| Tag | Content |
|---|
EnhancerAtlas ID | HS182-04044 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:68933770-68934570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr11:68934161-68934172 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr11:68934161-68934172 | GATGAGTCACT | - | 6.32 | | MEF2A | MA0052.3 | chr11:68934175-68934187 | TCTAAAAATAAA | + | 6.07 | | MEF2C | MA0497.1 | chr11:68934173-68934188 | GTTCTAAAAATAAAA | + | 6.47 | | Myod1 | MA0499.1 | chr11:68934071-68934084 | AGGGGCAGCTGCA | - | 6.22 | | NFKB1 | MA0105.4 | chr11:68934239-68934252 | AGGGGGATCCCCA | + | 6 | | ZEB1 | MA0103.3 | chr11:68934299-68934310 | CGCACCTGCCC | + | 6.02 |
|
| | 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 |
| GH11I069166 | chr11 | 68933484 | 68934765 |
|
Enhancer Sequence | GGTATGTGAG AAAGGATGCA GCCAGGCAGG TGCAACACAC CTGGGCAGCC CGTGGCTGTG 60
GCCATGGCCA TGGCCGGTCT GCATGTGGAG GAAAAGATGG TGAGGTGAGA CCCTGAGAAA 120
CAACTCTCTG ATCTCATCCA CCTCTCCCCT CCTAGGCGGG ACGAGATGGA TGCACCCTCT 180
GCCGCAGCCA CCTCTTCTGC AGGTGCCCGG CTTCTCCAGA CTTGCTATTT TGGAGGGGCA 240
GGTCAGTGGG AACGACCGAC TGCCTTGCAT CTCAGCCACT CATGGGCCTC AGAGTGTGGG 300
CAGGGGCAGC TGCAGCCCTC TCGAGCCTCT CACTCCCTGC TTGGCCTCTG TAAGCCTGTC 360
CGGGAGCAGC TCACAGAGCC CCTGTGGTGG AGATGAGTCA CTTGTTCTAA AAATAAAAGA 420
AGTGAAGTCA TGAAATAGTG TATTTCCTTT TTAAGCCCGA TGTGCCTGCA GGGGGATCCC 480
CAGCAGTGTG CTGGCGGCAG GGACCCTGAC AAGGTCTGGA GCCTCAGAGC GCACCTGCCC 540
CCACTTACAA GCCCCGGCCT CGGGGATTGG GTGGAGTGTC CCCTGCCTCC AACGGCTCCC 600
AGATGAGTGA GTAAAAGATG GCACGTAGAC CAGGAGCGGG GGCTGACACC TGCAATCCCA 660
GCACTTTGGG AGGCTGAGGT GGGAGGATCA CTTGAGGCCA GGAGTTTGGG GCCACCCTGG 720
GCAACATGGT GAAACCCTGT CTCTACTAAG AATACAAAAA AATTAACCAG CGTGGTGGCA 780
CATGCCTGTG GTCCCAGCTA 800
|
