Tag | Content |
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EnhancerAtlas ID | HS092-01990 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:64785720-64786980 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:64786953-64786973 | CGTTGGGGGGTGGGGGGGGG | - | 7.45 | ZNF740 | MA0753.2 | chr1:64786966-64786979 | GGGGGGGGGGTGG | - | 6.44 | ZNF740 | MA0753.2 | chr1:64786962-64786975 | GTGGGGGGGGGGG | - | 6.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68389 | chr1:64783020-64830623 | TC32 |
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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 |
GH01I064320 | chr1 | 64786283 | 64786484 |
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Enhancer Sequence | CTAAAATATT CATTGAATAA ATGAATACAA ACAGTGAGAG AAAGAGAAAT TTAGAAACTC 60 TATTGTCCAG AACAATAGAA TGAGTTTGGA CTAGAGGGCA AGAAATAACT GGGATCACAT 120 CCTGGTTCTG CAATCCACTT ACTGTTTAAC TACGGACTGT CACTGCAGAG CCTCTTAACA 180 TATTTTCCTA TCTTTAGTCT CACCCTGTGG AAGCTATGTG GGTTTCGGAT TTGGGTGGAC 240 CAAGGTCAGC CACTCCTTAA TGGTTATTGA CATAGACTAA TATTTTCCAT CTGTAAAATA 300 GGTTTTAAAG GCACCAAAAT GAGCGCATAA AGACAGAAGT CAAAATTGTT CAGTTTCCGT 360 GCAGCAAAGC ATTTAATGAA TGTGGCCTAT AATGAAAAGT TTTAATTCTT TCTTCAGGTC 420 TTCCTCAAAC ATTTAAGGAT CTCTGTGACG GCTGGCCTCC AAGGCCCCCA GTGATTCTCA 480 CTTCCTGGTA TTCATACTCT TATATAGGTC CCTTCCCCCA ACACCAGAGA GGTCTGACTT 540 GTGTTACTAG TTGGATATTG CTAAAATGAC TGTGTGTGAC TTCTGACATT GCCACATCCA 600 TCTTGCTATT TCCTGGATTA CTCAATCTGG GCGCGGGGGG GTGGGGGGAT GCAAGTTACC 660 ATGCCATGAG GATGCTCAGT GGAGAGATCC ACGTGGTGGG GAACTGAGGC CTCTTGCCCA 720 CAGCCATGTG GGTAGGTCAT CATGAAAGTG GCTCTTGTCA GCCTAGTCAA GCCTGGCCAA 780 TACCTCACTG CATGATGGAC TCTGAGCCAG AACCTCCCAG CTAAGCTACT ACCAAACCCC 840 TGACCCACTG AAACTGTGTG AGATAAATAT TTATATTATT TTAGGCCAAG TTTTGCAATA 900 CTTAGGTGCA TATAATGAAT ACAGGGTCCA AAAATTCAGT TCACAGAAAT GCATTAAATC 960 ACTTGCCCTG TCCTCTGCTC TAGCACTCCA TTCTTGGGAG CCTCTTACCC TTCCGTCCTA 1020 ACAGAACCTT CTCACCAGCT TTCCCTGTTG CAGCTGGTTA TACTCGCATC CCCTTTAACC 1080 TCACCACAGC GACTCCCACA TGACAAGTGC CTGAGAAGTC ACGTCTTCTC ACAGAGAACA 1140 GCCTGTCCAG GGATTATATT TCTTCTGTTT TTGTTGCTTT TCCCCTAAAA AAAAATCTGT 1200 TTCTGCCACT TTCATCTTTT CTATACTTAG AGACGTTGGG GGGTGGGGGG GGGGGGTGGT 1260
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