| Tag | Content |
|---|
EnhancerAtlas ID | HS060-27587 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:76034410-76035590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr5:76035035-76035049 | AGGAAATGACTCAT | + | 8.12 | | Zfx | MA0146.2 | chr5:76035128-76035142 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_14016 | chr5:76032505-76035729 | CD34_Primary_RO01536 | | SE_38085 | chr5:76032526-76035927 | HUVEC | | SE_45479 | chr5:76033507-76035720 | NHLF |
|
| | 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 |
| GH05I076735 | chr5 | 76031495 | 76036586 |
|
Enhancer Sequence | GCCTATTATC CCAGCACTTT GGAAGGCTAA GGCGGATGAA TGGTTTGAGC CCAGGAGTTC 60
GAGACCAGCC TAGGCAAAAT GGCAAAACCC CGTCTCTACG AAAAATACAA AAATTAGCCG 120
AGCGTGATGG CTCATGCCTG TAGTTCCAGC TACTTGGGAG GCTAAGGTGG GAGGATGGCT 180
TGAGCCTGGG AGGCGGAGGT TGCAATGAGC CAAGATGGTG CCACTACACT TCAGCCTGGG 240
TGACAGAGTG AGACCCTGTC ACAAAAAGAA AAGAAAAGAT ACTGATTCAC GTCATCAGGT 300
ATGGTGTGGT CCACAGAACA GGAAGCTCTG TGTGAGGTCT GATTTTCAGC CACCTGCTGT 360
GTAAAGGAAA GAGAGAGGTG CTTGCTGAGC AAAGTTTCAG ACCAGAAGAC CAAGAGACAA 420
TTCAGAACAG CAGCAGATTC TACCCATGGT GGCATTCCTG TAAAGTGAAA CTCAAGCGCC 480
AAGTTTGTTG TCATGGGGAC TGTTGATTGC ATGCTAGTCT TATGGAAACA CACGGAAAAC 540
CAGAGGTCAA ATTCAGTAGC ATCTCAGAAT TCAGATAACA CAGCATGTAC AGTTTCAACC 600
CAGCAGGCTG TGTGTTTATC ACTTCAGGAA ATGACTCATA AGCAGTAAGG AGATGAGCTT 660
TGAAAGCTGC ATCTGGCCAG GGCACGGTGG CTCACCGCTG TAATCCCAGC ACTTTAGTGA 720
GGCCGAGGCG GGTGGATCAC CTGAGGTCGG GAGTTTGAGA CCAGCCTGGC CAACATGTGA 780
AACCCTGTCT CTACTAAAAA TACAAAAATT AGCCAGATGT GGTGGCACAC ACCTGTAATC 840
CCAGCTACTC AGGAGGCTGA GGCAGGAGAA TTGCTTGAAC CCAGGAGGCA GAGGTTGCAG 900
TGAGCCGAGA TTGTGCCATC CAGCCTGGAT GACAAGAGCG AAACTCCATC TCAAAAAAAA 960
AAAAAAGAAA AGAAAGCTGC ATCTATAGTA GCCTGCATGG TGGCAGGGCC AGTCTGGCTG 1020
TTTTGCCTAT CTTAATGACT ACATCTGCAG GTCATTTTGG TGTGCTGCTA TGCGACCCAT 1080
CCAAGGAAGT GAAAACACCA CGAAGGGTGG GCTGTCCAAT ACTGAGATGC ATTCGTGAGC 1140
AAAACCATAA TCATTTGATA TCTATTTTTG TTGTTTTGTT 1180
|
