Tag | Content |
---|
EnhancerAtlas ID | HS045-41907 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr21:45531780-45532850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr21:45532615-45532625 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr21:45532615-45532625 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr21:45532615-45532625 | ATTTTCCATT | + | 6.02 |
|
| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_03198 | chr21:45532109-45532864 | Brain_Angular_Gyrus | SE_03880 | chr21:45531881-45533118 | Brain_Anterior_Caudate | SE_04775 | chr21:45530903-45533039 | Brain_Cingulate_Gyrus | SE_05779 | chr21:45531249-45533097 | Brain_Hippocampus_Middle | SE_06690 | chr21:45531017-45533054 | Brain_Hippocampus_Middle_150 | SE_07737 | chr21:45531139-45533045 | Brain_Inferior_Temporal_Lobe |
|
| 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 |
GH21I044112 | chr21 | 45532061 | 45532653 |
|
Enhancer Sequence | GAAGGAGTTT CATCATTGTT GGCCAGGCTG GTCTAGAACT CCTGACCTCA GGTGATCCAC 60 CCGCCTCAGC CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACCATGCC CGGCCAGCAA 120 GTGGTTTCTT GAGATGGAAT CTACTTCTGG TGAGGATGCT GTAAAGACTG TTGAAATGAC 180 AACAAAGGAT TTAGAATATG ACATCAACTT AGTTGATAAA ACGCTGGGAG CATTTGTGAG 240 GATTGACTCC GGTTTTGAAA GAAGGTCTGT TGTGGGTAAA ATGCTATCAA ACAGTATCAC 300 ATGCTACAGA GACATCTTGT GAAAGGAAGA GTCCATCGAT ACGGCAAGCT TCACTGTTGT 360 GTTAGGAATT GGCAACGGCC ACCCCGTTTT CAGCAGCTGC CACTGTGCCT GGTCAGCAGC 420 CATCCACATC GAGGCAGACT GTCTGCCAGC AAAAAGATGA AGACTCACTG AAGGCTCAGA 480 TGATTGTTAG CATTTTTTAG CAGTAAAGTG TTTTTAAATT AAGGGATGCA CGTTGTTGCT 540 TTAGACAGAA TGCTTGTGCA CACTGATAGA CTACAGCACA CATGAGTAGA CTGCAGCGCA 600 CACCAATAAA GTACACACTT CGACGACAGT ACACACGAAC AGACTACAAC TCACACGAAT 660 AGAGCACAGT GCACGCTTAC AGACTACAGC ACACGCTAGT AGACTACGCC GTACTGTTTA 720 CAGTATGGTG TAAACACAGC TCGGCTGCTT ATGGGGAAGC TGGAATGTGT GTGCCTCACT 780 CAGTTGCAGT GTAAGCGTTA TCTGCAGCAT CTCCGCGGGA TTCCTGTAGC CCCTTATTTT 840 CCATTTTTCT AGCAACAGTG TTACATGGGT GCACTGTCAT GGTGGTTAAT TCCTGTTGGG 900 CACTTAGCTT GCTTCTGGTA TTTTGATGTC ACACTGAGGC GGAATAATCC TCTCATCATA 960 TCATCCTGGA AGCAGAATTG ATGTATCCAA AGCCCATTTT TAAGGCTTTT AATGCATTTC 1020 ACTAGAGTTC CTCCAGGGAC AACGTCATTT CTTTTTCTTT TTTTTTTTGA 1070
|