Variant report

Variant	rs10010022
Chromosome Location	chr4:160352519-160352520
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160347600-160356800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:160349000-160356600	Weak transcription	HepG2	liver
3	chr4:160349200-160355800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:160350600-160367800	Weak transcription	HSMM	muscle
5	chr4:160350800-160354600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:160350800-160355400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:160351000-160356000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr4:160351200-160354600	Weak transcription	NHEK	skin
9	chr4:160351200-160355600	Weak transcription	HUVEC	blood vessel
10	chr4:160352200-160353400	Weak transcription	Foreskin Melanocyte 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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