Tag | Content |
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EnhancerAtlas ID | HS101-23228 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:28931600-28932770 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr2:28932137-28932149 | ACAAAGTAAACA | - | 6.18 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I028705 | chr2 | 28928308 | 28934662 |
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Enhancer Sequence | CGAGATTGCA CCATTGCACT CCAACCTGGG CGACAGAGTG AGACCTTGTC TCAAAAAAAG 60 AAAAGAGAAA ACAGGAACAG GAACAGAGAA ATCTGGATTT CAGTCCTACT TCTTCCCTTA 120 TATGCTGTGT GATCTTGGAC AAGGCACTTC CCATCTCTGA CCTTCAGTTT TTTCCATCTG 180 TAGGTAATCT CTATGGTACC TTCAAATTCT ACCAGAATAT TTTTAACTAA AATAGCATCA 240 TAGCTACGCT TCGCATTTTT GCTTTTGCTT TTCTTCTCAC AGTCACATAA TCAACCAAGA 300 GAATGAGGCA AGGAGTTGTG GTTGCTGCTG AACACACACA TTTATCTAGA GGGCAAATGT 360 AGACTTTGGT TTAAATTCTT CTGATGAAAC TGTGTCTCAC ACCCAAATCC CAAGTTCAAC 420 GGACTGCTCT TGAGATGCCA GCCGTGGCGG CCTTGCTAGG GAGGAGGCCC ATGATGGCCT 480 GTGTCTGAGT CTGTTTCATT GCAACACTCC CAGAAAGCCA GCCCTGTCAT TAAGCTCACA 540 AAGTAAACAC TGTCCTCAGC AAAAGCCTGA GTTAGCAGTC ACCTAAAGGC AACTGTGCTC 600 CTTTAAGGGG AGAGCTTTCA CCATTCATTG CTCCACCAGT GCCGGCCTTA AAACTTGAAA 660 TCAAACGCAG GGCTCCCAAG GCGCTGGCCT TTCATCCAAA ACCACCGAAG GCTGTGGGCA 720 GGATTCAGAA TTATGTTTCA CCAGCTGGTC CAGGCCGCAG TTTGTCTGGG GAGAGAAACA 780 GACACAGGGA ACAAAGAGAT GGAGGTGGGA AGGTGGTAAG AAAAGGGCCT TTCTGCTGTT 840 ATTGCCACAG AGCTATGGGT GGTATTAACG TAATCAGAAT ATTTTACCCA GAAGTCCAGA 900 ACGTAGAAGT ATCAATAAGC ATTTCTTGCC CCAAACATTT ATTGTAGGCA TATCAAGTTT 960 TTACCATGTC ATTTTGGTCT TTTTTTTTTG AGACAGAGTC TTGCTCTGTC ACCCAGGCTG 1020 GAGTGCAATG GCACAATCCC AGCTCACTGC AACCTTCACC TCCCAGGTTC AAGAGATTCT 1080 TCTGCCTCAG CCTCCTGAGT AGCTGAGATT ACAGGCACCC ACCACCACAC CTGGCTAATT 1140 TTTGTTTTTT TGTTGTTGTT TTTTGTTTTT 1170
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