| Tag | Content |
|---|
EnhancerAtlas ID | HS040-35273 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr9:127104670-127106160 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr9:127105672-127105682 | GGGGATTAGC | - | 6.02 |
| | | 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 |
| GH09I124340 | chr9 | 127103109 | 127107948 |
| Enhancer Sequence | CCCAGCTCCA GGGCCCACCC ACGGAAGGAT CCAGGCAAGT CAGCCCCTCC CGGGTGGGCC 60
TCAGGTGTCC CATATGTAGA ATGAGTGGCC AGCCCACCTT GTCATAGTGA GGAAGGAATG 120
AGGCCCTAGG GGTGAGGTGC CCGAGTCAGA GAAGGCCCTC GGGCCTGTCC ACCAGCTGCA 180
GGCCAAGCAC GGGCACTTCT GCCCGCCTCC GGCACGAGGC TCCTGCAGCT TGCCACATTT 240
CCCTTTTTGC TTTGGCCAGC GGGAAGCCAA AGTGCAGCCC AGCCTCAGTC TCCGAGGAGG 300
CTCCACTTTG TCCTCCTTTC CTCATGTGTC TTGTCCCTGG GTCAGATGGC TTTTCGTTTC 360
TTTTTCCATT CTGCTTTGTG TTTTTGTAAG CTGCTTCCTG TCTCCCATGA ACCATGGGCT 420
CTCCACACAT AAACACACAC ACAGCATATG AACACACACA CAGGCTGGCC AGGCTGACAG 480
AGCTGTGCCC ACTTCCCTGG GGCTGGGGCC GGGAGGCCAG CAGCTGGCTC CCTCTGCCTG 540
TGCCAGGCCC TCCACTTGAG AACCGGCCCT GTGGTTCCCA GCCCCGTTCC CTGCCTCAGT 600
CTTTGTCTCG GCTCTGCAGA GGCAGGCACA GCCCATCCTG TGCCAGGCCT CACTGAATTC 660
TGGCTCGGGC AGTCCTCCTC CGAGTCCTCA TTTGTGGGCA CCTAAATGTG CATCTCACAA 720
GGCAGTCCCG CCTTCGTGAC TCCCTGGCAT TGAGGCTCGG GTTACGCCGA GCTGACTCAT 780
TTGTTGGAGT GAGTGGGGCT GTGCGGCTCG CAGCTGGGGG GGCTGGACCA CAGCCGGGGG 840
GCGGTGAGGG GACGGATCGC AGCCGGGGGG TGGTACGGGG GATGGATCGC AGCTGGGGAG 900
GTACCGATCG CAGCGAGGGG TGGTGTGGGG GGACAGATCA CAGCCAGGGG TGGATACCAG 960
TCAGCAGTAG GAAGTGAATG AAACACAGCA GTCAAGCCCT GAGGGGATTA GCGTCCTCAG 1020
GGACATCAGG CGCTGACCTA ACCCTAGCAG CCCCGGCCTC ACACAGCAGC AGGCTGCTGT 1080
GGCCACCCAT AGCCGGCCCA TCCAAGGGTA ACGGGGCAGG GGCTCTGTGC CAAGTGACCC 1140
CCTCCCCACT CCTGCAGTCC CTAAAGGGGA AGGTGAAGCA GGCGTTTCCC CAGCAGACAG 1200
GGAGGAGAGC CACATCTGAG CCCACGGCCA TGTAATTGGA AAGAGGCCTC CCGCAGTCAC 1260
GCCCGGAGCC TCCCGCCCCA CAGCCTGTGG TGTCTTCCAG GGGCACCAGC CTGAAGAGCT 1320
GTGACAAAGC CCCCTGCCCT CTCTGGACAA CAGCTGAGGA TCCTGCACAG GGCACATACC 1380
CAGGTCACCT GGGCCCTGGT GACAGACACA GCCGGAGAAA ACCTGCCCTT CCCCAAGCCC 1440
CAGCACAGCC CGGAAGGCTC AAAAGCCCCT GTGCTCATCC CTGTGGCTGC 1490
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