Variant report

Variant	rs62239184
Chromosome Location	chr22:32066052-32066053
allele	C/T
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	chr22:32058800-32072400	Weak transcription	Fetal Heart	heart
2	chr22:32059000-32066600	Weak transcription	Hela-S3	cervix
3	chr22:32059000-32067000	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr22:32059000-32070000	Weak transcription	Primary B cells from cord blood	blood
5	chr22:32059000-32072400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr22:32059000-32072400	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr22:32061800-32066600	Weak transcription	HepG2	liver
8	chr22:32061800-32066600	Weak transcription	K562	blood
9	chr22:32061800-32066800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr22:32061800-32067000	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr22:32062000-32067000	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr22:32062200-32066800	Weak transcription	Placenta	Placenta

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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