| Tag | Content |
|---|
EnhancerAtlas ID | HS034-19576 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr22:20961460-20962310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr22:20961882-20961894 | CAGCACGTGGCC | - | 6.37 | | ZNF263 | MA0528.1 | chr22:20961641-20961662 | GGAGGAGGGGAACGAGGAGGA | + | 8.13 |
|
| | 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 |
| GH22I020606 | chr22 | 20960382 | 20961659 |
|
Enhancer Sequence | GCCTTTTTGG CCAGTCTGGA GAGAGAGGCT CTGGGAGCCA GAGATCAGCC GGCAGCCCCA 60
CCAGGCTAGC TGAGAAGGCA CTTGCGTAGC CCTCCAGAGG CCTCACGTGC TCTGTGAGCA 120
GGAAGGGATT CCCCTCACCC TGCCCCCCAT GCCCCGGGGA GAGGTCGCCG TGGGCAACAC 180
CGGAGGAGGG GAACGAGGAG GAGACAGCAG CGGCTGGAAG CCGCAAGGGC CACCCACTGT 240
TTGAACTCCC CCAGCGGGCT GGTGGTGTGG GAGTGGACGA AAGGTGAGAC CTGCTCTGGC 300
TTCAGGCTGT CGGCAAAGGC GTGCAGGTGC TTCAGTGGCA GGCGCACCAC CAGCATGTGC 360
CCCTTGGTGG GCATGAACGA CTCCTAGGTG GAGGAAGAGG AGTCAGGGCC TGGGAAGGGC 420
TGCAGCACGT GGCCTCCAGG TCTGACCACA GCCCGCCCTG GGACAGCTGA TCTGCCTCCA 480
CACAGGAGGC ACGAGCCAGG CAAAGAGTGG GGCCACCACT GTGCCTCACA CCCAGCGGGT 540
GTGCCTTGCA CTGCTTGGTC TGAACTGCGA CCAGCTCGTG GTAGGGAAGT GCTTGGCCCA 600
GCGCCCACAC AGCCTACCTG GGGAGAACTC GCTGAGACAG ACGCATCTGC TTCTGCACCG 660
CTGCACACCC GCGGTGGGTG GCACAGGGCT ATGGCCCGCC AGACTGTGCC CTTGGCCATT 720
GCTGCCTATC TTGATCCTCA TGGCAGGAGG AGGCCGATGT CACCCCCAAG CTCTGGATCC 780
AGGGTCTCCC AGGGAAGATG GCTAAGGCCA GGAATTCGAG ATTCGCTTGG GCAACATAGG 840
GAGGCCCTGT 850
|
