Variant report

Variant	rs73598555
Chromosome Location	chr10:22819848-22819849
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22816800-22823000	Weak transcription	Right Atrium	heart
2	chr10:22818400-22823400	Weak transcription	HepG2	liver
3	chr10:22819000-22830000	Weak transcription	HUVEC	blood vessel
4	chr10:22819200-22820000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr10:22819400-22822200	Weak transcription	Primary T cells from cord blood	blood
6	chr10:22819400-22827800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr10:22819600-22825000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr10:22819600-22825200	Weak transcription	Fetal Muscle Leg	muscle
9	chr10:22819800-22820400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
10	chr10:22819800-22822200	Weak transcription	Brain Substantia Nigra	brain
11	chr10:22819800-22822800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr10:22819800-22823200	Weak transcription	Fetal Thymus	thymus
13	chr10:22819800-22824000	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr10:22819800-22825200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr10:22819800-22825400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:22819800-22825400	Weak transcription	Spleen	Spleen

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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