| Tag | Content |
|---|
EnhancerAtlas ID | HS042-11472 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr12:119534280-119535370 |
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 | AGAAGTGCTT AGTTAGCTCA GTGTCTGGTG TGCAGGAGGT GCTTGATAAA TACTAGCTGC 60
TGTGATGATC AAGTGATGTG GAGAGAACGC TGGGCTGGGA GTCAAAAGGT GGCAACTCTA 120
CTAGCCAGAG CTATGATATG AGTCACTATT TGCCTTGGGC AAGTCCCCTT GCCTCTTGGG 180
CCTCCCTTTC TCCACTCTGT ACAGGGCTGA GCTGGATCTG GGGTTCTTCC CGCTCCACCA 240
TTGTTGGTCT CTGATTCCCC AAACAGTGTT TAACTCAATC TAGTGCTTGG GGCATGAGGA 300
TCTGCACCCA ATGCTGGGCC AAATGAGAAC TTTGTTGGGA GCAGCTGGCT GATTGGCTCA 360
GTGAGCAAGA GCTTTGATGG GAAGCAGGGA AGCAGCTAGG GAGCCAGGCC TCTTGAGGAG 420
TTTTGCAGAA AAGTTCAGCC CTGACTCTTA TCGGAGCCTT GGAATCTGCC GGTTGCCATG 480
ACTACAGAGA CAGCATCTAA GCTCCAGGTC TCTGATTAGC AGGAACAGAG CCGCCGGGAG 540
GCCTTGAGGA ATTCGGCACT CGTGGCTCCC TCCCTCCATC TGTGAAGTGG AGTGTGCCGG 600
CCCTTGACTC CACTGTTTTA GCTGTCCCCA AAGATTTCGG CTTCTTTTAA GTATTTTTTA 660
AATGCGATAT AGAAGGAAAA TGAGGCAACT GCCAGTACTT CTCAGCAAAG ATGGAACACA 720
GAATTTTTCT TAAGGACCTG CAAAGATGCA AGGCTGGAGG TAGGGAAGGG AGATAGGTGG 780
GGCTGTGGAG GGCTGAGGGC TGTGGCTGAA GCCTGATTCC ACTGCAGCGT TGAGTGACCT 840
CAGACTCTTT ACTTGTACCT CTGCTTCTTT ATTTGTAAGG AGAGTTAGGA TCCGATCTGT 900
GGTTCCCACA TGAGATCGGT AATCACAATT CATTTGTTCA TCCATCCATT TATTCATTTG 960
TTCATTCAAT GAATGTTCAT TGAGCAGGAA GCTACACGAC GGTTTCCTTC TTCCTCCCCT 1020
CAGCATTTCC TCTCTGCCTG GCAGAATTCA TTTTATTTCT GTTGGTTTTA TTGCAAAATT 1080
CCAGGTGGGA 1090
|
