Tag | Content |
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EnhancerAtlas ID | HS101-01196 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:38220800-38221870 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:38221247-38221258 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr1:38221247-38221258 | CTGAGTCACCC | - | 6.02 |
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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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Enhancer Sequence | GGCTAGGAGA GGTGAAGTTG CCTACAGCTA CTCTCCCGCA GCCTGTGGGA TCCCAACCCA 60 AGCCCACATC ACACCACCCT CAGGACCACT GGAAGAAAAT AAGTCAAACT CTGCAGTGCT 120 GGTGTGAGAA AGAGAGGGGA GGAGAGGTGC CCCAAGAGCT GTTCCACAGT TACGCAGGGA 180 CAGACACACA AGCATACATG CACACACACA CACACACCCT CCCACCACCA CCATCATGTG 240 AGTGAGTGTG TCATAAATTC CCAACTGGAA GTAAAGCCAG CCAGGTGGAG GGGGGTGGGT 300 GGAGAGAAAA GGGCCAGTAA AAGTTCCCTG GACCATGAGT CAGACCTGGT TCCAGTCTTG 360 ACACCTACTC AGTTTGCTTC TCTCACTTCT CAGAACACAG GTTGTTAAGA TCACAAGTGT 420 TTCTATCTGA ACAACCTGGG TTTGTAGCTG AGTCACCCCA CTTATTTGCT GTGTGGCCTT 480 GAGCACATCA GTTGACCCCT CTGAGCCTTG TGTTGAATAC CTACCTCAAA AAGGTTGTTG 540 GAGGATTGAG ATAAAACATG TAAACCACCT AGCCCAGTAC CAACCACATT TTCACAATAA 600 TGATAGTAAT TACTGTTCCT CCCCCACAGG CCTTAAGTGG TAACTGCTAA ACACCCACTT 660 TAAAAAAATT TCTCACCAGC TGGGCCAGTT GGTTCCTGGC CCTACCTCTC AGAACTTGGG 720 TGGTCCTCAC CTTGTTCCCT GGCCCTCTCC TCTAGTTTAG CTGGCTGCTC TCCAGCTCCA 780 AGAAGACGCA GTACAACAGA AAGGGTGCAG ACTAGCCCTC AGGAGGAACT TTCAGCCTGT 840 GTGGCAGAAG AGGGGAGGGG ACTAGGATTT CCACTGTCTG GAAGGCATAG GTTTGAGAGG 900 GTCCATCTTG CCCAGAGTTC TGGGCAGCAC AACTCTGGGG AGGGGCTCGG CAGCCCAGGA 960 GCCTTCAGAA GTCTCCTCTG CCTGCAGAAC AGAGCATGGG CCAACTATCC CCGTGGTCTG 1020 GTGGGCAGCA GAGACCCAGG CTGGGACTTG GAAAGCTTGG GTTCTAGTGT 1070
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