| Tag | Content |
|---|
EnhancerAtlas ID | HS053-35924 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr7:2995800-2997240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr7:2996499-2996514 | CAGCATGACTCAGCC | + | 6.42 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2995922 | 2997146 | | chr7 | 2996430 | 2996653 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I002952 | chr7 | 2992428 | 2997354 |
| Enhancer Sequence | TGAGACCCTG TCTCTAAAAA ATTAAAAAAA TATATACATA TATATAAAAC AAGGCTGAGT 60
GAGATGGCTC ATGCCTGAAA TCCCAGCACT TTGGGAGGCC GAGACGGGAG ACTGGGAGTT 120
TGAGGCCAGC CTGGACGATA TAGCAAGACC CCATCTCTAC AAAAAAATAA AAACTTAGCT 180
GGGTGTGGGG TTGCGTGCTT GTAGTCCCAG CTACCCAGAA GGCTGAGATG GAAGGATTGC 240
TTAAGCCAGG AGGTTGAGGC TGCAGGGAGC TATCATCATA CCACTGTACT CCAGCCTGGG 300
AGACAGAGCA AAATCCTGTC TTAAAAATAA TTTTTTTTTT AAACATACAA AACAAAACCC 360
TACTGTTAAG GATATACGGC AAAACTATAC CAAGAAACAA GGGGACTGAT AAAAATCAGA 420
ATGGTGGCTT CCCATGGGGA GGGGCAGCCA GACAGATGTG ACCTCGGAAG GTCCCCTGAG 480
GACATTGGTG ACACAAGGAA TTATGTTATG CTTCAACTGG GGACATGAGT GTCTGTTTCA 540
TTGTTCTCTG CCTCATAGAT ACACATTATA TATACATATT TATATGTATG AAATATTTCA 600
TGGAAAAAAT CTATGGAGAG TGTAGCTAGC CTCAAAAGAA AAAAAATGTC TCAGACGCAA 660
TTCGAAATGT ATTTTCCCTT CTAACACTTC CCTCTAACTC AGCATGACTC AGCCTCATCA 720
CCGGGGATGA ACCCAGTGAC TCTGTCAAGC TCTGGGCAGT TTCTTTGAAG GCAGTTTTCT 780
CAGAAATGTG CCCAGAGGCC CCGAGGCTCT GAACTTTAAC AGCATGGCAG GTTGGATGGC 840
CCGTCCCTAC CTAAGTCTTA GCTGGAGCTT GTCGCAACTC GCAACTCAAA CCCAACCTTT 900
GGCAGGGTTT GACTTCCAGT GTGAGACAGG TCCTAGGCCA CACCAATCTC TTTGCAAATG 960
GCTGAAAAGC AAGTGCCAGA CCCCCAGGCT AGGCTCCACA GAAAGGGCTG TGTTGCTCAC 1020
CTTCCCTGGG AAGCAAAGGA CCAGGAGGTG ACCCACCTGA GGACGAATTC CATGAGAGTT 1080
GCTGGCCTCA CGTCCTGACT TACTCATTCA AGACCTCTAC TGTGGCTTCC TCTTGCTGTT 1140
ATGATAAAGT TCCAATCTTT TTTTTTTTTT TTTCTTGAGA TAGGGTCCTG CGCTGTTGCC 1200
CAGGCTGGAG TGCCGTGGCG TGATCTCAGC TCACAGCAGC CTCTGCCTCC TGAGCTCAAG 1260
CAATCCTCCT GCCTCCACCT ACTGAGTAGC TGGGACCACA GGCAAACACC ACCGTGGCCA 1320
GCTAATATTT TAAAAATTAT TTTTGTAGAG ATGGGGTCTT GCTATGTTGC CCAGGCTGGT 1380
CTCAAACTCC TGGGCTCGAG TGATCTTCCC ACCTTGGACT CCCAAAGTGC TGGGATTACA 1440
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