| Tag | Content |
|---|
EnhancerAtlas ID | HS108-04695 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr10:121880-122790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr10:121912-121924 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr10:121912-121924 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr10:121910-121925 | CAACTAAAAATAGAA | + | 6.56 | | ZNF263 | MA0528.1 | chr10:122187-122208 | GCCTCTCCACGTTCCTCCTCC | - | 6.13 | | ZNF263 | MA0528.1 | chr10:122190-122211 | TCTCCACGTTCCTCCTCCTCT | - | 6.43 |
|
| | 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 |
| GH10I000076 | chr10 | 121942 | 122940 |
|
Enhancer Sequence | CCAGCCTGGC CAACATAGTG AAACCCGTCT CAACTAAAAA TAGAAAAAAT TAGCTGGGCG 60
TGATGGCGGG TCCCTGTAAT TCCAGCTACT CGGGAGGCTG AGGCGGGAGA ATCGCTTGAA 120
CCCGGGAGGC GGAGGTTGCA GTGAGCCGAG ATCGTGCCAT TGCACTCCAG CCTGGGAAAC 180
CGAAGCGAAA CTCCGTCTCA AAAAAAAAAA AAAAAAAAAA CACGAGCACC GATCAGGGGG 240
CGTCTGTTTC CTCGGCCTCA GGCTGTGGCC CCTGCCAGTC CCCAGCCTCC CGACCGACGG 300
CACAACGGCC TCTCCACGTT CCTCCTCCTC TCCGGGGACC AGGGTCTCTC CCCAGAAACA 360
AAATCGCATC GGTAACCGGC ATCTTGTCCT GTGCTGGGGG TGAGCCGCCC AAGCCTCCAT 420
GAAGGGACGC TCGTACAAAG TGAAGTCTGG GTACAAATGG CCAGACGGGA AACGCGCCGC 480
GCTCGCTCCG CTGCACTCAC AGCGGCGGCA GGAAGCCTTT TTCTCACTTT CTCCCCGGCG 540
GCCCCAGGTG TCCCGGAGCG TCTCCCTGTC CTCACAGCGG ACGTGGCCCC AGGTGTCCCG 600
AAGCCCCGGC CCCTCCGGGG TGGGTGCTGA GAGGAAGCTC CGTCCTCACA GTGGACGCCC 660
CACGCCGCCG CCGTGCGGTT CGGACACGGT TCGCGCGCGC GCCGCCCTCC GGGTTTGGCA 720
GGGCCGGGCG CCCCCTCGCG GCAGCTCTGG AGAATCTCTG AAAATCAGCG TCTGGATTTT 780
TCCAGGCCGA GATTTTGGAA ATTTCAACTG AACTGGAGAC CACCATCCCG TGCCTTGACG 840
GGAACGCATT GAGATAGTAA TCAAAGAAGA TGGCCAGTTC ACGCCTGTAA TCCCAGCACT 900
TTGAGAGTCT 910
|
