| Tag | Content |
|---|
EnhancerAtlas ID | HS053-05149 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr10:64181290-64182830 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr10:64182158-64182169 | TCTGACTCATT | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 64181777 | 64182381 | | chr10 | 64182475 | 64182697 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH10I062421 | chr10 | 64181570 | 64182875 |
| Enhancer Sequence | CTGCAAAACC ACAGTGTGCT AATCCCTGAA AGCATGGTTG AAATAGATTT AATTATGTAC 60
TGACAGCCTC CCGACATTGG CATACTCACT GTTGAAGTAA AGGCTTTAAT GATAGAGATA 120
TGCAAGAAGT CCTTGGGATT TCTTTCTCCA AATAGTAAAC AATAATTGAT ACTACATCCC 180
TGAGGTAATT GAAAAGATCA GTGCCACCAT CAAAATCTTG AAAGCTGCAG AGCTATTGAT 240
TTCTTTCAGG TCAGCATTAA CTTATCTGTT TGCTCTATGC AGAATACAGA TGAATCTGGA 300
ATAATGACAG CAGATTATTA CAACTATAGT TGTTACAGAT GTGAACTCCT TGCTGGATCT 360
ATAGCTGATA CTCAGCTATT GATTTGGATA ATGTTTTACC ACTGTATTCT GAATAGCAAA 420
AAAATATCAG AAGCAGCTTC CTCTTATCTG CAAGGTACTG CCATATATCT TCATTGTCTT 480
AGTTCAGAGT TATGTTAGTA TTCTGGTTTT CAGCAATAAT CTAGTCCAGA GAAACCAAGT 540
ATTACCATTC TACAGGGCAG CATGTTGGTC CATTATATGG ATGAGTCATG CTGAGTGGGC 600
TGTGTGAGTA GGAAGGAACC AGTATTTTAG ATGCCTTGAT AACTGCATGC ATGCCAGAGG 660
TGGGAGAAAC ACCCCATGAA AATTCAAGGC ATGTCATCTT GTTCATCTTG ATGAAACTTC 720
TAGGGTTGGG TAGACTGGGA AATGTGATAT CTCATAAGAA AGAGAATATA AGTCGCTATG 780
CCTTACACCC TCATCATTAA GGAGGCACAA TATTTTGTGA ACTTCTTTGG TTGTTAAAGG 840
CAACATTCCC CACTTTTGAG TGTACTGCTC TGACTCATTT ACCAGATGAC AACCAGTAAA 900
TTTGCCAGTT TTGAATGGAC CTAGACTAAA GGAGGCACTG CAGCTGGTCT GGACTGCTGT 960
GAAAACCACT CCACTATTTA GACCTAATGA CCAAGCAGAC CCAATGATGC ACAACATGTC 1020
TATGGCAGCT AGAGGTGCTG TACAAATGGA GCTGTGAGAA AACCCAGTAG GAGAAACAGT 1080
GCAGATACCT AGGGCTTTAG AGCGCGGCCA TGCTCTATTC TGAAAATGAT CATTTATTCA 1140
GTTTGGAAAT AGTTCTTAAT TCTCTACTGG GCCCTAGTAG AGACTGAATG CCATACCACC 1200
TAAGTAGCCC ATCATGAGTT AGGTGTTATC TCATCCACCA AACCTTACAA TTGGGTGTTC 1260
GTAGAGTACT CCATGATCAC AAGAAAAGAA AACTGCATAT GAGATGGAAA TGAAGTTGAT 1320
CTTGAAGACG AAACTAAGTT GTGTGAGTAC CTGGCACAGA CTCCCTTGGC ACCTACTTTT 1380
GCTGTCTTGC CAACTTGTTC TCAACTCACA CCTCTAGTCT CCTAAGAAAT ATCCCTGATG 1440
AGTTGTCTGA GGAAGGAAAT ATTTGGGCCT CTTTCATGGA TGGTTTCACA CAATGTGTTG 1500
GCACCAGCTA GGGGGAGACT TACTATAATG TTAAATGAAT 1540
|
| |
|
|
|
