| Tag | Content |
|---|
EnhancerAtlas ID | HS051-11517 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:27475300-27477510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr17:27476732-27476742 | GGGGATTTCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 32 | 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 | chr17:27476179-27476434 | 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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I029146 | chr17 | 27473356 | 27480087 |
|
Enhancer Sequence | TATATGATCC TTGTATTACA AATTTGCGGT GTGTAAAGTG TCAATAATAG AACTATATTT 60
AGGGAGTTGG GGAGAGTCCT GTTTAAAGCA CTCAGAGCTC AGGGCCAGGA GGGCCTGGAG 120
CACTTGCTTT TGAAGTGGGA GGGCCCAGCC ACTAGGGTGG CAGGTGCACT TCCAGGATGA 180
CCACTTCAGA GGTCCTCAGC ACCAGCCCTA GGGCCAGTAC TAGAGTCTAC ACCTGTCTCA 240
AAGAAAATGC CAGCGCAGGA GTCCCTTCCC TTTCTTGGGA GGAATTATCC TTTATTCTTT 300
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTAAGTA ACAAAATGTC ACCTCGTATG 360
AAACAGTAGT GTTAGGAGAC AGCGATTGGT ATTGAGGTGC CAAGATTTTT TATGAAATTC 420
TACCAGTGCC GATAGCCAGT GGATTCTGAA GGGTTATAGG GCAGACTCCC TTTAAGAAGC 480
CTAGGGATGG TCTCAGAGAG GAGAAGGAGG GCTGAGAGGA AACCTGGAGT GACCAACGGC 540
GCATGCCCAG GGCCACCCCA GCCACTCAGC ACCCTACGCA CGGGTCAGGC TCTGTGAGGG 600
CCGAGTCAGC CCCAGGCCCG GGGCGGCACT TCCCGGGTTG GCCCACCGGC CAGCCGGAGC 660
CTGGGCGGGG CCAAGGGGGT GGGGCCAAGC CCAGCACATG CGCCTAGAGC CCTGGAAGCT 720
CCGCCCTGCA GCGCCGCTGG CGCCCAGCAG AGGGTGGCAG CCCCCTTCTC ATCTACCCTC 780
CCGCTTTGCT GGGGCCGCTT TCACCTCCGC CAGGCCGGCC TCCAGGCCCC ACCCCCAGGA 840
GGCGTCCCCC AGGAGCTCCG GCCCGAGGGG GCTGCGGCGG CAAGATGGCC TCTCGCCGTC 900
CCCAGGACGC GTAGGGCAAG AAGAGGCAGG GATGAGCTCG GTGCCCACTT TGTTTTTATC 960
ACCGCTCTAT CCCCAGAACC TAAAACAGTT CCTACATATA GTAGGCATTC AGTAAATGCT 1020
TATTGATGGA ATAAATGAAT GAATACATGA ATGCAAGGTC AAAAGACGCC AGGAAAGCCT 1080
GTTCTAGAGA GGGGCTTGTC TAGAGACAAG CAATCAGGAA GGTCAGTGGG TATGGGACGG 1140
CGAGCCACAG ATCACTGCCC CAGAGGTGGT CGCCGAGGCT TGGGGCTCTG ACACTCCCCC 1200
CAGCCCCTAC ACCCACCCAG TCCCTGCATT GGCACACCCA TCAGTTTGCT CAGAGCCATG 1260
TGCCACCACA CCTTTTCGGG CACAGAGCCC AAGTAGGGAC GCCTGGGCTT GTCCTCTCTG 1320
CCAAGACCCT GAGTCAATCC CCAAAGACTA GGCAGGCATA TGCGGCCGAC TGCAGGGACC 1380
ACCTGACTGG CCCGACAGCA GGCCTGCTGC TCTCTGAGGT CTCTCAGCTG CTGGGGATTT 1440
CCTCATGGCC CCCGGGGACT TCCAAATTGC CTCTGCTTTG CCAAGCTCCC CCAAGGCCCA 1500
AAGCCATGAG CCAGCCTTGA GGATCCTTTC CCAAAATCCT CCACAGCCCT GCCCCACATC 1560
TCATCAGGAC TTGGGTCACT TCTGGGTCTC CTAAATGTAC CACATGCACT ATGTTCTCCT 1620
ATCCACCCCC TCTGGTAGAC AGGAGGGAAT AAACATAATG AAGCATTGTT CTCTTTTTCA 1680
TATAAATGAC AACTCTTCTC CATTTCCACA GAAGAAAAAA AAGGAAGCCA GCTTAAGGGT 1740
CAGCCACAGC AATTTAAATA AAATATCAGT AAGGTCTTCC TGGGTGTGAG AGATGGAGGC 1800
CTGTGGTGCT TATTCTCAAA GTCAGAGAAG TTCTTCTAGA CAAGCCTCAG GTTCCTCGTA 1860
ACACTGGACA TCCAATAAAT ATTTGAGAAT CTGTGTGTTC ACCTCTGGAG CCCCTATTGG 1920
GCCTGTTTCT AAAACCCTCT GAAGTAAAAA ATAAAGCACA AACCCTATGT CCATAGAAAC 1980
AGGAAGAAGC AAAAGCCTCT ACCTTGCCTA CCAACCCACC ACCTCTGTGC TAACAGCCTG 2040
GGCCAAATCC ACTGGGGCAT GTGAGTACCT GTGTGTTACA AAGCTGGGCA GAAGACATCC 2100
TTGGCGAGGA AAGGAAGCGC TGCCCCAGTT GTGGTGGCAC ACAGCCAGGG ACCTGCTGGC 2160
CCTGGGGCAT TAGGATTCCA GAGCTGGTGG TGGTTGAGGT GTAGAAATTG 2210
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