Tag | Content |
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EnhancerAtlas ID | HS101-09747 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:12680670-12682940 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr12:12682025-12682036 | TTTCCAGGAAA | + | 6.62 | Stat4 | MA0518.1 | chr12:12682025-12682039 | TTTCCAGGAAACTG | + | 6.5 | ZNF263 | MA0528.1 | chr12:12681098-12681119 | TCCCCCTCCCAACCTTCCTCT | - | 6.23 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_18383 | chr12:12678668-12684076 | CD4p_CD25-_Il17-_PMAstim_Th | SE_27729 | chr12:12679372-12682844 | Fetal_Intestine | SE_28607 | chr12:12679271-12682890 | Fetal_Intestine_Large |
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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 |
GH12I012526 | chr12 | 12679338 | 12682949 |
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Enhancer Sequence | AAGTGATGGC AATAATGAGA CTGCTTGAAG CAAAACTATT TAGATGATAC TAGACCTGGA 60 GACAGCAGTT ATCCGCACCG TAGAACCCAG TTGCCTCGCA CTGACATACC ACACTGTTGA 120 AAGCCGCCCC TCCAATCAGA GGTTCAGGTT GTTTACATAC ATCTCAAGGA CCCACAGATA 180 AAGGCTGGAA TAGCAGTCAG CCTTCAAAGA CTACCTATAA TGCCTGCGCT TTTAGGCACA 240 GGCCAGCCCA GGCAGAGGCC AAATCTGTGA GAAGCCTTCA CCAAAGTTTC TGTTCAGGGC 300 AAGGAGCACT CCCCTCCTGG TATTGGCTCA ATCAGAGCTC TTGTCTTTTT CTTAGTACTG 360 CTTCCTGTTT ATGATCACCT GTTTCACCCG CTTCCCCTTC CCTGACCCAC CTGAGCTCTC 420 CTCCTCCTTC CCCCTCCCAA CCTTCCTCTT TCCCTCTGCC ACCCATGTAT GTATCCTAGA 480 CACACTCCTC CTGGCCCACA GGCTCCTTCA CCTACCCCTC TACACTTAAT GCTTCCTCCA 540 GACACGCTGC CTGAAAACTC AGGACCCTAC CTACTGGGAG AGGGGCCGGT GTATGGAGGT 600 GGTCTTGGGA GGGTAGAAAT GGAAGGATCC CTGGATGAAG TTACTGGGCA AGAGGAAATA 660 CGGCCAGGGA TTGGCTTAAT CTGAGAATTG AGGAGAAAAT GTTTTAGAAG GGTATTTTCA 720 GTAAAGGTAG GCTGGAGGCA GGAGAAGAAA GATTTAGAAC AAGCCAAACA GAGGTCAGAT 780 GGGGATTAAT TCGTGCATCC TGGTTTTCTT GAACATCTGC CAAATCACTA TAATTCATCA 840 GGCCTACTGT AACTAATTCA GTCAACTAAC AAGTACTTAT TTGGCACCTA ATATGTGCCA 900 GGCACTGTGA AAATGTAGCA ATAAATGAAA AAAGTATTCA TTATAATTTA TAAGTTATTA 960 ATGTACTGCC TGGTTATAAA TTAACAAGGC AAAAATTACT GCCTTTCTGG AGCTTCTAAT 1020 TTAGTGATGG GGGACACGAT CAACAACAAA AACAAAACAT TTCCTATGAT AGACGCCGAT 1080 AAGAACTAGG GAGAAAAAAT AGAGCAAGAG CAAAGGGTGT GCGGGGGTGG CTGTTAAATT 1140 GTAAACAGAG TAGTCACAGA AGGCCTTACC TTGAGAACAT GAGAGAGGAG AGTGGTAAGA 1200 GACTGAGCTA TGTGGATACC TGGAAGATTG TAGCTTTCTG GGGCCAATGA ATATACTAGC 1260 CAAGATAATG CTGAATTGGG CAAATACCAA TAAAAGATGT GGCAGGTGTT CATGCTTTGT 1320 TCAGAACTAT GGTTATATCT ATTGGAAATG ATGCATTTCC AGGAAACTGA ACTTTTGTTT 1380 TTGTTGTTTT TTGAGACAGG GTCTTGCTCT GTCACCCAAG GCTGGAATGC AGTGCTATGA 1440 TCTCAGTTTA CTGCAACCTT CAACTCCTGG GCTCAAGTGA TCCTCCCACT TCAGTCTCCC 1500 AAGTAACTGG GACCACAGGC ATGTGCCACC ACACCTGGCT AATTTTTATT TCTTGTAGAG 1560 ACGGGGTCTC ACTGTGTTGC TTAGTCTGGT CTCAAACTCC TGGGCTCAAA CAATTCTCAT 1620 ACATTGGCCT CCAAAAGTGC TGGGATTACA GGCGTGAGCC ACTGTGCCCG GCCAAACTTT 1680 TTAAATTAAT GGATAAAACT GTATGTATTT ATCATGTACA ACACGATATT CTGAAGTAGA 1740 TATACACTGT GGAATGGTTA ATTCTACTAA CAAGTGCATT ACCACACATA GCCATCATTG 1800 TTGTGATGAG AACACTTAAC ATCCACTCCT TGAATTTTTC AGGAATACTA TATATCCTCG 1860 TTAACTGTGG TCACCATGCT GTACAATAGA TCCTTGAACG TATTTCTCCT AAATAATTAT 1920 TTACTTTCAC CAACATCTCC CCAGGCTTCC CCTCCCCATT AAACATCCCA GCCTTTGGTA 1980 ACCATTCTAC TCTCTACTTC CATGAGATCA ACTTTTTCAG CTCCCATATA TGAGTGAAAT 2040 TACACAGTAT TTGTCTTCCT GTGTCTTGTT TATTTCACTT AACACAATGT CCTCCAGGTT 2100 CATCCATGTT GTAGAAAATG ACAGGATTTC CTTATTTTTT AAGGCTGAAT AGAATTTCAT 2160 TGTGTACATA TATACCACGT TTTCTTTATT CATTCATATT TTGATAGACG CTTAGGTTGA 2220 TTCCTTATCT TGGCTATTGT AAATAGCACT GCAATAAACA TGGGTATGCA 2270
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