Variant report

Variant	rs8037399
Chromosome Location	chr15:44278799-44278800
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16958828	1.00[AMR][1000 genomes]
rs16959357	1.00[AMR][1000 genomes]
rs7169151	0.85[YRI][hapmap]
rs7172717	1.00[AMR][1000 genomes]
rs7180583	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs8035946	1.00[AMR][1000 genomes]
rs8036490	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs8038605	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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
6	nsv1052511	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
7	nsv542371	chr15:44266441-44719023	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	nsv984063	chr15:44276858-44282232	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44257400-44281000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr15:44259200-44285600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr15:44263000-44295600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr15:44267400-44290600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:44268800-44290400	Weak transcription	Fetal Heart	heart
6	chr15:44269600-44283600	Weak transcription	Brain Angular Gyrus	brain
7	chr15:44269800-44291800	Weak transcription	NH-A	brain
8	chr15:44269800-44292200	Weak transcription	HMEC	breast
9	chr15:44274600-44281200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr15:44276200-44281800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr15:44276400-44287200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:44276400-44287800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr15:44276800-44281200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:44276800-44281200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:44276800-44290800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr15:44277400-44292400	Weak transcription	NHLF	lung
17	chr15:44278000-44278800	Enhancers	Brain Substantia Nigra	brain
18	chr15:44278200-44295400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr15:44278400-44278800	Flanking Active TSS	GM12878-XiMat	blood
20	chr15:44278600-44278800	Enhancers	Brain Cingulate Gyrus	brain
21	chr15:44278600-44279200	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr15:44278600-44281600	Weak transcription	Brain Hippocampus Middle	brain
23	chr15:44278600-44283200	Weak transcription	Brain Anterior Caudate	brain

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