| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14868 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:123882710-123884280 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX2 | MA0706.1 | chr12:123884249-123884259 | AGTAATTAAC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 123882766 | 123883905 | | chr12 | 123883000 | 123883784 | | chr12 | 123884027 | 123884111 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I123397 | chr12 | 123882456 | 123884323 |
|
Enhancer Sequence | CCCAGCTACT TGGGAGGCTG AGATGGGAGA ATCACTTGAA CCCAGGAGAC GGTAGTTGCA 60
GTGAGCCGAG ATCGCGCCAC CGCACTCCAT CTTGGGTGGC TGAGCAAGAC TCCGTCTCAA 120
AAAAAAAAAA AGACAGCACT GCAGATGGTG AGGTGGTGCC AGACCACAGA ATCCCAGACA 180
CCTCCCAGCC AGGGTTGGAG CTGCGGTGTG CCCACACACA GGGCCTCTGC TGAGCGTCCA 240
CCAAGGGCTG CTGTGGACTT TAGGGTGGGG GGAGCCGAGT TGGCCTTGTT AATAAGAAGC 300
AAGAGTTTGT GCTGGGCAGA GTGAAGGCTG CGATGGGACA GGATGCAGGT CTGCTAAATC 360
TTGCAGCAGA TGAGCAGAAG GGAAGAACAC ACTTGCTTCC CTAAAGCACA GTCTGCAAAC 420
ACAAGAAAGC TCGCCCTGTT CCTGGACCGG GAGCCGTGCT TTGCCCCCCA CTGTTTGTGT 480
TGGCTCTGCT GAGTGCAGCC ATGCAAGCTG TTGCTGGCCA GGGCAGGGAG GCCATAGCTG 540
GCCGGGATGA CGTGGCTAGA GCTGGTCAGG GTGGAATATT TTCTGACTGC ACAGATAAAG 600
CCCAAGAACG GGACAGCTGG GGCTCATCTG AAGGGTGGGG TCAGTCCTGA CTTGACTGCC 660
ATGCTGGGCC CAGGCTGTGG ATCCAGGAGG GTGGGGCATA ATACAGCCTG TTGTTGGCCA 720
GATGGTCTGG GGTGAAACTG CAATTCAGAG CCTCTTATAT ACCTCCACTG AGGCTGAAGA 780
CAGCAGCCAG GGCGGGCCTA GCGCCAGGGC GTGGGTCCTG GGCAACAGGG TGGGATCAGG 840
GCTGCTGGAT TTGGACACAA GGTGGGCCTT GGAGAGATGC CCTATCCACC AAGTGCTTCA 900
CTGCAGGGGC CCCTTGGCCG GCCAGCCTGG CTGTGGGTGG GGTGGCAGCC AGCAGCGGGG 960
CAGGGACCAT GCCTCTTGGC AATGGCTGGG CTTCCTCATG CCCAGCTCGG CCCCAGGGCC 1020
AGATGTGCAA GCAGCCTGCT GATTCCGCTT GGGAAGGTCC CCTCCTTCCT GGTCACAGGC 1080
GCTTCTCAAC TGCCCTAGTT CCAACCTTGT ATCCCTCCCA CTCCATCTCC TTCTAGGCCC 1140
ATTTGTGGGT TCCTGCCAGA AGTCCCTTTA GAAAACCCAG GGCTGGTTGT TTGCAGGCCC 1200
CAAATTCCAG GCCTTTGGGA GACTCAGCCT CCCTGGCTTT GTGCCGGGGC ATCTGGCCTG 1260
GTCCCAGCTT CCCTCTGCGC ATCTCCTACC TGCCGTGTTT GGTCCCAGCA GAAAAACCCC 1320
CATTCCACTA CCCCGGTCTT TCCATGATCA CTCCCGTTTA CATGGGCCCC CGTACTTCTC 1380
AGCACTCTCT GCACACTTGC AATGAATGGG TCACACAGCA AGGTGGTTAT GTGTGTGATG 1440
GTGGTGGTGT TGCTTTGAGG GCCTGCTGTG TGCACTGTTC TAGACCAGGA GATTCCACAG 1500
TAAACTAGAC CAGCCCGTAG GGCTTGTTTT CCAATGGGGA GTAATTAACA ACAAAAAAGA 1560
CACCAGCTAC 1570
|
