Variant report

Variant	rs531842764
Chromosome Location	chr8:130628446-130628447
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	nsv612230	chr8:130624121-130661901	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv525691	chr8:130627555-130631930	Enhancers Genic enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130626400-130629400	Weak transcription	Dnd41	blood
2	chr8:130627400-130629600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:130628200-130628800	Enhancers	Lung	lung
4	chr8:130628400-130628800	Enhancers	Fetal Muscle Leg	muscle
5	chr8:130628400-130629000	Enhancers	Fetal Stomach	stomach
6	chr8:130628400-130629600	Enhancers	Fetal Lung	lung

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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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