| Tag | Content |
|---|
EnhancerAtlas ID | HS047-19538 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:105864740-105865480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:105865280-105865301 | GGGGGAAGAGGAGGGGGAGCA | + | 6.72 | | ZNF263 | MA0528.1 | chr2:105865277-105865298 | GGAGGGGGAAGAGGAGGGGGA | + | 7.03 | | ZNF263 | MA0528.1 | chr2:105865274-105865295 | TGAGGAGGGGGAAGAGGAGGG | + | 8.72 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GATTTCAGGG TTGAGTTGAC ACTAACACCA CATCCACAGA AGCCAGGAGC ATGAGTTTGG 60
CTTTAAAGAG CAAAATTCTA CTTGCTGGCC TCAACTGCAC CACTTCACTC CATTCAAAAC 120
TCTCCCTAGG TTGTAAGCTG ACCTCACAGG GATGCACAGA GGGATGAGAT GGATGTATGA 180
TGCAACCCAT TCCCATGCCT AGAAAACACA GCCTCTGGTG CACATCACTG CTCTCAGGGC 240
TGTTCTGAGG TCCCCAGGGC ACTGTGGAGC CTGTCTGGGA ATGCAGAGAG GCAAGAGGAG 300
GGTGGAGGCA GATTGGGTAA AAGGCTGCTG TCACAAAGAC AGCCAACACT AAGGGCCTGA 360
AACAGACAAA CTTTGTTTCC CTCCAATTAA TAGCCCAGGC AGCCAGGTGG GTGCTCTGCT 420
CTGTATGGTT GTTTAGGATG CAGTTGCCTT CCATCTAGTT TCCCACTGTC CCCGGGGCAC 480
TGTCCTTATC TTTATGGTCA CTCTGGGCTG CAGCCACTTC CATGTTCCGG CTCATGAGGA 540
GGGGGAAGAG GAGGGGGAGC ATGTGCAATA AGACACCCCA CACTCCACCC TGGTCTTCCA 600
CCACCAAGAG TGGAGGCTGC TGGCCACACC TAGCTGCAAA GGAGCCTGGG AAATGGAGTC 660
CCTCATCGGG AGGCCGTCTG CCCAGCTGCA ACCTACTGTG GAAGAAGATG GGAGCTGGGT 720
GCAGTGGCTC ACATCTATAA 740
|
