Variant report

Variant	rs549622
Chromosome Location	chr1:57605402-57605403
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12090414	0.94[CEU][hapmap];0.83[GIH][hapmap];0.93[TSI][hapmap];0.86[EUR][1000 genomes]
rs476568	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs484064	0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs490793	0.84[CEU][hapmap]
rs502701	0.94[CEU][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs506832	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs510824	0.84[ASW][hapmap];0.84[CEU][hapmap];0.96[TSI][hapmap];0.83[EUR][1000 genomes]
rs513259	0.84[CEU][hapmap];0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs519401	0.94[CEU][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.87[EUR][1000 genomes]
rs535415	0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs537307	0.84[CEU][hapmap];0.93[TSI][hapmap];0.82[EUR][1000 genomes]
rs546020	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs550511	0.93[TSI][hapmap];0.81[EUR][1000 genomes]
rs553453	0.84[CEU][hapmap];0.90[TSI][hapmap]
rs553508	0.94[CEU][hapmap];0.92[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs556204	0.94[CEU][hapmap];0.92[MEX][hapmap];0.93[TSI][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs561258	0.88[CEU][hapmap];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs563921	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.86[MEX][hapmap];0.86[MKK][hapmap];0.96[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs564665	0.81[EUR][1000 genomes]
rs578962	0.81[EUR][1000 genomes]
rs579057	0.83[CEU][hapmap]

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	nsv869295	chr1:56894955-57656562	Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	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
3	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs549622	C1orf177	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:57551400-57622000	Weak transcription	Fetal Intestine Small	intestine
2	chr1:57589400-57608600	Weak transcription	Fetal Intestine Large	intestine
3	chr1:57602200-57609200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr1:57605000-57608400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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