| Tag | Content |
|---|
EnhancerAtlas ID | HS051-24020 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:130341200-130342610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr6:130341573-130341583 | TTTAATTACC | - | 6.02 | | ZBTB18 | MA0698.1 | chr6:130342477-130342490 | CAGCCAGATGTTG | + | 6.25 | | ZNF263 | MA0528.1 | chr6:130341866-130341887 | TCCTTTTCCTCCCCCTCCCCG | - | 6.21 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGCTTTTCCT GCAACTTGTT TACGCCTGCC TTATTCTGGG GAGGAAAAGA GGGGTCGGGG 60
CCGGGGCCGG CGCCGGGGCC ACCGCCCGCC TCGCGCCGCG TGTGTGTGCG GTTCCGGAAT 120
AATGGGCTTT GCACACTCGC GTCCTGGGCC CCGCGGGCCG TCCTCGCGCC GCGGCGGCGG 180
GGCGGGGGGA AGTAGAGGCC GGCGGGGGTG GGGATCGGGA AGCGCAGGAG CCGAGGCATC 240
CGCCGCGCGC CCCGCGAGCT GGTGGAGTGT GGGGGCCGCC GGGCGGGGAG AAAAACTTGA 300
GAGCCCTGGA AGGGGAGGAG GGCACGGTGG CACGGGCGGG GGGAGGGCGC AACTTTTGGA 360
CTGGTGGTAA AACTTTAATT ACCTTTAAAG AAAAAAAGGC CCTGCGATTC CCCCCTCCCC 420
CAGTCCCGGT CAAAGCACAG CCCGCAGCGC GACCGTGAGA GAAAGTTTAA AAGCGGGCGT 480
GTTCCTCCCG GGTCCCCGCG GAGGGCTGGG GGCGTCGGTC TGTCCGTCGC GCTCAGAGGG 540
AGGTGGGGGT AACTAGCCGC TTTCCAGGGC GCGGGGACCG CGGCTCTACC CCACCCTTCC 600
ACGGGAGACG GAGGTAAACG TTGCTTCGGT TTCCCTTCTG AGTCCCCCTG CTGCCACCAC 660
CCCGCTTCCT TTTCCTCCCC CTCCCCGCCG ATTTTTTGAG GGGACCCGAA AAACGGAGTC 720
CCTTTCCTTA GGCAACTTCC TCGGGCGCTG TGAGCACGGC CCTCCCCCTC ACCGCCCCCA 780
CCCCCAACGC CTCGCATCCC TTGGCCCGCT TCTCCACCTC GGGGCCACCG CCAGAAAAAT 840
GCATTCGAGA TCATTCAGAG TGCACAGAAA CAAAAATAGA TTTTTAATTG TTAGGTTAGG 900
GGAAACTGAG ATGAGAAATA AGAATTTGGG GTGGGGGGGC GCGGCCGGGG CGAGTGCGTC 960
CAGTTCTCCT TTTGGTTTTC CTAGAGCGTT GTTTGTGATG TCTTTATTGG TTTAGGGAGT 1020
CCGAGAGGCT CTATGCTGGC TATCTCGGTC GCGTGGATTT TTGCGCAAGT TTTTAGAAAA 1080
ACACTGACTC GAGTAGAGAG CATTTCTCCG GAAAGTTTCA AGTGCAGCAA AATAGCGAAC 1140
GTGCAAAACT GGCCAAGGGG AGACCTCTAG TGGTTGAACG CGTCTTTTAA GTTCGGAAGG 1200
CCGAGAGCAA AGTTTGGCCT TTACTCGTAG CTACGTAGTC CGTTCAGACG TGGAAGTAAT 1260
TAGAGGACCT GAGCGAGCAG CCAGATGTTG TGTGAAAGGA TGCTGATCAG AAATTGAAAG 1320
TTTAGTAAAT CGAAGCAATG AATTCTGAGG ACTCAGACCC TGTAACTTCC ATCCGACATG 1380
AGTTATATGG GAAAGACACT TTGCTTTTAT 1410
|
