| Tag | Content |
|---|
EnhancerAtlas ID | HS108-42133 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chrX:16214870-16215530 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chrX:16215142-16215153 | CTGAGTCATCC | - | 6.32 | | JUN(var.2) | MA0489.1 | chrX:16215142-16215156 | CTGAGTCATCCTCT | - | 6.25 | | JUNB | MA0490.1 | chrX:16215142-16215153 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chrX:16215138-16215153 | TCTGCTGAGTCATCC | - | 7.27 | | NFYB | MA0502.1 | chrX:16215219-16215234 | CATTGAGCCAATCAG | + | 6.39 | | Nfe2l2 | MA0150.2 | chrX:16215140-16215155 | TGCTGAGTCATCCTC | - | 7.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAAGCAGAA ATATACTTCC ATCCACAGTT TCAAGGGTAC ACAGACTATC ACTTTTATAT 60
TTTTTTGTAC TTTAACTTAA TTTCTGACTC CAAATACCCA TTCCAACAGG CTAATGGATT 120
ACTAAGCCTC TGTACTTCCT GTGGTGCCCC ACCTTCTCCT CAACATTGTA TCAGGCTTCT 180
TATGTCTTGG GACAAAATGT TGATTGGAGG CAGGGGTGAG GAGGGCTTAG AATGACCATC 240
TGATTTTCAG TCATGGCCCA TGAAGGCTTC TGCTGAGTCA TCCTCTATCT CTAACAACAT 300
CTCCACTGGG ACAAGGACAT AGTTTGCTAC TTTCAACTGT AAAATGCACC ATTGAGCCAA 360
TCAGCTTTGG GGGCTTGCCA GCAGAACATC CAGGAAGTTA TCCCAAGATC CTTAGGTTCA 420
CCTTCTTGTT CCATTTCTCA GGGGAAATTA ATTTCTAGTC TGGGAGAGAA GAAAACCTCT 480
CTTCCCTCTG CTTTTTCAAA ACTCTGAAAA TGGCTGAAAA CACACAAAAA CTACTTTTTA 540
CCTTCTTTGA TAACCCACGA GGATATCCTC AGAATATCAT GGAGACCCTA CAAACTTAGT 600
CTTTTGGATA AAGTCAGAAA AGGGATTACT TCTGTTTTTC AGCCCTTTCC ATATATATCA 660
|
| |
|
|
|
