Variant report

Variant	rs17130853
Chromosome Location	chr1:69573265-69573266
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:69569800-69575000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:69570000-69575000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr1:69570000-69575000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr1:69570200-69574800	Weak transcription	NHEK	skin
5	chr1:69570200-69575000	Weak transcription	HMEC	breast
6	chr1:69571400-69575800	Weak transcription	Fetal Brain Male	brain
7	chr1:69572600-69576400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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