| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00843 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:24431650-24432400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:24431890-24431911 | TTCCCATCTTCTCCCTGCCCC | - | 6.13 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27677 | chr1:24424566-24436755 | Fetal_Intestine | | SE_28574 | chr1:24424526-24439807 | Fetal_Intestine_Large | | SE_30016 | chr1:24427249-24433190 | Fetal_Muscle | | SE_40929 | chr1:24431581-24433075 | Left_Ventricle | | SE_51642 | chr1:24431481-24432773 | Skeletal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 24431845 | 24432126 | | chr1 | 24432285 | 24432380 |
|
Enhancer Sequence | CTTTCCCAGC CCCCTTCAAG CCCTGAGGTT TCCATGCTGT TGTGGCGTTA AATTCTCATC 60
ACATGCAGGC CGGACAGGAG GTCTTCAATC CACTCTTCAG AACAGGAAAT GGAGTCAGGA 120
CCAGGCAGTT TAAGAGGCAT GGCTGAGACC TCACGCTGAG TGAGGAGAGA GGCAGAAAGC 180
GAGGCTGGGA ACACAAGGTT CTCGCTACAG GCGTGAGCTC CTTCTCCGTA GGCCCTTCCC 240
TTCCCATCTT CTCCCTGCCC CACCCACTGT CTCCCTGCTA CTTGGCCCCT GTCCTGCCTC 300
TCACCGTCAT CCTCAACCCT GGAGACGCCC AGCTTGCAGC ACCTGCCTTC TCATGAGACC 360
AGAATCATAT TTTTATGAGG GCTGGCTCCC CAGGGGCCCA GTCTTCCAGC CCCAGGCTGG 420
CTGCGGGGCA GCTAAGAATA ACCCAGGCCT AAGCTGGGCG TGGTGGCTTG TGCCTGTGGT 480
CCCAGCTACT TGGGAGGCTG AGATGGGAGG ATCACTTGAG CCCAGGAGTC AAGACTGCAG 540
TGAGCTATGA TTACTCCACT GCACACAGCA GCCTGAGCGA GGCCCCGCCT CTAAAAAAAA 600
TAACCCAGGC CTGGTTCCCC AGCAGCTGCT CTATTCGGTG GGTGGACAGA GCTCAGGGTT 660
CACAGGTCTG CAACAAGAAG TCCTGGCAGA AGTATTGGAT GTGAGGAACT CACTTGTGAC 720
CCCAGAGGCC CAGAACCCCT TCCTGCCCCA 750
|
