Variant report

Variant	rs12255705
Chromosome Location	chr10:91334004-91334005
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11185765	1.00[EUR][1000 genomes]
rs11185775	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11185776	1.00[EUR][1000 genomes]
rs11185781	1.00[EUR][1000 genomes]
rs11185782	1.00[EUR][1000 genomes]
rs11816406	1.00[EUR][1000 genomes]
rs12249756	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13376985	1.00[EUR][1000 genomes]
rs1475760	1.00[EUR][1000 genomes]
rs60233299	1.00[EUR][1000 genomes]
rs7093503	1.00[EUR][1000 genomes]
rs74146983	1.00[EUR][1000 genomes]
rs7893438	1.00[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	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91328000-91334200	Weak transcription	NHLF	lung
2	chr10:91328200-91347200	Weak transcription	HSMM	muscle
3	chr10:91332800-91334800	Enhancers	HepG2	liver
4	chr10:91333200-91334400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr10:91333200-91339400	Weak transcription	Liver	Liver
6	chr10:91333200-91344600	Weak transcription	Left Ventricle	heart
7	chr10:91333400-91348400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr10:91333400-91351200	Weak transcription	Ovary	ovary
9	chr10:91334000-91334400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr10:91334000-91334400	Enhancers	Fetal Lung	lung
11	chr10:91334000-91334400	Enhancers	Fetal Stomach	stomach
12	chr10:91334000-91334600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr10:91334000-91335200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:91334000-91335200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:91334000-91335400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr10:91334000-91335600	Enhancers	Muscle Satellite Cultured Cells	--

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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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