| Tag | Content |
|---|
EnhancerAtlas ID | HS105-42222 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:26231620-26232440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr2:26231909-26231927 | GACAAGCCAGGGCTTGCT | - | 6.15 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_09566 | chr2:26230391-26233253 | CD14 | | SE_26712 | chr2:26230608-26232892 | Esophagus | | SE_28420 | chr2:26231425-26232647 | Fetal_Intestine | | SE_29154 | chr2:26231420-26232678 | Fetal_Intestine_Large | | SE_32014 | chr2:26231685-26232630 | Gastric | | SE_35193 | chr2:26230790-26233105 | HeLa | | SE_36382 | chr2:26230622-26233114 | HMEC | | SE_64640 | chr2:26230706-26232972 | NHEK |
|
| | 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 |
| GH02I026007 | chr2 | 26230471 | 26233268 |
|
Enhancer Sequence | CCCAAGGATC TCTTTCAGAG GGGTTCCCTT AACTCTGGCA GGCCATGAGG ATGATGCCTG 60
GGAGCCCCAG GATTCTCCTG TTACTTTCTT GTGTCCTCAG AAACCACCCT GGTGACTCAG 120
TAACACAAAC CTAGGGTGTT GAGTGGGTGG GGCACCGCTT CCCACCCCAG TTTATCTGGT 180
TTTCCCAGGC AGAATAGTAC ACTGAAGCTG TAGGCAAAGA GGAAGCCCAA GATAGGGGAA 240
GGCCAGGGTG TTGGTTCCTC AGTTTGTTGA AATCAGAGTC ATGAAGCAAG ACAAGCCAGG 300
GCTTGCTCAG CATTTCTCCT TCCTGGCATG GGTTCACCTC AGCCCCAATT CAGTGGCAGC 360
TCTGTTGGTT CAGAGGGGTG AGGTATCCAA GAGGAGGAAG CTTGTACAAT CCTGCTAGCA 420
GGGGAGGGCT GATGGTAGGG TGGAGTTTCA AAGGAAGCCT CTGACATCTG ACAAAGGCTG 480
AGTCAGTTAT ATTGCCCCAT CTCTGAATCT GGCTTCTCCT GCTCCTCTAC CCTACCCATC 540
CTGCCTTCCA GACACACCAA AGTTCTTTTT ATCCCTGACC ATGACAGGCA TGGCTGCTGT 600
GTGCAGCTTC ATAGGTTGTG CACTGCACAG TTCCAGGAGG TGCTATTCCC ATAGACAAAG 660
GAGTGAATAA CAACTCCAAG AATCATGCAC AATTGTACCA GGCAGCCCCG AGCCAAGCCC 720
TTTTATGACT TCCTTCCTTT CCACATATTG CTTCCCCTGC CACAACTGCC CTTGTTTGCC 780
TTTCCTCCCC CCATTTCTTT ATATGGTGCA ACATCTAACA 820
|
