| Tag | Content |
|---|
EnhancerAtlas ID | HS051-05472 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr11:128059730-128060840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr11:128060061-128060076 | GTTTCTCAAGAAATG | - | 6.72 |
|
| | 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 |
| GH11I128189 | chr11 | 128059782 | 128060864 |
|
Enhancer Sequence | AGTTATTTTC TTATTTATTT ATATGGCTCC AAACCTAGAG ATCAGAAGGT GTTGTATGAC 60
TGGCTGGGGA TATCAATGAA ACAGATTATG ATGTATGCAT GAAGTGTGCA TGCAGGCCAA 120
AGTAGAACTT GATCCTGTGC CTCTCTGACA AAATAGGTGC TACTCACAGC TTTTACTTCC 180
CTTTTGAAAA GGGCACTTCT CAATGAGGGG AGAAAGGGCA CTTCTCAATG AGGGGAGTAG 240
GCCAAGGGGG GTCAAGTTTC AGGACAATGT TTCAGCTCTA CATGGGGCCT AGAGCAAAAG 300
ATCATAACGC ACGTTTAGGT CTACACAAGA TGTTTCTCAA GAAATGTTTT TGTTTAAAGT 360
TTGTTTCCTA CAATTCTCTC ACGCACGTGC ATGCACGTGC GTGTGCACGC GTGCACACAC 420
ACACACACAC ACACACACAC ACACACAGCT TGTAGACTCT TCGTTATGGG GAATGTCAGG 480
AAACCACACC CTGAAAGATT TTCTCTGTCT TACAATATTA AGGGATCATG ACCATATTAA 540
AGTCCCTTCC AGTACAGGGT TTGTCCATGT GAGCTTCTGA GAACAGGCGA GCTGTGGTTT 600
TCTCACTAGC ACAGAAGAGG TGAGAACACA GCCTTGGAAC CCCTCCTTCT CACCACCGAC 660
CCTCATCAAA GGGCGTATGC AGTGCTCACA ACCAGTCCTG GATGAGAGGG CTTCAGGCAC 720
TCAGGAGAAC CAGTATCTAG ACCACAGAGC AGCAGGGAGA GTGTGGCCAC CTAAAGATGT 780
GAAGGCACCG TAAAGACCCA CTTGAATCTT TGCTCACCTC AACGCCATCC AACAATTGAA 840
GCCTGGGCAA AGTGAAACAC CCATCTCCTG ATTCAGTCTC TTGGCTCTTG GTGAGCCAAT 900
GCTCACCTCT TGGCTTGAAG TCAGAGTGAG GGGTGTCAAT AGGACTCCCT TATGTCCCAC 960
TTTCCCCACA TTTCAGTTCC TGGCCCTGGA CCCCACTCTC CACTTGACTC CATCCCAGAT 1020
AGCTGATGCT GGTTCTCCCA CATCTCCCCT ATCAGGCAGC CAATGCTGTT GCCTAATTTA 1080
GCACAGAGTA AATTTATTTT GCCTTTATAC 1110
|
