Tag | Content |
---|
EnhancerAtlas ID | HS108-17848 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:74650440-74651190 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr17:74650552-74650565 | AGCTAATTAATTA | - | 6.09 | Lhx3 | MA0135.1 | chr17:74650555-74650568 | TAATTAATTAGTC | + | 6.46 | MSC | MA0665.1 | chr17:74651128-74651138 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr17:74651128-74651138 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr17:74651128-74651138 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr17:74651128-74651138 | AACAGCTGTT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:74651056-74651071 | TGACCTCGTGACCTG | - | 6.32 | Zfx | MA0146.2 | chr17:74651071-74651085 | CCCGCCTCGGCCTC | + | 6.01 | mix-a | MA0621.1 | chr17:74650556-74650567 | AATTAATTAGT | + | 6.62 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGGCAACA GAGCGAGACT CTGTCTCAAA AAAAAAAAAA AAAGAGTAGG GAAATGTGTT 60 TTGTTATGCA AAAATCAATT GTATTTCTGC TCTCTGAAAG TAGGAATTGA CAAGCTAATT 120 AATTAGTCCT TTTTGTTACC AAGCACCTCT GCTGCTCAAA TTCTTCCTGT ATCTTGAGTC 180 ACTGCTTGCC TCTGAAGAAC CCACAAATCT AGATAGCATC CAGACACTGT CATCTTTGAT 240 TTTGAAGACA CAGGGCAAGT GATGTGGAGA AGCCTTTCTC TGGGGCCTGA ACAGTGTGAG 300 TCAGAAATGC CAGTGTTGAA GGCTCTAGAT TGTGCTGCAT TATCACTGTT CACCAGATCC 360 AAGCAACATA AATGCCTGTT GTTCTTTTTT TATTTTTTAT TTTTTTGAGA CGGAGTCTTG 420 CTCTTTCATC CAGGCTGGAG TGCAGTGGCG CGATCTCGGC TCACTGTAAG CTCCGCCTCT 480 CGGGTTCACG CCATCCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA GGCATCCGCC 540 ACCACACCCA GCTAATTTTT TGTATTTTTA GTAGAGACGG GGTTTCACCG TGTTAGCCAG 600 GATGGTCTCG ATCTCCTGAC CTCGTGACCT GCCCGCCTCG GCCTCCCAAA GTGCTGGGAT 660 TACAGGCGTG AGCCGCCGCG CCCGGCCCAA CAGCTGTTCT TTCAGGCAGC TGAAAAAATC 720 AGATAGGCCC TAATAGACTT GTTTGACAAC 750
|