| Tag | Content |
|---|
EnhancerAtlas ID | HS040-26293 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr3:141656120-141657160 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr3:141656537-141656548 | TTCTGTGGTTT | + | 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 |
| GH03I141937 | chr3 | 141656083 | 141657614 |
| Enhancer Sequence | AGCCACTGTG CCCGGCTCAC TGCAACCTCC GACTCCCTGG TTCAAGCGAT TCTCCTGCCT 60
CAGCCTCCTG AGTAGCTGGG ATTACAGGCA CATGTCACCA CGCCCAGCTA ATTTTTGTAT 120
TTTTTGTAGA GACGAGGTTT CACCACGTTG GCCAGGATAG TCTCGATCTC CTGACCTTGT 180
GATCCACCTG CCTCGGCCTC CCAAAGCGTT GGGATGACAG GCGTGAGCCA CCGCGCCCGG 240
TGTGCCCGTT TTACCAACTG CTGCAGCTGC TGCTGGTTTT CTCATCCCCT CGGCTGAACC 300
ACCAGCCCCT CCCTCAGCAC CTGGAAGGAG AAATCTGGCG TCTTGCTGGC GGGCTACTGC 360
CCTGCAGCAC CTCCATGGCT CCCTGGCTGA TAACATAGGG GTGTTGTAAA CTTACATTTC 420
TGTGGTTTTC TGCTCATGTT GTTTCTCCCC AGACTTTTCT CCCATCTGCT TCTGTGTTAT 480
CTTTTGTTAC GATGACAGGG AGTGGTCCCT GCCTGCCCTG GCAGGCACCT GCCTCCCTGG 540
CCAAGCCCCA GCCCAGGAAG TTGCTCATGC TGGGCCCTCC AGGTTCTGAG AAAACTTTCA 600
GGGATTGGGG TAGGGAAGAA AATAGGTGAA AACCCTCTCT CCTCTGCAAG CTTATTTCTT 660
TGGCCTGGCC TGTCTTTAAC CTGCACAGTT TATGTGTAGA CAAGTCTCCC GGTGCGGGCC 720
CAGCAGGCAG GTGACAGCCG CCCTTGCGGG AGTCATCCTT AACCAAGCAG TTTCAGAAAT 780
GTTTCTTGAG AAACTGTTTC CGGAAGTCCC GGAGCCTGTG TTGCCCATTG ACAAGCCTTG 840
TCGGTCTCAG AAGACAGACT CCGGGGGTCT ACATCCAGAG ACCCGGCTGA GGACTGAAGC 900
CCGGGGTTTC CAAGCGGCTG CCTTCTCCGT CCTGCAGCAG GGTGCGAGTC AACCGCCCTG 960
GCTAAGGGAG CAAGGAACCC CCGCCATGCT GTGTCCCCTC CCCCCATTCC CCGAATGCCC 1020
GTCTGTTCAA AGAGGGTGAG 1040
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