Variant report

Variant	nsv968594
Chromosome Location	chr9:6727674-6751753
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:6739329-6739619	HepG2	liver:	n/a	n/a
2	ATF2	chr9:6750387-6751234	GM12878	blood:	n/a	n/a
3	ATF2	chr9:6750570-6751254	GM12878	blood:	n/a	n/a
4	BATF	chr9:6750653-6751296	GM12878	blood:	n/a	n/a
5	BCL11A	chr9:6750615-6751060	GM12878	blood:	n/a	chr9:6750723-6750732
6	BCL11A	chr9:6750696-6750991	GM12878	blood:	n/a	chr9:6750723-6750732
7	BCLAF1	chr9:6750276-6751333	GM12878	blood:	n/a	chr9:6750723-6750732
8	BHLHE40	chr9:6750315-6751151	GM12878	blood:	n/a	n/a
9	CBX3	chr9:6735364-6735786	K562	blood:	n/a	n/a
10	CEBPB	chr9:6741248-6741539	K562	blood:	n/a	n/a
11	CEBPB	chr9:6741286-6741517	A549	lung:	n/a	n/a
12	CEBPB	chr9:6741175-6741436	HepG2	liver:	n/a	n/a
13	CEBPB	chr9:6740249-6740281	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:6741317-6741361	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr9:6741216-6741438	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:6741242-6741528	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr9:6750252-6751279	GM12878	blood:	n/a	n/a
18	CHD1	chr9:6750324-6751143	GM12878	blood:	n/a	n/a
19	CHD2	chr9:6750474-6751082	GM12878	blood:	n/a	n/a
20	CTCF	chr9:6739360-6739510	GM12872	blood:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
21	CTCF	chr9:6739380-6739530	HCPEpiC	choroid plexus:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
22	CTCF	chr9:6739335-6739535	K562	blood:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
23	CTCF	chr9:6739360-6739510	SAEC	small airway:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
24	CTCF	chr9:6739340-6739490	HA-sp	spinal cord:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
25	CTCF	chr9:6739340-6739490	HFF	foreskin:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
26	CTCF	chr9:6739252-6739737	A549	lung:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
27	CTCF	chr9:6739400-6739550	HFF-Myc	foreskin:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
28	CTCF	chr9:6739660-6739810	AG09309	skin:	n/a	n/a
29	CTCF	chr9:6739360-6739510	GM12871	blood:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
30	CTCF	chr9:6739400-6739550	HRE	kidney:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
31	CTCF	chr9:6739360-6739510	HFF-Myc	foreskin:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
32	CTCF	chr9:6739340-6739490	NHDF-neo	bronchial:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
33	CTCF	chr9:6739356-6739540	Spleen_OC	spleen:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
34	CTCF	chr9:6739360-6739510	HPAF	blood vessel:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
35	CTCF	chr9:6739360-6739510	AoAF	blood vessel:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
36	CTCF	chr9:6739360-6739510	GM12873	blood:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
37	CTCF	chr9:6739380-6739530	BJ	skin:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
38	CTCF	chr9:6739400-6739550	GM12866	blood:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
39	CTCF	chr9:6739300-6739450	RPTEC	kidney:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
40	CTCF	chr9:6739340-6739490	SK-N-SH_RA	brain:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
41	CTCF	chr9:6739368-6739392	A549	lung:	n/a	n/a
42	CTCF	chr9:6739315-6739573	HUVEC	blood vessel:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
43	CTCF	chr9:6739420-6739570	GM12873	blood:	n/a	chr9:6739422-6739430
44	CTCF	chr9:6739400-6739550	SK-N-SH_RA	brain:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
45	CTCF	chr9:6739360-6739510	HepG2	liver:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
46	CTCF	chr9:6739320-6739470	HEK293	kidney:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
47	CTCF	chr9:6739400-6739550	Hela-S3	cervix:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
48	CTCF	chr9:6739400-6739550	GM06990	blood:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
49	CTCF	chr9:6739297-6739566	MCF-7	breast:	n/a	chr9:6739412-6739433 chr9:6739422-6739430
50	CTCF	chr9:6739319-6739386	GM12892	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6731623-6731673	CMK	blood:	n/a
2	chr9:6731623-6731673	SK-N-SH_RA	brain:	n/a
3	chr9:6731623-6731673	ovcar-3	ovarian:	n/a
4	chr9:6731623-6731673	AG09309	skin:	n/a
5	chr9:6731623-6731673	HCF	heart:	n/a
6	chr9:6731623-6731673	NB4	blood:	n/a
7	chr9:6731623-6731673	GM19239	blood:	n/a
8	chr9:6731623-6731673	Caco-2	colon:	n/a
9	chr9:6731623-6731673	SKMC	muscle:	n/a
10	chr9:6731623-6731673	SAEC	small airway:	n/a
11	chr9:6731623-6731673	NT2-D1	testis:	n/a
12	chr9:6731623-6731673	NH-A	brain:	n/a
13	chr9:6731623-6731673	MCF-7	breast:	n/a
14	chr9:6731623-6731673	PrEC	prostate:	n/a
15	chr9:6731623-6731673	AG10803	skin:	n/a
16	chr9:6731623-6731673	Hela-S3	cervix:	n/a
17	chr9:6731623-6731673	U87	brain:	n/a
18	chr9:6731623-6731673	NHBE	bronchial:	n/a
19	chr9:6731623-6731673	ProgFib	skin:	n/a
20	chr9:6731623-6731673	HepG2	liver:	n/a
21	chr9:6731623-6731673	SK-N-MC	brain:	n/a
22	chr9:6731623-6731673	Jurkat	blood:	n/a
23	chr9:6731623-6731673	HIPEpiC	eye:	n/a
