Tag | Content |
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EnhancerAtlas ID | HS187-06368 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:121211620-121212630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr12:121212061-121212082 | TCTCCTTTCCCTCCCTCCCTC | - | 7.28 |
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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 |
GH12I120774 | chr12 | 121212101 | 121212190 |
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Enhancer Sequence | GGTCTTGAAC TACTAACTTC AGGTGATCCA CCTGCCTCAG CCTCCCGAAG TGCTGGGATT 60 ACAGGCATGG GCCGCCGCGT CTGGCCCTTC CTGAACTTTT GTACTCAATT TGCCATAGAA 120 TCACTTCATC CTAACTGCGC AGGAGCCTTG AAAGGTCACA AGGTCTGAGC ATCCACCTGC 180 TGCTTTGTCA TTCATCTCAT GCTAATCCTC CTCCACCTGC GTCTAAACTA AACATGGAAC 240 AGACTGCTCA GTGACTGGGT TTTCCATGAC TCCAGACAGT GTCATTCTAT CCTAACCTTC 300 CAAATAAGAA AGTCTGGGTT CATCTTCAAC ACATCACAGC CTCTCATCAT ACACATGAAA 360 TCTGCAGCCA TTCTGAGGTG TTATCCTTTA CTGTTACTGC AGACCTTGCT CACACCTCCA 420 CCCACTTCCT ACTTTGCTGT GTCTCCTTTC CCTCCCTCCC TCTTACTCTT TCCCATGTAC 480 TGTTCACTGC CACTGTCAAA CATCTGTTCA CATAATTTCC TGCCTGAAGG TCACCAGGTT 540 CCCTTCTCTA TGACGAATCA AGTCTAATTA TAAAGTTGCA TAAACTCAGG AGGCACAACC 600 TCCACAGAGT GGAGCTGAGC ACCATGCTGG CTCTGCCTTG GCATCTGTCT GAACGGGTTC 660 CTATTCCTCA GCCTATCCCT TCTCTCCATC TGCGTTAAGC TGAACACCCT CTTTCCAATT 720 AGACCATCTA GGTCCTCCCC ACTCTAGTCT AAGTTCCGTG TATGAAGAGG CAGAAGGCAT 780 CCTTTTGACT GTCTCAGAGA AGGCTCTTAG AGGCATGTGG AATAAATACC ACTCTGACCC 840 AGCGAACACT GCCACAAGCA ATGTCGTATT CCCAGAACAT GCTCTCAATC TAGTTTGCCT 900 GCCTTTCATT CTGTCATTCA AGTAACCCTT AAAAAATCTT ACCTCCTCCT CAGGGCTTTT 960 CAAGGCTAAA GTGAAGGGAG GTGCTCTCTT TCCCTTGCGG CTTTAGACAC 1010
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