Variant report

Variant	rs10430649
Chromosome Location	chr10:93059828-93059829
allele	A/G
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	chr10:93058600-93060200	Enhancers	H1 Cell Line	embryonic stem cell
2	chr10:93058800-93060000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:93059000-93062600	Weak transcription	Fetal Intestine Large	intestine
4	chr10:93059400-93060200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr10:93059600-93060000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr10:93059600-93060200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr10:93059600-93060200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:93059800-93060000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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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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