Variant report

Variant	rs57213108
Chromosome Location	chr20:53284057-53284058
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:53283290..53284914-chr3:64513834..64516578,2	MCF-7	breast:
2	chr20:53282910..53285557-chr7:133594422..133596091,2	MCF-7	breast:
3	chr20:53267329..53270165-chr20:53282445..53284109,2	MCF-7	breast:
4	chr20:53283455..53285734-chr3:64506182..64507970,2	MCF-7	breast:
5	chr20:53263266..53270310-chr20:53278109..53284478,8	MCF-7	breast:
6	chr20:53283718..53285867-chr3:64515756..64517189,9	MCF-7	breast:
7	chr20:53281054..53285156-chr3:64517678..64520991,4	MCF-7	breast:
8	chr20:53283717..53285430-chr3:64475712..64477407,2	MCF-7	breast:
9	chr20:53272079..53274152-chr20:53283538..53285655,2	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11907565	0.97[AFR][1000 genomes]
rs11907588	0.97[AFR][1000 genomes]
rs55924953	0.97[AFR][1000 genomes]
rs59724662	1.00[AMR][1000 genomes]
rs61035069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73913652	0.91[AFR][1000 genomes]
rs73913655	0.97[AFR][1000 genomes]
rs8116736	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8123380	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067497	chr20:53146241-53751820	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
2	nsv1064144	chr20:53175264-53750137	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
3	nsv544302	chr20:53175264-53750137	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
4	nsv1060552	chr20:53234716-53655115	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:53280600-53285000	Weak transcription	Ovary	ovary
2	chr20:53280800-53285000	Weak transcription	Fetal Heart	heart
3	chr20:53281800-53285600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links