Tag | Content |
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EnhancerAtlas ID | HS176-35323 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr6:116725940-116727040 |
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) |
Myod1 | MA0499.1 | chr6:116726384-116726397 | TGCAGCTGTTTCT | + | 6.29 | Myog | MA0500.1 | chr6:116726383-116726394 | CTGCAGCTGTT | - | 6.02 | RORA | MA0071.1 | chr6:116726926-116726936 | ATCAAGGTCA | + | 6.02 | Tcf12 | MA0521.1 | chr6:116726383-116726394 | CTGCAGCTGTT | - | 6.62 | ZNF263 | MA0528.1 | chr6:116726950-116726971 | GGAGGAAGCAGATGAAGAGGA | + | 6.44 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00627 | chr6:116724535-116729710 | Adipose_Nuclei | SE_11480 | chr6:116724556-116735497 | CD20 | SE_46315 | chr6:116724971-116729226 | Osteoblasts |
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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 |
GH06I116403 | chr6 | 116724812 | 116729263 |
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Enhancer Sequence | CTCTGGAGTT GTGTTTTTGA AAAGTATTTG TTGTGACTCT TTAGTTCTCT CTTTATAGTA 60 TTTTTCCTTA CTTATCATCA GACAGAAAAT AAATCACAGA GGAAAGAAAT TACTTCACTC 120 TTGCATTGGA GCCAGTTAGC TACAGGAAAT CAGGAGAACT GGTGAGGGAA ACAAAGAAAG 180 TTGAACTTTT GGACAGAGAA GTAATTGTGT TTTTTTTTTT TTTTTGCAAC AGACTGAGTA 240 TTAAATTCTT GCCTGTGATT GCAAACTTCT GGATGGTGTC ATCCGAGGGT GTATTTGCAA 300 AAATAAAATA TAATTATAAA ATATAAAGAG AGAAAAAAGG TCTCTAGCAT ATTGAAATGA 360 ACCAGTTTCA TTGCTGTACG TATGAAAATG AGGAGTGTGC CTGCCTTGCT CAGCATTGCC 420 TGCTGGGCTT CAAATGCAGT TCTCTGCAGC TGTTTCTCGG GTTTTTCACT TCTCAAAATT 480 GCAAGTTAAA ACTGAAAATC AAAAGCCGGG AGAATGTAGC TGGGCCTCAA ACATGTGGAG 540 CCACAGCCCT GTGAGTAAAA AGATCAGGTT TTCTTCTCAT GACCTTACAG TGAGGAAGGC 600 TGGGCGGCTT AGCCCAGAAT GCACCTGGAA TCCATTAAAG TGGACTCGTG GAGACAAATG 660 CTGGGCTGTC AGAAAACCCA GCCTCTAATT CCCCTGGCTT TTTCTCATTC ATGTTTTTCC 720 CTTTCTCTTA CCCTTCCCCC TCACTCTTTC TGCCTCTCTT TTTCTCTGTT CTTTTCATTC 780 TGTGACCTAA GGGAAGCTAT TCCCTTTTAT GCTGCTGCAG AGACTTAAAA ATACTATAGA 840 AGGGTAAAAT AACTTATGAG GCTTTTTACA ACGATCAAAT TATTTAAAAT TTACAGAAAC 900 ACACAGCCAT TGGGAATTCA CTTCTTGAAT GCCGTTTATT AAGCAGGTTG TTGCCATCAG 960 TGTTACAAAT GGATTCTTGG GCAGGAATCA AGGTCAGGTG CCCTGTGGTG GGAGGAAGCA 1020 GATGAAGAGG ACCCGAGGGA GAGGCATAGG CAGGTGTACA GATTAGTTGA GCAGCCCAGT 1080 TACAGTGCCA TTGGACAGTT 1100
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