| Tag | Content |
|---|
EnhancerAtlas ID | HS108-39384 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr8:68225740-68226740 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr8:68226251-68226262 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr8:68226251-68226262 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr8:68226247-68226262 | TCTGCTGAGTCATCC | - | 7.27 | | Nfe2l2 | MA0150.2 | chr8:68226249-68226264 | TGCTGAGTCATCCAG | - | 7.05 | | Sox3 | MA0514.1 | chr8:68226076-68226086 | CCTTTGTTTT | + | 6.02 | | TFAP2A | MA0003.3 | chr8:68226409-68226420 | TGCCTGAGGCT | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CATGGATGTG GCTTCCTGTG AGCCGAACTG CAGTGATTGT TGTCTCTCTT CTGGGTCTAG 60
CCACCCAGCG AGTCTACCCA GCTCCAGGCT TGGTACTGAG GCTTGTCTGA ACAAAGTTCT 120
GTGATCAGCC ATGGATACCA GTGCCAGTTC TGGTAGAGGT GGCGGAGGGT GCAATGGACT 180
CCGTGAAATT CTTAGCTTTG ATGGTTTAAC GCTCTATTTT TGTGCTGGTT GGCCTCCTGC 240
CAGGAGTGGT GCTTTCCAGA AAGCATCAGC TGTAGTAGTG TGGAGAGGGA CCTGCAGTAG 300
ACAGGGCCCT AGAACTCCCA AGATTATACA CCTCACCCTT TGTTTTACAC TATCAGGGTG 360
GGTAGGGAAG GACCATCAGG TGGAGGCAGG GCTAGGTGGG TCTGAGCTCA GACTCTTCTT 420
GGGTGGGTCT TGCTGTGGCT GCTGTGGGGG ACAGGAGTGA GATTCCCAGG TCACTGGAGT 480
TGTGTATCTA GGAGGATTAT GGCTGCCTCT GCTGAGTCAT CCAGGTTGTC AGCGAAGTGG 540
GGGAAAGCCA GCAGTCACAG GTCTCACCCA GCTCCCATGA AAACTGAAGG GTCAGTCTCA 600
CTCCCACCTT GCCCCCTGCA ACAGCCCCAA GTCTGTTTCC AGGTGAAGCG CAAAAGGAGC 660
TTGAAAACTT GCCTGAGGCT TTCCGCCTCC CAGCTGTGAA AGAAAAGGAC TTTAGTTCTT 720
TCCCTAACTG TGAAGTCTAC AAGCCGCAGA TGGATTCAAG TCCTCCCCTG AGTTCTGACT 780
AGGAGGCTTC TCATTCAAAT TGCTACAAAA TTCAGCTAGA GAATTCCTTC TCCCTGTGGA 840
GTTTTACCCC CCTGCTCCTC TAGCCAACCT CCTGATGGAT CCCTGTGATG CCAGGCAGGA 900
ATGGGCTGCT TGGGGACCCA GCAAGCTCCC AGGGCCTTTC TGCTGCTTCC TCTACCCCTG 960
TATTTCGCTT GGCTCAACTA ACTTGACTCA GCTCCAGGTA 1000
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