| Tag | Content |
|---|
EnhancerAtlas ID | HS051-17860 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr21:36474620-36475990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr21:36475038-36475050 | GTCTGTTTACAT | - | 6.44 | | FOXP2 | MA0593.1 | chr21:36475039-36475050 | TCTGTTTACAT | - | 6.02 | | Myod1 | MA0499.1 | chr21:36475578-36475591 | AGCAGCTGTCCCT | + | 7.52 | | SPI1 | MA0080.4 | chr21:36475277-36475291 | TACTTCCCCATTTT | - | 6.72 | | SPIC | MA0687.1 | chr21:36475277-36475291 | TACTTCCCCATTTT | - | 7.06 | | ZNF263 | MA0528.1 | chr21:36475720-36475741 | CCCACTCTCCCTCCCTCCTTT | - | 6.21 |
|
| | 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 |
| GH21I035102 | chr21 | 36474698 | 36475950 |
|
Enhancer Sequence | TTGGGAGAAA TTATCTCCTA GATTTCTATG ATAGTTTACT CCAGGTTAAC TCTTTCCTCC 60
TCCCACCATT TCTTCTCATG ATCTTCAACA GGTTTCTCTT CCTCTGCTTT TCTTTAAAGT 120
GTTTCTCAAT CCAAGAGCCC TATCGGAATC CTGCAAAACC TACCACTGAG TTCTCCTTGA 180
TGAAGTGTTT CCTAAATGAA TCCCTTAACC AATTGAACTC TCTCATTTAG AGATACCCAA 240
TACTATGGAA ATTTACCATC CTGATCATCA TTTGTTCTTT GTATACTTTC CTTATCTGGC 300
CCATGAGTTC CTCATGAGCA GGGTCATGGC CCTATGTCTG GTTGTGGCTT ACAGAGAAGA 360
CAGCCAGTCA GTACTTGTTT AATGTAACCC AGTTGAGCTG TTATCCTTTC TCTCTGTTGT 420
CTGTTTACAT TATATATTAG CTGCCCTTAC AGAAGATCTG TCCTGCCTTT GTTCTTTTAC 480
TTGACTCTCA TTTTAGGTCT TAGCAAATTT TGCAAACTTC TTTGAAGCAC AAAGATTCTC 540
AACACTATTT CTTACTTGCA TTTATGTTCA TCTTCTTTCC TTTTTTTTTT TTTTTTTGTA 600
CAAGTGTTCT TACGTCTGAC TTTACCAGAG AATTTCCTGT TTGGCTACCT CTTGAGATAC 660
TTCCCCATTT TCTTCCCAGT CGGGATTGTG CTATGAACAA GGACCCTTCC CTCTCCAGAC 720
TTGTTTCATG CTCACGTCTT AGAATTCCAC CAATCTTTGC TCTAAGCTTT TAGAGTTCTG 780
CCTCCTCAAA AGGCGGTCAC CCACCTGACA ATACCCAGCT CACCCATGGT TGGCTGTGGG 840
AGGCTCTAGA GTAACCTGCT CCTTTTATCT CCAGGGCCCC CGTCACTTCC TCCTTGGTTA 900
GAATAGATCC AGAGAAGCAG CTCTGCCTCG CTTCCTCTTT GGACTGAAGT CGATTTCTAG 960
CAGCTGTCCC TGTGGGCTCC CTGCACCCGG GCCCCTCCCT CTGCAGTCAC CCAACCTCTC 1020
TGGCAGCATC TGTGCTGTTT GATCCATGCC TGGAAAACAT CAGTGCTTCC TCCATCTGGA 1080
TGGGTGGTCT CCAGCATCGT CCCACTCTCC CTCCCTCCTT TAATCTTCAA CCAAACTCTC 1140
TGTGCACATT CTTCCATCAT GGTCACACAT TTCACTCCAG GTGTATATGG CTTTGACTGG 1200
CTTAGCTATT GATCCTATTT CTTTTGAACA TGGCATTTCC TAGACCTTGG TGTTCTAGGC 1260
CAATTAAAAA CCTGCTTCCT TATATCCTGG TGAGGGCAAA TAATGGTGTT TACCTTCCTG 1320
CATTAATATC CAACATGCAT TTTATTTGTT AACTATATTT TATCCCTACT 1370
|
