Tag | Content |
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EnhancerAtlas ID | HS176-39274 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr8:22084670-22085700 |
Target genes | Number: 21 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr8:22085113-22085133 | CTCCCACCCACCCCCACACT | + | 6.28 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27590 | chr8:22083898-22089937 | Esophagus | SE_28211 | chr8:22084688-22085560 | Fetal_Intestine | SE_35070 | chr8:22083825-22086458 | HeLa |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I022226 | chr8 | 22084161 | 22086549 |
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Enhancer Sequence | GGCTCCATAC CCTGGCCACC ATTTTCCTGG GAAGGCCACC CAGACACTCC ACAGCCTTGG 60 CCCCTCCTCG AACCCCCCTG ACACCCCGTT CTCTTGGGAA CGGAGGGGAA AAGCCACAAA 120 GTTGAGGACG GCAAGGCCTT CATTTTTTAA GGAGACTTTG AGAGCTCTGC ACACTGCAGT 180 GCCGTCTCCA CGGCAACGGC AAATGCTGAG AAGCCAGGGA GGAAGGGAAA ATATGCCTTA 240 TTCTTTGGGG GGGAGGGTTA AGGGGGTGGT GTTGAACATT CACGTCACCG TGGCAACTGG 300 CCTGCCAAAA GACACCCAGA TCGGGAGAGC CGGTTCCAGA GAAAGAGAGC GGGTGAGTAA 360 CCCACGCCGG TGCCGTCGGC CTGGGAGCCA GCTGGCCGCC TCACTCCCCC TGCCTCTGCC 420 AGCTTGAGAG GATGGGGGTC TTCCTCCCAC CCACCCCCAC ACTGGCTTTT AACCCCAGGA 480 AAGGACACAC CCACGGAGGA CTCTCTCCCA TTCCTTTTCT AAGTCAAGCA AATGGCAGGC 540 CAGCAGGTGA GGGGCCCGAG AGGGAGAACT GAGGCCACAG CAAAAGGGCT CCGCCCCGAC 600 CGAGGCCCGT GTGGCCCACC CAGCCAACAG CGAGGCTGTG CCCTGAGCCG GGGCTTTGTC 660 GAGACTTGAG ACGTCATCCC CATAGGCGAA GCCTGCGGCC CCACCCTACC CGGGCTCTCT 720 GCCCCTGCCT GAAGTCTCAG TTGTGGCGCT GATAACAACG CTCCCTCTGT GCTAGGCGCC 780 GGGCCAAGCA CCACGCAAAC ATGACTCACT GCATCCTCTC CACGACCCCG TGAGGCTTGG 840 CATTGTTATT CCCTCTTTAC CAGGGAAGGA GCTCAGGCTC AGAGAGGTCA AGTAACTTTC 900 CCAAAATGAC ACAGGAAGAA GAGTGTGGAT TTTAACCAGC CTCTGACTCC AAGCCATCAC 960 TTCCAGGTGT TCCCTTATCC GGCCTCCTTC AGGAACAGAA GCTGGGGAGG GGCTCCCAGG 1020 ACACCTTCTA 1030
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