Variant report

Variant	rs2758457
Chromosome Location	chr6:114204808-114204809
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10046248	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs34732449	0.87[EUR][1000 genomes]
rs352090	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs60077422	0.91[AFR][1000 genomes]
rs6926826	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6927150	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6927480	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6927568	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs71566752	0.87[EUR][1000 genomes]
rs71566753	0.87[EUR][1000 genomes]
rs7758501	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9488238	1.00[CHB][hapmap]

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	nsv1021774	chr6:114063971-114407280	Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv538422	chr6:114063971-114407280	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	esv3363275	chr6:114101331-114302866	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114200600-114205200	Weak transcription	HSMMtube	muscle
2	chr6:114200800-114205000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:114200800-114205200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:114201000-114205200	Weak transcription	Fetal Lung	lung
5	chr6:114201000-114205400	Weak transcription	Fetal Brain Female	brain
6	chr6:114201200-114206400	Weak transcription	Adipose Nuclei	Adipose
7	chr6:114203800-114208800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr6:114204800-114206000	Enhancers	Brain Germinal Matrix	brain
9	chr6:114204800-114206400	Enhancers	Fetal Brain Male	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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