Variant report

Variant	rs73429198
Chromosome Location	chr7:121247319-121247320
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs2402581	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60461337	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73429197	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032054	chr7:120926379-121432971	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv539103	chr7:120926379-121432971	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv608333	chr7:121132213-121379616	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2761362	chr7:121172202-121252112	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121244000-121247400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:121245400-121248800	Weak transcription	HSMM	muscle
3	chr7:121245600-121249000	Weak transcription	Stomach Mucosa	stomach
4	chr7:121245800-121250600	Weak transcription	Fetal Lung	lung
5	chr7:121246000-121247800	Weak transcription	Fetal Brain Male	brain
6	chr7:121246000-121248800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr7:121246000-121248800	Weak transcription	Fetal Muscle Leg	muscle
8	chr7:121246000-121248800	Weak transcription	Pancreas	Pancrea
9	chr7:121246000-121249000	Weak transcription	NHEK	skin
10	chr7:121246000-121250000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr7:121246000-121250200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr7:121246000-121250400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr7:121246000-121250400	Weak transcription	Fetal Stomach	stomach
14	chr7:121246200-121248000	Weak transcription	Fetal Brain Female	brain
15	chr7:121246200-121250200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:121246800-121248800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr7:121247000-121248400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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