Tag | Content |
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EnhancerAtlas ID | HS044-06163 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr18:22810320-22811710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr18:22811026-22811042 | GCCTGAGTAAATAAAA | + | 6.11 | PROP1 | MA0715.1 | chr18:22811625-22811636 | TAATCAAATTA | + | 6.02 | TCF7L2 | MA0523.1 | chr18:22811652-22811666 | TAAGATCAAAGAGA | + | 6.12 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_13164 | chr18:22809711-22811929 | CD34_Primary_RO01480 | SE_13629 | chr18:22804729-22815127 | CD34_Primary_RO01536 | SE_14234 | chr18:22806781-22814596 | CD34_Primary_RO01549 | SE_38153 | chr18:22807145-22816415 | HUVEC | SE_66798 | chr18:22811027-22811761 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I025227 | chr18 | 22807496 | 22814791 |
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Enhancer Sequence | CTCCAAAGAA CACACAGGGA CTCACTACTC CAAGCGGGTT GGTCCACACT CTTCAGGTAT 60 CAGACTCCTC CAAGACTTTT GTGGTGATGG TCTCCCCGCC AACATACTCT GAGGTCTACC 120 TAAGACTTTG AGAGTTATCC ATCCCCATTA ACTTAGGCTT TTTGGCAGCC ACAGTGCAAA 180 CTAAGCTTAA ATGGTGAATA TAGGTTTAAA CGATGTCAAT TTCTTTTTAC ACGTGGAAGA 240 AACTGTAGAA GATTCTTTCA ACTCAGGTTC CTGAATCAAC TTTAACTTTT TTTCCCTTTG 300 GCACTAAGTG CTACTTACAG GGACTGTCTT TCTGGGTGAT GGCAAGTTTT CTGCATTTCA 360 ATGTGAAGTA CTTAACATGT CCATGTTAAA TTTTAATTTT TGAAACCAGT CTCTTCACTT 420 GAGCTGACTC TCCGAGAGCT GTAGCTCTTA CTGCCGAAAA AGCTTTGCTA GAAACCAGCT 480 CTGTGGCCTA AAAAGTCTAT TTAAAGATGC AAATGTGTGT GCATGGTTAG TGCAGATGTT 540 TTTCTACAGC AACTGTACTT GCTGAGTTTC ACCATTTCCA TAAAGCACAT TAAAACAAGT 600 GTGTGAACAC TCCGAGATGA AAGTCTCCAA CACTCCTGAG ACTTTCAGTG GAAAGTAGAG 660 CCGCCTGACT TTTCTCCAAG CAGACAGGAA TGCCCATGAT TCAGCAGCCT GAGTAAATAA 720 AAGAGGTCCT TATTTCCTAA TTTCGCTGGC TGGCCACACT GCAGCAGCCT CTGTGTTTCT 780 GCCAAAGGGG ATGCAGAACT GGAACTACAC CCAGCCGCTG AAGGCCTGTC TTTGTTAGCC 840 AGCCAGGCTT TCCGGACCAT CTTCTGGCAG CAGAACGGCC ATATCCTGCA AGGAAGACCT 900 CCATCTCAGG CTAGGCGCTT CTCTAGTCTG CCTAAAAGGA CGAAACAACA GATTTTGCTG 960 GGTCTGTGTT GGAGGAGGAC AGCTGGAAAC TCAGTTAGCA GCAGAGTAAC ACCTGTTCAG 1020 GCATATTTAT GGGGGAAAGT GCTCACTAAC AGAAAAGTGA AGTCATACCA GAAGGAGTTA 1080 TTCCACAGAA AAAAGGCAAC AGAACACAGA GTACCTTTGT GACGTGAGCC ATCAGCCCCT 1140 CGTGTGCCAA CCTGGGGAGG AGGAAGCAGA GACTGGACGT GATTTGATCC TAGCTCCTGC 1200 TGATGGACAG ACAAGCACGC AAATGAGGGT CTGAGAGTCT GTTTACAGCC TGCCATTGTG 1260 GAAGAGAAAT GCTGAGGGTT CTGGCCACTC GCTGGTGTTC AAGACTAATC AAATTAGCCA 1320 GAAATTAGAA AATAAGATCA AAGAGAGAGG AAGAGAATAT GTGCAGAAGG GCTAGACTAA 1380 TGTTAATGCT 1390
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