Tag | Content |
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EnhancerAtlas ID | HS031-22630 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr8:37448760-37449910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr8:37449693-37449705 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr8:37449697-37449709 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr8:37449701-37449713 | GTTTGTTTGTTT | + | 6.32 | PLAG1 | MA0163.1 | chr8:37449294-37449308 | CCCCTTAGGCCCCC | - | 6.18 | PLAG1 | MA0163.1 | chr8:37449293-37449307 | TCCCCTTAGGCCCC | - | 6.53 | TEAD1 | MA0090.2 | chr8:37449431-37449441 | CACATTCCAT | + | 6.02 | ZNF263 | MA0528.1 | chr8:37449528-37449549 | TTCTCTTCCTCTCCCGCCTCT | - | 6.35 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27732 | chr8:37446072-37450520 | Fetal_Intestine | SE_28603 | chr8:37446035-37459435 | Fetal_Intestine_Large | SE_56841 | chr8:37449368-37449715 | VACO_400 |
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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 |
GH08I037588 | chr8 | 37446287 | 37459940 |
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Enhancer Sequence | CTATAAAGAT GGACAACCCC GGTCTTCTCC CTTTGACTTC AGAGGGCAAA GAGAAGGCTT 60 GATTTGTGCC TTGGCTGGCA AAGCCCCCCA GTGGGGTAGG AGTCACTCTG TCCACAGTGA 120 CCACACACAG CTTTCAAATC CATAGGTCCC TTCATGGCTT TGGAGGAGGG GGAAAAACTG 180 CACCTTAGAC CTTCTTTATT CTCCATTCCT TTCTGTCCTC CAGGACCAAT GGGGTAGGTC 240 AGCCCCAGTG AACTCTCAAA TGACCACTGA AGGAGGAAGT GAGTGCAGAG TGTGATACCA 300 CTCACATCCC AGCCCAGACT GTTTGCTCAG CTGGGAGGAG TGTTGCAATT CTTCTTCCTG 360 CAGAGATAAC ACCCCTTCTC ATGGCTTCAG GCATCACCTA TCTCCTCTAG GCTGCGCTCC 420 TACTTGTCCA TCTCTGCTTT GACCTTGTTT CCAGGCTCCA GGAAGGACAT TTGCATGTAG 480 CTGCCTTGCC CCATTGCAGT CTACAAGCCT GAAGTCGGGG CTGTTCATTC CATTCCCCTT 540 AGGCCCCCAC TTCCTCTCAC TTTCTCTCTC CCCAAGCTGG AAACCTCAGA TCATTTCTAA 600 ATTCTTTCTT CCCCTTTGCA TTTCAATGAA CAGAAGTTCC ATCAATACAT TTTATCACTG 660 TTCAGTCTCA TCACATTCCA TGCTTAAGGC TCAAAGAGAC CTATAGAAAC AGCACTGTTG 720 CTCACTCAAT GGGCAAAGGC AGGGAGGCCC AGCCCATTTG CAGTGGGATT CTCTTCCTCT 780 CCCGCCTCTG TGGCCCTGAC TCTAGACTTG GGCTCCAAGA TGTTGGAATG GTGTCTCTCC 840 CCCTCACTAC CCTGCACATA GCACAGTGCC CTGGTAAACA TGAGGCCTCA GAAACACTCC 900 CTGCTCCAGG CACTTAGAAC TTAAGAGTTT TTTGTTTGTT TGTTTGTTTG TTTGTCTTGA 960 GACAAGGTCT CGCTCTGTCA CCCAGGCTAG AGTGCAGTGG CGCGATCATG GCTCACTGCA 1020 GCCTCGACCT CCTGGGCTTA AGCAATCCTC CCACCTCAAC CTCCCAAGTA GCTGAGACTA 1080 CAGGCATGCA CCACATGCCT GACTAATTTT TGTATTTTTT GTAGAGATGG GGTTTCAACA 1140 CGTTGCCCAG 1150
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