Tag | Content |
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EnhancerAtlas ID | HS024-11346 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr22:50595490-50596480 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr22:50595755-50595765 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr22:50595755-50595765 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr22:50595755-50595765 | ATTTTCCATT | + | 6.02 |
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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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Enhancer Sequence | GTGTAGCTCA CTGTAGTTTT GATTTGCATT TCCCTAATGA TTTGTGACAT TGAGCAGCTT 60 TTCATGTACC TGTTGGCCAT TTGTATGTCT CCTTTGGAGA ATTCAGGTCC TTTGCCCATA 120 TTTAATTGGG TCGCTTTTTG TCAGTGAATT TAAGACTTCC TCGTAGTTTT GGATATTAAC 180 TTCTTATATA CTATTTGCAA AGGTTTTCTC CCCCCTCCGC AGACTATCTT TTCACGTTGT 240 TGATTGCGTC CGTTGATGCC CAGACATTTT CCATTTGGAT GTAGTCCAGC ATATCCCTTT 300 TAGTTATTGC CAGTGGCTTT GGTGTCGTAT CCAAGAAGTC ATTGCCAAAC CTAATGTCGT 360 GGGGCTTTTT CCCTGTTTTC CTCCAAGAAT TTTATGGATT TAGGTCTTGG GTTTAAATCT 420 TCGATCCACC TTGAGTTTCT GTTTCCAGGT GGTGTCAGGT GAGGGTCCGT CTTCATCCTT 480 TCCGTGTGGC TCTCTAGTTT TTCCAGCAGC GTTGGTTGAA AAACTGTCCT GGCACCCTTG 540 TCAGAAGTCA TCTGGCCGTA TATTCGAGGG TTTATTTCTA AGTTCTCCGT TCTACCCTGT 600 TGATCTATAT GTCTGTCTTT TATGTCAGTA TATCTCATTA ATGTTTTCTA AGGAAGAGTA 660 TTTTCAAGAT GAGAAGTAGC TATATCAAAG GTCTAATATC AAAAAAAAAA AAAAAAAAAA 720 GATCAGAAAT ACCAGCCAGC CCTCCACTCC GGGGCTCAGA CCTGAGTGGC GGACTCCTGT 780 GACCCGTCCT CCTCTGTAGC GTTTAGCATG ACTGTGAGCC ATTTCATCAT TTAACATATG 840 CCATCTGCCC TGCTCACATG TAAGTTCTGC ACGAGAGCAG GGATTTATTC TGTCATATTC 900 AGTGTGTATT CCCAGCACCG ACTTCAGCTC CTGGATTGTA GCCTTCTGGT GAATATTCAT 960 GAAGTAAAGT AGGTTTTCTC TCCTCATCAA 990
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