| Tag | Content |
|---|
EnhancerAtlas ID | HS023-06667 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr13:28046740-28048150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr13:28047845-28047859 | ATTGTTTATCTTGA | - | 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 |
| GH13I027473 | chr13 | 28047201 | 28047350 |
|
Enhancer Sequence | GCTGGGAGCA AAGCATGTCA TCAAACCAAA CTGTGTCCAT TTGCCTGTGT GTAACAGAAA 60
GCCAAACATT GAGTCACTAG GTTTTGGCTG TGAGAAAGGT TCATTGTGAG TTGACTGACA 120
AGGAGACAGG GGGCTATGCT CAAATCTGTC TCCCTGAGTT GGGTGCTGGG TTGGGTTTTT 180
ATAAGCACAA GGTAATGAGG TGTGATCTGA TTGGATCTTG CAATGAGGTG ATGCCAGAAG 240
GCATGATCTG ACTGGATCCT TCCATGGAAT GTTTGCATCT TAACTCAATC CCAGCTCCTT 300
AAGCACTTAG GTCCCACCAG TGGTTACATG CTTGGTTCAT CTGGGCATGC TCAGGTTATG 360
TGATCTTCAA CCTGGGAGCC CGTGGCAACT GAAAAACTCA CAGGTTTGTT AAATGAAAGT 420
TGAACCAGAT TGGTTTGATG GGTTACCAGC AGAGGCCTTT GGGGGTTGGC TGGAGCAGCA 480
CCACCCCTCT GTGGTGTGCA CCTGGAGCAC CCATCCACAT AGGCCCCAAT GATAAGATAG 540
CGTTAACCAC CAGCTGTGCT GTAGCAACCC AGCCCCTGTG GATGGCCACA TAGTGGGTGA 600
AGAAGTCCCA GGTTTTAACC CGGGCTTCTT TATTGGAAAC TACATGCTTC TTCTCAAGTG 660
GCTTTGTGGG CACAGAACCC AAGAGCTGAA ACAATTCTTT CCCAAAAGAG GACACTGAGA 720
TTATTGGGCA GGAAGGAAGT TTTGGGCTTA CTGAAGAAGG CTTGTCTGTA TAAAATTGCT 780
ACTATTCGTG ACATCTGTTC TTTAGATTAT GTTTCCTGTG CTCTGTTTGT CAACTTGGAG 840
CACCATAATG CACTTTGATT TATGGCTGCT GTCCTTAAAA CCCACCTGAA AATAAGAACC 900
CCCTCTTAAC CTGTGAACAG AACTAGAACC CTGCCCCAAT AACAGCTAAT ATTAATTTTT 960
ATTTAGTGCT TGCCAATCAT CTCACAGCTA GGGGTGATGA AAGTGGATTT AACCAATATG 1020
CCTTAATGCT ACTGTTTATG TGTGTCTGGC ACTGTGCTGG GTGGTTTCCA TTTTATTCCT 1080
CATCCTGAAG ATAGCCCTGA AAGATATTGT TTATCTTGAT TTTTCAGATG AGGAATCAGG 1140
GCTCAGAGAT GTTAAATAGC TTGCCTGGTA TCACAAAGCT AACATGTGAT TGGCTCAGAT 1200
TTCTAAACCT GCCTCTGTCT GACCCCGATG CTATGTCCTT CCCACTACCC CACACTGCCC 1260
TTCCAGCAAA GGTAGCATCC ATGTGGAGGC AAGAATTGGG CTCCAATTTG CAGGAAGTGC 1320
AGATATGTTG GGGAGAGACT CAGGATATCA GAGCTGGAAG GAACGATTCA ATTGAGGGTT 1380
TTCCAACTTC ACGGTCCACG GACAACCATC 1410
|
