Variant report

Variant	rs574727171
Chromosome Location	chr7:25221160-25221161
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000234406	TF binding region
C7orf31	TF binding region
ENSG00000234406	Chromatin interaction
ENSG00000172115	Chromatin interaction

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv606424	chr7:24982529-25466521	Genic enhancers Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	nsv887845	chr7:25220519-25276424	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:25220400-25222000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:25220600-25221400	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr7:25220600-25221400	Enhancers	Spleen	Spleen
4	chr7:25220600-25233200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:25220600-25233800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr7:25220800-25221200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr7:25220800-25221200	Enhancers	Fetal Kidney	kidney
8	chr7:25220800-25221200	Enhancers	K562	blood
9	chr7:25220800-25222000	Weak transcription	Brain Anterior Caudate	brain
10	chr7:25221000-25225600	Weak transcription	Brain Cingulate Gyrus	brain

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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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