Tag | Content |
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EnhancerAtlas ID | HS133-20686 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:44885960-44888650 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr21:44887313-44887330 | TGACCTCAGGATGACCT | - | 8.03 | RREB1 | MA0073.1 | chr21:44887594-44887614 | CCACACACCACACACACCAC | + | 6.01 | RREB1 | MA0073.1 | chr21:44887637-44887657 | CCACACACCACACACACCAC | + | 6.01 | RREB1 | MA0073.1 | chr21:44887787-44887807 | CCACACACCACACACACCAC | + | 6.01 | RREB1 | MA0073.1 | chr21:44888089-44888109 | CCACACACCACACACCCCAC | + | 6.12 | RREB1 | MA0073.1 | chr21:44888086-44888106 | ACACCACACACCACACACCC | + | 6.14 | RREB1 | MA0073.1 | chr21:44887910-44887930 | CACCACACCACACACAACCA | + | 6.21 | RREB1 | MA0073.1 | chr21:44887856-44887876 | ACACACACCACACCCACACA | + | 6.37 | RREB1 | MA0073.1 | chr21:44887858-44887878 | ACACACCACACCCACACACA | + | 6.52 | RREB1 | MA0073.1 | chr21:44888015-44888035 | ACACACACCACCCACACCAC | + | 6.58 | RREB1 | MA0073.1 | chr21:44887946-44887966 | CCACAAACCACACACAACAC | + | 6.65 | RREB1 | MA0073.1 | chr21:44887731-44887751 | CCACACACCACACACACACC | + | 6.68 | RREB1 | MA0073.1 | chr21:44887803-44887823 | CCACACACCACACACACACA | + | 6.68 | RREB1 | MA0073.1 | chr21:44887572-44887592 | CCACAAACCACACACCACAC | + | 6.77 | RREB1 | MA0073.1 | chr21:44887615-44887635 | CCACAAACCACACACCACAC | + | 6.77 | RREB1 | MA0073.1 | chr21:44887658-44887678 | CCACAAACCACACACCACAC | + | 6.77 | RREB1 | MA0073.1 | chr21:44887981-44888001 | CCACAAACCACACACACCAC | + | 6.77 | RREB1 | MA0073.1 | chr21:44887997-44888017 | CCACAAACCACACACACCAC | + | 6.77 | RREB1 | MA0073.1 | chr21:44887579-44887599 | CCACACACCACACACCCACA | + | 6.8 | RREB1 | MA0073.1 | chr21:44887622-44887642 | CCACACACCACACACCCACA | + | 6.8 | RREB1 | MA0073.1 | chr21:44887957-44887977 | ACACAACACACCACATACCA | + | 6 | RREB1 | MA0073.1 | chr21:44887583-44887603 | ACACCACACACCCACACACC | + | 7.01 | RREB1 | MA0073.1 | chr21:44887626-44887646 | ACACCACACACCCACACACC | + | 7.01 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23438 | chr21:44888247-44889261 | Colon_Crypt_1 | SE_24060 | chr21:44888279-44888683 | Colon_Crypt_2 | SE_24764 | chr21:44888323-44891277 | Colon_Crypt_3 | SE_28233 | chr21:44888186-44889479 | Fetal_Intestine | SE_29330 | chr21:44888056-44889500 | Fetal_Intestine_Large |
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| Number: 3 | ID | Chromosome | Start | End |
GH21I043460 | chr21 | 44880833 | 44886047 | GH21I043466 | chr21 | 44886429 | 44887522 | GH21I043468 | chr21 | 44888121 | 44889206 |
