Tag | Content |
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EnhancerAtlas ID | HS095-08702 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:111607030-111608320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr13:111607924-111607944 | TCTGGGGGTGTGGATGGGGG | - | 6.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_40065 | chr13:111606384-111610750 | K562 |
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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 |
GH13I110953 | chr13 | 111605826 | 111608950 |
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Enhancer Sequence | GGGGACCCAA ACTCCTCAAG CTGCAGACAC CCTGGGATTC CCTGAGATGG GCGGATGGAG 60 GCCCAGCTGC GGGGAGGCGC GTTCCTGCTC GGAGAGCAGT CAGGGCTTTG GGGGCCAAAG 120 AGAGGCAGGA GGCCGAGCCA CCCCGTGGTG AGCTGCCCAG GGCGAAAGGC TGCCTTGACC 180 CTTCCACGGG CCTCCCTACC CTCGGGGAGA TTGGTCAGGG CTAGAAAAAC GCTTTAGGTA 240 GAGATGAAGC CAGCAAGTGG AACAAGGTTA GGAAGCTCTT TGTTTTAAAA CCATGTGTAA 300 CTGCTGATGG TTGAATTTTT TGAGATAGGA GAGGCTGAAA TACAAACAAT GACGAGCACA 360 ACCATCAAAA CAGAGCCAAG CACACCTGCA GCAGCCAGTC CAGGGGGCTG GCCTGCTCCA 420 CAGTCAGACT TGCCAGAAGT CAGACCTCCT CTAGCGACGA CTCAGGCAGC CACAACGCAA 480 TCCCTGGACC AGCCGGCCCC AGAGGGCCAG GAATGCATCC ATCACCGACA GGTCCTATGG 540 CTTTTGTCCT CGCTTCCAAC TCAGAGCCAA CCAGAGAAAG CCACACATGC TCCCTCACCA 600 ACCCCTCACC GCCCGTCTGA TGAGCCACCC CCAGCACACC CAGCTGCAGC CTGCACGGGA 660 CCTGGGCTTC CTTTGCCTTA GTGAGGCCCC ATCCCCTGCC TGACTCAGAG GCTCTGAAAT 720 TGCATGTGAT GGTGACTCAG AGGCTTTGAG ATTGCACGTG ATGGTGGTGA CTGCCCTCCC 780 ACAGCAAGCT CTGGACAGAG AGTCTCGGCC TGGCCTGCCT GGGTGGGCTT CACTGACCTC 840 CACAGGGATT TGAATTCTCA CTGTCAATGC TTTCAGCTTT CTACCTAGAA GAAATCTGGG 900 GGTGTGGATG GGGGTAAGAG CTGCTGCTTC CTTCTAGGTT TAGTTGGTCA GGACCCAGGA 960 AAAATATCAG AAATGCCAGC CACTCTTTCC TCTTCCAGAA TCCTTTTCTG AGGCCACTGT 1020 TTCTCTGGGG GTGGCTGAGA CACTGGCTGG AGCAGGTGCT GGTCTCAGGA CTAAAACTCT 1080 CAGAATCTGG CAACCGCCAG ATTCACCAGG AAAGTGAGTC CAGTCACAGC CATTCCTTGA 1140 CCTTGGGGAG TCTAACTCCT GCCTGGGGCA GTTCGCTTGA GTACCCAGAA AGTGGACGGG 1200 GCGGCAGAAG CGAGAATGGG AACACCCATT CATTCACTGG AGCGCTCACT CATCCATCCA 1260 CCTAACCCAT CAAACACGCA GGCAGGCAGA 1290
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