Tag | Content |
---|
EnhancerAtlas ID | HS175-11351 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr17:36756390-36759490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr17:36759380-36759390 | TCTAATTAAA | + | 6.02 | BCL6 | MA0463.2 | chr17:36758065-36758081 | CAGTCCTCGAAAGCAG | - | 6.07 | BCL6 | MA0463.2 | chr17:36758950-36758966 | GATTCCTCGAAAGAGC | - | 6.21 | EWSR1-FLI1 | MA0149.1 | chr17:36758451-36758469 | ACTGCCTCCCTCCCTTCC | - | 6.42 | EWSR1-FLI1 | MA0149.1 | chr17:36758455-36758473 | CCTCCCTCCCTTCCTCCC | - | 6.92 | POU2F2 | MA0507.1 | chr17:36757308-36757321 | ATATGCAAATCAC | - | 6.04 | RARA(var.2) | MA0730.1 | chr17:36756577-36756594 | AGGTCCCCAAAAGGTCA | + | 6.67 | SP8 | MA0747.1 | chr17:36757378-36757390 | CCCACGCCCCCT | + | 6.04 | ZNF263 | MA0528.1 | chr17:36759449-36759470 | GGAGGGGGGAGAGGGGGAGAG | + | 6.2 | ZNF263 | MA0528.1 | chr17:36758442-36758463 | CCCTCCTTCACTGCCTCCCTC | - | 6.37 | ZNF263 | MA0528.1 | chr17:36759453-36759474 | GGGGGAGAGGGGGAGAGAGAG | + | 6.47 | ZNF263 | MA0528.1 | chr17:36758454-36758475 | GCCTCCCTCCCTTCCTCCCTC | - | 7.07 | ZNF263 | MA0528.1 | chr17:36759446-36759467 | AAGGGAGGGGGGAGAGGGGGA | + | 7.45 |
|
| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_03264 | chr17:36756313-36756860 | Brain_Angular_Gyrus | SE_03264 | chr17:36758625-36759340 | Brain_Angular_Gyrus | SE_04205 | chr17:36755246-36757135 | Brain_Anterior_Caudate | SE_04205 | chr17:36758079-36758971 | Brain_Anterior_Caudate | SE_04205 | chr17:36759085-36761082 | Brain_Anterior_Caudate | SE_04913 | chr17:36754051-36764631 | Brain_Cingulate_Gyrus | SE_05891 | chr17:36754606-36762180 | Brain_Hippocampus_Middle | SE_07890 | chr17:36752363-36761054 | Brain_Inferior_Temporal_Lobe | SE_41884 | chr17:36757561-36758944 | LNCaP | SE_63462 | chr17:36710227-36758662 | NCI-H69 | SE_69079 | chr17:36756374-36759004 | 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 |
GH17I038600 | chr17 | 36756623 | 36759835 |
|
Enhancer Sequence | TCTTGCTGCA TTTCCTCTGG CCCAGTCCTC CTTGGTGGCA TTTTTGTTCC TGTCTTCAGA 60 GACTCTTCTC ATGACTCAGT GGCCTACATG ATCTTTTTCC AGGCTATCAA CCTTTACCCA 120 GCCCTGCCCC AGGACGGGGT AGATATGTAG GTAAAAGCGA CCAAGGCATG CGAAGAGGCT 180 CTGGGGGAGG TCCCCAAAAG GTCAGGCAGG GCTGTTGGAG GTACGGGCAG GACTAGGGTG 240 GCAGGCTCTC CTCCCTCATA ATGTCCATGA CCCCTGCAGG GGGCCTGGGC CCCATCTTCT 300 GTGTGGTAGC TAAGAGGGCC CAGAGAGGCA ATGAATGACC TAGTCCTTCT CACTGACCAT 360 CTCTGAGGCC CAGGTTTCAG CACACACATC CCCAGAGCCC AGGGGAATGG GCAAAAGCAG 420 GCAGGGGCAC AAGGGCAGGA CTTGCCATGG GTTGAGCCTG GGAGGTGAAG CCGGAGGAGG 480 AGCTCTGACA CCTGGCTAAG CTCCCGGCAG AGGGCTAGCA GGCCCTGGAG GGTGCACAGC 540 CTCAAGCCCC TCTGCCGGCT GCAGTATCAG GCCTCCGTGG GGTTCTGCAC ACCCCATCCT 600 AGCTAGCCAC AGGCAACTTT GGTGAATTCA CCCACCACTT GGCTTCTCTG TTTTGACCTT 660 TTGGAGCAGA AGTGCTGAGG GCAGGGGTCC CCTCGACTAC AGCCATCCCC CCAACCCTGC 720 