Tag | Content |
---|
EnhancerAtlas ID | HS053-03149 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:183001620-183002900 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:183001801-183001812 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr1:183001801-183001812 | CATGAGTCACC | - | 6.02 | TFAP2A | MA0003.3 | chr1:183002453-183002464 | CGCCTCAGGCA | + | 6.62 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00038 | chr1:182989993-183005830 | Adipose_Nuclei | SE_45631 | chr1:182990482-183002565 | Osteoblasts | SE_58641 | chr1:182991228-183075156 | Ly1 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 2 | ID | Chromosome | Start | End |
GH01I183031 | chr1 | 183001067 | 183002160 | GH01I183033 | chr1 | 183002441 | 183002590 |
|
Enhancer Sequence | AGTAATTCAA AATCAGTCTT CTTCACATTG CTTGCTTTTT TTTTTATTTT TAAAGAGACA 60 AAGTCTCACT CTGTTGCCTA AGCTGGAAGT GCAGCGGTGC AGTCAGAGCT CACTGCAGCC 120 TTGACCTCCT AGGCTCAAGT GATCCTCTTG CCTTGGCCTC CCACAGTGCT GGGATTATAG 180 GCATGAGTCA CCATGCCTGG CCTCTTTTTT TTCTTTTTTT GAATTTGGTA CGTGGCCTTA 240 TATAGAGTTA AGGACTCAGT AAATTTTGTT TCATGATGAT AAATCACAGT ACTGTGTATA 300 TATGAAAGTT TCTGCTAACC AGAATGATTG TTTGTGGCAG TGACTATACA GGTACCTGTC 360 TGTTTTCAGA GACATGGTTA ATGACCAGTC TCTTTTTTTT CCCATCTTCT TTAGAGTTCT 420 GATTTTGTGT TCTATTCTTG AGCTGGGTGG AGCTCAAGAA TAAATTTTAC ATATGTAAAA 480 TTTCAGAGCT ATGCATTTAA TATTTGTATA CTTCATTATA TGTAAATTAT TCCTTGAATA 540 AAAAAATGAA TTAAGAAACT TTCAGCCAAT TGTAGTACAC TATAATATAG TTGATTTTGT 600 TTGTTTTTCA TATGATTTTT GGCTTAGGAG AGAACACAAT GTGAGGCTTC ATCATCTAAA 660 ATATATTTCT CTTAGTGTCT TTCTCCTCTG TACCAGAAGT TGCTGGCATT AATAGACATT 720 AACAGATATT TGTTGAGTGA TCAAATCAGT GAACTGGCTG GTTTTAATTG AGTTATGAGC 780 CCATTTTCAT TGAAGTACCT GCAGAGCCCT CTCATACAAT CAAGCTTGGT AGACGCCTCA 840 GGCAGTGGAG CATGGGAAAC CTGGGGAAGA GCTGTCCTCT GTTCTCACCT CACTTTAAGC 900 AGGTAGTGGT TTTGGTTGAT GCTTCATCGT TTGATGTGGT AAAATGGTAA GTCTGTGGGT 960 TTTGCTGCAG GTTTAGAGAA TTCTTTAAGA ATGTCTTTGT GTGGCATATG CTTTGGTCAC 1020 AATATCTGGT GCTTAGGTAA CTTGCTATTT AATTTCCATG GTGAAATGTA AATGTTCCAC 1080 ATATCACTTA AATAATGGGA AGACCCCATC TTCATTCATT TAAACATGGT CTAGGTAATG 1140 GCTTTCTCTT ATTGAGCCTT TTAGAAATAA AAAGTCTGAA GTTTGAATCA TGTGGCTTTC 1200 TTGGAGAAAC TTTTATTTTT TTTTGAGACA GAGTCTCACT CTGTTGCCCA GGCTAGAGTG 1260 CAGTGGCGTG ATCTTGGCTC 1280
|