| Tag | Content |
|---|
EnhancerAtlas ID | HS052-06149 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr11:9836650-9838040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr11:9837472-9837486 | AAGAGATGACTCAG | + | 6.67 | | ZNF263 | MA0528.1 | chr11:9837060-9837081 | AGGGCAGGAGGAAGAGAGGGA | + | 6.35 | | ZNF263 | MA0528.1 | chr11:9837066-9837087 | GGAGGAAGAGAGGGAAGGAAA | + | 7.15 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_37183 | chr11:9836873-9838166 | HSMMtube | | SE_44219 | chr11:9835850-9836841 | NHDF-Ad | | SE_44219 | chr11:9836907-9838428 | NHDF-Ad | | SE_45197 | chr11:9837000-9837712 | NHLF | | SE_45779 | chr11:9835452-9838261 | Osteoblasts | | SE_47204 | chr11:9836841-9839200 | Panc1 | | SE_55915 | chr11:9835599-9838999 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 9836857 | 9836932 | | chr11 | 9837328 | 9837627 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I009814 | chr11 | 9835851 | 9836841 | | GH11I009815 | chr11 | 9837029 | 9838082 |
|
Enhancer Sequence | TGACAACTAT TGTGCCAGAA TGGTGGGATT ACATTTTTAA AAATAATAAT ACTTGTCCGG 60
GTGTAGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCAGGGCGGG TGGATCACAA 120
GGTCAAGAGA TGGAGACCAT CATGGCCAAC GTGGTGAAAC CCCATCTCTA CTAAAACTAA 180
AAAAAAAAAA AAAAAAAAAA AAAAAAGCTG GGCGTGGTGA CGCGTGCCTG TAATCTCAGC 240
TACTCAGGAG ACTGGGGCAG AATTGCTTGA ACCTGGGAGG TGGAGGTTGC AGTGAGCCGA 300
GATCATGCTA CTGCATTCCA GCCTAGCGAC AGAGTGAGAC TCCATCTCAA AAACTTAAAA 360
AAAATATAAT AATAATATTT TATTGAGGAA GGGCAGACAG AAAGAAAAAG AGGGCAGGAG 420
GAAGAGAGGG AAGGAAAAAG GCAGCATCCC AACTCTTTCT TACTCAAATA CGTATGATCA 480
CATAGCTAAT CTGAGAAATT ATGTGCAAAG AGAATGGCAG AGGGGAGTAT TAAGGAGCTA 540
AACCTCGGAG AGTGATTCGG ATCACGAGTA AGTGTTGTGC TGAAGCATGG AAAGTCTGTG 600
CTCTGGAAAA GACACTGGCA CCAGCAACCC TGGATTGCTG TAGAAAAGGG TTCTATTTTT 660
TGGATATAAA ATTATCTACT GTATCAGAAG ACACATATGC AGATTTAAAA CTTGAGCATT 720
ACCCAGCAGT TTTATGCCCT CTACCCTAAA GGTTAGTGAC TAAGTGGTTG CAGCAGTCCA 780
GGCAGTGGGA GAAGAGCTAG CAAAGCCACT AGCCTGCTCC AGAAGAGATG ACTCAGTTAC 840
TGGCATCTTA AGGGCCAAGC ATGTGGGATC TTGCTAATGG CACCCTGCTC ACAGTTTCTG 900
CTCCACGGTT CAGCCAGAGG TCTGTCTAGG TTGTCCAGTG CCAACTGGAG CACTGGATTA 960
AACGTTGAGA TTTCTGAGTT AACAGATAAC TTTCATGTCC TATATACCTA CTGGTAGTAA 1020
TGAAATTTAT TTTGTAATGT GTGACTTGCA AAACATTAAA TTCAAGGAAT TGTTGTTGCT 1080
TTTGGAGGAA AAGACCATCT TTACAATTTA TGGGCCCTCA GCATGGTGAA GCTCTTTAGC 1140
GCAACAATTT AACAGTAAGA ATAAAGTTGA TTAGCATCTA GTATTTTGAA TTTTCTGACA 1200
CATCTTAGGA CATGTGTCTC TTTCTATATA GCTTTGCGAA GTTTTAACAA GTGTTACTCA 1260
GAAAACCTAG ACTTGGCCTT GCCTTGCCTC CATACATGGT ACCACAGTCT TCCTCTCTCC 1320
ATTCTTCTAT GTTTCTGTAG CCTGCTTTAG GTTTACCATA ACAAAACTAT CTGTTTTGCC 1380
ATGGGCAGAT 1390
|
