Variant report

Variant	rs112696234
Chromosome Location	chr6:29414689-29414690
allele	A/C
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	nsv830624	chr6:29274525-29445565	Enhancers Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	esv15709	chr6:29413527-29415648	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:29413400-29415600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr6:29414200-29415200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr6:29414200-29415400	Enhancers	H9 Cell Line	embryonic stem cell
4	chr6:29414200-29416000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr6:29414200-29418000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:29414400-29415400	Enhancers	H1 Cell Line	embryonic stem cell
7	chr6:29414600-29415000	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:29414600-29415400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr6:29414600-29415600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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