Variant report

Variant	rs77518806
Chromosome Location	chr4:124939334-124939335
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv830049	chr4:124793932-124955708	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv868977	chr4:124841128-125550637	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv879879	chr4:124893772-124971109	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv3437088	chr4:124939102-124940350	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a
6	esv2401226	chr4:124939159-124939673	Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	n/a
7	esv3391030	chr4:124939277-124939600	Weak transcription Enhancers Active TSS	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:124935400-124941400	Weak transcription	Aorta	Aorta
2	chr4:124935600-124939800	Weak transcription	Esophagus	oesophagus
3	chr4:124937000-124940000	Enhancers	Stomach Mucosa	stomach
4	chr4:124938400-124939800	Weak transcription	Fetal Intestine Small	intestine
5	chr4:124938400-124940200	Enhancers	NHDF-Ad	bronchial
6	chr4:124938600-124939600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:124938600-124939800	Weak transcription	Hela-S3	cervix
8	chr4:124938800-124939600	Weak transcription	HSMMtube	muscle
9	chr4:124938800-124939800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:124938800-124939800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:124938800-124939800	Weak transcription	Fetal Intestine Large	intestine
12	chr4:124938800-124939800	Weak transcription	Fetal Lung	lung
13	chr4:124938800-124939800	Weak transcription	Fetal Muscle Leg	muscle
14	chr4:124938800-124939800	Weak transcription	Psoas Muscle	Psoas
15	chr4:124938800-124939800	Weak transcription	NHLF	lung
16	chr4:124939000-124939400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:124939000-124939400	Weak transcription	Fetal Heart	heart

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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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