Tag | Content |
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EnhancerAtlas ID | HS101-03216 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:172631420-172633260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid3b | MA0601.1 | chr1:172633216-172633227 | ATATTAATTAT | + | 6.02 | FOXH1 | MA0479.1 | chr1:172632154-172632165 | TGTGGATTGGG | - | 6.14 | KLF4 | MA0039.3 | chr1:172633043-172633054 | GCAGGGTGTGG | - | 6.62 | Lhx3 | MA0135.1 | chr1:172632892-172632905 | AGATAATTAATTT | - | 6.64 | NFAT5 | MA0606.1 | chr1:172631482-172631492 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:172631482-172631492 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:172631482-172631492 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_18375 | chr1:172627340-172634508 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20237 | chr1:172631268-172634391 | CD56 | SE_22718 | chr1:172627370-172634262 | CD8_primiary |
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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 |
GH01I172662 | chr1 | 172631389 | 172633630 |
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Enhancer Sequence | GTGATTTTCT CTGGGAGATA CTATTATAGA TTATTTATAC TTTCTAATTT GCTCCTTTTT 60 ACATTTTCCA TTTTTTTCCG GTTAACTAAT TAAATCTTTT ATTCATTCAC ATGTGTGAGG 120 CTAGATGTTG GGTGTTGGAT GCTGATTGAG GATGAGCCAG CCCAGGGGGC CTGTCCTTAT 180 GGAGCTTTTA GCAGGGGGAA GAAGCTAAAC AAAAGCAAGC AAACAGACCA TGCAATTCCA 240 AAGTTGTACT AAGTACAACC TGAGAATCTT CTTTAAGGAG GTGTTGTTTA CGCTAACACC 300 TTGGGGGTCA GAAGCCCGAT GAGTGAACGG CTGTGTGCAT GTGCTGTGGA GTGGGGTGGG 360 GCTGGGGGCG GGCATTTCAG CGCTGGGAAC GGCACATGCA AAAACCCTGG GGCAGGAAGC 420 ACTCATAACC AGTGTCTAGG ATATCCTTGC AATTTATTTA TTCCAGTATA GGTACAGCAG 480 ATATTCTTAG TGAGCATGTT CTGTAAGAAT AACGTTGTAC TAGGCTCTGT GAGGGATATA 540 AAGACATGCA ACATGTGGTT CTCTGTTCCG TTTCCTGCCG GTGCGTGGCT GAGTGCCAGA 600 TTAGTTGCTC GGGTGGTTTG CGGTGTAGGA ATGCAGAGGA GACTCAGTTT TGCCTTTCCT 660 GTTCGCTAAC ACCTCCTACA TGGTGGGTTG TCTTGGATGA CTAGAGAGGT CATGATTGCT 720 CAGCTAATGT TCTCTGTGGA TTGGGCCATT CTCATACCAT ATGTGAGTTT TACAGGCTAA 780 TCACGAACCT GACATAGACA AGCATCTCCT GTGAATATTT ATTGAAGTCT CAGTTAGCTG 840 AATTCATTAG CTAAGTGGCA GCTGTCTATC TTGTCTGAAA CAGTTGAAGT CAGAGAAATA 900 GTGTCTGTTT TGAGAACTAT TGTCTATCCT TCCATTTAAT TTGTCCAACA TTTGCTAGTA 960 ACATGCCCTG TGTTAGAAAC TGGGCTTCTC TGGTGAACTC AACGTATCGT AAGGAACTTG 1020 TCGTTATTTG AGGGGAATAA GATAATTTAT GTAGTTACCC CAGAGACAAG AGGAGTCAGA 1080 AATGACAAGA GAGGGGAAGA CAGAGGGATC CTAGATTTCA AAAGAGGGGC AGATCATATT 1140 TGATCAAAAA AGGCTTGAGA GGGTTTCCCA AAGAAAGCGG TAATAGGTAG TCCTTATGGG 1200 ATGTTTAGGA ATTTGACACA GAAATCTGCT TGAAAGAACA TTACGGGCAG AAGACATGGC 1260 ATGAACAAAG GCACAGAGGA AGGAAAGTGG GGGTATGTGT AGGCCACAGA ACTCCCGTTG 1320 TGTGGCAATG CTCAGTGGGA GTAAGGAGAT AAGGCTGGAC AGATGGGCTG GGATTGTGTG 1380 ATGGGGATAC TTGTATACGA CGGCATCTTC GGGGAGGAGC AATTAAAGGT GTTTGAGGAC 1440 TCAGTGATAT GAGGTGATTG TCAGAGGTCT TAAGATAATT AATTTGGGGC AGATTGTAAA 1500 ATGTCACTGG GGGAAGATCT GGTGACACGC AGACAGATCA GTAGTCTTCT TCAGCCTCTG 1560 TCCTGTAAGT CTTTGGAACA AGAGAATCAG AGTGGACAGA GCCCTGGAAT TGGCGTCAGG 1620 AGAGCAGGGT GTGGTCCCAT CTGTGATGCT GACTAGCTGG GTCTTCTTGG ATTAGTCACC 1680 CAACTTCTAA GCTCATTTTG CAATCGATAA GGTGGGACAA TAATACCTAC CTCAAAGGGT 1740 TGTGGTGAGT TCTAAATGCA ATAACTGACA TGACAGCTCT TTATGAATAA ATGTTTATAT 1800 TAATTATGTT TTATTGTAAC ATTATAATTT ATACATATGT 1840
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