| Tag | Content |
|---|
EnhancerAtlas ID | HS154-02046 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr1:223306570-223308020 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:223307176-223307195 | AGACCAGCAGAGGGCGCAA | + | 6.93 | | Gfi1b | MA0483.1 | chr1:223307445-223307456 | AAATCACAGCA | + | 6.62 | | ZNF263 | MA0528.1 | chr1:223306991-223307012 | TTCACTTCCCCTTCCTCCCCA | - | 6.21 | | ZNF263 | MA0528.1 | chr1:223307075-223307096 | TGAGGAGGAGGGGATGGATGG | + | 6.55 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTTAAGCAC TTGTCTAAGA TCTCACATTT ATTACACTGT GGAGCTCGGA TTTGAATCCC 60
GCTGCAAACT TAGTTGTCAC TGTGACCTTT GAACAAAACA AAATTGAATA TGCTGCAAAA 120
CATCCACAGA GCCTCAAAGC GAGCTCGGAA CCTGAAACGG CCCGCCTGAG ACCTCCTTGA 180
AACGGTGATT CTGATTCATC AGGGCTGTGG CTGAAGGACC TGAGAGTCTG CATTTCTAAC 240
GGGCTCCCAC GTGATGCTGC TGCTGGTCCA CTGACCACAC TGTTAGCGGT GAGAACCTAA 300
GAGTCTGTAA TTGCCTCCCT GCTCATTACC CCCATGCCCA CGTGAGCTGC CTCGTTCTTC 360
CAGGATAAGG CATGGCTAAG ATGCTGCACG ATTGGTTTTG AGAAGGGGCT ATACTAATAC 420
ATTCACTTCC CCTTCCTCCC CATTTTTCTC AGCGCTGAAG AGTGAAGCAT CAGAGAGTAC 480
CTCAAAGAAG ATTCATGTGA GGCTTTGAGG AGGAGGGGAT GGATGGGTCA TATCGCTTTA 540
CTAGGAGCTA AGGAAACGGG ACAGCTTGGG TGCGACTTCT GATTTCAGGA GATGCGCTTT 600
CCCTAGAGAC CAGCAGAGGG CGCAAAAGGG GCAGGGACCG AGGGGGAGGA GCCCGCGGAG 660
CCGCGGCCGG AGAGTCGAGC GGGGCGCGGG GAGCTGCAAG CGTCCCTGAG CTGAGCTCCG 720
CTGGGAAGTT CCTATCGCTT GCGCAGTAGA GTGCATTTAG ACATTTCAAT GACAACTAAA 780
TTTGTAGCTG GATTCAAATC CTAGCTCCAC AGTTTAGTAG GTGTGTGAGC TTGGGCGAGT 840
GCTGAACCTC TCTAAGCATC AGTTTACTGC CTATAAAATC ACAGCAATAA GTTTCTACCT 900
CCCACCCCCG CCGCCCCTAC CCCGGCAGCA ACAGCCTGCT TCCGGCTTCC AGGGATCCTC 960
CAGTGCCCAA ACCAGAATAT CCAGTTACCC ATGCTTAATA CTCCAACAGT TCTTGCTTGC 1020
TGAAGTAGGC AGCCATCATT TACGCAACTA CACCTTACCA GAAACGCCTT CCCTTTAGAA 1080
CACTGAAGGG GAAAGTTAGA GAGGGAAAGG AAATTTCTCA AGGCACTGGG GTGATTTTGT 1140
GTTTCTTTAG CATGAGTTAC CGGAAAGCTT CCTGTGTTTT CTTTACTATC TTTAGGTGGT 1200
GGTTCCCAGC ATCAAAAAAC AGCAAAAACA GCAGCAAGCA AAGGCGCTGA TACTCTGAAA 1260
AGTTATGTTG AAAACACATG GTTTAGGTAC AGAATGGCTT CCCCGTTGTT TGCACATTAT 1320
AACTCTTTAG CACACAATTT TAAAGCATCT GATTGAAAGA AATAATTTTT AGTGATTATT 1380
AAAAACGAAC AACTAGCACA ACATTTAAAA TCGTCGGGAA AAGGTGGCTC GCCCAGAAAG 1440
TGAACATCCC 1450
|
