| Tag | Content |
|---|
EnhancerAtlas ID | HS184-07753 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:57334530-57336000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr12:57335533-57335548 | CTATGACTCAGCAAT | + | 7.88 | | Nfe2l2 | MA0150.2 | chr12:57335531-57335546 | TACTATGACTCAGCA | + | 7.13 |
|
| | 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 |
| GH12I056940 | chr12 | 57334572 | 57336364 |
|
Enhancer Sequence | CTTTCCCCAA AAGGAACAGG ATTCATCACT CGGTGTTTGA TGTGAAGTCC CTTCAGCTCT 60
CCAAGCCCCA GTGTCCTCGT GAATCAAGCG GAGATCATCT TAAAGCCCTC AACAGGGACA 120
AGTGTGAAGG AACCAGTAAG AGAATGCTGA GATCAGAAGC CTGGATCCTG CCCAGCCCCA 180
TCCCCGATGG TCTCATGCCA ACCGTCAGGA CCCAACGTTA TCCAGAGACT GGGCTCTAAC 240
CACAGCCTGG ACTCCTCTAA CCCTGGGCCC AGCCACAACC ACTCTAGGAC TTCTGCTTTG 300
GAAAGCAGAA AGCTCAAGCC CCCGAAAATA AAAGTCCTGG AAATGTTCCC AGTTAGCAGA 360
CACTAGGTCT CCCCTAGTGA CACAGAGAGA AGAGAAACAA ACAGGCACTA GGAGGGATTG 420
AGGTGGTCCC TCTGTCCCCC ACACACTCCT TCACCCACTG GGCAGCTGCA GCAATGCTCT 480
CTGTCTTGGT GATGTCCATG GTCACCGTCT CCAGCCTGTC TGAAGTCTGG CCCCTCAGCT 540
GCTTGGTCCC CTTCTCTGTC CTACATGCAG CTCCCGCAAG CCTGTGCATT CAGTTGTCTG 600
GCCAGTAGCT TCCTGAAGCG TGAGTCACAG CTCATGATGA ACACTATGTG TCTCTCAGCT 660
GGCTCACCAC CTGCCTCTCC CAGTATGAGC ACAGAAGGTA GTACAGGCCC TGGAGGACCA 720
CCAGGTAGAG CCACATGGCT TTGCAGAGGA CAGACCCAGG TAGGCTGGGG TGAAATGAGA 780
GTCTGGCCTC TGTTCAGACA GGAGGATTTA AGAACACAGA GGGCTGAGGT AGGCAGAGAA 840
GCCCTCAGGC ATTTTGGCAG AAAGTCTTCA CTTTCCTCCC TGATCACTGT CTTTCTGCAA 900
CATTTTTTTT TATCCTGGCT TCATCTCTCT ACTATTTTGA ACTGCCTTTG CAAGTACTCA 960
TGCATGCAGT TGCAAACCCC AAGTCCTGCC CAGTAGGAAA CTACTATGAC TCAGCAATGC 1020
TTCCCTAGTC CACAAATTTC TCTCTGCATT GCTGTGCCCA CACAGATGTT TATGTGGGTG 1080
CAAACGTGTA TTGACACAGG CTTACACACA GCAGCCCCCA CACACTCTCC ATAGCAAACA 1140
CACCCCTCTG CTCTAAGTAC AAGGGTCAGA ACTGTCTCTA CAAAGCTGCT GTACTGACAC 1200
TTCTGGTCCA TGACCTTCTG AGCACAGAAA GACCTTATTG GGAAGCTACA TATGGTTTCC 1260
AGCCACATTA GGTGGAAATC CCTCTCTGAG CCTGAGATTC CTCATCCCGC TCAGCACCCA 1320
GAATCAATCA CTCCTCAGAA AACTGGGTCA TGGTCAGGCT GTCTAGGATG AGAAGGAGAA 1380
GCCGAAAGAG TGGACAGGAA CAGATCGTCT CCTGCTATAA TAGTTTTTTG GGGCAGAAGG 1440
AGTGAAGGAT CCCATGGGGG CACTGTGGAA 1470
|
