Tag | Content |
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EnhancerAtlas ID | HS050-40864 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr2:242436090-242437030 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE41 | MA0636.1 | chr2:242436700-242436710 | GTCACGTGAC | + | 6.02 | BHLHE41 | MA0636.1 | chr2:242436700-242436710 | GTCACGTGAC | - | 6.02 | MITF | MA0620.2 | chr2:242436696-242436714 | CAGGGTCACGTGACTAAC | + | 6.7 | MITF | MA0620.2 | chr2:242436696-242436714 | CAGGGTCACGTGACTAAC | - | 6.7 | USF1 | MA0093.2 | chr2:242436699-242436710 | GGTCACGTGAC | - | 6.14 | USF2 | MA0526.2 | chr2:242436698-242436714 | GGGTCACGTGACTAAC | - | 6.21 | USF2 | MA0526.2 | chr2:242436696-242436712 | CAGGGTCACGTGACTA | + | 6.66 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAAGTGAGGT GGCCCAAGGA AGCCTCTGCC CCTGCCCTGC CAACGGGGAC CCTAGTGGTC 60 CTTCCCCACA GCACCTACCT TCCCCCTACA CTCCGGGGAA TCTCGGACCT CGGTTCTCAG 120 GAGGGGACCA GATGGCTTCC TCCCAGCCGA GGGTCATGGA AGCCACTCAA TGGGTCTAAT 180 CAGACCCAAA AACACGAAGC CCAGAAACCC CCAAAGCACA CGGCACCGCC AGGCCCAGAT 240 CTGACCTCCA TCAGGACACC AGCATCTGAG CCTCCTGTCA CCGGGTGTCA CCCACCCTCG 300 GGGGGCTGTG GCTGGATCAG CAGGCTGCCC AGGACCTGGA CCCGAGTGGC TGCTTCCCGC 360 TGGGGCCTCC ACATGGGCTG GGGCCAACGT CCCTCGACCG TGCTCCTCCC TTTGCCGTCC 420 TCAGGCAGGC CCTGCCTTCA CCACCTCTCA CCCACATCCT CCATCCTCCC TCCCCAGGCT 480 CCAGGTGGGG CTCCTGGAGG GCACACCTGG GCCCAAGCCC GCTGGCCACG CCCTGGGCAC 540 ACAGATCCTG GCTGTATCAC ATTTCTGAGG ACGGTGCTGA CTGCCCATCA GCAGGTGACG 600 TTGATGCAGG GTCACGTGAC TAACCAGGGC GGCACCTGCC CGGGGATGGA CCCCGACTAA 660 ACCTTCTCTG CTTTCTCTAT AGAAGGATCA TCTGTGTTTG CACCTGAAGA AAAAAAAGTC 720 ACCCTAGGAA CCCAGAGAAC CTTGGCAGGT CTGGGAGTAC AAAAGGAGTC ATTGCAGCAG 780 ATTCTGCTCC TTCCACTCAG AAAACCCAGC CCACAATCAG CTGCAGGAAA GCTAGAAGCT 840 GAAACCACCC CACAGTGCTG TGAGGGAGAC ATCTCCGTGC AACAGTGTCA CAGCCTTGTC 900 CTTGACGGGA CTCCAGGCCC AGTCCCAGCC CCATCCTCAC 940
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