Tag | Content |
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EnhancerAtlas ID | HS050-33659 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr19:34011450-34012640 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPIB | MA0081.2 | chr19:34012231-34012243 | AATGGGGAAGTG | + | 6.18 | ZEB1 | MA0103.3 | chr19:34012415-34012426 | GGGCAGGTGGG | - | 6.14 | Znf423 | MA0116.1 | chr19:34011541-34011556 | TCAACCTTGGGGGCC | - | 6.44 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCCTGTGAG TACCTTAAGG GAAGACCCAC TGCTATTCCT GGAATATAGC AGGTGCCCAC 60 AAAATATTTG ATTTGTATGC TCTAAGCTCC CTCAACCTTG GGGGCCAACT TAGAACCCAC 120 TTTCTGTTGC CATTTTCCCT GTATCTTAAA AAGAGAGATG CATTCAGTCC ACTAGATCCC 180 CCATTCTGAC CTCAGTTTCC AACCTGGCAT CTGGAATACT GCTCCCTCCT ACACCATGCC 240 CCCTCTACCC CACTGTACCA CCAGACCCAC ACCTTCTCCC ATTGAACTCA CACATAGCTC 300 AGGGGAGCCT AATCTTTAAA AAACAGATCA AGCAGCTTGT AACAAAACCC TTCCAGCCCA 360 TCAGGGCAAA GTCTGAAGCC GCCACCTGGA ACACCACACC TTCCAACCAG CCCCAGGCAT 420 GCACCCCTGT CCCCAGAACA CTCTGAACTC TCAACCTTTG TCCCTTACCC TGGGCTCAGA 480 TGCTCCCTAT CTGGGAGATT CCGCCCAACG CTCTGGTGAA CCCATCTGTC CACCCTTCCT 540 CCCACTACGA CCACTCAGCT TTCTTTCATT TAGCCCAGTA TGGAGCACCT ACTGTGTGCA 600 AGGCACCGGG CTACTGAGAA GCAGGTAACA TACCTGCCCT TGCACTCTAA ATGCAGAGAA 660 GATAAAGAAC AAGTACAAAC AATGCTCTAT ATAGTTTATC AGGTGATGAT GAGGGCACAA 720 AAAGTGGGAT AGATGGTTAG AGAAGGATTC CCTGAGGGGG TGACATTTGG CCCCTGAAAG 780 AAATGGGGAA GTGCCCTGCT GGGAAAAGGG AATTCCAAGT CCGTCTCGAA TACCGCCTCC 840 TCCGGGAAGC GCCCGGGTCC CTGGGGTCCT CGCAACGCCG CCCTCCTACC CGGGGGTCTT 900 GGCAGCGAAC ATGCGTGTCG ACCCCAGCCC CCACCGCAGC CGCACACGGT GGGGCCGCCA 960 GACGCGGGCA GGTGGGGCCG GAGCCAGCCA GGAGGGTGGA GAGGAGCTGC GGCCCCCGCG 1020 CTGACCCTGA CTCGGAGCGT GCAGCTCGCC GACCGGCGCT GGGACTCCGG GCCAACGGGA 1080 AGAGGCGCCT ACCCGCGGCA TTCAGCGACC CCGGCTGACG CTCTCACCCG CGGTCCGGCC 1140 GGGACACCCA TGCCCCTCTC CACGCCAGCG GGAAAGAGCG AGGGAGGCGC 1190
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