Variant report

Variant	rs1764787
Chromosome Location	chr1:197300267-197300268
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1337169	0.85[EUR][1000 genomes]
rs1415214	0.91[EUR][1000 genomes]
rs1615444	0.92[EUR][1000 genomes]
rs1764622	0.91[EUR][1000 genomes]
rs1764623	0.90[EUR][1000 genomes]
rs1764624	0.91[EUR][1000 genomes]
rs1764625	0.90[EUR][1000 genomes]
rs1764786	0.82[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs1764788	0.91[EUR][1000 genomes]
rs1764791	0.91[EUR][1000 genomes]
rs1764792	0.91[EUR][1000 genomes]
rs2786108	0.88[EUR][1000 genomes]
rs2786110	0.89[EUR][1000 genomes]
rs2786111	0.89[EUR][1000 genomes]
rs2786112	0.89[EUR][1000 genomes]
rs2786113	0.89[EUR][1000 genomes]
rs2786115	0.89[EUR][1000 genomes]
rs2821127	0.88[EUR][1000 genomes]
rs2821131	0.89[EUR][1000 genomes]
rs482526	0.90[EUR][1000 genomes]
rs550098	0.81[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs554009	0.91[EUR][1000 genomes]
rs570845	0.91[EUR][1000 genomes]
rs572447	0.85[EUR][1000 genomes]
rs580067	0.91[EUR][1000 genomes]
rs643025	0.81[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs658409	0.91[EUR][1000 genomes]
rs664767	0.90[EUR][1000 genomes]
rs675699	0.91[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528460	chr1:196542567-197446702	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 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	chr1:197298000-197302000	Weak transcription	Brain Anterior Caudate	brain
2	chr1:197298200-197304800	Weak transcription	Brain Hippocampus Middle	brain
3	chr1:197299000-197323400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr1:197299800-197307200	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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