| Tag | Content |
|---|
EnhancerAtlas ID | HS108-33202 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr5:159614820-159616140 | 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 | GCTATCTCGG CTAACCACAA CCTCCGCCTC CCGAGTTCAA GCGATTCTTC TGCCTCAGCC 60
TCCCAAGTAG CTGGGATTAC AGGCATGCAC CACCATGCCA GGTTAATTTT GTATTTTTAG 120
TAGAGGCAGG GTTTCTCCAT GTTGGTCAGG CTGGTCTAGA ACTCCCGACT TCAGGTGATC 180
CACCCGCCTC GGCCTCCCAA AGTGTTGAGA TTACAGACGT GAGCCACTGA GACCCCGGCC 240
TGCTAATATT TTTTATTTCT CCAGGCTACA AGAGAGGGAA TCTCCTGAAT TCCTCTGGGG 300
CAGCCCTCCC AATTCACCCG GGAGAAAAGC AGGCAGGGGC CGGGCTAGGA TTCCAGAGGG 360
GCGGGAAGCC CTGGTGGAAT GGGGTAGCTG GAGCCAAGCA CCCCAGGAAT GCCCTCCCGG 420
CCTCTCCTCC CGATTCCTTA TCAGCTACAA GCTCGAGTTT CCTCAGCCAC ACGCGATCAA 480
ATGCTGCTTC AGAGCTCTAG GAAGCTGGGT GTGTCTTCTG TGCTTTGTAA AAAAGAAACG 540
AAAAAAACAT TAGCAAATCC CCAGCCCAGG TAGCCGGCTG GCTGAGGGCG GACTCTTGGA 600
ACTGGGCGGT GGGAGGTGGG GGACGGGGGA GGGATTGGGG GGCCCTTGCT CCAAAGCCAA 660
AGAGCGGGAA ACAGGAACTG CAGGGAGGCC ACTCCGCAGG CGCCTCCCCT TTCCCGCTGG 720
GGAGAGGCCG CCGCCGCGCG GCGCTCGGCC TGCACCGACC CTCCGGGGAC CCCGCTAAAC 780
GGAGGAGACC CCAGGCCCGG AGGTGTCGCC CCTGGGCTGC GACCCCCGAC TTTGGCCGGC 840
TTCTCCCTGC GGAGAAGGAG GCAGCGCCGG GACCGGGCTG TTAGCCACGT GCTGGGTGGC 900
CTTGGGCAGA TTGCCTCCTG TCTCTGGGCC TCAGATTTTC TCATCTAAAA AGAGGGGGCT 960
GGACTCATTT CTGCAAGGCC CCTCCCGGTT GGAGCGGTTC CCTGCAATTC CCTTCCTTCT 1020
CTGAACTTGA AACTCTTCCC TCCCCCATCC CCTTGGGGTG GCCCCTGGAT TATCTGGGTG 1080
GTGCTTATCC AGTCTGCCGC CTTGAGAGAA AATGTTGCCC TGCAGCTGTG ATTTACAGCA 1140
GGGCTCTGCA CCCTTTTTCT TTTTTTGTTT TTCTTTATTT TCCCTCCTTC TTTCCTTTTT 1200
ACATCTAGAG TACACACTTT ATGCACCCTT TTCCTATAAA GGGTCAGAGA GTAAATACTT 1260
CGGGTTTTGC AGGCCACACT CTCTGTCACA GCTATTCAAC TCCGTCATTG TAGCCAAGGC 1320
|
| |
|
|
|
