Tag | Content |
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EnhancerAtlas ID | HS098-10785 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:76478940-76480620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:76479388-76479406 | ACAGCCTTCCTGCCTTCC | - | 6.11 | EWSR1-FLI1 | MA0149.1 | chr11:76479787-76479805 | TGTCCCTTCCTTCCTTCC | - | 6.87 | EWSR1-FLI1 | MA0149.1 | chr11:76479392-76479410 | CCTTCCTGCCTTCCTGCC | - | 8.41 | EWSR1-FLI1 | MA0149.1 | chr11:76479791-76479809 | CCTTCCTTCCTTCCTGCC | - | 9.17 | RREB1 | MA0073.1 | chr11:76479514-76479534 | CCCCCACCCAACCCCCCTGC | + | 7.3 | ZNF263 | MA0528.1 | chr11:76479766-76479787 | TCCACCCTCTCTCCCTCCCTC | - | 6.84 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23234 | chr11:76478337-76483138 | Colon_Crypt_1 | SE_23987 | chr11:76478488-76483118 | Colon_Crypt_2 | SE_24911 | chr11:76478422-76484811 | Colon_Crypt_3 | SE_26826 | chr11:76477083-76483151 | Esophagus | SE_29250 | chr11:76478154-76484512 | Fetal_Intestine_Large | SE_32156 | chr11:76478741-76483150 | Gastric | SE_33832 | chr11:76478498-76486146 | HCC1954 | SE_34932 | chr11:76478452-76485751 | HeLa | SE_50399 | chr11:76478504-76483315 | Sigmoid_Colon | SE_52588 | chr11:76477874-76485218 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I076768 | chr11 | 76478435 | 76484606 |
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Enhancer Sequence | AGGTCCTGGA GGAGAGGCCT TCCAGGCGCT AACGACCCAC CCACTGTGCA TCTGAGGAGG 60 AACCTGGGCT CAGAAAGGGG AGTGGTGGCT GCTCCAAGAT CCCACGGCCA CCCTGGCCAG 120 GCCAGGCCTG GACCCCAAGG CTAGACTCTC TCAGGAGAGG GACAGAAACA GAGAGAGACA 180 GAGATACCAG CTCAGACAGG AGAATGTGCT CACCTGGCAA AGTCAGAGCA GTAGGGAGGA 240 AACATCTGCA ACCACTTGGC AAGCACAGGC AGCTCCTGGC AGCTTTAGCT CTCCACAGTC 300 AGGAGCCTTT GAGCACTGGG AGAGAAACAG CCTGGATTTG CTGCGTTCCG TGAGATCCCT 360 ACCGTTCTCT CAGGGGACCC TCCCACCACC AACCTCTACC TTCCCAGTCA CTGCACTCAG 420 TGACAGCAGC AGGTGCCTCT AACTCCACAC AGCCTTCCTG CCTTCCTGCC TTTGCACACT 480 CGGCTCTCTC TGCCTGGAAT GCTGCCCCTC CCTTGTCCCC CTGACTCTTC CTTGCCTTGT 540 CTTCTCAGCT GATGCTTCTC TGAGGCTTCC CAGCCCCCCA CCCAACCCCC CTGCCCCCAG 600 CCAGCCCGGC CTACTCCTTG AAGCAGATCA GATGCCATCT GCCCTGGCTT CCCCAGCCAG 660 AGTGCCTCCT TCCCTCTGTC GCAGTGCTGG TCACACCCAC AGTCACTGTC TGTGTCTGTG 720 TCTGCCTCTG GCACTGGAGG GGAAGCCTCT GTCAGCAGGG TTGGGCTCTA ACCTAAGGCA 780 ACATCCCCAA TTGCAGCAAA GGGCTGACCA CAGAGGACCC ACAATTTCCA CCCTCTCTCC 840 CTCCCTCTGT CCCTTCCTTC CTTCCTGCCG CAAATACTGA CTGAACTCCT GCTGTGTGCC 900 AGGCACTGCT CTAGGTGCAG GAGCTACAGC AGTCAACAAC ACAAAGCAGT GAACAAAGTC 960 CCTGCTCCAT GACTGCCACT CTAGGAGGGG ATGAGGAAGC AGACAATAGT GACAATACAA 1020 TCAATAATCC AGAGAAGTTT GGGTGGCGAC AGGTGCTATA AAGAAAGTAA AACCACGTTT 1080 ACTGAACTCA GAACTGCAGA CAGGGAAACC AGGGGTGCAG ACAGGTACAG TGGGCAGGAA 1140 GCAGGGGCAT GGTAAGTTCC AGACCCTCTG GGCCCCTCTG TTACCTTCCC TCTCAAGGGC 1200 TGCCAGGCGC TGGGGGAGGC AGGCATGTGG GAAGGAAGCC TTGGGGCCCC CCTGGAAGTG 1260 CCAGACGTCT CTCCCACCCA CAGACATACT TCCTGGCTCT CCAGGAATTT GATTCAGCAA 1320 CAGCAACTTA GCAGTTACTT GTGAAAGTCA CAAGAACTCC CTTGAGAGTT CCAGGGGTGG 1380 AGATGGCCTC CGCCGCCTCT CACTGAGCCT CCCAACAGCC TGGCGAGGTG GGCATGATTA 1440 ACCTCCCATC GAAGGAGGAC CCAAGGTCAC ACTGTTGGTC CCTGGCCCGG CTGAGATTTG 1500 AGCCCAGGTC AGGTGACTGC TGGGCCCACA GGCCTCCCGC CACCCCCTAT AGCCTCCCAA 1560 AGCCTTGGAG GGCAAGCAAG TGGTCCAGCC ATGGCTGCAG CCTGGACACC AAGGACCTAA 1620 GCCCAGCACA GGTGAACTGA ATGGGAGTCC CTCAACTCCT CTGGGCCTCA GGTTCTCTCT 1680
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