| Tag | Content |
|---|
EnhancerAtlas ID | HS158-59451 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chrX:1367580-1368860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chrX:1368382-1368394 | GACCACGTGGCC | + | 6.52 | | MYCN | MA0104.4 | chrX:1368382-1368394 | GACCACGTGGCC | - | 6.52 | | Myod1 | MA0499.1 | chrX:1368305-1368318 | TGCAGCTGTTTCT | + | 6.29 | | Myog | MA0500.1 | chrX:1368304-1368315 | CTGCAGCTGTT | - | 6.02 | | Tcf12 | MA0521.1 | chrX:1368304-1368315 | CTGCAGCTGTT | - | 6.62 | | ZNF740 | MA0753.2 | chrX:1368034-1368047 | CCCCCCCCCCCAC | + | 6.92 |
|
| | 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 |
| GH0XI001247 | chrX | 1366861 | 1369293 |
|
Enhancer Sequence | TCCCCCACCC CTGGAATTCC AAAGGCGCAG CCAGGCTCGG ATTTCCACGC GGGCGGTACT 60
GAATTAACGG CTGGGCCCCG GCGCCTTTCT TTTAACTAAT TACATCTGCA AGGGCCTTAA 120
TTCCAAACGA GGCGTCATTC CCGGAGACCA GAGGCGTTTG GAACTCAACG TATATACTTT 180
GGGGCCGCGA TCGAGGCGCG TCTCCCGTCT TCTGCCTCTG CGTGTCCTCA GCTGCAGAAA 240
GGCCGCCCCT GAGCCTTCGG GTTTTCCTGG GGGGAGAGCT CATGAGGAAC CCGTGTATGC 300
CTAGCGTTCC ATTATTGGAA CGCTAAGCTT GTCTGAAGGC TGAAGGTCAT CGCCAAGATC 360
TGGTTTTTTA CACCAAAAAA ACTTGCAACC TCCGGCATAA ATGGGCTTAA AGTGTCCGTG 420
AGAGCTCATT AAACGACAGG CCCCGGGTCC CTGACCCCCC CCCCCACCAA GCCCTTGCTC 480
TGGGACGCGC CTTGGACACG TCTGCAGATT CAGCCCTGGC CGGTTCAGCC CCCAGCGGCT 540
GTCAGCAATG AAAGGGGTCC CAGAAAGGAC TGGAAAAAGC AGATCACAAC GGGAATCCCG 600
AGGCAAGAAT GCAGGAGCCA GGCTATCTGG CAAGCCTCAA ATATAGCCAG CAGGTTGTGT 660
TGATCCCGCA TCACGGACGC TGTGAGCTGT GGAAGGAGCT TGGGATGAGG ATTGCTGGGG 720
ATGCCTGCAG CTGTTTCTGC TGGAGCTGCC TCTGGGGCAG GAAGTGTCAC GTTGCACCCC 780
AGGAAGGTCT CTGTCCAGCG CAGACCACGT GGCCCTTCCT GGTGCTACTC AAGCCCTGGA 840
GAGAGCCTCT AGGCTATTTG AGGTTCCTGG ACTCCAGCTT TAGCCAGAGC CAGCTAGGAG 900
GAGGCTGGGA GCTTGTTAAA GCCTGAAGGT AAGCCGGGTC AGGAAGTTGA GATTTGGAAA 960
CAGGCCTGAT AGTCTGTGCT TCCTCTTCGG GGAAAAAGAG ATGTTACAAC GCGCTGGGCT 1020
CCACCCTCCC CCGAGAGCTT GCAGATTTCC GGCTTCTGAG GAGCTGCCCT ACCACAGCTC 1080
CTTCTGTTGC TAGATAAGGG GTTGGGGTCA CACCCTCCTC CCTTCTGTGG CTGGAGGGAT 1140
GGTCTGTGGA CAGAAGAATG TGTGGCCACA GGGAAAGTGA GCCAGTATCA GCAGAAAAAC 1200
AAACTGAGGC TGGCACGGTG GCTCACTCCT GTCATCCCAG CACTTTAAGG CTGAGGTGGG 1260
CTGATCACGA GGTCATGAGT 1280
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