| Tag | Content |
|---|
EnhancerAtlas ID | HS047-04908 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:114498410-114499390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROD2 | MA0668.1 | chr10:114499214-114499224 | ACCATATGGC | - | 6.02 | | NR2C2 | MA0504.1 | chr10:114498758-114498773 | CAGGGTCAGAGGCCA | + | 6.25 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I112738 | chr10 | 114497895 | 114500043 |
|
Enhancer Sequence | TTTCTTCCTC TCATGAGCCA TCTGGATCTT AATGGTTATT TTCTTATAAG ACTGTTGAGT 60
TTACAGTACG ACAGAACTGT GTTTACCTTG GAATGAGGGC TGTCCTCTAT TAAGAAGCTT 120
TCAGTACAGC CCAAGAGTCA AGTTATGGTG TTGTGGGCAG AAAGCCAGTA GGGAAAGCCT 180
TGAGGAGAAA GCCCTCATGG AAGAGAAATG CTTTATCATC TGGTCCCTGA ATCTTATGGA 240
ATTCAGCAGT GACCTAGCCG CATGATCCCG CAGTGAGGGC TTAACACGTT CCACGGCCTG 300
AACTCGCTCT GAATGGACTC CAGATTCCCA ATGATGCATG CAGCCCCTCA GGGTCAGAGG 360
CCATCATGCT GCCAATCAGA CAAGGCAGGT GGAATGTTGC ACAGCTGCAC TCTGGTTGCA 420
TTTCCCAACA CCTCCCTGTC TCACGATGCT TGCACATTGG CATGCTGTTC CTGCCACCTT 480
GTCATACTTG TGTGTGTGGA GAGCCTGTCC CCAGTGCTGT TTTCTCAGGA CAAGCTCAAC 540
TTCACTTCCT CCCGCCTTAT CGAACCCTTT GTTTCCAAAA TTGTTAATCA AGCCACTTGG 600
GGGGTTGAAC TCAACTCCTC CCTCCCAATA TCCTCCCAGC TCAAAGTAAT GAGAAAAACA 660
ATTGCCCACA GTGAGGATGT CCATGGTCCC CATTTTCCCC AGTCTATCAT GCCTTAGACA 720
GATACTGTTG AATTTTGTCA GTTGCATGTC CCACATGCTA ATGGTGGTTA TTTGGACATC 780
TCTGCTTCAA GCCCAGCTTA AAAAACCATA TGGCCCCAGA TTCTTCAATG CCACAGCTAT 840
GGTGCTCTTC CATGTTAAGA GACTTAACAG ATGAAATATG GTTTTCCGAA CCTCTTTTCA 900
TTTACCATCA AAATAACAAG CGATGTCTTG TATTTCAACA GAGACATTCT TTTCACTCAG 960
TTACTCTGCA AAGAATGTGC 980
|
