Tag | Content |
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EnhancerAtlas ID | HS053-06121 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr10:120782040-120783540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX2 | MA0688.1 | chr10:120782070-120782081 | TTTCACACCTC | - | 6.14 |
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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 |
GH10I119022 | chr10 | 120782122 | 120783434 |
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Enhancer Sequence | ACTTGAGGCC CGCCTTCAAG AAGCTCAGCA TTTCACACCT CGGCCAGAGC CAAAGCTTTG 60 GGCTTTGAGC AAATTAGGAA AAGACACTTC TTCCACAAGG TATCTTTTTC CATCTGTCAG 120 TGAAGTGTCA TAATATACTG ATTTCGTTAG AAGATACTTT ACTCAAGGTC GGCCAGAAAA 180 TGATCACAGA GTTACTATGT CTATGAAGTA AAGGTGCCCC CTTAGATGGG AAGCGGTTGT 240 GCAGTACACA ACCTGCAGAA CTGTACACAA CCTGCAGAAC CACACATAGC ATTCTTTGCT 300 TGGCAGTCTG GTCCCATCCT TTCCACAGCC CTCATATCCC CGCTTCCCCT CCCTCTGCCT 360 AGAGCCCTCA GACCTGTTGG AGAACAGTCT CAATCTACAG GTTACCATTT TACATGTAAC 420 TCCTTCCTGT CAGCTTTTTA CTTCCCTCCC CCTGCAGACA GCAGGGATTG ACGACGGGTG 480 AGAGAAGGCT GATGGCCCCA TTTAGGGAAG CACAGGAGGA GGTGGGGAGG CCGGATGTAG 540 TGAATTCCAA ATGAATGAGT ATCCACGGGC CAGGGGATGA TCAAGGAGGT GTGAGGGTTA 600 ACAGTGCGGG CCTTGAAGAA ATGCCACCTA CCAGCTAGCT GTGAGCTGCT GGGCATGCTT 660 TTAGCCTCCC AAAACCTCAT TTTCCCTTTT GTGAAATGCT TATCATTGTA GGCCTGCTGG 720 GAGGATTTCA GAAATGATAT GAGTGAATGC TTAGTGCACG GTAAGGGCTC AGCACCTGTG 780 AGCTACTGTT ATTGCTATTA TCAGCATCAT CAGCCCAGGG ACATCTGCCC TTCCGCCTGT 840 CAGCCTCCAG GCAGCTCCTG CTTTAAACAA AATTGGGACA CTCCAGATTT CTAAAAGAAA 900 ACCACATGGC AGGGAGGAGG GCAAGTGCTG GAGGGAGAAA GGATTACTCA CTTTACCAAA 960 GTACCCACTA CTGGATAAAC AGAAACACCC AGACTGCTTT TAAATGGGGT TGGTTTTGTT 1020 CAGGGGACAT TGCTGACACG GACTGGAATG TGTCCTCTCC TGCCCCTGCC GCTGTGTGTT 1080 GCTGGCCAGT CTCCCGCACA TCTGGACCCC AGAAGTCCCA AGAATGACCG GGTGCATCCA 1140 AGGAGGCACA AACCCAGGTT CGGGGAGTGA GAGAAAAATG GGTGCAAATC TCAGTCCTGC 1200 TGCTCCTGAG CTTCTCAGCC TTGGGCTCCA TGCTGAGCTT TGCCCCCGTC TCCAACAGGT 1260 CACCAGCGCA CCTGCCTTGC GGGGCAGGGT TGGGGGTGGG GGGCACATGG AATAGTGCAT 1320 GTCAAGCACC TGGTGCTGAT GGTGGTGGTA TTATTACCAG CTGGGAGACT TTAGCCCAAG 1380 GCAGGGGGTG TGAGATGACA CCACGGCACC CGTTTCCCAT TCTCCGCATC CCCTTCCAGC 1440 CTTGTCCACA CACAGAGAAT TCTGACATGG TCGTCACCTC CACCTGGCCA GAATATGGTA 1500
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