| Tag | Content |
|---|
EnhancerAtlas ID | HS098-46115 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:133394280-133395600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr5:133395346-133395359 | TTCCAGAATTTTC | + | 6.14 | | Nfe2l2 | MA0150.2 | chr5:133394714-133394729 | CAGAGTGATTCAGCA | + | 6.28 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_39383 | chr5:133394309-133395192 | Jurkat | | SE_49860 | chr5:133394764-133396600 | RPMI-8402 | | SE_66306 | chr5:133394309-133395192 | 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 |
| GH05I134058 | chr5 | 133394251 | 133395866 |
|
Enhancer Sequence | CAGACGTGAG CCACCGCACC CGGCCCAAGG ACTCTGACTC TTAAGGCCAC CTGAGAGACC 60
TTAGGCAGAC CATGCATTGC ACCAGCCTTG ATCATGCAAA CTGCATTCTA ATCAGGGCCA 120
GATAGGGAAC AGAGCAAAGA TGGAGCCTAT CATTCCCAGG GACTGAGGGG ACCTGAGCAA 180
GCAGGGCCTT CCTGAGGCAG AGGGTGTCTG AACCTGACAC AGCAACGTGA CCGGCACTCC 240
AAGGCCTCTC CACAAGCCTC TCTGCAGGGA ACTGCAGCCC CAGCAGACAG TCCCTGGCCC 300
CACCTTGCCC TCTCCCCAGG AGCTGAGCCC AACTCCACCC AGCCATCAAG GGTGGGCTTT 360
ACAATAACCG CCTCCTCATG CCCGCGTGCC AATGCAGAGG CTATGCACCC TGCATGCCAG 420
CAGAACAGGC AAGCCAGAGT GATTCAGCAC TGCCTAGATT GTGGCTTGCC AACCCATGGT 480
CGGCAACAGG CCATGAGTCA CAAATTACAG GCCTTCTGTC CTAGCAGGCT TTGCCAGCCT 540
ATGGGGTGGC AACGCTGGCA AGGAGCTCCA GAGCTCCAGG CTGAGGGCTG TAAGGAAAGA 600
AAGGCCCAGA CAGGAGCAGC AGACTGGGCA CTCTTACAGC TTCCCTCCCC ACCAGCCAAC 660
GTGAGGCTCC CAGGCTCCCA GGACACAGAG CCAAGGTACA GTTTCAGTGA TGTGATCCCA 720
GGAGAGAGGC TTGGACATGC TCTGACCCAG GGCTTCCTTG GCTCTAGACC AAGAGGAAGC 780
GGCTGGCATC AGAGCCTAGC ACACTTTCAT TCTGCATCTT TCAAGTGAAA CTATGGGAGA 840
GCCTCCCACG TGCTGTAGGC AGTGGCCCCA GGGAAGTGGT CCTCTGCCCT CTAAGACATC 900
CCCACACCCA GGGAGGGCCT GGAGCAGCCT TGTTCATAGG GCCAGGAAGC TAGAAGCCCG 960
TCGCGCTGTT TCATGAGCTC CTACCAAACA GGAGCTGACC CCACAGGCCT CTGAGCATCA 1020
GCACACCCCC GAGCCATTTG GGCATCCTTG TCCATGACAA CAGGGTTTCC AGAATTTTCA 1080
AGAGAACTGG GTCATTATTT TGTGCTAGTA TAATGAAGCC AACCACACCC TATACCCCCC 1140
ACCTCAATCC TGCCCCCAAC AAAATTCCTT TCAGTTCAAG AACTGATTCT CAGCAACAGC 1200
AAACTTAAAT GCTACCCAAA TTTGATGTCT TGTTTGGGTT TCTTTGTTAT ACATGTTTGA 1260
TTGTGTGGCT GAAGGTGACG CAGAGAGGCA CAAACAGCAA GGAATGAGAG CCAAAGCCAG 1320
|
