Tag | Content |
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EnhancerAtlas ID | HS105-47749 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:219922420-219923400 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr2:219923216-219923226 | GCCCCGCCCC | + | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23646 | chr2:219921771-219926449 | Colon_Crypt_1 | SE_24654 | chr2:219923154-219926304 | Colon_Crypt_2 | SE_25299 | chr2:219921472-219926421 | Colon_Crypt_3 | SE_27657 | chr2:219922726-219926611 | Fetal_Intestine | SE_29068 | chr2:219922636-219925481 | Fetal_Intestine_Large |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I219058 | chr2 | 219922821 | 219922970 | GH02I219059 | chr2 | 219922997 | 219926270 |
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Enhancer Sequence | GAGAGGAATG TGCGCGAAAT CAACCAGAGC GAAATCAGCC GGAGGAGCCG GCCGAGGTGC 60 AGGTGTAGGC GCAGCCTCGC CCAGAACTCT CCCGCCACAC CCAAGGGAGC TGGAAGCCCG 120 GGAGGGTGCT GTCCCTCTCC CTTAGGAACA GAGGGCCCTG AAGTGCTCCC TCCCTAGCAT 180 ACAGCCGCCC CCGGGGATCT GGACCGCACG GCGGTATCAC AAATCTGGAG GAGGCATGGA 240 GGCAAGCGCC CTGGCGGCGC CTTCACTGGT AGGTGGAGGT CCCCTCTCTC CTGTGCTGTC 300 TTCAGCTCCG GGTATCCATC CCTCCACAGA CAGGACTACA CCTTTCAGCG CCCGGTCCCT 360 CTGTGCCTCC AAGGCAGGAG GGCCAGCCAG CGGCCGGGAG GGAGGAGTGG CAGCAGAGCC 420 GACTGCCTGC GGCCGGCCTG CGAGGCGTGC AAGGCCCGAG GTGCCCAGTA GGTGTCACCG 480 CAGCCTCAGG GCTGAGGCCT GGGGACGACA GGCTCTGGAG GCGCGGCAGG TGCAGAGCGT 540 CTCGGTAGCT TCAGGGGGTG TGTTGGAGGG GAATCGCCGG CCTGCCTGGA TCCCTCGAGC 600 ACCACCGAGG ATTCCCGCCG GGACCCTCTT ATAATCTTAA ACCGGCCCAC AACCCCGCCA 660 GAGATGACAG GGCCAGGGAA CCAGAAACCG GCGGATTAGC GCCAGGGCCG CCCAATGGGG 720 GGCCACATGC AACGTCTTCC TCTGCAAGGC GCAAAAGGGG CTGACAATCC CAGACCTCCA 780 GGACCTCTGC ACCGGTGCCC CGCCCCTATA CCGTAGGAAG GAACTCCATA AACCAAGCTT 840 CTGATCTCAG GGAGCCAGCT CCACCATCCT CCTCACGTGG AGTTGGGGTA GAGCCGCGCC 900 CTGGGGGAAG GACCGAAGCG GTCATCCTTG GTTGCTGCCT CCTGGTGTGC CTGGGTCCTG 960 AGAGCCCAAG AGACTGTGCA 980
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