Variant report

Variant	rs139435052
Chromosome Location	chr19:44519345-44519346
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	nsv469650	chr19:44405994-44555426	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv819782	chr19:44517906-44519375	Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:44509200-44520600	ZNF genes & repeats	Liver	Liver
2	chr19:44515400-44529000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr19:44516400-44519800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr19:44516800-44519600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr19:44516800-44519600	Weak transcription	Fetal Kidney	kidney
6	chr19:44517000-44528600	Weak transcription	Dnd41	blood
7	chr19:44517200-44520000	Weak transcription	Left Ventricle	heart
8	chr19:44517200-44520200	Weak transcription	HSMM	muscle
9	chr19:44517200-44521600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr19:44517400-44520800	Weak transcription	Primary T cells effector/memory enriched 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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