Tag | Content |
---|
EnhancerAtlas ID | HS050-00577 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:11415010-11416380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:11415613-11415626 | TTCTAGAACTTTC | + | 7.04 | LBX2 | MA0699.1 | chr1:11416332-11416342 | GCCAATTAGC | + | 6.02 |
|
| 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 |
GH01I011355 | chr1 | 11415181 | 11416790 |
|
Enhancer Sequence | TATTTCTGTA AGTTCCATCA GTTATTCTTC AGAGTGAAGC AGGATATGCC TGAATCCATC 60 CATCCATCCC CTGAAGCTGT ACTTAGAACC TCCCTGAGGA CGGTGACTGC TAAGTGGCTC 120 CGAAGAGCCT CCCCAGGCAT CTGGCAGGCT GGGGAAAAGC TGAGAAAGGC CTCTTTCTCT 180 GTAGCTTCAA GGAGGTATTT ATTGGCTGTC TTTCAGGCAC ATTTTAGCTG TCATCCAACA 240 TTCTCAACCT TAGTCCCCTT CTCTGGGCTA AGGGGAGAAT GATGGTCCTA CCCCAGTCTC 300 CCAGATGCCA GGTCTGGGAA ATGGAGTGGA AAATCCTTTG AAATTCCCAA TTAATAAATA 360 AAAATAATGT GGAGGGCTCA TCACCATGGA GACCAAAGGC TTGTTTGGTC GTCATGGTGA 420 CCCTGGGATA GGCTGTCTGC CCAAAATGAT CAGCATCACT AGGAAAGAAG GGCCAAGAGG 480 TGGAGAGACA GGACTGCATG CCACAGGGTG AGAGCCAGGC GCCGGCAGAT TTCTCGAGGC 540 AGGTCGAGAG CAAGAGTGGG ATGATGTGGA GGTGTGGGAG ATCAAAGGGG AGAGCACACT 600 ATCTTCTAGA ACTTTCTTCC TGCCACTCTG CCCCCTCTTT CATCCACCTG ATTCCTTCTG 660 GGCCCCGTGC CCCCCGGGCT GGGAGGGGAA CCTGGCCTAC TCCTTGGCAG TGCTGCCAGG 720 GAGTCTCCAT GACAACCCCA GCCCCCATCT GTGGGAGTGG AGCCCTCGGC TAGGGCCTCA 780 AGGGAGTTGC CTGGGTAACC GGGCTCCCTT GCCCCACTTC CCCGCCAACC AAACCTCCTC 840 GGCCCCTCCC CCTCTTTGCG ATGGGAGGGT GAGAGGATGG GGTCACCATG GAGACCCAGC 900 TTCCCTCCCG CTGCCCCCTT TCCAGAGCAG CTGTCACAGG ATGATGGTCG GGAGGAGACC 960 TGGGAACGAG GGTGTCTGCT GGCGAGGAGA CAAATGACCA AGACCCTCTC TCTGGCGGAG 1020 GAAGAGCATC CTGGCTCTTT AAGAAGTGAC ACTTCTTGGG ATGTTTGGGG TGTTGAGTGC 1080 AACTCCTCTC AGCCACCCCC TGCTGGAAGT CCTGGGCTCA GTGGAGCGGG CCTGGGCAAC 1140 GAGTTCTGGA GCGGGGACCT TCTCCCTCCC TGCCTGGCTG TTCCCCTGCA GAGGAGCTGT 1200 GGCTCATTCA GCAACGGAGA ACACTCAGGT GGTTAACGAG CATTTACTTC CCAAACGAGG 1260 AGACGGTTAC ATGACTAGTT GTTGTTTTAT CTTGCTAATG AAAATACATA AAAAACAAAA 1320 TGGCCAATTA GCAAGGCCAT TTGTTCCCAG GTCTTGGCTG TTTCTTTCTG 1370
|