Variant report

Variant	rs6900251
Chromosome Location	chr6:134206187-134206188
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	chr6:134205266..134207334-chr6:134212529..134214834,2	K562	blood:

Variant related genes	Relation type
ENSG00000227954	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1001331	0.93[EUR][1000 genomes]
rs11751744	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11757968	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1208227	1.00[ASN][1000 genomes]
rs1208228	1.00[ASN][1000 genomes]
rs1208234	1.00[ASN][1000 genomes]
rs1208235	1.00[ASN][1000 genomes]
rs1208237	1.00[ASN][1000 genomes]
rs1208239	1.00[ASN][1000 genomes]
rs1208242	1.00[ASN][1000 genomes]
rs1208244	1.00[ASN][1000 genomes]
rs1208246	1.00[ASN][1000 genomes]
rs1208247	1.00[ASN][1000 genomes]
rs1208251	1.00[ASN][1000 genomes]
rs1208252	1.00[ASN][1000 genomes]
rs1208253	1.00[ASN][1000 genomes]
rs1208260	1.00[ASN][1000 genomes]
rs1208265	1.00[ASN][1000 genomes]
rs1208267	1.00[ASN][1000 genomes]
rs1208268	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1208279	0.94[CEU][hapmap]
rs1208282	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs151105	0.82[EUR][1000 genomes]
rs151106	0.80[EUR][1000 genomes]
rs151107	0.82[EUR][1000 genomes]
rs151108	0.82[EUR][1000 genomes]
rs151109	0.82[EUR][1000 genomes]
rs1535615	0.82[EUR][1000 genomes]
rs1575446	1.00[ASN][1000 genomes]
rs1613895	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1616030	1.00[ASN][1000 genomes]
rs1746011	1.00[ASN][1000 genomes]
rs1746012	1.00[ASN][1000 genomes]
rs1746015	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1746016	0.84[EUR][1000 genomes]
rs17481786	1.00[ASN][1000 genomes]
rs1763937	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1763938	0.84[EUR][1000 genomes]
rs1763941	1.00[ASN][1000 genomes]
rs1763944	1.00[ASN][1000 genomes]
rs1763945	1.00[ASN][1000 genomes]
rs183473	0.80[EUR][1000 genomes]
rs2104261	1.00[ASN][1000 genomes]
rs228853	0.82[EUR][1000 genomes]
rs229919	0.82[EUR][1000 genomes]
rs229921	0.80[EUR][1000 genomes]
rs229923	0.81[EUR][1000 genomes]
rs229924	0.82[EUR][1000 genomes]
rs229925	0.82[EUR][1000 genomes]
rs229926	0.82[EUR][1000 genomes]
rs229927	0.82[EUR][1000 genomes]
rs229928	0.82[EUR][1000 genomes]
rs229929	0.82[EUR][1000 genomes]
rs229930	0.80[EUR][1000 genomes]
rs229931	0.88[GIH][hapmap];0.94[TSI][hapmap];0.82[EUR][1000 genomes]
rs41286216	1.00[ASN][1000 genomes]
rs41286218	1.00[ASN][1000 genomes]
rs4518518	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4610586	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs464168	0.82[EUR][1000 genomes]
rs6569914	0.87[AFR][1000 genomes]
rs6899948	0.87[CEU][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6915061	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6919282	1.00[CEU][hapmap];0.83[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920657	1.00[CEU][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs716050	1.00[ASN][1000 genomes]
rs7748433	0.90[EUR][1000 genomes]
rs9321418	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9321419	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs942130	1.00[ASN][1000 genomes]
rs942132	1.00[ASN][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	esv34122	chr6:134089019-134378252	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs6900251	AKAP7	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134198600-134206400	Weak transcription	Fetal Lung	lung
2	chr6:134200600-134206200	Weak transcription	Fetal Stomach	stomach
3	chr6:134204400-134206400	Weak transcription	Ovary	ovary

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