Tag | Content |
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EnhancerAtlas ID | HS078-00946 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:53776360-53778220 |
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) |
MYC | MA0147.3 | chr1:53777639-53777651 | AGGCACGTGGCC | - | 6.07 | ZNF263 | MA0528.1 | chr1:53777302-53777323 | TCTCTCTCTCCCTACTCCTCT | - | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 53776578 | 53776628 | chr1 | 53776668 | 53777368 |
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Enhancer Sequence | TCTCGGGAAG AACCAGAAAG AACTTCGTTT CTGAAAATCT TGGAACCAAT TGTTGTATAA 60 AGGAGTGAGG CCTCCATCCC AGGAGGTATG CAAGCAGGGG GATCCATTCA TTCATTCAAC 120 AAGCATACAA TGGGCCCCTC CTCTGTGCTG GGCCCTGTGA TGGGCACTGG GGGGTTGGGA 180 AAGAGTGCAT GAAAGCCAGT CCTGCCTGAA GAAAGCCATA CTATAAAGAC ACAGGAGATG 240 ACAAAGGTGC CAAATCGACC CCGGGTCATG CCTGCCCAGC CCTGCACATG CTTCAGAGCC 300 CGGAGGAAAT GCAGGAGGCC CTATGCCATG AAAAGGGGCT TGGGAAACAT CCAGGGTAGC 360 ACAGTGAGGG CTGAGCTCCA GCCAGCAGAT GCAAGACCCA GACCCCAGCC TGCTCTGAGC 420 TGCCATGCCC TCCGGTATCC CGGGGGCCTC CCTGCCCTGG TCCACCCCCA TCACAGCTCA 480 GGGCCAGTCC CCAGGCCCCT GCCCACCCCC AACACCGAGT GAGGGGTGCG CAGGAGGAAT 540 CCATAGTTTA CAGGGAGGGC CCTGCTGGCA GCAGGGTGTG AGGAGCGGGG AGGGGTAGCT 600 GTCTCTGCCT GGACAGGGGC ATGGGCACGG CCAGTCCCAG GCAGGTGGCG GGCTTACCCT 660 TTGCCCACTT TCTTGTCCCC TGGCAGTTCC TGGGGTGTGG GCTCCAAGGA GGCCCAGCAG 720 CCAGACCACC AGCTGCTTCC CCTCCCCACA CAAGCCCTGG CCACAAAGCG CCCTCCCCCA 780 ACTCTGCCCG CCTGTGGTGA CAGCCTCTTG GCACTAGCTC TCTCCTCCCT CCATCTGTCA 840 GGAATCGGTG CAGACAGACT GTGAGAACCA CAGAGGAAGG AGCGATACTG CGTGGACCCT 900 CCCTGCCCCC AGCCTCCCCA GTGTGCTCCC CAGCCCACCC CATCTCTCTC TCCCTACTCC 960 TCTGTCTCTG CCTTCTCTTC CATCTGTCTC CATCTCTCCC TACTGATGAA GACATCGACA 1020 GAGTGGGCAT AGGGAGGGGA AGAGGACCAG CCAACCAGTG ACCCCACTCG TAACCACCAC 1080 ACGCCACGGC CACAGCCCAG CCACCCATGT GGCTTCCCTT CTCCCCACCA TTAAGGAGTC 1140 AGATGCTGTG GGACTATGGG CTCAGTGTCC CCATCTGTAC AATGGGTGGA GTCATTCCTG 1200 CTGGCCCACC TCCCAAGGGC CACCATGAGC CTGGAGGCAA CATGTGGGAA GGGCCTTGTC 1260 GACTGCAGAG ACTCATACAA GGCACGTGGC CAGCGCCTCC AGCTTCTTTC TATTCATCAT 1320 GAGAACAACG ATCTCAGTGC TGCCCTCCAC TTGGGAGGAG TGAGGCCAAC ATGGGACACA 1380 GACAGACAGC CACATGCCTG GAAGAATAGA AATGGCGGTG GTAACACAGG CAGGCCCATG 1440 AATGTTATGA TTCTCACCAC AGTCATACGA GGTGAGCAGG GCAGAGATGG GGAAACAGGC 1500 CAGGGAGGGA GGTCACACAG CTGGGCTAGA GGCAGTCTGT AACAGCGGCC AGGCCTCCTG 1560 GCCCTATCCA CACAGCTCCC TACTCAGAAT GTTTGGCCCT GCTCTTCCAG ACCTTCCAAG 1620 ATCCTCTGTT TCTTTCTTGA GTTCTCCCAA AAGGTGAGGA AGAAATCAGT CTTTTCTTTT 1680 GGCAGGCAGG GGTTGAGACA GGGTCTGGCT TCCTTACCCA GGCCAGAGTG CAGCGGCATG 1740 ACTATAGCCC ACTGCAACCT CAAACTCCTG GGCTCAAGCA ATCCTCCTGC TTCAGCCTCC 1800 CAAGTAGCTA TAGGCATGGA CCATGACACC TGGCTAATTT TTTTTTTTTT TGAGAGACGG 1860
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