| Tag | Content |
|---|
EnhancerAtlas ID | HS052-30028 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr5:39779940-39780840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr5:39780355-39780367 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr5:39780359-39780371 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr5:39780363-39780375 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr5:39780367-39780379 | GTTTGTTTGTTT | + | 6.32 | | POU4F2 | MA0683.1 | chr5:39780653-39780669 | ATGAATATTAAATGTG | + | 6.25 | | Pou2f3 | MA0627.1 | chr5:39780576-39780592 | GGGAATTTGCATACAA | - | 6.89 |
|
| | 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 |
| GH05I039780 | chr5 | 39780417 | 39780827 |
|
Enhancer Sequence | CCGGCAAGGA CACTGAAGTC CTGATGAGAC TTCTAACTGT AACAGAACAG AGTCAGTAAG 60
TCTTCTCCTC AAACATCACA AAAAAAGTAT AAAATTGGAC AAAATTGTTG AACAACCATT 120
TAGCTATTTG TGCCTAGTGT TTCATTATTG GAGTGCTAAG CATGTGGGTT GTGGATATTA 180
ATCAAAGGCA GACACATTGA GAAGTGTTTA CTCATGCAAA ACTGCTACAG CTTCATGTAA 240
GGACAGTGAA AGTTGGACCT TCTTGCCCAA GGGTGCTCCC ACAGCCCACC CCATCTCAGG 300
TGGAGAGAGC TGTTCCTTTT TACTCACATA AACCTGTCCT TGAAAACCAG CAGCTTGGCT 360
ACCAAAAGGA GCAAAGATGA CCTGGTGAAT GGCGTGAAAA GCTGTGGGTG TTTTTGTTTG 420
TTTGTTTGTT TGTTTGTTTT TTGTTATTTG TCTGTTTTTT CCACTAAGAG TGGCAAACTT 480
TGTAGAAAAC AAATGAGGTA AATCTGCAGC TTTTCTAGCC TGCAGTTACA ATCCCAGTTC 540
CCTGAGAAAG ACTACATAGC AATTTAGCAA GGAGATCATG GAAATGAGAG AGACATGGAA 600
AGTCCAAATA AGCTCTCCAG GCATCACTGA GTGACTGGGA ATTTGCATAC AATTGCAGGA 660
AAGACCCAAG GCAGCACAGT GGAATGCTAA AGCCAGGGAA ACTTGAGAAC TGAATGAATA 720
TTAAATGTGC TCCTTAACTC CCACAAGGAT CTATCAGCAG AGGGTGGAGG CCTTATACAC 780
AAGAGGCATT TCAGTAAAAC CTCTGCTTAC ATCATTGGCT GACCTCTAAG CTCTGTGGAC 840
ATAGAAGTGA AATTTTAAAA ACTGAGCAAA GACAGCAACT ACCTGCTTCT GAAAAGAAAG 900
|
