| Tag | Content |
|---|
EnhancerAtlas ID | HS111-04090 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr5:159614850-159616030 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr5:159615178-159615189 | GGGCGGGAAGC | + | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr5:159615997-159616015 | TTTTCCCTCCTTCTTTCC | - | 6.33 | | Gfi1b | MA0483.1 | chr5:159615943-159615954 | AGCTGTGATTT | - | 6.14 | | ZNF263 | MA0528.1 | chr5:159615431-159615452 | GGAGGTGGGGGACGGGGGAGG | + | 6.22 | | Zfx | MA0146.2 | chr5:159615002-159615016 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCGAGTTCAA GCGATTCTTC TGCCTCAGCC TCCCAAGTAG CTGGGATTAC AGGCATGCAC 60
CACCATGCCA GGTTAATTTT GTATTTTTAG TAGAGGCAGG GTTTCTCCAT GTTGGTCAGG 120
CTGGTCTAGA ACTCCCGACT TCAGGTGATC CACCCGCCTC GGCCTCCCAA AGTGTTGAGA 180
TTACAGACGT GAGCCACTGA GACCCCGGCC TGCTAATATT TTTTATTTCT CCAGGCTACA 240
AGAGAGGGAA TCTCCTGAAT TCCTCTGGGG CAGCCCTCCC AATTCACCCG GGAGAAAAGC 300
AGGCAGGGGC CGGGCTAGGA TTCCAGAGGG GCGGGAAGCC CTGGTGGAAT GGGGTAGCTG 360
GAGCCAAGCA CCCCAGGAAT GCCCTCCCGG CCTCTCCTCC CGATTCCTTA TCAGCTACAA 420
GCTCGAGTTT CCTCAGCCAC ACGCGATCAA ATGCTGCTTC AGAGCTCTAG GAAGCTGGGT 480
GTGTCTTCTG TGCTTTGTAA AAAAGAAACG AAAAAAACAT TAGCAAATCC CCAGCCCAGG 540
TAGCCGGCTG GCTGAGGGCG GACTCTTGGA ACTGGGCGGT GGGAGGTGGG GGACGGGGGA 600
GGGATTGGGG GGCCCTTGCT CCAAAGCCAA AGAGCGGGAA ACAGGAACTG CAGGGAGGCC 660
ACTCCGCAGG CGCCTCCCCT TTCCCGCTGG GGAGAGGCCG CCGCCGCGCG GCGCTCGGCC 720
TGCACCGACC CTCCGGGGAC CCCGCTAAAC GGAGGAGACC CCAGGCCCGG AGGTGTCGCC 780
CCTGGGCTGC GACCCCCGAC TTTGGCCGGC TTCTCCCTGC GGAGAAGGAG GCAGCGCCGG 840
GACCGGGCTG TTAGCCACGT GCTGGGTGGC CTTGGGCAGA TTGCCTCCTG TCTCTGGGCC 900
TCAGATTTTC TCATCTAAAA AGAGGGGGCT GGACTCATTT CTGCAAGGCC CCTCCCGGTT 960
GGAGCGGTTC CCTGCAATTC CCTTCCTTCT CTGAACTTGA AACTCTTCCC TCCCCCATCC 1020
CCTTGGGGTG GCCCCTGGAT TATCTGGGTG GTGCTTATCC AGTCTGCCGC CTTGAGAGAA 1080
AATGTTGCCC TGCAGCTGTG ATTTACAGCA GGGCTCTGCA CCCTTTTTCT TTTTTTGTTT 1140
TTCTTTATTT TCCCTCCTTC TTTCCTTTTT ACATCTAGAG 1180
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