Tag | Content |
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EnhancerAtlas ID | HS179-01798 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:101647220-101648580 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBXT | MA0009.2 | chr1:101648222-101648238 | TCACACATATCTGTGA | + | 6.48 | TBXT | MA0009.2 | chr1:101648222-101648238 | TCACACATATCTGTGA | - | 6.56 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 101647248 | 101648435 | chr1 | 101647596 | 101647783 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I101182 | chr1 | 101647556 | 101647957 |
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Enhancer Sequence | AATATTACAG AAGTGATCCA TACCTCATGG AGTTATTGTT ACAAGGAAGT GCCAACGGAG 60 TTTGGGAATT TGGGAAGCCC TCTCTGAAGA AATGAGGATT GTATTGAGAT CTGAAGGATG 120 AGTTAAAATG ACCTAAGTGA ACTGGAGAGT TTCATGCATG GTAAATACCA AGCTGAGGTG 180 ATATACAAAT GCCAAGCTCA GATCCCCTTT TAAGGAAGGA CTTGATGCCC CTGGAGCTAG 240 CAGTGCCAGC CCTTTCAGGC ATTGCCTCAG CTACAGGGAG ACACCTCACC CAAGATCACA 300 CCCTTCCACC CATTTGTGTG CCACTTCTGA TGAGCCACTT CAGTTACAGA GCACTGTGTG 360 CTGTTGGCTA AGGCTGTCAG ACTTGCGTCT CAGCTTGATT TCTCCCTCTT CCCAATTCTG 420 CTTCCGCCTC CTCCCTTCCC TGGGTGTTGA CTCAAGAGCA CTCTCTAATA AACATCCTGA 480 ACTCTAAACT CTGCCTTAGA GTGTGCTTCC TGGAGAACTC AATGTGCATT ACGGCATGAA 540 AAGCCTTGAT GAGTAAGATG CTAAGAAGCA TTCAGAATGG CTGTAGACTG TGTGGGAAAT 600 AGTGAGATGA ACCCAGGCCA AAAACGAAGA CGTGGGTCAA GTCATGAAGT ATCTGGTAAA 660 CCATGTTGAG GATTTCCCTA AAAACAGTGG CTAGTAGGAA GCCATTGTTG AATTTTAAGC 720 AGGAATGACA TAATCAGATT TGCAGTTTTG AAATATCACT TTGGGGCCAG TGCGGTGGCT 780 CACACTTGTA GTCTCAGCAG TTTGGGAGGT TGAGGCAAGC AGATCTCTTA AGCCCAGGAG 840 TTCGAGACCA GCCTGGGCAA CATGGCAAAA CCCCTCTACA AAAAAATCTA AAAATTAGCT 900 GGGTGGTGGC ACATGCCTGT ATTCCCAAGT ACTTGGGAAG TTGAGGTGGG AGAATCACCT 960 GAACCCTGTC CAAATGAACT GTGCTAATAT AACTACTATA TATCACACAT ATCTGTGAAT 1020 TAAGGTGAAG AATAAAAATA AGAAAGCAAA ACCAGAGATG TATGATTGGC AGGAGGACAG 1080 GTCTTTCTTT TGATGTTGTA TCTGGAGGTC AACCCTGGAA GGTTGAGGCT GCAGTAAGCC 1140 ATGTTTGTGC AACTGCACTT TAGCCTGGGC AACAGAGTGT TCCAGAGGTG TCCCCAGCCA 1200 CATGCAACTG CAAGTCAATT ACACCTCTTT TCTTTATAAA CTTCTCAGTA TCAAGCAGTT 1260 CTTTATAGAA ATGTGAGAAT GAACTAATTC TTTCTTTCTT TCTTTCTTTC TTTCTTGTGG 1320 AAGACCTTGT GAAAGAAAGA AAGAAAGAAG GGAGGGAGGG 1360
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