| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00429 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:9078440-9079260 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr1:9079086-9079099 | AACTAATTAATTA | - | 6.22 | | Lhx3 | MA0135.1 | chr1:9079089-9079102 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr1:9079090-9079103 | AATTAATTAATTA | - | 6.78 | | POU6F1 | MA0628.1 | chr1:9079091-9079101 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr1:9079091-9079101 | ATTAATTAAT | - | 6.02 | | RUNX3 | MA0684.1 | chr1:9078466-9078476 | AAACCGCAAA | + | 6.02 | | mix-a | MA0621.1 | chr1:9079087-9079098 | ACTAATTAATT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGGGCACAGC AGAAATCAGG GCAGGCAAAC CGCAAACGCA GAATCTGAGA TGCAATTCAA 60
TTCCGTTTCC TAATCCCGGG GCTTCTCCAT GCTGTCAGCC CCTCCGTGGA GATGGAGCTC 120
GGCCAACCTC GACTGTTTAG TTTGGACTTA CACCAAAATC CCTCCAGAAT CCTCAGCCCC 180
CACGGGGGAG TCACCAGGAT GTGATGAGGA GACCTTTTCC TTTCTAGCCA CCGGGCTGGG 240
CCGCTTGTTA CAGGGGAGGA GCCTAGGCCT CCGTGTGTCC CTGGGACTTA ACGATAAAAC 300
TTTTGCTTTG GTCTATTTTC TGATTTTTCT AAAGCACAGA TTGCTTGTCT AACTTTTATT 360
CATAGAAGAA ATTACTGTAG TTAAGAAACT ACTGAGTTTA AATTGTCCAT CTTCCTGGGA 420
CGATACCTTG TAAAACCTTA TTGGTTATTT GTACTTCAAG GTGAAAGTGT TTCTAAAGAT 480
CCATAAATAA AGGGAAGGGG CTAGTAAGCG TGAGGCTTGG CCAGGTACAG TGGCTCATAC 540
CTGTAATCCC AGGACTTTGG GAGGCCGAGA CAGGAGGATC ACTTGAGCCC AGGAGTTTGA 600
GATCAGCCTG GGCAACACAG TGAGGCTCTG TCTCTAAAAA AAGATTAACT AATTAATTAA 660
TTAAGAAAAA CAAGCATGAG GCTTGCAAGG GCCTGGGGAT GCAGATGGGA GGACGTCTTG 720
AAATGAAAAG AGGCAGAGCC AGGCAGACAC CTCATCTGCT CCTGCTTCCA GCCTTGGCCA 780
AACAGACCCT TCCCCCAAGG CTGAGCCGGA GCCTGGGCCC 820
|
