Tag | Content |
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EnhancerAtlas ID | HS042-34037 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr4:651280-652740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RARA(var.2) | MA0730.1 | chr4:652316-652333 | AGGTTACCCAGGGGTCA | + | 6.24 | RARA(var.2) | MA0730.1 | chr4:651571-651588 | AGGTCATCCAGGGCTCA | + | 6.27 | RARA(var.2) | MA0730.1 | chr4:651765-651782 | AGGTCATCCAGGGCTCA | + | 6.27 | RARA(var.2) | MA0730.1 | chr4:651341-651358 | AGGTCGTCCAGGGGTCA | + | 6.36 | RARA(var.2) | MA0730.1 | chr4:651433-651450 | AGGTCGTCCAGGGGTCA | + | 6.36 | RARA(var.2) | MA0730.1 | chr4:651479-651496 | AGGTCGTCCAGGGGTCA | + | 6.36 | RARA(var.2) | MA0730.1 | chr4:651617-651634 | AGGTCGTCCAGGGGTCA | + | 6.36 | RARA(var.2) | MA0730.1 | chr4:651663-651680 | AGGTCGTCCAGGGGTCA | + | 6.36 | RARA(var.2) | MA0730.1 | chr4:652075-652092 | AGGTCGTCCAGGGGTCA | + | 6.36 | RARA(var.2) | MA0730.1 | chr4:652172-652189 | AGGTCGTCCAGGGGTCA | + | 6.36 | RARA(var.2) | MA0730.1 | chr4:651525-651542 | AGGGCATCCAGGGGTCA | + | 6.53 | RARA(var.2) | MA0730.1 | chr4:651306-651323 | GGGTCACCCAGGGGTCA | + | 7.36 | RARA(var.2) | MA0730.1 | chr4:651398-651415 | GGGTCACCCAGGGGTCA | + | 7.36 | RARA(var.2) | MA0730.1 | chr4:651444-651461 | GGGTCACCCAGGGGTCA | + | 7.36 | RARA(var.2) | MA0730.1 | chr4:651490-651507 | GGGTCACCCAGGGGTCA | + | 7.36 | RARA(var.2) | MA0730.1 | chr4:651536-651553 | GGGTCACCCAGGGGTCA | + | 7.36 | RARA(var.2) | MA0730.1 | chr4:651628-651645 | GGGTCACCCAGGGGTCA | + | 7.36 | RARA(var.2) | MA0730.1 | chr4:651674-651691 | GGGTCACCCAGGGGTCA | + | 7.36 | RARA(var.2) | MA0730.1 | chr4:652006-652023 | AGGTCACCCAGGGGTCA | + | 7.84 | RARA(var.2) | MA0730.1 | chr4:652141-652158 | AGGTCACCCAGGGGTCA | + | 7.84 | RARA(var.2) | MA0730.1 | chr4:652207-652224 | AGGTCACCCAGGGGTCA | + | 7.84 | RARA(var.2) | MA0730.1 | chr4:652242-652259 | AGGTCACCCAGGGGTCA | + | 7.84 | RARA(var.2) | MA0730.1 | chr4:652273-652290 | AGGTCACCCAGGGGTCA | + | 7.84 | RARA(var.2) | MA0730.1 | chr4:651869-651886 | GGGTCACCCAGAGGTCA | + | 7.93 | RARA(var.2) | MA0730.1 | chr4:651387-651404 | AGGTCATCCAGGGGTCA | + | 8.04 | RARA(var.2) | MA0730.1 | chr4:651811-651828 | AGGTCATCCAGGGGTCA | + | 8.04 | RARA(var.2) | MA0730.1 | chr4:652106-652123 | AGGTCACCCAAGGGTCA | + | 8.37 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_05764 | chr4:641718-651662 | Brain_Cingulate_Gyrus | SE_05764 | chr4:651764-654071 | Brain_Cingulate_Gyrus | SE_06434 | chr4:641638-654836 | Brain_Hippocampus_Middle | SE_07471 | chr4:641894-651593 | Brain_Hippocampus_Middle_150 |
