| Tag | Content |
|---|
EnhancerAtlas ID | HS040-00173 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:3692550-3694010 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPDEF | MA0686.1 | chr1:3693424-3693435 | ACCCGGATGTG | + | 6.32 |
| | | 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 |
| GH01I003776 | chr1 | 3693501 | 3693625 |
| Enhancer Sequence | CCTTGTACAC ATGGACCCCC CCACAGACAC GGACCCTGCG GCACACACAG CGCACAGGGC 60
ACACGCGCTG GCAGCCAGGC ACACGAAGAC ACCAGGTGCA CAGCTGTCAT CGGCCCCACA 120
CGGGGGCGCA CAAACACCTG GCACACAGCC CTTCAAAGGA CCTACAAACA GCTGGGCACA 180
CGTGGCTGGG AGGCCTGGGC CCAGCCTCAG CAGGAGCTGC AGGACACACC CAGGCTGGGC 240
CCTGCGGCCT GGAGCCCCCA GCTACAGCCT CCTCTCTCCC AGGGCCCAGC CCCTTCCCTT 300
GTGAAGGCCA GGATGAGGGG TTCCTTCAGC GGACAAACCG AGCCCACCTC CCTGGCAGCC 360
CCCCGGGGTG GGATCCTCCC GGCTGCTTTC CTCCGTGGGA GCAGTGTGCA GAGCTGTGTG 420
GCCCTGGGCA GGCCCCTGTC CTCTCTGGGC CTTTCTGACT CCTGGTTTTG TAAGGGTGGC 480
TATGTGTCCC CCGCCCTTGT CTCAGATGCA CCATATCTTC CTTAGTAAGT GGGCACAGTT 540
CTTCCTAGGC AGCCCACCAC GCGCAGAGGC TGGGTGTGTC CCTCTTGGGG CCGGCGGCTG 600
CCAGGGAGGA CCCGGGTCTA CCCTCCCTCC CCAGGGATGG GCCTGGTCCC TCCAAGTACT 660
CCTTGTGGGC CAAGAGCCTG TGTACAGAGG CATTAAGTGT CTGTTGAATG AACGGTGGAT 720
GACAGCCCTT GCCATAGTTA CCTGGCCAGG CGTGACATCC AGGAAGGCTG TGGGAAGGGC 780
TTGTTTCCCC GGGGCAGGCC CCCCTCCCAT GTGGCTCTAG GAATGCACCC CTACCAATTG 840
GGCCCTCTGG CGAGGACAGC CGGCAGGCCT GGGGACCCGG ATGTGGCTGG ACCTCAGCTG 900
TGTCCCAGGG ACTTCGGTCC CATTCCCCCC ACCCCGATCC TGGCCTCCAG TCCCAGCCCC 960
CGGTCCCAAC CTCCATTCTC TTGGTAGGTG CTTTCCTGGG TCTTGTGTTT GGCCCTCACC 1020
TACCACAAAA GATCCCAAAA AGCCTTGCCA GAAACATCCC CTTAGGGAAG GGGTCCTCAC 1080
CCCAGGGCTG GGGGTGGGAG ACACGGGCAG CCACTATCCT CACGGGCACA GAGAAGGGAG 1140
GCCACAGGGC CAGATGAGGT TATTGGAGGG CTGAGGCTGC GCCTGCCCCA GGCCAGGTCC 1200
CGCCGAAAGC ATCAAGTCAG GTAAACAGGA GGGGCTGCGC CAGTCTTGGT AGGGAGGCAG 1260
ACTCCACATC ATCCGCCTTT GGGGCGAGCA GGCTCACTTG AGATCTGCCT GGGCCAGCCG 1320
GTGGCAGGTG GAGCTGCATG GCTGATTGCA CACTGCCCCA AGGCTCCTGG CTCCAAACCC 1380
AAGGAGGGAG CCCAAGGGCC TGTCCTGGGC TGCGGTCTGA AGCAATGATG CTTTCCTGGG 1440
AGCCTGTTGT TGGGTGGGCT 1460
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