Variant report

Variant	nsv823510
Chromosome Location	chr6:32358261-32370568
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:127)
CpG islands
(count:2811)
Chromatin interactive
region (count:11)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:127 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:32361449-32361736	K562	blood:	n/a	n/a
2	ATF2	chr6:32364838-32365545	GM12878	blood:	n/a	n/a
3	ATF2	chr6:32365031-32365426	GM12878	blood:	n/a	n/a
4	BATF	chr6:32364973-32365409	GM12878	blood:	n/a	n/a
5	CEBPB	chr6:32358447-32358706	K562	blood:	n/a	chr6:32358561-32358572
6	CEBPB	chr6:32358422-32358696	IMR90	lung:	n/a	chr6:32358561-32358572
7	CEBPB	chr6:32358387-32358668	HepG2	liver:	n/a	chr6:32358561-32358572
8	CTCF	chr6:32369490-32369557	GM19238	blood:	n/a	chr6:32369497-32369515 chr6:32369499-32369512
9	CTCF	chr6:32361520-32361670	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr6:32361600-32361750	HUVEC	blood vessel:	n/a	n/a
11	CTCF	chr6:32361605-32361698	K562	blood:	n/a	n/a
12	CTCF	chr6:32368628-32368640	GM10248	blood:	n/a	n/a
13	CTCF	chr6:32361580-32361730	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr6:32369516-32369529	GM12878	blood:	n/a	n/a
15	CTCF	chr6:32361582-32361742	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:32361546-32361749	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr6:32369440-32369590	GM12871	blood:	n/a	chr6:32369497-32369515 chr6:32369499-32369512
18	CTCF	chr6:32361677-32361711	GM19239	blood:	n/a	n/a
19	CTCF	chr6:32361625-32361671	GM10266	blood:	n/a	n/a
20	CTCF	chr6:32364001-32364067	Fibrobl	skin:	n/a	n/a
21	CTCF	chr6:32361520-32361670	HMF	breast:	n/a	n/a
22	CTCF	chr6:32359380-32359530	K562	blood:	n/a	n/a
23	CTCF	chr6:32361520-32361670	AG09319	gingival:	n/a	n/a
24	CTCF	chr6:32361580-32361730	AG09319	gingival:	n/a	n/a
25	CTCF	chr6:32361610-32361734	MCF-7	breast:	n/a	n/a
26	CTCF	chr6:32361520-32361670	HMEC	breast:	n/a	n/a
27	CTCF	chr6:32369460-32369610	MCF-7	breast:	n/a	chr6:32369497-32369515 chr6:32369499-32369512
28	CTCF	chr6:32361569-32361778	NHEK	skin:	n/a	n/a
29	CTCF	chr6:32369460-32369610	GM12874	blood:	n/a	chr6:32369497-32369515 chr6:32369499-32369512
30	CTCF	chr6:32369380-32369530	GM12872	blood:	n/a	chr6:32369497-32369515 chr6:32369499-32369512
31	CTCF	chr6:32363933-32363993	GM19239	blood:	n/a	n/a
32	CTCF	chr6:32361534-32361736	K562	blood:	n/a	n/a
33	CTCF	chr6:32361560-32361710	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr6:32368603-32368626	GM10266	blood:	n/a	n/a
35	CTCF	chr6:32361580-32361730	RPTEC	kidney:	n/a	n/a
36	CTCF	chr6:32369505-32369554	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr6:32361513-32361763	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr6:32362618-32362620	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:32361626-32361730	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:32364080-32364107	ProgFib	skin:	n/a	n/a
41	CTCF	chr6:32361605-32361688	LNCaP	prostate:	n/a	n/a
42	CTCF	chr6:32361642-32361709	GM19238	blood:	n/a	n/a
43	CTCF	chr6:32361520-32361670	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr6:32361564-32361763	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:32361626-32361734	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:32361560-32361710	RPTEC	kidney:	n/a	n/a
47	CTCF	chr6:32361586-32361682	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr6:32361520-32361670	HRE	kidney:	n/a	n/a
49	CTCF	chr6:32369494-32369554	GM19240	blood:	n/a	chr6:32369497-32369515 chr6:32369499-32369512
50	CTCF	chr6:32361580-32361730	SAEC	small airway:	n/a	n/a

