Tag | Content |
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EnhancerAtlas ID | HS104-14075 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr12:52636960-52638720 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr12:52637919-52637939 | GAGCTGTGGGTGGTGGGGGG | - | 6.12 | SPDEF | MA0686.1 | chr12:52638127-52638138 | TACATCCGGTT | - | 6.14 | TFAP2C | MA0524.2 | chr12:52638011-52638023 | TGCCTTGGGGCA | - | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_02068 | chr12:52636208-52638805 | Aorta | SE_33886 | chr12:52635925-52644054 | HCC1954 | SE_36332 | chr12:52636699-52641658 | HMEC | SE_47640 | chr12:52636838-52644749 | Pancreas | SE_57989 | chr12:52637542-52638451 | VACO_9m | SE_65936 | chr12:52636117-52644962 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I052242 | chr12 | 52635980 | 52644122 |
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Enhancer Sequence | ATGCAGGGGT GGCCAGCTGA GGCCAAACTC AGGATGTGGA GCAGGAGGTT CCCATCTCCC 60 GGCCAAAGCT GGTGCCACTG TCTCAGACCC CCTTGTGAGA TCTCCAGCAC AGAATGTTCT 120 TGGCCAGGTC CTGGCATGGG CTGATGGGAG AAAGGTCCTG GATGTGCACA GAGCCTGTGG 180 AGGGAGACTC AGGCTGGCTG GCCAGAAGAA AGCCACCACT GGTTCCACAT TGATACTGAG 240 CACTCTGCTT GCACCTGGTT CTGGCTGCAG GGCGCTGTCC CTGGGAGCTC ATCATTCATT 300 GCAGGGACAG AGGACAGCAG AAGACCTTAT AATGACTCAC ATGGCCCTTT CCCACCCACT 360 CCAACCTCAC TTTCCACGAT TCCCCTCACT CTGCTCTGGC CATGCTAACC TGCTTCCTGC 420 ATCTTGCATT TGCCAAGAAT GGTCATGCTT CAGGGCCTTT GCACTTGGCG TTGCCTCCCC 480 CTGGAATGTG GTTCTCCCAG CTCTGTCCAT GGTTGTTGTT TTCTCCTCCC TGGGGTTTAG 540 GAAAAGACCC CTTCTCAGAG ACGGCACTCT CAAACACCAG CCCCTCTATC GGCAGCCTGT 600 CTGAAGTTCT TTGAAGCCCC TGTCACTCTC TGAAATGTTC TGTCTTATTC ATTAAGTGAT 660 TGATGGTCCC TACCTCCACT GGAATATAAC AGATGCCTGG AGAGCAGGGA CCCTGTCTGT 720 CTGGTTCACT GCTCCTCTCT TCCAGCACCT GGCACATGGC AGGGGCACGG GTCTCAGATG 780 AGAGACTGCC TGGGAGGATG AGCTTTGCTG GAAGCTGGGG TTGGAGGTGT TGATGGGGGA 840 AGGGCCCCCA GCCCTGGCTG AGTAGTGTGT GGCCAGGGCA GCTCAGCCTG TGCAGGTGTC 900 TGCAGTGGAG AGAGGGGGAG GGCACACATG TGGAAGCTTC GGAAAGCTGA TTTCCAGATG 960 AGCTGTGGGT GGTGGGGGGA TGTGAGGGTG ATTTACCCAC AAATGTCCTC CCCTTGGAGC 1020 CCTGTGGGCC TGTTTACAGG AGGGCGGAGG CTGCCTTGGG GCACAGAGGC AGGGCCGTGA 1080 GTCACCCCAT GAAGTGGGCC AGCTTCCAGG CCAGGAGGGG AAGCACAGAA TAACAAATGG 1140 TGGTTTCCCA AACCCTGCAG CCTCTACTAC ATCCGGTTCT CCTCTCACAC AACAGGGCGG 1200 ATCCAGGCCT ATAGCCAGGT GTCTACCACC ACTGAGGGGC GTCATGGGGA GCTACAAGGG 1260 GTCTCCAGAG GCAGCGGGGA TGGCGTTGGC TCTGGGGGCA CCAGTGTGAC AGGGCAGGGC 1320 ACCGAGCTGT GGCCGAGGGG CAGAGTGTCA GAGGGCCTCC TGGGGAATGC TGTCTCTGGC 1380 AGAGAGGCAG ACTGCCTCCA CTGAGGGAAG AGGATCTGAG GATAGAGAAT GGCCGGTAAG 1440 AAGGGAGAGA AGTCCTTGCC CAGGGGACAG GGATGGTGGT TTTCTGAGCT AAACAAGATG 1500 AGGCCTGGGA CTATTCAGGC TCCTGGCAGT GGGGGCTGAG CCTAAAGCAG AGGGCACTCT 1560 AAGGCCAGGG AGAAAGTGGC AGCTGCTCCA GGCAGGCACA GGTCTGGAAC CAGAGCATCC 1620 CTGACCAAAC CCGGGGACTG TGAGTCATGC ATCTCATGGC ATCTGGGGGC ATCTAGGAGG 1680 GTCTCTCTGC TCCAGGCCCT CCTATTCTGC GCCTGCTCTC AACTGGTTCC TATTTTATAG 1740 GTGGTTTCTG GTCTTTGTCA 1760
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