| Tag | Content |
|---|
EnhancerAtlas ID | HS050-53121 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr4:185587710-185588480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr4:185587978-185587999 | AGTCTGAAAGTGAAACCAGAT | - | 6.71 | | IRF2 | MA0051.1 | chr4:185587982-185588000 | TGAAAGTGAAACCAGATT | + | 6.66 | | PRDM1 | MA0508.2 | chr4:185588460-185588470 | GTGAAAGTGA | - | 6.02 | | STAT1 | MA0137.3 | chr4:185587802-185587813 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr4:185587799-185587813 | CAGTTTCCTGGAAA | - | 6.5 | | Zfx | MA0146.2 | chr4:185588008-185588022 | CAGGCCTGGGCCCA | - | 6.06 |
|
| | 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 |
| GH04I184666 | chr4 | 185587456 | 185588699 |
|
Enhancer Sequence | GACATCTTTG GCATTTGCAT CTCTAATCCT AGATACTGGG ATGGCCATCC ATGTCCAGAT 60
AGTGGTTTCT GCTCCAACAT GATTTATTTC AGTTTCCTGG AAAGTGCATG AGAGGCCTTT 120
CCATTTCAAG CCTTATCTGC AATCTCATTT CTGGATTTCT GACCTTTGCT TCGGCCTTGC 180
TTTGGGGCTT CGGTCCCAGG TCGTATCAAA GATGGCTTGT TTATTGTTCC AGGCAGAGCT 240
TCAGGGTTGG GATAATTCTA GATGTACGAG TCTGAAAGTG AAACCAGATT ATTTATCTCA 300
GGCCTGGGCC CAGGTGTAAA ACAAAGTCAG TCCAAAGGAG AAACACATAG TTAGAATGGG 360
AACACCATAT GAAGGTCTGA ATAAAAGCCA AATCCTGAGT GCTTATCAAA GCAGGGGTGG 420
GACAAGAGTC CAAACAGCAG ATGATTGACT GAAGCTCAGG TAACAGGTAA TTCAGTTCAG 480
AGCTGCTAGC GTCTTAGAGT TTCACGGCCA CCTAGAGTAA AAGGCGTGGA CATGGTCACT 540
AAAGCACTGG CATGAAAGCC AGGAACCTGA TTTCTGGATT AGGGGAAGGT GGCCACAGAG 600
ACCCAGCATG CTGTTTTCAC AAGGCTCTCG TCACCTGCCT GTTTCCTGGT AGCTCAGCTG 660
GACGTTCCTT CTCAGTCTCT CTCCCTCATC CTGTGAGAAA CACAGTCACC CATCCAAACC 720
CAAAGAATGG ACTTAGAGGC ATGGAGAACA GTGAAAGTGA GACTTTTTTT 770
|
