| Tag | Content |
|---|
EnhancerAtlas ID | HS193-22547 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr22:46853270-46854270 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr22:46854105-46854120 | AGGCCAGAGTGACCT | - | 6.69 | | PRDM1 | MA0508.2 | chr22:46853387-46853397 | GTGAAAGTGA | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 46853413 | 46853936 | | chr22 | 46854004 | 46854197 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046456 | chr22 | 46852796 | 46854389 |
|
Enhancer Sequence | CCCTGGGGTC CTAAAAGCAG GTGATCAAGA ATAAACTCAA CCCTAACAAA GCAGCCCCGG 60
CCCACTGGCG CACACAGGAG GGGCACCCAG GTCTGCCTCT ACCCAGACAT GAGGTGAGTG 120
AAAGTGACTT GTTGCCGTCC CCCTCCAAGA TGTTCAGCCT TGCAGAAAAA CCCGCCTTTC 180
CTGTGATATC AGAGCTGCCA CTCAGGAATG CGCCCCATGG GAAGACGAAG ACGCTACCGT 240
GATGACAAAT CACCCGCTCA CAGCGCGGAC AGAGATGAGG AAGGCTTCCC GGGAATGCCC 300
AGAGGCCTGG AGCCCACACT CCCGCTCACA GCTGTGATGA GCACGAGGGC GGACCCACAT 360
GGGAGCTTAG CCAGTGCTCA CAGGGGCAGG ACAGAGTCAG ACATACCTCG GCGTCCCCTA 420
GGAAGGGGCA GAGGAGACAG GGAAGGGAAG TGTACGTGAT TGGAGGGTCC GGTTCCTCCT 480
AGCTCAGCAC CAGAGGCAGC ACAGGCAGCA CTCTGACCAC AACACAGAAT GAGTTTCAGG 540
CCCCGAGGGC ATTATCTCTG GCCTACGTGG AGGGGCGGGA TGGCCAGCCC TTGTCTCATT 600
TGCACACGGT GCCTGCTGCA GACCCGCGGG CATGTTCTGT TGGGCGGAGG ACGCTGCTGT 660
CTGCATCTAG TGCAGAGGGA GGAAGGTGAC AATGACAAGC AAACACCACC ATGGGGGTGA 720
GGGCTGCAGG GAGGACAGAG GAGTGGGGAC AGGGAGGGAA CATTCAGGGA AGACCTGGGG 780
GAAGGTGCGC TGGAGGGGCA AGCACCACGG TGAGAGAGGC CAGTGTGTGT CCCGAAGGCC 840
AGAGTGACCT CAGCCTGGGG AGCCGGGGGT GAGGCTAGAC CTCTGAGTGC CACAGGCCCA 900
GTGACTGCAC TTTATACTGG AGCACCGGTC ACCCCAGGAA GGCCTGAACA CTGATGTGAC 960
AAATGCCTGC TTCACCAGGC ATCCTGGGCG CTCCGTGAAG 1000
|
