Variant report

Variant	rs60367173
Chromosome Location	chr4:96595345-96595346
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17024339	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs57872115	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs61355602	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72882070	0.81[AMR][1000 genomes]
rs72884050	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72884051	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72884057	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72884062	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830012	chr4:96547783-96746163	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv1844506	chr4:96554889-96704333	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1007133	chr4:96556072-96614235	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv997304	chr4:96575198-96861349	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:96593600-96597800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:96594000-96596800	Enhancers	Fetal Kidney	kidney
3	chr4:96594200-96596800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:96594600-96596400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:96595000-96595800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr4:96595000-96597000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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