Variant report

Variant	rs35578830
Chromosome Location	chr1:95543616-95543617
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:95543478..95545914-chr1:95548996..95550848,2	K562	blood:
2	chr1:95537638..95539562-chr1:95542128..95544518,2	MCF-7	breast:
3	chr1:95542549..95544382-chr1:95554227..95556548,2	K562	blood:
4	chr1:95534244..95536738-chr1:95541895..95543899,2	K562	blood:
5	chr1:95539591..95541319-chr1:95541795..95543723,2	K562	blood:

Variant related genes	Relation type
ENSG00000172339	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10465759	0.95[ASN][1000 genomes]
rs11801110	0.92[ASN][1000 genomes]
rs12239887	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17112857	0.91[ASN][1000 genomes]
rs2391390	0.88[ASN][1000 genomes]
rs34726676	0.95[ASN][1000 genomes]
rs34850224	0.92[ASN][1000 genomes]
rs34923964	0.98[ASN][1000 genomes]
rs3890785	0.95[ASN][1000 genomes]
rs4300274	0.98[ASN][1000 genomes]
rs4387224	0.98[ASN][1000 genomes]
rs4540701	0.98[ASN][1000 genomes]
rs4615892	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55902261	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55911502	0.93[AFR][1000 genomes];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs60846886	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6662345	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6672635	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6674467	0.95[ASN][1000 genomes]
rs6678809	0.98[ASN][1000 genomes]
rs6679106	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6684137	0.98[ASN][1000 genomes]
rs6687351	0.93[AFR][1000 genomes];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6689195	0.88[ASN][1000 genomes]
rs6704022	0.89[ASN][1000 genomes]
rs71654403	0.95[ASN][1000 genomes]
rs71654404	0.92[ASN][1000 genomes]
rs71654405	0.98[ASN][1000 genomes]
rs71654406	0.98[ASN][1000 genomes]
rs71654407	0.98[ASN][1000 genomes]
rs71654408	0.95[ASN][1000 genomes]
rs7417186	0.91[AMR][1000 genomes];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	nsv830636	chr1:95495849-95703126	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95539800-95549000	Weak transcription	K562	blood
2	chr1:95542000-95549600	Weak transcription	HepG2	liver

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