| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00589 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:11782200-11783480 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr1:11783376-11783391 | GGCCCACCCACAAAG | + | 6.27 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAGGCAGAT CTGCCAGCAG CTTCGTACTT GAGACCAGAC AACCCACACA TGCTGTGTGT 60
GCCTCACATT AAGTGGTGAC TCGGGACTGT GCTGGCTCTG TGGGGCTAGA ACCCTAAGGA 120
GTACCGCCGG AAGAAAGCCC AGCATTACTA TGGCTGGGGG ACAGCTGTTA GATGGTCCTA 180
GGACATCAGC CATGGAGAAC ACAGAGGGTC AGGACAAAGC TAAAATGCCC ATAGAACTGC 240
CACTGGTTGC CAGGGTAGTT CCATGGTTGG AAATTCAAGG CCCGTCTCTT TGCCCTAGCT 300
ATCTCTATTT GACATTTCCA AAGAGGGATG GGTGGATGGA ACCTCTTAAC TCCAGAGCTG 360
GGAATCCCAA AGCCCTCTCA AGTGTCTAAC CAACCTCTCT GCCAGGAAGT TCTTCCTTAG 420
GTCTATCTTA AATTTATTTT GCTCATACAG AAGCCAGTTT CCTCTAATCC AGGGTTTAGC 480
AAACTTTTAC TGTGAGGAGC CAAATAAACA TTTTAGGATT TGCAAGCCAT CTGATCTCCA 540
CCAGCTACTC AGCTCTGCCG TAGCTCGAAG CAGCCACAGA GAGTGTGTAA ATGAATTCAT 600
GGCTATGCTC CAGGAAAACT ATTTCTGGAC ACACATGTGA ATTCTGTATA CTTTTCACAT 660
GTCACAAAAT ATTATTCTCT CTTTCCTTTT TTTTTTTTTT GGAGATGGAG TTTTGCTCTG 720
CTGCCCAGGC TGGAATGCAG TGGCTCAGTC TCAGCTCACT GCAACCTCTT CATCCCAGGT 780
TCAAGCAATT CTCCTGCCTC AGCCTCCCAA GTAGCTGTGA CTACAGGCAT GTGCCACCAC 840
ACCTGGTTAA TTTTTGTATT TTTAGTAGAG ATAAGGTTTT ACCATGTTGG CCAGGCTGGT 900
CTCAAACTTC TGACCTCAGG TGATCCGCCC GCCTCAGCCT CCCAAAATGC TGGGATTACA 960
GGTGTGAGCC ACCGCACCTG GCCATAAAAT ATTATTAGTT TAATTTTCTA AAACCATTTA 1020
AAAGTGCAAA AACTGCTCTT TGCTTGCCAA CTGCGCAAAA CCAGGCAGTG GGGCAGATTT 1080
GGCCTGAGGG TCACGGTTTG CCAACCCCTG CTCAAGCCTG CTCACTCTCA ACGCTGGCTG 1140
CACGTTGCAA TAATCCAGGA ACATTCACAG GCCTGGGGCC CACCCACAAA GCTTCTGTTT 1200
TGTTTGGTCT GGGCTTCATA GTTTTTCTCC CAGGTAACTT CAGGTGCAGC TGGGGCGGAG 1260
AGTCTCTGCT CTCCCCTTCC 1280
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