| Tag | Content |
|---|
EnhancerAtlas ID | HS050-12298 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:61872330-61873780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr11:61872339-61872351 | AAACAAACAAAC | - | 6.32 | | MEF2C | MA0497.1 | chr11:61873527-61873542 | TTTTATTTTTAGTAC | - | 6.09 | | SRF | MA0083.3 | chr11:61872758-61872774 | TTACCCTATATGGTCT | + | 6.07 | | STAT1 | MA0137.3 | chr11:61872815-61872826 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr11:61872812-61872826 | CCTTTTCCTGGAAA | - | 6.91 |
|
| | 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 |
| GH11I062104 | chr11 | 61871666 | 61874160 |
|
Enhancer Sequence | CCATCTCAAA AACAAACAAA CAAAAACCAC CAGCAACAAC AACAACAAAA CACCTCTTTC 60
CTTTATATAA GTTACCCAGT CTCAGGTATT TCTTCATAGC AGTGTGGGAA TGAACTAATA 120
CAGGTGACTA CTCACATGTG GCAAATGCAG ACAAGGGCAC TCTGTGCTAT TGGGATGCTG 180
AGGTGGGGGT GTGATAGGAG TTTGGCAGGA CTTGTTTCCC AAGACATAGG TCACAAGGAC 240
CCCCCTGATA AAACAGGATG TGGTAAAGGA GCCAGCCAAA ACCCCCCAAA ACCAAGATGG 300
TGATGAAAGC GACCCTTGGT CCTCTCACCG CTCATTATAC ACTAATCATA ATCCATGATT 360
TGTCCATGGT GAAGGAAACT CCCACCAGAA ACACGACAGC TTACATACGC CATGGCAACA 420
TCCGGAAGTT ACCCTATATG GTCTAAAAAG GGGAGGAACT CTCATTTCTG GGAATTCTCT 480
GACCTTTTCC TGGAAAATTC ATGAATAAGC CACCCTTGTT TAGCATGTGA GCAAGAAACA 540
AACATAAAAA TAGCAACCTG CAACTCTCAC GGCTGCTCTT CCGATGGCAT AGCCACTCTT 600
ACTCCTTTAC TTTTAAAATA AACTTGCTTT CACTTTACTC TGTTAACTCT TGAATTCCTT 660
CCTGTGCAAA GCCAAGAACT CACGTCGCCT CCTGGGCTGA ACTCCAATGT GGGGGTTCAC 720
CCTGTGACAG GTGGATGGGC TGGAGTCCAG GAGTTCGGGT CCAGCCTAAG CAACATAGTG 780
AGACCCCCCA TCTCTATTTT TTTCTCAGAC AGTATAAGAG ACAGATGAAG CAAAGTGCAT 840
AAATGGCTGT GAGGAGCATG TGGTTTGTCA AAGCTGGAAC TTTATTTACA AACAAGTTCC 900
AGCATTATCT GAGTGGGTGC TGCTAACAAT TATAGCGTGT TCTTTCAAAC TGCAGACTGG 960
GATTAGACGG TTTGCCAAAA AGCCACTGAG TACATCAAAG CGAGAATTCT GAATTCTCCA 1020
TTTATCTTCA GATTTATCAC TCCCTCCCTC TGTGCCCTTC TCTGCATCTG CTGTATGTGA 1080
GTATGGAGAG TCCACACAAT TCAGTCTGTA CCAGTGGTCT AGGTTTTCAA CTACATCTCA 1140
TTGGTCAAGC ATGTTTGCAT TCACAGAAGG AACCCTACCC CCATTTTTGT TTTCCTGTTT 1200
TATTTTTAGT ACATTTTAGG CCTTAAGAAT GTAGGGTTTT TTTGTTTGTT TTTTTTTCCT 1260
ATGAGACGGG AGTCTTGCTC CATAACCCAG GCTGGAATGC AGTGGCATGA TCTCGGCTCA 1320
CTGCAACCTC CCCGTCCCGG GTTCAAGCGA TTCTCCTGCC TCAGCCTCCC ATGTAGCTAG 1380
GAATACAGGC ATGCACCACC ATGCCTGGCT AATTTTTTTT TTAATTTTTT TTTTAATTTT 1440
TAGTAGAGAC 1450
|
