Tag | Content |
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EnhancerAtlas ID | HS051-03574 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr10:90030570-90031990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr10:90031426-90031447 | GTCCGGTTTCATTTTTATTTA | + | 6.25 | RARA(var.2) | MA0730.1 | chr10:90030796-90030813 | GGGTCATCAAGAGGTCA | + | 7.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 90030953 | 90031359 | chr10 | 90031651 | 90031893 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I088271 | chr10 | 90030115 | 90032095 |
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Enhancer Sequence | TACCTTTTCT GGGTACGTTT ATTTGGAAAG GGTTTCTTCA CTTGAAGAAA GAATTAACAA 60 ACCCCTGTTT GGGAGGATAA AACAAGAAAT TCCTTTGGGA TGTCTCAAGT TTCTAGAGAG 120 CCAGGCTCTC GCAGGCTGAG GTGGCTTCCA CACTGTTCAT GAACTGCTCT TGGCGGGCTG 180 GTGGCCTGTT TGATATTCTG AGGTCTAGCA AAGATTTAGC TCCAGGGGGT CATCAAGAGG 240 TCATGGTCTT GATCATTTCC TCTGTTATTT ATCTTTGGCT TGTGGTACTG GAGCCTGCCT 300 TTGATACAGG GCATTTCTAC CACAGCTGCA CAGAATCAAG CATTTCAGTG ATTTGGTTTG 360 AGGTGAAGGA GGCTTGGCTT CTAATGCTGC GAAAATGTCA CTGGGTACAT CTGAGAATAT 420 CTAGCTCTGT CCTTCACTGA TGAGCAAATT CATTTCTGGG GGTTTACCAG TGGCACTTCC 480 CAGACTTGGG TCAGGAAAGG AATCCTCCTG GTGAGGACAG CAGTTTTCAG TTTGAGTAAT 540 TCCATTTTCA GTTCCTTCTG AGACATTTTT CTTGCTCTGA GCTGGAGATA AAAGCAGCAT 600 GTCTCAGGCC TCTAGGGTGG ATCTCTACTT TTCAACACTG TTTATGACTC ACCTGTGACT 660 GCCCTCAGTG CAGCCAAGGG GACCATTTAT GCTGAATTAG CCTTTGGATT TTTCTTCTTA 720 GTGACAGCAA AACTTCCGTG ACAGCAAACA AGTAAACCAC AGGAACATCC CTGGTCTGCT 780 CAGCACAGCA GGCTCTTGGG TTCTCAGAGA GCCTGGGAGG ACTTTTCAGC TTGTCTTATG 840 TGGGTTTGTT CACCCCGTCC GGTTTCATTT TTATTTAAAA CAATTGGTAT CTTTCATCTT 900 GGTTGCCAAG TATGGGTTGC ATATGGTTTT GACCTGATAT GAAGGGCCCA AATCAAATAC 960 CCAGGACTTG GCCTGGAAAA TTGGTTGTAT AAGACCTGCT CTCTTGTTCC CCTAAAAAGC 1020 AGCCTAGCAA ATGGAAGCAA TGGGTCCCAG GAGTTCGTTT CTGTATGCGG CTCTAACTCT 1080 GCCACGAAGG CCAGGACAGA TAGTGTGCAG TGCTCTGTCA TGTCTACCAG AGAAAATGAT 1140 GCAACATGTG CTGGAGACTT TACCATCTGT GCAAGAGTGC AGCCCTAGGC TCAATCCAAA 1200 AGAAAAAGGA AGTGGCATTA TAGCAGGGAT ATTCCCAGTG AGTCAAATTC CCAGAACAGC 1260 CTGTCCCTCC TCAAGGTGGT CAGTGTGCCC CAGCATCTCA CCTCCAGATT TGGACTAAAA 1320 CAGAACTGTT GCGTGCAGGG GTTAGAGAGG ACTAGAGCAG TGATGTATTT TATATATCAT 1380 ATTTTCTAGC AATGGTTTTC CATCTGAAAC CCAGTTTACA 1420
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