| Tag | Content |
|---|
EnhancerAtlas ID | HS165-03762 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr12:121323320-121324920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr12:121323575-121323587 | CAGTAAACAGAA | + | 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 |
| GH12I120885 | chr12 | 121323553 | 121324760 |
|
Enhancer Sequence | ACATGTCCTT AAGGCATCTA ATAGTCAGTA ATAATGCAAT GGTCAAATCC TGTTAAAGTA 60
TTTGTATCTA AACATGCAAG TGCCCATAAA AAGTTGTTTT TTTAATCCTC TGTCACTGGA 120
GCACTGATCA GCTATCCCTA TCTTCAACCA TCCTTGAGGC AATGACCTAC AACTATGGTT 180
ACTAAGGGAT CACAACTCAA TTGCCTCCAG GAGCTAGGTA AACAGCATAA ATGAGTGAGG 240
TAGAGATTCA GTGTACAGTA AACAGAAAGT GATGGGGACT CAGCCAAATT AGAAAATGTA 300
AGCTGTGAGT AAAGTCATTC AAACATTAAA ACTTTTTTTT TTTTTTTTTT TTTTGAGACA 360
GAGTTTTGCT CTTGTTGCCC AGGCTGGAGT GCAATGGCGC GATTTCAGCT CACCGCAACC 420
TCCACCTCCT GGGTTCAAGC AATTCTCCTG CCTCACACTC CTGAGTAGCT GGGATTACAG 480
GCATGTGCCA CCATGCCCAG CTAATTTTGT ATTTTTAACC TGTCCATGTT GGTCAGGCTG 540
GTCTCGAACT CATGACCTCA GGTGATCTGC CTGTCTCAGC CTCCCCAAGT GCTGGGATTA 600
CAGGCGTGAG CCACCACGCC CGGCCAAAAA AAAAAAAAAT TTTTTTTTCC AAATTCAGTC 660
CTTCTAGTAA TCAACTGACT GACTAGGAGA CACAATCTAT ACAACAGCCC ACTCTGAAAT 720
CTCCTTGTCT CTAAATTGTC TTAATTACAT CTGCTGGCAT TTGACACCCA GTCTCTAACA 780
CTATAAACTT CTGATGAAAA AGGATGTGGT TTATTCTATT TTAGTTACTA TAGCAGAGCC 840
CCAAAAGGCA TAAAGTCATT CATTAAACAC AGAGATCAAA TTCACAACCT TACTCTGTCT 900
AACCAAGTGA GCTGTGTGGT TAGGCAGTAC AAGTGGTATA TAACTGATAC ACAACAGGCC 960
AAAGCAGACC TTGAACACCT ATAACCATCA GAACAAGGAC CAAACGATAA CAGTTCCAAC 1020
AGATTTACTT GCTGAGAACT ATAGAATCTG GTACATCTCT AATGAGGAGG GAGGCAATTT 1080
TCTTCCTCCT GTGAATTTAA CTGCTCGCAA CCAAAAATCT GAGCTATGAG GAGCTTCCTC 1140
TCTGAAACCC TCTAAACACC CTCTTCCCCA CTGAAAGAAA ACCCGGCAGT AACAATATAA 1200
AACTAAAGAA CTAGAAATAC AGACTGATCA CACACTCATC TGTTTTTCCT AAAGACACAC 1260
AGATCATACA TGTGAGCAAA AATCTAGATC ATAAGTATTT ACCACCTCTG GAACCGCACT 1320
GTTCAATATG GGAGCTGCTA GCCACATGTA GCTACTGAGC ACTTGAAATG TGGCTAGTCT 1380
GAATTGAGAA GATCTTGTAC TAAAAAAAGT TAAAATGTCT CATTAATTTG TATATTGATT 1440
ACATACCATC AGTGATATAA TAATTTTTTT TTTTTTGAGA CAGAATTACC CTGTCACCCA 1500
GGCTGGAATG CAGTGGCACG ATCTCGGCTC ACTGCAACCT CTGCCTCCCA GGTTCAAGCA 1560
ATTCTTGTGC CTCAGCCTCC CACCATCACG CCCGGCTAAT 1600
|
