Variant report

Variant	rs373410924
Chromosome Location	chr1:84311344-84311345
allele	-/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523508	chr1:84310193-84314754	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84281400-84316600	Weak transcription	Pancreas	Pancrea
2	chr1:84297600-84313000	Weak transcription	Aorta	Aorta
3	chr1:84310400-84311400	Strong transcription	Primary T cells from cord blood	blood
4	chr1:84310800-84312200	Enhancers	Liver	Liver
5	chr1:84310800-84312200	Enhancers	Fetal Intestine Small	intestine
6	chr1:84310800-84324400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr1:84311000-84311400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr1:84311000-84311800	Enhancers	Duodenum Mucosa	Duodenum
9	chr1:84311000-84312200	Enhancers	Adipose Nuclei	Adipose
10	chr1:84311000-84314200	Enhancers	Fetal Intestine Large	intestine
11	chr1:84311200-84311400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr1:84311200-84312200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:84311200-84315200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr1:84311200-84315600	Weak transcription	Small Intestine	intestine
15	chr1:84311200-84321200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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