| Tag | Content |
|---|
EnhancerAtlas ID | HS062-10091 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr20:31489840-31491340 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr20:31490935-31490946 | TGTGGATTGGG | - | 6.14 |
| | | 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 |
| GH20I032902 | chr20 | 31490401 | 31490550 |
| Enhancer Sequence | TTTCAAACAC ACACAAAAAT AGATAAAATG GTATAATTCT TCCATATCAC CTAGTAGCTA 60
GTCCACGTTA ATATTTCTCT AAGTACCTCA GAGTATCTTC TTACAATATT TGGAACTAGA 120
TATAAGCACG GTTCTGGGAT GGTTTTGAGC AGAGAACTGG TGTGGTCTGG CTTATATGTT 180
GCAGGTGGAG TGTCCATGGG CAGGGGTGGT GGTGAACACA CCAGTGAGGA GGCCATTGCA 240
ATAGTTGAGG CTGCATAGGA TGGTGGCCTG GAGCTGGGCT GTGTTGTGGG ATGGAGGGAC 300
TGGAGATGTA TTTTTGGGGT AGGGTAGAGA ATATATTTAC ACACACAAAC ACAGAGACAC 360
ATGTTCCCTT CCTTCAGCCT GGGTGACAGA GCAAGACCCT GTCTTCAAAA AAAACAAAAG 420
ACTCCATTCA GGTCAGACAC GGTGGCTCAC TTCTGTAATC CTAGCACTTA GGGAGGCCAA 480
GGCAGGAGGA TCCCTTGAGG CCAGGAGTTC AAGACCGGCC TGGGCAATAC AGCAAGATCC 540
CATCTACACA AAATATTTAA AAATTAGCTG GGAGTGTTGG CACACCCCAT GCATTCTTGT 600
CTGCATGCAG TGCAATGTAC AGGCCGGCAG GTGGCACAAT TGACCACTTG CTGGTCTCCC 660
GTTTTGGCGA TGCCATCTTA GGGCATATCC TCTGCGGGTG GGGCCTGGCA TTGGCACCCC 720
AACCTCTGCC TCTGGAGTCA GCCTCAGCCT CCAAGGCAGT GTGGGCCTGA GGGTCTGGCT 780
TCCTTGCAGC CAGCCTCACC TGAGTTCTCA GATGGTTCGA GCCAGGAGCA AATCTGACGG 840
AGCGGGTGTG GTAGCAGGAG CCGGTGCTGA GTGTGTGGAC TGACCCCCGG CGTCTCCCCG 900
ACTGTCCCCT CTTCCTTCAC TTCTGCCACC ACCACCTAGT TGAAGCCACC GTCATCTCCC 960
ACCTGAACTG CTTGCCCTGG CCCTCTTAGC AGCCTCACCG TGTCCCCTCA GGCCACATTT 1020
CCTGACCCAC GGCCATCAAC AAATCTGATC CAGCCAGGGC CCTGTATGGA GCCTTCAACG 1080
GCTCCTGGCC AGGGCTGTGG ATTGGGCCCT GCCCATCTCG CCCATGTCCT CTCATGCCCT 1140
CTCCTCCTGG CCCACCTGGT GCCCACCACA CCGGCCTTGC ATAGGCTGCT CCCTCCGGCT 1200
GAAGCCTCAC CCCTCCCCTG GGCTCCCCGG GGCTGACTCC TTCTCACCCT TCAGGTCTCC 1260
GCTGCCCTGG ACCCTCCTCA GAGAGGCCGG CAGAAGTGAG CCTCCTTCTG TTGTCCTCCG 1320
TCAAAGCCAT GTGCTTATGT CCCTTGCAGG ACTCGCCATG ATTTGTAAAT GTCCATCTCC 1380
CTTCTGTGTG TCCACTTCCT CCTGTTGTTT CCCTCTAGAA GGAAAACCCC CTATGGCAGA 1440
AGCCTCGTGT CTGTGCCCCT GGTAATCCTG GCAGGAGTAG GAGCCAGGAA ATCTTTGTTG 1500
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