Tag | Content |
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EnhancerAtlas ID | HS101-40946 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:100612970-100613650 |
Target genes | Number: 32 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFKB1 | MA0105.4 | chr7:100613453-100613466 | CGGGGAATCCCCA | + | 6.34 | NFKB1 | MA0105.4 | chr7:100613453-100613466 | CGGGGAATCCCCA | - | 6.41 | TFAP2A | MA0003.3 | chr7:100613032-100613043 | TGCCTCAGGCA | + | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23113 | chr7:100609186-100614093 | Colon_Crypt_1 | SE_24054 | chr7:100609212-100613543 | Colon_Crypt_2 | SE_25182 | chr7:100607655-100613568 | Colon_Crypt_3 | SE_50739 | chr7:100608082-100613728 | Sigmoid_Colon |
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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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Enhancer Sequence | GTGAGTGCTC CTGGGCTGAT GCTCCAGGTC CAGTGCTCCT GGGTGGTAAT AGTACATGCC 60 CCTGCCTCAG GCAGCAGGGC TGCAGGTGGC CTCCTCCCCT TTGCATGGCA AGGGGCTGCC 120 ACAGGGCTGG AGACCCGTGC TGTGACCTCA TCTTGCTTTG GGGGTGCTGA AGAGGTCACT 180 GTGGAGACCT GTGGGTGCCT GTGGTTGTGC AGGGGATGGT CTGCACACAG CTCCTGGCTG 240 AGGGGCGGCT GAAATCCACA GCTTCTGCTC TCCAGGCTCC CCCCGGGAGG ATGAAGGGGC 300 TTTTGTCACA TAGACAGTCA TCTCTGCCTG CCCTCATCCT GGGGGCTTTA TCTGCTGGAG 360 GGATGGGTCT TTCCAAACCT CACGGAGGCA CTGCACATGC TGCTAGCCCT GGTCGGGAGA 420 GAGGGAGTCC AGAGGGGTGT GTGACAGTAT CATCTCTTGA CTTGGAGTAG CCTCAGGTGC 480 ACCCGGGGAA TCCCCACCAG TTAAATGGCT GACGGGGCCA GGCGTGGTGG CTCATGCTTG 540 TAATCCCAGC ACTTTGGGAG GCCAAGGTGG GTGGATCACC TGAGGTTGGG AGTTCAAGTC 600 CAGCCTGGCT AACATGGTGA AACCCCGTCT CTACTAAAAA TACAAAAATT AACCAGGCAT 660 GGTGGCGCAC ACCTCTAATC 680
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