Tag | Content |
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EnhancerAtlas ID | HS187-17446 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:100318770-100319960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr3:100319297-100319307 | AGCACGTGGT | - | 6.02 | SP1 | MA0079.4 | chr3:100319352-100319367 | GGTGGGCGGGGCCTT | - | 6.45 | SP3 | MA0746.2 | chr3:100319352-100319365 | GGTGGGCGGGGCC | - | 6.14 | SP4 | MA0685.1 | chr3:100319350-100319367 | GTGGTGGGCGGGGCCTT | - | 6.1 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28516 | chr3:100319469-100320143 | Fetal_Intestine | SE_29227 | chr3:100319453-100320197 | Fetal_Intestine_Large |
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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 |
GH03I100599 | chr3 | 100318559 | 100320404 |
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Enhancer Sequence | CTCCCTAATT AGCTTAATAA CTAACCTCTT GAATTCTTTC TCAGATAAAT CAGGGATTTC 60 TTCTTGGTTT GGACCCATTG TTGGTGAGCT AGTGTGATTT TTGGGGGATA TTAAAGAGAT 120 TTGTTTTGTC ATATTACCAG AGTTAGTTTT CTGGTTCCTT CTCATTTGGG TAGGCTCTGT 180 CAGGGGGAAG GTCTAGGGCT GAAGGCTGTT CAGATTCTTT TGTCCCATGG GGTGTTCCCT 240 TGATGTAGTA CTCTCCCCCT TTTCCTACGG ATGTGGCTTC CTGTGAGCAG AGCTGTAGTG 300 ATTGTTATCT CTCTTCTGAG TCTAGCCACC CAGCAAGTCT ACCCAGCTCC AGGTTGGTAC 360 TGGGGGTTGT CTGCACAGAG TCCTGTGATG TGAACCATCT ATGGGTCACT CAGCCATGGA 420 TACCCGCCCC TGTTCTGGTG GAAGTGGCAG GGGAATGAAA TGGACTCTGT CAGCGTTCTT 480 GGCTTTGGTG GTTTAATGCT CTATTTTGTG GTGGTTGGCC TCCTGCCAGC ACGTGGTGCT 540 TTCCAGAGAG CATAAGCTAT GGTAGTATGG AGAGGAACTG GTGGTGGGCG GGGCCTTGTA 600 ACTCCCCAGA GTATATGCCC TTTGTCTTCA GCTACCAGGG TGTGCAGGGA AGGCCCATCA 660 GGTTGGGGCA GGGCCAGGCA TGTCTGAGCT CAGACTCTCC TTGGGCATAT CTTGCTTCAG 720 CTGCTGTGGG GAATGGGGGT GAGCTTCCCA GGTCACTGGA GTTGCGTACC TAAGAGGATT 780 ATCACTACCT CTGTTGAGTC ATGCAGGTTG TCAGGGAAGT GGGGAAAGCT GGCAATCACA 840 GGCCTCACCC AGCTCCCACG CAATCTGAAG GGCGGTCTCA CTTCCACCAT GAACCCCCAC 900 AAACAGCCCC GAGTCTGTGT CCAGGCAGTG GGCAAGCAGG GCTTGAGAAC TTGCCCCAGG 960 CTACCTGCCT CCCAGCTTGG AAAGAAAAGG ACTTTGGTTC TTCCCCTGCT TGTGGAGTCT 1020 GCATGCCGGA TTCTTGTTCT GCCCCGAGTT CTGGCCAGGA GGCTTCTTGC CTGGTTCAAA 1080 TTGTTACAAA GTTTAGCTAA AGATTTCCTT CTGTTTGTGG CATTTCCCCC CACACCTCTG 1140 GCTGCCCTCT TGAAGGATCC CTGTGGTGCC AGGCAAGAGT GGCCTACTTG 1190
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