Tag | Content |
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EnhancerAtlas ID | HS082-02369 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:168862120-168863150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr1:168862417-168862428 | AGCTGTGATTT | - | 6.14 | RARA(var.2) | MA0730.1 | chr1:168862184-168862201 | GGGTCATGTAAGGGTCT | + | 6.26 |
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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 |
GH01I168892 | chr1 | 168861982 | 168863769 |
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Enhancer Sequence | TTTGTGCAGG GTCCATTTCA TCCATCCAAA TATCCCAAGG ATCTGGGATA TTTGCAGATT 60 CCCTGGGTCA TGTAAGGGTC TACTCTGACA TCATCTCATG TTATTCTACA GCTTGAGTCT 120 GTCTCCATGT GTTACTTCTG TCTGGCCAGT GATCTCTCAG TGTGTTTTTG ATTCCTCAGT 180 GTTTATATCA TCTCTAGTGA TTAAAATTTT AACATAGCAC AACACAGCAT AGACACGGCA 240 CCTCTTTTCC TATGATGCAG CTCAGCAACA TAGCATGATT CATCTTCCAT GTAGAACAGC 300 TGTGATTTGT GCTTCGTTGA TGTCTGCCTC CCTACTTTTC CTCATAGCTC TCCTCTCATC 360 TCCCCCATTT AGCATCTTTC ACCGTTACAA GCAATGATCA GATAAACAGA GAGATGAAGG 420 TAGTACAAAA GAAATCTCAG CCCTATCCTC CCTGTGGCTA TGTTGGATCA ATTTTCAGCC 480 CATCTTCCCT AGTCCCTTCT CTGCTGGACT TAATGTTCCC TTCCTCCTGC CAGCTTAATC 540 CTATCCAGGT CCTGAGTCAG TACTGACTAC AGCTGCCTTA GTTCCAGCAG GCTCCAACTG 600 GTTCTGGAGT TGGTCTGGGA TATGATCATC TTTTATTTCT GACTCAATGT AAGACTCAGC 660 TTGGGTATGT ACTCCTCTGT ATTAGAGCTC CCAGGATGGC TTGATGCCAT TCTCGTGTGC 720 TGCAGTGGCA CCGTCTGCTT GCCTCTGTTA TTATATACTT CCCGCTTGAT TCCAACTGCC 780 TGGTGACAAG GCAGCCTTCC CCACTGGAGA TGAGAGCTCC AGGAGGTCAG GGGCTAGCTC 840 ATCATCCATG TATCCCTGGC AATTTACACA GTCCCTGGAG CCTGGCCCAA GCCTCCCTGT 900 TTCTACTCTT GTTTTCCTAC AACATACTCC TCACACAGCA GCCATGATGA TCATTTAGAA 960 ACATAAATCA TCCTTTCCCT GTAATTTACC AGTTTTCAGA GCAAGGGGTT GGTGCCCTAC 1020 TTTTCTGAAA 1030
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