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Enhancer Sequence | AAAAAAAAAA TCAATGTGTG TACATGTATC GGGAGTGTGC ACTCAAACTT TTGATTGTTA 60 AAGGAGGGTT TTCACAAAAG CTGGGAGACC ACCCTTCTAG AACCCTGCCC TTGTAGGTCC 120 AAGGCTACGC GCCCTGGCAG ACTTCCATGA GCTGCGACTA CCAGCCACCA AGACGGTGTG 180 CCCAGCCAAC CCTGGTCCCC AGCTAGCTCT GACCCCTGCC CTGCCAGCAT CACCCTGAGA 240 TTCTTCTGCA AATTACAGTC TTCTCAGACT GTCTGTCGAC CCTGGGGTCT CAATGCTGGG 300 TTCTCAACAG GCAGAACCAC AGGGCTGCAT TGCGGGTTGT CTTTGAAAAA TGACCTGCCA 360 ATAGAAAGTT GGGGACGAAA GCCCTCCAAC AGTCTGTCCA AGCGACCCCC AAGAGAAACC 420 ACAGTGGGGT GCTGGAGGGT CCCCAACGAG GCACCCCCCC CCCTCCGACC ACCCTGCTGT 480 TACTTCCACC CACATCGAAG TCCTAGGGTC TCTTCTAATT TCCTACTTGG CCGTGCCTGA 540 AATGCCACTT CCAAAACCCG CATTCCTATG GTTGCAGAGG CCACAAGGGA GGGCCCTCGT 600 GGTATTTTTT CAGGACCCAA AACCACGAAG ATGCCAAGAA TCACAACTTT CACACAAAGG 660 ACACACTTTC TTTGATGGAA TCTTCAGATC ACACATCACA AAGGCAGCAC GCCATCAGTC 720 TTTGAAATGT CCCAAAACAC GTAAAGAATG TTCCGCTGCA GATCCGGCTT GTTTCACGGG 780 TGTGTGGCCT CCTCTTCCGA AGTCATTTCA TTCTTCGGGG TCTTTGACAC GCTCTGGCAA 840 CAAGCGCGGA GAGGTGAACG GGGCAGCGTT TGTGCTGAGA GTGGGCTGAG AGCGCCGCCC 900 TGCCCACTCC GGCCTGGGGC ATCCCATCTC TGCCAGGTTC TGGGCTTTGC ATTTTCTTTT 960 CATTTCATTC TTCCCAGGCA AGAGCACAAG GAAACAAGCA GAAGGAATTC AGAGAAACAG 1020 CTCCAGGCTC CAGCTCAAAG GCCGACACCA AAAGCGAACA CCTCTGGGCG CTCTTGCCTT 1080 CAAGAAGGTG GGGAGGCTCA CAGACGCAGC ATCCACCCCT CGCAGGGAAC CTCAGTTCCT 1140 GGCCTGTGGT CCCATGAAGG ACATCAGGCT GGCAGATTGG AGCACACCCC TTCTTTCTAA 1200 CCCCTCTTGA AAGCTTCCTT GAATCTGCCA GTCCTGCCCC CTGGAGCAGG AAGGAAAACA 1260 GAAGGCCTAG GACGCTAGAG GGGTCCCGAG CTTTCCGGAG CTCCAGCCAC CATCAGGTCT 1320 GACTGCTCAG GGACAGACAC ACCGACCACA TCCTGACCTC AGGATGACCT GCGGAAGTAC 1380 TTGGCATTTC TTCTTAGCCA AATCCCTTCA TTAAAAGACG GGTGAGGGTT CCAGCGCTGC 1440 CCTCTTCCTT CTCAAAACTC TTATTTCAGG GCTGAAGCCC AGACGTCCAG CCCGTCAGAA 1500 ATCCCCTTAG CCTGAGCTTG GCACCCAGAA GCTAGAGAGT AAATGCACAG GGGCCGGGGT 1560 CTGAGCCCTT CCGCAAGGAT GGGGATGGGG GCCACAATCC ACACACACCA CACCACAAAC 1620 CACACACCAC ACACCCACAC ACCACACACA CCACACCACA AACCACACAC CACACACCCA 1680 CACACCACAC ACACCACACC ACAAACCACA CACCACACAT TACACAGCAC ACCACACACA 1740 CACACCACAC ACACCACACA CCACATACAC ACCACACACC ACACACACAC CAAACACACC 1800 ACACACACCA CACACCACAC ACACGCACCA CACACCACAC ACACCACACA CCACACACAC 1860 ACACCACACA CACCACACTT ACACCACACA CACACCACAC ACACCACACC CACACACACC 1920 ACACACACCA CAAACCATAC ACACAGCACA CACCACACCA CACACAACCA TACCACACAC 1980 ACCATACCAC AAACCACACA CAACACACCA CATACCACAC ACCACAAACC ACACACACCA 2040 CAAACCACAC ACACCACACA CACCACCCAC ACCACACACC NNNNNNNNNN CTACACATCA 2100 CACACCTCAC ACTACATACC TCATACACAC CACACACCAC ACACCCCACA TACCTCCCAC 2160 ACACACCATA CACACACACT AGATCTCAAA CATAACATAC ACCACATACC TCACACCCCC 2220 CCGACACTAT ACAGCTCACA TATACACAAC ACACACCTAC CTTACACACA TGCCACACAC 2280 TCCACATCCC TTACACACAA TCAGTATATA TCACACATAC ACAATACATT CCTCACACCC 2340 CACATACCTC ACACAACCAC ATACACTACA CACACATCGC ACACTACCTC ACACACATAC 2400 TGTATACCTC ACACATACAT TTCACACACA CCACACACCT CACACACAGT GCACACACAC 2460 CACACCCCTC ACACGTTTCC TTGCAGAGCC GTATTGTGTG TGTGTGTGGT GTGTTCATGT 2520 GTGTACTTGT GTGTATATGG GGTGTGTGGT ATGTTCGTGT GTGTACTTGT GTGTATATGG 2580 GGTGTGTGGT GTGTATATGT GTGTGGGGTA TGTGTGTGTG TGGTGTGTGC GTGTCCTGCT 2640 CATGCAGAGT GTCCGCAACC ACTTCTCGCC TCCTCTGTCC CACCCGCCCA 2690
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