| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00388 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:17997310-17998720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr1:17997986-17998002 | TGTTTCTATGGCAACC | - | 6.31 | | RFX1 | MA0509.2 | chr1:17997986-17998002 | TGTTTCTATGGCAACC | + | 6.32 | | RFX2 | MA0600.2 | chr1:17997986-17998002 | TGTTTCTATGGCAACC | + | 6.73 | | RFX2 | MA0600.2 | chr1:17997986-17998002 | TGTTTCTATGGCAACC | - | 6.8 | | RFX5 | MA0510.2 | chr1:17997986-17998002 | TGTTTCTATGGCAACC | - | 6.79 | | RFX5 | MA0510.2 | chr1:17997986-17998002 | TGTTTCTATGGCAACC | + | 6.87 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_01537 | chr1:17996091-17998633 | Aorta | | SE_33681 | chr1:17997492-17999126 | H2171 | | SE_65277 | chr1:17995994-17998670 | Pancreatic_islets |
|
| | 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 |
| GH01I017669 | chr1 | 17995995 | 17999126 |
|
Enhancer Sequence | GCAGCCATGC TGGCCCCTTC CCACCACCAG GCCTTCACCT CTGTTGTTCC CTCTGCCTGG 60
AGCACTGTTC CCCTCCTGTG TGGCTCTTCT TTAGCTTGGG TCTCGGCTTA ACTGCCGCCT 120
CCTCAGTGAA GCCACCCTGA CTGCTCCAGC CGAGTCATCC CTACCCCTTC ATGGTCTCAG 180
CACATCACCC GGCTTTATTG CCTTCAGAGT GTTGGTCACT TTCTGCAATT ATCTCCTTGA 240
GTGCAGTTGT CCGTCTGCAC CGGCGCCTCA CTGCCTTGTT AACCAGTGAG TCCCAGGGCC 300
GGGCACGGCG CAGCCTCTCA GCCAGTTAGG GGTGAGTGTG CCGGCACCTT CCTCCGCCAC 360
GGCGGAGCCG CCTGTGCAGG GCGGTCGCAG GGCCCTCGCA GGACTCTGCA GGAAGGTGAG 420
ATTCGGGGGG TTAGGCATTC TTTCTGCGCT GGGGCAGTTA GGGAAGTGTC CTGGGAAGAA 480
CTGTGCCTTC AAGGAAGTAG GGCAGGGAGT CCCCTCCCAA GAGAAGGGAG GGAGGAATTC 540
GCAGAAGGGG CTTGTCCAGA GGGTCTGTGG CCAGTGGGGA TAGTCCCTGC CTGGATGGCA 600
GCCGGGGACA GATGGACAAC AGTGTCACTC AAGGGTGAGA ACCCTGCCTG GACCTGCACC 660
CGCACCAGCC TTGTGGTGTT TCTATGGCAA CCCCCTTCCC CCAAGCAGAT TTTCAGCCTC 720
CCTGGTGCAG TTGCAAGAAG CACAGGCCTG GGTCCTTCCT GGAAAGTGCT GGAACTCAGG 780
GCAAGTGGCG TCAGCATTTG GACCCCAGGC CTGGTTCCTG CCTTGAGGGG CTGTGGTGGG 840
GTTAACTGGG GCAGCCCCTC CCCCATTAGA CCCGGGCTTC CCATCCTTGG AGAAGCCTGT 900
CTGGACCATT TCACCTCCTA CATACACCAC AGCTACATGC TGACATCCTG GGGCCGGTTA 960
TGGGATTAAC CAGACTGAAG CTGAGTAGGG TGGGACTGGG CCTGGCTGGC TCCCATTGTT 1020
ACCATCCTAT CCCCATGGCC CAAGGCCAGG CCTGACGCAG AGCAGGTGCT CAGTAAAGGG 1080
TGGTTAAGGC CAGAAGCCCC TCAGGGAGAT GGGCTCTGTC TGTAATGTTT CCCCAAGTGG 1140
GGGGTGGGGG CATTGCAGAG CAGCTGACCG AGGCTTGGTT TTAACCGGCT TCGGAGCATG 1200
AAGGTGCTTC CTGAAGCGCG TGCGGTCAGC AATCTGCTCT GCATCTGATG CCTCCTGCCG 1260
GTACCTCTGC ACTGGCCTCT CATACCGGCT CTCATGCTTT TTGTCCCTAA GCAGGACAGA 1320
GAAGAAACTT CTCTGGGCTC CTGAACACCA ACAGCCCCTT GATTTCCCCT GCCCACCCCC 1380
CGCCCCAGCC GCCTTCCCCA CCCTTAATTT 1410
|
