Variant report

Variant	rs10225181
Chromosome Location	chr7:108418671-108418672
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10155811	1.00[EUR][1000 genomes]
rs10226797	1.00[EUR][1000 genomes]
rs10229154	1.00[EUR][1000 genomes]
rs10230997	1.00[EUR][1000 genomes]
rs10238635	1.00[EUR][1000 genomes]
rs10241318	1.00[EUR][1000 genomes]
rs10255237	1.00[EUR][1000 genomes]
rs10268467	1.00[EUR][1000 genomes]
rs10273105	1.00[EUR][1000 genomes]
rs10279331	1.00[EUR][1000 genomes]
rs10281086	1.00[EUR][1000 genomes]
rs1100228	1.00[EUR][1000 genomes]
rs16872645	1.00[EUR][1000 genomes]
rs28722885	1.00[EUR][1000 genomes]
rs6967977	1.00[EUR][1000 genomes]
rs6972924	1.00[EUR][1000 genomes]
rs7780568	1.00[EUR][1000 genomes]
rs848371	1.00[EUR][1000 genomes]
rs848372	1.00[EUR][1000 genomes]
rs848413	1.00[EUR][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	nsv817371	chr7:108199882-108649799	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1031096	chr7:108334543-108596014	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv888944	chr7:108348785-108433790	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108418200-108419200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr7:108418400-108419000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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