Tag | Content |
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EnhancerAtlas ID | HS193-08039 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr12:64646090-64647550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF8 | MA0652.1 | chr12:64647319-64647333 | TTGAAACTGAAAGT | + | 6.45 | SRF | MA0083.3 | chr12:64647080-64647096 | TGTCCAAATAAGGACA | + | 6.06 |
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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 |
GH12I064252 | chr12 | 64646173 | 64647208 |
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Enhancer Sequence | CTCTGGGGCA GAGAGATCTC TGAAAATCAT ATGAAACCTC CTAAACCTTC TGACAGATAA 60 CTTAAAATAT CTTAAAAGAC ATTTTCCCCA CACCGAGCGC CCATGCCTGG GACAAATTAT 120 ACATTTTCCC CTCTTCCTTC CTTGCCCATT TTGACAAGTT GCCCCAGCTG GGGCTTAATA 180 GATATTAAGT AGTGCTAATA ATAGTCATCC TCTGAAGGAA TGAGGACTTG AGATTGCCAA 240 GATGATCTTT TTTGCTCCAA CACACCAATC TCAGCATATT TCAGTTTGTG TGCCACTTTC 300 GTTCTTGGAT ATGGTCCAAC ACACACACAC ACGTACACAC ACTTTCTCTC AAAACACTTT 360 ATATATTTTT TAGAGAAAAT ATTTCTCAAT CTCCTTAAAA ATCATTATTT CATTCCATCT 420 TTTCATCATT GTTAACACTA AACCATTTGG AGTCACGTTG GCAACTGGAT TTCATCTTGA 480 GACTTGTCAT TGAGGAATCA TTTTGTTGTG TAGCAATCCC TATTCACAAC ATCAGCCAAA 540 TTATGTCATG TGGTTGCAAA ACTGCTGTCC TGTCTTCCAG CTTTTCTGAG TAAATTTGAC 600 TCTTTGAGAA GCTTCGTTCT TCCTATCCTA AAATGACCTT ATATGCTCTC GTATCTCAGG 660 GGATCCTAAT TGTGATGAAA TCTTTCTCTT TATTTCCTTT CTTATAGCCT GTGTTTTGAG 720 GTGGTGTTTT AGGGGTGTGG GGAGTAGGGG AACTACTGAG GTCTGAGTCA CAAAAGGAGA 780 TCTGAACAAG ATATCTGAAG TTCAGTTGGG CCCTCAAAGC TTCACTCGTA TTGGACTAGA 840 TATGCTTCCT GAGAGAAGTC TCTAAAAGTT CTGTAAATGA CACTGACCCT TTTGTTTCCT 900 AACTCCTACT GTTAAGGCAC AGGTTCTTTA CTGATCTTAA AACCCTAGGC CAGGATGGCT 960 GTAACCAGGG TGTATAACCT TATGTTTTAT TGTCCAAATA AGGACACATT TTAACATTTC 1020 AATAGTTTGG GGGTACAGGT GGTTTTTGGT TACATGGATG AGTTCCTTAG TGGTGAATTT 1080 TGAGATTTTA GTGCACCTGT CCCCCAAACA GTGTACATTG TACTCAATAT GTAGTCTTTT 1140 ATCCCTCCCC CCGTCCAACC ACCCCCCTAC CCCATCCCCA AAGTCCATTA GATCACTCTG 1200 TATGTCTTTG TGTCCAAATG AGGACACTTT TGAAACTGAA AGTGGGTGCT GGGGGTAAAA 1260 GACATAAGCC AGGGCCCACA CAGGCAAACC ATGCTGTCAG GTCAGCATAC CTAAAACACT 1320 TTGAGCCTCT TATCCTCTAT TAGCAGAGGT TAAGTTGGGG TCTCTAGATT TCTTTTTTTC 1380 TTTTTTTTTT TTTTTCATTG TTGTTGTTGT TGTTGGGATA AGGTCTTGTT CTGTTCACCC 1440 AGGCTGGACT GCAGTGGCAC 1460
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