Variant report

Variant	rs56218371
Chromosome Location	chr2:49022282-49022283
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:48974519..48977429-chr2:49021339..49023541,3	MCF-7	breast:
2	chr2:49022010..49024033-chr2:49025700..49028628,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs12613652	0.84[AFR][1000 genomes]
rs13001105	0.85[AFR][1000 genomes]
rs13009992	0.88[AFR][1000 genomes]
rs13025362	0.88[AFR][1000 genomes]
rs17483876	0.81[AFR][1000 genomes]
rs34075428	0.84[AFR][1000 genomes]
rs36080348	0.85[AFR][1000 genomes]
rs4331561	0.85[AFR][1000 genomes]
rs4374422	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4432506	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4449184	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4491769	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4525742	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4558635	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs55930451	0.91[EUR][1000 genomes]
rs55971673	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56963017	0.88[AFR][1000 genomes]
rs57100371	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57463767	0.85[AFR][1000 genomes]
rs58176203	0.88[AFR][1000 genomes]
rs58718281	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs59230684	0.85[AFR][1000 genomes]
rs60283047	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66481918	0.81[AFR][1000 genomes]
rs72811814	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72811828	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72811832	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs72811860	0.94[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs72811867	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72811870	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72811872	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72811873	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72823283	0.84[AFR][1000 genomes]
rs7567401	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010494	chr2:48767055-49027310	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1002793	chr2:48771220-49466550	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv1004965	chr2:48796170-49443587	Bivalent Enhancer Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv535684	chr2:48796170-49443587	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv498119	chr2:48808834-49422647	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv998864	chr2:49015878-49230000	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1014434	chr2:49016279-49053699	Enhancers Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48994600-49080200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr2:49018200-49027000	Weak transcription	Right Atrium	heart

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