| Tag | Content |
|---|
EnhancerAtlas ID | HS139-09139 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr11:34881340-34882860 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIL3 | MA0025.1 | chr11:34881378-34881389 | TTATGTAACCT | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAAGTATCT GGTATCTGTC TGCTTTGGTT TAATATGCTT ATGTAACCTC ATTGAAGGGC 60
TGATTTCCTC AGTTAATAAG GATGCAAAAG ACCAGAGTGC CCACTTAAGA GAGACTATGT 120
TTAGACCTCT CAAGGAATAA TTAATAAAGG GAATCAAGGG TCAAAGATTA TTTCAACTGA 180
CAAGTCTAGG CCCTTCTCAT TAGTAAAAAC TGCCCGGTTG CCTTGCAGTA TTTTCTTTGC 240
CAGGAGACAA CACCTATCCT AAATGTTTAA GTGACTTCTT GTTGGGCTGG TTTCGGAGGA 300
TTAAGCTCAG TGTAATTTCA TCCTTCCCAG GTGTGAGACA CTTGCGTGTG CAGTAATATG 360
ATTCTGTACT GTCAGGGAAA AGAGTGTGTC TTTGTCAGCA GTGTTTGGCA GTCAAACCCC 420
TGAATCATGA CCTCACTTTC AGGTAATCAC TCTTTGCAGG CTTAAAACCC CTGGCGTTAC 480
CACTTGCTCT TATGCTGAGA GACTTAAAGG TTTGGCTGCT GGCACGTGGT CCTGCTGGTC 540
AGCAGAATGG AGATGATCTG TGCTGGCAGC CCAACTGGAC TTCAGAAAGC ATTCCCTCCC 600
CAGCTGTTTG GATTCAGTTT CTAAGTGCTG AGCAATACCA TCTCTATGTT CAAGAAGGGC 660
AAAAACCAAA ATGAGTAGTA ATTATTTGGA TTTGCTTTAG CCTGTAGTTA GATCAATTCT 720
TCTTCTGATG CTTTGGGTAA TGTCCTCAAA ATGATTTCCT ACTGAATGTT TACAATTTCA 780
ACATGTAATA CATACTCTGG ATAAAGCAGT AGCTCACAAA TCATCTGATC AACAAGGTGA 840
ATCCTATCTC TGTCTTGGTC CACATGGAGA CTAGCACATG TGATTGACAG GCAGATAAGG 900
GCCGTATTGT CATTTGGTTG CACCTGTCCA TATGGCGAGG GATCGGAAAT GAGAAATGGC 960
TGTATTCTAA GCTGGGGATT ATAGAGCTGT GTTACTCTAA GTCTTACTGT CTTACAGTAG 1020
CAAGGAGCAA GAAGAGTCTT GAAAGAACGG AGCCTTAAAT ATCATAGGTC AAGCCCTATA 1080
GTTTCACAGA TGAGGAACTA TTGCCTCAGA GACAGAAAGC AACTTACACA AAATCACAGA 1140
GAAAATGCGA GTGGCCTTGC TGGGGTTAGA GTCAAAGTTT CCTGACACCC ATCTAGTGGT 1200
CTTTCTGCTA CACCTTTTTG TTTCCACAGA GTTTTACTGA CCCCTGTATT AAAGAAAAAA 1260
AAAAGATAAA GGAAAAAAAG CCTGTTTTGG CATGGTCCCT TGTTCTATGG TTTAAGGTCA 1320
GTCTTGTTCT TCAGCATCAG CACTTTAAGG TTTTTTTTTT TTTTTTTTTT ATCAGAAGTC 1380
TCTATATGGT TAGCCTGAAC CAGATGAAAT TGCTGCTTTT ATGAGGCAAA AAGTTAAATA 1440
TAGTAAATTT CAGATAGTTC TACCTGAGAG TTTTTCATTT AGAAAGTGGC AGTTAATGCC 1500
GGGCGCGGTG GTTCACGCCC 1520
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