| Tag | Content |
|---|
EnhancerAtlas ID | HS101-08961 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:112188450-112189550 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr11:112188826-112188838 | AGGTAAACAGAA | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_37173 | chr11:112185977-112190482 | HSMMtube |
|
| | 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 |
| GH11I112316 | chr11 | 112187563 | 112190095 |
|
Enhancer Sequence | CAAGGTGCCT AAACCATCAT TCTTTGATTC ATTAACTTAG TATGTCTTGT TTCTCTATCA 60
TGTAATGTAA GGAAATTAAC TCCATGTTGC CTCCTTTCTC TTCCCCCCAA TATTGGTCAG 120
CGCTAACTTT ACTTTTATGT TGTCAAAGTG TAGAACATTT ACATTTCATA TTGTACCCAA 180
AACTAGACCC TTTCTTGCTT TGTTTATATG TAAGTTGATG CTGAAAATTG AAAATCAATA 240
CATGGCTTTA ACAATAGTGT GATTTTGTAA AGATTATTTG CTGCAGAACC AGAAGAGTGT 300
TTGTCTTTAT GGAGGAGATG TAATCCTATG TCCAGATGTA ATCTTTGCTC TTCAAAAGAG 360
GTTGTTCCAA GCATCAAGGT AAACAGAATC TTGCTGTATG CTAACAATTC TTCAATATAA 420
TAACTCATTT TCAATCTGGA ACACGAGTCT TATTCTGGAA TTTATAATTG CGTGTGTCTG 480
TTTTCTGGTT GACATGCCTT CACCATGTTA CTAAGAATTT CCAACTTCTT AATCATTCTA 540
TTTGGAAAGT GGCCAATTTG GAACAGACTT TCTAGCTGTG TCATCCTGAA CTTTTCTGAT 600
GCACTCCTTA GTTCTACCAT TTGCTAGGTC CCATATCTTT CTTTCTTAGG TTTGAGGGAC 660
TGAATAAATA AATGGATAAT AGCCAAACCA TATTAAAAAA CAAAACACTG ACTCACAGGC 720
TGCAGCAACC ATCCCAGGAA ACCAAAACAT TATCTACAGT AACCAGCCCA AGAAGCCTGC 780
TTATTATCTA TAAGTCAGAT GGATAGTAAG TCAGACCACT GTCTCCAGCA CCCAGCCCAA 840
GAGGCCTAAC AATAACCTCA GAAACAATGG GCCTCCAACA GCCAGGACTT GATTAATATC 900
TGACAGCATC CCTAATTTTT GTCTCTGCTT CCAATTTGGG ACCAACCAGA GAGAGCTGTA 960
TATGCACCTG TAATCAATCC TATGGGATGC CGAGCTTCTA GTTAGTCCAC CTGCAACCTC 1020
CCCATGCCAA CAGCCTCCAG TCAGGGCATA CCTGAAACCT TTCCTTTTTT CCACTATACA 1080
GCTTTCCCAT TTTTCTGCTT 1100
|
