| Tag | Content |
|---|
EnhancerAtlas ID | HS095-16732 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr2:110405040-110406190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LBX2 | MA0699.1 | chr2:110405597-110405607 | GCCAATTAGC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 110405328 | 110405638 | | chr2 | 110405677 | 110406070 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I109647 | chr2 | 110405143 | 110405931 |
| Enhancer Sequence | CTCCTCACTT TTTTTATTTT TTTGAGATGG AGTCTCACTC TGTCACCCAG GCTGGAGTGC 60
AATGGCGTGA TCTCGGCTCA CTGCAATCTC CGCCTCCCGG GTTCAAGTGA TTCTCCTGCC 120
CCAGCCTCCC TAGTAGCCGG GATTACAGTT GCCTGACACC ATGCCCAGCT AATTTTTTGT 180
ATATTTGGTA GAGATGGGGT TTCACTATGT TGGCCAGGCT GGTCTCGAAC TTCTGACCTC 240
AGGCGATCCA CCCGCCTCAG CCTCCCAAAG TACTGGGATT ACAGGCATGA GCCACCCCGC 300
CCGGCTCGGC TCTCCTCACT TAAACAACAT TAGAGCCAGA GAAGCAAAAC TAGGCTTGCT 360
TGTATGCCCT TGCTTCTTGA AAGTCTTTGG CAATCTGGTC TGACCAAGAA TTTGAGAACA 420
AGCATCATTC CACAAATGCC CGTTAGCTGC CTCACTCAGT GCCCACTGAG GCCTGGCTCT 480
GGGGTGATGT GTCACACACC CTAACCCTTT GCTGAGCTGC TTAAGTATGT TGGAGGAGGC 540
AGAAAATAAA CAAGTGGGCC AATTAGCAGT AATCACACAT TAGGAGGGGT TACAGGATGG 600
AAACAGAGAG GGTGCAAGAA CTAAGTGGCC AAGGTTGGCT TCACTGAGAG CATGAGAGGC 660
ACAGCCCCGC AGAAGGGATA GTGACCGCTT GGGTCCTCGG GTGGGAATGC TTGGCGTGGG 720
CTGGGAGCTG AAGGGAGAAG AATGTGAACA CCGAACCACT GAACCAACAG CAGAGAACTC 780
AAAGGCAGGA AGGAGGCTTG GCTGGCTGCA GCCTGGCAGG GATCTGTGGA CAACATTCTC 840
TGTGCAGTGG GAGTCCCTGG AAGATTTTAA GCAGCAGAAA GACACCATCT GATTTACACT 900
TTTTTTTGAG GCAGTTTCAC TCTTGTTGCC CAGGCTGGAA TGCATGATGC AATCTCGGCT 960
CACTGCAACC TCCGCCTCCC AGCAGTTCTC TTGCCTCAGC CTCCCAAATA GCTGGGAATA 1020
CAGGCATATG TCATGATGCC CGGCTAATTT TGTATTTTTA GTAGAGATGG GGTTTCACTA 1080
TGTTGGCCAG GCTGGTCTTG AATTCCTGAC CTCAGGTGAT CCACCCGCCT TGGCCTCCCA 1140
AAGTGCTGGG 1150
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