Variant report

Variant	rs8042714
Chromosome Location	chr15:44242458-44242459
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:44237370..44240153-chr15:44241264..44242889,2	K562	blood:
2	chr15:44240850..44243740-chr15:44243781..44246529,3	K562	blood:
3	chr15:44240850..44243740-chr15:44243781..44246073,2	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1077421	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11070414	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11635039	1.00[CHB][hapmap];0.89[JPT][hapmap];0.97[ASN][1000 genomes]
rs1545182	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2016837	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2412822	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28548859	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2918945	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2918946	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4544217	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs472797	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs530074	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs563940	1.00[CEU][hapmap];0.88[CHB][hapmap];0.94[JPT][hapmap];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs589649	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs597705	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs638224	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs678513	1.00[CEU][hapmap];0.88[CHB][hapmap]
rs747714	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs920339	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037786	chr15:43888926-44318587	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv542370	chr15:43888926-44318587	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	158 gene(s)	inside rSNPs	diseases
4	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
5	nsv1044435	chr15:44176103-44507403	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs8042714	ADAL	cis	Nerve Tibial	GTEx
rs8042714	ADAL	cis	Artery Tibial	GTEx
rs8042714	ELL3	Cis_1M	lymphoblastoid	RTeQTL
rs8042714	ADAL	cis	Esophagus Muscularis	GTEx
rs8042714	CKMT1A	cis	Esophagus Mucosa	GTEx
rs8042714	ADAL	cis	Thyroid	GTEx

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44225400-44246200	Weak transcription	Right Atrium	heart
2	chr15:44225600-44246200	Weak transcription	NH-A	brain
3	chr15:44227200-44251000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:44227400-44244200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr15:44229000-44245000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:44236400-44246200	Weak transcription	NHLF	lung
7	chr15:44238200-44245800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr15:44239200-44242800	Weak transcription	Fetal Heart	heart
9	chr15:44240400-44243800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr15:44241200-44243000	Enhancers	Brain Cingulate Gyrus	brain
11	chr15:44241400-44243000	Enhancers	Brain Angular Gyrus	brain
12	chr15:44241600-44246000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr15:44241800-44242800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:44241800-44243000	Enhancers	GM12878-XiMat	blood
15	chr15:44242000-44243000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr15:44242000-44250400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr15:44242200-44242800	Enhancers	Brain Anterior Caudate	brain
18	chr15:44242200-44243000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr15:44242200-44243000	Enhancers	HSMMtube	muscle
20	chr15:44242200-44243400	Enhancers	Brain Hippocampus Middle	brain
21	chr15:44242400-44243200	Enhancers	Brain Substantia Nigra	brain

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