Tag | Content |
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EnhancerAtlas ID | HS101-00105 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:2135500-2136380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr1:2136333-2136343 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr1:2136330-2136345 | CAAGCCCCGCCCCTC | + | 6.34 | SP2 | MA0516.2 | chr1:2136329-2136346 | TCAAGCCCCGCCCCTCA | + | 6.16 | SP4 | MA0685.1 | chr1:2136330-2136347 | CAAGCCCCGCCCCTCAA | + | 6.09 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_02984 | chr1:2135742-2136307 | Bladder | SE_24063 | chr1:2135543-2136326 | Colon_Crypt_2 | SE_28207 | chr1:2135320-2136370 | Fetal_Intestine | SE_29530 | chr1:2135575-2136399 | Fetal_Intestine_Large | SE_40333 | chr1:2135518-2136309 | K562 | SE_46689 | chr1:2135346-2136306 | Ovary | SE_47622 | chr1:2135695-2136333 | Pancreas | SE_54645 | chr1:2135111-2136378 | Stomach_Smooth_Muscle | SE_62490 | chr1:2120386-2191742 | Tonsil | SE_68393 | chr1:2120436-2162432 | TC32 | SE_68394 | chr1:2120436-2162432 | TC32 | SE_69135 | chr1:2135338-2136316 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I002203 | chr1 | 2134602 | 2142348 |
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Enhancer Sequence | GTTGGTGAGG CCAGCTCCTG CCATCTCGGG TCCCCATGCG CTTCTCAGAT GTGAAAGCCC 60 CTTGCTGGCC TCCACAGACC CTCACAGACG GCCTCACAGG CCAACACCCA GCGGCTGCAC 120 TGCCCATGGT CACTATCTCT GCAGCCCGCG TGTGCGGCCA GTGTCCCTCC GGTGACCCCA 180 GGCCCAGGTG CCCGGCTGTT GGTCCTGCCA GCATCGTGAG CCGTGGTCTG CCGTCCTGGC 240 ACATCCTGAA TGGAGGTGCA CGCATAGAGG CTGCCTGTGA ATCTCCTGCG CTTCCTCAGA 300 GGGATTTGCC CCCTTCTGGG ACGTGCCCTG GGGACGGTCA GTTCTCCCAA ATAGTGACTT 360 CCTTTCTCCA CATAATGAGA GCCTTTGGCT GAGGGATTGG GAGGACCAGG AAAAAGCCGC 420 CAGGCCACGT GGGGCGTGAC TTGGCGATCC CGGTGGCTCC GGGCGTCAGC TTGGACCTCA 480 GACGCCCCTC ACAGCTCACA GCCCTGTGGC CTGCTCTGAG GGCCCCGCCC GCCGCCGAGC 540 CCCCGGGAGC CGGAGAACCC GCAGGACGTC AGCCGGGTGG ATTCCCTCCC ACTGCCCCTG 600 ACCCCACTGC CCAGCGCCTT CAGGACTAGC GGATGATGGA CTTGTGCTAA ACTGGCTACG 660 ACCCCTCCGG AGCAGGGTCC TGGGTAAATC AGCAGTGAGC TGCAGGCTCA GCCAGCCGCC 720 GCCTTTGGTT TCCTCCCGCC GCCGGCTCAC CCCACCTCAG ACCCGAGCTA GCTCTCCAGC 780 CTGGTTCCTC TGCCGGACCC TCCTCCCGGG CACCTCCCAC GCCCCGCCCT CAAGCCCCGC 840 CCCTCAAGCC CCCCTCCCTC CCTTCGGGCC CCCCATACCC 880
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