Variant report

Variant	rs7082714
Chromosome Location	chr10:6355100-6355101
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10795983	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1535694	0.87[ASN][1000 genomes]
rs2021951	0.87[ASN][1000 genomes]
rs2224781	0.86[ASN][1000 genomes]
rs6602620	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7087682	0.81[ASN][1000 genomes]
rs7923615	0.88[ASN][1000 genomes]
rs947477	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1054044	chr10:6155144-6487217	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv894836	chr10:6246678-6435374	Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv430123	chr10:6309402-6448384	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv430125	chr10:6322167-6477267	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1053440	chr10:6354798-6669469	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6342800-6356600	Weak transcription	Brain Substantia Nigra	brain
2	chr10:6349400-6360200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr10:6349400-6369800	Weak transcription	Adipose Nuclei	Adipose
4	chr10:6352200-6355400	Weak transcription	Esophagus	oesophagus
5	chr10:6353800-6357400	Enhancers	Fetal Lung	lung
6	chr10:6354000-6362400	Weak transcription	Aorta	Aorta
7	chr10:6354200-6355400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr10:6354200-6356800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr10:6354200-6369200	Weak transcription	Brain Hippocampus Middle	brain
10	chr10:6354400-6357600	Enhancers	Fetal Intestine Small	intestine
11	chr10:6354600-6355800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr10:6354600-6356800	Enhancers	Stomach Mucosa	stomach
13	chr10:6354800-6355400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr10:6354800-6355400	Weak transcription	Fetal Intestine Large	intestine
15	chr10:6354800-6356200	Enhancers	Fetal Brain Female	brain
16	chr10:6355000-6356000	Enhancers	A549	lung
17	chr10:6355000-6356800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr10:6355000-6363600	Weak transcription	Brain Cingulate Gyrus	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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