Tag | Content |
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EnhancerAtlas ID | HS040-16137 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr17:73599820-73600960 |
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) |
EWSR1-FLI1 | MA0149.1 | chr17:73600624-73600642 | CCCTCCCTCCCTCCCTCC | - | 6.03 | KLF14 | MA0740.1 | chr17:73600548-73600562 | TGCCACGCCCCTCC | + | 6.06 | SP3 | MA0746.2 | chr17:73600548-73600561 | TGCCACGCCCCTC | + | 6.08 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_23082 | chr17:73597298-73601104 | Colon_Crypt_1 | SE_24179 | chr17:73599887-73600883 | Colon_Crypt_2 | SE_52698 | chr17:73599237-73601046 | Small_Intestine |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I075603 | chr17 | 73599888 | 73600030 | GH17I075604 | chr17 | 73600161 | 73600310 |
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Enhancer Sequence | GCACATGGAG CTGCCAGGAA CCCCAGAGGC AGCTCTGTTC CCAGAGTTCA GAAACCTCCA 60 AGAAAAGCTG GTGGCATTGT CCGTTTTGTT GTTTGCCTAT CTGGCCTTTG GCTATTGACT 120 GGATGGCATC TTGGGAATCC TCTGAAGGGC TGGAGTTTAC CCCAAGCACA GGGACAGAGG 180 GAGCAGGTGG AGTCACTTCT CGTTGATGTC CAGCTGAGCT GGGCTGGTGG CTGCCTCAGA 240 AGGGAGGGGG CAGCTACTAG GAGCAGCAGC CTCACCCCAG GGCTCTGTGG ACCTCCTTAG 300 CCTGTGATGG CCTTGGCAAT GGGGATGGCC TGGTTGGGGG ACTGAGCAAA AGGCAGGCAG 360 TAGGGATGGG TGTTCCCAGC CTTGAGTCAG ATCCTGAGAA GCTCCAGGGC GGGGCACGTT 420 CTGTCTCTGC CATCTGGAAA CCTACCAGCT ACAGCAATTG TCACCTCCAA CAAGAACCCC 480 TGAGCCCGGA AGCTGGGTGA GAGGAACCTC CAGGTACAAC TCTCCACCCA GCACAGACCA 540 GGTCTGCTGA TCTGTGCCAT TCCCTGATGC ACTGTGGCAT CCCGTGACCA CAGACTGTCA 600 CCCACATCCC CAGAACCTGC ACGGTGCTTG CTTGGTACAG ACTAACTACT GAGTGTCCAT 660 TAAGCCAAAC TGGTACCACC ATCTGGACCT GTGAAATGTC CTTCAACACT CCCCCACCCA 720 CCCCTTCCTG CCACGCCCCT CCCTCCCTTC CACGTCCCTC CCTCCCACGC CCCTCCCTCC 780 CTTCCATGCC CCTCCCTTCC ACACCCCTCC CTCCCTCCCT CCCACAAACT TGTCTTGAGA 840 CCTACTGTGT TGGGTGGCGA GGAGACGAAG GCCTTGGGAA CCACATTCCT GTTGCTCCCG 900 TGGCCCAGAA CCAGCCCTCA TGCCTCCTGC GCACACCATG TTCACCTGTT CTCCCCCTGA 960 GCTCCAGCGC AGAGACCCTC CCTGCCCAAG TTCACTGCAG TGTCTCAGCC CCCAGCTGAG 1020 CGCCTGGCAT AGAGCAGGCA CTTTCCAAAT TTTTTAATGA TCTAGAAATG AAATAAATAC 1080 TGAGGGGCTC AGGGTGTCGT ACAGCAAGTG TGAAAGGGCT TGGGTGCAGT GGCTCACGCC 1140
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