| Tag | Content |
|---|
EnhancerAtlas ID | HS148-07774 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr17:74247880-74249150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr17:74248745-74248766 | ATTTTCTCTCTCTTTCACTTT | + | 6.21 | | IRF1 | MA0050.2 | chr17:74248751-74248772 | TCTCTCTTTCACTTTTTTTTT | + | 7.63 | | ZNF263 | MA0528.1 | chr17:74248049-74248070 | CTTTCTTCCTTTTCCTCCTCA | - | 7.04 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_11415 | chr17:74247580-74249549 | CD20 | | SE_15056 | chr17:74247576-74249126 | CD4_Memory_Primary_7pool | | SE_18937 | chr17:74247402-74249906 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19565 | chr17:74247575-74249815 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_21340 | chr17:74248712-74249921 | CD8_Memory_7pool | | SE_23599 | chr17:74247703-74248615 | Colon_Crypt_1 | | SE_24131 | chr17:74247750-74248058 | Colon_Crypt_2 | | SE_24131 | chr17:74248072-74248530 | Colon_Crypt_2 | | SE_27367 | chr17:74247623-74248919 | Esophagus | | SE_28090 | chr17:74247720-74249008 | Fetal_Intestine | | SE_29152 | chr17:74247624-74248997 | Fetal_Intestine_Large | | SE_31864 | chr17:74247673-74248817 | Gastric | | SE_32663 | chr17:74247575-74249525 | GM12878 | | SE_43246 | chr17:74247582-74249663 | Lung | | SE_47749 | chr17:74247791-74248535 | Pancreas | | SE_48284 | chr17:74246270-74250806 | Psoas_Muscle | | SE_50371 | chr17:74247468-74249790 | Sigmoid_Colon | | SE_52552 | chr17:74247474-74249789 | Small_Intestine | | SE_53757 | chr17:74247335-74249794 | Spleen | | SE_55588 | chr17:74247785-74248788 | Thymus | | SE_60322 | chr17:74239092-74270751 | Ly4 | | SE_60510 | chr17:74247565-74275632 | DHL6 | | SE_62440 | chr17:74241844-74272934 | Tonsil |
|
| | 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 |
| GH17I076250 | chr17 | 74246726 | 74249804 |
|
Enhancer Sequence | CACCAGCCTC TGTGGGGAAA GCCTGCCTGG GTGCCAGCCC TACTGCCCAC CAAGCTAGCG 60
GAGTGATTCT CCCAGGGTGG TGCCAGTGAC AAAGGGCAAT GCATGGGGAC GTCTCCATCA 120
TTGTCACACC ACCACCTCCA CCTTCACTGT GCCTCTCTCT AGGTTTAATC TTTCTTCCTT 180
TTCCTCCTCA CTTCCCTCTG TATTATCAAT CTCCTTCCTG TATCGGGACT ATTTCCTCAA 240
CAGGCCCGGG GAAGCTCTTG TCTATGGAAG TCCTCTTTGG CCTTAAGCTT CCCTCTAAGA 300
GCTCCAGCAG ATGAGTAACC TGTCCTCCTG CAAACACTGC CATGAAGTGC GTAGGCAGCT 360
GCCTGCCTTC AGGGCTGGAT GGACACCCTG TTTCCTTGCT CAATCCCTTC TGATGACTGG 420
ACTCTGTACA CAGTGTGGTC AGTGGGTCAG CTCTGATCTG GAAGCTCCCA AAGGCAGGAC 480
ACAAGATTTT CTCTGACTGT TCCCAGGCCC CAGGGCGTGT TGGGCACGGG AGCGTGTGGC 540
ACGGATGTTG TTCGTGATGA GGCATATTCT AGTGGTTTCC CAATTCGGTT GTGTACAACC 600
CAGTGCTCTA GTGTTCAGTA AATACTTCCT TCCTCTTTAG GCAGAACACT GGCTCTGTGT 660
TTTATTAACA GCACCTCATG CCTGGCCCAA AGAATGATTT GTGTGGCTTG GGCTGTTGGG 720
GTCAGAAATG GCATTCATTC ATCATTCACT CTGGAGGTGC TGTGTTTCTG AAGGAGAAGG 780
GGACCTATCC TGGCAAACAA ATCAGGGGCT TTATGGTAAA CAAACTCCTC TCTTCCCAGC 840
ACTTGTTTCT TGCTCTCTGT TTTTGATTTT CTCTCTCTTT CACTTTTTTT TTTTTTTCAC 900
TATACCCGGG CTTCCTGAGT TCCTGACAAT TTCTAAAGCC TCAAGCATGA TCTCATCAGA 960
AACTCTGGCT TCTTTTAACA TTTCTTTCCC TTCTGCTGAG TCCTAGTCCA TTTAAATTTC 1020
CTCTGTGACT CTGGGAATTT TTTTTCCTTG AGACACAGTC TCGCTCTTGT TGCCCAGGCT 1080
GGAAGTGCAA TGGGCTGATC TCAGCTCACT GCAATCTCTG CCTCCCAAGT TAAAGCGATT 1140
CTCCTGCCTC AGTCTCCCAA GTAGCTGGGA CTACAGGCAT GCACCACCAT GCCCGGCTGA 1200
TTTTGTATTT TTAACAGAGA CGGGGTTTCA CCATATTGGT CAGACTGACC TCAAACTCCT 1260
GACCTCAAAT 1270
|
