Variant report

Variant	rs183810164
Chromosome Location	chr6:121895837-121895838
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886594	chr6:121837314-122043117	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv3432329	chr6:121895353-121897601	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121892800-121896000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr6:121895200-121896000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr6:121895400-121899800	Weak transcription	Small Intestine	intestine
4	chr6:121895400-121905400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:121895800-121896600	Weak transcription	Fetal Intestine Large	intestine
6	chr6:121895800-121898800	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr6:121895800-121902400	Weak transcription	Ovary	ovary
8	chr6:121895800-121905400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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