Tag | Content |
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EnhancerAtlas ID | HS093-14802 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:2616630-2617500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:2617475-2617496 | TTCTTCTCCCCATCCTCCTCT | - | 7.46 |
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| Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
SE_03960 | chr19:2616846-2617848 | Brain_Anterior_Caudate | SE_05956 | chr19:2616466-2618282 | Brain_Hippocampus_Middle | SE_09725 | chr19:2613912-2622730 | CD14 | SE_10479 | chr19:2616428-2632474 | CD19_Primary | SE_11482 | chr19:2612601-2637196 | CD20 | SE_25680 | chr19:2611984-2620135 | DND41 | SE_31670 | chr19:2616655-2617741 | Gastric | SE_42475 | chr19:2616776-2617873 | Lung | SE_43602 | chr19:2617008-2623577 | MM1S | SE_53390 | chr19:2615816-2624370 | Spleen | SE_60827 | chr19:2607440-2634936 | DHL6 | SE_61224 | chr19:2586887-2637887 | HBL1 | SE_67209 | chr19:2617008-2623577 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 2616819 | 2617162 | chr19 | 2616918 | 2617026 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I002615 | chr19 | 2615800 | 2633597 |
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Enhancer Sequence | GGGCATGGTG GCGGGTGCCT GTAATCCCAG CTACTCAGGA GGCTGAGGCA GAATTGCTTG 60 AACCCGGGAG GCAGAGGTTG CAGGTTGCAG TGAGCCGAGA TCACGCCATC GCACTCCAGC 120 CTGAGCAAAA CCCCATCTCA AAAAAAAAAA CCAGACAAAT ATAGCTGGTG GGTTCTTGGG 180 CAAGGCTGGT GACCAGGGCC CTAGGGGAGG ATGTTTCCAA GAGCTGCCAA GAGCAGTGGG 240 GCCCGGGTTC TGCCCGCCTC TTCCTCTGAC TGTTTCCTCA TCTGGGGTCA CGGGATAAGT 300 GCAGCTCCGC CTCCCTGGTC ATGCAGGTGA CTGTGAATGA AAGTGTCTTG GAATCAGAAG 360 GTTCTGGCAT GAAAGCTTTG CACCAGCCTT CCACCAGTGT GCTGCCCAGC ACGTGACTAT 420 CGGAAAAACT TTAGCTTATT TCAGCCTAAT TACATTCCGT TAACCCAAAG TCTCTGACGT 480 TCAGGGCTGG ATCATTCTCT GGGATGGGGC CATCCTGGTG CACTGCAGGG TGCTGAGTGG 540 CGTCCCTGAC CCCCACCCAC TCCATGCCAG GAGCATCTCC AGTCGTGACA ACCACAGATG 600 TCCCCAGATA TCACCCAGAG TCCCCTGGAG GCAAACCTGT CCCACTTAAG AACCGCTGGC 660 CTGGACCAGA AACTGGATCT TTCAGGGAGG CAGAGCTCAC CAGCCATCCA GGCACTGAGC 720 CCGGCCCAGC CCTGCAGCTC TGACCCTGCC TTGGGCTGTG AGCTCTGAGG ACCCCATCAA 780 TCTGATCAAG AAGCCACACT AGGTCACCTC AGACCAAGGA CATTCTGCCA TGATGCTTCA 840 GACTGTTCTT CTCCCCATCC TCCTCTCCAC 870
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