| Tag | Content |
|---|
EnhancerAtlas ID | HS051-11785 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr17:40260130-40261280 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr17:40260829-40260844 | GCCCCCCAAGGGTTC | + | 6.6 |
|
| | 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 |
| GH17I042107 | chr17 | 40259219 | 40260904 |
|
Enhancer Sequence | GCAAGAGGAG AGTTGGAGGG GATTCCCATA CACGTTGGAG GATGGGCACC CAGTGGGGGT 60
GCTGACCCCG GCGTGTAGCA CACCGCGACT GCCTCACCCA TCTGTCTTAG CTGTGGTGTG 120
AGCTCCAGAG GGAGGCCGGC TAGGGTGTGG GGGAGTCCTG CCCTGTCTCA CCCGCGATGT 180
GCTCTTACCC TTTGGCCTGG GCACGGTGAT GCCTAGTGTA AGGCACATGG ACGTGCTTTG 240
GTCAAGGAAT AGGCCGAGGC GGACATCCGG GCCAGAGTGA CTCAGCGAGT TTGGGGGGCA 300
GGCACGTACT CCACTTGCTA TATAACCTGT TTGTGTAAGT TCATACTGGA CTCTACTGTC 360
AGTAGAAGGT AAAACTGCCC TGCTGACGCT GTTCACGGAG CTTGGTTCAG CTCGGCACGG 420
CAGGGCACGC TTGCTCGCCC AGAGAGAGAA TAATGCTACT AACCCCTGCA AGGGACAGCC 480
GGTCGCCTTG AAGGTGGGCA GTGGGGAGCC AGGAACCCGC TTGTGCCCAG AGGGAAAGAG 540
TTAAGCTGCT GACCCTGACA GAGCTGGCCT TGCCGGCCAG GGAGAGCAGC TGCAGGCGTG 600
GGGGCAGCAG GAGCCACAGG GCCGGAGCAG ACAGCCCAGA TAAAGGTGGA CAGTGTGAGA 660
GAGCCGCTGC TGAATAAAAC TACATTTCAC CTGCCTATGG CCCCCCAAGG GTTCTTTCAG 720
CTATCTGCTC ACTCACTCCC TCCCTCCAGA CCACAGCATG GGCTCAAACC TGACCCCAAG 780
TGTAACATTT GGTATAGTTA TGGACCTGAC ACCTAGTCCT TGTCCAGTCC AGTCATGGCA 840
GACACGAGGC CGTGTCCACA CTAGAGAGGG CTCAGTAGAG CCTCAGCACA AAGTATCCCT 900
GCTCTCTGGT TTGTAGTGCA CTCCCCAGCA TGACAGTGAT GTGACAGACA CCAGTGGTGC 960
CTTCTGAGTC AATCCAAAGA GCGGGCTGTG GGCATGGGCT GTATCTGCCC CATTTCACAG 1020
AAAGGAGAAA TTGAGGCTTG GATACATAGC AAGTGACCTG AAGTCACAGA GCTAGTGAGG 1080
GCAGAGTCAG GGCCCAAGCC TAGGTGTCCT AACTTCACAC CGGCTCCCGC TCTCGCCGTG 1140
TCCCTGCCCC 1150
|
