Tag | Content |
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EnhancerAtlas ID | HS050-21683 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr14:99933640-99934480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr14:99934257-99934270 | AGCAGCTGTTCCC | + | 6.92 | Tcf12 | MA0521.1 | chr14:99934256-99934267 | CAGCAGCTGTT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 99933712 | 99934074 | chr14 | 99934127 | 99934367 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I099467 | chr14 | 99933861 | 99934010 |
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Enhancer Sequence | ATCAAAAGCA GAAAATTTAA GTGAGGGGAG GGCAGGATGA CAGACAGCTT AAGCACCTTT 60 TCCTATGCTT AAGAAATGTC TTCTTAGAAG AGAAAAAAAT CTCCCCATGG TTCTGGCTCA 120 CAGCCAAGAG CAAGGGCACA GCCTGGACAC AGCACCTCCA CCCTTCTGGG CATTTCAGGC 180 TTCCCATATC TGCGGAGGGC ATCTCTGGAG GACCATCGAA CTTGACCTGA AAATAACTAA 240 AACCACCAAG GAGTCTGGTA ATAAGGACGT TAATCACACT TCCAAATATA GTGGGTCTGC 300 TGGCTTGGCA GGAGGAGACG CAGAAGCATC CTGTCAGCAA TGGCTTAGCT GGCCTCTCCC 360 TTCAGCCTTG CCTGAAAGAC CTTCTGCTGT GGGAGCCTGT AAACGAGGCA AGAACGTCAC 420 TTTGATGAGG AGCTCCAAGA CCCTTTCCCT TCTCTTAACA GTAAGTGAGC CTGGGACAGG 480 GCTGTTCTGC ACCGGCCCTC ACAGGGTGCC CACCAACAGC TACAAAACAG GCTCTATTCG 540 CTCTGCCTGC AGCCCCTCAC CTCCTCCAAA GTCTTCTCTC AGCTATCCAC CCAACTCCAG 600 TTGCTCATTG ATGTAACAGC AGCTGTTCCC TGGAGCTCAG TATTTACCCT CTGCCAGGTG 660 CTGGACTAAG ACAGAGCTCT TCATTTGATC TTCCTCGCAC TTTAAGCAGT AGATACCATC 720 CTCATCTTTC AGATGACATT GTCAGAAAGG TTAAGTCCCT TCTCTTTGTC CAAGGTCATG 780 CATCAGGTAA GAGGTACAGC TAGAATCTGA ACCCAGAACC ACTACCACAC TGCCTCTGTT 840
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