24	chr9:6731623-6731673	HL-60	blood:	n/a
25	chr9:6731623-6731673	BE2_C	brain:	n/a
26	chr9:6731623-6731673	A549	lung:	n/a
27	chr9:6731623-6731673	HRE	kidney:	n/a
28	chr9:6731623-6731673	MCF10A-Er-Src	breast:	n/a
29	chr9:6731623-6731673	BJ	skin:	n/a
30	chr9:6731623-6731673	ECC-1	luminal epithelium:	n/a
31	chr9:6731623-6731673	GM12878	blood:	n/a
32	chr9:6731623-6731673	Hepatocyte	liver:	n/a
33	chr9:6731623-6731673	HPAEpiC	pulmonary alveolar:	n/a
34	chr9:6731623-6731673	HUVEC	blood vessel:	n/a
35	chr9:6731623-6731673	AoSMC	blood vessel:	n/a
36	chr9:6731623-6731673	K562	blood:	n/a
37	chr9:6731623-6731673	GM06990	blood:	n/a
38	chr9:6731623-6731673	H1-hESC	embryonic stem cell:	embryo
39	chr9:6731623-6731673	HEEpiC	esophagus:	n/a
40	chr9:6731623-6731673	HCPEpiC	choroid plexus:	n/a
41	chr9:6731623-6731673	HCM	heart:	n/a
42	chr9:6731623-6731673	HEK293	kidney:	embryo
43	chr9:6731623-6731673	RPTEC	kidney:	n/a
44	chr9:6731623-6731673	LNCaP	prostate:	n/a
45	chr9:6731623-6731673	HRPEpiC	eye:	n/a
46	chr9:6731623-6731673	GM12891	blood:	n/a
47	chr9:6731623-6731673	IMR90	lung:	fetal
48	chr9:6731623-6731673	AG09319	gingival:	n/a
49	chr9:6731623-6731673	HAEpiC	amniotic membrane:	n/a
50	chr9:6731623-6731673	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:6354073..6354743-chr9:6738989..6739892,3	K562	blood:
2	chr9:6749197..6752825-chr9:6755235..6757236,4	K562	blood:
3	chr9:6725196..6728190-chr9:6756447..6759048,2	MCF-7	breast:
4	chr9:6749158..6750730-chr9:6754623..6757370,3	K562	blood:
5	chr9:6714855..6717847-chr9:6737862..6741209,3	MCF-7	breast:
6	chr9:6751286..6753075-chr9:6755508..6757503,2	MCF-7	breast:
7	chr9:6747740..6749345-chr9:6756036..6758918,2	MCF-7	breast:
8	chr9:6751679..6753304-chr9:6755614..6757783,2	MCF-7	breast:
9	chr9:6679734..6682958-chr9:6730915..6733550,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLDC-1	chr9:6748703-6748981	NONHSAT130164
2	lnc-SNRPEP2-1	chr9:6734598-6735076	NONHSAT130163

Variant related genes	Relation type
SNRPEP2	TF binding region
ENSG00000231108	TF binding region
SNRPEP2	CpG island
ENSG00000231108	CpG island
ENSG00000225489	chromatin interactions
ENSG00000107077	chromatin interactions

Extended variants
information (count: 1366 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:1366 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13287784	chr9:6727696-6727697	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs13288506	chr9:6727738-6727739	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs369669405	chr9:6727795-6727796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs820518	chr9:6727864-6727865	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs151212985	chr9:6727870-6727871	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs563118069	chr9:6727936-6727937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192483410	chr9:6727951-6727952	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs530745554	chr9:6727986-6727987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs560984953	chr9:6727997-6727998	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2918174	chr9:6728016-6728017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567177435	chr9:6728021-6728022	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs367565356	chr9:6728039-6728040	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574486528	chr9:6728067-6728068	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534622570	chr9:6728101-6728102	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546272563	chr9:6728110-6728111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10975807	chr9:6728118-6728119	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs538333424	chr9:6728153-6728154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs140406345	chr9:6728154-6728155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs143540773	chr9:6728193-6728194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs72697574	chr9:6728201-6728202	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs555304003	chr9:6728210-6728211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12341867	chr9:6728232-6728233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs202041077	chr9:6728239-6728240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs62566462	chr9:6728257-6728258	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs182888061	chr9:6728262-6728263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62566463	chr9:6728263-6728264	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs146790355	chr9:6728274-6728275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530624778	chr9:6728275-6728276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs62566464	chr9:6728276-6728277	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs370793732	chr9:6728297-6728298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs113200701	chr9:6728306-6728307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542310908	chr9:6728313-6728314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62566465	chr9:6728318-6728319	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs546604145	