Tag | Content |
---|
EnhancerAtlas ID | HS062-01972 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr10:49759570-49761200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:49760069-49760088 | TCTCCACTAGATGGCACTC | + | 6.79 | ESR1 | MA0112.3 | chr10:49760940-49760957 | GGGGTCAGGCTGACCTG | - | 6.11 | ESR1 | MA0112.3 | chr10:49760940-49760957 | GGGGTCAGGCTGACCTG | + | 7.07 | ESR2 | MA0258.2 | chr10:49760941-49760956 | GGGTCAGGCTGACCT | + | 6.69 | ESR2 | MA0258.2 | chr10:49760941-49760956 | GGGTCAGGCTGACCT | - | 7.63 | Nkx3-2 | MA0122.3 | chr10:49759601-49759614 | TATAAGTGGTTTT | - | 6.3 |
|
| 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 |
GH10I048551 | chr10 | 49759757 | 49760839 |
|
Enhancer Sequence | GTCACCCTTT CTCTCAGCCT CCCTTAAACT TTATAAGTGG TTTTCCTGCG TGTCCCCGCA 60 GCTTCAGGGA GGAGACCGTC ACCTCTGCCC AAAGCAATTG CTCCCACCTC TCAGTACGCT 120 TTATATACTG ACCATGTCGG GAAAGCAGTG GCAGGCCACA GCCACAAGAG GACAGAAGTC 180 CCACTGGCAC TAAAGCCCCC TTATAAGAGT GTTTTCTCTG TGTCTTGCTC AGTGGCTGGA 240 TGTGCAGGTT CTCAGGTGCT TTTGGAACCA GAGGTGTATG CTGTATCAAG TTCCAAGACC 300 TCCCAGCCCA GATGGGAACA ATGCTAGAAT CTGTAGGAGG CCCCATATGG CCAGATGTCT 360 GTGTTGGAGG GCAATTTTAG TGTGTGGCTT TGGAAGCCAG ATGGCTTGGC CTCAAGCTCC 420 ACTCCTATCT AGCTGTGCTG GCTGAAAGGC TGGGGGTGGG CAACAGGGCC TGCACTTTCT 480 GGCCCAGAAC TGGCAGATCT CTCCACTAGA TGGCACTCAC AGTATAATGT TTCCTCATTT 540 TTAATTCTAC TTTGAAAACA TTGTCATTTT TTATACCGTT GAATTGCACA AATAGAACTA 600 TGGCTTAAAA TTTACGTAGT TAATTCTAGG CATGACCTTC CTTGGAATTC TGTCACATTT 660 CCAAGAGTTG TCAAGTTTTT CCCCCTCTTG GGGGTGCTGG TTGGAGAGTG AGGGACCCAT 720 TGTGGTGTGA CCAGTACCAC AGGCCAGCAC AGGCATAGCC TGGAAGTGAT CCGGGGTTTG 780 TCCTCCTTCC TCATATCCTG CCCTGATTTC CTGGCCTAGG CCCAGACCCC AGGCGGGGCT 840 GTTAGGCTCC TTCCTGCGCC TGTTAGTTCA CTGCTCACAG AGCCTGCCAC CTGGCACCCT 900 CGGAACTGTA GGAGAAGCCC CTTGTCCCCC CAGATGCACT TGCCACCCTT CACCCACCCA 960 GCCTGGATTT CCTCTTGGTC TTTGCACATT TACCCCGGGG GCTGTGCTTG GTGCACACTG 1020 GCATGGCCCA CTTGGTGATA CTTCCTGCTC CTGCCCCCAG GTAACTGTGC TCAGCCTAGT 1080 GAGGATAAGT CCTTATTGTG CCTTGAGCTC AGGAAGAAAA TGTCCCCAGA CTCCCTAATG 1140 GCAGAGACTG ACCCCTGCTC ATCTCAGGGC CCTGCAAGGC TGGCTCAAAG CTGAGGTCAC 1200 ACGAGAGGTT TGCTGAGTTG GATGTGAATG GGTTTCTTGG CCTTCCTGTG ACTGCACGTT 1260 GCTGTGGTTT AAGGTGGGTT CATCCAATCT TCTTATTCGT TTTTAGCCCC AACATGGCCT 1320 ATAGCTGAAG CCTCAGTCAG CAACTGCTGT AACAGGAAGC CCACCCTTCT GGGGTCAGGC 1380 TGACCTGGGA GGGTCCAGGC TCCTGTACCT GCCAGCTGTT TGGCCTCAGG AGATTCACCT 1440 TACCCCTCTG GCCTGACATC TTCATGGGCT GTGAAGGATG GGGAGCTTTG CCAGCTGCAG 1500 CCAGAACCAA GCATGAGCTT CGAGTGCAGC CTCCCAGGTC CCATCTGAGC AGGCTGATAG 1560 GAAGCATCCT AAATCCGGAG CCCCCAGTGG GAGGGGAGCA GAGGGGACCA CTCTTGGGCC 1620 CCGGGCAGCA 1630
|