| Tag | Content |
|---|
EnhancerAtlas ID | HS080-05821 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr11:22362060-22363070 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr11:22362222-22362235 | TAATTAATTATTC | + | 7.12 | | Lhx3 | MA0135.1 | chr11:22362219-22362232 | GAATAATTAATTA | - | 7.12 | | POU4F2 | MA0683.1 | chr11:22362217-22362233 | GTGAATAATTAATTAT | + | 7.18 | | POU4F2 | MA0683.1 | chr11:22362221-22362237 | ATAATTAATTATTCAT | - | 7.47 | | RREB1 | MA0073.1 | chr11:22362480-22362500 | GCTCAGGGGGTGGATTGGGG | - | 6.33 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33521 | chr11:22355269-22373154 | H2171 | | SE_67091 | chr11:22355269-22373154 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I022340 | chr11 | 22362163 | 22362363 | | GH11I022341 | chr11 | 22362581 | 22362730 |
|
Enhancer Sequence | AAATATTTAA GTGAGATCTT CCCCTTTGAT GTGGAATATC TTACAAAAGT TGATTTGGGG 60
GAGCCTTTGT ATATCTGGGA GTCGCATTTT GCGTCTTGGG AAATGGACCC TTGACATTTT 120
TCGGTGTTTG TAAGAGAGAT AGTAATGACG CAAGATTGTG AATAATTAAT TATTCATGTT 180
CTGGCAGTAG GAAGCTTAGG TGTCGGCCAT ATGCTGTGGA GCCCTTTGTC TCCAACTCGA 240
GTAATAAGAA AAAAAAAATA GTAAGAAGTG TAACAGGGGA GTAAGCATTG AACTAGAGCC 300
CTGGGGCGGG ATGAAGGGGA AGGAGAGTGC ATGACACTCT CAGCGAGAGC TCTCAGGCCT 360
TCTCCTCACG CACAGGCACT AGCCTAGAGA GGCCTTAGTC CAGGGGGTGC TCCAGGCTCA 420
GCTCAGGGGG TGGATTGGGG AGCGGAATAC CAGCATCGTC AACCTGGAAA GCTTCAACTT 480
GCTAGAAACG GAAAAGGCAG CGCGGGTGGG AAAGGCTCTC TAGTTGGGCC CGCCTGCAGC 540
GGAGCAGCTC TCTGGTGCTG TGTTGCAGGA GGACACCGCG GTAGTCAGGG TAAAGCCCTG 600
CTGGGCGCGT GTAGGAGTGG GAGGCGCCTA CTCAGGTGCA GAGGAGGCGC TGGTAACCCC 660
TGCCCTCACA AAATGCAGAC CCTGCAGATC CTGCAAGAAA GTTAGGCCCA AGCGGCCTGT 720
GTATCTCAAT CAGAGCGCCC AGGGGTGGAT CCCGAGATGG GGACTCGCTA CCTTAGGCCT 780
AAAGGTGTTA AAGTTGAAGA GACGCCGCCG CCGCGGCCAA GGGCACCTGC AGAATGTGAG 840
AGAGCCTGGG AGGTCTTGCA GCTTGGTGTC ACCCCACCAC CCTAATCCCC GAGGGTGGGG 900
GGAGGTCGAC GGCCCTCCTC CCAACCCCGA CGGGTCCTGA AAAATGGGAA TGGGTCAGCA 960
TCGGGGGTAC CTAAGCCGCC AAGTCCTTGA CTCGCCCCTG CTCTGCCGCG 1010
|
