| Tag | Content |
|---|
EnhancerAtlas ID | HS154-03587 | Organism | Homo sapiens | Tissue/cell | Osteoblast | Coordinate | chr11:27179800-27181250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mecom | MA0029.1 | chr11:27180202-27180216 | AAGACAAGATTACA | + | 6.19 |
| | | 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 |
| GH11I027158 | chr11 | 27180401 | 27180610 |
| Enhancer Sequence | CAAGTGCCTT AGCTATGGAG TAATCTGTAT CAGTCAGAAA AACTTAACTC CACCCCCAGA 60
AAAAGAGGTT AGCTACCTTC AGATTTGTCT CTGTTTATTT ACTATGTAGA CTCTAAATCC 120
CATACTGGGG AGATTACCTG TGTTGTCAAG GTTTCCTTTC AAGAAACAAC AAACTCTTCA 180
CAGGTCAGGT AGCACTTAAA GCTCATGAAA TGGAGAATAA AGACAAAGTT GGCATTCTGG 240
CATTCAGAAG GGAAAAGTCT TTAAAGAGTA AAAAACATTC CTATAGTTAG TTGTATAAGT 300
GTACGGAACC ATGGGGCATT GCATGACCCA ATTTTGGGGC AATTCATGAG TAAGAAAGTG 360
GAGAATTGAC AAAGCGGTTA GAAAGGAGGC GTGTTCTACA ACAAGACAAG ATTACAGAGC 420
CTTTTGGATA AATTAGGATT TCAGCTGGTG CCCCCAATTC ACGTTTTTTT GTTTGGTTGG 480
GTTTTTTGTT GTTGCTGTTT TTTGTTTTGT TTTGTTTTAG TAGAGATAGG GTTTCACCAT 540
GTTAGCCAGG ATGGTTTCGA TCTCCTGACC TCATGATCTG CCCACCTATG ACTTCCCAAA 600
GTGCTGGGAT TACAGGCCTG AGCCACTGCT CCCGGCCTTC CAATTCACGT TTGGAAGAGG 660
AAACTTGCAG ATCGGAGTGA CTCATTCTTC AAGTGTGTTC TTTAGGCAGG GCCTCCATCT 720
AGTGGTTTGC CCTGGAAATT AACCCGCAGC CTTTATTAAA TACACACTAC TTCTTTTCAC 780
AAACTTTATG AAAATAGAAA ATTAGAGCTC CCTCATGTAG CATGGCAGAG GAAAATTTCC 840
CTCCTGAACT CATGAATTCT GTCCTTTCAT TGCTTGCTAA GAAGTGCAGC ATTCTTAACG 900
TCTAGATTTT GTCATGCCCT CTCCATTCAT GGAGTTTTCA TACCCAGTGT ATCTCTTTGC 960
ACATAGAAGA AAACTGTGAT TTCTAACAAC CAAAGAAACA AAACTGTGTG TGTCTATGTG 1020
TGTCTGTGTC TCTGTGTGTG TGTAGAGTGT GCTAAGAAAG AGCTCAGCTG TAGAATAGAC 1080
AATAGCAATT GGTAAAGGTG TGGACATATC ATAAGTATTA GTAAGAACAA CAGGAGAATG 1140
GATGAATGTT AACTGGACAG TGAGATAAAA GCAGATGAAC AAACTTGCAA GGGAGGAACA 1200
GCATGTCTCA CCAGGAAGCA GAATGGGGCC AAAACAAGCT GAATCTCAGC TGGGACATAC 1260
ATAGTCACTG AATCAGTGAC GTCAGATTTT CAGAGCTCTC CTGCTCCTAT CTGTAACTTT 1320
GAACAAGTCC TTCTCCATGT GAGCTTCTGA CATTTTATCA CTGGATTTGT TTTTTTTTTT 1380
TTTTTTGGAA ACGAAGTTTC ACTCTTATTT CCCAGGCTGG AGTGCAATGG CATGATCTCG 1440
CCTCATTGCA 1450
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