Variant report

Variant	rs10265129
Chromosome Location	chr7:116670659-116670660
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10255165	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12164064	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28519509	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6961817	0.86[ASN][1000 genomes]
rs7457973	0.86[EUR][1000 genomes]
rs7797217	0.93[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116661600-116670800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:116662000-116675200	Weak transcription	Fetal Stomach	stomach
3	chr7:116664000-116670800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:116665800-116680600	Weak transcription	Osteobl	bone
5	chr7:116666200-116680400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:116666800-116673800	Weak transcription	Pancreas	Pancrea
7	chr7:116667000-116671200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr7:116667000-116671200	Weak transcription	Fetal Brain Male	brain
9	chr7:116667000-116673800	Weak transcription	Right Atrium	heart
10	chr7:116667000-116674000	Weak transcription	HUVEC	blood vessel
11	chr7:116667000-116681000	Weak transcription	NH-A	brain
12	chr7:116667200-116671200	Weak transcription	NHDF-Ad	bronchial
13	chr7:116667200-116676000	Weak transcription	K562	blood
14	chr7:116667200-116680800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr7:116669400-116674400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:116670400-116671600	ZNF genes & repeats	Brain Hippocampus Middle	brain
17	chr7:116670400-116671600	ZNF genes & repeats	GM12878-XiMat	blood
18	chr7:116670600-116671400	Weak transcription	Fetal Heart	heart
19	chr7:116670600-116671600	ZNF genes & repeats	Fetal Lung	lung

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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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