| Tag | Content |
|---|
EnhancerAtlas ID | HS048-38096 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr9:130180100-130181650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PRDM1 | MA0508.2 | chr9:130180691-130180701 | GTGAAAGTGA | - | 6.02 | | TCF3 | MA0522.2 | chr9:130181442-130181452 | AACACCTGCT | + | 6.02 |
|
| | 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 |
| GH09I127416 | chr9 | 130179001 | 130181842 |
|
Enhancer Sequence | CTGTTGCTAC CAGTACCCAC TTACCCGTGC CAATAATGTG ATTCATACTC TTCAGAGGTC 60
CCTTTGTTTC CCTTTAAGTC TTCCCATCAG AGCACAGAAT GCTTCGCGGA CCCAGAGCCA 120
GCCCCCATTG ACCATCCTGT AGGGGCCCCA GAAGCCCAGC CTGGCGCCAT CAGTAAAGGA 180
TTATGGAGAG GAGCACTGGA TAGAACAGCC CCAGGGGACA GGTGCAGCAT AAGCTTGCTT 240
TACCCAGCCC AGGGCCGAAA TCTGCACGGC CCACGGACGC CCACTACCCC CTTACACCAT 300
CCCAGCTCCT GCCCCAGAGT AACTTGGCTT CTGCAAACCA GAGAGACTTG TCCCTGATGC 360
CCCCCGGGGA CCAGGGGTGG AAGTGCATCA GCTGGAGCAA GACACACTAG GCTACCTCAC 420
GGTGGGCGTG TGCGGGATCC CAGGGCTAAG CCAGCAACCC TGTAGTGGCC ATTGGGGTTG 480
GCACCTACTG AGCCTGGGGC TGCACGCAGA ATCGCACCAG CTGAGGTGTG ACGCTCTCTG 540
CCGCTGCCTT GTGGCCTGGG CAGGATGACA CTGCCTCTGG TCCCCAACAG AGTGAAAGTG 600
ATTGATTATG ACTCCAAAGC TCATTCAGCC TGCTGGACAA GGCAGGATCA GCCGAAGGGG 660
TTGAAACCTG CTTCTGCTTG GTTTCTTTTG TTTGTTTGAT TGTTTTTGAG ACAGAGTATC 720
ACTCTGTCGC CCAGGCTGGA GTGTAGTGGC GTGATCTCGG CTCACTGCAA TGTCCGCTTC 780
CATGGTTCAA GCGATTCTCC TACCTCAGCC AACTGAGTAG CTGGGATTAC AGGCGTGCAC 840
CACAACGCCC AGCTAATTTT TTGTATTTTT AGTAGAGACG GGTTTCACCA TGTTGGCCAG 900
GCTCGTCTCA AACTCCTGAC CTCAGGTGAT CCGCCTGTCT CGGCCTCCCA AAGTGCTGGG 960
ATTCCAGACA TGAGCCACCG CGCCTGCTTG GTTTCTGGCT CCTTCTGCTC CTCTTTCCTC 1020
TGTCCCTTCC AGACCACACT CCCAGAGGGA GCACAGATCA CGGCCCTCAG ACTCCATCTC 1080
CCAACACGCT GCTGTGACAA GCACTAATGG CCTCCAGAAG GGCAACCCAA CTCGCCCTCA 1140
AGGACACTGG GGGTGGTGGC ATGGGAGCTG CAACCTCACA TGGGACCCTG TGTTAGGGGG 1200
GACACCCGGT AGGGTCTGGC CTGGCTTCCT CTGCTGTAAC TAAGTCACCG CTTCAGTCCT 1260
GCTGTCCTGA CCACCCACAA GATGATCGGT CTCAGTCCCT GGGTCATTAG GATTGTCGAT 1320
GTGTCAGAAG TCCCACTGTT GGAACACCTG CTATGCACGG TCTCTCACTG GGAGACCGAG 1380
GCACACCTTG CTTGACACCA GATGAAATGA CCCAGACCCT CCTTGGTCTT TGGGGAGCAA 1440
ATCTAGGAGA AAAGGACTTA GGGCAGGTCA GTCACTGAGC AGTGAGACAG GAAAGGCTCT 1500
GCAGGCTTGC ACAGAAGGGA TCGTTATGCG CATAGGGCTT CCCAGAGAAG 1550
|
