Variant report

Variant	rs12191923
Chromosome Location	chr6:49860382-49860383
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12191200	1.00[MKK][hapmap]
rs12195555	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12196205	1.00[MKK][hapmap]
rs12201007	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12204651	1.00[MKK][hapmap]
rs12207683	0.82[AMR][1000 genomes]
rs1547776	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1572882	1.00[MKK][hapmap]
rs17736662	0.81[AMR][1000 genomes]
rs55727321	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62404942	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62406371	0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62406372	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62406377	0.81[AMR][1000 genomes]
rs62406378	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7738293	1.00[MKK][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	nsv933942	chr6:49480550-50004231	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv933833	chr6:49515134-49961765	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12191923	TMEM14A	cis	parietal	SCAN

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49857800-49860400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
2	chr6:49858600-49860400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr6:49858800-49860400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
4	chr6:49858800-49860400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
5	chr6:49859200-49860400	Enhancers	Fetal Intestine Large	intestine
6	chr6:49859600-49860600	Enhancers	Hela-S3	cervix
7	chr6:49859800-49860400	Enhancers	Esophagus	oesophagus
8	chr6:49859800-49860600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:49860000-49860400	Enhancers	Fetal Muscle Leg	muscle
10	chr6:49860000-49860600	Enhancers	Dnd41	blood
11	chr6:49860000-49860800	Enhancers	Fetal Heart	heart

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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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