Variant report

Variant	rs371233392
Chromosome Location	chr8:91545787-91545788
allele	A/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	esv3480542	chr8:91545158-91546166	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv3480543	chr8:91545306-91546012	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91533800-91545800	Weak transcription	HSMMtube	muscle
2	chr8:91543000-91545800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr8:91543000-91546200	Weak transcription	HUVEC	blood vessel
4	chr8:91543200-91545800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:91543200-91545800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:91543200-91545800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:91544800-91546600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:91544800-91552400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:91545400-91550000	Enhancers	HSMM	muscle
10	chr8:91545600-91550000	Enhancers	NHEK	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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