Tag | Content |
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EnhancerAtlas ID | HS147-01480 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:49396960-49398140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:49397459-49397470 | CATGAGTCACT | - | 6.14 | IRF1 | MA0050.2 | chr1:49397178-49397199 | TCTTTCTTTCTCTTTCTCTCT | + | 6.86 |
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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 |
GH01I048931 | chr1 | 49397073 | 49397978 |
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Enhancer Sequence | AGGATTGGGA GCTAGACAAA TTCTTTCAGC CATAAAAATG ACAGCTATTG TACAAATAAA 60 CCAGTTACTA AATGGACAGA AACACTCTTC CTCCATGTAC CCTCTCACTT CATTCAGGTC 120 TCTGTTCAAA TGTGACCTAC TTAGAGATCT TTCTCTGTCC ACCCTATCTC AAGTAGCCCT 180 TAACCTTCTC TATCTCTTAT ACTGCTGCAT TTTTCTTTTC TTTCTTTCTC TTTCTCTCTC 240 TTTTTTTTTG AGACACAGTT TTGTTCTGTC ACCCAGGCTT GAGTGCAGTG GTGTGATCAT 300 GACTAACTGC AGCCTTGTTC TCCAGTGCTC AAATGGTCCT TAGACCTCAG CCTTCGGAGT 360 AGCTGGAACT AAAGGCGTGT GCCACCACAC CTAATTATTT GTAGATAACG GGGTTTTTCC 420 ATGTTGACCA GCCTGGTCTT GAATTCCAGG GCTCAAGCGA TCTGCCAGCT TCGGCTTCCT 480 GAAGTGCTGG GATTACAGGC ATGAGTCACT GTGCCTGGCC TCTGTGGCAT TTTTTTCTTC 540 ACAGCATCTG AAACCGTATT ATTTATGGTT TATTTGTTCA TTTGTTGGCT GAGTGACTGA 600 ACGAATGTGG TTACCTTCCT TTCCTCCTGG CTCCCATTCT GGTGCTCTTC TCCCTGCATG 660 CAAAATCAGC CCATCCTTCC CAGGAAAGAG TATGGGAGTG AGTCTCCAGA AAGCTAGGTT 720 TCCTGTCTGA CTCCCCAAAG AGACTCTAAG GTTCTGCTGC ATCCACTCAG GATGGTCCCT 780 CTCTCCACCT GAGCAGTATG CAGTGGGAAT CCTGCCAGCA CCAGAGGAGG CTGCCTGCCT 840 TCTTCTGGCC TGATTGCTTC TTGGTTACCC CAGGGCAGAG ATGAAACAGA GATAGGTATG 900 CAGGATGGTA CAGCATGTCT TCCCTGAAAG AAAAGCTTTG CAAGTTTAAT TAAACCCTAG 960 TAATTTTCAT AGACCACAGG TTGAAGAAGG AAAACTGTGT TCTTGGAGCT TTTCCTACCC 1020 TTAAAAAAAT GTGTTCCTTT AGTCTAGTTT TGATTTCCCG TGTAAAAGGG TCATGAAATT 1080 AATGGAAAGG AAATGCCCAG GAAAGGAAAG ATGCTGTTAC TCGTTGAATT TGAAAGAATA 1140 TGGGGATGAT ATTTCTGATC ATATTTTTGG CTGTCAAAAG 1180
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