Variant report

Variant	rs17614895
Chromosome Location	chr2:58915608-58915609
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:58883585..58885520-chr2:58914478..58916170,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10490092	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10490093	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13026438	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13421824	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17049642	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17190597	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17190618	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17269154	0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17269182	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17549476	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17549656	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17549677	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17549712	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17549754	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17549803	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17550194	0.90[AMR][1000 genomes]
rs17550487	0.87[AMR][1000 genomes]
rs17614872	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17615036	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17615120	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17615185	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17615279	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17615309	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17615381	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17615638	0.90[AMR][1000 genomes]
rs1922781	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1922783	0.90[AMR][1000 genomes]
rs1950160	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2204913	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35026255	0.82[AMR][1000 genomes]
rs55645922	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55745617	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56174720	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56266136	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56365214	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs60018257	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs60888271	0.90[AMR][1000 genomes]
rs7419776	0.81[ASN][1000 genomes]
rs984881	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs984882	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs984883	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs993531	0.90[AMR][1000 genomes]
rs993532	0.90[AMR][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	nsv431180	chr2:58857542-59178687	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:58914600-58916200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr2:58915000-58917400	Weak transcription	Right Atrium	heart
3	chr2:58915400-58916200	Active TSS	K562	blood
4	chr2:58915600-58916800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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