Variant report

Variant	rs57861468
Chromosome Location	chr1:77499026-77499027
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1102447	0.87[AFR][1000 genomes]
rs1102449	0.87[AFR][1000 genomes]
rs55770009	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55819295	1.00[AMR][1000 genomes]
rs59424670	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59726610	0.90[AFR][1000 genomes]
rs736453	1.00[AMR][1000 genomes]
rs74090583	1.00[AMR][1000 genomes]
rs74090586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74090590	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74090592	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs858588	0.87[AFR][1000 genomes]
rs858599	0.83[AFR][1000 genomes]
rs858601	0.83[AFR][1000 genomes]
rs858602	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003826	chr1:76965331-77656929	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv535006	chr1:76965331-77656929	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv830292	chr1:77425571-77584307	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77490600-77499200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:77493400-77499200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:77493800-77503400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:77495800-77502600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr1:77496200-77502400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:77497000-77516800	Weak transcription	Fetal Stomach	stomach
7	chr1:77497200-77503400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:77498200-77499200	Strong transcription	Cortex derived primary cultured neurospheres	brain
9	chr1:77498400-77500800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr1:77498600-77502600	Weak transcription	NHEK	skin
11	chr1:77498800-77499800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr1:77499000-77500000	Weak transcription	Brain Germinal Matrix	brain

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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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