Tag | Content |
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EnhancerAtlas ID | HS180-47823 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr8:103809650-103810560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr8:103809995-103810006 | TGTTGTGCAAT | - | 6.14 | PRDM1 | MA0508.2 | chr8:103809795-103809805 | GTGAAAGTGA | - | 6.02 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_27892 | chr8:103808914-103811281 | Fetal_Intestine | SE_28869 | chr8:103808952-103811449 | Fetal_Intestine_Large | SE_35476 | chr8:103809034-103810665 | HepG2 | SE_40837 | chr8:103809672-103810545 | Left_Ventricle | SE_47342 | chr8:103810357-103812039 | Panc1 | SE_47635 | chr8:103809725-103810357 | Pancreas | SE_48146 | chr8:103809623-103811065 | Psoas_Muscle | SE_48645 | chr8:103809677-103810355 | Right_Atrium | SE_51194 | chr8:103806096-103810653 | Skeletal_Muscle | SE_62939 | chr8:103793900-103843923 | Tonsil | SE_68638 | chr8:103800188-103823262 | TC71 |
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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 |
GH08I102796 | chr8 | 103809086 | 103811083 |
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Enhancer Sequence | GGCTGAGGCA GGAGAATCGC TTGAACCCAG GAGGCAGAGG TTGCAGTGAA CTGAGATCAT 60 GCCACTGCAC TCCAGCCTGG GCGACAAGAG TGAAACTCCA TCTAAAAAAC AAAAAAAACA 120 GAAACAAAAA CAAAAAAAGT GCCAAGTGAA AGTGAAGACA CAGCCACGTG GAGAGAAAGC 180 CATGTGCAGA GGGTGCCGTG ATGCAGCTGG AAACCAAGGA ACGCCAATGA TTGCCCTCCA 240 GGAACAGGTG AGGAAAGCAG AAGGAGCCCT GCTGCCACCT GGACTTCAGA TCTCTAGCCT 300 CCAGAACCGT GAGAGAATGA ATTGCTGTTA TTTTGTCCGG TGCTTTGTTG TGCAATCCTA 360 GGAAACTAAT CTACTATATG TTCCCTGGTG TGGTGTCAGC TGAGCCCGAA AACCTAAGGT 420 ACAAAGGACA GTTCTTGCTC CCTCTCAGAA AGGCATCCAG TCCAGCCTGC TAATCTGTTT 480 TCCCTGGGAA CATTTCTTGC TTCTGGTCAC AGGAGCAAGA GCCCAGTAAG GGTCCATCAG 540 AGGCCTGTCA TCCATTAGGG CAGGGTCTGG TTTAATGCTT TCTTCAGGGC CACATCTCAC 600 GTGGTAAGAG GAACACACAA AAAATCAACG TAGTGTTTTT CTTCAAACTC TTGGATTTTG 660 GCCAGCTGCA GTGGCTCACA CCTGTAATCA CAGCAGTTTG GGAGGCTGAG GCAGGCAGAT 720 TACTTGAGGC CAGGAGTCCA AGACCAACAT GTTGAAACCC CATCTCTACT AAAAATACAA 780 AAATTAGCTG AGCATGGTGG CACATGCCTG TAATCCCAGC TACTCAGAAG GCTGGGGCAT 840 AAGAATCACT TGAACCCGGG CGGCAGAAGT TTCAGTTGCA GTGAAAGGGC AAGACTCTGT 900 CTCCAAAAAA 910
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