| Tag | Content |
|---|
EnhancerAtlas ID | HS051-09470 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr15:74781550-74782910 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr15:74782322-74782341 | TAGTGCCCTCTGGTGGCCT | - | 8.06 | | RREB1 | MA0073.1 | chr15:74782384-74782404 | ACCCCCCACACCCCCACCCT | + | 6.58 | | ZNF263 | MA0528.1 | chr15:74782388-74782409 | CCCACACCCCCACCCTCCTCC | - | 6.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 74782042 | 74782799 | | chr15 | 74782465 | 74782881 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH15I074489 | chr15 | 74781781 | 74782896 |
|
Enhancer Sequence | AAGCAATTCT CCCACCTCAG CCTCCAGAGT ATTTGGGATT ACAGGCACCT GCCATCATGC 60
CTGGATAATT TTTGTACTTT TGTAGAGACA GGGTCTCGCT CTGTTACTTA GGCCGGAGTG 120
CAGTGGTACA ATCTTGGCTC ACTGCAACCC CAACCTCCTG GGCTCAAGTG ATCCTCCCAT 180
TTCAGCTTCC TGAGTAGCTA GGACTACAGA TGCACACCAC CACGCCTGGC TAATTTTTGT 240
AGAGACAGCC TCTTGCTATG TTTCTTAGAC TTGTCTCGAA TTCCTGGGCT CAAATGATCC 300
ACCAGCCTCA GCCTCCCAAA GTGCTGGGAT TGCAGGCATG AGCCACTGCG CCTGGTCTAA 360
AAACACCCTT TTCATTCAGC ACTATAGGTT TTAAAAGGCA GTGTTCCCAT AAGAAATAAT 420
GGCAAAGAAA GGAACTCCCA GTCACATTCA GCAAACCTGT TTTCCCAGCT ACATTCATGC 480
ACTGGTTGAT GCAGGTAAGT GTACAGGGGA GGTTGATGGA GAGATAGGAG GGTCCTGGAA 540
ACAAAGGAAG ACTGTGACAT TAGATGACTG CAATCGTGGA GACTCAGATG GTGCTTGTAC 600
TACCACGGTT CATCTTTTGA GTATGGGCAT GTCATAGTCT GGACCAGAAT CTAAATTCTA 660
GTAGCAAAGC AGGTAGGGTG GTTATTGCAT AAGGAGGTAT CACAACCTGT CATTTGGGGA 720
GGGTGAGGGA AGGACTGGCT GTCACAGCTT AGCCTCACCA AGGACGTATG TGTAGTGCCC 780
TCTGGTGGCC TGCAATGGCA CGCAAGCCAG CCAAATCAGA ATCCCCCATC TCTCACCCCC 840
CACACCCCCA CCCTCCTCCC AGCCACCCCC ATCTCAGGCA AGACAAAGCC AGAGTCCTAA 900
CTGGTCTCCC TGCTTCCACT CCTGTCCACC AGAATGATTT GTTAAGATCA TCAGATCATG 960
TCACTCCTCT GCTCAAAATT CAGGGTAATT TCCCTTCTCC CTGAGTTATT TAGCCACAGT 1020
ACTCACAGTG GTCTCCATGG CTGTACTCGG TATGGCGCCT CCCAGCAACC TTTCTGTCTC 1080
CACTTCCTGC CCCTCTTCCG GCTGCTCACC CTGCTGTAGC CACACCGGGC TGCCTGCTCT 1140
TCCTCTGCCA GCATAACCCA CCAAGCACAC TCCCACCTCT GCATTTGCTG TCTCCCCCAC 1200
CTGGAATGCA CAGATGACTC CTTCATGTCC TTCATATATG TGTCAAATAT CACCACATCA 1260
TCTTTTGCAC TAAATTAAAA AACAGCCCTC CTCCCAGCAC ACTATATCCC CTTTAGCTGG 1320
ATTCATTTTT TGCCATAGTA TTTAATACCA TCTGACGTAT 1360
|
