Tag | Content |
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EnhancerAtlas ID | HS017-06448 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr11:94975700-94976820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr11:94975788-94975799 | AAGCAATAAAA | + | 6.32 | NFAT5 | MA0606.1 | chr11:94976659-94976669 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr11:94976659-94976669 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr11:94976659-94976669 | ATTTTCCATT | + | 6.02 | SOX10 | MA0442.2 | chr11:94975782-94975793 | AAAACAAAGCA | + | 6.02 | Sox3 | MA0514.1 | chr11:94975855-94975865 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09975 | chr11:94974123-94976451 | CD14 | SE_11552 | chr11:94974109-94976217 | CD20 | SE_29469 | chr11:94974127-94979167 | Fetal_Intestine_Large | SE_62584 | chr11:94960773-94991031 | Tonsil | SE_63441 | chr11:94962357-94990341 | NCI-H69 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I095241 | chr11 | 94974449 | 94977451 |
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Enhancer Sequence | TTTTCCACAC ATTATCCTTC ATTCAGACTT AATGCCTGCA GGTCCGGTTT AATGATTTCC 60 CAGAGTTTAT GAACGAAAAA GAAAAACAAA GCAATAAAAA CAAAAATCAA AGTTAAATTT 120 CCTCAAAAGT TTTCAAGAAG GAAGTAGTCA GGACAAAAAC AAAGGGAATG AGGGCACTTT 180 GTCTCAGGAT ACAAATTAAA GATCACTGTG GTGGCCTCTG TGGGGTGGTT ATAAAGGGGA 240 CCAGGTGTAT ACTAGGAAGT CATTTAGTTT TAGAAATGTA AATATGTGTA AATGTTTTAA 300 TTTTACTCAA CTTGCCAGAG GTAGAATGTC CCTGGACAAC TAACTGATAC ATTTCTTTAG 360 GGCCAATCGC TGGCTTTAGA AGAGCCTCAG CTAATCACAG TAGAGCTGGA CTGTTGTGGT 420 TTTCCATTCC TTTGCATCGT ATTCCTCAGT CTCTGCGGAA GGCACTGCTC CTTCCTTTCC 480 TTTCTAAATC TCTCTCTGTC TCTCTCTCTC TCTCTCTCTC TCTCGCTCTC TCCTCCCCTA 540 GTTTATCCTG GACTCATGCT GAGCTCAGCA ACCCTTGAAC TCATTTTCTA TCTGACATGT 600 GAAATAGTTC TTAGGTTTCA TTAAACATTT GGAAAATAAA CGAGGTACTT CGCTCTGCCA 660 CTTTTCAGGT ATGGTGAAGA AAATAAAATG GCCTCCCTGG GCAGTACTAG ATGGGTTGTG 720 GTTGTGCTGG CCTTGCTCTT GATGAGATAG CACTACTGTT ATTTCTGTAT ATACCAGACC 780 TGTCACTTTG CATTTTCTAT TTCTCAGTGA AGACATGAAC ATCTAGACAT TCCACATGTC 840 TATGGGGAAC TAGAGTGTCC AGGAATGGAA GCAAATGGAA ACATTCTCAT TATGCAAGTG 900 TAACTTTAGC TGTGACCTAA AATGTATTGC CTAAGACTTC TATAAGGGTG AAATTGAAAA 960 TTTTCCATTT TTTTTAACCT CAATATTGTA TAATCTAGTC ACTGTTCAAA AACTCCTCAA 1020 ACTTCATTTT TCATTACTTC ATAGGGTTTT TTTGTGAGGA TTAAATTAAA AGACATATGT 1080 AAAGCACTGA GAACAGTGTC TCCCCTATCA TTAGTACTCA 1120
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