Variant report

Variant	esv3407839
Chromosome Location	chr9:15530438-15665653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1640)
CpG islands
(count:428)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:15606729-15607013	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:15552687-15552948	K562	blood:	n/a	n/a
3	ARID3A	chr9:15552151-15552649	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:15642421-15642732	HepG2	liver:	n/a	n/a
5	ATF1	chr9:15606159-15606277	K562	blood:	n/a	n/a
6	ATF2	chr9:15552105-15553502	GM12878	blood:	n/a	chr9:15552396-15552403
7	ATF2	chr9:15552008-15553342	H1-hESC	embryonic stem cell:	n/a	chr9:15552396-15552403
8	ATF2	chr9:15552934-15553370	GM12878	blood:	n/a	n/a
9	ATF2	chr9:15552023-15553562	H1-hESC	embryonic stem cell:	n/a	chr9:15552396-15552403
10	ATF2	chr9:15531390-15531836	GM12878	blood:	n/a	n/a
11	ATF3	chr9:15587162-15587411	K562	blood:	n/a	n/a
12	BACH1	chr9:15552248-15553824	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:15533280-15533522	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr9:15612994-15613254	GM12878	blood:	n/a	chr9:15613158-15613169
15	BATF	chr9:15613003-15613305	GM12878	blood:	n/a	chr9:15613158-15613169
16	BATF	chr9:15531423-15531671	GM12878	blood:	n/a	n/a
17	BATF	chr9:15529561-15530461	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:15529456-15530507	GM12878	blood:	n/a	n/a
19	BCLAF1	chr9:15552224-15553528	GM12878	blood:	n/a	chr9:15552861-15552874 chr9:15552858-15552871 chr9:15553084-15553093 chr9:15552986-15552999
20	BHLHE40	chr9:15552208-15553359	HepG2	liver:	n/a	n/a
21	BHLHE40	chr9:15531576-15531579	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:15552022-15553397	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:15529542-15530441	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:15552719-15553088	K562	blood:	n/a	n/a
25	BHLHE40	chr9:15553594-15553760	K562	blood:	n/a	n/a
26	BRCA1	chr9:15552798-15553456	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr9:15552718-15553410	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr9:15553012-15553375	HepG2	liver:	n/a	n/a
29	BRCA1	chr9:15554639-15554686	GM12878	blood:	n/a	n/a
30	BRCA1	chr9:15533324-15533607	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr9:15552681-15553468	GM12878	blood:	n/a	n/a
32	CBX3	chr9:15552616-15553168	K562	blood:	n/a	n/a
33	CCNT2	chr9:15552710-15553034	K562	blood:	n/a	n/a
34	CCNT2	chr9:15553242-15553567	K562	blood:	n/a	n/a
35	CEBPB	chr9:15532952-15533152	K562	blood:	n/a	chr9:15533019-15533030 chr9:15532971-15532982
36	CEBPB	chr9:15543068-15543387	IMR90	lung:	n/a	n/a
37	CEBPB	chr9:15552157-15552649	MCF-7	breast:	n/a	n/a
38	CEBPB	chr9:15543159-15543324	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr9:15552156-15552882	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr9:15587130-15587433	IMR90	lung:	n/a	chr9:15587301-15587312
41	CEBPB	chr9:15578740-15579055	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:15552145-15552651	A549	lung:	n/a	n/a
43	CEBPB	chr9:15552069-15553236	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:15552003-15552754	A549	lung:	n/a	n/a
45	CEBPB	chr9:15552214-15552605	K562	blood:	n/a	n/a
46	CEBPB	chr9:15634610-15635086	IMR90	lung:	n/a	chr9:15634719-15634730
47	CEBPB	chr9:15532813-15533531	H1-hESC	embryonic stem cell:	n/a	chr9:15533019-15533030 chr9:15532971-15532982
48	CEBPB	chr9:15552290-15552500	K562	blood:	n/a	n/a
49	CEBPB	chr9:15532880-15533152	A549	lung:	n/a	chr9:15533019-15533030 chr9:15532971-15532982
50	CEBPB	chr9:15552191-15552597	A549	lung:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:15553181-15553231	GM19239	blood:	n/a
2	chr9:15553181-15553231	GM19239	blood:	n/a
3	chr9:15553060-15553110	HPAEpiC	pulmonary alveolar:	n/a
4	chr9:15553451-15553501	NT2-D1	testis:	n/a
5	chr9:15553069-15553119	SK-N-SH_RA	brain:	n/a
6	chr9:15553181-15553231	Hela-S3	cervix:	n/a
7	chr9:15553181-15553231	AG04450	lung:	fetal
8	chr9:15553069-15553119	AG09309	skin:	n/a
9	chr9:15553451-15553501	Caco-2	colon:	n/a
