| Tag | Content |
|---|
EnhancerAtlas ID | HS050-52510 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr4:148280850-148282030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr4:148281514-148281530 | GATTGTTTATTTAATG | - | 6.24 | | Foxd3 | MA0041.1 | chr4:148281514-148281526 | GATTGTTTATTT | + | 6.62 | | JUN | MA0488.1 | chr4:148281574-148281587 | TATATGATGTCAT | + | 6.04 | | NFE2L1 | MA0089.2 | chr4:148281714-148281729 | ACTGCTGAGTCACTG | - | 6.71 | | Nfe2l2 | MA0150.2 | chr4:148281716-148281731 | TGCTGAGTCACTGAG | - | 6.6 |
|
| | 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 |
| GH04I147359 | chr4 | 148280497 | 148285022 |
|
Enhancer Sequence | GGAGCCTTAA GATGAATCGC CTTTGCCTTA CCCTGCTCTT TCTTTGGCAG TGATGTTTGT 60
TGAATTTCTG TTTCCCTCTC TGCTTTCAGC CCATGGACTT GGAGTTGTGT TTCTCCATCA 120
GTTCACTAAC TTTGCTTTGA ATTTCTGGCT CTCCTTAAAG TAACACCCAG TCCCCCTGTT 180
CGAATGTCCA CTGATCACTG ACCCTGCCTC CTGGGTCTCA TGCAAAGTCT GACACCTGAA 240
CACATTTTGG CATCCTTGAT CAGCACACTC CTGGACTTTG TCAAGTGGAG TGTCAGTCTC 300
CTCCCAGAAA TGCTAGGTTA GAACCAAGGT GGGGACTCTG ACGGACCTCA GGCCACACTC 360
TTCAAGCAAA GAAGACTTGG CTTGATCTTG TGACAGCCAC TTGTATTTAA ATGAGATGCT 420
GGGAAACATA TGGAGACCTA CACAAGGGAA TACCCAAAAG CTTCTTGGGC ATTACACTGA 480
CCTACATAGT ATACGGTTTT CCATTTGGGC TGAGTCACAC TGCCCCTGAT CAGGATAGAT 540
GTTATAGGGA GATGGAACAG AAGGCAGGGA GTTCATAGCA GTACTATCTG GTACCCCAGC 600
ATCAGGGATG TCCCCAGCTT CCCGTGATAT TCATGTAGGC CCTGGAAGCA CCGCTTCATA 660
TAGTGATTGT TTATTTAATG TCCAAGTTTG GAATGGCTTA GAAAAAGAAA AAGACCTAAG 720
AGCTTATATG ATGTCATGGA AAGATAGAAG TCAGACATGT GGTTTTCTTG GGTTCTTCAG 780
CTTTTCCCAA TTTTCTCCAC CCCACATTCA GAGCTCTATT TGCCTTCATC TGCAGAATCT 840
CTGTAGGAAG CAGTTTTGAA AGGCACTGCT GAGTCACTGA GTTGTACTGT GGTCTGACTC 900
TCTGATACTT TAAATTCTGA TTTGAAGAAA TTGCTTGAAA GCACTGATAT CTTTTTCTCA 960
CCGCTGGCAA ATGGCAAAGT TTTCACTGAG TGAAAAGCAA TGTTTCGTAA GTGAAAAATA 1020
TAAGAATCAA TTTGTCCATC ATTCCATTAT CCTGCCCAAA CACTTAACAA TTAAGGGACA 1080
GGCCAGAAGG CTTCAGTTAA TTACATAAAA GGTTTTTTTT GTTGTTTGTT TTTAAGTTAG 1140
GTTTAAAGAG TCCATGAGCT GCTGACAGTC TAAGAAAAAT 1180
|
