| Tag | Content |
|---|
EnhancerAtlas ID | HS092-23576 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:26231540-26232620 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:26231542-26231554 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:26231546-26231558 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:26231550-26231562 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr2:26231554-26231566 | AAACAAACAAAC | - | 6.32 | | 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 | CAAAACAAAC AAACAAACAA ACAAACAAAA AGACACCACA TACAGGAATA AAATGTACTG 60
AGGAGACAAA AGAGTGTCAA CCCAAGGATC TCTTTCAGAG GGGTTCCCTT AACTCTGGCA 120
GGCCATGAGG ATGATGCCTG GGAGCCCCAG GATTCTCCTG TTACTTTCTT GTGTCCTCAG 180
AAACCACCCT GGTGACTCAG TAACACAAAC CTAGGGTGTT GAGTGGGTGG GGCACCGCTT 240
CCCACCCCAG TTTATCTGGT TTTCCCAGGC AGAATAGTAC ACTGAAGCTG TAGGCAAAGA 300
GGAAGCCCAA GATAGGGGAA GGCCAGGGTG TTGGTTCCTC AGTTTGTTGA AATCAGAGTC 360
ATGAAGCAAG ACAAGCCAGG GCTTGCTCAG CATTTCTCCT TCCTGGCATG GGTTCACCTC 420
AGCCCCAATT CAGTGGCAGC TCTGTTGGTT CAGAGGGGTG AGGTATCCAA GAGGAGGAAG 480
CTTGTACAAT CCTGCTAGCA GGGGAGGGCT GATGGTAGGG TGGAGTTTCA AAGGAAGCCT 540
CTGACATCTG ACAAAGGCTG AGTCAGTTAT ATTGCCCCAT CTCTGAATCT GGCTTCTCCT 600
GCTCCTCTAC CCTACCCATC CTGCCTTCCA GACACACCAA AGTTCTTTTT ATCCCTGACC 660
ATGACAGGCA TGGCTGCTGT GTGCAGCTTC ATAGGTTGTG CACTGCACAG TTCCAGGAGG 720
TGCTATTCCC ATAGACAAAG GAGTGAATAA CAACTCCAAG AATCATGCAC AATTGTACCA 780
GGCAGCCCCG AGCCAAGCCC TTTTATGACT TCCTTCCTTT CCACATATTG CTTCCCCTGC 840
CACAACTGCC CTTGTTTGCC TTTCCTCCCC CCATTTCTTT ATATGGTGCA ACATCTAACA 900
CTTAGTTCTC AAATTCTGCC CAAATATAAT CCTGGTGAAC ACAAACATAA CAGAATGCAT 960
ATGGAAGACC TGACATACAG GAGTCTCGAA CTGGCACATT GCCAGCTCAT TAAGCTTGGT 1020
AGTTTTATTA TGCCTGTGGG GTGTTCTAAA AGGTAATGTA AGTAAAGTCC ATTAGAACAG 1080
|
