| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06127 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:227002340-227003670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:227003463-227003474 | GGGGGCGGGGC | - | 6.02 | | KLF4 | MA0039.3 | chr1:227003030-227003041 | AGAGGGTGTGG | - | 6.02 | | KLF5 | MA0599.1 | chr1:227003464-227003474 | GGGGCGGGGC | - | 6.02 | | Klf1 | MA0493.1 | chr1:227003032-227003043 | AGGGTGTGGCC | - | 6.32 | | Myod1 | MA0499.1 | chr1:227002636-227002649 | TGCAGCTGTTTCT | + | 6.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_54921 | chr1:227001401-227004634 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH01I226813 | chr1 | 227001144 | 227005115 |
|
Enhancer Sequence | AAGAATATCA ATATCATTTA TCAGCCTACA AAAGCACTAC AAGTAGGGAT TTCTTTGTAA 60
CTGCCCTGAC CCTGGATTAT GCCCTACTCC TTATTTTGTC TAAAACATTA GCTGGGCATG 120
GTGGCATGGG CCTATAGTCC CAGCTACGCA GGAGGCTGAG TCAGGAGAGT CACTTGAGTC 180
CAGGAGCTTA AGGCTACAGT GAGCTATGAT CCAGCCACTA CACCCCAGCC TGGGCGACAG 240
ATCCTGTCTC TATAAAAGAA AAAAAAAATC CTTGAGAGTA GCTTGGCTTT GCAGAATGCA 300
GCTGTTTCTT GCTTTTGAGG GTGTTTGTTT GCCATTTGAC CCTCTTTTTT TAAACCTTAT 360
GTTTATAAGG GAAAGCCTCT TACAGTAAGT GTGTTTAGGG TTCTAGTTAC AATTAATCTG 420
TGGTCCTAGA GAAGGCAAGA GGGCCGAGGG AAGGGAGAAG AAGGGCTGGC AAGACAGTGA 480
GAGCAGAGAG CTTGTGACTT CACTCCCCCA GGCAGAGGGA AGAGTGACTA AGCCGGACGC 540
TCCATCCAGG CAGGAAAACC GTCCAAGCTT GCTCATTTCC CATCAGCCTC GCACCTGCTG 600
GGATCTCCTG GCTGGCATGG ACTCTGTACA GTCACCTGGT GTCCCCAGCA CAGGACACCC 660
TGGGGCCTTT TTCCTACTCA GTCAGATGCC AGAGGGTGTG GCCGTCATCC AGTTACAGAC 720
GGAGCTAATA ACAAAGTCAC TCTGCCTTTC ATGTGTGCAG CACTTCAAGC ATTTCTAAAT 780
GCTTGCACGC CACTAAGAGA TCTTGCATAA GCACAGGGTC AAGTCCTTTT GATTTATTCA 840
ATAAGACACA AACCAACTTA GAAAGTGAAA ACTCTGACTT TTTGGCATGC ACTTGGTGCT 900
GCTCCACATT TACTGCTGGC CTGTCCCTGT CCCTCCTTGT CTTTGTCACT TAGCTGTGGC 960
CCTTCTTGCA GGAAGACTTC TGGAATTGTC ATATTCCCAC CTCTTTCTCC TTCCTCTGCT 1020
TTCTGCAGGT GACACTAAGG AAACTCATCT CAATGCATGC ACAGGGAACA ATGAAGATGT 1080
AGAGGATGTG CTATGACCAT TGCAAACATA GAAAAATTAA GCTGGGGGCG GGGCACAGTG 1140
GCTCACGCCT GTAATCCCAG CACTTTGGGA GGACAAGGCG AGCAGATCAC TTGAAGTCAG 1200
GAGTTCAAGA CCAGCCTGGC CAACATGGTG AAACCCTGTC TCTACTAAAA ATACAAAAAT 1260
TAGCCAGGCA TGGTGGCACA CACCTGTAGT CCCAGCTACT CAGTAATCTG ACTCTGGAGA 1320
ATCACCTGAA 1330
|
