| Tag | Content |
|---|
EnhancerAtlas ID | HS050-02157 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:46992130-46993230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr1:46992797-46992813 | TTTTCCTGGAAAGCTA | - | 6.16 | | KLF16 | MA0741.1 | chr1:46992915-46992926 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr1:46992915-46992925 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr1:46992912-46992927 | GAGGCCCCGCCCCCA | + | 6.44 | | SP4 | MA0685.1 | chr1:46992912-46992929 | GAGGCCCCGCCCCCACG | + | 6.36 | | STAT1 | MA0137.3 | chr1:46992798-46992809 | TTTCCTGGAAA | - | 6.62 |
|
| | 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 |
| GH01I046527 | chr1 | 46992721 | 46992930 |
|
Enhancer Sequence | GAGCGCCAGC CTCCCCTTGT TGCACCCCCA CCCTGCCTGT CCCCCCACCA CTGTCATTGT 60
GTCGGGCTAA TGAGGTAAAC TGAAGCGAGC CCTGTCCCCC CTGACAGGTT TATGAGAATT 120
TAATAAAGCG TGGCCGGGAC CAAATGAGTT GCCTCAGCCT CGGAGAGCTC ATTGTCTTTG 180
GCGTCAGCGT TTTTTGACTC GAGCTGCCCC CATCCTCCGC CCCAGCTCCT CCCTGGCTCG 240
GCCCCCACCC CCGCCCTTGG TGCCTCCCTA GGTGAGCCTG GAGGCCAGTG GGCCCTGCAG 300
CGGGAGGGCA CCCAGGCTGA ACCCTGGGGA TGGCAGAAAT TAAGTTGGTC AGTGTGCCCT 360
GGGGAGGGAC TATGCTGTCC TTTGCCCTCA CCTACCACAC CTTCACAAGC TGCAGACTCC 420
AGGAACATAC TCGGGCCTCG GGGACTTCCC ACACAACTGC CTCATGCTCC TATGTCTTGG 480
CCGCTGTCAA CCTGAGGCCC TGCTGGAGCC GCCTTGAGCC TGATTCACCT TTTCTCGCCT 540
GTTTGGAGCA AGCAGCCAAA GTGAGCTCCC AGAGGGAGGG GCTTCTCTTC CGGCCAGGGC 600
ACAGGTTGGG GGCATGGGGC CTTCAGTCTG GCCTGGTTCC ACCCCTTGCA TGGAATGTCC 660
CTCCTTATTT TCCTGGAAAG CTAGCAAGGG GTGGAGCACA GACCGTGGAG CAGAAGGGAG 720
TCCGAAGTGC AGATGAAGAG GCTGCCAGTC GGGAGGCTCC CCAGATGGAC AGGCAGGCAG 780
AAGAGGCCCC GCCCCCACGG CTGTGGGGAT ACCTTGAGAA GGTACCCAGC TGCCCTTCTT 840
CCCTCATGTC CTGGGCAACC TAGAACCAGC CTTTCTCTGC CTGGCCTCTT AGGGGTCCAA 900
GGCCGAGGAG TTTCTGGACC ATTTGGAGAC CCAGAATTCC TTCTCTCCCC AACAAAAGTG 960
TTTCCAGGAA TTACTTCCTT CTGAGACTAA AGCTTGGCCT GACACAAGAG CCTCTTCTGG 1020
AAGGTCCTTA ACTCATTGGG GTGTTGGAAG GCAAGTCTTA GGGATCAAGG CCAGTTTGTG 1080
ACCATGATAA AAGCTCAGTT 1100
|
