| Tag | Content |
|---|
EnhancerAtlas ID | HS062-13335 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr5:141080960-141082670 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr5:141081546-141081557 | TTTGTTTACTT | - | 6.62 |
|
| | 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 |
| GH05I141702 | chr5 | 141081568 | 141082567 |
|
Enhancer Sequence | TCCACCCTGG CTCAGCCCAG CCTTGAGGGC AGTGCCCCTG AAATCCTGGG CATCTGACAC 60
CTGAGTGCTG CAGGCCCCAG CCCACAGCAA GCACTGGCAC TCCCCTAAAT CTTTCCAGAG 120
CCAAGACCCC TCCCGCCGCC ATCTCAGAGC CTCACTTGGT CAGAGCGGCC AGGGGAGGCG 180
GGATCGATGT GCAGAGAACT CAGTAATAAT CCCAGCACAG GCAGCCAGGC TGCTGTATAA 240
AGACAGATTA AAAACTCATC GGGTTGAGAT GAGGAAATAA TTCAGATGCT TGGCCATAGT 300
GGGAACGTCT AGGGCTGCAG GTGCTAGTCG GAGTACATGT GAGGGGGTGG CCGGGACCCA 360
GATGACAGCG GCTTTTGGCC TTGGGAATCT GCACTCCCCC ACTTCGTTCC ACCCCCAGAG 420
CTACCTTCCT TTGCTGCCTG CCTTGAAGCC AAGGCTGACA AATCTCAGTC CCCCAGGGAG 480
CAGCGAGGGG GAGGCAGGCT GGGGGAAACC GAGAGAGCAC AGTTGCTGCC TAGCTCCACA 540
CCCTGGTTTA TTTCCTCCGC AGCACTGAAA TTATTTTGCT CATTTATTTG TTTACTTGTA 600
TGCTGTTTCC TCACCTAGAC TATAAGCCCC GCGAGGCCAG GGACCTGTTC ATCTGTGTAC 660
TGCAGTACCT CCAGCCCCCA GCCTACAAGA GGGACTTCTT AAGAACTGTT GAGTAAATGA 720
ATGCATGGAT TGGAATCCTG GCTCTTGCTG TATGACCTCG CTGAGGTTCC GTTCTCTTAG 780
CTGTAAAATG GGCACGGTAG TGGCTTCCAA AGGAGATCTC AGCCCAGCGC CAGGCTTCTA 840
GGAAGCGCTC AATTGAGGAT TTTGTTACAT TGATGTCAAA AGAAAATGGA AACCGTGTCT 900
GCCGCTTGAG ATGCCATCAG GGGGCGCCCT TGTGCAAGGC GCTCGGCGTG CTGCGCCTTC 960
CGCAGGCTCC CGGGTGAGCG CATCCAAGGC CGCCCCCACT CCCCGCCCCC ACCTTTGGGG 1020
GGCTTATCTC CTCCCCTCTC CGTCCCGTTC ACACGCCCAC CCTCACTCCG CCCGCGTCCC 1080
CGCTCCGGGG ACCGTCTCCG CAGCCCCGTG CCCACCCTTC CCCACCGCCA GGCCCAGACT 1140
CCTTCCGCCC ACGCGGCCCC ATATGCTGGA AAGAGCCTCC CACTCCCCAT CTGTCAAGCC 1200
ACTTCCTTGC CCCCATTCCC GGCTTCGCCG CTGTCCCCTC CTCCAGGAAG CTGGTCCTGA 1260
TTGAGGGGCA GAGGACTGCC AGCTTCGCCG GTCAACCGCC CGGTATCCCC GTTCCCCCAA 1320
CCACAGGGCT TTAGGGAAAT GCCCGCTGCC CTGGGCAGAT GACCCCCAGT GCTGAGCTCT 1380
GAGCCTCGAG TCAGGGTTTG CGAACAGATG CGAGAACTCT CTGTGCGCTT CAGACCCGTG 1440
GGGAAACCCT GCCGAGGAAA GGAGTGGGAG GGCCTGCGTG GAAGGACCCC TCGTGTCACG 1500
GCCGGCTGGC TGGGGGTGGG GAGCGGGCTT CGGGGCATTG CCGGCTGTTC GCCTGGAGGA 1560
CGCAGGGCTT GGGGAGCGCG GTACAGACAA ACACAGGCTG CTTTTCTCGC CCGAAAGACC 1620
GGTTTCATTT CGCAGATTGA TTATTGCTGC GTGAGTGTGT GTGTGTGTGT GTGTGTGTGT 1680
GTGTGTGTGT GTGTGTGTGT TTGGGCGTTG 1710
|
