| Tag | Content |
|---|
EnhancerAtlas ID | HS136-14381 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr3:193549310-193551230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr3:193550099-193550120 | TCCCAGTTTCACTTTCACTGA | + | 6.8 | | PRDM1 | MA0508.2 | chr3:193550107-193550117 | TCACTTTCAC | + | 6.02 | | ZNF263 | MA0528.1 | chr3:193550774-193550795 | GGAGGACGAAGAGAGGGAACA | + | 6.27 | | ZNF263 | MA0528.1 | chr3:193550771-193550792 | GAGGGAGGACGAAGAGAGGGA | + | 6.95 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_26640 | chr3:193545583-193555892 | Esophagus | | SE_28285 | chr3:193549235-193550677 | Fetal_Intestine | | SE_29192 | chr3:193549119-193550715 | Fetal_Intestine_Large | | SE_33797 | chr3:193545336-193550466 | HCC1954 | | SE_36824 | chr3:193545523-193550492 | HMEC | | SE_65134 | chr3:193545781-193550434 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I193828 | chr3 | 193545921 | 193550968 |
|
Enhancer Sequence | CGCAGTGAAA CCTGGCTGGG GAGGGTCACC GAGTGTGTAT TACTAATTCG ATCTCCGCCG 60
CACCCTTGGT CTCATGCCCA GCACCTTTGT GTGGTGGTTA CTCAAGGATG TGGGAAGCCG 120
CTGGAGCGAG GCTGCTGACG CACCCCATTT CAGAACTGCC AACGCGGGCT CCTTGGCAAC 180
CAGAGCTCAC CATCTGCCCA GGCAACCAGG GAGGGCACAG AGGGCAGTGA GCCTCTGCCA 240
GGATGGACAG TTCTCAGCAT TGAAAACTAG CTGTGGGTTC TGCCAGTACC GTGGAGCCAA 300
TTGTACGTCT CATTCAGCCT CGGGTCCTGC CTTGCCAGCT GCGTGTGGGC CATCTTAACT 360
TGGATGATCC CTGGACGCTT ACCATTTAAG AGCATAAGGG TGGATCAGTC ACTTTCTCTT 420
AGAGGGCTCC ATTTTCCTGT CTTTGTCATG AGAAGATTGG GCTGCAATAG TCTTCCATGT 480
GCCTTCCAGC ACCGTGCAGT AGGATACGGC GGGTGTGGAC CTTGAAAGCC AAAACGTCGA 540
TGTTCATATC TGGCTCTGCT GTGTGACTGC AGGCAGGCCC CTGAACTTTT TCACCCTCAT 600
TTCTTTGCCT CTGAAATAGG GCTAGATAAA GCCTCTTGGC CCCTGGCCCC TGTTATTACC 660
CCCAGTTAAC AACAGCGCTG ATAATGACCC ACACTTACTG TTGGCTTCCT GTGAGCCAGG 720
CCGTGCTCTA AGGGCTTGGT ATATGATAAC TCATCTCATT TGTGAGAAAA TCTCTCCAAA 780
GCAGAAACTT CCCAGTTTCA CTTTCACTGA GAGTGCTCAT GGGCCTTCCC AAGGCCACAC 840
AGCCAGCAAG TATTATGTCT GGGACTTGAA CTCAGTAGTG AGAGCTTACC TTCTACACGG 900
TTCTCTCTCT GCAAGAGGAA CCCCGTAAAT GTCATGTCCA TTTTCTTCTC CTTTTCTCTT 960
TCAGCTCGGC ACACTTCTTC ATTTGGTGTC CAAAGTAACA TCCACCTACT CTTAATGTTT 1020
TCGGCCGGGT GCAGTGGCTC ATGCCTGTAA TCCCAGCACT TTGGGAGGCT GAGGCAGGTG 1080
GATCACCTGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC ATGGTGAAAC CTCTTCTCTA 1140
CTAAGAATAC AAATATTAGC CAGGCGTGGT GGCAGGCAAC TGTAATCCCA GCTACTCAGG 1200
AGGCTGAGGC AGGAGAACTG CTTGAACCTG GGAGGTGGAA GTTGCGGTGA GCCGAGATTG 1260
GCACCACTGG CACTCCAGCC TGGGTGACAA AGCGAGACTC CATCTCAAAA AAAAAAAAAA 1320
AAAGTTTTCA CGACTCTCCT CATCCCACAC AGTCACCTGT GACTCCTGTC TTTTCTCCCA 1380
ACCCCTTTTA CTTCCATATT TCTTAGTGTT CCAGTTAGAG GGAACTGCTT GTGCAAATGT 1440
CCCGTGGCAA GAGAGAGTGC AGAGGGAGGA CGAAGAGAGG GAACAACACA GTGGCTGCCT 1500
CCAGGCAGGC TGAGCTTGAT GAACCAACAG GACCCTGACC ATCTGAGCTT TGAGTTCTTT 1560
CTGCCTGCTA AGAGAAATGA GAAACTTCTG AAGCACTTTA AGTGAAAGAG TGACATGATC 1620
CAGGCTACCT TTTAAAAATA GTTTTTATCC TGCTAGAAAC CTTTCCAGGA GCCAGCAGGG 1680
CCTTCCTATT CTGAGCCAAA GTTTTTCTGC CTCATATTCA AAGCCTCTGT CCAGCATCCA 1740
ACTGGGACAT GTGTCTGGGT TGGGGGCAGG GAGAAGGGCT TCCCAGGTGG GTGGATGGGA 1800
TATGTAGTGA AAGACCCTTT CGTTCCAAGT CCGCAGGCCT CCAATGGGCT CTTCCACTCC 1860
TAATGCACAG CCCCTCACCT GTTCTCTGCT TTCAAATGGC CCTTTGCCTC CTTCCACAGA 1920
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