| Tag | Content |
|---|
EnhancerAtlas ID | HS103-09892 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr17:20043980-20045550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr17:20045097-20045112 | CACTTCCTCAGAATT | + | 6.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr17 | 20044114 | 20044330 | | chr17 | 20044871 | 20045290 | | chr17 | 20044372 | 20044828 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I020141 | chr17 | 20044661 | 20044810 |
|
Enhancer Sequence | CAGCCAAAAG TGTTCATCTT GCCAAGGGTG TCAGTCAGTG TGTCCTGTAA ACATGGGGTG 60
CATTGGTTAT TTTGGTGAAT TGATTATCTG TAAAATGTTC AGTAGAGAGT GCATAAGAGA 120
GCAACTTCTG TATTACCAGA GTAATCTTCC TAAGCCACAG CTGTCATGAG ATCACTTCTC 180
TGCTCGAAAA CCTTCAAGCA CTCCTCACTG GTTGAGGGGC CAAGGGCAAC ATCTTGCCTT 240
GTGATTCATT GTGATCTATG GCTGTCTTAC CTCCCTCCCC CGTTGGTGCC TTGACTGTGA 300
CCTTTTCACA GTCACTCTGG TGAACAACGA CGGGGCCTGC TGCCGGGGCC TTGCTTGTCT 360
AGGCTGTGCA TGTCCAAGCC AAGCCCCTCC CTCCCTGCTG CCCCCTTCTC TCCTCCTGCC 420
ACTGCAGACC TTGATGGATA TGCTGTTCAC CTGGAAAGGA CCCGCTCATA GTAGCACCTC 480
CTTCAAAAAG CGTTTCTTGA GCTCCTTTCA ACAGGGCATG CTTTTTCCTT TAAAAACCCT 540
TCTGCAGCAC CCCATGTGTA TTTGTTAAGT CACTCCCATA TCCTACCTAT ACTGCTTCTC 600
CTGCCTAATA ACTCTCTGTT GCCGTGAGTT GAACCCAGCT CACTGGACCT GCTCGCTGCT 660
CATTCAGCAA GCAGGCAACT CCTGAGTATG GGCGATGCTG TCCCCTTTAT CTCCTCTTCT 720
TCAAAGACTG TGTGTCTTTG AATGCGAGCT CACCAGGCTC CCCCAGGCTT CAGTCATGCT 780
AACTGATTCA GAGCGAGGAC ATGGCTCTTT TGAGGTTGTA AATAATACAT CAAGTCTTGA 840
AGGCTTATCT GCTTGTCTCC CTTGACTTTT TCAAGAAGCA GCTTTATTGA TAATAATTTA 900
CATACCATAA AATTCACCCA TTTACAGTGT GCAATCCAGT GAATTTTAGT GAATTGACTG 960
AGTTACAACC ATCACCGCAG ATGAGTTTTA AGATATTCCT GTCACTCCAG AAATACCCCA 1020
TGCTGCTGTT TCCAGTCAAT ATCTGTTTCC ACCACCAGCT CCAGGCAACC ACTAATCTGT 1080
TTTTTATCCG TATAGCTCCT CCCTTGACTC TCCCTGCCAC TTCCTCAGAA TTGGAGTGTT 1140
TTCTGGACTA ATGTGTGTGC TATTTGCCTA AGGAACTTTT CTTCCGATTC AGTTACGTAA 1200
CTTTGTGATC TTCTCTTTCA CTCATTCTCC CCATGTTCAA GTTTCTCTTG GTTTTCTTTG 1260
TTGTGTGAAC CTAGTCTCTG TTCACCGAGT TGGCCTTTGG CTTATTAAGA AAACTGAGCT 1320
TTTTCCCCTC TTTCAGAATA TGGAAAACTT GAATAGTGTC ATGTACAAAT ATTGTAGTGT 1380
CATGTACAAA CCAGATGCTG AATGTTATCT ACCGAATGAA GGAATCTGAG CCCTGCTAAG 1440
GCATGGGAAA TCTTGTCTTC TGTTACATTC AGCATAGTGC GTGTAAAGTC ACTAAATTAT 1500
TATTTTGGTT AATAAATACT TTTTATTTTT TGGTAAGGAA AATTACATTG TTTTTATTAA 1560
GATGATTCAT 1570
|
