| Tag | Content |
|---|
EnhancerAtlas ID | HS050-22053 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr15:25017540-25018880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr15:25018385-25018396 | GCGCCTGCGCG | + | 6.14 |
| | | 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 |
| GH15I024772 | chr15 | 25017241 | 25018946 |
| Enhancer Sequence | TGAATTGCAG AAGTACCTGC TATACTGTAG TTTTTGGGCA TGAGGGACCC CTGTGCTCAC 60
AGCGCCATCT AGCATCAACA GAAAGGGGGG CTGATGGCAA TAGAAAGGGG GGCTGATGGC 120
AGCCTTAATA AATTCAGGAG AGGAAAAAAA AAAACACAAA ACAAAACAGA TGGCGGCCCA 180
GCATCCAGGA ACTGCTGTGT TCATTTGAGT AGGATTTTTC TTATATTCGT TTAAAAACTG 240
AAACATAATT CATAATTGCT GCAGGGGTTA GGGGTGAAAT GCAATTGGTA ACCATTCCCA 300
GTAAAGACTC AGGGAATCCT GGCCCAAGAC CACATTTCCT GTCATTTAAC GCAAGGGTTA 360
AAAGGTCGAA GTGAATCCCA TTACGCTAAC TGATTTCATT TACAAACATG GATGTATAGG 420
AGTGTGTTAC TATGCACGGA ATCATACTTC GGATGTGAGT GTAAAACGAG TTCAGCTGAT 480
TTTGCACTGT CACATTAAAC CCGGAACCAT GTGTTTCCAT ATACATCACG CTCCTCTTTG 540
GTAGCACTAC AGTTCATAAG ATGAATGTAA TTTCTTAGAT TACAGCCTTA ACGGGTTATT 600
ACTCTTTCAA TGTTTTCTAA TGTGATATAG ATGTCGGACG TATTCGCTCA AGTATACGTG 660
GCGGGGCCGG GGTCCCGACC GTCTGTCGGA GCGAGCTGTG CCGCAAAGCC CAGCTACTCC 720
GATCTCACAG GGATGGTGGC AGGAAATGCG CCATTGTTCG GCGCAGCGAA ACAGCCCGCA 780
GTGCGCTGTA GGAAGGTCAC ATGACAGAGG GGGAAGACGG TGGCCGGCAG CAGCCGATCC 840
ACTGCGCGCC TGCGCGGCTC CGGTGGCGTG AATGTCGCTG GTCTCCCGTC ACCGTTTCCG 900
TTTCCGGGCG AGTCTGTTCG GCTTATGGCG TCTGCTAGGA GTCTCCTATC CGGCGTTTGT 960
GCCGCAGAAA ACCTTTAACC TGCGTTTTAC CCGTAAACAT TTTCCTTTTT AGGCTTCCTA 1020
TCATTGTTTT GGTTCTTGCT CCTGTATTAA CTTTGTTTTT GGTTTTTTCT TTTTTTTTTT 1080
TTTTCAAGAC GGAGTCTCGC TCTGTCGCCC AGGCTGGAGT GCAGTGGTGC GATCTCGGCT 1140
CACTGCAAGC TCCGCCTCCC GCGTTCACGC TATTCTCCTA CCTCAGCCTC CCGAGTAACT 1200
GGGACTACAG GCGCCCGACA TCACGCCCGG CTAATTTTTT TAATTTTAAT AGAGATGGAG 1260
TTTCACCATG TTAGCCAGGA TGGTCTCGAT CTGCTGACCT CGTGATCCGC TCGCCTCGGC 1320
CTCCCAAAGT GCTGGGATTA 1340
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