| Tag | Content |
|---|
EnhancerAtlas ID | HS093-11290 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:11707080-11708120 |
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 | AGATGGGGTT TCACCATGTT GACCAGGCTG GTCTCGAACG CCTGACCTCA AGATCACTCT 60
AGTTTTTGTT TCCACTTCTG GATCCCCATG GGATGGAGAG AGACGGGACA CTCGCATTGA 120
CAGAGAGACC AGACCTCCTG GGTCACCTGG GGGAATAAGC AATGCAGCCA GCTGCCAGGT 180
CCCAGGGCTG CCTTCTCCTG ACCATCTGGG CAATTCAGAC ACAGCTGGGT CTGAGGTGCC 240
AGAGTGTGTT GTTCCGCCTG TTTAGACCTG CCCCACCTCG AAGACATCGG TGATTCACAA 300
TCTTCCCTAG AACGGACAAC TCCTGGAGGG TGGGGCCCCT GCTGATTCAA ACTGGGCTCC 360
TATGAAAGCT CCCAGAGGGT GAGGGCAGTC AGGGAAGGCT TCCAGGAGGA AGTGGCTCTT 420
GTTGAAGGCT AAGCCAGAGT TAGGTGGGAG AGGAGCAGGA AAGGTGTCCT TACAGGGAGC 480
ACAGCCGGAC GGAGGGTGTG GCGTGTGCCG GCTAGGCAGT TCACACTGGT GGAACCGAGG 540
GCACAGAGGT GGCTGGGGCA AAGCCCAGAC AGAAAGGACA TCTCAGAAAT GAGGATCTGT 600
ACTCCGAGAG CCGGCCTCAC CCTGCCACAT GTTGTCAGAT GACCGGGCGG GCCACTTCTC 660
TCGCTGAATG TTTATTTCCT TATCTCTAAA ACGGAACTGA CAGTTGAGAT CAACGCCTGT 720
GTTCTGTGGG GTCCCTCTGC TTCCTGGCAG GTCCTGAGAT TTGGACACTT GCACATGACT 780
CATTCATTCC CAGCAACACC AGTCAACAGT GGAGCCGTTG TGCCCATTGT ACAGACGGGG 840
CAGCTGAGGC TTGTGCAGGC TCAGAAGGAT GTCCTAGTCT CTCTCACTCT CCTTTCTCCC 900
TCCTACGGAT GCTGTGACAA ATGACCACAA ACTAGGTGGC TTAAAACAAC AGAAACTGAT 960
TGTCACAGTT CTGGAGGCTA GAAGTCTGAA ATCAAGATGT CAGCGGGCTG GTCCTTCTGG 1020
AGGCCTTCTC CTTCTCCTTC 1040
|
