Variant report

Variant	rs73844833
Chromosome Location	chr4:124598177-124598178
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73844826	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34581	chr4:124271321-125247395	Flanking Bivalent TSS/Enh Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv469710	chr4:124474286-124623722	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv482747	chr4:124474286-124623722	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv830047	chr4:124504051-124699142	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv879874	chr4:124550693-124607201	Genic enhancers Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124573000-124598200	Weak transcription	Right Atrium	heart
2	chr4:124580800-124605000	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:124593400-124604800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:124594800-124605000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr4:124595000-124610600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:124595800-124604800	Weak transcription	Fetal Intestine Large	intestine
7	chr4:124597000-124598400	Enhancers	Fetal Muscle Leg	muscle
8	chr4:124597000-124603400	Weak transcription	Fetal Intestine Small	intestine
9	chr4:124597200-124598400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:124597600-124598400	Enhancers	Aorta	Aorta
11	chr4:124597800-124598200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
12	chr4:124597800-124598200	Enhancers	HSMM	muscle
13	chr4:124597800-124598400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
14	chr4:124597800-124598800	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr4:124597800-124598800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr4:124598000-124598400	Active TSS	Psoas Muscle	Psoas

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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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