Variant report

Variant	rs532313997
Chromosome Location	chr11:75867369-75867370
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049039	chr11:75827548-76023665	Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv1051472	chr11:75851880-75922608	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1037940	chr11:75855316-75909619	Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv897926	chr11:75862571-76004202	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv897927	chr11:75866999-75908083	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:75833400-75872800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:75862800-75869200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:75864000-75868000	Weak transcription	Fetal Heart	heart
4	chr11:75864400-75868000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr11:75864400-75871800	Weak transcription	Right Atrium	heart
6	chr11:75864600-75872600	Weak transcription	Fetal Intestine Large	intestine
7	chr11:75864800-75868000	Weak transcription	Fetal Thymus	thymus
8	chr11:75865000-75868000	Enhancers	HepG2	liver
9	chr11:75865000-75868200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr11:75865000-75868800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr11:75865000-75869000	Weak transcription	Pancreas	Pancrea
12	chr11:75865000-75869600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr11:75865000-75876000	Weak transcription	Spleen	Spleen
14	chr11:75865200-75868000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr11:75865800-75870400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr11:75866400-75867400	Enhancers	Adipose Nuclei	Adipose
17	chr11:75866600-75868000	Enhancers	Fetal Stomach	stomach
18	chr11:75867200-75868200	Weak transcription	Fetal Lung	lung
19	chr11:75867200-75868200	Enhancers	Fetal Muscle Leg	muscle

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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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