| Tag | Content |
|---|
EnhancerAtlas ID | HS074-00650 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:92925340-92926120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr1:92925632-92925643 | CTCTGTGGTTT | + | 6.14 | | SP3 | MA0746.2 | chr1:92926105-92926118 | CACCACGCCCACC | + | 6.48 | | SP8 | MA0747.1 | chr1:92926106-92926118 | ACCACGCCCACC | + | 6.32 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_25489 | chr1:92924665-92927892 | DND41 | | SE_31273 | chr1:92924793-92926322 | Fetal_Thymus | | SE_50017 | chr1:92924910-92926122 | RPMI-8402 | | SE_66520 | chr1:92924952-92926106 | Jurkat |
|
| | 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 |
| GH01I092459 | chr1 | 92924451 | 92926517 |
|
Enhancer Sequence | TTTTACACCC TCACGTATCT AATAGGACTT TCTCTCAAAT ACAGACTTTG GATGTCATTT 60
TCTTCATTTT GGGGGGTTGG TGGCTTTTGT CCTTAGCAGC TGTGGCCTTA GACTTTATCT 120
AGGTTTGCAA TCAGGAAGCT GTGATACTTC CTGAGACTGT TCTGGGTAAA ATTTACACAA 180
TACAAGTTGA GTTCTCTTTC TTCACTTAGG AGTTGCTCTG GGCTCTTGAA AGGACAGGCT 240
GTGCTCTGTC CAGTTTGCTA CAGGTTGAAT CCAACAGTTG GTAAGAACCA GCCTCTGTGG 300
TTTACAGCTA CTTGTGCTTC CTGAGCAACA CTCGTGGAGA ATTTGGAAAG AAGGCAATGA 360
TTAGGATTAG AGTCTAGAAA ACCGTTAAGA AGGAGGAAGT TTATCAACTT AGTGGGAGTA 420
AATCTCCAAA CCACTCTCAG AATGCTAACA CGCACAGTTT CTCTTTGCCA TGACCAATCG 480
TCAGGCTGTT GAAGGAAACC AACCTAATAG CAGAGGCAAA GGGAGAAGCT GGAGAAGAAT 540
AATCATTTAA AAATATTCAC ATCCTTTGAC CAAATAAATA AGTCAGGAAT GGACATTGTT 600
AGGTGCCCCC CCCAACTTTT TTTTGTTGTT GTTGTTGAGA TGGAGTCTTG CTGTCACCCA 660
GGCTAGAGTA CAGTGGCACC ATCTCAGCTC ACTGCAACCT CCACCTCCTG GGTTTGAGTG 720
ATCCTCCTGC CTCAGTCCCA AGTAGCTGGG CTTACAAGTA TGTGCCACCA CGCCCACCTA 780
|
