Tag | Content |
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EnhancerAtlas ID | HS103-19343 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr5:64235000-64236420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr5:64235728-64235744 | CTTTGTTTACACTGTG | - | 6 | YY1 | MA0095.2 | chr5:64236382-64236394 | TCAGCCATCTTG | - | 6.04 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH05I064939 | chr5 | 64235201 | 64236227 |
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Enhancer Sequence | GAGGAGAAGA GGTGTTCTGA TTTTTGGAAT TTTCAACCTT TTTGTGCTGG TTTTTCCTCA 60 TCTTCCTGGA TTTACCTACC TTTGGTCTTT GATGTTGGTG ACCTTCAGAT GGGGTTGTCT 120 TGTCGGCGTC CTTTTTGTTA ATATTGATAT TGATGCTATT CCTTTCTGTT TGTTAGTTTT 180 CCTTCTGACA GTTAGGCCCC TCTGCTGCAG GTCTGCACGA ATTTGTTGGA GGTCCACTCC 240 AGATCCTGTT TGCCTAGTTA TTACCAGTGG AGGCTGCAGA ACAGCAAAGA TTGCTGCCTG 300 TTCCTTCTTC TGGAAGCTTC ATCCCAGAGG GGAACCCGCC AGATGCCAGC TGGAGCTCTC 360 CTGTATGAGG TTTCTGATGA CCCCTGCTGG GAGGTGCCTT CAAGTCAGGA GGCACAGGTG 420 TTAGGGACCC ACTTGAGGAG GCAGTCTGTC CCTTAGCAGA GCTCGAGTGC TGTGCTGGGA 480 GATCGCTGCT CTCTTTAGAG CCAGCAGGCA GAAACATTTA AGTCTGCTGA AGCAGCACCC 540 ACAGCCGCTT TTTCCCTCAG GTGCTCTGTC CCAGGGAGAT GGGAGTTTTA TCTATAATCC 600 CCTGAATGGG ACCGCTGCCT TTCTTTCAGA GATGCCTTGC CCAGAGAGGA GGAATCTGGA 660 GAGGCAGTCT GGCTACAGCG GCTTTGCCAA GCTGCACTGG GCTCCGCCCA GTACTAACTT 720 CTGGTCGGCT TTGTTTACAC TGTGAGGGGA AAACCGCCTA CTCAAGCCTC AGTAATGGTA 780 CACGTCCCTT CCCCCACCAA GCTGGGGTGT CCCAGGTCAA CTTCAGACTA CTGTGCTGGC 840 AGCGAGAATT TCAAGCCGGT AAATCGTAGC TTGCTGGGCT CTGTGGGGGT GGGATCCACT 900 GAGCTAGACC ACTTATCTCC CTGACTTCAG CCCCTTTTCC AGGCATGTGA ACAGTTCTGT 960 CTCACTGGCA TTCCAGGTGC CACTGGGGTA TGAAAAAAAA CCTCCTGCAG CTCTGTGTCT 1020 GCCCAAACAG CTACCCAGTC TTGTGCTTGA AACCCAGGGC CCTGGTGGTG TAGGCTCCAG 1080 AGGGAATCCC CTGGTCTTTG GGTTGCGAAG ACTGTGGGAA AAGCTTAGTA TCTGGGCTGG 1140 AGGGCACCGT TCCTCACGGC ACAGTCCCTC AGGGCTTCCC TTGGCTGGGG GAGGGAGTTC 1200 TCTGACTCCT TGCACTTCCC GGTGAGGCAG CGCCCCACCC TGTTTCGGCT CACCCTCCGT 1260 GGGCTGCACC CACTGTCTAA CCAGTCCCAA TGAGATGAAC CAGTTACCTC AGTTGGAAAT 1320 GCAGAAATCA CCCGCCTTCT GCATTGATCT TGCTGGGAGC TGCAGACCAG AGCTGTTCCT 1380 ATTCAGCCAT CTTGCCAGCT ACCACCTGCA CCTTAGTTTT 1420
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