| Tag | Content |
|---|
EnhancerAtlas ID | HS047-04916 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:114751380-114753000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr10:114752517-114752538 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | MYC | MA0147.3 | chr10:114751555-114751567 | GGGCACGTGGGG | - | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr10:114752742-114752757 | TGAACTCCTGACCTC | - | 6.22 | | Zfx | MA0146.2 | chr10:114752765-114752779 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I112991 | chr10 | 114751297 | 114752537 |
|
Enhancer Sequence | AGGGACAGCC AGCTCTCTTT AGATGGTCCC CACCATCTAG TCAGGGCTTG TTACATATGG 60
AGCAGAGACA GCGCAGGCTG CTGCTGTTTT CCTGGAGAAG GCCCCTGTCG GTCTGTTCAG 120
CTGTAGCTGA CCTTTCCTCC TTGTGCTTTT TGGGGAGGGA GCCTTGGAAG GAGTAGGGCA 180
CGTGGGGCAC TCTGCTTCCC GGCCCCACAC TGGCGAACCT ATGGATTCTG CCTCTGATTC 240
CTGAGGAAAC ATCACTGTGA AGGTGGAATG AGCCACATAC AGAGGTGGCT GTTGGGGCCG 300
GGGAGGGGTG AAACGCCCCC AGGGTGTACA TTGCACCAAA AGCCAGGCTG CATATAGACC 360
TCAGGATGGG CTGGCTTTTC TATTTATTTA GAAGTATTTC CAGAGGGTAA CCTCATTGGC 420
TACAAAGCAT GTCTGAACAA GAGCTCCGTT GTTCATTCCC AGCCCTGTTA CCCTGGCAGG 480
ATGCAGACTC CAGGCGGCCT GTTGGTCAGG CCTTGGACTC AGAGAGCAGT GAAGCCTGAG 540
GAGGGGTGGG GGGCAGAGGC GTGAGTGGTC TAGGGCCTCA GTCCCTCCAG GACACCCCTT 600
GCCAAGCGCA GAGAAAGCTC TGCCCATCCG TCCCCTCAGG CAGTGGGATT GGGCAACCTG 660
GGAAGCAGTG AATGTGCGTC GGTAGCATAG ATTCCATTCC GCACGCCACC CTCGCCTCCG 720
CCCCCCAGCC CTGGGAGGGA TGCATGCCCT CCGGGAGACA CCCAGACCCG ACAGAGAGGC 780
CTTTGTTGGA GCTGGAGGTG AGAATCTGTG GGCGTTGGGA TTCCTGGGTT CGAGTTCCAG 840
CTCACTGCCA ATTGCCCGAG TGCTGGGCGA ACATTTCTGG AATCAAAAGG AGTGCAGCCT 900
GCCCAGCAGG GCCTACGGGA GCCGGAGGCT GCAGGGTGCT AAGATTGCGT TATCTTTACC 960
AAGTGCCCGG AGCTCCTGGG AGGGAAGAGA GAGTCCTAGG ACTCAGGATA GGAGGTGGTT 1020
GGAGTTTCTC GAGGAAGACT CCATGCTTTG GTTCTGGCCC CTGGAAACCC CTCCTGAGGA 1080
CTGGACCTCC AAGCAGACCC CCTCTGTGAC TCCGGAATGC AGTGTTACTC TCTTATATTT 1140
TTCTTTCTTT TTTTTTTTTT GAGACGGAGT CTCACTCTGT CACCCAGGCT GGAGTGCAGT 1200
GGCACGATCT CGGCTCACTG CAACCTCCGC CCTCCGAGTT CAAGCGATTC TCCTGCCTCA 1260
GCCTCCCAAG TAGCTGGGAT TACAGGTGCC TGACACCGCG CCTGGCTAAT TTTTTGTATT 1320
TTTAGTAGAG ATGGGGTTTT ACCATCTTGG CCAGGCTGGT CTTGAACTCC TGACCTCATA 1380
ATCCACCCGC CTCGGCCTCC GAAAGTGCTG GGATCACAGG CGTGAGCCAC CGCACCCGGC 1440
CACTGTCTTG TATTTCTAAC GTCCCCCTGA CTTTTCTGAT CATGTAATTC TTAACTTTCT 1500
CAAAACTGAG ATTTGTCACG TGTCCTCTCC CCACTCCATT TTGTGAATCA GAGTCTTCCA 1560
GGGGCAGGAC CTGGAGAATG GGTCTTTATT AACACACATG TGAAAATGCT TTTGCCAGCA 1620
|
