| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06822 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr13:47224820-47225880 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:47225428-47225449 | TTTTAGTTTTGTTTTTAGTTT | + | 6.15 | | IRF9 | MA0653.1 | chr13:47225774-47225789 | AACAAAAGCGAAACT | + | 6.52 | | Stat6 | MA0520.1 | chr13:47225822-47225837 | ATTTCTGTAGAAGTG | - | 6.05 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 47224954 | 47225004 | | chr13 | 47225277 | 47225344 |
|
Enhancer Sequence | GTGAAAAAGA GTTTGGTTGT CAGGACAAAC AAGGAGCAAA AAAAAAAAAA AAAAAAAGAG 60
AAAGCCTGGG TGATCTTTGG CAATTATTGG TAACATTGGG CTTTGCTACC TAGTACTAAT 120
TGAGCCCATT CACTTTAAGC CTTCTTAAGA AAGTTGAGGA GCACTGAACA ACTCTAGCCA 180
GATACAAAGT TTGCTATCTA TCTTTACATC CCGCTAACTT AGGTCAGTGT TTGCTGAGCA 240
TGGTTTAGTA ATGTGCATTG ATTGATTATG CACAACATAA TATCATATAT TAATGCCCCT 300
GAGTAGCTCT GATATTAAGA AAATCAGTTA TTTTAAGGCC TTGGTTTTAG ACTTTGCAGC 360
TAGGTTCTCT GGTCAAATTC TAAATCCTTT CCCCATATCT GGGATGTCAG GAGAGAAAGG 420
GAAGCTGTTT CATCAAATAT ATCTTTACGG TGAATACAAG ATCCCCAATT GCAAGCCTGA 480
ATGTAGCCTT TACTCATGTC ATTGCGTCAT GTTAGTGTGC AAAGGGGAGC AAGACTTGTG 540
TTGAATAACA GATATACCCA ACATCAAAGT TCAGAAAGTT CAATGAACCA GGTATAATGT 600
CAGTGGTTTT TTAGTTTTGT TTTTAGTTTT GATTTAGTTG GCTACTGAAA ATTACTGGTT 660
TTGTCTTGTT TTCCTTGCAG TCAAAAATGA GTTTCTGGCC GGGTGTGGTG GCTCAGGCCT 720
GTAATCCCAG CACTTTGGGA GGCCGAGGCG GAGGGATCGC CTGTCAGGAG TTCGAGACCA 780
GCCTGGCCAA CACGGTGGAA CCCCGTCTCT ACTAAAAATA CAAAATTAGC TGGGCGTGGT 840
GGCGCATGCC TATAATCCCA GCTACTCAAC GAAGCTGAGG CAGGAGAATC GCTTGAACCC 900
GGGAGGCAGA GGTTGCGGTG AGCCAAGATA GCGCCATTGC ACTCCGGCCT GGGTAACAAA 960
AGCGAAACTC CATGTCAAAA AAAAAAAAAG AGTTTAAGTT GCATTTCTGT AGAAGTGCTT 1020
TTTTTTTTTT TTTGATATGC AGTCTCACTC TGTCACCCAG 1060
|
