| Tag | Content |
|---|
EnhancerAtlas ID | HS052-24649 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr22:24026960-24028050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr22:24027559-24027570 | CATGAGTCACT | - | 6.14 | | KLF5 | MA0599.1 | chr22:24027543-24027553 | GCCCCGCCCC | + | 6.02 |
|
| | 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 |
| GH22I023684 | chr22 | 24026783 | 24029423 |
|
Enhancer Sequence | ATCTGGCTCA GAGCAGATGA TCCCCTGCAC CTCCCACCCT GAATCACACA GCTACACCCA 60
GCACATGCTA CAGAGGCCCA GCACACTCTG GATCACATCC AGAAACTCCA CAATAGGGGA 120
GGAGACATGC TGTTTCCCAG GAAGGGCAGC TCCCCAGACT TGGTCATTCT CAGACTCCTC 180
CAGTCAAAGG CCGGGCACAG CCAGCTGGGA TCGCCATGCT TCACTCTGAC CCACACGACT 240
GGCCTTGCCT CCTCTATGGG AAGAGACCCC TCAGCACAAC CTCAAACCGA GACATAACAG 300
GACAGGACAG GCTGGATGCT AGAGAGGCCA GCCAGATCTC CACACAAAGG CTCTGCTCTT 360
AAGCAGGAGG TAGCCTGAGG GTCAAAGGTT TCCTGAAGCA ACTCAGGTGA GACCTCACAT 420
ACAAGAGCCC CAAAGAGGCT GCAAAAGCAC CAGCTCAGCC AGCCAAGAAC CCAGGTGTCA 480
CACCCTTCTC AGACCACTGA GGATCGCTGG GATTCAGCAG GAAAAGGTGG ACATGACAGC 540
TGATGGACCA ATACTTCCCA ACACCCTTCC AGCAAGCAGC TGTGCCCCGC CCCTCCCCAC 600
ATGAGTCACT CAACTTCAGT CCTGCACATG GATGCCTTTG ACCATGGGGT CATGGCTTTG 660
GTCTCCTGCC ATAGGGGCAG TGAGAGGAAC AATGGTGGTC TGGGAAGGAG GATCCTAGAC 720
TGGGTGTCCC ACAAGACCAG GCTGTGACAG ATCCCAGAGC CAATACTCAT GCGCCAGCCA 780
GTCCCCAAAC CCAACAGCTA CCCAAAGCCC AGGATATAAA TAGCCTGTGC ACTGCTAAGC 840
AGATACTTCA GGGAATGATC TGCTGGCTGT GAAGAAGATG CGGCCTCAGT AGGGTTCCAC 900
GAGCCTTCTG CCAGCAAAAT CTTCTTTGCT TGGATGCCCA TTAGAAACAC TAAGGGAGCT 960
CTTCAAAGGA ACAGGCCAGA CATGGTGGCT CACATCTGTC AACTCAGCAT TGTGGGAGGC 1020
TGAGGCAGGA GGACAGCTTG AGGCTAGGAC TTTTAAGACC AGCCTGGGTG GAACAGTGAG 1080
ACCCCACCTC 1090
|
