| Tag | Content |
|---|
EnhancerAtlas ID | HS050-25065 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr16:11707140-11708080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr16:11707745-11707757 | GAATGTTTATTT | + | 6.74 | | Gata1 | MA0035.3 | chr16:11707756-11707767 | TCCTTATCTCT | + | 6.02 | | KLF4 | MA0039.3 | chr16:11707570-11707581 | GGAGGGTGTGG | - | 6.32 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_10082 | chr16:11705586-11708566 | CD14 | | SE_23656 | chr16:11705744-11708148 | Colon_Crypt_1 | | SE_27070 | chr16:11705764-11708228 | Esophagus | | SE_31920 | chr16:11705719-11708162 | Gastric | | SE_42648 | chr16:11705745-11708264 | Lung | | SE_50207 | chr16:11705709-11708328 | Sigmoid_Colon | | SE_52871 | chr16:11705643-11708238 | Small_Intestine | | SE_53430 | chr16:11705562-11708227 | Spleen | | SE_61608 | chr16:11668804-11735966 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 11707140 | 11708076 | | chr16 | 11707277 | 11708060 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I011611 | chr16 | 11705658 | 11710497 |
|
Enhancer Sequence | AGTTTTTGTT TCCACTTCTG GATCCCCATG GGATGGAGAG AGACGGGACA CTCGCATTGA 60
CAGAGAGACC AGACCTCCTG GGTCACCTGG GGGAATAAGC AATGCAGCCA GCTGCCAGGT 120
CCCAGGGCTG CCTTCTCCTG ACCATCTGGG CAATTCAGAC ACAGCTGGGT CTGAGGTGCC 180
AGAGTGTGTT GTTCCGCCTG TTTAGACCTG CCCCACCTCG AAGACATCGG TGATTCACAA 240
TCTTCCCTAG AACGGACAAC TCCTGGAGGG TGGGGCCCCT GCTGATTCAA ACTGGGCTCC 300
TATGAAAGCT CCCAGAGGGT GAGGGCAGTC AGGGAAGGCT TCCAGGAGGA AGTGGCTCTT 360
GTTGAAGGCT AAGCCAGAGT TAGGTGGGAG AGGAGCAGGA AAGGTGTCCT TACAGGGAGC 420
ACAGCCGGAC GGAGGGTGTG GCGTGTGCCG GCTAGGCAGT TCACACTGGT GGAACCGAGG 480
GCACAGAGGT GGCTGGGGCA AAGCCCAGAC AGAAAGGACA TCTCAGAAAT GAGGATCTGT 540
ACTCCGAGAG CCGGCCTCAC CCTGCCACAT GTTGTCAGAT GACCGGGCGG GCCACTTCTC 600
TCGCTGAATG TTTATTTCCT TATCTCTAAA ACGGAACTGA CAGTTGAGAT CAACGCCTGT 660
GTTCTGTGGG GTCCCTCTGC TTCCTGGCAG GTCCTGAGAT TTGGACACTT GCACATGACT 720
CATTCATTCC CAGCAACACC AGTCAACAGT GGAGCCGTTG TGCCCATTGT ACAGACGGGG 780
CAGCTGAGGC TTGTGCAGGC TCAGAAGGAT GTCCTAGTCT CTCTCACTCT CCTTTCTCCC 840
TCCTACGGAT GCTGTGACAA ATGACCACAA ACTAGGTGGC TTAAAACAAC AGAAACTGAT 900
TGTCACAGTT CTGGAGGCTA GAAGTCTGAA ATCAAGATGT 940
|
