| Tag | Content |
|---|
EnhancerAtlas ID | HS154-03296 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr10:133836500-133837650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr10:133837375-133837393 | AGAAAGTGAAACCCGTTC | + | 6.06 | | Mafb | MA0117.2 | chr10:133836627-133836639 | AATATGCTGACG | + | 6.18 | | Nr2f6(var.2) | MA0728.1 | chr10:133837606-133837621 | TGAACTCCTGACCTT | - | 6.04 | | Zfx | MA0146.2 | chr10:133837629-133837643 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I132022 | chr10 | 133836367 | 133837304 |
|
Enhancer Sequence | CCCAGCACTT TGGGAGGCCG TGGCTGGAGG ACCGGAGCTT AGGGGTTCAA GACCAGCCTG 60
GGCAACATAT GGAGACCCTG TCTCTAAAAA GAAATTGTCG TATCGAACAA AGTTCCTTAA 120
TATCTGGAAT ATGCTGACGC CTTTCTTCCT GGATCTATTC CTGAGAAGGT GGTCACTGAG 180
CTTCCTCTTC CGAGACAGCC TGGCGCTCTG GACGCTTGGC TTCCGCTCGC TGGCTCGCCG 240
ACGCCCTCTG CTGTCCACGG TTGGGAGACC TGAAAGTCGC AAGAGCGTGC CCGTGACAGG 300
AGGCTGTGCG CAAGAAGACG TTTACAGCCG TTTTATTTGT AATAGCCCCA AACTGGAAAG 360
CAGACGGGTG TCCTTCAACA GGAGAATAGA TACATACACC GTGGCAAATT TGTACAAGAG 420
AACAATCTCC AGCAATAAAT AAGAGCACGC CACTGATGCG CGTGGCAATT TGGAAACCTT 480
CCACAGAACA GCACACGGAT TGCATGGATG CGAAGCTCCC CTCAACTAAT CTATGGGGAA 540
AATCATCAGA AAAAATGGGT GCCTCTGGGA GAGTAAGGGC AGGGACTAGC CAGAAGGGGC 600
AGCAGGGCCA GGTGGAGACT CACTCGCCTC TGTGGATACT CTGGTCATGC GGCTTGGGGA 660
GTGCGTGTCC CTTGAAGAGC CTGATCCAGA AACAGTGCCG TGTTTTCTGA AACTGAATGC 720
AACGAAGTGC GGCTTCATCC ACTGAGTCAC TGCCCATCCC CTCAAGGATC CCCAAGGAGG 780
CGACGCTGAG TCCGGAACGC AGGAGGGAGA CCGTTCTTCT TCCCGTGAGG AACATGCTCC 840
AGGGTCCGGA GTCTACGGAA AAATAGGAGG GTTTGAGAAA GTGAAACCCG TTCATTTTCT 900
GTGGAGCAGA ATCAGCAAAT GCTGTCTCGG GGGGCCCTGT GGGCCTTGGG AAGCATTTTG 960
GACTAAACCA GAGGATAATG AGACACCACT GGAGGTTTAC CAGCAGAGGC GGTGCCATGG 1020
GGTTTGCGTC TCTAGAAGAT TCTATGGGGG ATCACCAGCA CGCCCAGCTA ATTTTTGTAT 1080
TTTTAGTACG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT TCTGATCCAC CCGCCTCGGC 1140
CTCCCAAAGT 1150
|
