Variant report

Variant	rs72708768
Chromosome Location	chr4:173944285-173944286
allele	C/G
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:17)

rs_ID	r²[population]
rs10005134	0.95[EUR][1000 genomes]
rs10019125	0.95[EUR][1000 genomes]
rs28540604	0.95[EUR][1000 genomes]
rs68064819	0.83[AMR][1000 genomes]
rs6811671	0.81[EUR][1000 genomes]
rs72708748	0.85[EUR][1000 genomes]
rs72708762	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72708764	0.95[EUR][1000 genomes]
rs72708766	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72708769	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72708772	0.95[EUR][1000 genomes]
rs72708774	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72708775	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72708780	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72708781	1.00[EUR][1000 genomes]
rs72708785	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7659038	0.95[EUR][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	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173936400-173945000	Weak transcription	HSMM	muscle
2	chr4:173941400-173950000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr4:173942600-173949400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:173942800-173946000	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:173942800-173948800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:173942800-173949400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr4:173942800-173950000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr4:173943000-173945800	Weak transcription	Fetal Thymus	thymus
9	chr4:173944200-173944400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:173944200-173944600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:173944200-173944800	Enhancers	H1 Derived Mesenchymal Stem 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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