| Tag | Content |
|---|
EnhancerAtlas ID | HS048-00278 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:11003880-11005020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr1:11004227-11004238 | AAAGATAAGAA | - | 6.62 |
| | | 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 |
| GH01I010943 | chr1 | 11003892 | 11005030 |
| Enhancer Sequence | CAGGTGTGGT GACGTGCTAC TCAGGAGGCT GAGGCAGGAG AATTGCTTGA ACCCAGGAGG 60
TAGAGGTTGC AGTGAGCCAA GATTGTGCCA TGGCACTCCA GCCTGGACTG CAGAGTGAGA 120
CGCCTTCTAA ACAAAACAAA ACAAACAAAA AAAAAACACT AGTAAGTCAG GACCTTCAAC 180
CAGGGACAAA CAATGAGCCT GGATGCTGAA GGGCGTGAAA GGCTTTGTGC TCAAGAAGGA 240
AAGCCCAAAA GAGAAACTGG ACCAGCTCCA GCTGCTCTGT GTAGCAGGAG AAAAGTACAA 300
TAAATGCAAC ACAGCCTTTG GACTTCATGC GGAGTCGTGG GGGCATAAAA GATAAGAATC 360
CAAGCCGCTG AGGGCGGGGA ACCACTGAGT GATACCTAAG CTGTCCAAGA TCTCCCGGCA 420
GCTGCTGACC CCGAGGGAAA GAGCTGCTCC CTGCCAGACT TTCACTGATC ACAGACGTGT 480
CAGCCATAAA CAACTGACTG CAAGACCTGG GAGGTCTCAG CAGGAAAACC AGCAGAGGCA 540
ACACCCGTGC GTGTCCCGGG AGCAGGCATG GGTGCCAGCC AGGTCTGCCC TGGTCACAGA 600
AATGGGGTTG TCCCATCTGG AGGGAGAATG GGAGCCTTCC CGAGAACCCT GAGCACTTTC 660
TAATTAAGCA CGACTGCCCC GCTTTTGAGC GGGTGCAGAT CGAAGCTGGG GGAAGGAAGA 720
GAAGTAAAGT GGTTTGTTCC AGCTGCACGG AGCGCTGAGC TGGGAAGAGT GCCCAGAACA 780
GTTAATGCCC AGACCCTCTC AGCCTTGCAA ATCGCCGCCC GCCTGGGGGG TGAAGAGCCA 840
TTTATGCCAG GTAAAGGCTG GTGATTTCAT TAACTCCCTT CCCTCTGTCT CGTCTCCAAG 900
GGCGCAGGGT GGTTGTTAAA CACGGGAGGA CTTGGTAAAG GGTCAGCCCT TGTTTACAGG 960
ACTTTCTTGT GCATGTGTGC CCCTGGTCTA CCCTGTCCCA AAGCTGGGGG GCTCTACAGG 1020
GATGGAGAAA GGGCAGGGGT GGATGGAAGT GGATGGAGGT GGAGGGGAGG AGGCAAAGAG 1080
AGACAGAGAC TGATTCCTGG GAGAAACACC ACGGCCAGTG TTGAGATAAA AGATGCGAGA 1140
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