| Tag | Content |
|---|
EnhancerAtlas ID | HS037-18203 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr19:45995390-45996410 |
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 | CTAAATGTAT TAATCACGCC ATACTCCTTT CCAGGGCCTA ACTCAAATTT CTGACCCCTT 60
TCTGAGACCC TAAAACACAC CTCCTAAACC CAACCTCAGC CCTGACCAGT GACCTTTGTA 120
CCCCAACCTT CATCTCATCT GTCTAAACTT TAGGCTCACT CCTGTAATCA CAACACTTTG 180
GGAGGCCGAG GCGGGAGGAT CACCTGAGGC CTGGACAACA TAGTGAGACC CTGTCTCTAC 240
AAACAAAATA AGAAAATTAG CAGGGCGTGG TGGCCTGTGG CTCTAGTCCC AACTACTTGG 300
GAGGCTGAGG TGGGAGGATC ACTTGTGCCC AGGTGTTGGA GGCTGCAGTG AGCTATGATC 360
CCACCACTGC ACTCCAGAAA GGGCGACAGA GGGAGACTCT GTGGCTTAAA AAGAAAAAGA 420
AACTTTAGTA ATCTGCTTTC CTTTGAGTCC TGAAAACCAG GAACTCAGTA CCTTTCTATT 480
TCTTTCCAGA TCCTCTCTAT CCTCCCACAC TCCCTCCAAC TGACCCCTCC GACCGGTCCC 540
TCTTAGAGGC TCACCCCTCA CTTCCGTCTC CTTCCAATGC ATCTCCTCTC ATTTACCTCC 600
AAATAGGGCA GCCCCTCCCT CCCCATAGCA GGGCCCTCCC AGGCAGGCTC CTAGTGGCCG 660
GCGCCGGTGG ATGGGGGAGG GGCCAGGTCG CCTGAGGCGG GGGCTAAGTT TAGGCACGCT 720
GGGGGGAGGG GGCCTCCCCG CAGCTGTTCT GGCCCGTCTG GCCCCTGAGT GACAGCGCTG 780
CCTGGGGCCG AGGCTGGGGG AGGGGGTCCT CCCTGCTCCT GGGCCCCAAA GTGCTGGCTC 840
GAAGGAGAAG GGACCCCATG CTCCCTCTGG GTCCTCCCTA TACTGCCCCT CGGCCCCCTA 900
GCCCCAGCCT GCAGCGCTGC GGAAGCAGAT CAGTAATAAA AATGCTCCGG ATGTGCAGGA 960
GATAAGGGCG AGTTTGGACC CCGTTCCGCC GACCTCAGCC CCCGTCCAGC CCGTTCCGCA 1020
|
