Variant report

Variant	rs357410
Chromosome Location	chr7:138038706-138038707
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:138030718..138033704-chr7:138034861..138038720,3	K562	blood:
2	chr7:137941053..137942559-chr7:138036086..138038896,2	K562	blood:
3	chr7:138035919..138038912-chr7:138143414..138146146,5	K562	blood:
4	chr7:138034267..138036102-chr7:138038390..138040259,2	K562	blood:

Variant related genes	Relation type
ENSG00000122779	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1035329	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs11536612	0.93[AFR][1000 genomes]
rs357370	0.93[AFR][1000 genomes]
rs357374	0.93[AFR][1000 genomes]
rs357375	0.93[AFR][1000 genomes]
rs357380	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs357405	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs357406	0.82[ASN][1000 genomes]
rs357407	0.90[ASN][1000 genomes]
rs357409	0.94[ASN][1000 genomes]
rs357413	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs357415	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs357416	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs357417	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs357419	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs357420	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs357422	0.85[ASN][1000 genomes]
rs357434	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs357436	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs357439	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs357444	0.81[EUR][1000 genomes]
rs357452	0.81[EUR][1000 genomes]
rs368043	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs378745	0.93[AFR][1000 genomes]
rs396783	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs402615	0.81[EUR][1000 genomes]
rs403675	0.81[EUR][1000 genomes]
rs407702	0.93[AFR][1000 genomes]
rs410156	0.93[AFR][1000 genomes]
rs410187	0.93[AFR][1000 genomes]
rs424335	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs424847	0.93[AFR][1000 genomes]
rs443184	0.93[AFR][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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	esv3348355	chr7:138022746-138072487	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	1 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	chr7:138034400-138038800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr7:138037600-138038800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:138038200-138039600	Enhancers	HepG2	liver
4	chr7:138038600-138038800	Flanking Active TSS	K562	blood

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