(count:2811 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32362744-32362794	GM12892	blood:	n/a
2	chr6:32363892-32363942	H1-hESC	embryonic stem cell:	embryo
3	chr6:32369487-32369537	AoSMC	blood vessel:	n/a
4	chr6:32365553-32365603	SK-N-SH_RA	brain:	n/a
5	chr6:32362744-32362794	PANC-1	pancreas:	n/a
6	chr6:32362744-32362794	GM12892	blood:	n/a
7	chr6:32363892-32363942	H1-hESC	embryonic stem cell:	embryo
8	chr6:32369487-32369537	AoSMC	blood vessel:	n/a
9	chr6:32365553-32365603	SK-N-SH_RA	brain:	n/a
10	chr6:32362744-32362794	PANC-1	pancreas:	n/a
11	chr6:32362638-32362688	HEEpiC	esophagus:	n/a
12	chr6:32367729-32367779	NH-A	brain:	n/a
13	chr6:32365553-32365603	Hela-S3	cervix:	n/a
14	chr6:32362593-32362643	Hepatocyte	liver:	n/a
15	chr6:32369487-32369537	HUVEC	blood vessel:	n/a
16	chr6:32362593-32362643	A549	lung:	n/a
17	chr6:32362744-32362794	AG10803	skin:	n/a
18	chr6:32369487-32369537	H1-hESC	embryonic stem cell:	embryo
19	chr6:32363933-32363983	GM12878	blood:	n/a
20	chr6:32363186-32363236	AG04450	lung:	fetal
21	chr6:32369487-32369537	ovcar-3	ovarian:	n/a
22	chr6:32362626-32362676	A549	lung:	n/a
23	chr6:32366347-32366397	NHBE	bronchial:	n/a
24	chr6:32363228-32363278	PANC-1	pancreas:	n/a
25	chr6:32362707-32362757	HMEC	breast:	n/a
26	chr6:32362678-32362728	T-47D	breast:	n/a
27	chr6:32367970-32368020	SK-N-SH_RA	brain:	n/a
28	chr6:32367729-32367779	RPTEC	kidney:	n/a
29	chr6:32368318-32368368	GM19239	blood:	n/a
30	chr6:32363186-32363236	GM06990	blood:	n/a
31	chr6:32363888-32363938	GM12878	blood:	n/a
32	chr6:32363942-32363992	A549	lung:	n/a
33	chr6:32363212-32363262	NT2-D1	testis:	n/a
34	chr6:32363255-32363305	NHDF-neo	bronchial:	n/a
35	chr6:32367672-32367722	HRE	kidney:	n/a
36	chr6:32363875-32363925	HCT-116	colon:	n/a
37	chr6:32363212-32363262	HEK293	kidney:	embryo
38	chr6:32363186-32363236	NHBE	bronchial:	n/a
39	chr6:32365665-32365715	CMK	blood:	n/a
40	chr6:32363228-32363278	NH-A	brain:	n/a
41	chr6:32368482-32368532	ProgFib	skin:	n/a
42	chr6:32367672-32367722	HepG2	liver:	n/a
43	chr6:32368482-32368532	HL-60	blood:	n/a
44	chr6:32367729-32367779	GM12892	blood:	n/a
45	chr6:32362744-32362794	HCT-116	colon:	n/a
46	chr6:32366347-32366397	CMK	blood:	n/a
47	chr6:32367672-32367722	PANC-1	pancreas:	n/a
48	chr6:32363212-32363262	HUVEC	blood vessel:	n/a
49	chr6:32363228-32363278	HCPEpiC	choroid plexus:	n/a
50	chr6:32362318-32362368	ECC-1	luminal epithelium:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:32369487..32371543-chr6:32654022..32656870,2	K562	blood:
2	chr6:32363881..32366700-chr6:32368239..32370976,2	K562	blood:
3	chr6:32212577..32213569-chr6:32361133..32362153,5	MCF-7	breast:
4	chr6:32363881..32366700-chr6:32368239..32370976,2	K562	blood:
5	chr6:32358023..32360400-chr6:32361196..32362901,2	K562	blood:
6	chr6:32360990..32362711-chr6:32363289..32364863,2	K562	blood:
7	chr6:32360881..32363601-chr6:32363763..32366001,3	MCF-7	breast:
8	chr6:32212479..32213374-chr6:32361354..32361920,2	MCF-7	breast:
9	chr6:32360881..32363601-chr6:32363763..32366001,3	MCF-7	breast:
10	chr6:32356860..32358519-chr6:32360443..32363333,2	MCF-7	breast:
11	chr6:32360990..32362711-chr6:32363289..32364863,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-DRA-1	chr6:32361226-32361468	NONHSAT108902
2	lnc-HLA-DRA-1	chr6:32361226-32361463	ENSG00000228962.1
3	lnc-HLA-DRA-1	chr6:32360320-32361134	XLOC_005254
4	lnc-HLA-DRA-1	chr6:32359390-32359517	ENSG00000228962.1
5	lnc-HLA-DRA-1	chr6:32358287-32358530	NONHSAT108902
6	lnc-HLA-DRA-1	chr6:32359390-32359517	NONHSAT108902
7	lnc-HLA-DRA-1	chr6:32358287-32358530	ENSG00000228962.1
8	lnc-HLA-DRA-1	chr6:32361226-32361247	XLOC_005254

No data

Variant related genes	Relation type
HCG23	TF binding region
HCG23	CpG island
ENSG00000228962	chromatin interactions
DKK2	miRNA target sites

