Tag | Content |
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EnhancerAtlas ID | HS098-39704 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:121713510-121714890 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:121714563-121714582 | TAGCTCCCTCTTCTGGCCA | - | 6.92 | EWSR1-FLI1 | MA0149.1 | chr3:121713839-121713857 | GGAAGCAGGGAAGGGAGA | + | 6.02 | HOXA13 | MA0650.2 | chr3:121713510-121713521 | GCCAATAAAAC | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 121714355 | 121714445 | chr3 | 121713958 | 121714176 | chr3 | 121713923 | 121714776 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I121994 | chr3 | 121712875 | 121715130 |
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Enhancer Sequence | GCCAATAAAA CTAGAAGCCA AAGGCCAGAA ACAGAAGGTC CAGATGCGAA GGACTTAGAG 60 GATGCTGTGA GTCAGGGGCT GGGGGCATCT GCTCAGAGTG AAGGAAAAAG GGAAGGGCAT 120 GATACTGAAG ATAATGGGCA GAATTACTTG GCAATTGCAT GGAAGAGTAT TTCTAGCTGG 180 CATGCCAACC CTGGGTGGAA GAAAGTTTGT GGGAAGAAGG CAAGGGCGTG CAAAAAGCTC 240 AAGTAGATTC CAGTGAGTCC TTTCTACTCT TCCCGCCTTA TTAAGTATTG AGATTGTCCC 300 TAAGTAGGGG AATTTCTCAG GGGTGGGGTG GAAGCAGGGA AGGGAGATGA GAAATACTAT 360 TTCCTTTTAT GGCAAAGAAA ATCATATAAA AAAAGTAGTG CAAGGGATCC ATAAAAATGT 420 CACTCCAGCC CCTTAGGTGG GGCTGGTCTG AGGCATACAA CCCGCAGTGA GTACAAATTA 480 AAAACAAAAG CATTTCGTTG TTTTTGTTTG TGCTTTTCTA TTTTGGGGTA GTTGTGGCTG 540 AGTGCCTCAT GTTTCCTAAG GGCTCTGCCT ATCCACGCGT GTTGGACGTG TGCCTGTACG 600 TTAAGTGCAG GAAGTGCCAG CCTCAGTGTG AACGAGGTTA GGCCCCAGCC TGGCATTCTC 660 AGTTCCTCCT TGCTTCCCTG GGCCCTGTGG CCACCCCTAA AACAGCAGGG CCACGTACAG 720 TAGAAGGGGG CAGAAAGCTG GCATCCTGAA CACAGCCACA TAGGGTGTAG GGTTTGCCAA 780 GGCCAGCAGC AAAGGGGTCA TCCAGTGGGC TGCTCAGTGA TTCCAGTATG AAACTTCCAG 840 CACAACAGGA AGTGGTTGTA ACAGAGTCCC CAGAAATGTC CGGAGCTCCA ACCCTCAGTG 900 TGAGTCACAG CCTAGCCTGG AAGAAATCAG AGGCAAACTT GCAGCAGCTC CCCCAGCAGC 960 TACACCTTCA TGCCAGCTGA TCACCTGGAG CCTCCCTGAA GACAGGTCCA CAGGCTCAGC 1020 ACTGCCCTCT CCCTCTGCAG AGATGCCTCT CCCTAGCTCC CTCTTCTGGC CACCACCAAC 1080 ACACATACTG GAATGCCCAG CCTTATACAT GTAATTTACT TTACATAAGC TAACTAGTTC 1140 TCTGAAAAAT CTCTTCACGT GGGAATCCAA TGAGGAAGCT GGGCTCAGAG AGATTACCTT 1200 CCCAGCCTAA GGTCCTACAG CTAGCGACTG GCAGAGCCAG GGTGTGAACC TGTGTGACGC 1260 TCAAGCCTAC ACTCTTTGTG TGCCGCACCG CCAAGTCCCC AGACTCCTTT ATTTTCTGTG 1320 ATGAAGCAAA AAACCTTCCC TGCAGGCACC TCCTCAATTT ACCTCTCTCT AACTCGGCTC 1380
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