Tag | Content |
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EnhancerAtlas ID | HS101-44241 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr8:134375280-134376020 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr8:134375484-134375496 | AAATGTTTGTTT | + | 6.27 | RUNX1 | MA0002.2 | chr8:134375761-134375772 | AAACCACAGAC | - | 6.62 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_04561 | chr8:134374472-134376017 | Brain_Anterior_Caudate | SE_05389 | chr8:134374393-134376244 | Brain_Cingulate_Gyrus | SE_08729 | chr8:134374879-134376251 | Brain_Inferior_Temporal_Lobe | SE_29358 | chr8:134374923-134376586 | Fetal_Intestine_Large | SE_35585 | chr8:134374722-134376353 | HepG2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH08I133363 | chr8 | 134375245 | 134376335 |
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Enhancer Sequence | TCCTTTAACG CCCAAAACAC CCTGTGGTGT TTAAGGGAAG AATTGCTGCA GAGCTGACTT 60 TCCTAATAAT GAGGGTGATT GAGTCTGTTT GTTGCAATAT AGGGTCTGCT GCTCCAACTG 120 AGACCAAAAA CAATGTGATG GAAACAAAAG AGTATTTTAT TTCTCTTTTC ATGCAATGGT 180 CTGGGCTTGG GAAATTCCTG GAAGAAATGT TTGTTTCATG GGGGCCCTGG CTCCTTCCCC 240 TGTACTTCTC CACCCTCCCT GGGGTGTTGC TTCATCCATA GGGTTGGTGA TGATTTATGG 300 CCAGGTGCTG CAATGCATAA CTCGTGGGCA TGTTGCATAG AACACAAAGA GAGTGGTGTT 360 CTCTGGAGCC ATGCAACACA GTGCTGCCTC TGTGAGGAGA GAAACAGGAA AGGAGTGTGA 420 AGAGGACATC CCTTCCCTTT TAGGGCTCAC CCTGGAAGCT GTGCACCTCA CTTCTGCTCA 480 CAAACCACAG ACTAAAACCA TCCTGTGGCC TCAGCTGGCT GCAATAGAGG TTGGGATGTG 540 TCATCTTTAT TCTTGGCAGT CTTGTATTCA GCTGAACCCC AGCCACTTAA TGAATGCAAT 600 CTATCCTCTT TTACTTCATT CTTTTAGAGT AAGTTTTGTG TAGCCATTCT CTCTAAGATG 660 TCCTACTCCA TCGCCTTGCC TCCCTCCTTT TTTTATTGAA GAGATACAGA TATTTCCTTG 720 TGGACAATTA TTTTACCCCA 740
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