Tag | Content |
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EnhancerAtlas ID | HS187-10051 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:7977080-7977650 |
Target genes | Number: 27 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:7977127-7977146 | TGCCCGGCAGAGGGCGCCA | + | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I008073 | chr17 | 7977041 | 7977210 |
|
Enhancer Sequence | CGGCGGGGGA AAAGCCCAGG CGACATCAGT CGTGCCCTGG TACTGGCTGC CCGGCAGAGG 60 GCGCCACCAT GCCCCGCTCT CACCGTTTTG CAAAAGCTTC AAGCTGCCGC ATCCGTACCC 120 TCATCCTGCC TGCGTGACCC TCCTATGGCA GCAACCCCAT CTCCCCTCAC CCAGATCATA 180 AGGCTGGGGA CGGAGGACTT GGCCAGAAGT CCTCCAGGGC TGCTCCTGGC CCCTGTCTAA 240 CCAGTGGCCC TCAGATCTCT CTTCCAGTTT CCCTGGGGAT GCCGCTCCGG TCCCAGACCT 300 GGGGATGTTG GGAGAGGCAG GAGGCTTTCC TGGGTTCCTT CGGAAGAGTC CTGCCCCGAC 360 TCAACCCAGC GCCCCCTCTC CACTCCCTCC CATCACCTCC TTCCAGACTC TGTGCCCACT 420 CCAGATGGAT TTCTCAGTCC CACACATCTT CCCTACCAAG CTGCTGGCTT CCCTTTCCTG 480 TTGTCCCGTG TGAACCTCAG GTTGCTTCTC TTTCCTGTTG TCCGGTGTGT CCTGGTTGCC 540 ATGGTGATCT CAGGTTCCAA AAGTCCCACA 570
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