Tag | Content |
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EnhancerAtlas ID | HS108-08203 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr11:76480750-76482020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr11:76480949-76480960 | GGATGACTCAG | + | 6.32 | JUNB | MA0490.1 | chr11:76480949-76480960 | GGATGACTCAG | + | 6.14 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_00254 | chr11:76480614-76486015 | Adipose_Nuclei | SE_23234 | chr11:76478337-76483138 | Colon_Crypt_1 | SE_23987 | chr11:76478488-76483118 | Colon_Crypt_2 | SE_24911 | chr11:76478422-76484811 | Colon_Crypt_3 | SE_26826 | chr11:76477083-76483151 | Esophagus | SE_29250 | chr11:76478154-76484512 | Fetal_Intestine_Large | SE_32156 | chr11:76478741-76483150 | Gastric | SE_33832 | chr11:76478498-76486146 | HCC1954 | SE_34932 | chr11:76478452-76485751 | HeLa | SE_50399 | chr11:76478504-76483315 | Sigmoid_Colon | SE_52588 | chr11:76477874-76485218 | Small_Intestine | SE_57784 | chr11:76481611-76482778 | VACO_503 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I076768 | chr11 | 76478435 | 76484606 |
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Enhancer Sequence | CACTCACGGC AGGTGTGCTA CTCAGCACGA GCAGAGGCAA AGCAGCTATG GACTCTGCTC 60 ACCTCACAGC CTGGCACACA GAAAGCTGTG AACTCTGCTC ACCTCCAAGG ATGGGGGTGG 120 AGCTGAGGGC AGGATTGCCC GTCTGGGGAA AGAGGAGGGC CCGATCGAGG GTCAGGTGCC 180 CTGGGTCCAT GCTGAGGCAG GATGACTCAG TAATATTGCC ACTCGCCTCC CCTGAGACAG 240 CCAGCTGCTG TTCCCAGGCC TGGAGAGAAG GCAAAGCCAG CATTTGCTGA GGGCCTACTA 300 TGTGCCCATG CTTCGTAGGG TGTTATTGAG TCTACTATGT GACACACAGA GAGTTAAGTC 360 ACTGGCTCCA TGTTGCATGA GTGTATTAGT TTGCTAGGGC TGCCATAACA AAGTACCAGA 420 GATTGAGTGG CTTAAACACC AGACACGTTT CCTCGCAGTT CCAGAGGCTG GAAGTCGGAG 480 ATGGAGGTGT CAGCAGGGCT GGCTTCTGGA GGCCTCTGTC CTTGGCTATA GATGACCATC 540 TCCATGCTCA CAGGGCATTC TCCCTCTATG TGTGCCTGCG TCCAGATTTC TTCTCCTTAT 600 CAGGACAATG GTCATACTGG ATTAGAGCCC ATCCTGCTGA CCTCATCTTC ACTAAATTAC 660 CTTCTCCCTG AGCCTCTATG TAAGTGAAGC AATTCAGAGC ACAGGCTGTG AAACTAGAGG 720 GCCTGGATTC GAGTGTCAGC TCCACCACTT ACTAGCTCTG TGAACTGAGA AATTTGCTGA 780 ATCTCTCCAT GCCTCAGTTT CCCTCTCTGT AAAATGGGGA TAACAGTAGT GTCTTCCACA 840 TAGAATTGTG AGGATTAAAG GAGTTAAGAT AAGAACCCTA TCTTGCCCAT TGTGAGCTTC 900 AGCTAAGTTG TTAACTTAAG TTTTATTTAC TGGGGCCACT CCCACACATG CCAACAGCAC 960 AAAAACTGTG TGTCACAGCT CTGCCTCTCT CTCAGTGTGT GGCCTCGAAC AACCAATTTC 1020 CCTCTCTGAG CTTCAGTCTG TAAAACGGGG GTAGGAGTCT CACCTCCCAG GGTCACTTTG 1080 AGCGTCAGAC GTGACCACAG CATAAACACT GGTAAATTCT CTAAGAATGT TTCATCCCTG 1140 TAATGACACC AGAAATGAAA ATGAAATCAT GCCGACAAAG TCTCCTTTTT CCTTTCTGCT 1200 ACAGGGCCTG TCCTGCAGCT CCAAAACGAG GACTTAGAGC TGGCTAGGGT GGGAGGGAGG 1260 ATCTCAGCTC 1270
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