| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17687 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:45180200-45181810 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr19:45180521-45180532 | TCTGATTGGCC | - | 6.02 | | NFYB | MA0502.1 | chr19:45180522-45180537 | CTGATTGGCCAAAGT | - | 6.1 | | ZNF263 | MA0528.1 | chr19:45180725-45180746 | AGAGGAGAGAGAGGAGAGAGA | + | 6.78 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I044676 | chr19 | 45180211 | 45181273 |
|
Enhancer Sequence | ATTGTTTAAT ACTACATAAC TTATTCAGGT AGGCTGCATC CAGGGGCTCA ATGTTCTCAA 60
ATGACTCCTT TATATACTCG TCAACTCTGT ATTTTTCTTC GGTGGCTTCA TTCTCAGGCA 120
GGCTCTCCCC TGTTGCCACA AGATCACTCC CAGGGGGCCC AGGCTCATAC TCCACTGGTT 180
TAGCCATTCC TAGCAAGGAG ACCACCTTGT TCCTGGTAGT TCCAACAAGA GCCCCAAGTC 240
TACCTCTCAT TGGCTTAACT CAGATCACAT GACTTTTCAT GAACCAATCA CTGTGGCCAG 300
GGGTTGGTGG CCAGGGAAAG CTCTGATTGG CCAAAGTTGG GCTATTTGTG CAGCCCCAGA 360
GACTGGGCTA GATCCAACTC CGTTTAATCA AGTGGATTGA GAGTGTAGAC CGGCTCTCCA 420
AAGGAAAACA AAACTGGTTG CTATTGTCAA AGAAGGGGAG TGGGCAGCAG CAGGCACAGC 480
TATCAGATGC TACCTACTTG TATGGAGAGA GAGAGAGAGA GAGAGAGAGG AGAGAGAGGA 540
GAGAGAGACA GTCCTGTTTC CCCCAGGGAG AGTCTATTCG TGAAAAATTC CTTTCTTATG 600
ACATCAGCGT CTTCAGAACT TTGTCTCTTG AAATTGATTC TGAACTGATT GTAGATAAGA 660
TGTCTAATTT TTCTGCCACT CACCAGTTCC CAGAATATGA AAGCAGCAAT TTTGTCTCCT 720
TTCTCAACTC TTCCTTATGT GCCATGGATT CTGTTTTCTT CTTCTTCTTT TTTTTTTTTG 780
AGACAGAGTC TTGCTGCAGT GTAGTGGCGC AATCTTGGCT CACTGCAACC TCCACCTCCG 840
GGACTCAAGC AATTCTCGTG CCTCAGCCTC CCAAGTAGCT GAGACTACAG GCGTGCACCA 900
CAACGCCCGG CTAATTTTTT GTATTTTAGT AGAGATGGGG TTTCACCATG TTGCCCTGGA 960
TGGTCTCAAA CTCCTGATCT CAGGCAATCC GCCAGCCTCG GCCTCCCAAA GTGCTGGAAT 1020
TACAGGCATG AGCCACTGCG CCTGGCCTAT TTCTTTTTCT TTTTTAAAGA GACAGGGTCT 1080
TGCTTTATCA CCCAGGCTGG AGTGCAGTGG CATGATCATA GTTTACTGCA GCCTCAGACT 1140
CCTGGGCTCA AGTGATCCTC CCACCTCAGC CTCCTGGGTA ACTGGGACCA CAGGCCTGTG 1200
CTACCACACC TGGCTAATTA TCTGTATTAT TATTTTTTGT AGAGATGGGG TCTTGCTATG 1260
TTGCCCAAGC TGACCTCAAA CTCCTGGCCT TAAGCGGTCC TTCTGCCTCA GCCTCCCAAA 1320
GTGCTCGAAT TACAGGCATG CATCACCATG CCTAGCTTAT TTTTTACTTT TTGTAAAAAT 1380
AAGATCTCCC TGTGTTGCCC TGGCTGTCTT GAATTGCTGG GCTCAAGCCA TCCTCCCATC 1440
TCAGCCCCCC AAGTAGCTGG GACTACAGGA GTGCACCATT TCCAAGCTTT TTTTTCTTCT 1500
TCTTCTTGTT TTGCTCTTGT CGCCCAGGCT GGAATCCAGT GGCGCGATCT CGGCTCACTG 1560
CAACTTCCGC CTCAGGGGTT CAAGCGATTT TCCTGCCTCA GCTTCCTGAG 1610
|
