Tag | Content |
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EnhancerAtlas ID | HS133-10178 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:65174340-65176860 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr15:65176113-65176127 | ACTCCCCAGGGAAT | + | 6.82 | EWSR1-FLI1 | MA0149.1 | chr15:65175366-65175384 | CCTAGCTTGCTTTCTTCC | - | 6.36 | Gfi1b | MA0483.1 | chr15:65175757-65175768 | AAATCACAGCT | + | 6.14 | PLAG1 | MA0163.1 | chr15:65176446-65176460 | GGGGCCCTAGGGGA | + | 6.8 | ZNF263 | MA0528.1 | chr15:65176158-65176179 | GAAGCAGGGAGAGGTGGAGGA | + | 7.51 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00179 | chr15:65172839-65178037 | Adipose_Nuclei | SE_00949 | chr15:65174130-65175109 | Adrenal_Gland | SE_00949 | chr15:65175332-65176800 | Adrenal_Gland | SE_04179 | chr15:65175534-65176600 | Brain_Anterior_Caudate | SE_06037 | chr15:65173704-65176966 | Brain_Hippocampus_Middle | SE_07417 | chr15:65174128-65177139 | Brain_Hippocampus_Middle_150 | SE_09222 | chr15:65172751-65178816 | CD14 | SE_12439 | chr15:65175616-65176658 | CD3 | SE_13731 | chr15:65173976-65175138 | CD34_Primary_RO01536 | SE_13731 | chr15:65175365-65176693 | CD34_Primary_RO01536 | SE_19509 | chr15:65174104-65177154 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20451 | chr15:65174035-65176951 | CD56 | SE_25922 | chr15:65173689-65176787 | Duodenum_Smooth_Muscle | SE_26878 | chr15:65174167-65175164 | Esophagus | SE_26878 | chr15:65175386-65176861 | Esophagus | SE_29936 | chr15:65174596-65175161 | Fetal_Muscle | SE_29936 | chr15:65175381-65177037 | Fetal_Muscle | SE_31256 | chr15:65174141-65175130 | Fetal_Thymus | SE_31256 | chr15:65175181-65176841 | Fetal_Thymus | SE_31840 | chr15:65174479-65175098 | Gastric | SE_31840 | chr15:65175828-65176741 | Gastric | SE_42313 | chr15:65174019-65176830 | Lung | SE_43954 | chr15:65173800-65175308 | MM1S | SE_50230 | chr15:65174179-65175183 | Sigmoid_Colon | SE_50230 | chr15:65175191-65176819 | Sigmoid_Colon | SE_52555 | chr15:65174086-65176814 | Small_Intestine | SE_55484 | chr15:65174598-65175047 | Thymus | SE_59387 | chr15:65156174-65198203 | Ly3 | SE_62974 | chr15:65169474-65198305 | Tonsil | SE_67436 | chr15:65173800-65175308 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr15 | 65176143 | 65176677 | chr15 | 65175297 | 65176800 | chr15 | 65175391 | 65175749 |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I064880 | chr15 | 65173183 | 65177998 |
