weak transcription	Adipose Nuclei	Adipose
4	chr9:14957600-14982400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr9:14958000-14960800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr9:14958000-14962200	Weak transcription	Fetal Muscle Leg	muscle
7	chr9:14959200-14960600	Weak transcription	HepG2	liver
8	chr9:14959400-14961800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr9:14959600-14961600	Weak transcription	Dnd41	blood
10	chr9:14960600-14961200	Enhancers	HepG2	liver
11	chr9:14960600-14961200	Enhancers	HUVEC	blood vessel
12	chr9:14960800-14961800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:14960800-14962600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr9:14961000-14962600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:14961200-14961400	Flanking Bivalent TSS/Enh	HepG2	liver
16	chr9:14961200-14962400	Enhancers	NHDF-Ad	bronchial
17	chr9:14961200-14962600	Active TSS	Duodenum Mucosa	Duodenum
18	chr9:14961200-14962600	Active TSS	K562	blood
19	chr9:14961400-14961600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:14961400-14961600	Enhancers	Liver	Liver
21	chr9:14961400-14961800	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr9:14961400-14961800	Enhancers	Placenta	Placenta
23	chr9:14961400-14961800	Enhancers	Pancreas	Pancrea
24	chr9:14961400-14961800	Bivalent/Poised TSS	HepG2	liver
25	chr9:14961600-14961800	Enhancers	Left Ventricle	heart
26	chr9:14961600-14962000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr9:14961600-14962000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:14961600-14962200	Enhancers	Dnd41	blood
29	chr9:14961600-14963000	Enhancers	Adipose Nuclei	Adipose
30	chr9:14961800-14962000	Enhancers	Fetal Intestine Small	intestine
31	chr9:14961800-14962000	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr9:14961800-14962200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:14961800-14962200	Flanking Bivalent TSS/Enh	HepG2	liver
34	chr9:14961800-14962400	Enhancers	Fetal Intestine Large	intestine
35	chr9:14961800-14963200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:14962200-14962400	Enhancers	Fetal Muscle Leg	muscle
37	chr9:14962200-14962400	Active TSS	HepG2	liver
38	chr9:14962200-14962600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr9:14962200-14962600	Enhancers	Small Intestine	intestine
40	chr9:14962200-14963000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr9:14962400-14963000	Flanking Active TSS	HepG2	liver
42	chr9:14962400-14967600	Weak transcription	Fetal Intestine Large	intestine
43	chr9:14963000-14963400	Enhancers	HepG2	liver
44	chr9:14963400-14967000	Weak transcription	HepG2	liver
45	chr9:14967000-14968800	Enhancers	HepG2	liver
46	chr9:14967600-14968000	Enhancers	Fetal Intestine Large	intestine
47	chr9:14967800-14968200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr9:14968800-14969600	Weak transcription	HepG2	liver
49	chr9:14969600-14969800	Enhancers	HepG2	liver
50	chr9:14969800-14975200	Weak transcription	HepG2	liver

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