| Tag | Content |
|---|
EnhancerAtlas ID | HS101-19504 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:73599390-73601120 |
Target genes | | Number: 31 | Name | Ensembl ID |
|
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 | | Myog | MA0500.1 | chr17:73599715-73599726 | CAGCAGCTGTC | - | 6.14 | | SP3 | MA0746.2 | chr17:73600548-73600561 | TGCCACGCCCCTC | + | 6.08 | | Tcf12 | MA0521.1 | chr17:73599715-73599726 | CAGCAGCTGTC | - | 6.02 | | ZNF263 | MA0528.1 | chr17:73599517-73599538 | CCCTCTCTCTCCTCGTCCTCT | - | 6.73 |
|
| | 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 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I075603 | chr17 | 73599888 | 73600030 | | GH17I075604 | chr17 | 73600161 | 73600310 |
|
Enhancer Sequence | CAGGTGGGGC CCAGCACCTC GGGGCAGGAC TGACAAGGAG GCCACCGGGA GTGACTGGCA 60
GCCCCGGGGG TCCTTCTGAT TGGAGATGGA CTCACTCTGC CCAGGACTGG GCCTAGCACC 120
CAACCCTCCC TCTCTCTCCT CGTCCTCTCA TCCTCTCTCT CTCTCTCTTT CTCTCTCCAT 180
CTCACTCTCT TCTACCATTC ACCATCCCTC CACGCATTCG TCATTTCTTC TCCTCTCTGC 240
AAACCTCTCC TGTGCTGATG CCTGGGCACC AGAGATGAGG TGGGAGCAGT ACCTGCCCTA 300
GGCGGGGCTC ACGGTCTAGT GCCCACAGCA GCTGTCCAGG GAGTGCAGGC TGAAGCAGTG 360
AGATGGCAGG GGGGACGGAG TGAGAAAAGA GCCTCTCAGA AGGGCAGGAG GGGCGGGGAG 420
GGGCGGGGTG GCACATGGAG CTGCCAGGAA CCCCAGAGGC AGCTCTGTTC CCAGAGTTCA 480
GAAACCTCCA AGAAAAGCTG GTGGCATTGT CCGTTTTGTT GTTTGCCTAT CTGGCCTTTG 540
GCTATTGACT GGATGGCATC TTGGGAATCC TCTGAAGGGC TGGAGTTTAC CCCAAGCACA 600
GGGACAGAGG GAGCAGGTGG AGTCACTTCT CGTTGATGTC CAGCTGAGCT GGGCTGGTGG 660
CTGCCTCAGA AGGGAGGGGG CAGCTACTAG GAGCAGCAGC CTCACCCCAG GGCTCTGTGG 720
ACCTCCTTAG CCTGTGATGG CCTTGGCAAT GGGGATGGCC TGGTTGGGGG ACTGAGCAAA 780
AGGCAGGCAG TAGGGATGGG TGTTCCCAGC CTTGAGTCAG ATCCTGAGAA GCTCCAGGGC 840
GGGGCACGTT CTGTCTCTGC CATCTGGAAA CCTACCAGCT ACAGCAATTG TCACCTCCAA 900
CAAGAACCCC TGAGCCCGGA AGCTGGGTGA GAGGAACCTC CAGGTACAAC TCTCCACCCA 960
GCACAGACCA GGTCTGCTGA TCTGTGCCAT TCCCTGATGC ACTGTGGCAT CCCGTGACCA 1020
CAGACTGTCA CCCACATCCC CAGAACCTGC ACGGTGCTTG CTTGGTACAG ACTAACTACT 1080
GAGTGTCCAT TAAGCCAAAC TGGTACCACC ATCTGGACCT GTGAAATGTC CTTCAACACT 1140
CCCCCACCCA CCCCTTCCTG CCACGCCCCT CCCTCCCTTC CACGTCCCTC CCTCCCACGC 1200
CCCTCCCTCC CTTCCATGCC CCTCCCTTCC ACACCCCTCC CTCCCTCCCT CCCACAAACT 1260
TGTCTTGAGA CCTACTGTGT TGGGTGGCGA GGAGACGAAG GCCTTGGGAA CCACATTCCT 1320
GTTGCTCCCG TGGCCCAGAA CCAGCCCTCA TGCCTCCTGC GCACACCATG TTCACCTGTT 1380
CTCCCCCTGA GCTCCAGCGC AGAGACCCTC CCTGCCCAAG TTCACTGCAG TGTCTCAGCC 1440
CCCAGCTGAG CGCCTGGCAT AGAGCAGGCA CTTTCCAAAT TTTTTAATGA TCTAGAAATG 1500
AAATAAATAC TGAGGGGCTC AGGGTGTCGT ACAGCAAGTG TGAAAGGGCT TGGGTGCAGT 1560
GGCTCACGCC TGTAATCCCA GCACTTTGGG AGGCCAAGGC AGGCAGATCA CCTGAGGTCA 1620
GGAGATTGAG ACCAGCTGAC CAATATAGAG AAACCCCGTC TCTACTAAAA ATACAAAATC 1680
AGCTGGGCGT GGTGTTGCAT GCCAGTAATC CCAGCTACTC GGGAGGCTGA 1730
|