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Enhancer Sequence | AACCAAACTG ACTGGCACCA AAGAAGGGCA AAGGACACTG ATGAAACACT CCCAGACACT 60 GGGGCAACGG CTGGCCAGGG CTGGAATATT CTGTGACCCC CACAGGGGAA AACTAAGTGA 120 AATATCTGAA AACATCACAA ACATAGACAC ACTATCACAG CCTCACAGGC AGAAAGGGAA 180 CTTACCAGGC ATCTGGCCCT GACACAGCAT GAGCTCTGGA ATGATGATTG CGGGTACACT 240 GCCCTCCCTC CCTTCGTTTA GCCACTGTGC AGAGTGAACA CCCACAGGTC TCAGCATGTG 300 ACTCTCTTCT GCAAGAGTCA GCCCAGTGGG GAGACAGACA CTCCGGAAAC CTAGATATGT 360 GCTGGGCTGG GTGGCAGTGC CACAGCTGGG CACTTTACTC CCCAACATAA ATGTAGGCAT 420 TTCTGTGTCT TGTGAGCCCA TGAATCCTCA TAAGACCCTG TTGAGTTGGG AATTACTGCA 480 GAGCTGTAAC AGACAGAAAA CCTAGGCCCA CAGACAGCCA GTGACCTCCC ATGGGCACAC 540 AGTTTGGGTG TGGCAGAGCG CGGTATGGAA TCCAAGCCTT CTGGTGCTAA ACCCTGCAGG 600 ATTCTGGCAG GTCACACTCC AGGCTCCCAA GCCAAGCAAG CGTTTGAAAA TGCCTTCCCA 660 TGTCCAGTCG CGGTGGCTCA CACCTGTAAT CCCAGCACTT TGGGAGGCCA AGATGGGTGG 720 ATCACTTGAG GTCAGGAGTT GGAGAACAGC CTGGCCAACA TGGTGAAACC CCGTCTCTAC 780 TAAAAGTACA AAAAAAATGA GCTGGGCGTG GTGGCACGTG ACTGTGATCC CAGCTACTCA 840 GGAGGCTGAG GCATGAGAAT TGCTTGAACC CAGGAGGCAG AGGTTGCAGT GAGCCGAGAT 900 CATGCCACTG CACTCCAGCC TAGGTGACAG AGTGAGACCC TATCTCAAAA AAAAAAAACA 960 AAAAAAAAAC GAAAATGCCC CTCTGTGAGC CACAGGCTCT GCCCCTGCAG TGGGCTATCT 1020 ACCTGTCCTA GCTTGCTTTC TTCCTCAGAA ACAGATGTTT CATCCTCCTA CCATTCTCTT 1080 GACTGACTCC ACAATTGTGG CTAAGACAAA CTGGGTGAAT CACATCTAAA GCAGAAGCAA 1140 GTCTGCATGA ACCCCAACAC TTCCCCAGTC AATTTCCTGT GTTAGGTTCA GAGGGGTCAT 1200 TTCAAACTCT CAGCATGTTC AAGACGAGAC TGCCTATAAG GCCACGTCTT GGGACATGGT 1260 TTAGGGGAGG AGGTAGGAAT ATGTGGCAGG GCCCTCTGGC TATACGGATC TCCCTATCTG 1320 CTGGAAACTC CACCACTAAA ACCATTCCTT TGTATCATTT CCCCAGAGGG ATCTTGATAA 1380 TTGTGAAACG CCAAACAACT TGCCAGCCAT GAGTCCCAAA TCACAGCTAT GAAAGTGCTT 1440 TACAGTTTAT AAAGTGATTT CACAGCGAAA AATGGGTTTG CTCCTCATAA CAACTATGAA 1500 AGTTAGGGCA GCAATTTAAA TGTGTCCATG GAATAGATGA GGACACTGAG TGAGGCCCTG 1560 AGAGGCAGAG GAATTCCTCT GCCAATCAGA GCCCACACTT GAATACAGGT CTTTCTACTC 1620 CACATTGCAT GTACCCCTGA TAACTGGGAG TTGCCTTGGG AGCAGATGCT GATGGGACAC 1680 AAAACAGGCA GATTTTGATA AGAAGGCAGA TGATGAGGTG GAAAGGCTCT GAAGAAAGAG 1740 GTGGATGGCA GAGCTTGGCT AGAGGGGAGC AGGACTCCCC AGGGAATCGA GGATCTGGGC 1800 AGGGGAAAGG GTAGCCTGGA AGCAGGGAGA GGTGGAGGAT GAGCTCTGGG AGCCAGAACC 1860 TGAATTCTGT TCCGGCCCTG TTCTGAAGCC TGAGGGGCTG GAGTGGACTT CTCCTCTAGG 1920 ATCTGTCTGC CCTGTCTGCT CTGAGGACCT GCCAGCTCTC CTGGGAGGCG CTCAGGGCAT 1980 CTTGTGAGCC TGTCAGCACT GACCTTGTCA CGCGGCTCAT GACTGCTCCT CATCCGACCT 2040 CAGATGAGTC AAGAGGGGAA GCAGGCGCAA AGGGCTTCCA GGGGATTCCC GGGATGCAGG 2100 CAGCTTGGGG CCCTAGGGGA AAGAGCCTGG GGCTCTTCAA GGCTGGGCTA TGAAGCCACC 2160 CTCCTCCCAG GGTTGAGGGG CAGTCAAAAT ATCCCCAAAC CTAATGTGAT TTCTCACCTG 2220 CCAAGTGGCA GCAGTGTGGC ATCGGGGCAT AAAAGCTGCT AACAGTGGGG AAAGGCCTGG 2280 CCCAGTGCCA AGCAGGCTGT GGGCGTCCCT AGAAGAATGA GCAGCGCAAC TACAGCAGGA 2340 GTCCCAGGCC CTGGGCAGAG AGACACCCCT TTATCGAGAC CTACTACCTG CCAGGCACTT 2400 TATTTATTGG TAAATTTAAT CAGATTTTGA AAACCACAAA ATCTGGATAC ATTTGCATTG 2460 TGGTATTTGT TGTAATTGTT GGATATAATT ACATATACAT GCTATAAAAT ATAAGATAGA 2520
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