Tag | Content |
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EnhancerAtlas ID | HS176-21459 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:114575750-114576660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr2:114576602-114576615 | AATTAATTAATTC | - | 6.29 | Lhx3 | MA0135.1 | chr2:114576601-114576614 | TAATTAATTAATT | + | 6.78 | POU6F1 | MA0628.1 | chr2:114576603-114576613 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr2:114576603-114576613 | ATTAATTAAT | - | 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 |
GH02I113817 | chr2 | 114575371 | 114577334 |
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Enhancer Sequence | TTACAATGAA GCCTCGTTTG CCTGCCTTTG ACTCAAATTG CTATCACACT TGTACTCCCT 60 AACTCTCATT TACTCCCTAT CTGCCTTCCC AGCTTGCTTG CTTATTTATT TATTTACCTT 120 TTTTGTCAGC ACTTACCACT AATATAGCAT ATATTTGGCT TGAATATTTA TTATCTAGAA 180 TGTTAGTGAG GAGTCTGGCT TTTGCTTAAG CCAAATGTGT GATCTTTCAG ACCTGACTAC 240 AGGCAATTAC GAAGGCCTTA CCTGGCAGAC CTCATACAGA AAGCTGCTGC TCTCTGAGAG 300 ACATTTGGTG CACAGCCAGT GGGTCACGGT CTCTGAAGGA AGTTGCAGTC AAGGACTCAG 360 GCTCTCCCGG TCAGTCATGC TTTTCCTATG TTTACATTCC TGGCCCCAGA GTCTTCATTG 420 CTAGTCTCTG GCAGACCTTG GGTAGACGTC CTTTTCAGAT GCCTTTGCCA AGACCTCCTT 480 ATGCGGGGAG GAGGGAGACC TTGATGATAC ATTCCCCTAC TCTGACTCAT CACCCAGGAC 540 TTGTCCACTC CAAGCTCTCG CCGCTGCCCT CCTGCTTCAG GGTCCATAAA ACTGCTTTAA 600 GCTCTTGCTT TTACCATTGC CGTGAGTGAT TAAAGGCTCG GTTCTTTTAT CTCTGGCTTG 660 TTGCTGTAAC CGGCTACTCT GAGAGCTCTC TCTCTCCCAG CTCAGCTGAG CTCCTGACAA 720 TTCACTTCAC AAGGGTCAGG GTTTGCTCTT TGTTTTCACT GCTGTATCTC CAGCACCTAG 780 AAAAATATCT GGCACATATC AGGTGTTCAG CAATTTGTTG AATGAATTAG TAAGTGTCTG 840 TTCAATTAAT ATAATTAATT AATTCTTGGA ATAGATGCCT TGTTTTAAAA TTTTATTACA 900 TATTGTTAAA 910
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