| Tag | Content |
|---|
EnhancerAtlas ID | HS051-04043 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr10:134043110-134044760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr10:134043654-134043664 | GGGGCGGGGC | - | 6.02 | | Myod1 | MA0499.1 | chr10:134043587-134043600 | GGGGGCAGCTGCA | - | 6.08 | | TFAP2C | MA0524.2 | chr10:134044048-134044060 | TGCCCTGGGGCT | - | 6.11 | | ZNF263 | MA0528.1 | chr10:134044338-134044359 | TCCCTCTGCCCCTCCTGCTCA | - | 6.34 | | ZNF740 | MA0753.2 | chr10:134044183-134044196 | GGGGGGGGGGGGG | - | 6.03 |
|
| | 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 |
| GH10I132229 | chr10 | 134043063 | 134044703 |
|
Enhancer Sequence | AGGCCATGAT TCTGCCCCCA GAGGTTCCTG TACTGGTTAG TGTGTGGCCC TGGAGGCACC 60
TGTCTCAGTC ACATCCTGGC TCCGGGGCCC TTACTGGAGA CCCCTCCCTG AGACTCAGTC 120
CTTTTGTGAA GCAAAGCGGT GACCCTCCCT CCCGCAAGGG GCCACTGGGA GTCACACTGT 180
GCACAGAGCA CCGGGCTGGC CCAAACTAAG AAAGCATGTC TGATGGTGCC AAGCGGTGGC 240
CTGGGTGGAT CCGGCTGCAG CACTGTGGTG CGGGAGACAG TGGCTTGGCC TGGCACCATG 300
GGCTCTAAGT ATGGCCTCTC CAGGAAGCTG ACAACAGGCG TGGCCTCAGC ACCTCCCTGC 360
CCGGTGGGAG GGGAAAGCTG AGCCTGAAGG GACAGGAAGA GCCTTGTGTT GGGGGCTGCC 420
CAGAGGCGCG TGTGCTGATG GGGGCTCCTG AACACGCGGC CACACCTGCT GAGGAGCGGG 480
GGCAGCTGCA GGCAGCCCGA GAACAGACGG AGACTAAGCT TGAACGAGGC CGCCTTGGGA 540
GGGCGGGGCG GGGCGGGATT TCTCCTGAAC TTCCTGCATT TCCTATGACC ATTTTTTAAA 600
TTGTTATTTT GAAAGCCAGT TGAGGGTTTC AGAATGACAG TGAGCGTAAG CTGCAGCAGC 660
CCCTGGCTGC CCCTGGCAGG ACCCCCTCCT GCCGCTTCCC ACTGCCAACG GGGCAGAGTC 720
GCGTGGCTCG GCAGCACGGC CTTCCTCCCA TGCACACGGC CGCAGGAGGC CGAGGAGTCC 780
CGTGCCCGGG ATGGAAGCCC CAGCCTCACT CTGCACAGGC GCAGAAGCAA CGGTGCTTTC 840
CTGCGCCAGC CCCAGCACCC GCGGCCTCCT GCAGACGGTC ACTGCAGGCT CAAGGCGGCC 900
ACTGCAGGTC TGGAAACTGC TCCAGAAAGG CTGTTTGTTG CCCTGGGGCT GGGACCAGAC 960
AGGCTGTGAG ACAAATATGG TGGAAAATCC GGCCCTCACC CTCTGCCCCT CAGGAGCCTG 1020
GCTTGGGGCC ACTGGCTGGG GCCAGGGCTC TTGCTGCTGG GGGGGAAGCT GGCGGGGGGG 1080
GGGGGGCTGC AGAGCCCACC TCTGCCTGGA GCGGCGCCAG CACCCGCAGC CCAAGGCCGT 1140
CTTCAGCCGG TCCCAAGCCT CAGGCTTTCT GTCGCTTGTG CACCACCCCA GAAAGCTGCC 1200
TGCCCAGGCG ACCCAACCCT CTCCAGGCTC CCTCTGCCCC TCCTGCTCAC GATGCAGCTC 1260
AGCTCTTACG GGGGAATCTC TGGAAGAACA CGCCTTCCCT TGGGGTGCTC AACCCCCACA 1320
GCCCACTCAC CAGGGGACAG GGCACCTGGG CTTCCCGTGC CCTCTGGGCC CTGTCACATG 1380
TGCGGCGGAC ACAGACCGGG TGTCTACTCC AGACAGGACC TCACCCTCCT GCCAGACAGG 1440
CTCACCCAGG ACCACCCGCT TTCCCAAGCA TGTGGCCTGG GCTCCATCTG GGACCAGCCC 1500
CTTGGCCCTG TGACCCAAGC CTGCTCTCCC CGTCACACGC ATCCCATCAC CCACAGCCAG 1560
GGAGCAGGGA CAGAAGAGCC ACCTCGAGAC AGGGCCTGGC CTCGCACACC CACGGCTCTG 1620
CTGTCCACCA GAACAAAGCA GCAGATCCAC 1650
|
