| Tag | Content |
|---|
EnhancerAtlas ID | HS050-47404 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:64058950-64060430 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr3:64059923-64059935 | AAGTAAACAGGA | + | 6.07 | | Foxo1 | MA0480.1 | chr3:64059924-64059935 | AGTAAACAGGA | - | 6.32 | | NEUROG2 | MA0669.1 | chr3:64059366-64059376 | AACATATGTC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH03I064074 | chr3 | 64059128 | 64059452 | | GH03I064073 | chr3 | 64059662 | 64060253 |
|
Enhancer Sequence | CCAAAGAGCT GGCAATGTTT GCAGCTTGAG CAGGGAGAGG CATATCAATT ATTGATACTT 60
TTCCTTCTCT AGATGTGTGT GATTCATTCC ATGCTGGCTC TAACATATGC AGGGGAAAAG 120
GAGAGAGAAG AATGTTAAGA TTTTCTCACT GGCCAGAGTG CTGACACTGG TTTTCTGCTC 180
CAATTAAAGT GGGACCTTGA GAGTGTGGGG GTGATACTCT TTGTCCAGAT GAACTTTGGC 240
AAAGTGATGG AGGATGGGAG GCCCAGATGT GTGACCCAAC AGCAGATGTC AGCACTGGGA 300
TGGTCCAGCT GAGTGCACGT TTATGCCTTT CCTTCTCCAA GGGAGACCTC AGGAGATAGA 360
TAGTATCTCA CAGGCTTACA ACAGATGCTA ATCAGATTAT ATCCAGATGC TCTATGAACA 420
TATGTCAGCA GTTGAAAAGA CCTACTCTAA TTGAGGCAAA ATTACTTTTT CCAATGCTGT 480
AGGTAAAATG CACAAGTAAA AATATAACTC TGTGGTTGTT TAAATACACC CTAAGGTACT 540
TTTTCTTTAG CACACAGAAA GCCCAGGGTG AACAAATATT GTATGTGCTT GCCAAGAAGT 600
CTGTTGAAGA GACAAAAGTG GAGAGAGAAA GGAAGTAGGC AGCCTCTTCA GCTCCCTGTG 660
CTTACAAGAT GCAATTTCTT AATGGTTTAG GATTCTATCA TCCAATTTGA AAACCATGCT 720
TTTGTAAATT CTCTTTCTTG CTTGCTGATT GAGGAGCTCC TAATGTTAAC AAGTTTAATT 780
TATTACATAC TGAAGAATAT CCAAAGTGTT TTCTTATGTA TTTAGTGCAG AACTTGTGTT 840
TTTCAACAAA TGCATCAACC ACCATTTGTT GAGGGCCCAC CTTATGCACT GGCCAGTGAG 900
GAGACATCAG TGAAGAGTGT TGTAGACAGC TGTGAGCTTT CAAGGAGCTC ATAGTGTCAT 960
AAGGGAGGCA GACAAGTAAA CAGGAAATTA CGACACACGT GGAAACACCA TGATGGAGAA 1020
AGCTTAAGAT GCTATGGAAG TATAGAGGAA GCTTGCCAGA TGCAGCCTTG CTATGGGGAT 1080
GGCTGAGAAA GCTTGAGGAG GAACAGATAC AGGCTGAAGG GGCTGGATGG AGTAGAGGTG 1140
AGGGAAGGGA ACTCTTAAGA CATGAAACAT GCCACACGAG ACTATATCAG TGGCTATAAA 1200
TTACACAAGT TCTGATTAGA AGATAAATAA CTAAAACTGT AAAAATGGAA TGGGCTTCCT 1260
CAGAAAACCC CAAAGTTCCA TATTATTAGA GGTATGCAGA GACCAGATTA GCAGTTTGGG 1320
AAATTACAAA AATACATTTT TGACCTGGGT GGGAGGCCAT ACCAGCCAGC TCCATAGTGC 1380
CAACCTCAGA GCCAAGCCAA ATTTCCAGAG GTAGAGTTCA GAAATGTGCA TTTGTTTAAA 1440
AGCTTCCAAG GTAGTCATCA GGCAAATCAA AACCACAATA 1480
|
