Variant report

Variant	rs531133968
Chromosome Location	chr12:10224451-10224452
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3364971	chr12:10224370-10224647	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10219000-10236800	Weak transcription	Left Ventricle	heart
2	chr12:10220800-10234800	Weak transcription	Placenta	Placenta
3	chr12:10221400-10235000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr12:10222000-10225400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:10222000-10234800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr12:10222400-10227600	Weak transcription	Adipose Nuclei	Adipose
7	chr12:10222800-10225200	Weak transcription	HUVEC	blood vessel
8	chr12:10222800-10248400	Weak transcription	Psoas Muscle	Psoas
9	chr12:10223000-10232600	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr12:10223400-10226000	Weak transcription	Right Ventricle	heart
11	chr12:10223600-10232600	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr12:10224000-10234800	Weak transcription	Lung	lung

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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