| Tag | Content |
|---|
EnhancerAtlas ID | HS002-03721 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr16:11707090-11708110 |
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 | TCACCATGTT GACCAGGCTG GTCTCGAACG CCTGACCTCA AGATCACTCT AGTTTTTGTT 60
TCCACTTCTG GATCCCCATG GGATGGAGAG AGACGGGACA CTCGCATTGA CAGAGAGACC 120
AGACCTCCTG GGTCACCTGG GGGAATAAGC AATGCAGCCA GCTGCCAGGT CCCAGGGCTG 180
CCTTCTCCTG ACCATCTGGG CAATTCAGAC ACAGCTGGGT CTGAGGTGCC AGAGTGTGTT 240
GTTCCGCCTG TTTAGACCTG CCCCACCTCG AAGACATCGG TGATTCACAA TCTTCCCTAG 300
AACGGACAAC TCCTGGAGGG TGGGGCCCCT GCTGATTCAA ACTGGGCTCC TATGAAAGCT 360
CCCAGAGGGT GAGGGCAGTC AGGGAAGGCT TCCAGGAGGA AGTGGCTCTT GTTGAAGGCT 420
AAGCCAGAGT TAGGTGGGAG AGGAGCAGGA AAGGTGTCCT TACAGGGAGC ACAGCCGGAC 480
GGAGGGTGTG GCGTGTGCCG GCTAGGCAGT TCACACTGGT GGAACCGAGG GCACAGAGGT 540
GGCTGGGGCA AAGCCCAGAC AGAAAGGACA TCTCAGAAAT GAGGATCTGT ACTCCGAGAG 600
CCGGCCTCAC CCTGCCACAT GTTGTCAGAT GACCGGGCGG GCCACTTCTC TCGCTGAATG 660
TTTATTTCCT TATCTCTAAA ACGGAACTGA CAGTTGAGAT CAACGCCTGT GTTCTGTGGG 720
GTCCCTCTGC TTCCTGGCAG GTCCTGAGAT TTGGACACTT GCACATGACT CATTCATTCC 780
CAGCAACACC AGTCAACAGT GGAGCCGTTG TGCCCATTGT ACAGACGGGG CAGCTGAGGC 840
TTGTGCAGGC TCAGAAGGAT GTCCTAGTCT CTCTCACTCT CCTTTCTCCC TCCTACGGAT 900
GCTGTGACAA ATGACCACAA ACTAGGTGGC TTAAAACAAC AGAAACTGAT TGTCACAGTT 960
CTGGAGGCTA GAAGTCTGAA ATCAAGATGT CAGCGGGCTG GTCCTTCTGG AGGCCTTCTC 1020
|
