Tag | Content |
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EnhancerAtlas ID | HS133-09604 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:93510680-93512900 |
Target genes | Number: 11 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr14:93512491-93512508 | CAGGGCATCTTGACCTC | - | 6.27 | ESR2 | MA0258.2 | chr14:93511661-93511676 | AGGTCAGAGTGGCCT | + | 6.66 | Gata4 | MA0482.1 | chr14:93512804-93512815 | AGGAGATAAGA | - | 6.14 | HES2 | MA0616.2 | chr14:93511862-93511872 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr14:93511862-93511872 | GGCACGTGCC | - | 6.02 | Klf12 | MA0742.1 | chr14:93511071-93511086 | AAGAAGGGTGTGGCC | - | 6.25 | Klf1 | MA0493.1 | chr14:93511075-93511086 | AGGGTGTGGCC | - | 6.32 | LHX2 | MA0700.1 | chr14:93512053-93512063 | ACTAATTAAC | + | 6.02 | RUNX1 | MA0002.2 | chr14:93511647-93511658 | AAACCACAGAG | - | 6.14 | ZNF263 | MA0528.1 | chr14:93511134-93511155 | AAAGGAGGAAGAGGAAGAAGC | + | 6.88 | ZNF263 | MA0528.1 | chr14:93511890-93511911 | GGAGGAGGAGGTGAGAGGAGG | + | 7.65 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_03888 | chr14:93504983-93513044 | Brain_Anterior_Caudate | SE_04808 | chr14:93494251-93514329 | Brain_Cingulate_Gyrus | SE_05777 | chr14:93493302-93514911 | Brain_Hippocampus_Middle | SE_06743 | chr14:93509612-93512256 | Brain_Hippocampus_Middle_150 | SE_07721 | chr14:93492779-93514769 | Brain_Inferior_Temporal_Lobe | SE_09265 | chr14:93510048-93513026 | CD14 | SE_23185 | chr14:93505279-93514419 | Colon_Crypt_1 | SE_23918 | chr14:93509314-93512076 | Colon_Crypt_2 | SE_23918 | chr14:93512135-93512869 | Colon_Crypt_2 | SE_26366 | chr14:93505659-93512899 | Duodenum_Smooth_Muscle | SE_26889 | chr14:93505113-93512411 | Esophagus | SE_27639 | chr14:93505251-93519390 | Fetal_Intestine | SE_28556 | chr14:93505100-93524844 | Fetal_Intestine_Large | SE_34796 | chr14:93505024-93514368 | HeLa | SE_40660 | chr14:93505046-93514961 | Left_Ventricle | SE_41563 | chr14:93509310-93512004 | LNCaP | SE_41563 | chr14:93512123-93512958 | LNCaP | SE_42451 | chr14:93505095-93514218 | Lung | SE_48575 | chr14:93505057-93512067 | Right_Atrium | SE_48575 | chr14:93512083-93513885 | Right_Atrium | SE_49689 | chr14:93509996-93512067 | Right_Ventricle | SE_49689 | chr14:93512119-93512836 | Right_Ventricle | SE_50538 | chr14:93509223-93514489 | Sigmoid_Colon | SE_52403 | chr14:93505242-93519331 | Small_Intestine | SE_57475 | chr14:93510071-93511486 | VACO_503 | SE_65267 | chr14:93507414-93512032 | Pancreatic_islets | SE_65267 | chr14:93512106-93514234 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I093038 | chr14 | 93504881 | 93524683 |
