Tag | Content |
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EnhancerAtlas ID | HS012-22290 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr8:11754340-11755440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr8:11754639-11754660 | TTTTTCTTTCTCTTTCTGTCC | + | 6.59 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09230 | chr8:11752974-11756738 | CD14 | SE_26133 | chr8:11753966-11756300 | Duodenum_Smooth_Muscle | SE_26664 | chr8:11754373-11755368 | Esophagus | SE_28772 | chr8:11753187-11756743 | Fetal_Intestine_Large | SE_42363 | chr8:11754182-11756283 | Lung | SE_46238 | chr8:11754152-11755841 | Osteoblasts | SE_49106 | chr8:11754216-11755643 | Right_Atrium | SE_50500 | chr8:11754129-11756424 | Sigmoid_Colon | SE_52567 | chr8:11754004-11756317 | Small_Intestine | SE_54194 | chr8:11753967-11756413 | Spleen | SE_56280 | chr8:11754449-11755859 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 11754568 | 11755261 | chr8 | 11754378 | 11755121 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I011895 | chr8 | 11753368 | 11756709 |
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Enhancer Sequence | TCTGCTTGTG GAAGTTGGTT AATTTTTCTG GTTATGATAC TGAATGTTGC TACATTTTCC 60 TTGATAGTAT AGTATCATCT GGTTGATGAT TTTGCATCTT AGCATTATAC TCCCCTTCTC 120 CCAGCAGCCA GTGCCTCTCC AGTCTTCCTC AGCCACACCG GGGCTCACTG CAACCTCCGC 180 TCAGCTGGCC CAGATGCAGC CATCTTTCAA GAAATCCAGA TCTTGAGGCA AAATTTCAGA 240 GAGCAAAACT TTCACAGGGA CTTTCAGGCA TAATTTGACC AGGTCATTCG ACCAGGTTGT 300 TTTTCTTTCT CTTTCTGTCC CCCTATCTGC GTGGTTCTTG GCCTGCTGTC AGGGCATGAT 360 TTAAGAGGGT TGTTTGCTTA CCTTGAGTGG ACGCCCCCAC AGGCCAGTTC CCTCCCCAGA 420 AGGACTTGAG GGCAGGGTGC AGGGGGGCGG GGGGAGCTGC CGAACCATGG ATGTCAGACC 480 TGTCCACGCA CAGGCAAAGA GAGGGCACAA ACTTGACAAC ACAGCGAAAC TCCACTTGTT 540 TCTTCACAAG TCTTTAGAAA GGAGCTTTCA TTTCTGTAGT TTTGCTTCCT CTCTGAATCT 600 TTGGCCTGCA CAGTGACCTC AGTGTCTCCT GACCACGGAA TCACATGCCC GTATCTACTT 660 TGGAGTTTGA GCTTTTCAAA ACTGCAACTC TTTGCCAATA GCTGGTTTGT GGGCCTGGTG 720 TCAGCAGTGG GGAACAGTCT TCCTGCCACT TTCCATTCAT GTCTACGTGA CTCCAACCTA 780 AAATAGATTT TTGGGGGAGC CCTTGATTGT AACCTTCAAC AAAGGAAGTC ATGCTAGGCA 840 GATTCTCCTG AGACAGGTCC TTACGTGCTA GTAAGAGCCT TTGGTGAGTA CTTTAGGATT 900 TACAAAGCCT CTCCAAAGAC AGACTTTGAT TTGATCCCCA CAGCAATCTC ATGGGAGGTG 960 TTTCAAGTCC ATTTTACAGA TGAGAAAATC TGCCACTGAG TGGGAGAATG GTGGGGTGGG 1020 AAGCGTGGTT GAAGAAGAGA AACAGCATTT ATTACCTTTC TGGGCCTAAC ACTGCGCTGT 1080 TCGCTTTATA TATGTTTGAT 1100
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