Tag | Content |
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EnhancerAtlas ID | HS064-05286 | Organism | Homo sapiens | Tissue/cell | GM18507 | Coordinate | chr16:88520-89670 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr16:88793-88804 | ACAGATAAGGA | - | 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 |
GH16I000037 | chr16 | 87233 | 89811 |
| Enhancer Sequence | GGAGCAGACG GCTTGAGAGC AGGGAGTGGG GCGGCTCCAA GCTCAGCAGT CCTCATTTCT 60 AGAAAGGGAG AGGGGATGGT AGGGCAAGAC CCACATGTGA CACCTGAGAG CTACAAAGGA 120 GGAGCCCAGG ACACTCCCTA GGGGAGCATT AGAGTGTTGG GTATAGCGAC AAGGGGGTAT 180 GGCCATCTGA GGGGAAGGTC TCTGCTTTTC CTCTGCACTG AAAACTCACA GCTGCACCTG 240 GTAAGCTGAG CAGGGCAGGG TTACCACCCT CCTACAGATA AGGAGACTGA GGCTCAGAGA 300 CCTAGGACCT GCCCAATACC TGGCTCCTGA CACCTCTGTT CTTGGCACAT TCCCATCAGC 360 TTCTACACAA GCCTGTGAAC TTCCCGAGGG CAGTGCCTGC GAGGCACCAC TCAGCACATG 420 CCCCAGCAGA AGGCACCACA GTGCTTTACA AATAGGGTGG AGCTACAGGC AGATCTACCT 480 TCCCCCATCC TTGACCACAG GACCAGGAAG TCAGGGCAGG TGCACACACC CCCACCCACA 540 TGCTCCGTGC TCCTCTGTGT CACCAGGGAG GCCTCACCAC AGCTCAGACA CCAGGTCACA 600 GGACAGTTGT GAGAGCAAGA GGGGAAGCCA GTGTCTGCCA CCTGGGAAAG AGCTGCCCCG 660 ACACCCCCAG TCCTGCTAGG GAGCCTGGCT GACATCACTG CCCAGGACAC CCTCTCCTGC 720 ACTGGGTCTG TGGACATAGC CTCCAGCCCA TGGTCACTCT GGGCCCTTCT TAGAGCCTCA 780 CCTGTTCCAT GGCCTCAGCA TCAAGGCCTG GCCCAGATGA CCACTGGGCC TCACGGCCTG 840 CCTGCCCTGG TTCCCTGGGC CACTGTGAAG CTGTGCGCTG CCCTGCAGCT AGACCCCTCC 900 CTCAGACCAC AGGCTCTGCC ACACCCACGG GAGGGTCTTC AGGCAAGCTC AGCCATTCAC 960 CCTCCCTTAG CTGGGCAGGG TGGCCCACGC CTATAGTCCC AGCTCCTTGG GAGGCTGAGG 1020 TGGGAGGATC TCCTGAGCCC GGCAATTTCA GGTTGTGGTG AGTCGTTATT GCGCCACTTT 1080 ACTCCAACCT AGGTGACAGT GAAACCCTGT CTCAAAAAAA AAAAAAAACA ACTGCAGCAA 1140 GAATATTCCC 1150
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