Tag | Content |
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EnhancerAtlas ID | HS073-11556 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr5:95156520-95158150 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr5:95157872-95157886 | ATTCCCCAGGGACT | - | 6.31 | EBF1 | MA0154.3 | chr5:95157872-95157886 | ATTCCCCAGGGACT | + | 7.64 | Mafb | MA0117.2 | chr5:95157145-95157157 | AAAATGCTGACT | + | 7.22 | SOX10 | MA0442.2 | chr5:95157853-95157864 | AAAACAAAGAC | + | 6.14 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00235 | chr5:95155938-95161048 | Adipose_Nuclei | SE_01473 | chr5:95157173-95160926 | Adrenal_Gland | SE_06654 | chr5:95156702-95160856 | Brain_Hippocampus_Middle | SE_09663 | chr5:95148934-95164578 | CD14 | SE_11777 | chr5:95149010-95161143 | CD20 | SE_12316 | chr5:95157124-95160751 | CD3 | SE_18767 | chr5:95150222-95162090 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19610 | chr5:95155488-95160988 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20485 | chr5:95150373-95161000 | CD56 | SE_24621 | chr5:95156888-95157162 | Colon_Crypt_2 | SE_24621 | chr5:95157240-95157639 | Colon_Crypt_2 | SE_24621 | chr5:95157697-95158581 | Colon_Crypt_2 | SE_25672 | chr5:95156141-95162033 | DND41 | SE_26405 | chr5:95156637-95161022 | Duodenum_Smooth_Muscle | SE_27962 | chr5:95156530-95164802 | Fetal_Intestine | SE_28976 | chr5:95156477-95164865 | Fetal_Intestine_Large | SE_31877 | chr5:95157131-95160878 | Gastric | SE_34665 | chr5:95156768-95161227 | HeLa | SE_37859 | chr5:95156510-95161124 | HSMMtube | SE_40949 | chr5:95156696-95160869 | Left_Ventricle | SE_42421 | chr5:95156657-95160906 | Lung | SE_48283 | chr5:95156675-95160838 | Psoas_Muscle | SE_48806 | chr5:95156738-95160850 | Right_Atrium | SE_50448 | chr5:95156610-95160955 | Sigmoid_Colon | SE_52585 | chr5:95156686-95160861 | Small_Intestine | SE_53861 | chr5:95155534-95160960 | Spleen | SE_55361 | chr5:95156702-95157709 | Thymus | SE_55361 | chr5:95157729-95160862 | Thymus | SE_56476 | chr5:95156690-95161002 | u87 | SE_62882 | chr5:95143144-95179855 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 95157600 | 95157800 | chr5 | 95157800 | 95157833 |
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Enhancer Sequence | ATTTTTCCAA ATAAAAATCC CAGGTGTGGT GGCTCACCCG TTTAATCCCA GCACTTTGGG 60 AGGCCGAGGT AGGTGGATCG CCTGAGGTCA GGAGTTCGAC ACCAGCCTGG CCAACATGGT 120 GAAACCCCGT CTCTACTAAA AATACAAAAA TTAGCTGGGC ATGGTGGTGG GCGCCTGTAA 180 TCCCAGCTAC TTGGGAGGTT GAGGAGAACC CAGGAGGCAG AGGTTGCAGT GAGCCAAGAT 240 TGCACCATTG CACTCCAGCC TGGGTGACAA GAATGAAACT GTCTCAAAAC AAACGAACAA 300 ACAAAACTAA TGCTTGGCTC CCACCTCTGA CATTGTGATT TAGTTATTGA GGGGCATAAT 360 TTGGGCATAA GGATTGTTTT AAAAGCTCTC TAGGTGATCC TAATGTGCAG CAAAGTTTGG 420 GAACCAATGG CTAAAAGGTC CTCAGGGTGG CAGCCACAGT GGGGCCCGTA GTAGTGTTTG 480 CACTGCCCTT TACACCTCTC AGGGCCTGGG CATCCTATGC AGCTGGTGGT CCCACTAGGC 540 AGCAAGAGCT TCTCTCGTCA TTGTGTATAC TCCAGGACCT CAGCACACAG CAGTAGGATA 600 ACACACTAAG CCCCCTTTCT GCACCAAAAT GCTGACTTCT TATTAGAGAG AAGGGGAGAG 660 AAACAACCTC CAATGCTTTA TACTCAGAAC CCAGAGACAA CCTTGTAAGT CAAACTAAAA 720 CTGAAATAGG ATATGTGCTT GGCCTAACAC TGTGCTGTAG AATTCGTGCA TCGTAAAAGA 780 GAACTTAGCT GAGCTGGTGG GACATTTCTC ATCCCACCTC ACAGCAGAAC TGATACAGGT 840 GATGTGGCTG GCATCCCTCC TGAAGCCCAG GACGCAAAGC CAAGGATGCT GAAGAGAGGG 900 AAGTCTTTCG GATGGAGGAG AGCAATTTTT AGAGGGTCCC ACAGTCTATT CGTAGCAAAT 960 GGGACTCTGA GGTCACCTAA TCTGGTCTTG CAGCTGGGAT CTTTGAGGAC TACTGGGGTG 1020 GTGACTTGCC CAGGATCACA CAGCCAGCCA TTATAAGAGC CAGGCCAGAA CTCCAGGCTA 1080 TGATTCCCTA CAATGTGGGG CCTGGAAACA TCCATAATTA ATTTAGAACA AGGGGCAGAT 1140 AACGGTACAT TAGATTTTTC CAGTGGGAGG AATTAGATAA GGAAGAATGA GCAAATTAGA 1200 AAAAGAAAGC CTAGAGAAAA GAATGAAGAA CATGAATCTC ATGTTAAATA ACAAACACAT 1260 CACACCCGGC CCTCCACCCC AGCTTCCACC TCCAGCCCTG CCAACTGAAA ACTGTCATTT 1320 CCTGGCAGTG CTTAAAACAA AGACTCTAGA TAATTCCCCA GGGACTCACC GGCAAGCTGC 1380 TGGTCCCACT TACCCTGCCG CACAGCAGAC ATCAGCTGTA CTCCCTCTTC TGCCCCGTGA 1440 AGACCTTTGG CTGCAGTGCC GCCGCTCATT CAAGTGACCG AGATCCTCTC TAAGGCGCCC 1500 TCCCCCACAC CCCCCGCCCC GCACAGCCCT CTGGACGCCT TGAAGTACGG AGCCGCAGCC 1560 TTATCCTAAA GAAAGGCACA GCTCTGACAA GAAAAGGCAA TCCGGGAGCC TTTCCCTAGC 1620 CGTTTAAAAT 1630
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