Variant report

Variant	rs73144207
Chromosome Location	chr3:86437151-86437152
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12632769	0.83[ASN][1000 genomes]
rs12633748	0.97[ASN][1000 genomes]
rs12635791	0.97[ASN][1000 genomes]
rs1495887	0.95[ASN][1000 genomes]
rs1495890	1.00[ASN][1000 genomes]
rs1603323	0.95[ASN][1000 genomes]
rs34120884	0.83[ASN][1000 genomes]
rs35397503	1.00[ASN][1000 genomes]
rs35706703	0.83[ASN][1000 genomes]
rs59459179	0.92[ASN][1000 genomes]
rs61272271	0.97[ASN][1000 genomes]
rs6783564	0.83[ASN][1000 genomes]
rs6793988	0.81[ASN][1000 genomes]
rs7615350	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7634263	0.95[ASN][1000 genomes]
rs7636445	0.95[ASN][1000 genomes]
rs9814295	0.95[ASN][1000 genomes]
rs9821248	0.95[ASN][1000 genomes]
rs9823746	0.83[ASN][1000 genomes]
rs9832811	0.83[ASN][1000 genomes]
rs9833387	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532629	chr3:85763873-86608579	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv877115	chr3:86278951-86554319	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv834753	chr3:86386749-86546500	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:86431000-86437400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:86431400-86437800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr3:86435400-86439000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr3:86436000-86437800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:86436000-86438000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:86436600-86437200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr3:86437000-86437200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:86437000-86438200	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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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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