10	chr9:15553286-15553336	SK-N-SH	brain:	n/a
11	chr9:15553060-15553110	MCF-7	breast:	n/a
12	chr9:15552206-15552256	HRCEpiC	kidney:	n/a
13	chr9:15553286-15553336	LNCaP	prostate:	n/a
14	chr9:15553451-15553501	HCT-116	colon:	n/a
15	chr9:15553069-15553119	HL-60	blood:	n/a
16	chr9:15552606-15552656	HepG2	liver:	n/a
17	chr9:15553286-15553336	HEEpiC	esophagus:	n/a
18	chr9:15553060-15553110	HEK293	kidney:	embryo
19	chr9:15552206-15552256	HMEC	breast:	n/a
20	chr9:15552606-15552656	ProgFib	skin:	n/a
21	chr9:15553451-15553501	ovcar-3	ovarian:	n/a
22	chr9:15552206-15552256	GM19239	blood:	n/a
23	chr9:15553181-15553231	NT2-D1	testis:	n/a
24	chr9:15553451-15553501	U87	brain:	n/a
25	chr9:15553060-15553110	GM06990	blood:	n/a
26	chr9:15553060-15553110	HEEpiC	esophagus:	n/a
27	chr9:15552206-15552256	GM06990	blood:	n/a
28	chr9:15553069-15553119	AG04449	skin:	fetal
29	chr9:15553069-15553119	HCF	heart:	n/a
30	chr9:15553069-15553119	GM12892	blood:	n/a
31	chr9:15552606-15552656	HL-60	blood:	n/a
32	chr9:15553069-15553119	Hepatocyte	liver:	n/a
33	chr9:15553181-15553231	Hepatocyte	liver:	n/a
34	chr9:15553069-15553119	HRPEpiC	eye:	n/a
35	chr9:15552606-15552656	NH-A	brain:	n/a
36	chr9:15553060-15553110	HL-60	blood:	n/a
37	chr9:15552606-15552656	H1-hESC	embryonic stem cell:	embryo
38	chr9:15553451-15553501	MCF10A-Er-Src	breast:	n/a
39	chr9:15553060-15553110	SAEC	small airway:	n/a
40	chr9:15553060-15553110	K562	blood:	n/a
41	chr9:15553286-15553336	GM06990	blood:	n/a
42	chr9:15553286-15553336	NHBE	bronchial:	n/a
43	chr9:15553181-15553231	HEEpiC	esophagus:	n/a
44	chr9:15552606-15552656	HNPCEpiC	eye:	n/a
45	chr9:15553060-15553110	AoSMC	blood vessel:	n/a
46	chr9:15552206-15552256	BJ	skin:	n/a
47	chr9:15552206-15552256	MCF10A-Er-Src	breast:	n/a
48	chr9:15552206-15552256	A549	lung:	n/a
49	chr9:15553181-15553231	GM06990	blood:	n/a
50	chr9:15553451-15553501	HCM	heart:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:15538062..15540509-chr9:15552565..15554442,2	MCF-7	breast:
2	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:
3	chr3:5020895..5021614-chr9:15552897..15553484,2	Hela-S3	cervix:
4	chr9:15540944..15543831-chr9:15548082..15550784,2	MCF-7	breast:
5	chr9:15540367..15542446-chr9:15551493..15554062,3	MCF-7	breast:
6	chr9:15510875..15512396-chr9:15551516..15553319,2	MCF-7	breast:
7	chr9:15551936..15552629-chr9:15619996..15620642,2	MCF-7	breast:
8	chr9:15548082..15550677-chr9:15551279..15553386,2	MCF-7	breast:
9	chr9:15421567..15424446-chr9:15606338..15608598,2	MCF-7	breast:
10	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
11	chr9:15509318..15512022-chr9:15550389..15555494,9	MCF-7	breast:
12	chr9:15609722..15611520-chr9:15613088..15614614,2	MCF-7	breast:
13	chr9:15551939..15552527-chr9:15606365..15606962,2	MCF-7	breast:
14	chr11:61559649..61560247-chr9:15552431..15552962,2	Hela-S3	cervix:
15	chr9:15508603..15511423-chr9:15563063..15564927,2	MCF-7	breast:
16	chr9:15551543..15553297-chr9:15600119..15601625,2	MCF-7	breast:
17	chr9:15551936..15552629-chr9:15619996..15620642,2	MCF-7	breast:
18	chr9:15540944..15543831-chr9:15548082..15550784,2	MCF-7	breast:
19	chr9:15509144..15511285-chr9:15608383..15610950,2	MCF-7	breast:
20	chr9:15570769..15573187-chr9:15586351..15588425,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNAPC3-3	chr9:15563976-15564022	NONHSAT130275
2	lnc-C9orf93-3	chr9:15550639-15551154	NONHSAT130274
3	lnc-SNAPC3-3	chr9:15553289-15553604	NONHSAT130275
4	lnc-SNAPC3-4	chr9:15588353-15588613	NONHSAT130276

No data

Variant related genes	Relation type
FTH1P12	TF binding region
RN7SL98P	TF binding region
RNU6-246P	TF binding region
CCDC171	TF binding region
HMGN2P16	TF binding region
FTH1P12	CpG island
RN7SL98P	CpG island
RNU6-246P	CpG island
CCDC171	CpG island
HMGN2P16	CpG island
ENSG00000164985	chromatin interactions
ENSG00000207601	chromatin interactions
ENSG00000231376	chromatin interactions
ENSG00000168496	chromatin interactions
ENSG00000134107	chromatin interactions
ENSG00000164975	chromatin interactions
ENSG00000164989	chromatin interactions
