Tag | Content |
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EnhancerAtlas ID | HS101-30252 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:107968970-107970510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr3:107969330-107969341 | GACCAATCAGA | + | 6.14 | NFYB | MA0502.1 | chr3:107969325-107969340 | ATATTGACCAATCAG | + | 6.78 | SREBF2 | MA0596.1 | chr3:107969858-107969868 | ATCACCCCAT | - | 6.02 | Stat6 | MA0520.1 | chr3:107969437-107969452 | TGTTCTCTGGAACTG | - | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 107969267 | 107969929 | chr3 | 107970116 | 107970472 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I108250 | chr3 | 107968901 | 107970993 |
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Enhancer Sequence | AGGTAGCTTA GTGCCTCTCA AAAGTAAGTG GGTCTAGTTG TTCAATTGGC CACTGCCCTG 60 CCTCTAGGAT CCCTGAAAGG GACCAGATGG ACCTGAAGCA GGTAGCCAAC TACTTCTGCA 120 CTGTCGTACA ATGCAATGTG GTCCACCAAC AGATTTACGC CAGTTCTTCA AGATGGATCC 180 TGAGTGGCTA ACTGGGACTC CATTTAAAAT AGAGCAAAGC AGCCATTTGT TGAGTAGGGG 240 TGACATACAT GCCCTGAGTT CCAGGAAAGC CTGCAGCATT TAACTTTGAG GCTTTCAGGA 300 TTCACCTGAA CCAGTCAATT AAAGCTCACC CGAGTTGGCT AATCAGGGCT CAGCTATATT 360 GACCAATCAG AACTAAGTCA GTTTCAAGTT TCAACACTAC ATTTGCGTAG ACAGTCTTGA 420 TTTGGAACCT GGGTGGAAAC TTTTGCTATA AGACCTGGGG TTCTGTTTGT TCTCTGGAAC 480 TGGTAATGTT GTTAACTCTT TATGCCTTTA CCTATAACCA GATAAAAACA ACATCTGAAA 540 TGTAACTCTG ACACCAGGGC ACTAAACAAT TTCATTCCTC TGACCAAGGT CTACCCCGCT 600 AATCAGCAGG AAGTGGCTAA AGTAGTCATA GCTCGTATTC CCTCAAGATT GAGGAATGGA 660 TATAAAAAAG GGAGGGATGT GTAGCTGCAC CAGACCAGTC TGGTTCAACT TTTATGTAAC 720 AATGTTGTAA GTTGTTTTTC AGTTGCCATG GACCCTTAGG TCAATCAACC TGAGCAGGCC 780 CAGATGAACC AAGTATGTAA CCACAGGAGG AACCTCTAAG TACTTGGACC AAGGAGTGGG 840 AACTAAATAA ATAAGCAGAT CCAGGATCCA AACAGATCAA GCTTTTGCAT CACCCCATGG 900 CAGGATCCAG TCAGATCATA CCCCCTGGCA TCACCTCATT ACAAGATCCA ATCAGGTCAC 960 AGCTCATTAC CCTATGCTTA TAAAACCTGA TCCAGCCCCC AGCTTGGGGA AACACTGCTT 1020 TGGGAACTAA TGCCCAGTGT TCTCCTTACT TGTTACAAGT AATAAAATCC CCTTATTAAA 1080 TCCTCCTTGG TTGTGGTCAT CGGACTGATA CCCCCTAAAC GACCGAACCT ACTCATTGTG 1140 TGGGTAACAT GCCTAGTTGA GTTTCTCGTT TTTACACCTT GTCCTAGAAT CTGTTTAATA 1200 ATCACTTATC AGGTATAACA TAGAGAACAC AGGAAACAGT TGCTTGCTAA GTAATTGTTT 1260 TGATTCTCTC TCCTTCATGA CAGCTAGCAT TTAAGAACTT ATTATGTGTG AGGCGTAGTG 1320 CCAAGGTTCG AAGTACAGTG TTTTATATAT CTGATTTAGA TATTACCTTG CTTAAGCCTT 1380 AAAAGAGATC TCGTGCTTTG TAGATGAGGA CACTGAAGCT CAGATTGCCC AAGGTCACAC 1440 AGCTGGTATG TGGTGGGATG TATTTGACAC AAGGTCTCTA ATGACAAAGC CATAATCTTT 1500 CTACTACAAA GTGAACATTA CCATACTTCT CCCATACCAC 1540
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