Variant report

Variant	rs6540814
Chromosome Location	chr1:214436619-214436620
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:214433200-214437000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:214433200-214437200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:214433200-214437200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr1:214433400-214437000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:214435400-214437200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:214435400-214437400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr1:214435400-214437600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr1:214435400-214437800	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr1:214435600-214437000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr1:214435800-214444800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr1:214436200-214438000	Weak transcription	Fetal Heart	heart
12	chr1:214436400-214437000	Weak transcription	H1 Derived Mesenchymal Stem 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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