| Tag | Content |
|---|
EnhancerAtlas ID | HS180-25484 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:26231560-26232660 |
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 | ACAAACAAAA AGACACCACA TACAGGAATA AAATGTACTG AGGAGACAAA AGAGTGTCAA 60
CCCAAGGATC TCTTTCAGAG GGGTTCCCTT AACTCTGGCA GGCCATGAGG ATGATGCCTG 120
GGAGCCCCAG GATTCTCCTG TTACTTTCTT GTGTCCTCAG AAACCACCCT GGTGACTCAG 180
TAACACAAAC CTAGGGTGTT GAGTGGGTGG GGCACCGCTT CCCACCCCAG TTTATCTGGT 240
TTTCCCAGGC AGAATAGTAC ACTGAAGCTG TAGGCAAAGA GGAAGCCCAA GATAGGGGAA 300
GGCCAGGGTG TTGGTTCCTC AGTTTGTTGA AATCAGAGTC ATGAAGCAAG ACAAGCCAGG 360
GCTTGCTCAG CATTTCTCCT TCCTGGCATG GGTTCACCTC AGCCCCAATT CAGTGGCAGC 420
TCTGTTGGTT CAGAGGGGTG AGGTATCCAA GAGGAGGAAG CTTGTACAAT CCTGCTAGCA 480
GGGGAGGGCT GATGGTAGGG TGGAGTTTCA AAGGAAGCCT CTGACATCTG ACAAAGGCTG 540
AGTCAGTTAT ATTGCCCCAT CTCTGAATCT GGCTTCTCCT GCTCCTCTAC CCTACCCATC 600
CTGCCTTCCA GACACACCAA AGTTCTTTTT ATCCCTGACC ATGACAGGCA TGGCTGCTGT 660
GTGCAGCTTC ATAGGTTGTG CACTGCACAG TTCCAGGAGG TGCTATTCCC ATAGACAAAG 720
GAGTGAATAA CAACTCCAAG AATCATGCAC AATTGTACCA GGCAGCCCCG AGCCAAGCCC 780
TTTTATGACT TCCTTCCTTT CCACATATTG CTTCCCCTGC CACAACTGCC CTTGTTTGCC 840
TTTCCTCCCC CCATTTCTTT ATATGGTGCA ACATCTAACA CTTAGTTCTC AAATTCTGCC 900
CAAATATAAT CCTGGTGAAC ACAAACATAA CAGAATGCAT ATGGAAGACC TGACATACAG 960
GAGTCTCGAA CTGGCACATT GCCAGCTCAT TAAGCTTGGT AGTTTTATTA TGCCTGTGGG 1020
GTGTTCTAAA AGGTAATGTA AGTAAAGTCC ATTAGAACAG CTAAGATGAA AAATACACAA 1080
TACTAAGTGT TGGTGAAGAT 1100
|
