Variant report

Variant	rs77074012
Chromosome Location	chr18:29975923-29975924
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	esv3347612	chr18:29975003-29990362	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29963600-29976200	Weak transcription	Aorta	Aorta
2	chr18:29963600-29999200	Weak transcription	Fetal Kidney	kidney
3	chr18:29964800-29985400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr18:29966600-29981400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr18:29966800-29985400	Weak transcription	Right Ventricle	heart
6	chr18:29967000-29986600	Weak transcription	Brain Angular Gyrus	brain
7	chr18:29974200-29977400	Weak transcription	Ovary	ovary
8	chr18:29975400-29976600	Weak transcription	Brain Cingulate Gyrus	brain

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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