Variant report

Variant	rs59440875
Chromosome Location	chr6:36405555-36405556
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:36403741..36414959-chr6:36560215..36569964,50	K562	blood:
2	chr6:36404075..36406250-chr6:36407059..36409344,2	MCF-7	breast:
3	chr6:36403741..36405640-chr6:36561781..36563741,2	K562	blood:
4	chr6:36404398..36407410-chr6:36409121..36410704,3	K562	blood:

Variant related genes	Relation type
ENSG00000179165	Chromatin interaction
ENSG00000112078	Chromatin interaction
ENSG00000112081	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1003250	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10440841	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12214285	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12215889	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1742757	0.80[AMR][1000 genomes]
rs1744654	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4711450	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs515129	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs515186	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs517890	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs522179	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs544267	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs546272	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs546353	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs547026	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs547966	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs566742	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs584196	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs584418	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs595954	0.83[EUR][1000 genomes]
rs597153	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs600192	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs605684	0.80[AMR][1000 genomes]
rs614028	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs619011	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs621796	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs628314	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs629297	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs629721	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs632943	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6457918	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs659726	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs664370	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6923993	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7744363	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs853881	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs853882	0.80[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs863815	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9357214	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9470274	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9470278	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9470285	0.84[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885806	chr6:36349890-36621178	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs59440875	ETV7	cis	Whole Blood	GTEx

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36399000-36410200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:36400400-36408400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:36400400-36409200	Weak transcription	Placenta	Placenta
4	chr6:36400600-36408800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:36400600-36408800	Weak transcription	HSMM	muscle
6	chr6:36400800-36406000	Weak transcription	A549	lung
7	chr6:36400800-36409000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr6:36404200-36408600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:36404600-36408600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:36404600-36408600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr6:36404800-36408600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:36404800-36408600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:36404800-36408600	Weak transcription	NHDF-Ad	bronchial
14	chr6:36404800-36408800	Weak transcription	GM12878-XiMat	blood
15	chr6:36404800-36408800	Weak transcription	NHLF	lung
16	chr6:36405000-36408800	Weak transcription	NH-A	brain
17	chr6:36405200-36408400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:36405200-36408400	Weak transcription	Osteobl	bone
19	chr6:36405200-36408600	Weak transcription	Muscle Satellite Cultured Cells	--

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