Variant report

Variant	rs2937745
Chromosome Location	chr5:75604670-75604671
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:75601594..75605692-chr5:75607686..75610680,4	K562	blood:

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10942765	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13188781	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1469387	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1863919	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1971744	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1995381	0.80[EUR][1000 genomes]
rs2358712	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs246813	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs246814	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs246815	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2913252	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2913255	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913256	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913257	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913258	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913259	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913260	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913262	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913263	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913265	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2913266	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937741	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937742	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937743	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937744	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937746	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937747	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937748	0.80[EUR][1000 genomes]
rs2937749	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2937750	0.80[EUR][1000 genomes]
rs2937752	0.80[EUR][1000 genomes]
rs2972836	0.80[EUR][1000 genomes]
rs2972838	0.80[EUR][1000 genomes]
rs2972840	0.87[EUR][1000 genomes]
rs2972843	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972846	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972847	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972848	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972849	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972850	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972853	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2972854	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs31244	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34596551	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35764719	0.87[EUR][1000 genomes]
rs35930860	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35966882	0.89[EUR][1000 genomes]
rs35984318	0.87[EUR][1000 genomes]
rs4352583	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4566771	0.89[EUR][1000 genomes]
rs6453213	0.89[EUR][1000 genomes]
rs6453214	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs67560206	0.91[EUR][1000 genomes]
rs67771044	0.89[EUR][1000 genomes]
rs6876070	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6891108	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7730153	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv870415	chr5:75526088-75738412	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75595200-75605200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr5:75601800-75605800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:75604200-75614200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr5:75604600-75605800	Weak transcription	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links