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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 |
GH04I000657 | chr4 | 651765 | 654071 |
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Enhancer Sequence | CTGGTGCGGC GGGGCAGGAC GTCCAGGGGT CACCCAGGGG TCACGGCTGT GTGGCAGGGG 60 CAGGTCGTCC AGGGGTCACC CAGGGGTCTC GGCTGTGTGG TGGGGGCAGG TCATCCAGGG 120 GTCACCCAGG GGTCACGGCT GTGCGGTGGG GGCAGGTCGT CCAGGGGTCA CCCAGGGGTC 180 ACGGCTGTGC GGTGGGGGCA GGTCGTCCAG GGGTCACCCA GGGGTCACAG CTGTGCGGCG 240 GGGGCAGGGC ATCCAGGGGT CACCCAGGGG TCATGGCTGT GCAGCAGAGG CAGGTCATCC 300 AGGGCTCACC CAGGGGTCAT GGCTGTGCGG CGGGGGCAGG TCGTCCAGGG GTCACCCAGG 360 GGTCACGGCT GTGCGGCAGG GGCAGGTCGT CCAGGGGTCA CCCAGGGGTC ATGGCTGTGT 420 GGCACAGGCA GGTCGTCCAG GGGTCCATTG AGGGGTCACA GGGGTCATGG CTGTGCAGCA 480 GAGGCAGGTC ATCCAGGGCT CACCCAGGGG TCATGGCTGT GCGGTGGGGG CAGGTCATCC 540 AGGGGTCACG GCTGTGTGGT GGGGGCAGGT CGTCCAGGGG TCCATCCAGG GGTCACCCAG 600 AGGTCATGGC TCTGCGGCGG GGGCAGGTCA CCAGGGGTCA CAGCTGTGCG GTGGGGACAG 660 GTCACCAGGG GTCATGGCTG TATGGTGGGG GCAAGTCGCC AGGGGTCACG GCTGTGTGGC 720 GGGGGCAGGT CACCCAGGGG TCATGGATCT GTGGCAGGGA CAGGTCACCA GGGGTCACGG 780 CTGTGCGGCG GGGGCAGGTC GTCCAGGGGT CACAGGTGTG CGGGGCAGGT CACCCAAGGG 840 TCATGGCTGT GTGGTGGGGG CAGGTCACCC AGGGGTCACA GGTGTGCGGG GCAGGTCGTC 900 CAGGGGTCAC GGCTGTGTGG CAGGGGCAGG TCACCCAGGG GTCATGGCTG TGCGGTGGGG 960 GCAGGTCACC CAGGGGTCAC AGCTGTGTGG GGCAGGTCAC CCAGGGGTCA CGGCTCCCTC 1020 TGTGCAGTGG GCGGCCAGGT TACCCAGGGG TCACAGCTCT CTCTGTGTGG TGGGGACACG 1080 GCCCTGGGGC CAGAGCTGAG TACAGCCCTG GCATGCCCCC GAGGTCCCTC TGTCTGCACG 1140 GCCCTGGCAT CCCTTCCCTG TGCTCAATCT CCCCAGCCAG GGGCCTTGCA TGGCCAGAGC 1200 CCTCCTGGTC ATCATGAGAG AGTCCCATCA TTATACCTGA GGACTGCGTA AGGCAGTGCC 1260 CGAGAGAGGA CAGGTGGGAA AGTCAGCAGG CCATGCACAC GGTCATTTGT CTCCAGATCA 1320 GAGGCCGCCA GGGCCTTCCC AGGGTGAAAG CACAAGCTCT TGACAGCACC TTCCTCTAGC 1380 TCACACGGGG TGGACGCACC GCCGTCACCT TGTCCCACAT GCGAAGCTCT TTCTCGTGAC 1440 ACATCTGTGT CTCTGTGTAG 1460
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