ENSG00000134825	chromatin interactions

Extended variants
information (count: 7051 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:7051 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561486246	chr9:15530453-15530454	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs568372759	chr9:15530607-15530608	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs571790796	chr9:15530648-15530649	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs529548638	chr9:15530652-15530653	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs541520389	chr9:15530668-15530669	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs569126830	chr9:15530712-15530713	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs540062018	chr9:15530715-15530716	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs551964871	chr9:15530768-15530769	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs540651855	chr9:15530775-15530776	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs570573835	chr9:15530827-15530828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151063041	chr9:15530829-15530830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140833217	chr9:15530874-15530875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574755831	chr9:15530887-15530888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535763367	chr9:15530912-15530913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557326779	chr9:15530918-15530919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372600629	chr9:15530921-15530922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs200759148	chr9:15530970-15530971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546022585	chr9:15530976-15530977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35210539	chr9:15531002-15531003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183018662	chr9:15531028-15531029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs187589791	chr9:15531077-15531078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377461036	chr9:15531089-15531090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540186366	chr9:15531091-15531092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561770081	chr9:15531108-15531109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373121745	chr9:15531111-15531112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149708617	chr9:15531118-15531119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs550849414	chr9:15531120-15531121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563226841	chr9:15531148-15531149	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs78036719	chr9:15531174-15531175	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs200750101	chr9:15531193-15531194	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs190010286	chr9:15531195-15531196	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs202191304	chr9:15531199-15531200	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs533359636	chr9:15531226-15531227	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs551991812	chr9:15531244-15531245	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs79576909	chr9:15531250-15531251	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs532853516	chr9:15531304-15531305	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs552551839	chr9:15531307-15531308	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs546584832	chr9:15531317-15531318	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs563097823	chr9:15531338-15531339	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs193257671	chr9:15531376-15531377	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568045920	chr9:15531386-15531387	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs535470776	chr9:15531387-15531388	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs557289782	chr9:15531416-15531417	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs575532321	chr9:15531520-15531521	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs539214022	