Variant report

Variant	rs6906423
Chromosome Location	chr6:101656493-101656494
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs2797369	0.91[ASN][1000 genomes]
rs3905202	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4133169	0.88[ASN][1000 genomes]
rs6925287	0.81[AMR][1000 genomes]
rs72610833	0.88[ASN][1000 genomes]
rs72610834	0.95[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs72610835	0.87[ASN][1000 genomes]
rs72610837	0.95[ASN][1000 genomes]
rs9377260	0.85[AMR][1000 genomes]
rs9377261	0.85[AMR][1000 genomes]
rs9377262	0.88[ASN][1000 genomes]
rs9386270	0.84[ASN][1000 genomes]
rs9390731	0.88[ASN][1000 genomes]
rs9390732	0.88[ASN][1000 genomes]
rs9399712	0.90[ASN][1000 genomes]
rs9404083	0.87[ASN][1000 genomes]
rs9404085	0.88[ASN][1000 genomes]
rs9404089	1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[ASN][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	nsv1020400	chr6:101172705-101981665	Weak transcription Bivalent/Poised TSS Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv538390	chr6:101172705-101981665	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv886458	chr6:101623345-101716365	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:101653800-101657400	Enhancers	Fetal Intestine Large	intestine
2	chr6:101655000-101657200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr6:101655800-101656600	Enhancers	Rectal Mucosa Donor 29	rectum
4	chr6:101656000-101657200	Weak transcription	Fetal Intestine Small	intestine

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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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