| Tag | Content |
|---|
EnhancerAtlas ID | HS108-16394 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:21022540-21023350 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr17:21022785-21022796 | TTCTTATCTCT | + | 6.32 | | Gata1 | MA0035.3 | chr17:21022785-21022796 | TTCTTATCTCT | + | 6.32 | | HES2 | MA0616.2 | chr17:21022615-21022625 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr17:21022615-21022625 | GGCACGTGCC | - | 6.02 | | RUNX3 | MA0684.1 | chr17:21022897-21022907 | AAACCGCAAA | + | 6.02 | | ZNF740 | MA0753.2 | chr17:21023282-21023295 | GGGGGGGGGGCGG | - | 6.64 |
|
| | 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 |
| GH17I021119 | chr17 | 21022714 | 21023319 |
|
Enhancer Sequence | TCGACTCACT GCAACCTCTG CCTCCCTGCT TGGAACGATT CTCCTACCTT AGTTTCCCGA 60
GTTGCTGGGA CCACAGGCAC GTGCCACCAC GCCTGGCTAA TTTTCGTAGT TTTAGTAGAG 120
ACGGGGTTTC ACCATGTTGC TCAGGCTGGT CTTGAACTCC TGGGCTCAAG CGATCCGCCT 180
GTCGCCTGCC TCGGCTTCCC AAAGTGTTGG GATTACAGGC TGAGCCACCA CGCCCGGTCT 240
GGGCTTTCTT ATCTCTGAGA GTCACAATTT CTGTGAGGCA GCCACCAACA CTAGCTTTTA 300
AGTTTCAGGG AGTTGCAGTG AAACTTTCTT TCCTGCCAGG AAGCTGACAT TTTCCAGAAA 360
CCGCAAATAA CAGAACATTT TGTCTCTGTG TCAGCTTCAT GCACCCTAGT CTTAAACCAA 420
CAATGTTCTT AAAAATGCAT TGTTTTTCTT CTCTTATCGC TTCTCGGTTG TTCTAATAAT 480
TTGATAGCTT CAGTACACCA TTAATGTTCA CCTTACACCT CCCGGAGGAG GAGATGGCGT 540
GATACTCGCA AACACGGGAC TACAAACTAT TGATTCCATT CCGCGTGCTT CAGGAAGGTG 600
GCGCTGTTTC CGTGCAGCTC ATCAGGTACC TCAGAAAAAG AAATTTGGTG GAGACGTTTC 660
CGCAGCCTCC AAGCAGCATC ATTCAAAGGA CAGGTCAGCA GGAAACAGAT TTTATTTTAA 720
AATTCCCAGC AGCGGGAGGG ACGGGGGGGG GGCGGGGGAG GGACTTGTTA GAGTTCCTGT 780
CGCTAAAGGA AATTCTTCCT AGAGCTATAC 810
|
