| Tag | Content |
|---|
EnhancerAtlas ID | HS062-16678 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr9:117500920-117502270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:117501302-117501321 | AGCCCACCAGAGGGCGATA | + | 6.07 | | RARA(var.2) | MA0730.1 | chr9:117501120-117501137 | TGTCCTTGGTGTGACCT | - | 6.16 |
|
| | 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 |
| GH09I114738 | chr9 | 117500786 | 117501704 |
|
Enhancer Sequence | ACTGGGTGGG GAAATTACCC AATCTTGGGC AGAATCCAGC TAACCTGCTG CTGCTGACAG 60
CATGGCTGAG CTGGGTCAAG GGCTCAGGGA TGTAGGGATA TGAACCACAA ACATGAAGGT 120
TTGGTGTTTC ATGGCAGAGA GAAGGACCTT GGCCCTGGAT GGGGGTCGAG GGTTTGAGGT 180
CTGGCCTTGG CTCTGACAGT TGTCCTTGGT GTGACCTTAG GCAAGTCACT CTCACTCTTG 240
GGTCTTTCAT TGTCCCATCA GTAAATGAGG ATGTTAGACT AAATGGTGTC AAAGATCTCT 300
TTCACTTCTG AAATTCCACG ATTCTGTGAG TTCTGTTTTT GTAGCCTTGC AGCCCGTTTG 360
AAAACCATAC CCTTTCCATT TAAGCCCACC AGAGGGCGAT ATGCCCCACG TGTTGGTCCT 420
GCCCCGGTCC AAGAGACCTA ATCACTGGGT TAAGTGCCTT AGAAGAGGAA GCCATGACTC 480
AATCCCTGCT TCTAGGGAAG AGAGATGGAA GTGGACACTA TTTAAGTTGC TTCTTGGATC 540
TGCGATTGAC CAGGGCTCTT CACGTCCATT TTCTCTTTGA TTTCATGTCA GTTCCCTGGG 600
CCACATGCCA GTTTCTTATT TCACAGGGAA CCAAGACTTA AGGAATTGAA AGGACTTACC 660
TTGGACTAGG TGGGTTTCCA GTGGTAGGCC CAAGACCTTA CCTCTCCATC TGTGACTTGT 720
CCTTCTGGGC CTTTTCCAGT GGATCTCAAG AGGCTGCCTC TGTTTCTAAG GGGCTCCTGC 780
TGAACTAATA AGACAATTTA CACATGAGTT GATTAAGGCA AAATACGAAA CCGTATTAGA 840
GTCAGGACTA GGAGCTACAC TGCATGGATA GACAAACACT TCTTTCCAAT GAAGCTCTTC 900
TTCTGGGATT TGGACTAAAT GATCTGTTAA ATGTGAACTT CCATAGGAAC TATAATGGTC 960
TTGATTCTAT GTTGCAGACA GTGGAATCCA CTCTGGCTCA TTTAAGTAGC AAAGGAATTT 1020
TTGAAAGGGT ATTAGGAAAC TCTCAGAATC TCCAGGAGAG GCAGAGAGTG AGAATCTGAA 1080
ATTATGTAGC CAGAAACCAT GACTAATTCC AATGTGGGGG CTTTTCTAGA AAAAAACCCA 1140
CTGCTACATT TGCTTGCCCC CTCAGATGTT CGGAATTGGG CACATCATGG AAACTAATAT 1200
TGACTGAGCA TCTCCTATAC AGTGGGCTTT GTGCTGGGCA TGTATCTTAT TTAATCCTAT 1260
GGGATGGGTA TGGTTATCCC TAATTTATAT ATAAGGAATG CAGGCTTGGG GAGTTTGATG 1320
ACTTGCTCAA TGAAACCCAC CTCTCTCTGA 1350
|
