| Tag | Content |
|---|
EnhancerAtlas ID | HS047-13428 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:81169710-81171040 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr16:81170710-81170727 | TGCTTGCTTGGAATTAC | + | 6.66 | | Foxd3 | MA0041.1 | chr16:81170331-81170343 | GTTTGTTTGTTT | + | 6.32 | | IRF1 | MA0050.2 | chr16:81170654-81170675 | TTCTTGTTTTAGTTTCTGTTC | + | 6.04 | | POU2F2 | MA0507.1 | chr16:81170402-81170415 | TTTATTTGCATGT | + | 6.17 | | POU4F2 | MA0683.1 | chr16:81170170-81170186 | ATGAATATTTAATGGT | + | 6.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 81169722 | 81169772 | | chr16 | 81170077 | 81170916 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I081136 | chr16 | 81169696 | 81171662 |
|
Enhancer Sequence | TCGCGGCCTT TGCAGGTGCT GAGTGTGCAG TCCTTCCCTT CCCCCGTTCT CAGCAGAGAG 60
GTTAGGCACC ACCGCAGCAG AGAGGCCTGC CCTCTCTTGA TCTTCCCCAA CCCTATTTCT 120
TACCATAATT CACACTTATA TGTCTACTTG TGCATTTACC TGGTTGATGC CATCTCCCCA 180
AATGGGCTGT TCATTCCAAA GGCAGCAACC TGTGCTGTGT TGGCAGGGAC TGGGGTTGGA 240
AGTGGGGATT GACTTTACAT GGGCAACAAA GAACCTTTTG GGCTGACGAA GCTCTTCTAA 300
ATGTGAATTG CAGTGATGGT TACATAACCC TATACATTTA CTGAAATCAA CAAATTGTGC 360
ACTTACAATG GGTGAATTTT ATGTAAATTA TATTCCCAAG CCATCACAAG GCCTGGCCCG 420
CAGCCAGTGC TCCCTGAGGA CTTGCCAAAG GGGTGACTGA ATGAATATTT AATGGTCTGG 480
AGCCTAGCAT CTCTGTGGAG AATTGAGAAG ATTTTAATGG ACCTCTCAGA TCTGCAAATC 540
TAAAACGCTG TCCTGGAATG GAAGAATACA GGCCCTGAAG AGGTAGCCAC ATTGCACTGT 600
GAGGCACGTG CATGGCATTT GGTTTGTTTG TTTCTATTTT ATTTTCCCTG AAAGGCAAGA 660
CCATTGCCTC AATGATTCCA CGTTGATTCA GTTTTATTTG CATGTTTGTT TTGTCATTAC 720
TGTCACCACC CTTGGGAATT TTGGTTGGGA AGTGAGAAGT CAGGCTGGGA GGATGGGGAC 780
TGGCCAGTGG CCTCCTAGAG CAGGGGTGAG TGTGGCCGTA TTTCAACAAA CCTCTATTTA 840
CAAAAACAGG CAGCAGGAGA CATGTGGCCC CCCAGCTGTA GTTTGCAGAG CTTTGTCCTA 900
AAATTCTAAT TTGCGGCCAC TTTTTGCAGC CTCCTGTAAA CCGATTCTTG TTTTAGTTTC 960
TGTTCTAAAG CCCAGGGCCC TGAGTCTCGG AGAAGAAAGC TGCTTGCTTG GAATTACACA 1020
GAGAAGGACC GCCCATGTGG ACAGCTTCGT CCCTGAGGCA ACTCTTCTAG CTGGCAGGTC 1080
ATACTTGGGT GTCATGGAGA AATGCCAGGG AACGAACAAA CACAGATACT CAGGAGACAA 1140
TGGAGTCACT TTTTTCCTGG CTCTTTTGGG GATGGCTCAC AAACTGGGGG TGAAAAGCTG 1200
ATGAGGAACA AAGGTCTGGG GAGCTGGCCC AAGGCCCAGG ACCCCCAACA GGCTGCACTC 1260
TGCAGGGCTC ACTGAGCCTC ATCAGGGCCG CAGCTGGCCA GACCCTGCCT CCAGCCACCG 1320
AGGCACATTA 1330
|