Extended variants
information (count: 839 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:839 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3117099	chr6:32358270-32358271	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	disease
2	rs386699303	chr6:32358285-32358286	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs3129951	chr6:32358286-32358287	Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs534612405	chr6:32358331-32358332	Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs17423691	chr6:32358345-32358346	Active TSS Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs17423698	chr6:32358368-32358369	Active TSS Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541702044	chr6:32358376-32358377	Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs556786713	chr6:32358380-32358381	Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs575087398	chr6:32358387-32358388	Active TSS Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs377068266	chr6:32358414-32358415	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs371339370	chr6:32358418-32358419	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs7761671	chr6:32358419-32358420	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs185468646	chr6:32358423-32358424	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs117130854	chr6:32358432-32358433	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs386699304	chr6:32358458-32358459	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs115303880	chr6:32358459-32358460	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs3117098	chr6:32358513-32358514	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
18	rs551291976	chr6:32358526-32358527	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs563113343	chr6:32358528-32358529	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs17495592	chr6:32358533-32358534	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs9348883	chr6:32358549-32358550	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs117886263	chr6:32358666-32358667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs3117097	chr6:32358689-32358690	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs546604525	chr6:32358704-32358705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567963592	chr6:32358727-32358728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62402741	chr6:32358728-32358729	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs12662906	chr6:32358797-32358798	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs149986549	chr6:32358802-32358803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72847903	chr6:32358834-32358835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs140243223	chr6:32358840-32358841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs67019312	chr6:32358883-32358884	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs117030612	chr6:32358900-32358901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs573924756	chr6:32358927-32358928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs66568865	chr6:32358939-32358940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9268476	chr6:32358942-32358943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117680060	chr6:32358956-32358957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200237273	chr6:32359015-32359016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs574073110	chr6:32359078-32359079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544575015	chr6:32359087-32359088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9268477	chr6:32359121-32359122	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs191637688	chr6:32359131-32359132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1143257	chr6:32359133-32359134	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs560500519	chr6:32359145-32359146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs118171271	chr6:32359149-32359150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs117177076	chr6:32359150-32359151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1143258	chr6:32359156-32359157	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs62402742	chr6:32359163-32359164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs62402743	chr6:32359171-32359172	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs370909783	chr6:32359172-32359173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs118094977	chr6:32359185-32359186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Ovarian cancer	21781307	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32344000-32361400	Weak transcription	Fetal Stomach	stomach
2	chr6:32351400-32365000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:32356000-32361400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr6:32356400-32364200	Weak transcription	Fetal Lung	lung
5	chr6:32356800-32360800	Weak transcription	Right Atrium	heart
6	chr6:32357200-32358600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:32358000-32358400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:32358000-32358400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr6:32358000-32358400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:32358000-32358400	Enhancers	GM12878-XiMat	blood
11	chr6:32358400-32360600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr6:32358400-32361400	Weak transcription	GM12878-XiMat	blood
13	chr6:32358600-32360400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr6:32359600-32361200	Weak transcription	Fetal Brain Male	brain
15	chr6:32360400-32361000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr6:32360400-32362000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:32360600-32361000	Enhancers	Left Ventricle	heart
18	chr6:32360600-32361000	Enhancers	NHEK	skin
19	chr6:32360600-32361200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:32360600-32361200	Enhancers	HUVEC	blood vessel
21	chr6:32360600-32362000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr6:32360800-32361000	Enhancers	Right Atrium	heart
23	chr6:32360800-32361000	Enhancers	Spleen	Spleen
24	chr6:32360800-32361200	Enhancers	Fetal Muscle Trunk	muscle
25	chr6:32360800-32361600	Enhancers	HMEC	breast
26	chr6:32360800-32362000	Enhancers	Fetal Muscle Leg	muscle
27	chr6:32360800-32362000	Enhancers	Hela-S3	cervix
28	chr6:32360800-32362800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr6:32360800-32362800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr6:32360800-32362800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr6:32360800-32362800	Enhancers	Esophagus	oesophagus
32	chr6:32361000-32361400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr6:32361000-32361800	Enhancers	Primary hematopoietic stem cells	blood
34	chr6:32361000-32362200	Flanking Active TSS	NHEK	skin
35	chr6:32361000-32370600	Weak transcription	Spleen	Spleen
36	chr6:32361200-32361400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr6:32361200-32361400	Enhancers	Fetal Kidney	kidney
38	chr6:32361200-32361400	Flanking Active TSS	HUVEC	blood vessel
39	chr6:32361200-32361600	Strong transcription	Fetal Brain Male	brain
40	chr6:32361200-32366000	Weak transcription	Fetal Muscle Trunk	muscle
41	chr6:32361400-32361600	Enhancers	HUVEC	blood vessel
42	chr6:32361400-32361800	Enhancers	Primary B cells from peripheral blood	blood
43	chr6:32361400-32362000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr6:32361400-32362000	Enhancers	GM12878-XiMat	blood
45	chr6:32361400-32363000	Strong transcription	Fetal Stomach	stomach
46	chr6:32361400-32366800	Weak transcription	Fetal Kidney	kidney
47	chr6:32361600-32362000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr6:32361600-32362000	Flanking Active TSS	HMEC	breast
49	chr6:32361600-32362000	Flanking Active TSS	HUVEC	blood vessel
50	chr6:32361600-32366800	Weak transcription	Fetal Brain Male	brain

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