| Tag | Content |
|---|
EnhancerAtlas ID | HS148-11741 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr22:39784310-39785040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr22:39784326-39784344 | AGCAAGTGGGCGTGGCCT | - | 6.37 | | KLF14 | MA0740.1 | chr22:39784329-39784343 | AAGTGGGCGTGGCC | - | 8.12 | | Klf12 | MA0742.1 | chr22:39784328-39784343 | CAAGTGGGCGTGGCC | - | 6.48 | | SP1 | MA0079.4 | chr22:39784330-39784345 | AGTGGGCGTGGCCTG | - | 7.61 | | SP3 | MA0746.2 | chr22:39784330-39784343 | AGTGGGCGTGGCC | - | 6.92 | | SP4 | MA0685.1 | chr22:39784328-39784345 | CAAGTGGGCGTGGCCTG | - | 7.76 | | SP8 | MA0747.1 | chr22:39784330-39784342 | AGTGGGCGTGGC | - | 7.22 |
|
| | 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 |
| GH22I039388 | chr22 | 39784006 | 39785732 |
|
Enhancer Sequence | CAGGCCGGGT GGGAGGAGCA AGTGGGCGTG GCCTGGGCAT GGCCCGTCGG TCAAGGTACT 60
GGCCCTGCCC ACGCCCGGGA GAGGGGCGGG CGAGAGAGAT GCTAAGCCAA TCGGATTGCG 120
GTCATCGGGG GCGAGCGGAG TCTGCAAGAG GTCCGAGGAG TAGCGGGTGC CGAGGGAAGG 180
AGCGCGGCGG GGCGGGTGAG GGATCCCGGG GCTCCGTTCC AGGACACCCA GGTTCTGACC 240
CCGTTTAGGA GTGCGGAGGG CAGGGGCTGC CTGCAACCCA AGGAGCCCGA GCTACCCTGA 300
AGGCCGACCC TGAGGCCGCT GCTCAGCGAG AGGAGCCGAC CCTTGGGGGA CAGCGGGGTC 360
GGGTTCCAAG CCGGGGCTGC TGGGGCTGGT CAGGCCGCCC GCCCTGCTTG ACCCCTCTCA 420
CCTGATGGCT CCCTTCTCCA ATCTTCAAGA AGGTGAAACG TCACTGTGGT CCGCAGAGGG 480
CAGGCCGCGT GTGCGGAGTC GCTGTCATCC CTTAGTGGCC ACGCCCGCCT CCCTGTCCAC 540
TTCCCGTCTT CGTCGTTGCG GTTCAGGTGT TCGCTCCACT CTGCGGCACC AAAGGCCCGT 600
CACGTGCTTC CCCTGCCCAG ACACCCCAAA CACCGAAACT GTCATCCGAA GGCCCCGCAC 660
CTGCCGCCTG TCGGATGCTG AAGAACGAAT CCCAGGTGGA GAGGACAGCA CCCCAAAAGG 720
GATGGGGGAT 730
|
