| Tag | Content |
|---|
EnhancerAtlas ID | HS017-19578 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr2:203830470-203831330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr2:203831177-203831188 | AAATCACAGCC | + | 6.02 | | NFE2L1 | MA0089.2 | chr2:203830649-203830664 | GAGTGACTCAGCAAA | + | 6.86 | | Nfe2l2 | MA0150.2 | chr2:203830647-203830662 | AAGAGTGACTCAGCA | + | 7.17 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 203830527 | 203830982 | | chr2 | 203830557 | 203830927 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I202965 | chr2 | 203829885 | 203831046 |
|
Enhancer Sequence | TTTAAAAGTT TGTTGTATCC TACAGTAGTG TAAGATATTC AACTTAAAAT CTTAAGTTAT 60
ATAATTTTCA CATCTACTTA TTTGTATTAT CTATTGCTGT GTAACAAATT ATCCCAAACG 120
TAGTGGCTGA AAACGACAAA CGTTAATTAT CTCACAGTTT CTGTGAGTCA GGAATCCAAG 180
AGTGACTCAG CAAAGTGGTT CTGCTGCAGT TGTCTCATGA CTTGACTGAG GGAGGGTCTA 240
CTTTCAGATT CACTCTTGTG GCTGTCAGCA GGCCTTATTC CTTGCCACGT GGGCCTTTCC 300
ACAGAGCTCC CTTACCACTT GGCAGATGAT TACCTCCAGA GAGAGCAATT CAAGCAAGAG 360
TAAGAGAGAG TACCCAAATG ATAGTTACAG TCTTTTTGCA GCCTAATATC AAAAATTACT 420
TCCTACCACT TTGGCCATAT TTATTAAACG TAAGTTAGTA AGTCTAGCCC ATATTCAAGG 480
GGAGGGGATT ACTCAAGGAC ATGAATGCTA GAAGGCATGG ATTACTGGGG GCCATCTTAG 540
GGCTGGCTGC TGTATTAACA GCCCAAATAA AAACAAGAAA ATAATTATAA AAGGAAATAA 600
AAATTTAAAT GATACCAATA TTTATTAACC AAATGTAACA TTTGCTCACT ATTTATAAAA 660
TGGTATAAAA ACCATATGTC AGGTGGGATG CAGTGGCTCA TGCCTCTAAA TCACAGCCCT 720
TTGGGAGGCC AAGGCAGGCG GTTCACTTGA GTTTAGGAGT TCAAAACCAG CCTGGACAAC 780
AAGACAAAAC TCTGTCTACT AAAAATACAA AAATTAGCCT GGCGTGGTGG CACACGCCTA 840
TAGTCCCAGC TACTTGGGAG 860
|
