Tag | Content |
---|
EnhancerAtlas ID | HS050-39182 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:178557130-178558230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:178558197-178558215 | ACTGGCTTCCCTCCTTCC | - | 6.44 | FOS | MA0476.1 | chr2:178557654-178557665 | AATGAGTCAGA | - | 6.32 | Myog | MA0500.1 | chr2:178557990-178558001 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr2:178557990-178558001 | GACAGCTGCAG | + | 6.14 |
|
| 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 |
GH02I177692 | chr2 | 178557321 | 178557470 |
|
Enhancer Sequence | GTACTTTACA TTGTCAAAGC TCTTTCATAA AATTAATCTC TTTTCACTGC CACAAGGATC 60 CTAGGAGATT AGAATGGGTG ATATGCCTAT ACCCCTGTTG CTGACAAGGA AACTGAGGCA 120 AAGAGAGATC CGACTCTCAA AGCTGGTGAA ATTACTACTT AATTATCAAA TCCTTATTCA 180 CTGCAGGGAC TCAGAAACAG GCACAGAAAT CATTTCAGAA AGTTGCTCAG CAGTAACTGG 240 AAAACGTTTT CAGTGAGTTG GAAAATCAGA GTGAATCATT AACCCCCAGG CTCAGGTTGT 300 GAAACTTAGA AATTCACATT AAGGATTTTG TTTGTTTTTG TATTTTAATC TTGTGAATTC 360 TGCTTTCATA TGCCATTTGA ATGACATAGA ATCCCAAGGA CACACAAGGT CTTTAGAAAT 420 TAAAGTCATA AGTTTTTGTG GATGTTTTGA AAGCCTTTCC ACATTTCCAT GAATCTCATA 480 TATTTTTTTC CTTTTAGAGC ATGGCAAGAA ATCTTGCCTC TAGGAATGAG TCAGAAACCT 540 GTCTCCAAAA GGCAGGGCTC TACCCTGCCC AGCCTGGCCC TTTCCTAGAG TGACTTTCTC 600 CCTCTAGGGG AGGAAAGCAG TGAGCTTCCT TTTTGGTTTC TTCAACTGTA TCATGACTTT 660 TAGGTTGAGT AGTCAGGGCA GAAGAACCAA CAATAATCCA GACTTCCAGA AACTAATTGT 720 ACGGGGAGCC TAATATCCTC TTGGCTCACC CACCCCTCTC CTGCCATTGC TGCTACACGC 780 AGTGCCTCAG CGGTCCTGCG GATCACATAC TTTCTGCCCT GGCACTTCAC ACATGACTTC 840 ATGTGTGAGA ACAGGGATGA GACAGCTGCA GGAATGCCCA GTCATCAGGC ACACACAACA 900 TGGAAGTACA TGAGAGTTAA CATCCCACAG ATCAACATTT GGTTGATGAG GATGGTGGGT 960 GGCGGACAAT TTTGAAGTGC GATATATGAG ACTTCTCAGA TGGTCCCTGC AGGATCAAGA 1020 CTGGCTGACC ATAGTGGAGA ACAACAAAGA AATGTGTCCT TCCTTTCACT GGCTTCCCTC 1080 CTTCCCCATT TCACTGTCCC 1100
|