| Tag | Content |
|---|
EnhancerAtlas ID | HS105-40536 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:45397920-45399100 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF2 | MA0596.1 | chr19:45398743-45398753 | ATCACCCCAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCAATCCTCC CACCTTGACC TTCCAAAGTG CTGGGATGAC AGGCGTGAGC CACCTCGCCT 60
GGCCAGGGAA ACAGCTTTTC AGCCTGCAAG TAGTGCAGTC GGGACTCGTG AAAGGAACTT 120
GAGGGAGGAT GGTCCCCTGG TTGCATAAGG CTTTGCAGAG CCTTGGCCTT CGCTCTGAGT 180
GAGTCTGGGG CTTTCGGAAA CCAAGGCATA GCTTCTCACA GGACCCTGCA GCTGGCGTAG 240
AGAGCAGACT CCAAAGGGGG TACCACTGGG AGGGAGTGGA CGGGGAGAGG AGGTTGGATT 300
CTGGATGTTG TTTGAAGGCA GAGCTGCCAG GATTTGTTGA GACCGGATGG AGGCGATGAC 360
TCTGTAGTTT TTGGCTGGAA CTGGAAGGAT GGAGTTTCGG ATTGCCAGCT TTGTGTCTTT 420
GTGCAGCCAT CCACTGTGTC GTGGAGAGCA GGCTCTTGAG CGCTGAGTCC TGAGTGAATG 480
ACTCGTGCAG GCGGGGAGGG GAGCTAGGGT TGGCCTTGGA CCCCTGGGAG TGCCTAGGGA 540
GAGTCACCAC TTCTCGCTGC AGGAGCCCAG GGAGACTCAA AAGTGTTGAC TTTTGAGCTG 600
CCAGAGGAGG AGAAGGGGCT ACCCCGGCTG GGGGACAGGA GCAAGAAGAT TCCAGGCAGG 660
GAGAAGCAGG AACAGGGGTG AGGGAAGGGA AGGGCCATGG CAGAAAACCC AGGAGACAGG 720
GAAGCTGGAG GTGCAGCAGG TGCAGAGAGG CCTCCTAGGT GAGGCTGATC TGTAGGGGCC 780
CCATGAGGAA GAAACATTTC CTGTCCCCAA CTCACCTGGT GACATCACCC CATCTTCTCA 840
TACACTACAG TTGAACCACA TGAGCCTTTT TTGTTGGTTT GTTTTTGTTT TTGAGACGGA 900
GTCTTGCTCT GTTGCCCAGG CTGGAGTGCT GTGGTGCAAT CTCGGCTCAC TGCAACCTCT 960
GCCTCCCTGG TTCAAGCGAT TCTCCTGCCT CAGGCTCCCT AGTATCCCTA GTAGCTGGGA 1020
CTACAGGCGC GCGCCACCAT GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ACAGGTTTTC 1080
GCCATGTCGG CCAGGCTGAT CTCGAACTTC TTACCTCAAG TGATCCACCC GCCCCGGCCT 1140
CCCAAAGTGC TGGGATTACA GGTGTGAGCC ACCGCGCCCG 1180
|
