Variant report

Variant	rs566808234
Chromosome Location	chr2:234493123-234493124
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
UGT1A12P	TF binding region
ENSG00000085982	Chromatin interaction
ENSG00000234143	Chromatin interaction
ENSG00000072080	Chromatin interaction
ENSG00000242515	Chromatin interaction
ENSG00000123485	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv876013	chr2:234338227-234579915	Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv428072	chr2:234393609-234624769	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	esv11149	chr2:234492605-234501401	Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
5	esv1801264	chr2:234492805-234500262	Enhancers Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
6	esv1802734	chr2:234492805-234500262	Enhancers Bivalent Enhancer Active TSS Weak transcription	TF binding region Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
7	nsv522661	chr2:234493048-234496945	Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234486400-234494800	Weak transcription	A549	lung
2	chr2:234492200-234493200	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr2:234492200-234493200	Active TSS	K562	blood
4	chr2:234492200-234493400	Active TSS	iPS-15b Cell Line	embryonic stem cell
5	chr2:234492400-234493200	Enhancers	Liver	Liver
6	chr2:234493000-234493200	Enhancers	HepG2	liver
7	chr2:234493000-234494200	Enhancers	Spleen	Spleen

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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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