| Tag | Content |
|---|
EnhancerAtlas ID | HS047-20542 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:233285680-233286770 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr2:233286089-233286100 | GCGCCTGCGCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33043 | chr2:233285036-233286673 | H1 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I232418 | chr2 | 233283041 | 233286618 |
|
Enhancer Sequence | TGCCTGCCTG CCCGAGGGAG AGGACGCGCC GGTGGCTCCA CCCTCCTCCG CCCGTCCCGC 60
GCTCCCTTCC TTCCTCCTGC GACCCTCTGG CTACCTGGCA GCGCGGCGGC AGCGGGGACC 120
TGGGTCGGGG GCCGCGGAGA CAGGCTTCCG AGGGTCGTGC GCGGGCTGCG GTAGGGGACT 180
CCGGATCCAG TCGCATCCCG GGACTAGTGA GGGTAGCGGG TACACCCGGC AGGAGTCCCC 240
TCCGATCCCG TGTCCCCACT CGGAACCGCC CACCAACCGG TTGGAAAGGA GCTGGAGCTA 300
CGCAGCTGGG GGCCGTCATG GTCCAGCCCA CAGCCCTGGA GCACCACCCA GGGAGGACTC 360
CTCCTAAGGA TTGAGAGGGC GCTGACGGAG TGCCTGGGCT GCCCGCACAG CGCCTGCGCA 420
GAGCTCACCT TCACCAGGGA GCTTCCTTTA CCTCCTCGGA ACCCCTGTCC GGGATCAGCT 480
CTCCCCGGGG TGTCTGGGCT TCTGGTTGTC TCGCCCCCTT CCCCCAGCCT CTGATCCACG 540
GAGAGCAACG CAGAGCCCTG CCAGAAGCAG GCCTGGGGCT GTGAGTGTGG CCCCCATGGT 600
CCCAATAGGC GGTTGTCCCA GAGAACAGCA ATCACTGCCT ATAGGAGGTG ACGTGGGTTT 660
AGCCTCTGAC CACACAGTCC TGGTCACCCT GCACAGACTG TCAATAAAGA AGGGTCTGAG 720
GCCCAGCTCC TTGGCTCCTC TGCAGTTTCC CCAAAAGGGA AGCTGAGGCT GTGGGTGAGT 780
GGGTGATGTC CGTGGTCCAG GCTCCAGTTC CCTCACTGTG GGGTCTTCCC CTACCCCTGT 840
GATATGGTTT GGCTCTGTAT TCCCACCCAA ATCTCACCTC GAATTGTAAT CCCCATAATC 900
CCCACGTGTC AAGGGCGAGA CCAGGTGGAG GTAATTGAAT CATGGGGCTG GTTCCGCACG 960
TGCTGTTCTT GTGCGAATGA GTGAGTCTCG CCAGATCTGA TGGTTTTATA AGCGTCTGAC 1020
ATTTCCCGTT TGCGCGCATT CTCTCTCCTG TCGCCATGCG AGAAGGTGCT TTCCACCATG 1080
ATTGTCAGTT 1090
|
