| Tag | Content |
|---|
EnhancerAtlas ID | HS175-17985 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr21:45642960-45643930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFG | MA0659.1 | chr21:45643449-45643470 | GAATTGCTGTGTCTGCAAATT | - | 6.29 | | MAFG | MA0659.1 | chr21:45643449-45643470 | GAATTGCTGTGTCTGCAAATT | + | 6.71 | | MAFK | MA0496.2 | chr21:45643450-45643469 | AATTGCTGTGTCTGCAAAT | - | 6.33 | | MAFK | MA0496.2 | chr21:45643450-45643469 | AATTGCTGTGTCTGCAAAT | + | 6.76 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH21I044223 | chr21 | 45642886 | 45643934 | | GH21I005040 | chr21 | 45643145 | 45643345 |
|
Enhancer Sequence | TCTGGGGAGA TAAGGGTCCA AGCTGAGAAC TCCCCTGAGA AGTCTGTATG CAGACAGCCC 60
CGGGTGATCC TGGCTGTCCA AGGGCTGAGG GCGGGTTGGG AAGGGCCCTC ATCACCCCAG 120
GGGCCAGCTC CCCACATAGC AGCTGAGTAG CACCCAGAGA ACCCGGATCT TCACTCAAGG 180
TGGCTGGCAG CAGAGCCACA GCCCAGGCCA CCAAAGCCAC CAGAGCCCCT GTGTGGCAAG 240
GATCATGATG CGAGGGTGGT GAGTTGGTTG CTGTTCTCAG CAGGATCCTG GGTGTAAATG 300
GCCATGCCTG TCCAGCACGG CTTATGGGGC TGAGCATGTG AGAACTTGTG TGGCCTGTGC 360
CTGTGCAAAC GCGTGTGCCC TGGGTATCAC ACCCAGAGCC CTGCTGTGTG AAGAAGCCTC 420
AGTCATCACG TGTGAGCTCA CAGTGGGCTG GTCATGGGGC CCCTTCCACA TGGTGCACTG 480
CTGCTGCAGG AATTGCTGTG TCTGCAAATT CTGGACATAC CAGACCCTAA ATAGAATGCT 540
GGGAGCAGGC AGGTTACAGA AGCCTCTGAG TGCGGCAGCT CTATGGGAAC TGGGGTGCTT 600
CACTTACAAG TATTTGAGGT ATTACAATGT ATCCAATTTT TTTTTTTTTT TTTTTTGAGA 660
CGGAGTCTTG CTCTGTCACC CAGGCTGGAG GGCAGTGGTG CAATCTCGGC TCACTGCGAC 720
CTCTGCCTCC CGGGTTCAAG CAATTCTCCT GCCTCAGCCT CCTGAGTACC TGGGATTACA 780
GGCGCCTGCC ACCGTGCCCA ACTAATTTTT TTCTTTCTTT CTTTCTTTTT TAGTCAGAGT 840
TTCGCTCTTG TTCCCAGGCT GGAGTGCAAT GGCGCCATCT TGGCCCACTG CAACCTCTGC 900
CTCCTGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCGAG TAGCTGGAAT TACAGGCATG 960
CACCACCACA 970
|
