| Tag | Content |
|---|
EnhancerAtlas ID | HS049-05403 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr22:45948900-45950310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:45949809-45949828 | TAGCGCCACCTGCTGACCA | - | 7.18 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_02043 | chr22:45943776-45951130 | Aorta | | SE_03088 | chr22:45946883-45949439 | Bladder | | SE_03088 | chr22:45949443-45950539 | Bladder | | SE_26724 | chr22:45943946-45950832 | Esophagus | | SE_32122 | chr22:45946042-45950553 | Gastric | | SE_34210 | chr22:45944514-45950338 | HCC1954 | | SE_39193 | chr22:45944312-45950508 | IMR90 |
|
| | 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 |
| GH22I045547 | chr22 | 45943553 | 45950732 |
|
Enhancer Sequence | GGCCTGAGGG TGTAACACGG TGGACGGTGG CAGAGATAGA GCCGTCGATG GCCCCCCTGC 60
CTTGGCCAGT TCCTGGGGCT TGTCTCCCGG ACGACGAGCG TGTGAAAGTC AGGAAAATGC 120
CGGCAGGGAT ATCCACAAGC ACCTGGGGTG GCCAGAACTG CCGTGCCTCC CAGGAGAAGG 180
AGGGGGCCTA GAGGGCCTTT TTTCTCTGGT GTGTGGTGGC TTAGGATCAT TTCCATAGAG 240
CTTGAGGTGT TAGGGTCAAA TGTGTTGAAC TGGCAAGTTG GAGCACATTG TCCTCTAACG 300
CATGACATGG CCCAGGATGG GTGGCCTGCT GAGGGGACAT GTCTGGAAAC CAGGGCCTGC 360
GTGGCAGGGG GGGACGGGGC GGGCTCGCCT ATGCCCTGCT CTGTAATACA TTCAGTGATG 420
ACAACCCGTC CCTGACCTAG ACACACTGGC TAAAAGGGAT TTTTGGGCCG TTCCCAGTCT 480
GACAGGCAGT TTGCCAGACA GTTATGTTTC TGGTGTTTTA AAAAGTTTGA GTAGAGCGAA 540
GTACGATCAT TGAAGCCAGG ACTTACCAGG AAAATCAAGG ACATGTTTAT TTTTGTGCAT 600
TAGTCATTTG CAAAGCACAT AGCGGGTGCC CCAGGCCCTG CTCTTTGTCC AGAAGGAGCC 660
AGCCCAGAAA CTCCTAGTGT AGAGAAGGTT TTGGGGTGCT CTGAGGAATG ACTGTGTGGG 720
GTCGGAGGGG GAGCCTCCAG GGGAGGAGTG ACCAGTCGCT GTGTGTGATG ACGGCGGGAG 780
CTGCACCAGA ACACCACGCA CACCTCCCAT TGCTTTCCTC CGCTTCCCTC TGGCAAAACA 840
AATTCCATCC CTGGTTAGTA CCCGCCATGC TGAGAGAAGC GGGAAGCCGA AATCCCACCA 900
GGGCGACTCT AGCGCCACCT GCTGACCAGC CCCATCCAGG CTGGTCCTGA AGTTGCTGGT 960
GTGTGTGCGT GTGCGCGTGC TTGTGTGTGT GCATACATTG TGTGTGTAAA AGCTTTGAAG 1020
TAAGACAGGC CGACTTTGAA AGCCAAGCTT GCCCCTTACG ACACACCACG GAGCTATCAG 1080
CAAGTTCTGC ATCCTCAATG GGCGTCTGTC TTCCAGCCAG TAGAGCGGGA GGACGATGGG 1140
AGACAGTGGA GGGAGCGAGT GGAAGGAAAG TCTGCTGCTT GCAGCCTGCT CCCTGCACCC 1200
GGAAGCGCAG TTCACCTGCA CCCGGAAGCA CAGCTCATGG GTCCCATGCT CCTCCCCCAG 1260
TTCACGGACG CTTTGGTCAT AGCTCCTCAG AGGCCCCCCT GGGGGAGAGC TCTCAGATCG 1320
CCTGGAGCAC TCCCGTTTGG CCTGGACCTG GGCATCTCTG GGGCAGGCCA CCGCCAGCAG 1380
CACCCGTGCC CACCTTCTTT CCTGCCTCTG 1410
|
