Variant report

Variant	rs10210389
Chromosome Location	chr2:67195459-67195460
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10174577	0.99[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10175701	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs10180582	0.91[ASN][1000 genomes]
rs10496138	0.91[ASN][1000 genomes]
rs13409540	0.96[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs1362484	0.81[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs58683753	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6721312	0.93[ASN][1000 genomes]
rs6726820	0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs67764531	0.95[ASN][1000 genomes]
rs7419773	0.93[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	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10210389	EHBP1	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67192000-67196400	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:67194400-67195600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:67195000-67196400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr2:67195400-67195600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:67195400-67195600	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:67195400-67196600	Enhancers	Colon Smooth Muscle	Colon

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Input of quick search could be:

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

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