Variant report

Variant	rs74074577
Chromosome Location	chr1:56320759-56320760
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs12033494	1.00[EUR][1000 genomes]
rs17112799	1.00[EUR][1000 genomes]
rs55756946	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs55887759	1.00[EUR][1000 genomes]
rs56148162	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58186426	0.82[AFR][1000 genomes]
rs58590950	1.00[EUR][1000 genomes]
rs59376992	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59529055	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs59552930	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60518072	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74072513	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs74074556	0.86[AFR][1000 genomes]
rs74074558	1.00[EUR][1000 genomes]
rs74074571	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74074575	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74074579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74074580	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829926	chr1:56188492-56360745	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56310400-56321200	Weak transcription	Psoas Muscle	Psoas
2	chr1:56315000-56323200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr1:56319400-56321200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:56319600-56321400	Enhancers	Ovary	ovary
5	chr1:56319800-56321400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:56320000-56320800	Enhancers	NHDF-Ad	bronchial
7	chr1:56320000-56323200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:56320200-56320800	Enhancers	Fetal Muscle Leg	muscle
9	chr1:56320200-56321400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr1:56320200-56321600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:56320400-56320800	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr1:56320400-56320800	Enhancers	Rectal Smooth Muscle	rectum
13	chr1:56320400-56320800	Enhancers	HSMMtube	muscle
14	chr1:56320600-56321000	Enhancers	Osteobl	bone
15	chr1:56320600-56321200	Enhancers	Fetal Stomach	stomach
16	chr1:56320600-56323200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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