| Tag | Content |
|---|
EnhancerAtlas ID | HS154-02886 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr10:88739240-88740730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr10:88740307-88740318 | CCCAATCCACA | + | 6.14 | | ZNF263 | MA0528.1 | chr10:88739964-88739985 | GGAGGAGGGGACAGGGAGGGG | + | 6.51 |
|
| | 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 |
| GH10I086979 | chr10 | 88739157 | 88740602 |
|
Enhancer Sequence | GCCTGAAGTG GGCGGATCAC TTGAGCTCAA GAATTGAAGA CCAGCTTGGG CAATATGGTG 60
AAACCCCATC TCCACAGGAG TGGAGGAAAA ACCAGGCAGA GGGACCCCCA GGACATTGAG 120
GGGCTCTGGC CGCTGTATGG GACACGCTTC TGGAAACTTG CCCCTAATAG GGCATCAAAG 180
CCAGGCAGGC AGGGGCTCCT CTGTCAGAGG TTGGAAGCCA GGACTGCATC TTCCCATCTT 240
ACTTTTGGGA TGCAGGTCAG CTGTTTTCCC TCAGATGAGA GGTTCCAATT TTTTGTTTGT 300
TTAGTTTTTG AGACAGAGTC TCGCTCTGTC ACCTAGGCTA GAGTGCAATG GCGCTATCTT 360
GGCTTAGTGC AACCTCTGAC TCCCGGGTTC AAGCAATTCT CCTGCCTCAG TCTCCCGGGT 420
AGCTGGGATT ACAGGCACAC ACCACCATGC CAGGCTAATT TTTGTATTTT TAGTAGAGAT 480
GGGATTTCAC CATGTTGGTC AGGCTGGGAG GTTCCAATTT TATAAGATGA GAAGAAGGGC 540
TGAGGTCATG CCCATTCTGC CACTTTGCTG AGTCCAGAGC TATGATGAAG TGAAGAAGAA 600
GGCACAGGGC AGGACAAAGA AGGGAGCTCA GGGACCCGGG AGTTTTCCTT GGCAGAAGTC 660
AACTTGCCCC ACCCCTGAGA AAACTCTGAC CTTCTCAGCT GCCAGGGAGG AACGCAGGGA 720
CTGGGGAGGA GGGGACAGGG AGGGGAACAG TCTGCTGCTC TGTGCCCTGG GAGAGAAGTC 780
TGATGACGGC AGTAACTCAG GAAGGGTTAA GAATATTCCT AAAATAGCCA AGCCACAGTC 840
TAAGCCAGTC CATGAGCAGA GAGCAGATCT GTAGCAGGAA AAGTCAGCCT GATCTTTGCC 900
CCACTGCCTG CTGCCTAGCC CTGGCTGCTA ATTAAGCCTC CTACCCTGTC CCCTTCACCA 960
ATTCCTCTTG TCCTAGTGGG GATGGGGTAG GAGTAGTCAG AGGAGCCAAA TCACCCCAAT 1020
CAACAGGGAA CTACAGCTGG GACCAGGAGC ACTGGGCCCA GTGGCCCCCC AATCCACACT 1080
CCTGGTCTGA GAGTCAGGTA GGGGGACATA GGGAGAAAGA CAGGCAAAGT GCAGGCTTTG 1140
TGCATGGGAT GGAGGCTGCC AAGAGAGAGC AGCCAAATTC TCCCACCCAC ACACATGCAT 1200
CGCCAGCCAT GATCAGGTGG GACCTCCAAG ATCATCATCA GATACCGCCT TCTCCTAGCT 1260
CTGTGTTCCC CTACACTTAG GGCATCTTGG AGTGAGACAG GCAGGGAGGG GTTGAGGGAG 1320
CCCCTACATG AACAAACCAT ATCTTTGTTT CAGGGGCAGG ACCAGGTATA TAATTTGCAG 1380
GACCCAATGC GAACTGAAAA TGTGGAGTCT GTCATTCAAA AATTGTTAAG AATTTCAAGG 1440
CAGTGACAAC AGAGCATTAA ACCAAGTTCA GGTCCCCTCT GAGTGTGGGG 1490
|
