| Tag | Content |
|---|
EnhancerAtlas ID | HS050-61154 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr7:109770-110750 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr7:110169-110180 | CTTGAGTGCTT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 109773 | 109945 | | chr7 | 110432 | 110501 |
| Enhancer Sequence | GCATCCACAC TCACCCCTCT GATTGCTCCA GAACCTTTTC TTCAAAGAGA AATCTCTGCA 60
CTCTGCAGGG ACGGTAAGTG GCGACCCTTA GGTAGCTGAA AGCACGGGGA AAAGAGCAGG 120
AAGAGGTGGG AACATGGAGA TGGAGAACAC AGGGAGCGGC ACGCTCAACG CAGGTGGAGT 180
CTGTGTCCCC TCCAGCGATA GCCAGAACCA GGACCACCAG GGATCCGACA TCACTGGCCC 240
CATCCCGTAG GGTGGGCTGT GGGCAGGGAA CAGCTGAATC GCCAGGCCAC TCTCAGACCC 300
TTGGCAGACA CAAGGAATAA CAGCTGTGGC CGCCGCTGTG GCCGCAGTCC CAAAGTTTGG 360
AGAGAAATAG CAGCAAGTAG CAGCACCACT GTCCGTCAGC TTGAGTGCTT CTCGGACAAA 420
GGAAGACAGT TCTCCTGTTT CCCAAAGACT TGCAAAGGCT GTGTGTTCCT CAGGCAGCTA 480
CTGCGCCATC GGCCTCTGAG TGATAAGGAA AGGAACCAGG GCTCAAACCT ACTCCTGAGT 540
GAGTCAAAGC AACTCCGCAC TCCCTGCCAG CACTGAGGGT GACCCCCGAG CCCTGCTCAG 600
GAGCTGTGGG GCCCGAGATC TCCCCTCCGC CCCGTGGGCA GGGGAAGGGC AGCAAAGGCT 660
CTCTGCCACG CCTGTGTTCG GGCTCCAGAA CTCTTGGCCT GGTGTCTGGA AGATGGGATT 720
GCTGCCTTGG ACAAGCCTCT CCTCCTTGCT TTTCCCTTTT TCTCACAGTG GGGTTTAAGC 780
TAAGGTCCTA TTCCTAGATC ACTAATAATG ATAGCAGGTG CCATTTATGA ACACCTACTG 840
TATCCCAGTG CTGCTCTCAG TGCTGTACCT GTATTCTCTC ATCTCATTCT CTCAAGGGCC 900
CAGTAAGGTA GCCACTTCAT TAGCCATCTT TTACTAAAGA GCAGACTAGG CACAGAGACG 960
GTAGGTCACT TTCTGAAGGT 980
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