Variant report

Variant	rs12456713
Chromosome Location	chr18:44118635-44118636
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44093200-44120400	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr18:44094000-44126000	Weak transcription	Adipose Nuclei	Adipose
3	chr18:44108600-44119400	Strong transcription	Monocytes-CD14+_RO01746	blood
4	chr18:44109200-44126200	Weak transcription	Right Ventricle	heart
5	chr18:44111200-44126000	Weak transcription	Brain Angular Gyrus	brain
6	chr18:44118400-44118800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr18:44118400-44126000	Weak transcription	Spleen	Spleen
8	chr18:44118600-44121400	Weak transcription	Primary monocytes fromperipheralblood	blood

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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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