Tag | Content |
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EnhancerAtlas ID | HS016-00560 |
Organism | Homo sapiens |
Tissue/cell | CD14+ |
Coordinate | chr22:47249510-47250810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:47250569-47250587 | CCTTGCTTCCCTCTTCCC | - | 6.22 | FOXP1 | MA0481.2 | chr22:47250325-47250337 | TCCTGTTTACAT | - | 6.02 | Foxo1 | MA0480.1 | chr22:47250325-47250336 | TCCTGTTTACA | + | 6.62 | Lhx3 | MA0135.1 | chr22:47249586-47249599 | AATTAATTAATTC | - | 6.29 | Lhx3 | MA0135.1 | chr22:47249585-47249598 | AAATTAATTAATT | + | 6.92 | MYC | MA0147.3 | chr22:47249710-47249722 | GAGCACGTGGCT | - | 6.04 | POU6F1 | MA0628.1 | chr22:47249587-47249597 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr22:47249587-47249597 | ATTAATTAAT | - | 6.02 | ZNF263 | MA0528.1 | chr22:47250276-47250297 | CTTCCCGTTCCCTGCTCCTCC | - | 6.16 |
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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 |
GH22I046853 | chr22 | 47249163 | 47251194 |
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Enhancer Sequence | ACTTACTTCG CTGAAACTGG TCACCAAAGA CACCACATTT GCCTCATTGT ACTTGAGAGC 60 GGAACAGGAA CGGAGAAATT AATTAATTCA GTTTTATAGA TGAAGAAGGG GAGCCTGAAG 120 AGGTTCATTG TTCAACAGAT ACTTACTGAG CACTCACTCG AGGCAGGGCC TCGTCCTCTG 180 GGCCCTGGAG ACTCAGCAGT GAGCACGTGG CTGGTCGGAG TGATGGGCAC AGAGCTGGGC 240 GCAGGCAGTT TTGGAAAGCA CATGAGACTC TTTTCTGCCT CAGGGATCAC TTTCTCAGCC 300 ATGCCGCATG ACCTCAGAGG CATTTTGCAC CAATGGACAC TTCGTGAAAA ATTTTTTCCC 360 AGGGTTCTGT GACATTTTGC CCCGATTTCC CCCGCTGTCT CCGAGTGTCC CCTGTGAGTG 420 GACTCTTTCT CCTTCACACC CATGTGCGTT TCTGGACTTC TTGTTTTAAA CACGCTCTTC 480 CTTGGTTGGG ACTCTGCCTG TCTTTCCGCA CCTCTGAGCC TCATTGCCCA GTGTCCGTGT 540 CTTCCGGAGG TGCCTACTGC ACTGTCTTGG GATTTTGCCC TGTCAGAAAT GTGTCACGTG 600 TGATAGGAAA ATCATGGACG TGGTTGAGAG TCAGGCCCCT GAGTTTCCTT TCCTCATTTG 660 TAAAATGGGG ATGGGAACTG CTCTCCAGGA TGACAAATTG TCACGTGGAA ACCAGTGCAC 720 GGCGCAGACA CTGCTCCACA GTGTCGACAT CCCTTCTCTC CCTCCCCTTC CCGTTCCCTG 780 CTCCTCCTCC ACTGAACAAG CCACCCCTCT CCACTTCCTG TTTACATCAT AGATGGCGCC 840 AATCTCTCCT ACCCAGGGTA ATGTTTGGTC ATTGTCATTT TGGCCTTTCT TTTTCCCCAT 900 ATCTAGTTAT TGCTGAAGCC CACCCCCACC TGTTCTTGTT GTTTCCGGAT GTTCTCGCGC 960 TAATTCCTTC AGCCTTTCCT TTCTGCCTTT GATGGGTCTG CCCTAGATCA GACCTTTATG 1020 ATGTCTGCCC AGGCATTGAA GTAGCTTCCC AGCAAGTCTC CTTGCTTCCC TCTTCCCCCT 1080 GCGATGCATT CCAGGTCCTG GCAGGAGGTG AATCACATTG AAACGTGGCT TTGACCTCTG 1140 CTTTTACAGC TCCCCGTTGC TTGCAGGACA AAGATCACAC TCCTGATATT TAATGCCTTT 1200 CTTAATCGGA CTCCTAATTA CGTGTTCATC CTCTGTTTCA TCCAGACATA GGAACCTGCT 1260 GATCCCCCGG CTCATTGTTA ATCTCTGCCT AATACTTGTG 1300
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