Tag | Content |
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EnhancerAtlas ID | HS104-22410 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr16:2218780-2220610 |
Target genes | Number: 46 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr16:2218879-2218899 | GGGGTGGGGGTGTGTGGGGC | - | 7.02 | ZIC1 | MA0696.1 | chr16:2218871-2218885 | CCCAGCAGGGGGTG | - | 6.06 | ZIC3 | MA0697.1 | chr16:2218870-2218885 | GCCCAGCAGGGGGTG | - | 6.26 | ZIC4 | MA0751.1 | chr16:2218870-2218885 | GCCCAGCAGGGGGTG | - | 6.02 | ZNF263 | MA0528.1 | chr16:2219529-2219550 | TCCCCCTCCTGCCCTTCCCCC | - | 6.88 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26937 | chr16:2219364-2220733 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I002169 | chr16 | 2219906 | 2220018 |
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Enhancer Sequence | TCCCTGCCAT CCTGGTCAAT GGCGCTCATT GCTGGGCTCT GGGCCTACCC AGGGGACAGA 60 GGCCAACTCT ACCCTGGGCA TGAAGGACTG GCCCAGCAGG GGGTGGGGGT GTGTGGGGCC 120 TCTCTGGCAG CTGCCTCTCT CCAGTGCTTG GACACCAGGT GTGGCGGCCC TGCTGGCCCT 180 CTTGGGACCG AGGCCTTTTC TTTTTTCCTT TTTTCTTTTT TTTGAGACGG ACTTTTGCTC 240 TTGCTGCCCA GGCTGGAGTG CAATGGTGTG ATCTCAGCTC ACCACAACCT CCGCCTCCCG 300 GGTTTAAGTG ACTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGATTACAGG CGTGCACCAC 360 CACTCCTGGC TAATTTTGAA TTAGTAGAGA TGGGGTTTCT CCATGTTGGT CAGGCTGGTC 420 TCGAACTCCC GACCTCAGCT GATCTGCCCC CTCCTTGGCC TTCCAAAGTG CTGGGATTAC 480 AAGTGTGAGC CACCTTGCTC AGCCAGAAAA GAAGTTTTTA ATTAATTGAA CAAACACACC 540 TGTGTGCCGG GCGCTGTGCT AGGCCGAGGG CGAGTTGGGT ATGTCTGGGC CCCGTCCCCT 600 GGGCCTCTGC CTGCCTCGGT CTCCACAACC CGAAGCCACG AGTCCTCCAT GTCTGTGGTT 660 CCCATAATCA CCTGCTATCC CCATGGGTCA CGGTGGCTTT CAAGAGAGGC GGGTACCTTC 720 TCTGTTTGCT GATAGGCCCA CACAGGGAGT CCCCCTCCTG CCCTTCCCCC GTCCCCCAGG 780 CCTGCCTGCT GTCAGCCCCT ACGCCCAAGA GGGTGGGAGA CTCTGGGGTA GTATTGGGCA 840 GGCCCGGGAG AGTGGTTCCC GTGCCAGCTC CTGCTCTGCT CTCGCCCCTG GGGCTCCCTC 900 TGCTGCTGTG GGGCCTTGTG ACTCACTTTC TCTGACTCCC TTCTGTTCCC CATGTGCTGC 960 TTCCATGCAG ACGGGCCCTT GGGACCCAAA GGGAGGTGGG TACATGGCAC ACAATGCCCC 1020 CCGCCGGCCT TGGGACTGGT TTGCCTCTGT GCTCTGTGGG TTTCATACCC AGGCTGCCGG 1080 GAAGGGGGCC AGAGGCTCGG CAGAGCAGCA GCTGGGCCCC TCTGCAGTCA AAGCACCAGG 1140 AGAGAAGCCT TGGGCAGTGT GGCTCTTGGA AACTTCTGGA GGTTTCCAGG CCAGAGGGGA 1200 GGAAGGGACA GTGTCTGCCC CTCCCCCAGG CTCCCTTGTC GGTGGCTCAG CCAGAGGCAG 1260 GCACCTGTGG CCCTCACTCC TGCCCTCGGG AAGCTCAGCC GAGGTTCTCT GGGGGCCTGG 1320 CCCTGCCTTC CCTCTGAGCC TCCCAGCTGG GCCTGGTGTC CCCCACCAGC AAGGCCAGAC 1380 AAGCAGCCAG GCCCGGGGGG CACCTGGAGC CCAGCCGTCG CTCCCTGCCA GCATTCCTGG 1440 CCCTTCCATC CTGCGGTCAC GGCCTCGGCT GTCCAGGATT GGCTGGTGGA GGTGCCCCCT 1500 CACGGCCCAC ATTCCCCCAC GGGAAGCAGG AAGCAGCCCG GGTATATGGA ATTGAATAGC 1560 AGGAAGTCTC TCCATTTACA CAAAGAGAGG TGGCAGGCGT GAGCGGGCAG CCCAGCACCC 1620 CGGCCCAGGC CGCCCAGGCG GGCAGGCAGG GACCTGGGTT GCATCAGCTC CCCACGCCCA 1680 CCCACGGCCC CCGTGGACGA GGAGAGTACC CGCAGGGACC GGGGTGGCCC CAGGGGTGCT 1740 GCTGCCCTCG CGCTTCCGCC GGGCTGGGTC CTGTCCTCCC CGAGGCTCTG ACCCCGTGCG 1800 GAGCCCCCCG ACAGGCGCCT CTCCCTCCAC 1830
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