| Tag | Content |
|---|
EnhancerAtlas ID | HS050-00999 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr1:20960430-20961810 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:20960497-20960508 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr1:20960498-20960508 | GGGGCGGGGC | - | 6.02 | | MEF2C | MA0497.1 | chr1:20961011-20961026 | ATGCTTAAAATAGCA | + | 6.21 | | SP1 | MA0079.4 | chr1:20960496-20960511 | TGGGGGCGGGGCTAG | - | 6.58 | | SP2 | MA0516.2 | chr1:20960495-20960512 | GTGGGGGCGGGGCTAGG | - | 6.75 | | SP4 | MA0685.1 | chr1:20960494-20960511 | GGTGGGGGCGGGGCTAG | - | 6.99 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGCGGGGCC GGGTCCTAAG CCGAGCGGAG GACGGAGCTA AGCGCGGGGG CGGGTCCTCA 60
GCTGGGTGGG GGCGGGGCTA GGTGTGGAGG CGGGGCTCTG AGCAGATCGA GGGCCGAGGC 120
GAGGGTCCTT AAAGCTCATC TATTTCACCA TTACTGATCG GCTGCTATAA ATAAAGCCAG 180
CACCTCCCAT TTGTTTTAAT GTTTCCCTTC CTCAAATGAA GACATGTTGC CGATTACAGC 240
TCCTGTCGCA GCACAGCAAA AGGCTTTGTG TAAATTTTCT AAAATGTACG GACAACTAAA 300
TCATAACATT CCTATCCCTT TGAGGTAGTT GCCGTCCCTA ATTTATGGAG AAGGAAAGTC 360
CTCAGGTGAA GGGACTTGCT CGAAGTCACA CAGCTAATAA AATGCAGTGC CCTTAACCAC 420
TGAGCCAGGC TGCCTCCGCC GTTTAACCAA AGGATTAGTA GTGACAGAGC TGAAACCGCA 480
GTAAAAACTA TGAACGGCGA GAAAAACAGT CCTAACATTT TAGTTACCTG TGTAGAGTTA 540
TCCCTGCTGA CTGGATACAC AAGGGTTCTT AGGGTTTTTT AATGCTTAAA ATAGCACAAG 600
ACTTCTCTTT TTGCCCAACC AAAGTCTGTA TTAGGGTTCT CCAAATGGAA TCAATAGGAT 660
GTGTCTATAT AGAGGCAGGT TTATTTTGAG GACCTGGCTC CCTATGGGGA TTGGCAAAGT 720
CTTAAAAGCC GCAGAGTAGG CGGGCAGGCT GGAGAGCCAG GGAGGAGCCA GCGGTGCAGT 780
TCAGGTTTGA AGCCTGGCCG CTGGCAGAAT TCCATCTTCT TCCAGGGAGG TCACTCTTCT 840
TCCTGGGGGT GTAGAACCAC TCACTAAATT AGCATAGCCC CTGCATTTTA CAGGTTAGGG 900
CTGAGGTGGT GGAAGAGGGA GTGACTTGCC CAAGGACACA GCTGTTAGGG CCAAGCAGTG 960
GCTCCTGGGT TTCCTGGTTT CCATCCCAGT TCTTATTGCT CATCACCACT GTCTCATGTT 1020
TGAGCTCTGG CCAGTTTGGG GTGACAGGTG ACATCTGGCC TAGTCCCCAG CCCCTGACCT 1080
TGTCTTTTGC CACAGCTTAA CTGGCAGAAG CTAAGGATGG GAAATTTGAC TAATCCTGCT 1140
TAAAACTAAA GAGGCTTTTT TAACTGAGGA GATTGATCCT CCTAAACTTA CCATTCACAC 1200
ACACCTTCTT CGCACACTTC ACCCTCCTAT GCCTGAAAAT GTTATTAGTT ATCAATTAAT 1260
TTCACATTAA AAAAATTTTT TTTGGTCAGG CACTGTGGCT CATGCCTGTA ATCCCAGCAC 1320
TTTGGGAGGC TGAGGCGGGC GGATCACGAG GTCAGGAGTT TGAGACCAGC CTGGCCAACA 1380
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