| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06510 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:132662970-132664200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr12:132663148-132663162 | TGTCCCTTGGGATT | - | 6.24 | | Gata1 | MA0035.3 | chr12:132663975-132663986 | TCCTTATCTGT | + | 6.14 | | KLF16 | MA0741.1 | chr12:132663670-132663681 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr12:132663670-132663680 | GCCCCGCCCC | + | 6.02 | | Myod1 | MA0499.1 | chr12:132663005-132663018 | TCCAGCTGTCCCT | + | 6.16 | | SP4 | MA0685.1 | chr12:132663667-132663684 | CGAGCCCCGCCCCCTCC | + | 6.16 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 132663524 | 132663727 | | chr12 | 132663332 | 132663875 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132178 | chr12 | 132662746 | 132663750 |
|
Enhancer Sequence | CCGGCTGGCC CAAGTCGAAA AATAATGCAG ATGTCTCCAG CTGTCCCTGA GAACACTTCC 60
TGTTCCTTGA TCTGTGGCTT GTGATTCTCC CCCCGCCCCC ACTCCCCTTA CATGGGGCTG 120
TGGCTGCCCC CAGCCTTTCC CTTTCGTGAC CTCAGGATTG TATGACTGCA GGTTGGGCTG 180
TCCCTTGGGA TTCAGGGCCT CAAATGTACC TGCTGACCAG TTGAAGAGTG CTGACCAGCT 240
GTCCTGCTGA ACACCTCTCA ATCTGGATTT TTGACATTTC CCTGTGATTA AATTCAGGGA 300
ATCCAGCTTT GGTGACAGAG CCACTGAAGC AAGGCTGTTC CCTGCTTGGA GACGCACCCA 360
CTTTACACGT GTAGGGTGGC GAGTCTGACA AACGCAGCCA CAGGCAGCCC CCACCGGGGG 420
AGCCGGACGT TTCCATCCAC CCAGACAGCA GCGTTCACGC CCAGGACCAT GTGGGCCTGC 480
GCCCCGGGCC GCACCTGCCT CTCCTGCATT CCGTGTCTGG CATCTTGTGT CGTTGCCACC 540
CTGCGTGCCA TGTCTGGCTT CTCTCTCTCA GCGAGTGTCC TCCGTGTCTC CGAGTCGCGC 600
CCGTTCTGTT GTGCGTAAAT GCCGTTCTCA GAGCTGTTGT TTGTTTAGGG ATGTATCATG 660
TTTTCAGCTT AACATTTGTG CCATTCGTGT GCCCTGGCGA GCCCCGCCCC CTCCAAGTTA 720
CTGGCGTGCT GTGGGCGTTC TCGGGTTTCT ACTCTTCCTG CTGTCGCCAG CGCAGCCGAA 780
GCACCAAGCA GGAAGCTCTG CCGAGTTCTT GGCTTCAGGT AACGTGTCAG ACCCAGGGCA 840
TGAGCTCCAG TCCCTCTTGC CTCCACAAAG GACAGCACAT TTCCAGTTCA GGGTGCTGTG 900
GCCGACACCG TGCGTGTGGC TGGGGCCAGT GTCACCGCGA ATCTCGGCTG CTCCACGCCC 960
TTGCTGTGGG CTTGGGGCCA GTGCTTTACC TCTCTGGCCT CAGTTTCCTT ATCTGTTAAC 1020
AGGGTTGGTG TGAGAATGAA TGAGAAGGCA TGCACAAAGC GGGGCACAGC CTGCCCCAAA 1080
GCAAGGTCCC GATCCAAGTA GCTGCCGTTA TTGCTAATAG TGGTCCCAGC GGAGCCACAG 1140
TTGCTGAACG GTCCTGCAGA GATGTCCCCT TGGGTACAGG GCCCCCAGGG AGGAGCTGGG 1200
GACAGAAGGC AAAGCAGCTG GATCCACCCA 1230
|
