Tag | Content |
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EnhancerAtlas ID | HS118-10012 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr2:68342590-68344070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYB | MA0100.3 | chr2:68343234-68343244 | ACCAACTGTC | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAAGGCATAA AAAGGTTAAG GAACTTCCTC AATTGGCTAG GAAGGGGTAG AATTAGGATT 60 TTAACTCAGG CATTCTGGGC TCCAGAGCCC AGACTTAATT ACTACACTAC ACAGCTTCTT 120 AATGCATCTT TGATAAATAT CAATTGATTC AACATACAGA ATTGCAGAGT TACACCAAAC 180 CTAAAGCAGT AGGTGGTAAC CTCTAGGGAG TCACTCTGAT CATCTGAAAG GTTTTGTACC 240 CTTCTAGAAA GTGCATGTGC ACACACACAC ACCACATGCA CACCACACGC ACCCCTGACA 300 GAAAGAAGAG TGGTAACCAG AAGCCCTGAT TCTGGGGCTG CTTTGCTATC TTCACCCTAA 360 ACTTCAGTCC TTTGTTATGA TTAGGTATGG GGAAAAGTAT GAGAAAGATG TTGTCTCCAC 420 TCTCCAAAAG TTTGACCTCA GAGTAAGGCT AGAAGCTGAC ATGAGCAGCA AACAAATTGG 480 TTTTCAATGC CTCCTGCCTC CTTATTCTGT AGCATTCATG GGGCAGTGAG CATTCACCAC 540 GTCTGCCTGC CCAGCATCCA CTTCCCTCAC TCTCATGACA GTGCTTTGAT TTCCATTTGG 600 GGGACCACCA CTCCCCCATT GCATGCAACA ATATTGGACA GTCAACCAAC TGTCCACCCT 660 CCTCTGGCCA AAGAGTAAGT ACATGACCCA CATGAGCCAG CTGGACTCTG CCCTGGGAAT 720 TTGAGCAATA CAAGGAGGAA ATTCAGTTGG AGGCAATTCA AAGACTTAGA GCATGAGTGC 780 CCATCTGCCA CACCAAACCC CTGAGCTCCT TTGCTTTCTT TCCTGTCCGA AACCTGATTC 840 TTGAGCTTTC CCCTCAGTTC CACATGCTAC CTGAGTTGGC TTTATAAATG CCAACCTGGC 900 GAGGCTGAAT TACATTTCCC AGAATTCGCT TTCCTGTATG TTTCCAGTTA GGGTGGGCCA 960 TGTAGAAGCT CCTGGAGTGA GATTTGCAGG GTGGAAGTGA AGCAGCACCA GTTTTTGTAG 1020 CTTGCACACA TTGTCACTTT CCGCTGGCTC ACCGCGTCAG CAGGAGGCAG GGGCTGGGCC 1080 TGTAGCTGCT CTACCCTTCC CAGGATCCTC CTTCAGCTTT CCCGACTTCT GAGCCAGACA 1140 GGTCTGCTTA GCACTGTGAT GAAGTATCCT GACTTCTGCA GGAGACCCAT GCCACCCAAA 1200 TCAGAGGCAC GGTTTCCGTC CCTCCTCATG GTCTCCAGCG GGTGGTTTCC AGCTTTTTCT 1260 TGTTCACCCC CACCTTACAC CCATCTCCCT GGCCCAGCTG CCTGCCCTGT GGACTGCAAG 1320 CTTCAGCATC AGACCTGAGG GCAAGAGCCT TACAGAGACT GTGTCAGCAG CTCCCATGGG 1380 TAGGTAAGAT CAAATCCTGG TAAGAAATCC CTAGTGCTGA TTCCTGTTAC GGCTGCTTCC 1440 TGGAAGGCAG TGTCACGTGG AACCTCTAAA TTGCAGCATT 1480
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