Variant report

Variant	rs7938449
Chromosome Location	chr11:102648898-102648899
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102644800-102651000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:102647400-102650200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:102647400-102651000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr11:102647600-102650200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:102647600-102651000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr11:102647600-102651200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:102647800-102650800	Weak transcription	NHEK	skin
8	chr11:102647800-102651000	Weak transcription	HMEC	breast
9	chr11:102647800-102651600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

Quick Search:

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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