| Tag | Content |
|---|
EnhancerAtlas ID | HS154-13332 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr2:225306700-225307920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr2:225307302-225307314 | CACCCCCTGACA | - | 6.22 | | NFKB1 | MA0105.4 | chr2:225307158-225307171 | GGGGGAATCCCCG | - | 6.36 | | NFKB1 | MA0105.4 | chr2:225307158-225307171 | GGGGGAATCCCCG | + | 6.46 | | ZNF263 | MA0528.1 | chr2:225307477-225307498 | GGAGGAGGGGAGCGCGAAGGA | + | 6.23 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 225306713 | 225307810 | | chr2 | 225307433 | 225307612 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I224442 | chr2 | 225306718 | 225307917 |
|
Enhancer Sequence | AAAAATATAG TTTCCATGAC TTTTTGTTTG TGTAGGATGC AAAGTGACTG CTGTGTGCTG 60
TGAAAGATGG GACAAACGGC TTTGAGCTCA AGGGACATGG ATTTGGGAGG AATTCAAAAT 120
GTGAAGCCTA ACTCAGGATT CAGGAACCAG ACTAACAGAG GGCAATGAAA CAAAACCAGA 180
GAACTCAGGC CCAGAGCCAG CGAGGGAGAG GAAGGACGCC GAAGCGTAGC GTCCCGCGCC 240
GCCCCCCGCC AACCCGGGAG GACGCAGACC CCCCAGAGCC GGTGTCCAGC CCCACCTCTC 300
CGGGCGCCTG CAGGAGGGGA ACCGCGCGTC CCATCGCCCG GACCCCGGGC CGGCGGCGCG 360
GCCGAGTCCC GCTGCTTCCG CACTCGCCCC GGGACCCGGA CCCCCGCCCC ACCGCGCCCC 420
TCCACCTCCC CGCCGGCCGG TGCCACGTGT AACGCCGCGG GGGAATCCCC GGGGACACAG 480
GGCTGGCTGG ATTCGCCTCT CGGCCACAGC TCTGCGCTCC ACGAGCTGCT CCTGCCCGGT 540
CCCCGCAGGA CTCGAACCCG CGACACCTCT GCCGCGCCCT AGCCCTCGCG CCCCGCCGGA 600
GTCACCCCCT GACACTGCCA GGATCCCCGC CCGGCTGCGG GCACCACGTC CCCCGGGCCT 660
TCGCGGGGCC CCGAGGGCCA AGACCGAGGA CGCGCCGAGC CGAGGCTGCC TGGGGACCTG 720
GTCCATCCGG TTCTGATGGG GTCCGCAGGG AAAAGGCACT ATCCCGGAAA GCTTCCTGGA 780
GGAGGGGAGC GCGAAGGACG AAACTGGGCC TCCCTCTAGG CGGAGCTTAG TGTTTAAAGC 840
TGGCCGGCCT TTCTCCTTTT CATAGTAATT ATTCTCTCAC TAAGCTCAGG AAGCACGCCC 900
TCCACCATCT CATTAAGCGA ACCGGCTGTG GCTGACTCTT CCCTCCTCTA ACAACTGTGG 960
CTCCTCATAG CCGGCACAAT GACGTCCAAA GCTGTCGGCT CCCGCACGGG TTCCTCCCTT 1020
TGAGGCTTGT CTTTCGCACT CCTTCCACCT GCTCGGAGAA CTGCGCCCAG GTGGGTTCAG 1080
CAACTAGCAG GTGCCATGAA GAGACCCTCA GAGAAGCGGC CGGCCTACCT GGCGCCCGTT 1140
ACCCCTCTCG CCGCAAACCC ACTTCCCTGA ACTGTTTTGC AGTTCACAGC CTCTCTCCCC 1200
GCTCTAAAAA CTAAAAACAA 1220
|
