Tag | Content |
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EnhancerAtlas ID | HS101-00528 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:17949670-17950880 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr1:17950741-17950755 | GGTCCCAAGGGAGT | - | 6.15 | ZNF263 | MA0528.1 | chr1:17950555-17950576 | TGCCCTTCTCCTCCCTCCACC | - | 6.22 | ZNF263 | MA0528.1 | chr1:17950548-17950569 | TTCCCCCTGCCCTTCTCCTCC | - | 6.41 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_01537 | chr1:17947922-17953357 | Aorta | SE_09560 | chr1:17949821-17964167 | CD14 | SE_26573 | chr1:17950237-17952175 | Esophagus | SE_40808 | chr1:17949037-17953149 | Left_Ventricle | SE_49224 | chr1:17948837-17952605 | Right_Atrium | SE_65277 | chr1:17948671-17950143 | Pancreatic_islets | SE_65277 | chr1:17950412-17951739 | Pancreatic_islets |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I017621 | chr1 | 17948068 | 17950143 | GH01I017624 | chr1 | 17950866 | 17952070 |
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Enhancer Sequence | GTAAGTGTCC CCAAACTTTT TCCCCAGCCC ACCAAGGTAA AACCACAACC AGTCTGACCC 60 CGGGGCCATG CAGTCCAGCC TCCTGCCTCT GCCTGCTTGC CTTGTTCAAG TCAGTGGGAT 120 TAGAGGGTGG CAGGGTCTTC TGGGCCTGAT CTAGGGGTGA GTGTGACACC TTGAAGTGGC 180 CAGGATGTCC TTGGATATAC CTGGCAGGCC ATGGTGCTGA TGAAGCCAGG TGGCTGTCCT 240 GGCTCCTCCC AGGTGGCAGC ACCCCCTGGC CTCCCAGTCA CTGTGGGCAG CCACCTGGCC 300 GGTCACAAGC TCTCTTACCG AGCACTTGAG GGGTTTCAAG CCAGTGTGAA ATGCTGTGAA 360 AGACCACAAC TTTGGCCCGG AGAGGATGTG CCGCAGTGCT GGGGAAAGGG CACTGGCTCA 420 CGATCCGGGG GACCTGGTTC TGGTCCCAGC TCAGTTCTGC AACCTAGGGC AGGTCCAGGG 480 CCCACTCTGA GCCCAGGCTT GCCATCTGTG GAATGAGGGG TGCACTGGAT TTCTGGCTTT 540 TCTAGCTGAA GTCTGCGGAC CCCAGATGTT CATGGGGTGA GGGAAGGTCA AGTTGGTAGC 600 ACTCTACTTT GATGTGTTTT AGGTAACTAG GTTTTGCTAA AAGAAAAAAA CTTTTTTTTG 660 AAAGCCACAG CGCTCGATAG AGTCACTGAA TAGGTCTGAT GTTCTGGGTG TATATCAAGG 720 GGCTCTGGAG AGAGAGTTGA TTGACTCCAG GCCGACCATC CCTCCCTTGG TAACTCAACT 780 CTGGGCACGC TGCCCGGTGA GAGGCCAGGA GCACTTTCCT TAAAGGTGGA GGGCAAGGGG 840 CATTCGATTT CCTGAACGTG AATGCAGTAG AAGGGGTGTT CCCCCTGCCC TTCTCCTCCC 900 TCCACCTGTG GGCTTGGGCT GCTGCACTGG GGATGGAGAC CTGGGAGGCG AAGGTCCCCT 960 GGGCTCTCCT GTGGCACCAC CCCATCCCAC CTGTGACCTC AGGCCAGCCT CTCTACCTCT 1020 CTGAGCTCCA TGTCCACACC CCAGTGGGGG TGATGGATTT GCACAGCTCG AGGTCCCAAG 1080 GGAGTGTGGG GTGAGTGCAG GCGCCCTTCT GCTCCCTGCC TTGAGGCGGC CTCCCTGGCC 1140 CACACCTGCC TCGTTTCCTT CTGCTCCCTG CATTGAGGCG GTCTCCCTGG CCCACACCTG 1200 CCTTGTTTCA 1210
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