| Tag | Content |
|---|
EnhancerAtlas ID | HS047-21112 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr20:31273320-31274420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr20:31273613-31273624 | TTTCTAGGAAA | + | 6.14 | | Stat4 | MA0518.1 | chr20:31273613-31273627 | TTTCTAGGAAATTG | + | 6.22 |
|
| | 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 |
| GH20I032684 | chr20 | 31272616 | 31274823 |
|
Enhancer Sequence | GAGAGAGAAA GAAAGGTCTT GCCAGTACCT TCTGTCCAGG CCTTGCAAAC CCAGAGTGGC 60
CCCAAGTCAG TGGGGTCTCC TTCAGGCCCC ACAAGGCGAG CTGGAGAGCT GCTGGAAATC 120
AGCTGATGTG CTGGCAGAGC TCCAGCCCAG AGTTTCTCAT GACTTGGAGC CGACATATTC 180
CCAGCATCTC AGCTCATTTC AGGCAAAATC ATCGAGCATA TTTTAGGATC AGCAAAAACC 240
CACAATGCCT TTGGCCGAGC ACTTTCCCTC TTCTTGTTGA AGCCCAGGGG TATTTTCTAG 300
GAAATTGAGT CCATCTGTTT CTGATTCATT CGTACTTAAC TCATCACCGG GCTGTTTTGT 360
AAGAGCCCTT TGATGTGAAA GCCGCCTTAT TCCATAAGCC TCTCTAAGCC TTTATTTAGT 420
CAACAGCAGG TAAACGGGCC TCTCCAAAGA GGCCAGAGGC AGCATATTGA TCTCCTGCTA 480
CACAAAGTCC ATGTGAAGGG AAAGTGTGGC CCAAACGCCT GCCTGGAGAC ACTGAGACTC 540
CCCGTCTTTG GGCCTAGCAG GGCAAAGCAG ACCACTCCCT AGCCCTGACC CAGCGCTGTG 600
GGGCTCAGCC ACGCAGAGGG ACCTCCTCTG GCGACTCACT AACTCTCCTC CCCAGGCACT 660
GTAACCCAGC GTCCTCCTCC ATAACTCACA GCCTTGCTAC ATAGATTTAC GATTTCCTGT 720
ATGTTGCCTA AGAGTTCCTT TTTTTTGGTG GGGGACAGGG TCTTGTTCTG TCACCCAGGT 780
TGGAGTGCAG TGGTGTGATC ATGACTCACT GCAGCCTTGA CCTCCCAGGC TCAAGCAATC 840
CTCCCTTCAG CCTCCCACAT AGCTGGGACC ACAGGTGTGT GCCGCCACAC CTGGCTAATT 900
TTTGTATTTT TTGTTGAGAC AGGGTCTCAC TATGTTGCCC GGACTGGTCT TGAACTCCTG 960
GGCTCAAGTG ATCTGCCCAA TTCAGTCTCC CAAAGTACTG GGGTTATAGG TGTGAGCCAC 1020
CGTGCCCAGC CCCAAGTGGT TTTTTTTTGT TTTGTTTTTT GAGATGGGGT TCAAGCGATC 1080
CTCCTGCCTC AGCCTCCCAA 1100
|