chr9:15531522-15531523	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs7035261	chr9:15531635-15531636	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs10810395	chr9:15531679-15531680	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs540346558	chr9:15531689-15531690	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs561883496	chr9:15531721-15531722	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs147854630	chr9:15531727-15531728	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Ovarian cancer	19835627	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:15530200-15532800	Weak transcription	Fetal Thymus	thymus
2	chr9:15530400-15533400	Enhancers	GM12878-XiMat	blood
3	chr9:15532400-15533400	Enhancers	Primary T helper cells PMA-I stimulated	--
4	chr9:15532600-15532800	Enhancers	Placenta	Placenta
5	chr9:15532600-15533000	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr9:15532600-15533400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr9:15532800-15533000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:15532800-15533400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr9:15532800-15533400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr9:15532800-15533400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr9:15532800-15533400	Flanking Active TSS	Placenta	Placenta
12	chr9:15532800-15533400	Enhancers	Fetal Thymus	thymus
13	chr9:15533200-15533400	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr9:15535800-15536200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr9:15536200-15536400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr9:15541800-15542200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr9:15541800-15542400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr9:15541800-15542400	Enhancers	Fetal Kidney	kidney
19	chr9:15541800-15542400	Enhancers	Fetal Lung	lung
20	chr9:15541800-15542600	Enhancers	A549	lung
21	chr9:15542000-15543800	Enhancers	Fetal Stomach	stomach
22	chr9:15542200-15544000	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr9:15542600-15543000	Weak transcription	A549	lung
24	chr9:15542600-15543600	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr9:15542800-15543800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr9:15543000-15543200	Enhancers	A549	lung
27	chr9:15543200-15543600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:15543200-15543600	Flanking Active TSS	A549	lung
29	chr9:15543400-15543800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr9:15543600-15544000	Enhancers	A549	lung
31	chr9:15544000-15551800	Weak transcription	A549	lung
32	chr9:15549600-15550400	Enhancers	Primary neutrophils fromperipheralblood	blood
33	chr9:15549800-15550000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr9:15549800-15550200	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr9:15549800-15551200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr9:15549800-15551600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr9:15550000-15551800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr9:15550200-15550600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr9:15550200-15550600	Enhancers	Small Intestine	intestine
40	chr9:15550200-15550800	Enhancers	Duodenum Mucosa	Duodenum
41	chr9:15550200-15551200	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr9:15550200-15551800	Enhancers	Primary hematopoietic stem cells	blood
43	chr9:15550200-15552000	Enhancers	Fetal Thymus	thymus
44	chr9:15550600-15550800	Enhancers	Rectal Mucosa Donor 29	rectum
45	chr9:15550600-15551200	Enhancers	Fetal Intestine Small	intestine
46	chr9:15550600-15552400	Weak transcription	Small Intestine	intestine
47	chr9:15550800-15551800	Weak transcription	Duodenum Mucosa	Duodenum
48	chr9:15550800-15551800	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr9:15551200-15551600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr9:15551200-15551600	Weak transcription	Fetal Intestine Small	intestine

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