CCCCAGCATG GCTGGAACAC AGGGGCCAGA CTCACCTCCC CAGGGAATGC TCAAGCCCAG 780 CTTTCACCCC TCTGGGAAAT CGGAGCAGCA AAAGCATGGG CCAATGGGCA AGGGGAGTTG 840 GAATGGTGGG TGGGACTCTG GGCCGGGTGT GGGCGGCACC CTCCCCCTTC AAGCAGGCAC 900 CATTAATATA TGCAAAGCAT ATGCAAATCA CCCAGAAGAG AGACACAACA CCGCTGGAAT 960 GTCACAAGAA ACCTTGGAGA TCAGCCAGCC CACGCCCCCT CATTTCACAG GTGAGGAAAG 1020 AGGCCCGCGC TGGGATGGGA CTTGCTCAAG GTCACGCAGA CATCTGGGCA CTGAGGAAGG 1080 ATAAGAATGA GCTCTCTTGA CTTAGTGCAG TGCTTTTTCC ACCAGGGTCT TGTCTTTCTG 1140 CTGGGGGGTT TATAACATTG CAAAGGGGCC CCAGGGCGTG GATGGGGCTC CAGGCAGGCC 1200 CATCAGAGAC ATGGGTGGGA GATGGAGCTG AGAGGCTTCT TGGATGCCTC CCTTACCGCC 1260 TCTGCACCTG GAGATGGTCT GGTGGGTGTG AGGGGCAGTG CAAGGGCAGC ATAGCACCTG 1320 GGGGGCCGCG CGGTTGGAGG GGCGGGAGGC TGGAGGTAGG CAAAGAGAAA TATGAGGGGC 1380 AGGGCAGAAG AGCAGGGAAC CTGGGGTGTT TGAGGCAGGG GAGGAAGAGC CCAATGTCAG 1440 GGCAAGGTGC CTGCTGTGGT GTGGGGAGGG GGATGGCGCC CTCAACACAT ACACACACAC 1500 GCACACACAC ACACACGCTC GCGCGCACAC ACACACACAC ACACATCGCT AAGTGCTCTG 1560 CAGCCCTTCC TGGACTCTGA CAATTATGGC ACCTGACAGA CCATAATAGT TAACCCAGGC 1620 CCATCCCTTC TGAGGCCACT TCCCCGCCCC CAGCTTGGCT TCTCAACCTT CCAGACAGTC 1680 CTCGAAAGCA GGGCCAGAGC TGGGGAAAGG AAGGGGAGGC AGACAATGGG AGGGGTGGTC 1740 AGAGGGAGGA AGGGGGAGGC AGAAGAAGAG ACGAGGACAG GGTTAGAGAG AGAGACAGCA 1800 GGAAGGGCAG CGCAGGAGAA ATTGACGAAC AGGGAGCGGG AGGGGAGGAA TGGGAAGACG 1860 GAAAGGCACA GAGGAGAGAT GGGGGAGGGG CGAAGACTGA GGGCATCCAG GGGAGTGCTC 1920 TGGAGCCCAG GTATCGGGTA GAGGAACCCT GACCCCGAGG TTCTAGGCTG CTTGGCAGGA 1980 GTTGGGGACC ATGCCCCTGC CCCTCTGCCC ACCTCCCCCA GAAACTCCCC TGGCTGCCAG 2040 GAACTCAGTC CTCCCTCCTT CACTGCCTCC CTCCCTTCCT CCCTCGGGGC AGGCACTGCT 2100 TCCCAGCCAA ATCCGAAGCC TTCATCTCCG CTACTCAGAG CTTGGAATGA AAGAAGGGGA 2160 AGCGAGTACA GCCCTCAAAC CCGCTGACGG CCAGATTTTT ATTATCTTTG CTCGAATGGG 2220 CCCTAGGAAG CCAGTGAGGG ATTCTTCAAA GAGCATCTGA GTGCCTCATT GAAGCCTGCA 2280 CCTGCACCAG CCCACCCACA GCAGGCAGCC AGGACTTGGG GGGCACAACC TGTCCCCCAC 2340 CCCCCACAAA TCCTAGAGTC CAGAGCCTCA GCTACCAGGA GACTCACCCT CAGCAGCTTG 2400 TGCCCAAGCA GGGGTCCCTA GGTCAGGAAA CCAGGCTTAA AGCTAGACCT AAGTCTGCTG 2460 GGCCTCTGAG GCAGTCTGTG TCCCTCTCTG GGCCTCAAGG ACATAAATGA AGAAAGAAAA 2520 CAGATTTCCT TGCCAGGGCT TGGAGGAGAT AAATGCTTGA GATTCCTCGA AAGAGCAGCT 2580 TTTATGGCAA GCCCTGGATC CTTCCCCTGA ACTCCCTGCC TGCCCAGCAC CCACAGGCCC 2640 CTTTGCAAGA GCACCCCCCA CCACAGCTGC CTCTTCATGT GCCCCAGGCC TGCTACCCAG 2700 GATGACAGAC GCCATGAACT GTTCTTCCTT GAGCCCCAAA CTCAGCTCCC TCAGTTCAAA 2760 TCCTCAACAC TGTCTCCCTT CTTTCCCCAA AACCTAACCT GGGGTGGGGG TGGGGGCTCA 2820 ACAAACTGGG TACTTCAAAG AGCCCAGCCG CCTCCCTCCT AAGCACTTCC AGGGCTGGGG 2880 TTTTGGCAGA GAATTCCAAG GTTGGCATAG GCAGATGGCA GCCATGCCAC CCCCACCCTC 2940 TAGCTCTGAC CACACTGTCG ATGCCCACAG CCAAAGAAGG AATCAATGGT TCTAATTAAA 3000 CCCTTTTTCC AGGGTGGGTC CCTGGCGAGA GAGAGGGAAG AGGGAGAGAG ACAGGGAAGG 3060 GAGGGGGGAG AGGGGGAGAG AGAGAGAAAG AGAGAGAGAG 3100
|