Tag | Content |
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EnhancerAtlas ID | HS190-08769 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr22:50201650-50202340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EHF | MA0598.2 | chr22:50201820-50201832 | CACTTCCGGGTA | - | 6.37 | ELF1 | MA0473.2 | chr22:50201820-50201832 | CACTTCCGGGTA | - | 6.62 | ELF3 | MA0640.1 | chr22:50201819-50201832 | CCACTTCCGGGTA | - | 6.64 | ELF4 | MA0641.1 | chr22:50201820-50201832 | CACTTCCGGGTA | - | 6.74 | ELF5 | MA0136.2 | chr22:50201820-50201831 | CACTTCCGGGT | - | 6.32 | Gabpa | MA0062.2 | chr22:50201818-50201829 | CCCACTTCCGG | - | 6.02 | ZBTB7A | MA0750.2 | chr22:50201818-50201831 | CCCACTTCCGGGT | - | 7.22 |
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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 |
GH22I049807 | chr22 | 50200885 | 50202805 |
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Enhancer Sequence | CTATCAAAAA ATACTAACAA AAAACAAAAA AAAAATGTTG GTAAGGATGT GGAAACCCTG 60 AACCCTTGCG CACCGCCGGC AAGAACGTAA AAAGGTGTAG CCGCTGTGGA AAACAGTGTT 120 GTGGCTCCTC AAACACTTAA AGACAGAAAT GCCGTGTGAC CTGGCAATCC CACTTCCGGG 180 TATACACCCA AAAGAACTGA AAACAGGCTC AGATACTTAT CACCCATGTT CTTCACAGCA 240 TTATTCACGA TGGCTAAAAC ATGGAAGCAA CCCAAGAGCC CATGGAGGAA GGAATGGGTA 300 AGCAAAAGCT TATCTCCACA TACAGAGGGT TATTCAGCCT TAAAAGGCAA GGAAGTTCCA 360 ATGCATGCAA TGACATGGAA AAGCCTTGAA AATGTGCTCA GTGCAATAAG CCAGACACAA 420 AAAGACAAAT ACTGCCTGAT TGCGCTTATG TGAGGGACTG AAGAGGAGTC AAATTCATGG 480 AGACAGGGAG TAGAACGGTG AACGCCCGCA GCCAGGGAGG GAGGAATGGG GAGTTCCTGT 540 TTAACTGGGA CAGAGTTTCA GACTGGGAAG ACAAAAAGGC TCTGAAGATA GATGGTGGTG 600 ATGGCTGCAC AGCAACAGCA ATATCAAAGT GCTTCATGCC CCTGAGCTAT ACACTTACAA 660 TGATTAAGAT GGTACATTTT ATGTTATGTG 690
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