Tag | Content |
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EnhancerAtlas ID | HS047-16452 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:2616670-2617620 |
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 | GGCTGAGGCA GAATTGCTTG AACCCGGGAG GCAGAGGTTG CAGGTTGCAG TGAGCCGAGA 60 TCACGCCATC GCACTCCAGC CTGAGCAAAA CCCCATCTCA AAAAAAAAAA CCAGACAAAT 120 ATAGCTGGTG GGTTCTTGGG CAAGGCTGGT GACCAGGGCC CTAGGGGAGG ATGTTTCCAA 180 GAGCTGCCAA GAGCAGTGGG GCCCGGGTTC TGCCCGCCTC TTCCTCTGAC TGTTTCCTCA 240 TCTGGGGTCA CGGGATAAGT GCAGCTCCGC CTCCCTGGTC ATGCAGGTGA CTGTGAATGA 300 AAGTGTCTTG GAATCAGAAG GTTCTGGCAT GAAAGCTTTG CACCAGCCTT CCACCAGTGT 360 GCTGCCCAGC ACGTGACTAT CGGAAAAACT TTAGCTTATT TCAGCCTAAT TACATTCCGT 420 TAACCCAAAG TCTCTGACGT TCAGGGCTGG ATCATTCTCT GGGATGGGGC CATCCTGGTG 480 CACTGCAGGG TGCTGAGTGG CGTCCCTGAC CCCCACCCAC TCCATGCCAG GAGCATCTCC 540 AGTCGTGACA ACCACAGATG TCCCCAGATA TCACCCAGAG TCCCCTGGAG GCAAACCTGT 600 CCCACTTAAG AACCGCTGGC CTGGACCAGA AACTGGATCT TTCAGGGAGG CAGAGCTCAC 660 CAGCCATCCA GGCACTGAGC CCGGCCCAGC CCTGCAGCTC TGACCCTGCC TTGGGCTGTG 720 AGCTCTGAGG ACCCCATCAA TCTGATCAAG AAGCCACACT AGGTCACCTC AGACCAAGGA 780 CATTCTGCCA TGATGCTTCA GACTGTTCTT CTCCCCATCC TCCTCTCCAC CTCCAGCCCT 840 CAAAGACCTG GCCTGGGTCC CCTCCCGTGG CTCCCAGACC TCCGCTTCCA GGGAGCCCTC 900 CGGAATGTCC TTCCTCCTGC CTTCAATGCT CCTCCCCATC CTGCAGGGGT 950
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