Variant report

Variant	rs17785485
Chromosome Location	chr6:79854226-79854227
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	chr6:79784760..79788222-chr6:79851456..79855536,3	MCF-7	breast:
2	chr6:79852069..79854687-chr6:79872579..79874335,2	K562	blood:

Variant related genes	Relation type
ENSG00000146247	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs13437410	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1415311	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17723508	0.88[CEU][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17786528	1.00[ASN][1000 genomes]
rs45463891	1.00[ASN][1000 genomes]
rs56097110	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72890022	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72890023	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72890048	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72890085	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72890089	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72891829	1.00[ASN][1000 genomes]
rs72893703	1.00[ASN][1000 genomes]
rs72902838	1.00[ASN][1000 genomes]
rs72902857	1.00[ASN][1000 genomes]
rs72902878	1.00[ASN][1000 genomes]
rs72902895	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72904839	1.00[ASN][1000 genomes]
rs72904869	1.00[ASN][1000 genomes]
rs72904885	1.00[ASN][1000 genomes]
rs7751422	1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9443633	1.00[ASN][1000 genomes]
rs9443636	1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9443640	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9448603	1.00[ASN][1000 genomes]
rs9448617	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9448624	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9688399	1.00[JPT][hapmap];1.00[ASN][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	nsv830706	chr6:79825910-79994878	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1028607	chr6:79853272-80767716	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79846200-79856400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:79853400-79858600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr6:79853400-79859600	Weak transcription	HUES6 Cell Line	embryonic stem cell

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