| Tag | Content |
|---|
EnhancerAtlas ID | HS093-09639 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr14:92926940-92928470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr14:92927883-92927895 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr14:92927887-92927899 | GTTTGTTTGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09263 | chr14:92926107-92934512 | CD14 | | SE_53529 | chr14:92924774-92928910 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 92927535 | 92927833 | | chr14 | 92927282 | 92927953 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I092458 | chr14 | 92925232 | 92929788 |
|
Enhancer Sequence | CCTCTCAGTC AGTAAACAGT TAGGGCCCAG GCTCTGTTCT GGGCTTTGTG GATCAGGTAG 60
GAACAGGACA GCCATGGTCC CTGCCCTCTG GGAGCTTCTG GGCTTGCAGA GCAAATCTGA 120
GCAGATGACC ACACAATGTT CTTTATACAC TGTCTCCCAC CCCTAGCATA CAGCTGATAA 180
GTGGGGAGGT GGGAGGCCAC AGCCTGCTCC CTCCTCGCTG ACCCCAGATG ACGGGTCGCT 240
GGGATTGCCG GGGTGGAGCC CGGCAGCATC AGCAGGACCC AGCTTCGGTG CCCACCTGGC 300
CTGATGGTGG ATTTACAGGT GGACACCCAA TACAGGCAAA CTCTTCCCAC TTTAGACTGC 360
AGAGGCTGGT AATTAGGCCT CCCAGGAGTG GGTGTGGGTA GGGGGAAAAA GAGGAAGAGG 420
CGCTTTCGCC CGTGGAAACC ATGGTCTGCA GTGCTGGCAC CGCCCTGAAA CGGTCGGCAA 480
TGACCCTGAG CCGCAGCCCA GCTGGGAAAG TCTCCTGGTG CAGCTTGTTT GCTTGTTGTG 540
GCGCATAGTC TGGGGAATCT TGTGAGCCTG CTGAGGCTGC TCCCTGGCCC GCCAACAGGA 600
CTCTCTCCTG CGCCCGTAAC GGTAAGGAAA TCACATTGTT CTTACCAGGA CGCTGGCCTT 660
CGTGGCCACT TTTATTATAG CAGCCAACAA ACAGCTACTG GGGACTTGCC ATATGTCAGG 720
CACTAAGCAG GAAATGGGGA ATTCTTCTAT TGCTCTGTAA TTCTTATATT AGTCAGCTCA 780
GGCCGTCCTA ACAGAATGTC ACCGACGAAG CAGCTTAAAC AACGGAAATG TATTTTCTCA 840
CATTTCTAGA GGCTGCAAGT CTGAGATCAG GGTGCCAGCA TGGTTGGGTT CTGTGTCCCT 900
CTTCCTGACT TGTAGACAGC TGCCTTTTTG TTCACGTGGC CTTGTTTGTT TGTTTGTTTG 960
GTGCATGCAT GTGGAGAGAG ATCTTTCTCT TCCTCTTCTT CTGAGGCCAC TATTGAATTA 1020
GGACCCCACT CTTAGTACCT TAATTACCTC CTAAAAGCTC TATCTCCAAA TACAGTTACA 1080
TTGGGGGTTA GGACTGCAAC ATATGAATTT GGAGGCGGGT AGGGGGAGGA ATAATTCAGT 1140
TCATGGCAGG ATCTCACGGG GCATCTGTGC CCCATGCCCT TTTCTAAGAG CTTTACATGT 1200
ATCCCCTCAT TCATGCCTTG CCACAGAACG AGGTAGGAAT GCTTATTATC TCCACTTTAC 1260
AGAGAAGGAA GGGGAAGCAC AGAGAGGTAA GTGATTGCCC ATGGTCACCC AGCAGCTCTG 1320
CAGGTGCAAT GAGCCGGGTT TCCACCCCGA GCACCAGACA CTATCCTCTG AGTACTGCCT 1380
CTTCATTCCA GGCACTTTCA TTTAATCTTC ACAGCTGCTT TGTGAGGGAG GAATATTATC 1440
CTCATTTATA GAGGCGGAAA CAGGCTCAGA GAGGCTGCGG GGCTCCCCGA GTCACACAGC 1500
CATTGGGTAG GGAGTCACTT TTCCACTCTG 1530
|
