Variant report

Variant	rs201346561
Chromosome Location	chr11:120861498-120861499
allele	-/AATA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3376837	chr11:120860642-120865340	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:120857200-120862600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:120858000-120868800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:120860400-120861600	Weak transcription	Fetal Lung	lung
4	chr11:120860400-120864200	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr11:120860400-120864400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:120860400-120868000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr11:120860600-120862600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr11:120860600-120863600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:120860800-120864000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr11:120861000-120864200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:120861400-120862600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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