Tag | Content |
---|
EnhancerAtlas ID | HS101-31166 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr3:160866180-160868590 | Target genes | | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr3:160866224-160866238 | TTCCTTTGATCTCT | - | 7.42 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 160868054 | 160868232 | chr3 | 160866736 | 160866980 |
| Enhancer Sequence | ATTGTTTTTG TGTATTTTTC TGAAATGTAG ACTGACCCTG CTTATTCCTT TGATCTCTGC 60 CAGCTGCGTA GAAGAAACGA GGGATGGGTA ATGTAAAAAT CTGTATCAGT ATTCTAACTC 120 TGAGCATATA TTGAAATTGG CTAGCAACCC CATATCAGCT TGGTGCCCAA TTCATGGAAA 180 GCCTTCTCAT TTAGTTTACT TGGGATACTT ATTTTATTTA CTGTTGTTGA GTATATTGCT 240 GTCGTACTCT TTAAGTAAGA ATGCAAGATA AGCTTACTCA ACATTTTCTA TAATTGAACA 300 CTTATTGTCT TCCAGATATT TCCTTTTGTC AGGACCCAGA GTTATGAATG GCCATCACTA 360 TACTGATGCT TCCTGACTGA GCTCCTTTCT ACCCTAAATA CAAGAGAACC TAAGAGTTAG 420 GCAGGAATAT TATCACCTCT ACACAGCCCA AAGAAGCTAT AGAAAAATGA ATTTTTGTCC 480 TTCTGCAACT CTTAGGATTA AGTATCCCCT TGGAAAAGGG AGGGGAGAAT ATGTCAGTGG 540 TGTTTAATCC AGAGCAACCC CTTCTTGAAT AGGGGATGGG TAAAATACGG CTGAGACCTG 600 CTGGACTGCC TTTCTATGAG GTTAGGCATT CTTAGTCAAA GGATATTTGT GGTTAAGGGA 660 ACAGATTAAT AATGTTTACT GAACAGACCC AGGACTTAAC AGACCCAGGA AATGTCCTGA 720 TGTTACAATA TCTTAAGAAC AAAAGCATTC TTAGTTTAAG AATAAGTTTT GCTTTAAAAT 780 AATAATATAC ATTCTTGTGG AAGACAGTAG TTACACAAAG ATTAACCATT CTTTGTCACA 840 AGCCCTTGTA GTAGAGTATA TCTCATCATT TTTTGTTTTA TTATCTTGTA AACAAGCATT 900 GTACCTAAAG TGGACATGTT CTTCCTCTTG CTTTCAGGAC TGCCCCGCTC TATCTATGGA 960 GTAGCTATAC TTCTATTCCT TTACTTTCTT AATAAACTTG CTTATACTTT ACTCTGTGGA 1020 CTCACCCTGA ATTCTTTCTT GCGTGAGAGC CAAGAACCTT CTTTCGGGGT CTGGATCAGG 1080 ACCCCTTTCT GGAAACAAAA TGAGTAGTAC TTTTTTTTTT TTTACAGCTT TATTGAAGTA 1140 TAATTGATAT AAAATAAAAA ACTGTGCATG TTTAGTATGT ACAATTTGGT GAGTCTGACA 1200 TTTGCATGTG CATGTGGTTT TGGAGAGGGA TGAAAATGGG TGGTAGGGCA AAGGTTTCTA 1260 TTCACCCAGC TCACTTTATT TATTTTTCTT ACCCTCCTAG ATACTGTAGA TATTTCAGTT 1320 TGTGGTCCCT GCTGTTGAGC AATCTGAGCT CTGTGAGATA TGCAGATAAT GTCTCCAGAG 1380 AGCCATTAGC ATGGGTCTTC AGCCATGCCT CCCCATCCAT GCCACGAGGG AATTGTTTAA 1440 AGTCATTTTG TTCCTGATTA GCTGCCTCAC TCATTATCTT CCTGTTCCTG GAATTTGTGG 1500 CACAAAGAAC AATGTATAGC CAATCAGTAG CTAATACTAT TTTAATGTAA ATTCTTAATA 1560 AACAACTTAG GAACTGCCTC TTCTTTTTCT TTAAAAACCT ACTTTTTATC TGTTGCTACT 1620 CTGAGTGTAT ATTCAGGGCA ACTTGAATCT ATGTTGCTAG TTGCAATCCT CAAGCTTGTC 1680 CAAAATAAAC TCTCTATATT AGTTTGGTCT CAGCTTCTTC CTCTTAGATG GACACTGTAC 1740 ACCCAAGTCA AATCCATTTT CCTCAAAGTC CCTTGGAACC CTACTTGGGT TACCATCCTA 1800 GCTGTAGCTC TGACCCAGCA ATTCCCTTAA ATTAACCTTG GCACTGGCAC AGTGCTCAGG 1860 ACCTTTTCCA TAAGGGGCTT GCTCCTCTGA CTCACCCCTC CTCATCAATT CTTTTCTCCA 1920 GGGAAATCTT CCTAAGAACT GGCTGCATTA TAGAACCAGA CTGGAATCCA CTCATCTGGC 1980 ACAGTAAAAC CAGATATCTA CACCAAGGTT TTTGCAGCAG TAGAAAGGCA TTTATTTGCA 2040 GGGTGCCAAG CAAGGAGGAC CAGGAAGCTA AATGCTCAAA TCCTGACCTC CTTGATGACT 2100 TGCAAGCAAG AGTTTTTAAA GGTAGGAGTA AATCTCAGGA TATCAGAAGC TACATGCAAA 2160 ATTATACATC AATACAAGAA GGTTTTAGCT TTATAAGGGT AGAATATCTT GGAGTGGGGG 2220 CCTGGAGGGT GACTTATAGG TCATAGGTAG ATTCAAAGAT TTTCTGATTT GTAATTGGTT 2280 AAGGAAGTGA AGCTTTGTTT AAAAATCTGG AGTCAGGGCC GGGCACAGTG GCTCACACCT 2340 GTAATCCCAG CAATTTGGGA GGCTGAGGCA GGCAGATCAT GAGGTCATAA AATCGAGACC 2400 ATCCTGGCCA 2410
|
| |
|
|
|