| Tag | Content |
|---|
EnhancerAtlas ID | HS087-11419 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr19:50037650-50038810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr19:50038215-50038226 | CCACACCCTGC | + | 6.62 | | RUNX1 | MA0002.2 | chr19:50038451-50038462 | TTCTGTGGTTT | + | 6.32 | | TBXT | MA0009.2 | chr19:50037902-50037918 | TCACAATTAGGTGCTA | - | 6 | | ZNF263 | MA0528.1 | chr19:50038237-50038258 | CCCTCATTCTCTCCCTCCTCT | - | 7.64 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_62028 | chr19:50036137-50074396 | Toledo |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I049532 | chr19 | 50035922 | 50038257 |
|
Enhancer Sequence | CGGTACGCGG CGAGCCCCCG ACCCTGCTCC CCATACACCG TGACCCTGAC CTTCTGGACC 60
GCCTCATTCT GAGAACCCTG AACCCATTTA CCCGGAGTCC CTGGCCCCTA ACCAGGCTCT 120
ACCCACTTTT AGGAGCCCAT AACTGTGAGA TCTTCAGTTT CTCACCTCTG GCTTCTCTTT 180
TTTGTTTTTC GTCTGCTTAT TTTTCTGGTA TTTAGCTGCA TGCTAAAAAC GATCTTTTTT 240
TCAAACATGA AGTCACAATT AGGTGCTAAA AGCCACTGAA CGCACCCAAA CAGGGACTTG 300
AAACCTGGGC CCTCAAATTA AAAGTCCAAT GCTCTACCAA CTAAGCTACC CAGGTTCCCT 360
TCAGGGCTTT CATTCTGGGA CTCACCACCT CTGTGACAAT ATGACTAGGG TACTTGAGAT 420
CCCTGGCCAA GGACACCTAC TTTCCATGCC TTGTCATCCT GACCCCTAAC TTCTGTGACC 480
TCTCATCCTG AGAACCCCAA AGCCAGTTAC TCAGCCCCTG ACTCTCAGAT CCCTCCTTTC 540
TGTCCCAAGT CCCAGCCTCA GTGCCCCACA CCCTGCCACA CACACAGCCC TCATTCTCTC 600
CCTCCTCTCC TCTCTGTCCC TGGCCCCAGC CTCCCCGTCC AGTCTGTCCT CCACAGGGCT 660
CCGGGGGCGG GGTTCTTCAT GCCCAGCACT GACTCTGCCC CTCCCTCCCC CTCCTGGGCC 720
CCCAGGAGAC GGTCCCACTC CCCAGCCGGG ACGTTTCCTC CTGTGGCTTT GTTTTTCTGC 780
ATTTTCTGCA CCAAATGGAT TTTCTGTGGT TTTCCTGAAC TCACCACACT CTTCAAACCT 840
CTACCTTCTG CCCATATTGT TCCCTCCAGT TACAATGCCC GTCCCCTCCT CTCAGTCAAG 900
CCATCTCAGT CCCTGTAAGC TACCCCATCA CAGCCTTAGT CTGGGGCCAA AAGGCCCACT 960
GTCAACTCAT AGTGGGCCAT TCCTGTCTCC ACACGCTTGG ATCAGTTATT TCTTCTCTCT 1020
GAGAATCAAT TTTTGCATTC AGAAAGTAGA ATACATGGAA AAACCCACTG TATGTGCTTT 1080
TTTGTGATGA TTAAATGCAA TATTGTGCAT AAAGAGCTTA GCATATAATC TCTCACAAGT 1140
TAGCTAATTT ATTGGGTGGA 1160
|
