| Tag | Content |
|---|
EnhancerAtlas ID | HS134-15277 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr12:119534210-119535130 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr12:119534628-119534643 | CTGATTGGCTCAGTG | - | 6.71 | | RFX1 | MA0509.2 | chr12:119534750-119534766 | GGTTGCCATGACTACA | - | 6.79 | | RFX1 | MA0509.2 | chr12:119534750-119534766 | GGTTGCCATGACTACA | + | 6.81 | | RFX2 | MA0600.2 | chr12:119534750-119534766 | GGTTGCCATGACTACA | - | 6.42 | | RFX2 | MA0600.2 | chr12:119534750-119534766 | GGTTGCCATGACTACA | + | 6.51 |
|
| | 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 |
| GH12I119096 | chr12 | 119534681 | 119534830 |
|
Enhancer Sequence | TGTTCTTCAC AGTAGGGATG GTAATGCTGG CTCATGGGTT TCTTTGAAAA CTTCAATGAG 60
AAGATGAGTG AGAAGTGCTT AGTTAGCTCA GTGTCTGGTG TGCAGGAGGT GCTTGATAAA 120
TACTAGCTGC TGTGATGATC AAGTGATGTG GAGAGAACGC TGGGCTGGGA GTCAAAAGGT 180
GGCAACTCTA CTAGCCAGAG CTATGATATG AGTCACTATT TGCCTTGGGC AAGTCCCCTT 240
GCCTCTTGGG CCTCCCTTTC TCCACTCTGT ACAGGGCTGA GCTGGATCTG GGGTTCTTCC 300
CGCTCCACCA TTGTTGGTCT CTGATTCCCC AAACAGTGTT TAACTCAATC TAGTGCTTGG 360
GGCATGAGGA TCTGCACCCA ATGCTGGGCC AAATGAGAAC TTTGTTGGGA GCAGCTGGCT 420
GATTGGCTCA GTGAGCAAGA GCTTTGATGG GAAGCAGGGA AGCAGCTAGG GAGCCAGGCC 480
TCTTGAGGAG TTTTGCAGAA AAGTTCAGCC CTGACTCTTA TCGGAGCCTT GGAATCTGCC 540
GGTTGCCATG ACTACAGAGA CAGCATCTAA GCTCCAGGTC TCTGATTAGC AGGAACAGAG 600
CCGCCGGGAG GCCTTGAGGA ATTCGGCACT CGTGGCTCCC TCCCTCCATC TGTGAAGTGG 660
AGTGTGCCGG CCCTTGACTC CACTGTTTTA GCTGTCCCCA AAGATTTCGG CTTCTTTTAA 720
GTATTTTTTA AATGCGATAT AGAAGGAAAA TGAGGCAACT GCCAGTACTT CTCAGCAAAG 780
ATGGAACACA GAATTTTTCT TAAGGACCTG CAAAGATGCA AGGCTGGAGG TAGGGAAGGG 840
AGATAGGTGG GGCTGTGGAG GGCTGAGGGC TGTGGCTGAA GCCTGATTCC ACTGCAGCGT 900
TGAGTGACCT CAGACTCTTT 920
|
