| Tag | Content |
|---|
EnhancerAtlas ID | HS082-07078 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr11:110396240-110397390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:110397348-110397369 | ACTTGTTTTCACTTTTGTTTT | + | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I110525 | chr11 | 110395861 | 110397685 |
|
Enhancer Sequence | TCTGTCTCAG GAACAAATAA ATAAAAATGA AGTGCTGCTC TAGGTGAAGT AGGGTCAGCG 60
CTGTAGAGGT GAGGGCCTGA AGAGTGGAGG AAGAACCAGG GATCATTGTT GTGAATGGGG 120
AAGGAAGTCT TAGGGGCTGA ATCCCGGCAG CGGCCTCTCT CCCAGGAGCA GAGGGCCTGC 180
ATCTGTCCTG GAGCCCTTCC CTTGTCAAGA GCATGAAGAA ACACAGCGTC AATGTCTGGG 240
GGCCTACTTT CAATTTCCAG TGAAATTAGG ACAAAGTTCC TTTAGGCTTG ATATCATTTC 300
TTTTAAGCCT GAGGCTTGAA GTTGGAGCAT TCTAAATGCG TAGGAAACTG TTATGAATAG 360
CAACGAAAGG CAGAGTAACT AACACCTGAC ATAGCTATTT TCCTTGCCAT TGCCTCTGCA 420
TGATTTAATA TTTAATATGC TTGTGGTCAA ACCAAGTCTG AACAGAGCAA GCCTGAAGCA 480
CTTCTAGCAA CACAGCCAGG TGGCCAGGAG CCCAAAGTGA TATAACTGCG GTTTACTCAC 540
AGGCTTTCAG AGTAACCTTT AGGGCTGGTT GAACTCTCAG ACACCACTTA GCATTTCCTA 600
ACAATGATCT GTAATGCATT TGGGAAGCCT GTCTGAATCA CCCAATTAGA TCATGCTTTC 660
TAATGGGCCT CAATGCAGAG ATGCTGCCAA CAGCTTTGGC AGAGGCACAC AGAGCCCCCT 720
TCTTTACAAG GCATCTTCCA CTCTCTGTTT TTGATTTCAC TCTCACAACA TCACTGTGTT 780
GTATCCCAGG TGGATGCTAC TATTCCCACT TGCAGATGAG GAATCTGAGG CTCGCTGAAG 840
TTAAGTGACT TGTGCAACGT CACAAAACCA TTGAATGGTT GCTGTGAGCT TTCAACTCAG 900
GAAAGGGCTT GACTTTCCCC TCAGGTGCCC TTTCCACTGT GGTGTTGGGA GTTAAGTAGA 960
GGCAGACAGG TCATTACTGG ATGGGAAATG CCCTGTGAGC CATTGCCAGC TATGTTTCTG 1020
TGTTGGCCTC CAGCAGTGCT TGTCTGATCA GAGACAGGGG TTATGTGGTT AGAACTGGGA 1080
AGAAGGCACC CACTAAAATT CTCTAGTGAC TTGTTTTCAC TTTTGTTTTA GGTTTAGGGG 1140
TATAAGTACA 1150
|
