| Tag | Content |
|---|
EnhancerAtlas ID | HS026-16472 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr19:45995330-45996410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr19:45995499-45995514 | TGACCTTTGTACCCC | - | 6.07 | | IRF1 | MA0050.2 | chr19:45995797-45995818 | AAAAAGAAAAAGAAACTTTAG | - | 6.15 | | Zfx | MA0146.2 | chr19:45995571-45995585 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATCTGTCAG GTGTAAAGTG ATATCCCCTT GATACCCTTA GCAACACATG TTTCTAAGTC 60
CTAAATGTAT TAATCACGCC ATACTCCTTT CCAGGGCCTA ACTCAAATTT CTGACCCCTT 120
TCTGAGACCC TAAAACACAC CTCCTAAACC CAACCTCAGC CCTGACCAGT GACCTTTGTA 180
CCCCAACCTT CATCTCATCT GTCTAAACTT TAGGCTCACT CCTGTAATCA CAACACTTTG 240
GGAGGCCGAG GCGGGAGGAT CACCTGAGGC CTGGACAACA TAGTGAGACC CTGTCTCTAC 300
AAACAAAATA AGAAAATTAG CAGGGCGTGG TGGCCTGTGG CTCTAGTCCC AACTACTTGG 360
GAGGCTGAGG TGGGAGGATC ACTTGTGCCC AGGTGTTGGA GGCTGCAGTG AGCTATGATC 420
CCACCACTGC ACTCCAGAAA GGGCGACAGA GGGAGACTCT GTGGCTTAAA AAGAAAAAGA 480
AACTTTAGTA ATCTGCTTTC CTTTGAGTCC TGAAAACCAG GAACTCAGTA CCTTTCTATT 540
TCTTTCCAGA TCCTCTCTAT CCTCCCACAC TCCCTCCAAC TGACCCCTCC GACCGGTCCC 600
TCTTAGAGGC TCACCCCTCA CTTCCGTCTC CTTCCAATGC ATCTCCTCTC ATTTACCTCC 660
AAATAGGGCA GCCCCTCCCT CCCCATAGCA GGGCCCTCCC AGGCAGGCTC CTAGTGGCCG 720
GCGCCGGTGG ATGGGGGAGG GGCCAGGTCG CCTGAGGCGG GGGCTAAGTT TAGGCACGCT 780
GGGGGGAGGG GGCCTCCCCG CAGCTGTTCT GGCCCGTCTG GCCCCTGAGT GACAGCGCTG 840
CCTGGGGCCG AGGCTGGGGG AGGGGGTCCT CCCTGCTCCT GGGCCCCAAA GTGCTGGCTC 900
GAAGGAGAAG GGACCCCATG CTCCCTCTGG GTCCTCCCTA TACTGCCCCT CGGCCCCCTA 960
GCCCCAGCCT GCAGCGCTGC GGAAGCAGAT CAGTAATAAA AATGCTCCGG ATGTGCAGGA 1020
GATAAGGGCG AGTTTGGACC CCGTTCCGCC GACCTCAGCC CCCGTCCAGC CCGTTCCGCA 1080
|
