Variant report

Variant	rs10195394
Chromosome Location	chr2:72258959-72258960
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10202944	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13412195	0.96[ASN][1000 genomes]
rs13416099	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13417153	0.85[ASN][1000 genomes]
rs17007680	0.83[ASN][1000 genomes]
rs8179675	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874260	chr2:72242013-72268093	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv874261	chr2:72242013-72270790	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv874262	chr2:72242013-72279514	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv3584760	chr2:72249991-72271489	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv874263	chr2:72251751-72279514	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:72251400-72259800	Weak transcription	Spleen	Spleen
2	chr2:72255600-72260200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr2:72257600-72260400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:72257600-72261200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:72257800-72259200	Enhancers	NHEK	skin
6	chr2:72258200-72260200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr2:72258400-72259200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr2:72258400-72260200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:72258600-72260200	Enhancers	Placenta Amnion	Placenta Amnion
10	chr2:72258600-72260200	Enhancers	HMEC	breast
11	chr2:72258600-72260600	Enhancers	Esophagus	oesophagus
12	chr2:72258800-72259200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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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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