| Tag | Content |
|---|
EnhancerAtlas ID | HS098-29236 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:26231660-26232330 |
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 | GGCCATGAGG ATGATGCCTG GGAGCCCCAG GATTCTCCTG TTACTTTCTT GTGTCCTCAG 60
AAACCACCCT GGTGACTCAG TAACACAAAC CTAGGGTGTT GAGTGGGTGG GGCACCGCTT 120
CCCACCCCAG TTTATCTGGT TTTCCCAGGC AGAATAGTAC ACTGAAGCTG TAGGCAAAGA 180
GGAAGCCCAA GATAGGGGAA GGCCAGGGTG TTGGTTCCTC AGTTTGTTGA AATCAGAGTC 240
ATGAAGCAAG ACAAGCCAGG GCTTGCTCAG CATTTCTCCT TCCTGGCATG GGTTCACCTC 300
AGCCCCAATT CAGTGGCAGC TCTGTTGGTT CAGAGGGGTG AGGTATCCAA GAGGAGGAAG 360
CTTGTACAAT CCTGCTAGCA GGGGAGGGCT GATGGTAGGG TGGAGTTTCA AAGGAAGCCT 420
CTGACATCTG ACAAAGGCTG AGTCAGTTAT ATTGCCCCAT CTCTGAATCT GGCTTCTCCT 480
GCTCCTCTAC CCTACCCATC CTGCCTTCCA GACACACCAA AGTTCTTTTT ATCCCTGACC 540
ATGACAGGCA TGGCTGCTGT GTGCAGCTTC ATAGGTTGTG CACTGCACAG TTCCAGGAGG 600
TGCTATTCCC ATAGACAAAG GAGTGAATAA CAACTCCAAG AATCATGCAC AATTGTACCA 660
GGCAGCCCCG 670
|
