Variant report

Variant	rs76923203
Chromosome Location	chr2:173276196-173276197
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533927	chr2:173161637-173796894	Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
2	nsv875414	chr2:173267081-173307756	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3357124	chr2:173275963-173276528	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:173270000-173277600	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:173270400-173277600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:173272800-173276400	Enhancers	HUVEC	blood vessel
4	chr2:173273400-173277600	Weak transcription	Adipose Nuclei	Adipose
5	chr2:173273400-173278000	Weak transcription	Left Ventricle	heart
6	chr2:173273400-173280600	Weak transcription	Fetal Intestine Small	intestine
7	chr2:173273600-173277400	Weak transcription	Thymus	Thymus
8	chr2:173274000-173281000	Weak transcription	Fetal Kidney	kidney
9	chr2:173274600-173277800	Weak transcription	Pancreas	Pancrea
10	chr2:173274600-173290200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:173274800-173280000	Weak transcription	Stomach Mucosa	stomach
12	chr2:173275600-173281000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	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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