| Tag | Content |
|---|
EnhancerAtlas ID | HS154-21110 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr8:41604780-41606170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr8:41605602-41605614 | GGTGACGTCAGC | + | 6.14 | | CREB1 | MA0018.3 | chr8:41605602-41605614 | GGTGACGTCAGC | - | 6.14 | | FOS | MA0476.1 | chr8:41606140-41606151 | TCTGACTCATT | + | 6.32 | | IRF1 | MA0050.2 | chr8:41605411-41605432 | GAAGGGAAAATGAAACCAGTC | - | 6.71 | | IRF2 | MA0051.1 | chr8:41605415-41605433 | GGAAAATGAAACCAGTCT | + | 6.17 |
|
| | 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 |
| GH08I041747 | chr8 | 41605273 | 41605943 |
|
Enhancer Sequence | TAGTCTCATC ACAACCATGG GATCTGCTTT CAGCGTTTCC TCTAACAAGC AGAGAGGCAA 60
ATCTTCCTCA AGGCCCAGAC CGAGTGTCAT TTTGCCTGTG ACTTTACCTG TCCCCTCTCT 120
TTGCCACACT GTACCTTATT TCTAGCCCCC TAAAAGTGGA TTGCTTTCTT GGCCATGTTC 180
CACGGACCTT GATAACTCTC TCAAGACCCT CATCACACAG AATTGCATTT ATCTGCGCTT 240
GTGCCTGTCT ATCCCAAAGG CCTGAATTCT TTGAGATCCT GTGTTTTGCT CACCTTGGTA 300
ATCAGGTCCT AGCATGGAGC CTGGTGCATA AGGTTTGCAG AATTCAATGC ACCTTCATGG 360
AACCTGCCAC ACACAGGCCT ATCTTTTTTC TTTGTCTCTA AGCACTATGA AGATCATGTC 420
TAGTCTTCAT ATTCTAAATT CCTAGAGCAA TGAAACCATA ATGTGGAGTT TAGAGAGTGT 480
GTGTTCCTTG CACTACATTC CGGATCGTTC CTGAAGGTGC TAGTCACCCT TTTCCCAGTC 540
CCTAGGATTC CATGGAATGT CCCTGCTGTG ACTACAAATG AAGATTTTTA TGTAACTGAA 600
CTGGTCAATT AGCTCTTCCT TGGCTGCAGA GGAAGGGAAA ATGAAACCAG TCTGGGGCAG 660
ATCACCCAGA GCAATAACAG GCTTGCTGCG CAGTGTCAAA TCCATCCTCT GAGTCAGTAC 720
AGAGGCTTGG GCTGGGTGTC TCAGTCCTGG GCTCTGAGAC TCTTCACCTC TCTGAGTCTC 780
CCCAGCCTCC CTGGTCAAGC ACCTGCTCTA ACCAACTCTC AGGGTGACGT CAGCATTAAC 840
GGTGTCGCAG GTACCAGGTG CCAGGCATAG GGGCACCTAG CTGCATATCT GGTTTAACTA 900
TTTAACACAG AACACTCTTC TCCCAGGTGA GGGCTCCAAT GAAACGTTCT TTCTTCCTCA 960
TCCCTATTCC AGAGCTGCAC CAAGGCAGCA AGTCTAAAGA AGTTTAATAC CACAACACCA 1020
TCATTTTAGG AAGGCTTTCT GTGTGTTTTC GGGGTGCAGC TAGGATCAGA GAACTATGTA 1080
GTTTAATACA TTTTTCTATG CCTGTCAACA GTTCCTAAGA AAAAGACAAT GACAGAGAAA 1140
AGTGCCAGGT TCTAGATCTA TACAGATCTA GCTCTAACCT CCTTAGCTGG ATTGACCACC 1200
ATCCTCACCC TCTTTCATTT CATGTACCCC AACCTCCCCG AACTGCCCCC TGCCCCAGTG 1260
CCCTTTGGCA CTCCAGCCTT TGCAGTCTGT TCCTTCTCAC AGCAATTCCT GTTTCCCAGT 1320
TCTGTACTCG GAGACTTGTA TCCTTCCTTC ACAACCTTTC TCTGACTCAT TAGCAAGCCA 1380
GCCACTACCC 1390
|
