Variant report

Variant	rs1797320
Chromosome Location	chr15:50467966-50467967
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:50458824..50460746-chr15:50465947..50468257,2	MCF-7	breast:
2	chr15:50467355..50470733-chr15:50646637..50649542,3	MCF-7	breast:
3	chr15:50464723..50468254-chr15:50470192..50472116,3	K562	blood:
4	chr15:50467355..50471725-chr15:50472590..50476419,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000140284	Chromatin interaction
ENSG00000104064	Chromatin interaction
ENSG00000104043	Chromatin interaction
ENSG00000244879	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11858285	0.93[ASN][1000 genomes]
rs1648345	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16963406	0.86[ASN][1000 genomes]
rs1797314	0.93[ASN][1000 genomes]
rs1797315	0.81[ASN][1000 genomes]
rs1797316	0.93[ASN][1000 genomes]
rs1797318	0.93[ASN][1000 genomes]
rs1797319	0.96[ASN][1000 genomes]
rs1896171	0.89[AFR][1000 genomes]
rs2433281	0.93[ASN][1000 genomes]
rs2433283	0.96[ASN][1000 genomes]
rs2554884	0.93[ASN][1000 genomes]
rs2554885	0.93[ASN][1000 genomes]
rs2554886	0.93[ASN][1000 genomes]
rs2555487	0.96[ASN][1000 genomes]
rs2555488	0.93[ASN][1000 genomes]
rs2555489	0.93[ASN][1000 genomes]
rs28455006	0.93[ASN][1000 genomes]
rs2899458	0.96[ASN][1000 genomes]
rs6493415	0.93[ASN][1000 genomes]
rs8024818	0.93[ASN][1000 genomes]
rs8031851	0.93[ASN][1000 genomes]
rs933855	0.93[ASN][1000 genomes]
rs933857	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1035983	chr15:50223334-50595170	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv542382	chr15:50223334-50595170	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv904209	chr15:50444824-50482133	Enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50461600-50472400	Weak transcription	Hela-S3	cervix

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