Variant report

Variant	rs7573994
Chromosome Location	chr2:10961581-10961582
allele	C/T
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	esv3444752	chr2:10961415-10961838	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10953600-10968200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:10955400-10968600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:10960800-10961600	Enhancers	Fetal Muscle Leg	muscle
4	chr2:10960800-10961800	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr2:10960800-10962000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr2:10961000-10961600	Flanking Active TSS	Stomach Mucosa	stomach
7	chr2:10961200-10972400	Weak transcription	Right Atrium	heart
8	chr2:10961400-10961600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:10961400-10968600	Weak transcription	Gastric	stomach

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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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