chr9:6728361-6728362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs2918175	chr9:6728376-6728377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs532098330	chr9:6728388-6728389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537777834	chr9:6728396-6728397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs138262378	chr9:6728405-6728406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188585083	chr9:6728406-6728407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs193274325	chr9:6728407-6728408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555191664	chr9:6728421-6728422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567200655	chr9:6728430-6728431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534201942	chr9:6728440-6728441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149181617	chr9:6728454-6728455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184392980	chr9:6728465-6728466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544170574	chr9:6728475-6728476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2988408	chr9:6728480-6728481	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574584824	chr9:6728488-6728489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs4742249	chr9:6728508-6728509	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs560907214	chr9:6728509-6728510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Dyslexia	22102821	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
early-passage human iPS cells	21368824	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6717200-6728400	Weak transcription	Fetal Intestine Small	intestine
2	chr9:6717800-6728000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr9:6724200-6749200	Weak transcription	Primary B cells from cord blood	blood
4	chr9:6725200-6734600	Weak transcription	GM12878-XiMat	blood
5	chr9:6726800-6737800	Weak transcription	Liver	Liver
6	chr9:6732600-6733800	Enhancers	HepG2	liver
7	chr9:6733200-6734200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr9:6733400-6733600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:6738600-6739800	Enhancers	Primary B cells from peripheral blood	blood
10	chr9:6742800-6743600	Enhancers	HepG2	liver
11	chr9:6743600-6747800	Weak transcription	HepG2	liver
12	chr9:6749200-6750200	Enhancers	Primary B cells from cord blood	blood
13	chr9:6749200-6750200	Enhancers	Primary T cells fromperipheralblood	blood
14	chr9:6749400-6750200	Enhancers	Primary B cells from peripheral blood	blood
15	chr9:6749800-6750400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr9:6750000-6750200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr9:6750000-6750400	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr9:6750000-6750400	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr9:6750000-6750400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr9:6750000-6750400	Enhancers	GM12878-XiMat	blood
21	chr9:6750000-6750600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr9:6750000-6751000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr9:6750000-6751200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr9:6750200-6750400	Active TSS	Monocytes-CD14+_RO01746	blood
25	chr9:6750200-6750600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
26	chr9:6750200-6751000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr9:6750200-6751000	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr9:6750200-6751000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr9:6750200-6751000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr9:6750200-6751200	Enhancers	Primary monocytes fromperipheralblood	blood
31	chr9:6750200-6751200	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr9:6750200-6751200	Flanking Active TSS	Primary B cells from peripheral blood	blood
33	chr9:6750200-6751400	Enhancers	Fetal Thymus	thymus
34	chr9:6750400-6750600	Flanking Active TSS	Primary hematopoietic stem cells	blood
35	chr9:6750400-6750600	Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr9:6750400-6750600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr9:6750400-6750800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr9:6750400-6750800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr9:6750400-6750800	Active TSS	GM12878-XiMat	blood
40	chr9:6750400-6751000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr9:6750400-6751000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
42	chr9:6750400-6751000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
43	chr9:6750400-6751000	Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr9:6750400-6751000	Active TSS	Rectal Mucosa Donor 29	rectum
45	chr9:6750400-6751000	Enhancers	HMEC	breast
46	chr9:6750400-6751000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr9:6750400-6751200	Enhancers	Primary T cells from cord blood	blood
48	chr9:6750400-6751200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
49	chr9:6750600-6750800	Active TSS	Primary hematopoietic stem cells	blood
50	chr9:6750600-6750800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links