Tag | Content |
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EnhancerAtlas ID | HS101-12004 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:28173800-28175460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr13:28174060-28174076 | TGTTTCCATGGAAACA | + | 6.11 | RFX1 | MA0509.2 | chr13:28174060-28174076 | TGTTTCCATGGAAACA | - | 6.11 | RFX2 | MA0600.2 | chr13:28174060-28174076 | TGTTTCCATGGAAACA | + | 6.39 | RFX2 | MA0600.2 | chr13:28174060-28174076 | TGTTTCCATGGAAACA | - | 6.39 | RFX5 | MA0510.2 | chr13:28174060-28174076 | TGTTTCCATGGAAACA | + | 6.07 | RFX5 | MA0510.2 | chr13:28174060-28174076 | TGTTTCCATGGAAACA | - | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr13 | 28173976 | 28174510 | chr13 | 28174612 | 28174729 | chr13 | 28174909 | 28175141 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I027599 | chr13 | 28173583 | 28174991 |
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Enhancer Sequence | GTATCTTGTA GGAATAGAAT AGCACCTGTA CTTTGGCAAC TCTTACTTTC CTGCAGATTA 60 TGTTAATGGA AGGGAAGAAT TTCAAAGGCA CCCCAAAGAG GCAAATATTT AGCAACTTTC 120 TCTCAAATCA AACTTTTACA CTTTGGATCT CAAACTCAAG AAACACACAT CTAAATATTT 180 AAACTTGTGG GTCTTGGTTA ACAATGGCAG CAAATATCAC CCAAAGAGCA TTACGCCAAT 240 CCTGAAAATC TTTTGGTTGC TGTTTCCATG GAAACAGCCT AGATGAAGAA AACCTAAGAG 300 TAAAGAATAA TACATTTTTT AAAACCACTT TATCTTGTTT TCCCCTATCA GTTAGCCAGC 360 ATGGCACATA ACTAACAGGC ACATCAGTTA TGTACCAGAA AATTCATGAC TCATTCAACA 420 AATATGTGTT GGTTATCTGC TGCATGCCAG GCACTGCACC AGAGGATAGG GTTACTCTGG 480 AGAGCTCACA GAGCTCAGTC TAGCACAAAG ACATTTACTA GCCAATGACA CAAAATGATC 540 GAGAAATTTC ACATTCTTTT GTCATATTAT GTTTTTGAAA TTTTACATGT CAAAAACAGT 600 GTACATTTTA TACTTACATC ACATTTCAGT TGGGACTAGC CACATTTCAA ACCCAATGCC 660 AACAAAAGGC TAGTGTCTTG TACTGGACAA CATGGGTACA GATATTCCAA TGGGGACGAA 720 AAGCATGCAT ATCAGGAGTA AGTCGTTTCC TCAAAGAACA TAAAATCTAA CCAGTAGATT 780 AGCCACTATA CATGCAAAAT ATATATGGTA CAGAAACATA ACCGTAGAAT TACTCAGTAG 840 GTAAAGAAAT CTGTAAGAAA CATTAATATA TAAGATACTG GGTGAGCAAC TGTGTGTAGA 900 ATTCTTTCAG CTGCAAATGA TGGAAAACCT GACTGAAAGT GGCTTAAGTG AAAAATAAGA 960 TAGGTGTTAC TGACTCGGGG CTTTCTCCCA ACTCTGCTTC CTCTAGATTG GGTTCATTCT 1020 CAGGCTTCAT GTGGCAGCTA GTTCCCAGCA GTTTTAGGGG CACAGTGTCA GACCCCTTGT 1080 TCTGCTTCCA CAATATTGCC AACAAATGCC CCAGAATTAC ATCTTCCTAT TTCTAATGGC 1140 TGGCTTGGTC ATGTACCTAT GCTGAACCAA TCACAGTAGC CAGGGACATG TGATGCTTTA 1200 ATGGGCCAGA CCTGGGTCAC TTCTGTAACA AGGCATCAAG TCAACTTCCC CAGAATCACA 1260 AAGACTAAAG TGGCTTAACA CTGATAAGCC TGATGTATGG CCTATCTTCC TTTAACCATA 1320 TTACTTGACT GCTTCACTTG ATACTCAAAC AACCCGGAAG AGTCTTATAA AGTCCATTTC 1380 CAGTGATTTA TTCCTTCATA GCTCAATTTA TTCACTATTA CTACAGGCTG GACATTATAC 1440 TGATTGCTTT ACAAGCAGTA TTTCATTTAA TCTTTCCAAC AAACCCTATG AAGTAGTTAC 1500 CATCACCATT ACCATTTTAT AGATGAGGAA AACGGGGATC CAAGGGATTA AAAACAACTA 1560 GGCTATCAGT GATTGGAATG GGATTCAAAC TCTGGTCCAT CTAATTCCAA AGTCCACGTT 1620 CAGCAGTACC TGAAATTAAG ATATTTTTAC TGTTCCCTCC 1660
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