| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04328 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:123926260-123928180 |
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 | chr12:123927173-123927185 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:123927177-123927189 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr12:123927181-123927193 | AAACAAACAAAC | - | 6.32 | | Zfx | MA0146.2 | chr12:123926930-123926944 | GAGGCCGAGGCGGG | - | 6.01 | | Zfx | MA0146.2 | chr12:123927737-123927751 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09978 | chr12:123926998-123928009 | CD14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 123927429 | 123927555 | | chr12 | 123927238 | 123927294 | | chr12 | 123927800 | 123928005 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I123441 | chr12 | 123926134 | 123926514 | | GH12I123443 | chr12 | 123927548 | 123927947 |
|
Enhancer Sequence | AGACCCAACC AGTGCTATAG TCTGCATTGG TAAGCCTGCT CGAGGAACTC CGTGTATTCG 60
CCCAGGATTT AGTCCACGAA CGCTCAAGCA ATTTGCAATC CAAAGAAGAT TTGAAATATG 120
AGACTTCTGA GGCATCATAT GCTCACCAGT TTATGATAAA GGATGTTTCA GAGGATACAG 180
ATGAAAGTGA AGAATGGGGG GAGGGGGCAG AGCTCCCACG CCCTCCCTGG GGCAGTGCCC 240
TCCAGGAACC TCCAGTGTTC AGCTGTACTG AAGCTCGAAA AATGTGCTGT ATCTTGCTCT 300
TGGTGGAGGT CACGTGAGTA TACACGAAGG TAAAAAGTTG AGGTTGGGCA GGGTAGCTCC 360
CGCCTGTAAT CCCAGCATTT TGGGAAGTTG AGGTGGGAGG ATCGTTTCAG CCCAGGAGTT 420
CAAGACCAGC TTGGGCAACA TAGTGAGATC TTGTCTGTAT AAATAATTAA ACAATTAGGC 480
GGGTGTGTTG GTGTGCACTG GTGGTTCCAT CCATTTGAGG CCAAGGTGGG AGAATTGCTT 540
GAGCCCAGGA GGCTGGGGGT GCAGTGAGCT GTGATGGAGC CACCGCACTC CAGCCTGGGT 600
GACAAAGCGA GACTATCTCT AAACAAATAG CAGGGCGCAG TGGCTCACAC CTGTAATCCC 660
AGCACTTTGG GAGGCCGAGG CGGGCGGATC ACAAGGTCAG GAGATCGAGA CCATCCTGGC 720
TAACACGGTG AAACCCCGTC TCCGCTAAAA ACACAAAAAA TTAGCCGGGC GTGGCGGCGG 780
GCGCCTGTAG TCCCAGCTAT TCAGGAGGCT GAGACAGGAG AATGGCGTGA ACCCGGGAGG 840
CGGAGCTTGC AGTGAGCCGA GATCGCGCCA CTGCACTCCA GCCTGGGCCA GAGCGAGACT 900
CCATCTCAAA AATAAACAAA CAAACAAACA AACAAATTAT AAATAAATAA CAAAAAGCTG 960
TGGAACCATT CACTTATCTG TGCATTTCCT TTAGGTAAAT TACGTCTCAA TAAAGTGCTG 1020
GGGAGAAAGC AATGAAGCAC TGACATACGC TACACCAAGG ATGAACCTCG AAAACATCAT 1080
GCTGAGTGAA AGAAGCCAGA CACAAAAGGC CGCACAGTGT ATGATTCTAT TTACATGTAA 1140
TGTCCAGAAT AGGTAAATCC ATAGAGACAG AGTAGATTCG TCCCCAGTCT AGCCTCATTC 1200
TAGGGCTGGG AAAAATGGGA AGTGACTACC TCTGTGTATG GGGTTTCTTT TGCGGGGGGA 1260
TCACAATGTA CTAAAATTAG ATTGTGGTGA TGGTTGCACA ACTCTGAATA TACTAAAAAC 1320
CACTGAACTG TATATTTTAA ACAGGTTGAT TTTATATGTA CATAATGCTC AATTCTGTTG 1380
AGTAGAATTA GCCTTCCTAG AACAATGCCA TCAGGAAGAA TTAAAAGTGA GTTTCAGCTG 1440
GGCACAGTGG CTCATGCCTG TAATCCCAGC ACGTCGGGAG GCCGAGGCGG GTGGATCATG 1500
AGGTCAGGAG TTTGAGACCA GCTGGGCCAA CATGGTGAAA CCCCGTCTCT ACTAAAGACA 1560
CAAAAAATTA GCTGGGTGTG GTGGCCAGTG CGCTTATAAT CCCAGCTACT CAGGAGGCTG 1620
GGGCAGGAGA ATCGCTTGAA CTTGGGAGGC GGAGGTTACA GTGAGCTGAG ATCGCACCAT 1680
TGCACTCCAG CCTGGGCGAC ATGGCTAGAC TCTGTCTCAA AAAAAAAAGT TTCTTCTAAC 1740
TTTCTTTCTT TTTTTTTGAG ACGGAGTCTC GCTCTGTTGC CCAGGCTGGA GTGCAATGGT 1800
GCGATCTCAG CTCACTGTAA NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1860
NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN NNNNNNNNNN 1920
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