Variant report

Variant	rs112312550
Chromosome Location	chr11:57030202-57030203
allele	A/G
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	nsv915640	chr11:56814841-57139786	Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	esv3371973	chr11:57030181-57030602	Enhancers Weak transcription Flanking Active TSS	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	chr11:57029000-57030600	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr11:57029200-57030400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr11:57029200-57030800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr11:57029400-57031600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr11:57029400-57031600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr11:57029800-57030800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr11:57030200-57030400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr11:57030200-57030600	Enhancers	H9 Cell Line	embryonic stem cell

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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