| Tag | Content |
|---|
EnhancerAtlas ID | HS145-18128 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr3:141656320-141657330 | 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 | CCAAAGCGTT GGGATGACAG GCGTGAGCCA CCGCGCCCGG TGTGCCCGTT TTACCAACTG 60
CTGCAGCTGC TGCTGGTTTT CTCATCCCCT CGGCTGAACC ACCAGCCCCT CCCTCAGCAC 120
CTGGAAGGAG AAATCTGGCG TCTTGCTGGC GGGCTACTGC CCTGCAGCAC CTCCATGGCT 180
CCCTGGCTGA TAACATAGGG GTGTTGTAAA CTTACATTTC TGTGGTTTTC TGCTCATGTT 240
GTTTCTCCCC AGACTTTTCT CCCATCTGCT TCTGTGTTAT CTTTTGTTAC GATGACAGGG 300
AGTGGTCCCT GCCTGCCCTG GCAGGCACCT GCCTCCCTGG CCAAGCCCCA GCCCAGGAAG 360
TTGCTCATGC TGGGCCCTCC AGGTTCTGAG AAAACTTTCA GGGATTGGGG TAGGGAAGAA 420
AATAGGTGAA AACCCTCTCT CCTCTGCAAG CTTATTTCTT TGGCCTGGCC TGTCTTTAAC 480
CTGCACAGTT TATGTGTAGA CAAGTCTCCC GGTGCGGGCC CAGCAGGCAG GTGACAGCCG 540
CCCTTGCGGG AGTCATCCTT AACCAAGCAG TTTCAGAAAT GTTTCTTGAG AAACTGTTTC 600
CGGAAGTCCC GGAGCCTGTG TTGCCCATTG ACAAGCCTTG TCGGTCTCAG AAGACAGACT 660
CCGGGGGTCT ACATCCAGAG ACCCGGCTGA GGACTGAAGC CCGGGGTTTC CAAGCGGCTG 720
CCTTCTCCGT CCTGCAGCAG GGTGCGAGTC AACCGCCCTG GCTAAGGGAG CAAGGAACCC 780
CCGCCATGCT GTGTCCCCTC CCCCCATTCC CCGAATGCCC GTCTGTTCAA AGAGGGTGAG 840
AGGAGGGGGG AATACCAACT GCTCCGAGGA AAATGCAGTT CATCATATGC ATCTTTGCAC 900
GCTTTTTTTT TTTTTTTTTT TTGAGACGGA GTTTCACTGT TGTTGCCCAG GCTGGAGTGC 960
AAGGGCGGGA TCTCAGCTCA CTGCAATCTC TGCCTCCTGG GTTCAAGCGG 1010
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