Variant report

Variant	rs197632
Chromosome Location	chr1:57700186-57700187
allele	A/C
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:19)

rs_ID	r²[population]
rs127600	0.90[ASN][1000 genomes]
rs197624	0.82[AMR][1000 genomes]
rs197635	0.89[ASN][1000 genomes]
rs197636	0.89[ASN][1000 genomes]
rs197637	0.89[ASN][1000 genomes]
rs197639	0.90[ASN][1000 genomes]
rs197640	0.90[ASN][1000 genomes]
rs197641	0.90[ASN][1000 genomes]
rs197642	0.90[ASN][1000 genomes]
rs2764661	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs514350	0.91[ASN][1000 genomes]
rs552727	0.90[ASN][1000 genomes]
rs554689	0.84[EUR][1000 genomes]
rs565846	0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs606497	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs626210	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs657471	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6682379	0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs706379	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv461628	chr1:57463326-57816489	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv546305	chr1:57463326-57816489	Weak transcription Enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr1:57698200-57701400	Weak transcription	K562	blood
2	chr1:57698400-57702200	Enhancers	Fetal Intestine Large	intestine
3	chr1:57699600-57701000	Enhancers	Liver	Liver
4	chr1:57699600-57702200	Enhancers	HepG2	liver
5	chr1:57699800-57702200	Enhancers	Duodenum Mucosa	Duodenum
6	chr1:57699800-57702200	Enhancers	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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