Tag | Content |
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EnhancerAtlas ID | HS095-04703 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr10:129669550-129671070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:129670020-129670039 | CAGCCAGGAGGTGGCACTC | + | 6.35 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28206 | chr10:129670363-129671295 | Fetal_Intestine | SE_29082 | chr10:129670279-129674277 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I127872 | chr10 | 129670446 | 129673113 |
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Enhancer Sequence | TCAAGGCCTG CCTTCTGAAT TCCTTTGTCT CATAGGGTCC TCCCTTAATG TGTGCATTCT 60 CACTTCCCCT AGGAGTAGCA GCCCCTGAAG GCCAGACTAC TGTGAATGCT GCTGCTCCTC 120 TGGGTCTAGC CACCCAGTCG GGCTGCCACA TTCCAGGCTG GTGCTAGGGA TATCTACAAG 180 GGATCCAATG ATGTAACTTG TCCAGTCTCC CAGCAGTGGC AGGGGAGAGA CATAGACTGA 240 GATTTTCTTG GTTGTAAATA GCCTTAGCAT GTTGGCTTTC TCAAAGCCAA CAATAGTAGT 300 AACGTACTAG GTATATGGAA ACGTACTTTC CATATGGAAA GACTCAACAT CTGGTTAGCC 360 AGGGTGATGC AGGCAATGTC AGTAGGCGAG GTTGCACAGA GGTTTTCTTC TTCCTGAGTA 420 ATGTGTTATT GTGCCTGCAG ATGCTGCAAT GGATGGTGGC AGCTGGCCAC CAGCCAGGAG 480 GTGGCACTCG CAAAAGATCA CCAGCTGAGG TGGTAGTGAT GGGGTTGGTG CTTGCCTCAT 540 GTTACCCAGG GGAGGTACTC TGGAGTCTCA GGCAATGGGC GGGGTCCTGG AGTTCCCAAA 600 CGTCCCTGTC CCTTGTGTTT ACCAGGGCAA GTGAAGGGGC AAAGCGGGTC AGGCTAGATC 660 AGGTAAGTCC ACGCCCTGGC TCCCTACATG CAGGGGCAAG CAGTGTCCTC AGCGGGGGAT 720 TGGAGGGCAG TTCTCTGGCT GCTGGGATAA TGTTCCAGAG ATGAGTGTAG CTGCCGCTGC 780 TGCACAAAAG AATCCGCATG GGGAGTGAGG AGTAACAGGC GGCAGTCAGT CCCACTCAGC 840 TCCCACGCAC TTGGCAAGGA AGGCCTCACA CCCGCAGGGT TCAGCCAACA GCAGCGAGCT 900 GGGTTCCAGG CAGCCTGCTC TCAGAACTCA AAACCGCCCA GGCCATGAGT CTTCCTGATA 960 GAGACAGAAA CCTGGCTTTC ATGCTTCGGC CCTCCAGGTC CACCCGGGAA GCAGGGGTGC 1020 CAGCTCCTGC ACTCGTGGCC ATAGCACACT TCCCAGTTGC CCCTGGGTTC AAGCCAATAG 1080 GGTTCGTCCC CTCTCGAGAT TATGTGGCAA AACTCAGTTG GGAGCTTCTC TCACCCTGTG 1140 ACCACCGCCT GAGTCGGCTG GCAGACTTCC ACAAGGGCCC CTGTGGGATG GGATCAGGAA 1200 TGGCTTCGCT CCATCACCGC TGGAGCCTGG GAGTGCCCAC AGAGCCTGTC CCGATGCTGC 1260 TCCTCCCTCT GTTCTCCCCA CCACTCACTA ACTCGGCTCC AGTGCTGGGC AGGGTCATGG 1320 GCTTCTGAGG GTTGCAGCTC CCCTGTGGGA GTGAGCGTCT TGGCAGCTGT GTCTCCCCTC 1380 ACGCTCTAGA GACTCAAAGT CTTCCATCTG CTTCGCGGTA TAGGCTGCTG CCCGCCACTT 1440 CTTTCAAAGG GACTATGGTT TCTTTCCCTT TCTGTTAAGT TCCTGTGTTG CTCTTGGAGA 1500 AAAGTTCACA GTGTGACTCT 1520
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