| Tag | Content |
|---|
EnhancerAtlas ID | HS101-17997 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:15866440-15867900 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr17:15867248-15867266 | GACATGTCTGAACTTGCT | + | 6.18 | | TP53 | MA0106.3 | chr17:15867248-15867266 | GACATGTCTGAACTTGCT | - | 6.28 | | TP63 | MA0525.2 | chr17:15867248-15867266 | GACATGTCTGAACTTGCT | - | 6.77 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_34155 | chr17:15866015-15870747 | HCC1954 | | SE_34419 | chr17:15865569-15871441 | HCT-116 | | SE_47449 | chr17:15865749-15870863 | Panc1 | | SE_64592 | chr17:15866382-15867738 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I015962 | chr17 | 15865615 | 15871372 |
|
Enhancer Sequence | ATTACAAGAA CTCTTGCTTA TAATACAATG CCATCTAATT AATGAAAAGG AATGATTGAG 60
TTAAGCAAAT CACCATTTCA CGACTGTCAT AGTAAGAACT GATTCAGGCA AGAATCATCA 120
ATAGGTGCTA AAACTTGTAG GTGAAAGTTT GATGAGGAGT AAGATACTTA CAGTCCCCAA 180
ACACGTACCA CAAGATACCT GCTAATTAAA ATGGGAAAGT TATGATGGAG AAACCTGGCA 240
GACACCACAT CAACCAAGTG CCTTCTCATG TACCCCTCTT GCTGGTCGCT TGTGTTTATG 300
GCGGCTGATG CTTTTGACAG TTAATGTCAC ATCTGAGGCA GTGCTCCGTA ACCCCAGCCT 360
TGGGAGGGCA CTTTTTGGGG CAGAGGACAG AGTGTCCTGT TATCTTTTGG TCTGGTTCCA 420
GGCAGGAGCC CTTTCTCTCA GGGACTGCTT ATTTTATGGG AAGGAGATCA GAGTCTGGAG 480
CCCAGTAGCT TTGGGCTGTC TCTGTGTCCC ATGTGATCCA TGAAAACAGC ACATGAGAAT 540
CACCAGGCCC AAAGGGGAAC TCTGGGAGAC CTGGTCCTGG CCCCTAACCT CAGTCTCAAC 600
TGGTTGAATC ACTGGTGGAC CACCTTGGAT TGCCTCTTCT TGCCATAGGA AGCTGGTTGG 660
GAGTGCTGCC AACTTTCTTG ACCGCAACCT GCATTGCTCA TCTTTTGTTC TTAGGGGACT 720
GTGAAGGACA AATGGCATCT CTCCCAGCCA CCTTCACATA AGACAGTGGG CTCAGCTCAG 780
GCCCAGCCAG GTCCATCACT GGAATTCAGA CATGTCTGAA CTTGCTGGAG TAGATGAGAA 840
CCCCACAGGA GCCAGAGCAG CCCGGGGCCA GGGCCTCCTG GGAAGACTCG GCCTGAAAGT 900
AACCTTTGGT GACCACACCT TGCTATCCAG TGGGCAGGCA GATGCTGTCC TTTCCTCAGA 960
CTGGCCTGCA GGCTACAGCC GTGCCCATCT GCAGAGATAA GGTGGTTTGC CCTCAGGACG 1020
CAGATGGCAG AGAGGCCTGC TTCCCGTTCA TATAAGTAAA ATCTAATAGT ATCTACTTTT 1080
TTTATTGTTG TTTTTGTGTA AGAATGGTTT TATTTGTTCC TTAAATGTTT GGCAGAATTA 1140
GTGAAATCAT CTAGGCCTAA AGTTTTCTTT GTGGGAAGGT TTAAAATGAT GAATTTTAGG 1200
CTGGGCGCTG TGACTCACAC CTGTAATCCC AGCACTTTGG GAGGCCAAGA TTGGCGGATC 1260
ACCAGAGGTC AGGAGTTCGA GACCAGCCTG GCCAGCATGG TGAAACCCTG TCTCTACTAA 1320
AAATACAAAA AAATTAACCA GGTGTGGTGG CAGGCGCCTG TAATCCCAGC TACTCAGGAG 1380
GCTGAGGCAG GAGAATCGCT TGAACCTGGG AGGTGGAGGT TGCAGTGAGC CGAGATCATG 1440
ACACTGCACC TTCATTCCAG 1460
|
