Variant report

Variant	rs73849810
Chromosome Location	chr4:142027173-142027174
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs17006871	1.00[AMR][1000 genomes]
rs17006913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17006916	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3897805	0.85[AFR][1000 genomes]
rs56044111	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57425272	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57567945	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73849811	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73849812	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73849843	1.00[AMR][1000 genomes]
rs73849845	0.87[AFR][1000 genomes]
rs73849846	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73849847	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7669598	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7672823	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880167	chr4:141616979-142092124	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv880169	chr4:142005573-142038481	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:142000800-142031600	Weak transcription	Right Ventricle	heart
2	chr4:142010400-142027600	Weak transcription	Left Ventricle	heart
3	chr4:142013000-142040400	Weak transcription	Psoas Muscle	Psoas
4	chr4:142023200-142027800	Enhancers	Fetal Heart	heart
5	chr4:142024000-142027600	Weak transcription	NH-A	brain
6	chr4:142024200-142031200	Weak transcription	Colon Smooth Muscle	Colon
7	chr4:142024400-142030800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:142024600-142027400	Weak transcription	Fetal Muscle Leg	muscle
9	chr4:142026200-142039200	Weak transcription	H9 Derived Neuron 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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