Variant report

Variant	rs73460418
Chromosome Location	chr6:73879102-73879103
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000238464	Chromatin interaction
ENSG00000203909	Chromatin interaction
ENSG00000203907	Chromatin interaction
ENSG00000256980	Chromatin interaction
ENSG00000080007	Chromatin interaction
ENSG00000224221	Chromatin interaction
ENSG00000203908	Chromatin interaction

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

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

rs_ID	r²[population]
rs1970550	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs55756283	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs73460435	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410973	chr6:73716033-74419545	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised 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	191 gene(s)	inside rSNPs	diseases
2	nsv1022151	chr6:73876795-73996828	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv538304	chr6:73876795-73996828	Flanking Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 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	chr6:73846400-73879200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:73867000-73884600	Weak transcription	Primary T cells from cord blood	blood
3	chr6:73867400-73880600	Weak transcription	Aorta	Aorta
4	chr6:73867600-73890400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:73867600-73890400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:73869000-73904200	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:73876800-73879200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:73876800-73889800	Weak transcription	HSMM	muscle
9	chr6:73877200-73884200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:73877800-73884200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:73878000-73885600	Weak transcription	Primary B cells from cord blood	blood
12	chr6:73878400-73890200	Weak transcription	Psoas Muscle	Psoas
13	chr6:73878800-73879600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr6:73878800-73880200	Enhancers	NHEK	skin
15	chr6:73879000-73879200	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr6:73879000-73879400	Active TSS	Skeletal Muscle Female	skeletal muscle
17	chr6:73879000-73880000	Enhancers	Foreskin Keratinocyte 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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