Tag | Content |
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EnhancerAtlas ID | HS092-03702 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:168862180-168863100 |
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 | CCCTGGGTCA TGTAAGGGTC TACTCTGACA TCATCTCATG TTATTCTACA GCTTGAGTCT 60 GTCTCCATGT GTTACTTCTG TCTGGCCAGT GATCTCTCAG TGTGTTTTTG ATTCCTCAGT 120 GTTTATATCA TCTCTAGTGA TTAAAATTTT AACATAGCAC AACACAGCAT AGACACGGCA 180 CCTCTTTTCC TATGATGCAG CTCAGCAACA TAGCATGATT CATCTTCCAT GTAGAACAGC 240 TGTGATTTGT GCTTCGTTGA TGTCTGCCTC CCTACTTTTC CTCATAGCTC TCCTCTCATC 300 TCCCCCATTT AGCATCTTTC ACCGTTACAA GCAATGATCA GATAAACAGA GAGATGAAGG 360 TAGTACAAAA GAAATCTCAG CCCTATCCTC CCTGTGGCTA TGTTGGATCA ATTTTCAGCC 420 CATCTTCCCT AGTCCCTTCT CTGCTGGACT TAATGTTCCC TTCCTCCTGC CAGCTTAATC 480 CTATCCAGGT CCTGAGTCAG TACTGACTAC AGCTGCCTTA GTTCCAGCAG GCTCCAACTG 540 GTTCTGGAGT TGGTCTGGGA TATGATCATC TTTTATTTCT GACTCAATGT AAGACTCAGC 600 TTGGGTATGT ACTCCTCTGT ATTAGAGCTC CCAGGATGGC TTGATGCCAT TCTCGTGTGC 660 TGCAGTGGCA CCGTCTGCTT GCCTCTGTTA TTATATACTT CCCGCTTGAT TCCAACTGCC 720 TGGTGACAAG GCAGCCTTCC CCACTGGAGA TGAGAGCTCC AGGAGGTCAG GGGCTAGCTC 780 ATCATCCATG TATCCCTGGC AATTTACACA GTCCCTGGAG CCTGGCCCAA GCCTCCCTGT 840 TTCTACTCTT GTTTTCCTAC AACATACTCC TCACACAGCA GCCATGATGA TCATTTAGAA 900 ACATAAATCA TCCTTTCCCT 920
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