Tag | Content |
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EnhancerAtlas ID | HS098-14777 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:122048020-122049080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:122048809-122048830 | TCTTTCTTTCCCTTTCTTCTT | + | 6.08 | IRF1 | MA0050.2 | chr12:122048786-122048807 | TCTTTCTTTCTCTTTCTTTCT | + | 6.76 | TFAP4 | MA0691.1 | chr12:122048418-122048428 | ATCAGCTGTT | - | 6.02 |
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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 |
GH12I121609 | chr12 | 122047874 | 122049676 |
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Enhancer Sequence | AATGCTAGGG GCTAGAACTG ACTGGGTTTA TTGATGAATT GGATATTGTG GGGAAGGGTG 60 CAGTCTAGGA AAGTGACTGC AGCGTGACTC CTGGGGTGAT CAGAACTACA ATTTCTCCAG 120 CTTCTCTGGG GCCTCACAGA GCCACACTGT GTTTGACAGG CTGTTCCCAG GATGCGGGTG 180 TTTTTATGTG ATTAGGCTGG AACTGTTCTC TGGGAAATAA ATGCCCTCAG TCTAAAGGGC 240 TTTTACGAGC CAGGGCAGGG GATTAAAGGC GGCCGGGCTG TGGAGAAATC CCAGGGTTAG 300 GAGACAGCTG AGCATGGAGA CTTTTAATCT AAACCTTAAA CGTTTTTATT TTCCACTCCT 360 TGAACTCAGG GTGTCACTTT AAATACATGT TTGGCAACAT CAGCTGTTCT ATTTTTCTTT 420 TTAATTATAC AAAGCGAGAT CCTGGAAATG GCTCAGCCCC AGGCTGGGGG AGGCAAGGGA 480 AGTTTGGCAA TGGTAGGAGG CAGAGAAACC AACTAAAAAT CTAGTGGATT TGAAATCCTT 540 TTGAGGGAGC ACAGAGGCCA AACTTCGAGC CACCCTGAAC TTGGTAAGAG CTGCCCTGAC 600 TCAGGATTTC TAAAAGGAGA CCGACAGACT CACCAGCTTA GAATGGAGAG AGGACAGATG 660 GACACGTCTC CAAGACAAAA ATATCACCAG CCCTAGCACT GTTCCTGTAC CTCGAATTTA 720 TTCCCAGGCC CTGTCCTGTT AGCTCAGCTC TTTTCATTTC TTTTCTTCTT TCTTTCTCTT 780 TCTTTCTTTT CTTTCTTTCC CTTTCTTCTT GCTCTTTCTT TCTTTTCTTT TCTTTCTTTC 840 TCTTTTTCTC ATTTCTTTTC CTCTTTCTCT CTCTCTCTTT TTTTTTTTTT ATTAGAGGCA 900 GGGTTTTACT ATGTTGCCCA GGCTGGTCTT GAACTCCTGG GCTCAAGCGA TCCTCCTGCC 960 TCAGCCTCCC AAAGTACTGG GATTACAGGT GTGAGCCACT GTGCCTGGCC CTGTTACCTC 1020 CTTTCATCCT CTGAGCAGAA AACAGCTAAC TAGGTTGTTC 1060
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