| Tag | Content |
|---|
EnhancerAtlas ID | HS118-05300 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr13:47224840-47225890 |
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 | CAGGACAAAC AAGGAGCAAA AAAAAAAAAA AAAAAAAGAG AAAGCCTGGG TGATCTTTGG 60
CAATTATTGG TAACATTGGG CTTTGCTACC TAGTACTAAT TGAGCCCATT CACTTTAAGC 120
CTTCTTAAGA AAGTTGAGGA GCACTGAACA ACTCTAGCCA GATACAAAGT TTGCTATCTA 180
TCTTTACATC CCGCTAACTT AGGTCAGTGT TTGCTGAGCA TGGTTTAGTA ATGTGCATTG 240
ATTGATTATG CACAACATAA TATCATATAT TAATGCCCCT GAGTAGCTCT GATATTAAGA 300
AAATCAGTTA TTTTAAGGCC TTGGTTTTAG ACTTTGCAGC TAGGTTCTCT GGTCAAATTC 360
TAAATCCTTT CCCCATATCT GGGATGTCAG GAGAGAAAGG GAAGCTGTTT CATCAAATAT 420
ATCTTTACGG TGAATACAAG ATCCCCAATT GCAAGCCTGA ATGTAGCCTT TACTCATGTC 480
ATTGCGTCAT GTTAGTGTGC AAAGGGGAGC AAGACTTGTG TTGAATAACA GATATACCCA 540
ACATCAAAGT TCAGAAAGTT CAATGAACCA GGTATAATGT CAGTGGTTTT TTAGTTTTGT 600
TTTTAGTTTT GATTTAGTTG GCTACTGAAA ATTACTGGTT TTGTCTTGTT TTCCTTGCAG 660
TCAAAAATGA GTTTCTGGCC GGGTGTGGTG GCTCAGGCCT GTAATCCCAG CACTTTGGGA 720
GGCCGAGGCG GAGGGATCGC CTGTCAGGAG TTCGAGACCA GCCTGGCCAA CACGGTGGAA 780
CCCCGTCTCT ACTAAAAATA CAAAATTAGC TGGGCGTGGT GGCGCATGCC TATAATCCCA 840
GCTACTCAAC GAAGCTGAGG CAGGAGAATC GCTTGAACCC GGGAGGCAGA GGTTGCGGTG 900
AGCCAAGATA GCGCCATTGC ACTCCGGCCT GGGTAACAAA AGCGAAACTC CATGTCAAAA 960
AAAAAAAAAG AGTTTAAGTT GCATTTCTGT AGAAGTGCTT TTTTTTTTTT TTTGATATGC 1020
AGTCTCACTC TGTCACCCAG GCTGGAGTGC 1050
|
