Tag | Content |
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EnhancerAtlas ID | HS121-24990 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr21:45740030-45741610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr21:45741426-45741439 | GAATCTTCTGGAA | - | 6.06 | Klf1 | MA0493.1 | chr21:45741014-45741025 | TGGGTGTGGCT | - | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGAGGCAGG GAGCGGCGCC CACAGAGGGA GGAACGGGCT CAGTTATTCT GCAGCCTCTT 60 CACGCTGGCC CCGTGGCTGG GCCTGCCTGC CCCCACCTTC CCTCCTGCTG GGGTCCGAGC 120 TGTGAGCTGG GAGGGTGGGC CTGACCTCTG CCTGGGCTCA GGCACCACTG TGGCTGGCAG 180 GTCCCGGGTG CTGGGACCCT GGCTGCAGGG CTGGCTGTTG CTTCTCAGTG GTGGATGGAA 240 ATGAAGTCAG GCCACAGGCT TAACTCAGGA GAGGAGAAGC CATTGTGTAG AAAATGTCCC 300 CCGGGGCCAG GCTCACACCT GTAATCCCAG CACTTTGGAA GGCTGAGGTG GCCAGTTCAC 360 CTGAGGTCAG GAGTTCGAGA CCAGCCTGGC CAACATGGTG AAACTCCGTC TCTACTAAAA 420 ATACAAAAAT TAGCTGGGCG TGGTGGTGGC ACATGCCTGT AATCACAGCT ACTCAGGAGG 480 CTGAGGCAGG AGAATAGCTT GAACTTGGGA GGTGGAGGGT GCAGTGAGCC GAGATCGTGC 540 CATTGCACTC CAGCCCGGGC GGCAAGAGTG AAACTCTGAA AATAAAATGT TCCCAAACAG 600 CTGAAAACCT CAGGAAATGG GATCTCTCCA AAATAAGGAT GAAATGGCTT GTTTCTAAAG 660 TCCTGGGGGA CGAGGGTCCT GTAGAGAGAG TCACGGCCAG TGAGGTCCTG GCTCCCAAGC 720 CCCTTGAGCC ACAGCCGGAG CTGCAGGCCG GGGCAGACAG CGTGGCCCAG CCTGAGTCTG 780 GTCCTCCCTT CCATGGACAT CTTTGGGTGT CCCTGCTGCT CCAGCCTCCT GCTTATCCCC 840 AGAGCTAGTC AGCGGGCTCT ACCCTCCGTG GTGGGGCAAC CTGGTCTCCA CGAACCCAGA 900 ACCTGGCAGG GGCGTGACTG GCTTTGTGGG CAGCAGGGCT GGCTCGTACC AGGACCCAGT 960 GGGGCCATGT GGCTATGGAG CCCTTGGGTG TGGCTGCTGC CAAGTGGGAT GTGCTGCACG 1020 TGACAGGTGC ACGCCAGGTT CAGAGCCTCA GCACGGTGGG TGGAGGGGAG GTGGTGGCGG 1080 CCGTCACTGG ATTCACATGG ATGTGGTGGG GTTTTGGGTC CATCAGGTTA AATTAACTGT 1140 AGTCCTGATG GGACTGTCTC CATGTCTTTT CCCTTCCCTT AACGTGGCTA CTAGAAAACA 1200 GGATAGCCAG GGCCCCTTCC TTACTCGTGG CTGTGCACCC CCCACCCTCC CGCCCGCTGC 1260 CAGCCCCTTG TGTGGGCACT GACCTGTGTT CCCGCCCGCA AGCCTGGCTT CACAACAGTG 1320 CTCGCCCCTT CTGCCTCCTC TGTTGCCTGC GTGCCAGGGG GCCAGGCTTG CACCGTGTCT 1380 CTTTTGGTCT TCACCAGAAT CTTCTGGAAT TAGAACAGAT ACCGTATTCC CAGGGCAGTT 1440 GGGCGGTGTG CTGGGCAGCG TCCAGGCTGC TGGCAGGGCC TGGCCCCTTT TTCCAGAACC 1500 TGCCGGCCTG CTGACCTCCT GTGCAGGTTG GGGGTCCCCT CCCCGGCTGT GCCTCACGCT 1560 CATCTCCCCT TCTCTCTGAA 1580
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