| Tag | Content |
|---|
EnhancerAtlas ID | HS053-30928 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr4:185424700-185425850 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Spz1 | MA0111.1 | chr4:185425289-185425300 | AGGGTTACAGC | + | 6.14 |
| | | 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 |
| GH04I184503 | chr4 | 185424750 | 185425961 |
| Enhancer Sequence | GGGACTACAA GAGTGCACCT TCACGCCCAG CTAATTTTTC ATTTATTTTA TTTTTTACAC 60
ATGGGGTCTC GCTTTGTTAC CCAGGCTGGT CTCAAATTCC TGGCTTCAAG CAGTCCCCCC 120
ACTTTGGCCT CCCACTGGGA TTATAGGCAC GAACCACCAT GCTATATGGA ACTTTTGAAT 180
TGGGGTTTAG AAGAAAATGC AGTAAGTTCT GAGAGACTGA GGATGATGCT TGGCCAAAGG 240
GCTGGTTTGA ACATGAAATG TATCTCTATT AATGCCCGTG TGAGGGCCCA GAGGTGCCTT 300
GGCCCTGGAG TCAGGAGATG TGGGTCCCAG GCAGTGCTCT GACATGCCCT AGCTGAGCAG 360
AGCTGCTCTC TGGGAGCCAG TTTTCTGCTT GGTAAAATTA GGACAATATG CTCTATCTTT 420
CGGGTTGGGG AGGGTGGTGC GAGGAGCAGA AATAATGCGT GGAAAGCAAT CTGCACCGTG 480
CCTTGCAGGA GAGGAAGCTG CTGTTCCTGT TTGCATGTGC CAGGCCAGTT ACTGTAGAGA 540
TGTACGCTTC ATTAAAACAC CGTCATCTTC ACCAGGCTGC AGAGATACCA GGGTTACAGC 600
ACAGCTGAGA TGAGGAGCTG ACTGATCCTG TTGGGAGGAC CTGGAGATGA TTCATGGTAA 660
GAGCACTACA GGAAGAGAGA GAAGCATCTG CTTCCTCGAG TGCCAGGGTG GCAGAGAGGC 720
CACCGGAAGT CTTCACTTGG CTGAAGACTT GCAGTGAGTC TGGGGTTTAA TTCAGAGGAT 780
TGAGAGAAGG CCAGCACCAT GGGAATTGTT CAGCATGGGG GTCCAGGGCC AACAGAGAGA 840
ATTCTGATTG TATTCAAGAA GAAAGGCGAA ACTCGGAGCT AGGATAGCTG AGCTGAGCAG 900
GAGGTCAGAG AAGTAGGAGT AGCATGCAGA AAGTGGGCCA GCAGCCGGGA GAGGCCTGCG 960
AGGTGGGATG TGCACACGGC TGATGCTGGA CACCTGGAGC CAGGGCGTGA CGGGGGCACT 1020
GGCTGACTGC CCAGGGCCCA TGCCTTATCC CCCGCCCCCA CCCACCACGC CTGCCCACAC 1080
TTTTCTGTGT GGGTCCTCAC CCAGCCTGGC CACGCTCCAG TGGCATCCGC AGCTCTGCTC 1140
TTTTCCTCAC 1150
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