Variant report

Variant	rs2018244
Chromosome Location	chr1:172431892-172431893
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172422600-172435400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:172423400-172434600	Weak transcription	HSMMtube	muscle
3	chr1:172423600-172432000	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr1:172425800-172435400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:172426000-172436000	Weak transcription	Fetal Intestine Large	intestine
6	chr1:172426400-172434600	Weak transcription	Fetal Muscle Leg	muscle
7	chr1:172430200-172435400	Weak transcription	HepG2	liver
8	chr1:172430400-172435200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:172430400-172435400	Weak transcription	HMEC	breast
10	chr1:172430600-172435200	Weak transcription	NHEK	skin
11	chr1:172430600-172436000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:172431200-172435000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr1:172431200-172435400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:172431600-172435400	Weak transcription	A549	lung

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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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