| Tag | Content |
|---|
EnhancerAtlas ID | HS060-14233 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:17017720-17018690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr17:17018018-17018038 | CCCCCGCCCACCCACCACCA | + | 6.95 | | SP2 | MA0516.2 | chr17:17018014-17018031 | CTACCCCCCGCCCACCC | + | 6.39 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_03884 | chr17:17017571-17019353 | Brain_Anterior_Caudate | | SE_04928 | chr17:17017830-17019571 | Brain_Cingulate_Gyrus | | SE_05858 | chr17:17017776-17019376 | Brain_Hippocampus_Middle | | SE_07879 | chr17:17017409-17019369 | Brain_Inferior_Temporal_Lobe | | SE_19214 | chr17:17015912-17025378 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_31426 | chr17:17017812-17019019 | Gastric | | SE_42036 | chr17:17017803-17019326 | LNCaP | | SE_65457 | chr17:17017870-17018746 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 17017900 | 17018538 | | chr17 | 17018069 | 17018211 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I017114 | chr17 | 17017606 | 17018950 |
|
Enhancer Sequence | ATTTTGATGA AGTCTAGTTT ATCTTTTTTT TTTCTTTTGT TGCTTGTGCT TTTGGCGTCA 60
TATCCAAGAA ATGGTTGCTA AATCCAGTGT TACAGGGCTT TTTTCCTTGG TCTTCTGTGC 120
ATTTTATAGC CTTTGTTCTT GCATTGAGGT ATCTGCTCCA TTTCAAGTTC ATTGTTGCAT 180
ATGGTGTAGT GTCACCCTTG GTTGGTGGAT CCTGCTAGCT GACCATTGTG GTGGGTGAGG 240
GGGATGAAAA GCTGTTCTTC CCCAGTTCCC ATGCCTCTCC TACCTTCTTC CCATCTACCC 300
CCCGCCCACC CACCACCAGT TTTAGGAGGA AGGTGGGCCT TAACTGGGTG AGGGCTCCCA 360
AGGGAAGCTC CTCTGGCAGA GGGCCCTTGG CCATTTGGCG GGGGCCCTGG TATCTCGCTG 420
CCCAGGCAGC GGCCGAAGCC AGCAGGCCAG CCTGGCGTAG CAGGTGTGAG GAGGAACTTC 480
CTGGTCTTGG CAGCAAGTGA AAAAGGTCCT TGTTTTCTTA TTTTCTCCGT TAAAAAAAAA 540
GTAGTTTAGT GGTTCTAACT ATGCCCCTGG GAAAGCCCTG AACGGGTCAT TTCCTCAGCA 600
TCCCACAAAG TCACTTGTAG CAGAAGGCCC AGCCCACGCA CTGCAGCACC AAGGCTGGGG 660
CGAGGCCCAC ACTGCATTGT TGCTGCTGGC ATTAGCAGAT GCTGCACATC TTGGAGGCCC 720
CCTCCTGCTA ATCCACGAAT GCCTCAGAAA GCATGCACTG TCTCTGGGGC CAGAGCTGAA 780
TCTTAGAAGA GGGCCTACTT GGGATGGGAG CGGTAGCTCT GCGTCTGTGG TGACACCCAC 840
TGTCACATTC CAGTAGAGGG AAGGAAAGGT AGGGCCTCGG GATTTTGGCC CTGACTGCAT 900
GGTTCCTGCT TCTTCTGTGA TGGAGGCGGC ATGCTGTGGT GGGCTAGGAG TTAGGAAGCC 960
TGGGCCTGAG 970
|
