Variant report

Variant	rs7831724
Chromosome Location	chr8:118765215-118765216
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831438	chr8:118679896-118823600	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv831439	chr8:118747352-118899118	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv933516	chr8:118764605-119009093	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118744200-118769200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:118751400-118805400	Weak transcription	NHLF	lung
3	chr8:118760400-118767800	Weak transcription	Fetal Lung	lung
4	chr8:118764200-118765400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:118764200-118765400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr8:118764200-118765400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:118764200-118765400	Enhancers	Fetal Muscle Leg	muscle
8	chr8:118764400-118765400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr8:118764400-118765400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr8:118764600-118765400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr8:118764600-118765400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr8:118764600-118765400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:118764600-118765400	Enhancers	Fetal Muscle Trunk	muscle
14	chr8:118765000-118765400	Enhancers	Osteobl	bone
15	chr8:118765000-118780200	Weak transcription	Aorta	Aorta
16	chr8:118765200-118765400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:118765200-118775800	Weak transcription	HSMM	muscle

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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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