| Tag | Content |
|---|
EnhancerAtlas ID | HS045-67799 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr8:125721380-125722250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr8:125722120-125722133 | TTCTGGAACATTC | + | 6.67 | | KLF4 | MA0039.3 | chr8:125722026-125722037 | CCACACCCTGT | + | 6.14 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_05555 | chr8:125721851-125723879 | Brain_Cingulate_Gyrus | | SE_10859 | chr8:125712814-125729740 | CD20 | | SE_33465 | chr8:125721578-125724787 | H2171 |
|
| | 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 |
| GH08I124708 | chr8 | 125720497 | 125724067 |
|
Enhancer Sequence | TCCTGCCTTT TGGACAGCAA GACTACATAA AGGAGACCAT ACTCAAGTTT CAAAAGAAAC 60
CCGCAACCCA AGACACTGGA AGCTCTTAGA GCCCTTTAGA AAGCAATTCC CCAACTGTCC 120
TTGGTTTTTG CATCTGCATC CACCCACCAA GAAGTCCCCA GAAAGTTCAT TCCTGAGGTT 180
GCTGGCTGAG CTCTGTCCCC ATTTGAGGAA ATCCCTCGGA ATGCACTCCC AGAGCCGTGA 240
AAACAATTCA ACACAGACCC CACTGTGGAT TTCACCTGAG AACACATAAA GGCTTCACAA 300
CGTTCCAGAC AGACCCAAAT CAAAGAAAAC AAAACTCCCG CCACGCCCCG GCTTCTGCCA 360
AGTCCAAAGT CACAAGGCAA AATGAGAAGG CGCACCTCCT CCAGGAGCCC CCTGAATTTC 420
TTCAGAGAGG AGAGCCAGGA GTTTCTGGAG CCCTTGGCAG TGCGTTCGTT GAAAATACAA 480
CTCAGATTAC ACTGGGTTCT AAGAAAGGAA AAGGTCCCTA TTAAAGAAAC GGGAAGAGAA 540
AGCCAGTTTG TTTACAAGCG TGTAAAGAGG ACTCCCTCCA TCACTTCCTT GGGTGAGAGA 600
TGGGGCTTCC CTGAACACGT GATCTCACCC ACACTCCCCA CACACACCAC ACCCTGTGGC 660
TGCTTCTCTT CAAATCTCCA GGGGGATTCA GCAATATTGA AAACTCCTAT TCAGCTGTCA 720
CTACCCAGCT GTGACACTTC TTCTGGAACA TTCTCTGACA CACCCCCTTC CCACCTACCC 780
TCTGGTTTAG CTGCACCTAC TCCCCAACTT ATCACATCAT ACAGTTTGCT GTCTATAAGC 840
CTGAGGGCTT CCCCTTTGGA CTGTGGAACA 870
|
