Variant report

Variant	rs10144932
Chromosome Location	chr14:72871859-72871860
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10134133	0.94[CEU][hapmap];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11158954	0.82[CEU][hapmap];0.89[JPT][hapmap]
rs11621747	0.92[CHB][hapmap];0.82[JPT][hapmap]
rs12434786	0.84[CHB][hapmap];0.80[EUR][1000 genomes]
rs12435911	0.80[CEU][hapmap];0.83[JPT][hapmap];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2239216	0.92[CHB][hapmap];0.88[JPT][hapmap];0.91[ASN][1000 genomes]
rs6574073	0.93[CEU][hapmap];0.92[CHB][hapmap];0.83[JPT][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6574076	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7151688	0.82[CEU][hapmap];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7159300	0.89[EUR][1000 genomes]
rs8015756	0.82[CEU][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72861000-72873400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:72868800-72872200	Weak transcription	Fetal Brain Male	brain
3	chr14:72870800-72872000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr14:72871000-72872200	Enhancers	Placenta	Placenta
5	chr14:72871800-72873600	Weak transcription	Cortex derived primary cultured neurospheres	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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