Tag | Content |
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EnhancerAtlas ID | HS101-04009 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:222060250-222061220 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:222060687-222060698 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr1:222060687-222060698 | GGATGACTCAG | + | 6.14 | RREB1 | MA0073.1 | chr1:222060325-222060345 | GGGAAGGGGTGGGTTGGGGG | - | 6.22 | RREB1 | MA0073.1 | chr1:222060324-222060344 | TGGGAAGGGGTGGGTTGGGG | - | 7.16 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_36705 | chr1:222058928-222062088 | HMEC | SE_55946 | chr1:222059265-222061847 | u87 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I221886 | chr1 | 222059486 | 222061718 |
|
Enhancer Sequence | CTGTCCTGGG TGAGCAAGCT GCTGGCATCT CCTGTCGGCC ACAGGAGGTG TGTTGACAAG 60 GGCCAGGAAA TATGTGGGAA GGGGTGGGTT GGGGGGAGTT TCCTAGGCAG CGTTCCTCTA 120 GGAACTTTCT TCTCTAGGAA TTCTCTTAGA TCAGCATCCA TTGCCTGTCC ACTGGGTCAT 180 AAGCTTTCCT TATGCACGTT CAGTTGTTAA ATCTACAACA CCTCTCGCCC CCACACAGAC 240 TTTCACTCCC GCTCAAGAGA GGGGTCAGGG TGTGTGTGTG TGTTGTGAGC AAACTCCTTC 300 ATTGCCATGG ACCTGGCAGA GGCACAAGCC AGCCCCATTC CAGGACCATG TGACACTGGC 360 TGGGTTACTC ACTTGTTTGC CCTCCAGCAG GGGCAGCCGG GGACACCTCC CTAGAGTGAC 420 TACAGCGTTT ATCCCTGGGA TGACTCAGCC CAAGCCTCCC TCTGCCCAAA AAGGGAATCT 480 GAGGCTGGGG CTGGAGATGG GGCCTGTTGA TTAGCCGCAT CTATGGTTGG GAGAGCATAG 540 AAACTACCTC TCACCTGGGA AACATGAGGG ACAGAGTGAG TAATGCTCAG ATCAGTGGCT 600 CAGGAACTCA GCGTGAAACA TAAGTTTATT TGAGAAGCTC AAGTGACAGG TGGAGCTTTG 660 CTTCCAGAAC CCCAAGGAAG ATCCTACTCA GCCACCTAAT GATAACATTT TCATTTCAGA 720 TTTCCATTCA TTTCATCTCA CTGACTTCAC TCTCACCTTT ATTTTGTTTT CGTCATTTCT 780 GGAGTGGGTC AATTACTTAA CCCTGAATAG AGATGTGATA TAGCAGAGTC TTAGGGTGGG 840 TTCTGGCTGA TTCCTCATCA AGAATAAGAT TCTATTTCCT TTGTCCTGAA CAGGATAATC 900 TCTTCAGATT ACAAAGCTGT ACCTACCTAG TATTGTTTGT TGATGTTTCT GTTGTTTATA 960 AACACTGGTC 970
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