Variant report

Variant	rs11265487
Chromosome Location	chr1:160773098-160773099
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11265488	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11265489	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2027015	0.88[ASN][1000 genomes]
rs2779800	0.87[ASN][1000 genomes]
rs35237586	0.83[AFR][1000 genomes]
rs474131	0.87[ASN][1000 genomes]
rs485618	0.82[ASN][1000 genomes]
rs492874	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs492906	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs494091	0.88[ASN][1000 genomes]
rs496201	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs504848	0.84[ASN][1000 genomes]
rs505728	0.81[ASN][1000 genomes]
rs506081	0.87[ASN][1000 genomes]
rs509749	0.87[ASN][1000 genomes]
rs510143	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs512645	0.84[ASN][1000 genomes]
rs516509	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs516847	0.82[ASN][1000 genomes]
rs522897	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs539433	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs551827	0.87[ASN][1000 genomes]
rs551882	0.88[ASN][1000 genomes]
rs556810	0.85[ASN][1000 genomes]
rs567306	0.88[ASN][1000 genomes]
rs569659	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs569911	0.84[ASN][1000 genomes]
rs571841	0.88[ASN][1000 genomes]
rs574610	0.84[ASN][1000 genomes]
rs576334	0.84[ASN][1000 genomes]
rs577453	0.84[ASN][1000 genomes]
rs6427548	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6667581	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs790625	0.84[ASN][1000 genomes]
rs790626	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1822379	chr1:160545332-160831143	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831714	chr1:160581168-160776809	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv464161	chr1:160747615-160852046	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv548057	chr1:160747615-160852046	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11265487	LY9	Cis_1M	lymphoblastoid	RTeQTL
rs11265487	SLAMF7	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160768600-160774000	Genic enhancers	Primary B cells from peripheral blood	blood
2	chr1:160771000-160774400	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
3	chr1:160771000-160806600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr1:160771200-160773800	Genic enhancers	Primary T cells fromperipheralblood	blood
5	chr1:160771200-160775400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr1:160771400-160773200	Strong transcription	Fetal Thymus	thymus
7	chr1:160771400-160775600	Genic enhancers	Primary T helper cells fromperipheralblood	blood
8	chr1:160771600-160773600	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:160771600-160774000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
10	chr1:160771600-160777400	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr1:160771800-160777200	Weak transcription	Gastric	stomach
12	chr1:160772200-160773800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr1:160772200-160782000	Genic enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr1:160772400-160775600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr1:160772400-160776200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr1:160772400-160777000	Weak transcription	Thymus	Thymus
17	chr1:160772400-160777200	Weak transcription	Spleen	Spleen
18	chr1:160772400-160777600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr1:160772800-160773400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr1:160772800-160776000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr1:160773000-160773200	Enhancers	Primary T cells from cord blood	blood
22	chr1:160773000-160773400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr1:160773000-160775400	Strong transcription	Primary B cells from cord blood	blood
24	chr1:160773000-160775400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links