Variant report

Variant	rs6127036
Chromosome Location	chr20:52579475-52579476
allele	C/T
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	chr16:732113..733855-chr20:52577889..52580528,2	MCF-7	breast:
2	chr20:52578439..52580096-chr4:70380828..70382348,2	MCF-7	breast:
3	chr20:52578883..52580609-chr20:52582194..52583717,2	K562	blood:
4	chr20:52572078..52574056-chr20:52577646..52580045,2	K562	blood:
5	chr20:52578676..52580952-chr20:52822613..52824922,2	MCF-7	breast:
6	chr17:59938997..59940771-chr20:52578844..52581418,2	MCF-7	breast:
7	chr20:52578607..52581315-chr8:144821296..144823256,2	MCF-7	breast:
8	chr20:52576980..52579771-chr20:52581907..52583862,2	K562	blood:
9	chr20:52577489..52580206-chr6:39156376..39158164,2	MCF-7	breast:

No data

No data

No data

Variant related genes	Relation type
ENSG00000101132	Chromatin interaction
ENSG00000103266	Chromatin interaction
ENSG00000136492	Chromatin interaction
ENSG00000203499	Chromatin interaction
ENSG00000161999	Chromatin interaction

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs6123333	0.91[ASN][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	esv34060	chr20:52251863-52702186	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	296 gene(s)	inside rSNPs	diseases
2	nsv834009	chr20:52386050-52590795	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	182 gene(s)	inside rSNPs	diseases
3	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
4	nsv1055549	chr20:52555871-52586281	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52566400-52644800	Weak transcription	Gastric	stomach
2	chr20:52567000-52580200	Weak transcription	Stomach Mucosa	stomach
3	chr20:52570200-52591800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr20:52570200-52592400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr20:52570800-52590800	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr20:52576400-52591400	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr20:52577000-52580400	Weak transcription	Fetal Muscle Leg	muscle
8	chr20:52578400-52580200	Weak transcription	Fetal Stomach	stomach
9	chr20:52578400-52591200	Weak transcription	HSMMtube	muscle
10	chr20:52578600-52580400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr20:52578600-52592400	Weak transcription	Brain Hippocampus Middle	brain
12	chr20:52578800-52591800	Weak transcription	Brain Anterior Caudate	brain
13	chr20:52578800-52592400	Weak transcription	Brain Substantia Nigra	brain

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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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