Variant report

Variant	rs12165718
Chromosome Location	chr22:31180678-31180679
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10427627	0.89[AFR][1000 genomes]
rs10427877	0.89[AFR][1000 genomes]
rs12106514	0.89[AFR][1000 genomes]
rs5753281	1.00[YRI][hapmap]

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	nsv915818	chr22:30708245-31346302	Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv2763260	chr22:31141521-31185000	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31140000-31185400	Weak transcription	Fetal Brain Female	brain
2	chr22:31168000-31185400	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr22:31172800-31189400	Weak transcription	Fetal Heart	heart
4	chr22:31173800-31181600	Weak transcription	Spleen	Spleen
5	chr22:31173800-31198200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr22:31177600-31182800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr22:31177800-31185800	Weak transcription	HSMMtube	muscle
8	chr22:31178800-31187600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr22:31179800-31181200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr22:31179800-31181400	Enhancers	Fetal Intestine Small	intestine
11	chr22:31179800-31181800	Enhancers	Fetal Intestine Large	intestine
12	chr22:31180400-31181200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr22:31180600-31181200	Enhancers	NHDF-Ad	bronchial

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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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