Variant report

Variant	rs371929439
Chromosome Location	chr8:130398675-130398676
allele	C/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	nsv429942	chr8:130397818-130460011	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130394600-130399000	Enhancers	Dnd41	blood
2	chr8:130394600-130401000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:130394800-130399200	Enhancers	Fetal Thymus	thymus
4	chr8:130394800-130411800	Strong transcription	K562	blood
5	chr8:130395600-130399400	Enhancers	Thymus	Thymus
6	chr8:130397800-130401000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:130398200-130401200	Weak transcription	Monocytes-CD14+_RO01746	blood

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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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