| Tag | Content |
|---|
EnhancerAtlas ID | HS147-26198 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr20:60906190-60907420 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr20:60907127-60907140 | GAAAGTTCCAGAA | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 60907170 | 60907220 | | chr20 | 60906457 | 60906534 |
| Enhancer Sequence | GGCAGAGGGA CGAGATGCTG CAACGCCCGT GGTGCGGGGA GGATAGGGGG TGCAGGCGGT 60
ACGATGGGGG GGTGCAGGCG GTACGATGGG GGGGTGCAGG CGGTACGATG GGGAGTGCAG 120
GCGGTACGAT GGGGGGGGTG CAGGCGGTAC GATGGGGGGG TGTAGGCGGT ACGATGGGGG 180
GTGCAGGCGG TACGATGGGG GGGCCGGTCA CACAGCTCAG ACCCAGGAAA CTGCAAACCC 240
AGGCGTCCGA CCGAGCCCTG CTCTTTCCAA GATGCCCTTG CTCCTCCTCC AGCTGCACAA 300
ACCCCAACCG CAGACCAGCG TGTTGGCCAG TTCCTGGGCC CACAGGCCTA TGCGGCTCCT 360
CCCATAGCCC TCTTCCTCCC CCTCGCCCTC CCATCCGTCA CTGTTCCCCC ACTCTTATCT 420
CGAGTGCTGC TTGGTGCCAC CAGGCCGGGC CAGGCCCAGC TCTCCCAGGA CCTGACCCAG 480
GCAGGCACTC AGCAGGCACA AGCCGCAAAT GGGTGCTCCC TTTCCGTGCG GCCATGTGAG 540
GTTGGTGTCT CGGAACACGG CAACTTATCC GCTGACACAA CGGTGGGAGA CGCGGCTGCA 600
CAGAACATGT TGTGTGGCAT TTATAGAAAG TGCCAGGCCA GGTATGGTGG CTCCTGTCTG 660
TAATCCCAGC ATTTTGGGAG GCCCAAGAGG GCGGATCACC TGAGGTCAGG AGTTTGAGAA 720
TAGCCTGGCC AATATGGTGA AACCCTGTCT CTCCTAAAAA TACGAAAATT AGCCAGGCGT 780
GGTGGTGAGT GCCTATAGTC TCAGGTACTT GGGAGACTGA GGCACGAGAA TCGCTTGAAC 840
CCAGGAGGTG GAGGTTGCAG TGAGCCAAGA TCTTGCCATT GCGCTCCAGC CTGGGCGACA 900
GAGTGAGACT CCATTTCAAA AAAAAAAAAA AAGAAAAGAA AGTTCCAGAA CAGGCAACCA 960
ACGCTGTCTG TGCCAGGAGG TGGCTGCCCT GGGGCCAGGG AGCTGTGACT GCAGGTGCTT 1020
TCCTGAGCAC ATGGAACAGC TCGGGGGTAC GTCAAAAGGG ACTGAATCCA CAAAACGCTT 1080
GCAGGAGGGG TTCCAGAAGA AACATGCTGG GCTGGGCATG AGCGAGTGTG GCCGCCTTGG 1140
GGACCTGGGA CCCCAACTGT CCTCTCCCCT CTCATGCATG TTTCAAATCT TCTGAAAGAA 1200
GCTGACCCCT TGGGGTGGGG ACCTGAGGGG 1230
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