Tag | Content |
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EnhancerAtlas ID | HS049-03256 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr17:27475330-27477050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
REL | MA0101.1 | chr17:27476732-27476742 | GGGGATTTCC | + | 6.02 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_03450 | chr17:27475263-27475960 | Brain_Angular_Gyrus | SE_03450 | chr17:27476005-27478190 | Brain_Angular_Gyrus | SE_03910 | chr17:27475000-27480152 | Brain_Anterior_Caudate | SE_04884 | chr17:27475155-27487900 | Brain_Cingulate_Gyrus | SE_05843 | chr17:27474727-27488125 | Brain_Hippocampus_Middle | SE_07476 | chr17:27475143-27479986 | Brain_Hippocampus_Middle_150 | SE_07806 | chr17:27475148-27479935 | Brain_Inferior_Temporal_Lobe | SE_08959 | chr17:27475489-27475671 | Brain_Mid_Frontal_Lobe | SE_08959 | chr17:27476179-27476434 | Brain_Mid_Frontal_Lobe | SE_09987 | chr17:27475197-27478404 | CD14 | SE_13853 | chr17:27475176-27477721 | CD34_Primary_RO01536 | SE_19008 | chr17:27475112-27477128 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19489 | chr17:27475160-27476826 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_28031 | chr17:27475246-27476625 | Fetal_Intestine | SE_28952 | chr17:27475061-27476714 | Fetal_Intestine_Large | SE_30293 | chr17:27474971-27477134 | Fetal_Muscle | SE_32448 | chr17:27475261-27477030 | Gastric | SE_33834 | chr17:27475307-27475967 | HCC1954 | SE_33834 | chr17:27476050-27486414 | HCC1954 | SE_34898 | chr17:27474962-27479646 | HeLa | SE_37582 | chr17:27474947-27477539 | HSMMtube | SE_40250 | chr17:27475220-27476718 | K562 | SE_41080 | chr17:27475006-27477618 | Left_Ventricle | SE_42354 | chr17:27475115-27477716 | Lung | SE_47275 | chr17:27471944-27488173 | Panc1 | SE_48211 | chr17:27475177-27476941 | Psoas_Muscle | SE_49086 | chr17:27475201-27476989 | Right_Atrium | SE_50708 | chr17:27475226-27478094 | Sigmoid_Colon | SE_51291 | chr17:27474828-27477160 | Skeletal_Muscle | SE_52472 | chr17:27475233-27478072 | Small_Intestine | SE_53778 | chr17:27475227-27478308 | Spleen | SE_65361 | chr17:27474948-27476968 | Pancreatic_islets | SE_68762 | chr17:27475328-27476928 | H9 |
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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 |
GH17I029146 | chr17 | 27473356 | 27480087 |
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Enhancer Sequence | GTGTAAAGTG TCAATAATAG AACTATATTT AGGGAGTTGG GGAGAGTCCT GTTTAAAGCA 60 CTCAGAGCTC AGGGCCAGGA GGGCCTGGAG CACTTGCTTT TGAAGTGGGA GGGCCCAGCC 120 ACTAGGGTGG CAGGTGCACT TCCAGGATGA CCACTTCAGA GGTCCTCAGC ACCAGCCCTA 180 GGGCCAGTAC TAGAGTCTAC ACCTGTCTCA AAGAAAATGC CAGCGCAGGA GTCCCTTCCC 240 TTTCTTGGGA GGAATTATCC TTTATTCTTT TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 300 TGTGTAAGTA ACAAAATGTC ACCTCGTATG AAACAGTAGT GTTAGGAGAC AGCGATTGGT 360 ATTGAGGTGC CAAGATTTTT TATGAAATTC TACCAGTGCC GATAGCCAGT GGATTCTGAA 420 GGGTTATAGG GCAGACTCCC TTTAAGAAGC CTAGGGATGG TCTCAGAGAG GAGAAGGAGG 480 GCTGAGAGGA AACCTGGAGT GACCAACGGC GCATGCCCAG GGCCACCCCA GCCACTCAGC 540 ACCCTACGCA CGGGTCAGGC TCTGTGAGGG CCGAGTCAGC CCCAGGCCCG GGGCGGCACT 600 TCCCGGGTTG GCCCACCGGC CAGCCGGAGC CTGGGCGGGG CCAAGGGGGT GGGGCCAAGC 660 CCAGCACATG CGCCTAGAGC CCTGGAAGCT CCGCCCTGCA GCGCCGCTGG CGCCCAGCAG 720 AGGGTGGCAG CCCCCTTCTC ATCTACCCTC CCGCTTTGCT GGGGCCGCTT TCACCTCCGC 780 CAGGCCGGCC TCCAGGCCCC ACCCCCAGGA GGCGTCCCCC AGGAGCTCCG GCCCGAGGGG 840 GCTGCGGCGG CAAGATGGCC TCTCGCCGTC CCCAGGACGC GTAGGGCAAG AAGAGGCAGG 900 GATGAGCTCG GTGCCCACTT TGTTTTTATC ACCGCTCTAT CCCCAGAACC TAAAACAGTT 960 CCTACATATA GTAGGCATTC AGTAAATGCT TATTGATGGA ATAAATGAAT GAATACATGA 1020 ATGCAAGGTC AAAAGACGCC AGGAAAGCCT GTTCTAGAGA GGGGCTTGTC TAGAGACAAG 1080 CAATCAGGAA GGTCAGTGGG TATGGGACGG CGAGCCACAG ATCACTGCCC CAGAGGTGGT 1140 CGCCGAGGCT TGGGGCTCTG ACACTCCCCC CAGCCCCTAC ACCCACCCAG TCCCTGCATT 1200 GGCACACCCA TCAGTTTGCT CAGAGCCATG TGCCACCACA CCTTTTCGGG CACAGAGCCC 1260 AAGTAGGGAC GCCTGGGCTT GTCCTCTCTG CCAAGACCCT GAGTCAATCC CCAAAGACTA 1320 GGCAGGCATA TGCGGCCGAC TGCAGGGACC ACCTGACTGG CCCGACAGCA GGCCTGCTGC 1380 TCTCTGAGGT CTCTCAGCTG CTGGGGATTT CCTCATGGCC CCCGGGGACT TCCAAATTGC 1440 CTCTGCTTTG CCAAGCTCCC CCAAGGCCCA AAGCCATGAG CCAGCCTTGA GGATCCTTTC 1500 CCAAAATCCT CCACAGCCCT GCCCCACATC TCATCAGGAC TTGGGTCACT TCTGGGTCTC 1560 CTAAATGTAC CACATGCACT ATGTTCTCCT ATCCACCCCC TCTGGTAGAC AGGAGGGAAT 1620 AAACATAATG AAGCATTGTT CTCTTTTTCA TATAAATGAC AACTCTTCTC CATTTCCACA 1680 GAAGAAAAAA AAGGAAGCCA GCTTAAGGGT CAGCCACAGC 1720
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