| Tag | Content |
|---|
EnhancerAtlas ID | HS148-18177 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr8:101450150-101450810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr8:101450788-101450799 | GCAGGGTGTGG | - | 6.62 | | Klf1 | MA0493.1 | chr8:101450790-101450801 | AGGGTGTGGCT | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27991 | chr8:101449856-101452919 | Fetal_Intestine | | SE_28830 | chr8:101449753-101453025 | Fetal_Intestine_Large | | SE_32533 | chr8:101448020-101453094 | GM12878 | | SE_62291 | chr8:101421434-101542088 | 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 |
| GH08I100437 | chr8 | 101449399 | 101453077 |
|
Enhancer Sequence | TGGAGGGCAG GACCCACGTC TGTTGTGTTC ACTGTTAAAT CTCCAGTGCC TGGAGGATAA 60
ATGGTCCTCA GCACGCCTTT GCTGAAGGAA GGTGTCTAAT CCTGAGCAGG GTGACTGAAG 120
CAAGAGGGAA GAGAGCTGAC TGAGTTGATC TGCTTAGTCC CATGGAGAAA AGCAGCAGAG 180
AAGAGGAAGA AACTGAACTT GGCTCTTCCT TCCCCATTTC ACTCTCAGAT GCTGAAATGA 240
CTATTTTTGG TGAATGCAAA TCATAGCTGT GGCCAGTGTC TTCAGTCCAA GGCCACAACT 300
GCACGCGCTG AGCCAGGGTT ATAGTCACAA GAGTTTATTT TTAAAGTAAC CACGCCTGAC 360
CTTCAGGCTC AGAGGCTGCA GACTCAGACT TTCCTGGTCA GGGCCACCCC AGGGTGGCCA 420
GTCATACTCA GCAGAGAAAA GCCACGTGTT CCAAAATGGA AAAGGCGCTC AGGCTTCTTC 480
CTCCACCACA GCTAAGGAAT ACCTTCCCCT CCCATCTGTC GCCTACATGC TGACCGCTTT 540
CTGGCGCATT TAACACCCAC AAATCACAAG CTGTTGCTCT TGGCTTGGAG CTCCAGTTTC 600
TTGAACTAAA TTATAAGTAT GAGCATGCTG TGTAGCTTGC AGGGTGTGGC TGCTGGAAGA 660
|
