| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11106 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:17720910-17722020 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr19:17722004-17722015 | TTTGTTTACAT | - | 6.14 | | Foxd3 | MA0041.1 | chr19:17721999-17722011 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr19:17721844-17721856 | AAACAAACAAAC | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTTGGAGGAA GTAGAGGGTA AGACAGGTCA GGTTCTCCCA GTTGGAAAAA GTAGATGTTT 60
GTGGCTCTCA AAACCTGCCC AAGGCTGGGC GCAGTGGCTC ACGCTTGTAA TCCCACCACT 120
TCGGGAGGCC AAGGCGGGTG GATCACTTGA GTCCAGGAGT TTGAGACCAG CCTGGGCAAC 180
ATGGTGAAAC CCTGTCTCTA CGAAAAATAC AAAAATCAGC TGGGCGTGGT GGCACGCGCC 240
TGTAGTCCCA CATACTTGTG GGGCTAAAGC AGGAGGATTG CTTGAGCCTG GGTGGCGGCA 300
GTTGCAGTGA GCTGAGATTG TGCCACTGCA CTCCAGCCTG TGTGACAAAG CAAGATCCTG 360
TCTAAAAAAA ATAAAAAATA AAAACACCCC ACCCCTCGCC CGCCGCCAAA AACCCTGTCT 420
GAAATAAAGA CTACATTTCC CAGCATTGCC ATGAAGCTAA GTGTGGTCAT ATGACTATGT 480
TTTGGCCAAT GAGGTGAGAG AAAAAAATCA CGTGTACTAC TTCTCCACTG TGGCTTAAAA 540
GGCAGGGAGT GAACCCCAAA CTTTCTCCTT CCTCTAGCCG CAGTCTGCAA TGCTTGTGGG 600
GGCTGAGCTC TTTGTGACCC TATAGTGGAG GAAAAACACA TTTGGGTCCA GGTATGGTGG 660
CTCACGTCTG GAATCCCAGC ACTTTGGGAG GCCCAGGTGG GAGGACTGCT TGAGGCCAGG 720
AGTTTGAGAC CAGCCTGGAT ACCATAGTGA GACACCATCT CTACAAAAAT ATAATTTAAA 780
AAGTAGCCAG GTGTGATGCT GCATGCCTGC AATCCCAGCG ACTCCGGAAG CTGAGGCAGG 840
AGGATCGCTA GAGCCCAGGA GTTTGAGGCT GCAGTGTGCT GTGATTGCAC CACAGCGCTC 900
CAACCTGGGC AACAGAGTGA GACTCTGGCC TCTAAAACAA ACAAACAACA ACAACAACAC 960
ATTAGGGATG AAAATGCAAC AAAAGATGGC AGCAGCACAG ATCACCAACA CTGCGAAGCC 1020
TCCATATCAG CTCGAGGCTG GTTGCTACTT AAACTGTTAT CCCAGAGAAA AACCAATTCT 1080
ATCATTTTTG TTTGTTTGTT TACATGGAGT 1110
|
