Tag | Content |
---|
EnhancerAtlas ID | HS047-14071 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:17745330-17746750 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF143 | MA0088.2 | chr17:17746024-17746040 | CTCCCACAATGCACCC | + | 6.47 |
|
| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00344 | chr17:17737261-17745931 | Adipose_Nuclei | SE_00881 | chr17:17742643-17747546 | Adrenal_Gland | SE_02989 | chr17:17745481-17746328 | Bladder | SE_03206 | chr17:17743577-17745493 | Brain_Angular_Gyrus | SE_06266 | chr17:17737667-17755965 | Brain_Hippocampus_Middle | SE_07574 | chr17:17738149-17746374 | Brain_Hippocampus_Middle_150 | SE_14781 | chr17:17736973-17745691 | CD4_Memory_Primary_7pool | SE_17733 | chr17:17742453-17746557 | CD4p_CD25-_CD45RAp_Naive | SE_23173 | chr17:17742277-17746020 | Colon_Crypt_1 | SE_23799 | chr17:17742658-17745542 | Colon_Crypt_2 | SE_24725 | chr17:17742593-17746201 | Colon_Crypt_3 | SE_26625 | chr17:17738275-17747583 | Esophagus | SE_27885 | chr17:17742376-17745561 | Fetal_Intestine | SE_31441 | chr17:17742274-17746249 | Gastric | SE_33480 | chr17:17738227-17755543 | H2171 | SE_34007 | chr17:17738817-17747312 | HCC1954 | SE_34262 | chr17:17737342-17746262 | HCT-116 | SE_34795 | chr17:17737387-17746315 | HeLa | SE_36316 | chr17:17738464-17746027 | HMEC | SE_39928 | chr17:17737435-17746177 | K562 | SE_42125 | chr17:17738220-17748162 | Lung | SE_44649 | chr17:17742509-17745666 | NHDF-Ad | SE_47997 | chr17:17742680-17746082 | Pancreas | SE_48150 | chr17:17738162-17746924 | Psoas_Muscle | SE_50203 | chr17:17742343-17745587 | Sigmoid_Colon | SE_51164 | chr17:17737218-17746592 | Skeletal_Muscle | SE_52449 | chr17:17742250-17745593 | Small_Intestine | SE_53726 | chr17:17742513-17746183 | Spleen | SE_54926 | chr17:17742507-17746342 | Stomach_Smooth_Muscle | SE_57042 | chr17:17742306-17746192 | VACO_400 | SE_60863 | chr17:17723038-17753684 | DHL6 | SE_61850 | chr17:17725940-17761172 | Toledo | SE_62888 | chr17:17723024-17755643 | Tonsil | SE_64851 | chr17:17738314-17746194 | NHEK | SE_68738 | chr17:17742506-17746256 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CACAGGGTAG GGACAGAGCT CAGGCCTCTT TCAGTGCCCA CATTGCCTGG TACAGTGCTG 60 GGGGCACATA ATGAGCCAGG ATCTATGCTA TCTGTTTAAA GGGACCTGGG TTTGCAGCCC 120 CCCACCCCCA CTTCAGGAGC CCACTCCCCT TCTCCCCTGG GTGTGGGAAC CTTTATCTCA 180 CTCCAACTGG TCAGAAACAG GGCTCTGCAG AGCTCCCTGG AGCCCAGGGA GGCAACTGGC 240 CAGAGGTAGC TGGGTGCCGC CCCTTCTGGC TACGACTGGT GATGGCGGTG GTCCCAACAC 300 GGCCCCTGCC GTGACCTGAC TCCTATCAGT GGGCAGGAGA GCCCCTCCTG AGCCACGCTC 360 CCAGAAGGGC TGCTGTTCAG GGTAGGTGGG GCAGCTTTAT CTGCTGGCCA TGGAAGTGGT 420 GTCTTTCCTG CCCACTTCAT GGACCTGTCT GGGAGGTCTG GCTCTGGGTT GGGTACTGGT 480 TCTGCCACTA CTCCCTGTGC AGCCTGGGGC AAGCCTACAG CTCTTTCTAG TCCTCCATGT 540 CTTCACTGGC ACAGCAAGAG TTTGGGAAGA TCTCCAGGTT CATCGGGGGT TTGGTGAGTC 600 CACCCTGACT TGAGGTCTGT CCTTAAGCCC CAGCGAAGGG ATTAAAGGGC CCTCGGCCTC 660 CCAAGCCACT TGGAGAAGGC ACAGTTCCCA CAGGCTCCCA CAATGCACCC CTCATGACCC 720 CCTATGCCTC TGGGCCTGAG GGGCCTGCTT CCAGGAGGAC AGCTACCTTA CAACAAAGGG 780 CTGCAGGTGC CCACCTCCAG GACAAGGGGA GAGGGGGAAG GAAGCCTTTT TAGAAAGGGA 840 GAGCAGGCTG TGGGGATGGG AGGAGACAGG TTTCTTTTGG GGGGAATAAA AATGTTCTAA 900 ATTTGGTTGC GGTGATGATT GCCCAACTCT ATGGATATTC TGAAGACTAC TTAATTGTAC 960 ACTTTAAATG GGTAAATTGT ATGCTATGTG AATTATATCT CAGTAAAACT GTTAACAAAG 1020 TGTGAAGTCT ACCTGGCTTG GAGCAGCAGT TCTCAAATTC AGTGCCCAGC ACAGGCTCTG 1080 CAGATGATGC CCAGCCAAGC TGTGGGAGTC CAGCCGAGGG TGGGGGCTGG GGCTTAGAGG 1140 GGGTCAGGGG TGGCTCAGGC CTGCTTGCTC AAGGCCTGGG TGCCCTGGGC AAGGGTGAGT 1200 GGCCTCCTCC TGCCCATCTG GGACCTGGGG TGAGACCTAG GAACAACCAC AGCACTTGGT 1260 CCTAGAGCTC TCAGGCAGGT TGTAGCAGGC TTACAGCCAC TCCCACCGAT GTCACAACCT 1320 GGGCCACGCA CAGGAATTTT CCTGGCCAGG TAAGGGGCTG CTCAGGCAGC CTGGCCACTG 1380 GGGAAGGGTG GACTGAGGGT CCCCATGGCC ACCCCTGCTT 1420
|