| Tag | Content |
|---|
EnhancerAtlas ID | HS154-12441 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr2:70256620-70258100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr2:70257137-70257152 | TTCTATTTTTAATAC | - | 6.11 | | ZNF263 | MA0528.1 | chr2:70257063-70257084 | TCTCCCTCTCCACCCTTCCCC | - | 6.28 | | ZNF263 | MA0528.1 | chr2:70257035-70257056 | ATCTCTTTTTCTCCCTCCTCC | - | 6.94 | | ZNF263 | MA0528.1 | chr2:70257038-70257059 | TCTTTTTCTCCCTCCTCCTCT | - | 7.57 |
|
| | 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 |
| GH02I070028 | chr2 | 70255510 | 70258951 |
|
Enhancer Sequence | ATGAGCCAGG CGTGGTGGTG CGCACCTGCA GTCCCAGCTA CTCAGGAGGC TAAGGCAGGG 60
GAATCACTTG AACCCAGGCA GCAGAAGTTG CAGTGAGCCG AGATTGTGCC ACTGCACTCC 120
ACCCTGGTGA CAGAGCAAGA CTCCGTCTCA AAAACAAAAC AAAACAAAAT AGGAGTCCTG 180
GACTTAGTGG AGGACATCAG ATTCAACTCC CTCCCCTACT TGGCCACTTT GCTTGTCAGA 240
AGCAGGTAAG CACACCAAGG CTGAGCTAAG AAATATCCAC AAGGGGTCTT GTGTCCTCAG 300
AATTCTCATC AAGGACCCCT CCCTAGAGGA GGCTGAGGAG GGAGTACAGG TCCTTGGGCC 360
ACAAATGGTG GGAGAAAGGC ACAGTGAATT GTGAGCTGTC TTATCCAGTC ACATGATCTC 420
TTTTTCTCCC TCCTCCTCTG GTCTCTCCCT CTCCACCCTT CCCCTCCCTT TGCTCTGTTT 480
TCAAGATTTG GTTAAAATAG ATGCAAACTC CAGTCTTTTC TATTTTTAAT ACCGAGCCAT 540
TACATAATCC ACACAGTAAT TGCTGACTTG AAAAACTATT GGCAACATTA GAAAATCCCC 600
AGAGTTTTAA ACAGGAAAAG GATTACTACA GCACAAAAGC CTTTGGTAGT TTCACTGACT 660
AGTAAACCAT TGGTAATCGT CACTTGCCAG TGGAAGTCAC ATGGGCCCTG GGAAACACTC 720
CCCTATCTCA GGGAAAGCAG GCTGGGGGAA GGGATGAAAT GCAGCCTCAG CTGGGAGGAG 780
GAGGCTGCTG GTGGGGTGGT GTGCTGAGCT CTGAGTGGGG CTCCAACAAG TGACCTCCAG 840
CCAAAAGTGC TGAAGGAGTG AGCTTCAGGT TGTCCTCGGG CCACCTTTTA CTGCTTTTGT 900
TTCTTGCTAG GGAATGAGTG AAGTCTCCAG CGGCCCAGTC CTTTCCCTCT CGGTTTCCCA 960
CCTTCCTACA GCCTCCAACA TATTCCTGTA AGAGCCTGAG GGAGGGTGGA CTACTCCAGT 1020
TAAATAGATT TTATAAAGAC ACAGGAGCAG GGAAGGCTGC CTGTTTATCA CAAAGACCTA 1080
ATCCACTCCT CTGCAAGGCT TTCCAGACAT TAGGCCAGAA CCACACTATT TAATTCTTCA 1140
ATAAAATGAT CCAATGAAAG TTTAAGAACC AGTGGTTTGG TTTACAACCA AGCAGAAGTT 1200
AATTATCTAA TTGAGACAAA ATTCTCTGTA TGTGTATGTG TGTTGGGAGT GTGGGCAGTG 1260
TATAAGATAC AGAGGGGACA GGGACTACTC TCCCTGATTT TGCCACTTCT GCCACAATCC 1320
TAACCCCAAT AATCAAGGAG GATCTGAATA ACCACATGGC CATTCATTCA ATAAACATAT 1380
GCTGAATGCC ACATACCAGA CTAGGTGCTG GGGATGCAAC ACAGCAAAAT CACTGCCCTG 1440
CTAGAACTGC TAGGTCAGTG AAGGAGAGAC ATTAATCAAA 1480
|
