| Tag | Content |
|---|
EnhancerAtlas ID | HS047-14222 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:27475320-27477190 |
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 | AATTTGCGGT GTGTAAAGTG TCAATAATAG AACTATATTT AGGGAGTTGG GGAGAGTCCT 60
GTTTAAAGCA CTCAGAGCTC AGGGCCAGGA GGGCCTGGAG CACTTGCTTT TGAAGTGGGA 120
GGGCCCAGCC ACTAGGGTGG CAGGTGCACT TCCAGGATGA CCACTTCAGA GGTCCTCAGC 180
ACCAGCCCTA GGGCCAGTAC TAGAGTCTAC ACCTGTCTCA AAGAAAATGC CAGCGCAGGA 240
GTCCCTTCCC TTTCTTGGGA GGAATTATCC TTTATTCTTT TGTGTGTGTG TGTGTGTGTG 300
TGTGTGTGTG TGTGTAAGTA ACAAAATGTC ACCTCGTATG AAACAGTAGT GTTAGGAGAC 360
AGCGATTGGT ATTGAGGTGC CAAGATTTTT TATGAAATTC TACCAGTGCC GATAGCCAGT 420
GGATTCTGAA GGGTTATAGG GCAGACTCCC TTTAAGAAGC CTAGGGATGG TCTCAGAGAG 480
GAGAAGGAGG GCTGAGAGGA AACCTGGAGT GACCAACGGC GCATGCCCAG GGCCACCCCA 540
GCCACTCAGC ACCCTACGCA CGGGTCAGGC TCTGTGAGGG CCGAGTCAGC CCCAGGCCCG 600
GGGCGGCACT TCCCGGGTTG GCCCACCGGC CAGCCGGAGC CTGGGCGGGG CCAAGGGGGT 660
GGGGCCAAGC CCAGCACATG CGCCTAGAGC CCTGGAAGCT CCGCCCTGCA GCGCCGCTGG 720
CGCCCAGCAG AGGGTGGCAG CCCCCTTCTC ATCTACCCTC CCGCTTTGCT GGGGCCGCTT 780
TCACCTCCGC CAGGCCGGCC TCCAGGCCCC ACCCCCAGGA GGCGTCCCCC AGGAGCTCCG 840
GCCCGAGGGG GCTGCGGCGG CAAGATGGCC TCTCGCCGTC CCCAGGACGC GTAGGGCAAG 900
AAGAGGCAGG GATGAGCTCG GTGCCCACTT TGTTTTTATC ACCGCTCTAT CCCCAGAACC 960
TAAAACAGTT CCTACATATA GTAGGCATTC AGTAAATGCT TATTGATGGA ATAAATGAAT 1020
GAATACATGA ATGCAAGGTC AAAAGACGCC AGGAAAGCCT GTTCTAGAGA GGGGCTTGTC 1080
TAGAGACAAG CAATCAGGAA GGTCAGTGGG TATGGGACGG CGAGCCACAG ATCACTGCCC 1140
CAGAGGTGGT CGCCGAGGCT TGGGGCTCTG ACACTCCCCC CAGCCCCTAC ACCCACCCAG 1200
TCCCTGCATT GGCACACCCA TCAGTTTGCT CAGAGCCATG TGCCACCACA CCTTTTCGGG 1260
CACAGAGCCC AAGTAGGGAC GCCTGGGCTT GTCCTCTCTG CCAAGACCCT GAGTCAATCC 1320
CCAAAGACTA GGCAGGCATA TGCGGCCGAC TGCAGGGACC ACCTGACTGG CCCGACAGCA 1380
GGCCTGCTGC TCTCTGAGGT CTCTCAGCTG CTGGGGATTT CCTCATGGCC CCCGGGGACT 1440
TCCAAATTGC CTCTGCTTTG CCAAGCTCCC CCAAGGCCCA AAGCCATGAG CCAGCCTTGA 1500
GGATCCTTTC CCAAAATCCT CCACAGCCCT GCCCCACATC TCATCAGGAC TTGGGTCACT 1560
TCTGGGTCTC CTAAATGTAC CACATGCACT ATGTTCTCCT ATCCACCCCC TCTGGTAGAC 1620
AGGAGGGAAT AAACATAATG AAGCATTGTT CTCTTTTTCA TATAAATGAC AACTCTTCTC 1680
CATTTCCACA GAAGAAAAAA AAGGAAGCCA GCTTAAGGGT CAGCCACAGC AATTTAAATA 1740
AAATATCAGT AAGGTCTTCC TGGGTGTGAG AGATGGAGGC CTGTGGTGCT TATTCTCAAA 1800
GTCAGAGAAG TTCTTCTAGA CAAGCCTCAG GTTCCTCGTA ACACTGGACA TCCAATAAAT 1860
ATTTGAGAAT 1870
|
