| Tag | Content |
|---|
EnhancerAtlas ID | HS099-00429 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:24431290-24432130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:24431575-24431585 | GCCCCGCCCC | + | 6.02 | | 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: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTTCCCAAA GTGCTGGAGG TGGGCCTGGG CTTGTTTGGT TATTTGTGTG CCCCAGTGCC 60
TCAGTCAGGT CCTGGGATAG ATGACACCCT CAGTAAATAT TTGTTGAAAG CCCTTCCTCA 120
TCCCCCAGGG TACTGGGCAA TGGGCCTTAG ACCCAGGGGG ATCTCAGGAA AGAGTAGCTT 180
AGCCATGTGA ATGACACGTC TCCTTCTGTG GTGAGACTGA GACCTGGGCC GCGGCCATGC 240
CTACTCCAAT GTGTGCCTGT GCAGGAGACC CCTGCCCCTG CCCCTGCCCC GCCCCTCCCC 300
AGGCGAGGCC TAGCCTCTGG GATTCTGCCA TGGTTCCCCT CCCAGGAAGG GCATCTCCTG 360
CTTTCCCAGC CCCCTTCAAG CCCTGAGGTT TCCATGCTGT TGTGGCGTTA AATTCTCATC 420
ACATGCAGGC CGGACAGGAG GTCTTCAATC CACTCTTCAG AACAGGAAAT GGAGTCAGGA 480
CCAGGCAGTT TAAGAGGCAT GGCTGAGACC TCACGCTGAG TGAGGAGAGA GGCAGAAAGC 540
GAGGCTGGGA ACACAAGGTT CTCGCTACAG GCGTGAGCTC CTTCTCCGTA GGCCCTTCCC 600
TTCCCATCTT CTCCCTGCCC CACCCACTGT CTCCCTGCTA CTTGGCCCCT GTCCTGCCTC 660
TCACCGTCAT CCTCAACCCT GGAGACGCCC AGCTTGCAGC ACCTGCCTTC TCATGAGACC 720
AGAATCATAT TTTTATGAGG GCTGGCTCCC CAGGGGCCCA GTCTTCCAGC CCCAGGCTGG 780
CTGCGGGGCA GCTAAGAATA ACCCAGGCCT AAGCTGGGCG TGGTGGCTTG TGCCTGTGGT 840
|
