Tag | Content |
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EnhancerAtlas ID | HS170-00984 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr13:48477810-48478810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr13:48478198-48478219 | ATTTGCTTTCACTTTCTACCG | + | 6.31 | IRF2 | MA0051.1 | chr13:48478197-48478215 | CATTTGCTTTCACTTTCT | - | 6.45 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 48478393 | 48478707 | chr13 | 48478600 | 48478683 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I047903 | chr13 | 48477936 | 48478805 |
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Enhancer Sequence | AGGCGCCTGC CACCACGCCC GGCTAATTTT TTGTATTTTT AGTAGAGAGG GGGTTTCACC 60 ATGTTAGCCA GGATGGTCTC GATCTCCTGA CCTTGTGATC CGCCCGCCTC GACCTCCCAA 120 AGTCCTGGGA TTACAGGCGT AAGCCACTGC GCCCAGCCAA GAATTGTTTA AATTAATCCA 180 TTTTAAATTA ACAAAGCAAG TATTTCCTCT TTAGCATCAT GAAAAACGGA GCATGCTCAT 240 ATAAGAATCA TAAAAATCCA CCCAGCACAG GAAATGCCTT TAAAATTTGT AGGACTAAAA 300 TAGTCCTACA AATAATCGTT GACCCTCTTG CTTAATACTC TCAAATGATG GGGAGTGACT 360 CACTAATTTA TGAGGTGTCC TTGCCATCAT TTGCTTTCAC TTTCTACCGA TCGGTACTTA 420 GTATGTCTCA GAAGCAAAAC AGAACAAGCC AGCCTTTAAA TACCCTCTCA AAGATGGACA 480 ATGGCCACAG GCATCCGTCT GTCCTATCTC CTTTATATCA GACTGAACTT TTGCTATACT 540 CCTGCTACGT TGTTTCACCT AAAGCTGCTT CCTCGCATAT TTTAAGTTCA GCCTCAAGGT 600 TTCTGGGTAC ATAGTGAACT GAAACCTGAC TGGATGTGGA AACAGACCGG AACCTGCTCT 660 TGGAACAAGT AGCTAAGTCT CAGCTAATCC CAGCAGCCAG ACTTTGACCA CTCACAGGCA 720 GCCAACCTCT CAAACCGTGC TAAGAAGGCA AACGCGAGCT GTAAGCAACC CAGCAGTTTC 780 CGTACCTCAC TTCCGTTTTC TGTACCTCAC TTCCGTCTTC TGTACCTCAC TTCCGTTTTC 840 TGTACCTCAC TTCGATTTTC TGTACATCAT TTTCCTTTAT CTGTGCGTAT ATCCTTTTGA 900 ACTCCTGGCA ATGCCTGAGT AACTCCGAAC CTATTCGGGT TGGGAGGTGG GGGGTAGCTA 960 CTCAATTTAC AAATCGTTCT TCACTCAGTT AAAATCTGTT 1000
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