| Tag | Content |
|---|
EnhancerAtlas ID | HS047-22273 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr21:45642990-45643950 |
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 | TCCCCTGAGA AGTCTGTATG CAGACAGCCC CGGGTGATCC TGGCTGTCCA AGGGCTGAGG 60
GCGGGTTGGG AAGGGCCCTC ATCACCCCAG GGGCCAGCTC CCCACATAGC AGCTGAGTAG 120
CACCCAGAGA ACCCGGATCT TCACTCAAGG TGGCTGGCAG CAGAGCCACA GCCCAGGCCA 180
CCAAAGCCAC CAGAGCCCCT GTGTGGCAAG GATCATGATG CGAGGGTGGT GAGTTGGTTG 240
CTGTTCTCAG CAGGATCCTG GGTGTAAATG GCCATGCCTG TCCAGCACGG CTTATGGGGC 300
TGAGCATGTG AGAACTTGTG TGGCCTGTGC CTGTGCAAAC GCGTGTGCCC TGGGTATCAC 360
ACCCAGAGCC CTGCTGTGTG AAGAAGCCTC AGTCATCACG TGTGAGCTCA CAGTGGGCTG 420
GTCATGGGGC CCCTTCCACA TGGTGCACTG CTGCTGCAGG AATTGCTGTG TCTGCAAATT 480
CTGGACATAC CAGACCCTAA ATAGAATGCT GGGAGCAGGC AGGTTACAGA AGCCTCTGAG 540
TGCGGCAGCT CTATGGGAAC TGGGGTGCTT CACTTACAAG TATTTGAGGT ATTACAATGT 600
ATCCAATTTT TTTTTTTTTT TTTTTTGAGA CGGAGTCTTG CTCTGTCACC CAGGCTGGAG 660
GGCAGTGGTG CAATCTCGGC TCACTGCGAC CTCTGCCTCC CGGGTTCAAG CAATTCTCCT 720
GCCTCAGCCT CCTGAGTACC TGGGATTACA GGCGCCTGCC ACCGTGCCCA ACTAATTTTT 780
TTCTTTCTTT CTTTCTTTTT TAGTCAGAGT TTCGCTCTTG TTCCCAGGCT GGAGTGCAAT 840
GGCGCCATCT TGGCCCACTG CAACCTCTGC CTCCTGGGTT CAAGCAATTC TCCTGCCTCA 900
GCCTCCCGAG TAGCTGGAAT TACAGGCATG CACCACCACA CCTGGCTAAT TTTGTATTTT 960
|
