Variant report

Variant	rs57610255
Chromosome Location	chr20:23045465-23045466
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]
rs1331081	1.00[AMR][1000 genomes]
rs1537133	1.00[AMR][1000 genomes]
rs55783247	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55964438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56978650	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59053572	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7266993	1.00[AMR][1000 genomes]
rs73901579	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901582	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901583	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901586	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901588	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901589	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8123988	1.00[AMR][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	nsv912816	chr20:22757960-23062927	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2758516	chr20:23029404-23173240	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	esv2758789	chr20:23029404-23179604	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23038400-23046600	Enhancers	Fetal Lung	lung
2	chr20:23039800-23046000	Enhancers	Fetal Muscle Leg	muscle
3	chr20:23040200-23046800	Enhancers	Fetal Stomach	stomach
4	chr20:23042000-23046000	Weak transcription	Stomach Mucosa	stomach
5	chr20:23042200-23046200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr20:23043200-23045600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr20:23043200-23046400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr20:23043400-23063000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr20:23043600-23053000	Weak transcription	Ovary	ovary
10	chr20:23043600-23054000	Weak transcription	Lung	lung
11	chr20:23043600-23062200	Weak transcription	Placenta	Placenta
12	chr20:23043600-23066600	Weak transcription	Aorta	Aorta
13	chr20:23043800-23046200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr20:23043800-23055200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr20:23044000-23045800	Weak transcription	GM12878-XiMat	blood
16	chr20:23044200-23047200	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr20:23044800-23053000	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr20:23045000-23051800	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr20:23045400-23047000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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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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