Variant report

Variant	rs7542538
Chromosome Location	chr1:165426193-165426194
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165422200-165433200	Weak transcription	Right Ventricle	heart
2	chr1:165424000-165434800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:165425200-165426200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:165425400-165426200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:165425800-165426400	Enhancers	Brain Germinal Matrix	brain
6	chr1:165426000-165426200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr1:165426000-165426200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr1:165426000-165426400	Enhancers	Placenta	Placenta

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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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