| Tag | Content |
|---|
EnhancerAtlas ID | HS050-48477 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr3:124403060-124404960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr3:124404295-124404306 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr3:124404294-124404305 | GTCAAGGTCAT | + | 6.32 | | Esrrg | MA0643.1 | chr3:124404295-124404305 | TCAAGGTCAT | + | 6.02 | | Klf1 | MA0493.1 | chr3:124404055-124404066 | AGGGTGTGGCT | - | 6.02 | | Nr5a2 | MA0505.1 | chr3:124404291-124404306 | GAGGTCAAGGTCATA | + | 6.36 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr3 | 124403308 | 124403810 | | chr3 | 124403831 | 124404003 | | chr3 | 124404078 | 124404324 | | chr3 | 124404471 | 124404702 |
|
Enhancer Sequence | CTGAGGCAGC TTCTGGTTTT TCTGCTTGCT ATTCCCCCAC CTACACCATC CTGCGGCCAC 60
TTGGTACCCC ATCTCCAGGT TGATTTTAAC CTAAAACACA GATCCTGGCA GACGAGAAGA 120
CCTAACTCCT AGTGCCAATT TTTGTGTATA AGTGTGTTAT TCCATTTTCC AGCTCAATAA 180
AAAGGAATAT CATTTCTGCC CATCTTGGCT TTCCGAGGCT GAAGTGTAAC TTAAACAAAA 240
ACCACAAAGG CAGTATCACA TGGAAAACTG GAACAGGAGT CAAAAACCTG GATTCTAGTT 300
TGGATACCGC CAGCTATGAG ACTGCTGGCC AGTTAGCCTT TCTGAGCCCC AAGTTCCTCT 360
GGAAAGTTGC ACAGCTCCAA GTGTACAGGT GTTTATACAG TGATGTGTAA CCCTTTGAGC 420
ACCATGCACG TCTAAGGTGT GCTAACAAAG GACTTTGCTC TCCAGCACTT CTGACTTTGA 480
AAACATTGAG ATCCCGACCG AAGAGGACGT GGAAGATTCT GTGCTTTGGC CAGCAATTCA 540
CTTTTCAGGG GGTGTGGCGG GAATGGCCTG GGCAGATTTC CTTCTGAGAC TCAACTGGAG 600
TGTCCACTCC TGGCTCTGGG AAGTTTGAGC GGCCAGAGCT GGTACTTTTT TCCTTCCTCA 660
AACCTACAGT TCCCTGGCCC GCCTTTCATG TCCTCAGATC TGAAGAGCCA GCCTACTCCC 720
CGCACCCCAC TCCCCGCCAA CTACCACATC AGCTACTCTG GCCTCCTTAT CCTAGAGCTT 780
CAAAATAACC CGGCCAGACG GATTGAAGGA AACTTTTACA CCCCCAGCCA GGTGACCAAC 840
CTCCTGGCAT CCCCAGTGTG TGTCCACTGA TGCCTGGTTC CGCATTTTAT AAAAAGAATT 900
TTTTCATGAA AAGAACCCTT TGGATGAAAA GAAAGTGAAG CATCACATTC CTGTCGTTTT 960
ATTTTTGCAA AATATTTTCT TTGTAATATA TCTGAAGGGT GTGGCTTGAA GACTTCCTGC 1020
CTGGCTTTGT TCTGACTCTC CATGCAGACC GATTTATATT CCGCCACCAA GAGAAGGGAG 1080
CTGAGCTTAG TGGCTGCTTC CCTCTCCTGG GAGAATTTTA AGAAGATCGT CCACAGCAGA 1140
TTCACATCTA TTATGCTTTT TGTTCCTTGC AATTGCCCTG TGAAGTAAGT AGGGTAGAGT 1200
TTCTCACCCT CCTGGGGGAA ACATGTTCAG GGAGGTCAAG GTCATACAGC TAATAAAAAG 1260
AGCAAGTCTT GATGGTGGTG CTTTGAGAGA CCAAACTTAG CATGTGCTGT AGAGGAAGTC 1320
TACTCGTATG GCTCAAGTAC TTTCTTAACA AGGGTCAGGC TCAGGCCCTC TTTTGCTGCA 1380
CATCTGTTTT AGGAGGAGAA TTTCTTCAAC AACTTTTCAA ATCTCTTGAC TATTGGGATA 1440
ATTACTTGGC CTCACCCACG CCCTTTCTCA ATGACTCAAG AGCCCAGCCA GAGCAACCAA 1500
GAAAGGAAGT CCAATTACAT GAGTTGGAAA TGTCTGAACT GGTTTCTCAG GTCAACATAG 1560
TCACTCAGCA CGCCCTGTCA TGCATGTTCC ATCGCACCCT CACCCTAGAC TGGGGGCCTA 1620
ACCCGTTTCG TTTACGTTGT ACACTAATGA GATTACAAGG TACCATTGAC CCAGAAGTTC 1680
CTCTAAGAGC CTGCTATTGA AGAAGCAAAG ACCATCACCC CCCAACCCCA CCCCCATGCT 1740
GTCAAAGTTC ACTCAGCGTG AGTTCCTAGT CAGTTCAATT TCACACAATT TGATTAACAC 1800
AAGGCATTGC AGTGATTATT ATGGAGGACT AACGAACAAT GTAAGATTGG TTCCCATGCT 1860
TAAGGCTTAA GAAGCATAAG AAGGAGGCAG GTATAAATAA 1900
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