Variant report

Variant	rs61900900
Chromosome Location	chr11:120454144-120454145
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11599940	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11600436	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11601826	0.81[AMR][1000 genomes]
rs11602493	0.98[EUR][1000 genomes]
rs11603180	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12279396	0.89[EUR][1000 genomes]
rs1573789	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17311310	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17311317	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17311324	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3892497	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4278519	0.90[EUR][1000 genomes]
rs4297478	0.83[AMR][1000 genomes]
rs4500499	0.95[EUR][1000 genomes]
rs4561221	0.81[AMR][1000 genomes]
rs4936521	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4938818	0.97[EUR][1000 genomes]
rs61900897	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73000621	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1054057	chr11:119781953-120519770	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv541178	chr11:119781953-120519770	Weak transcription Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1054301	chr11:120396485-120465800	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1036102	chr11:120442895-120498908	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv468881	chr11:120446830-120551100	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv556476	chr11:120446830-120551100	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120437200-120468000	Weak transcription	Right Atrium	heart
2	chr11:120448400-120454200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:120450200-120458400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:120452400-120462600	Weak transcription	Fetal Lung	lung

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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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