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Enhancer Sequence | GGTCCAACCC CCTCCGCAGA GATAGGAAAG CTGAAATCCA GACACAAGGA AGGGACCATG 60 AATAAGTTTG TGCTGGCGAT TACTGAGAAA GTCTAGCATA AAAATTAAAC CGAAGCCTAG 120 GCCGAACACT GGCATCCCTC TGCTTGGCTG TGAAGCTGGT GAGGATGCTG CACTCGGCCT 180 GGCAGCAGAT GGAAACTCTG GAACTCGAGG GCCACGGATG AGCCACAGGG CCCCCCAGGT 240 AAAGGACTGA CAGCCAGCCA TGCAAGCCCC TGGGACTGAC CCAGATGCAG AACTGACCAA 300 TGTGGCGACA ACCATCACCC AACCCTGTGG GGCTGTAGAT CTCAGAGGAG GTGGGACAGT 360 GGCCCAGCGG ACAGCAACAC GGCAGAGAGG GAAGAAGGGT GTGGCCTCTG TCTATGGCCT 420 GGCCAGAAGG GCCACCGCAA GCACCAAGGC TAGCAAAGGA GGAAGAGGAA GAAGCAAGAA 480 AAACCCGACA CCGTGACGGA CTAGCGTGGG CCGCAAGTCA GGGTTGTGGT TCTTTAGGAT 540 ATATCTTAAC AGGGTAAGGG CCTTAAATGC CCTTTCCCCA CCAACCTGAC AGGGTTTAGC 600 ACCAGGACTC CTGGCCAGGG CAGGCCCCAG GGCTCTAGGA TCTGTCAGAT CAGGAAGAAA 660 GGGGCATTTA AGGTCTCCCT CCTGTAAGAT CTACCTTAAA GAACCAGATC CCTGACTTTG 720 CAGCCCAGTG CCATGCTGCT TTTGAGCCTG AAATGGAAGT CTGTGCCTTA GTTCCAAGTC 780 ACCAGGCACT GGTTCCTTGC CCTTGCAGGC ACAGGGCATC AAGATCAAAC CAAACCTCCA 840 AGCCTCACCT CTCACAAATA AGCAGAGGCC AGTTACCCCT CTGGGCAAGA CCTCAGGCCC 900 CTGTCCCTGC CAGTCAGCAG CTCTGCCTCC CGCAGCGCTT GAGGGCTGGT CCATGCAGCC 960 GGCCAGGAAA CCACAGAGGC CAGGTCAGAG TGGCCTTTTA ATTCAACTCC CCTGGTGACC 1020 CTGAAGAGCA CTGCCGCAGA CTGAGAGGCT GGAAGTAGGC TATGCTGCCC CTGCCCCATA 1080 ACAAAGACTC TACAGCAAAT CACCAGGATG GGGGAAGATT AGCGCAAAGT GGGTGGAGAG 1140 TCTCCCTGAA ACGTACTGAC AGCACTTAAA AACCAATTAG ATGGCACGTG CCTGTAGTCC 1200 CAGCTACTCA GGAGGAGGAG GTGAGAGGAG GATCACTGGA GCCCAGGAGT TCAAGGCTGA 1260 AGTGCGCTAT GATTGCATCT GTGAAATAGC CACTGTACTC CAGCCTGGGC AACACAGCGA 1320 AACCCTATCT AAGAAAATCC AATTAGAGAC CTTGGCTTAC ATGCAATCAG AGAACTAATT 1380 AACAAGGACC AGTAATTAAA ATTAAGCTAT ACTCTCTAAT TCAGACTTTT TTTTTTATTC 1440 TTTCAGAACT AATTTCAGGA TCCAGTTTCT AGCCTGGACA CAACCCAATC CACCCTGGGC 1500 CAGAACTGCC AGAATACCTT CCCTGAAACT GTCCTCTGCA ACTACCTAAA AACCTTCAAT 1560 CGCTCCCCAG TGCCCCCAAA TGAGGACCCA CGTTGCCTCC GACTTCCTTT CCACACTCAC 1620 AGCTCACTGC CTCCCAAGCG GTCACTGCTC TGGCGGGACG GGTCCACCAG TGGTCTGTGA 1680 GCCGGGCCTC AAGCCCTCAC CAGGCACACA CAGAGTCCTT TTTGACCCCA TCCCCACCCC 1740 ACGCTCTTTT CTTCTGCAAA CCTCCCAGTG TGGTCTGGGG CAGTCAAGCC GCACCCCTCC 1800 CTCCTGACTC TCAGGGCATC TTGACCTCAT CGCCCAGGCT GACCACAAGT TCCAAACAGG 1860 ACTTTCTTGT GGCCATTGCT CAGGTCCCAG GCATGCACAA ACCCACTCAC AGACACTTGG 1920 CTGAGAGAAA TCTCAACCAT TAGTGCTACT CCCATTTTCT ATTCTGAGGA GGTAGAAACT 1980 GAGGCTCAGA GAAACAGCGC TAGCCCGGGG CCCCACGGTG GGGACAGCAG GGTCTGCACA 2040 GGGTTGGCCT GGCTCAAGCT TCCTTTCCCA CATGGCCCCA TGTGCTCCAG ATAAAGGCAA 2100 CTATGAACCA TGTTCCTGTC ATAAAGGAGA TAAGACATAC ACACAGGATA TGGTGATTGG 2160 GCAGGACGCA ATTTAGTGCT CAGACTTTCC TAAGTGCTCT GGGCTTCAAG ACCTTCAGAA 2220
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