Variant report

Variant	rs1750084
Chromosome Location	chr14:46103130-46103131
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10142974	1.00[EUR][1000 genomes]
rs10143197	1.00[EUR][1000 genomes]
rs10145394	1.00[EUR][1000 genomes]
rs1266271	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1266285	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1613188	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs1686232	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1686236	1.00[EUR][1000 genomes]
rs17116172	1.00[EUR][1000 genomes]
rs17116174	1.00[EUR][1000 genomes]
rs1750086	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1770931	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2183485	1.00[EUR][1000 genomes]
rs57795005	1.00[EUR][1000 genomes]
rs7147938	1.00[EUR][1000 genomes]
rs7151112	1.00[EUR][1000 genomes]
rs7151323	1.00[EUR][1000 genomes]
rs7151398	1.00[EUR][1000 genomes]
rs7152047	1.00[EUR][1000 genomes]
rs7152379	1.00[EUR][1000 genomes]
rs74044190	1.00[EUR][1000 genomes]
rs74044192	1.00[EUR][1000 genomes]
rs8004089	1.00[EUR][1000 genomes]
rs8004461	1.00[EUR][1000 genomes]
rs8007164	1.00[EUR][1000 genomes]
rs8007355	1.00[EUR][1000 genomes]
rs8019757	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530814	chr14:45604432-46198418	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1042989	chr14:45774194-46489107	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv901847	chr14:45797782-46607899	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2422441	chr14:45848850-46325684	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1035463	chr14:45940562-46201777	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv542083	chr14:45940562-46201777	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv976289	chr14:45973774-46282154	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1044871	chr14:46007760-46432325	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv456282	chr14:46024675-46458696	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv564729	chr14:46024675-46458696	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	esv2757568	chr14:46050874-46120738	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv2759988	chr14:46050874-46120738	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46101800-46103600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:46102400-46103400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:46102400-46103400	Flanking Active TSS	NHEK	skin
4	chr14:46102600-46103200	Flanking Active TSS	HMEC	breast
5	chr14:46102600-46103600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr14:46102600-46103600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr14:46102800-46103200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:46102800-46105200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr14:46103000-46104000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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