Tag | Content |
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EnhancerAtlas ID | HS053-00173 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:8257580-8258530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr1:8258010-8258021 | TCTTATCTCCC | + | 6.62 | HES2 | MA0616.2 | chr1:8257655-8257665 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:8257655-8257665 | GGCACGTGCC | - | 6.02 | NFE2L1 | MA0089.2 | chr1:8257947-8257962 | AGTGCTGAGTCATGC | - | 7.27 | Nfe2l2 | MA0150.2 | chr1:8257949-8257964 | TGCTGAGTCATGCAC | - | 6.66 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_02150 | chr1:8257513-8259183 | Aorta | SE_33918 | chr1:8257041-8259053 | HCC1954 | SE_34231 | chr1:8248874-8265404 | HCT-116 | SE_34786 | chr1:8256055-8259168 | HeLa | SE_47106 | chr1:8252219-8265565 | Panc1 | SE_54787 | chr1:8257110-8266466 | Stomach_Smooth_Muscle | SE_55963 | chr1:8255991-8265376 | u87 | SE_65889 | chr1:8257508-8258772 | Pancreatic_islets | SE_67577 | chr1:8255991-8265376 | u87 |
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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 |
GH01I008196 | chr1 | 8256176 | 8259101 |
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Enhancer Sequence | GAGTTCAAGA CCAGGCTGGG CAACATGGCG AGACCCCATC TCTACAAAAA TACAGAAAAA 60 TGAGCTGGGT GTGGTGGCAC GTGCCTGTGG TCCCATGACT CGGGAGGCTG AAGTGGGAGG 120 ATCACTTTAG CTGGGGAGGT GGAGGTTGCA GTGAGTTGAG CACTCCAGCC TGGGCTACAG 180 AGTGAAACGC TGTCAAAAAA AGAAAAAAGA AAAAAAAGAT ACTCTCTTAT ACATGCAGTA 240 TAATGATCAA AATCAGGAAA TCCAACATAA ACAGAATGCC CTTATCCAGC CCACAATCCA 300 CACTTGAATT TCATCACCCG TCCCTGCAGC TTTCCTGGCG GGCCTGGGCC CTGATCCAGG 360 ATGGCCGAGT GCTGAGTCAT GCACCCCTCT TCACCCGAAG CTCCTCCGCC CACACCTTGT 420 ACAGGCGCCT TCTTATCTCC CAGGTCCGAG TCTAACCGCA GCTCCCCACC TGCTCATCCT 480 TACGGGGGCG GAGATGCGGT CTCACAGTGC CTGGCTCTGT AACTTCAAAG CACGTGTCCA 540 CATCCTGGTC TGTCCTGTCC TCTCCACGAA AAGTGATCCC CAGGGTCAGG GTGTGCCTCG 600 TTGCCACTGC AGGGACTGGG CATCCAGACC CTGCAGGGGG GACACTGGGA TCACCATCGG 660 CCTCTCTGCT CATGAGCTGC GTGACCTTGG GCAACTTAGC CCTTTTGTGC AGCTGTAAAA 720 TGAGGATGGT GGCTGCACCC CATCTGGAGT TTTCTGAGAG GCAAACGGGT CTGTTATGAG 780 AATCCAATGA GTCCTTATGT GTAAAGCACT CAGGACAGTG CCGGGCACAT AGAAAGTGCT 840 CAGTAGGCCC GGCACGGTGG CTCACACCTG TAATCCCAGC ACTTTGGGAG GCTGAGGTGG 900 GTGGATAACT TGAGATCAGG AGTTCGAGAA TAGCCTGGCC AACATGTCAA 950
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