| Tag | Content |
|---|
EnhancerAtlas ID | HS060-06723 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:94886180-94887100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:94886462-94886483 | GTAATGAAAGTGAAACTGCGT | - | 7 | | IRF8 | MA0652.1 | chr11:94886465-94886479 | ATGAAAGTGAAACT | + | 6.06 | | IRF9 | MA0653.1 | chr11:94886464-94886479 | AATGAAAGTGAAACT | + | 6.38 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_36837 | chr11:94885982-94887101 | HMEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCCATGATAC AGGCATGGGA CTGAAAGCCC CATCAGTCCC TTGGAGAGAT CATCAGAGAG 60
TGAGTAGAGA CATAGCAGGG CGAAGCCCTG AGCCCCGGTT CCCCCAGCAT GTACCTGCAG 120
TCTGTTTCCT CTTCTCAACT ACAATTCCCA TGGTCTTGTC TTGTTCACAG AACCTGCTCA 180
AGGAGCATCT ATTAAATGAA GGAACCCAAC TTTCATCACA TGTAAAATAA ACATCATTAT 240
AATCCTACCT CATAAGGTTG TTGTCAGAAA AAGTTAAACG TCGTAATGAA AGTGAAACTG 300
CGTTATGATT GGTAGATGCC TGCTATATTT TAAAATGTAG GCTTCATTAT CTCATTCTGT 360
ACAGCTTGTA TTACTTGATT GTATCTTCAC AGTTTCTGAT GCATGCAAGG CAGACACTCT 420
CGTTCTCACT TTATTGACGA GGAAAGTAGG ATTGGTGAGA CAAAATAAGT CCCTGAAGCT 480
GCATATCTAA TGGTAACACC AGTGGCTGAC CTGTTTGAGC ACATCTGCGG CAGGCACTGT 540
GTTAATGATT TTGCATGTGT TATCTGGCAA CAACACAGCG AGGTGGGGGT TATTATCTTC 600
ACTTGCACAT GAGGAAACTG AAGCATAGAG AGGGTGGTTA ACTTAGCCAA GGTCCCATAG 660
TGAGTGGTTG GAAGAGTCTG GGCCATGAAG CAGACCTGCC CATCCTGATT CAATGTTCTT 720
TTTGCAGCCT GATAGCTCCT CTTCTTCATC CCCCTACTAG ACTCCTGCCA GGGCCAAGCC 780
TCACCACTCC TTCCCTTGAC ATTGGCAACA TTCCTCTCTC CTTAACGTTT CTCTCCTACC 840
AAGCCTGCTT GCTGCAGGAT ACAAGAGTTC AGTCACTCCT TGGGAACAAC CTGCAGGTCA 900
AAACATTTTG GCTTATTGCT 920
|
