Tag | Content |
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EnhancerAtlas ID | HS155-05956 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr17:27475270-27476930 |
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: 34 | 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_08959 | chr17:27476470-27476640 | 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 | TAAGCACTGT TGCCATAAAT GGGTACTAAT TATATGATCC TTGTATTACA AATTTGCGGT 60 GTGTAAAGTG TCAATAATAG AACTATATTT AGGGAGTTGG GGAGAGTCCT GTTTAAAGCA 120 CTCAGAGCTC AGGGCCAGGA GGGCCTGGAG CACTTGCTTT TGAAGTGGGA GGGCCCAGCC 180 ACTAGGGTGG CAGGTGCACT TCCAGGATGA CCACTTCAGA GGTCCTCAGC ACCAGCCCTA 240 GGGCCAGTAC TAGAGTCTAC ACCTGTCTCA AAGAAAATGC CAGCGCAGGA GTCCCTTCCC 300 TTTCTTGGGA GGAATTATCC TTTATTCTTT TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG 360 TGTGTAAGTA ACAAAATGTC ACCTCGTATG AAACAGTAGT GTTAGGAGAC AGCGATTGGT 420 ATTGAGGTGC CAAGATTTTT TATGAAATTC TACCAGTGCC GATAGCCAGT GGATTCTGAA 480 GGGTTATAGG GCAGACTCCC TTTAAGAAGC CTAGGGATGG TCTCAGAGAG GAGAAGGAGG 540 GCTGAGAGGA AACCTGGAGT GACCAACGGC GCATGCCCAG GGCCACCCCA GCCACTCAGC 600 ACCCTACGCA CGGGTCAGGC TCTGTGAGGG CCGAGTCAGC CCCAGGCCCG GGGCGGCACT 660 TCCCGGGTTG GCCCACCGGC CAGCCGGAGC CTGGGCGGGG CCAAGGGGGT GGGGCCAAGC 720 CCAGCACATG CGCCTAGAGC CCTGGAAGCT CCGCCCTGCA GCGCCGCTGG CGCCCAGCAG 780 AGGGTGGCAG CCCCCTTCTC ATCTACCCTC CCGCTTTGCT GGGGCCGCTT TCACCTCCGC 840 CAGGCCGGCC TCCAGGCCCC ACCCCCAGGA GGCGTCCCCC AGGAGCTCCG GCCCGAGGGG 900 GCTGCGGCGG CAAGATGGCC TCTCGCCGTC CCCAGGACGC GTAGGGCAAG AAGAGGCAGG 960 GATGAGCTCG GTGCCCACTT TGTTTTTATC ACCGCTCTAT CCCCAGAACC TAAAACAGTT 1020 CCTACATATA GTAGGCATTC AGTAAATGCT TATTGATGGA ATAAATGAAT GAATACATGA 1080 ATGCAAGGTC AAAAGACGCC AGGAAAGCCT GTTCTAGAGA GGGGCTTGTC TAGAGACAAG 1140 CAATCAGGAA GGTCAGTGGG TATGGGACGG CGAGCCACAG ATCACTGCCC CAGAGGTGGT 1200 CGCCGAGGCT TGGGGCTCTG ACACTCCCCC CAGCCCCTAC ACCCACCCAG TCCCTGCATT 1260 GGCACACCCA TCAGTTTGCT CAGAGCCATG TGCCACCACA CCTTTTCGGG CACAGAGCCC 1320 AAGTAGGGAC GCCTGGGCTT GTCCTCTCTG CCAAGACCCT GAGTCAATCC CCAAAGACTA 1380 GGCAGGCATA TGCGGCCGAC TGCAGGGACC ACCTGACTGG CCCGACAGCA GGCCTGCTGC 1440 TCTCTGAGGT CTCTCAGCTG CTGGGGATTT CCTCATGGCC CCCGGGGACT TCCAAATTGC 1500 CTCTGCTTTG CCAAGCTCCC CCAAGGCCCA AAGCCATGAG CCAGCCTTGA GGATCCTTTC 1560 CCAAAATCCT CCACAGCCCT GCCCCACATC TCATCAGGAC TTGGGTCACT TCTGGGTCTC 1620 CTAAATGTAC CACATGCACT ATGTTCTCCT ATCCACCCCC 1660
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