| Tag | Content |
|---|
EnhancerAtlas ID | HS007-11686 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr3:124724630-124725730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr3:124724740-124724751 | AGCCACACCCA | + | 6.14 | | POU2F2 | MA0507.1 | chr3:124725541-124725554 | CTAATTTGCATGT | + | 6.2 | | RELA | MA0107.1 | chr3:124724777-124724787 | GGAAATTCCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27692 | chr3:124719214-124724973 | Fetal_Intestine | | SE_28593 | chr3:124718717-124724917 | Fetal_Intestine_Large | | SE_42314 | chr3:124724382-124725134 | Lung | | SE_46146 | chr3:124721931-124724884 | Osteoblasts |
|
| | 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 |
| GH03I125005 | chr3 | 124724383 | 124725134 |
|
Enhancer Sequence | CCTCAGGCCT CATCAGGCTT TCGACAGAGG AAAGCTCTCG TCCTCTGAGG TCTCCAACTG 60
AGTCATGCCC ACCACTTCAA GGGGGTGCTT CAGTTTCCTC TTGTCCTTAG AGCCACACCC 120
ATCCAAACCC CATTCCTCTT GGTCAGAGGA AATTCCCATT TTATCATTGA TAAAGGGGGC 180
TTCCAGAGGT CAGGCAACTT CCTAAGAAAG CTCACCCAGG CTCCCAAGGG CCACCACTGG 240
CATTGGAGCG TATGCGTGTC CATCTTCAAA GCTCTCCTTT CCCCTATAAC CTCTGTGCCC 300
TGAGGAATCT GATATCCTAA GGACACCCAA GGGACTTGAG AGAAAGAAAG GTGCCAAGCA 360
TGTGTCGTGG GGCTATACTC CATGGGGCTG CCGACTCCAT GATTATAAGC CACATAATGA 420
AAACAGCCCA TATTCAAGAC ACTGTTGGGT TCGGAAATGA AAAAAAGCAG CCTCATTTTC 480
AAGGCCCATT TCACTCATAA AATAAAATTC CAGTTAACAT CAATTTGTGC TGATTGAGCC 540
TGAGGGGAAC GGGACTTACA AATGGGCAGG CAACCAAAAT TTAGTATGGT GTGTTTTATT 600
GCTGGCTCTT ATCTTCCTTT ATATTAAATG CTTATCTTTC CCTCCGGATG GAAAACAAAT 660
AACTCAAGAC ACAGAAGTCC ATGAAGCTGC TCTTTCCCCG AAAGCCTGCA TGCCGAATTG 720
AGAAAAAGAC CCACAAATGA GCCAGGGAAA ACATTTAACA TCTTACACTT ACTGTCTAAA 780
GCGCTTAATC CTTACTTAAC ATCTTTTTGC TTGTTCTACA GTTCAGTGAA GCCAGCTGCT 840
TAGGACTCTT TCTGAGCAGC AGGGAGCTCT CTGAAAACAT TCTTGGCCAA ATGAAAGCAT 900
TTCAGCATGC TCTAATTTGC ATGTTCCTCT GATGTTTATG AACAATGAAG CTAAATGACT 960
TGAAAAGGGA AAGATGATTG TGAAGGCGAT AGTGCTGCTC TCCTCCTGAG CTGTGCTACC 1020
TGTGGAACCC TCTGCACGCA GGCTTCCAGA ACAATGGTCC TGCTTCTTCA CTTTCTCATC 1080
TCACGTGTCT AGGCTGATAC 1100
|
