| Tag | Content |
|---|
EnhancerAtlas ID | HS064-08881 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr2:203830510-203831340 |
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 | AACTTAAAAT CTTAAGTTAT ATAATTTTCA CATCTACTTA TTTGTATTAT CTATTGCTGT 60
GTAACAAATT ATCCCAAACG TAGTGGCTGA AAACGACAAA CGTTAATTAT CTCACAGTTT 120
CTGTGAGTCA GGAATCCAAG AGTGACTCAG CAAAGTGGTT CTGCTGCAGT TGTCTCATGA 180
CTTGACTGAG GGAGGGTCTA CTTTCAGATT CACTCTTGTG GCTGTCAGCA GGCCTTATTC 240
CTTGCCACGT GGGCCTTTCC ACAGAGCTCC CTTACCACTT GGCAGATGAT TACCTCCAGA 300
GAGAGCAATT CAAGCAAGAG TAAGAGAGAG TACCCAAATG ATAGTTACAG TCTTTTTGCA 360
GCCTAATATC AAAAATTACT TCCTACCACT TTGGCCATAT TTATTAAACG TAAGTTAGTA 420
AGTCTAGCCC ATATTCAAGG GGAGGGGATT ACTCAAGGAC ATGAATGCTA GAAGGCATGG 480
ATTACTGGGG GCCATCTTAG GGCTGGCTGC TGTATTAACA GCCCAAATAA AAACAAGAAA 540
ATAATTATAA AAGGAAATAA AAATTTAAAT GATACCAATA TTTATTAACC AAATGTAACA 600
TTTGCTCACT ATTTATAAAA TGGTATAAAA ACCATATGTC AGGTGGGATG CAGTGGCTCA 660
TGCCTCTAAA TCACAGCCCT TTGGGAGGCC AAGGCAGGCG GTTCACTTGA GTTTAGGAGT 720
TCAAAACCAG CCTGGACAAC AAGACAAAAC TCTGTCTACT AAAAATACAA AAATTAGCCT 780
GGCGTGGTGG CACACGCCTA TAGTCCCAGC TACTTGGGAG GCTGAGGCAG 830
|
