Variant report

Variant	rs17108448
Chromosome Location	chr14:39344082-39344083
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10136471	0.83[ASN][1000 genomes]
rs12885472	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12894222	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1957051	0.90[EUR][1000 genomes]
rs7152381	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7153130	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs927295	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv564416	chr14:39140536-39440106	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv470631	chr14:39153764-39440106	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv3429206	chr14:39160730-39648836	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv932194	chr14:39173578-39411337	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:39338400-39348200	Weak transcription	Pancreas	Pancrea
2	chr14:39339000-39347400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr14:39339000-39350200	Weak transcription	Brain Anterior Caudate	brain
4	chr14:39340000-39344600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr14:39340000-39346600	Weak transcription	Brain Angular Gyrus	brain
6	chr14:39342400-39344800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr14:39343000-39345200	Enhancers	Primary hematopoietic stem cells	blood
8	chr14:39343000-39345800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr14:39343000-39346600	Weak transcription	Adipose Nuclei	Adipose
10	chr14:39343400-39344800	Enhancers	Primary B cells from cord blood	blood
11	chr14:39343600-39345400	Enhancers	Brain Hippocampus Middle	brain
12	chr14:39343600-39348200	Weak transcription	Psoas Muscle	Psoas
13	chr14:39343800-39345200	Enhancers	Brain Substantia Nigra	brain
14	chr14:39344000-39344600	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr14:39344000-39347600	Enhancers	Primary neutrophils fromperipheralblood	blood

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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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