Tag | Content |
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EnhancerAtlas ID | HS180-00779 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:23157770-23159440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:23157853-23157874 | TAGCAGAAAGTGAAAGCATTT | - | 6.19 | IRF2 | MA0051.1 | chr1:23157857-23157875 | AGAAAGTGAAAGCATTTT | + | 6.29 | TBX21 | MA0690.1 | chr1:23158262-23158272 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:23158262-23158273 | AAGGTGTGAAA | + | 6.62 |
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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 |
GH01I022824 | chr1 | 23151232 | 23159621 |
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Enhancer Sequence | TTCAGGTCCT GGGAGGTAAG TGAGCACCAG ATACAAACCC AGAACTGGGA TGGGGAGTGG 60 CTGCCCCTTG CTACCTCCCC CCTTAGCAGA AAGTGAAAGC ATTTTGCACA AAAACTCAGC 120 TGTAGGCATT GTGTAATAGC ATTGATCTAT CCAAAAATAT TGAGTGCCTA CTGTGTGCCA 180 GGCAGCCTGT GAAGCCTTTT GCGTGAATCC TCTCATTTCA ACCCAGGAAC CCTTACAAGT 240 CAGTCTACTA TTATTTCCAT TTTATGGATG AAGAAACTGA GGCTCAAGGA GCCTGAGTGG 300 TTTGCCTAAG GTCAAGCAGA GCAGGGCAGG AATCCAGGGC TTTCCAAATT CAGAGCCTTA 360 ACACCATGCC ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA TTATAAGGGG 420 AGGGCCAAAA TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA TGCTGACCTG 480 GGCTTCCTCA GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC AAGGGCTCAA 540 GAGGGGCTGT GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT TCCAGAGGGA 600 GCTATCCACC CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG ATTCTCTGCC 660 CCACATAAAC CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG GAAGAATTGG 720 GCTTCCCCAG GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT GCAGTCCAGG 780 AGGACCTTCG AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG GAGAGCCAGA 840 AAGTAGGGAC AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG AACAGGGTGC 900 ACGTCATCAG AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG CATGGCCCTG 960 GGTGAGTCAT GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG GCAAACCAAT 1020 GCCACCTCTC AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA TGGTGGCTGT 1080 TGCCAATGCT ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT TGCAAGCCAC 1140 ATTCATCCTT TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA GGATTCTTAC 1200 CAGAGAGGTT AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC CTGGGATGCA 1260 CCCCTAGTGA TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC TTCTTCAGTC 1320 TGGGTGGTTG CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC CAGGAATCCC 1380 TCCCTGACCA CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA CCTTTGAGAC 1440 ATTTATCAGA GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC CTAAGACTTT 1500 GAGGGTTCAG CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA TTTTGTTAAT 1560 GACTACAGCA CCTGTACAAA GGGACAGATA GGTGTCCACA GACTCACATG TATAAGTAAC 1620 AGTCATGCAT GCACAGCCAT GCACATGTGG CTTAGTGAAT ACACATGTAT 1670
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