| Tag | Content |
|---|
EnhancerAtlas ID | HS170-00823 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr12:51762360-51763280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr12:51762478-51762493 | TACGCCCCGCCCACT | + | 6 | | SP2 | MA0516.2 | chr12:51762477-51762494 | CTACGCCCCGCCCACTT | + | 8.08 | | SP4 | MA0685.1 | chr12:51762478-51762495 | TACGCCCCGCCCACTTT | + | 6.58 | | Zfx | MA0146.2 | chr12:51762433-51762447 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_05159 | chr12:51762348-51764035 | Brain_Cingulate_Gyrus | | SE_06229 | chr12:51762108-51764112 | Brain_Hippocampus_Middle | | SE_07315 | chr12:51762614-51764013 | Brain_Hippocampus_Middle_150 | | SE_25710 | chr12:51761044-51764360 | DND41 | | SE_59549 | chr12:51734714-51764347 | Ly3 |
|
| | 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 |
| GH12I051368 | chr12 | 51762246 | 51766694 |
|
Enhancer Sequence | TGTATTTTTT GTGAAGATGG GGCTTCACCA TGTTGGCCAG GCTGGTCTCG AATTCCTGAC 60
CTCAAGTGAT CTGCCCGCCT CGGCCTCCCA AAGAGTTGGA ATTACAGGCG TGAGCCACTA 120
CGCCCCGCCC ACTTTTTCCT TCTTCAATCC TACTGGACAG ACAGGTGAGG TGATTATGAC 180
ATGGCGCTCA TTTATGAATG GATTCTTCAG GCAGTCATCT GAGGAGGGGG CTGTATCTTA 240
CTTAACTCCA GGAATGAGGC CTCTTATCTC TGGGGGCCAG GACCTCAGGA ATCAAAATCA 300
GCCTCATGCA GCAGCCTCAG CCCAGCACTC ACTCCACAAA TGTCTGTCAA TGTGCTGCCA 360
GGTGCCAGAT GCTGTTCTGG GAAGGGAGGG GCCTGGTCTG GGTCCTGCCC TTTGAGACTC 420
ATAGTGCACC TGCAGCCCCG GGTGCTGGCC CTGACAGGAA GGAGGGAGGA AGCCCAGGCT 480
CCTCAGCATG GCTGCTGTGT TTCCCCGAGA GCTTGCCCAG CTCTGCGCAC AGGAAGTTCA 540
CGGTAGTGGA GATAACCCAC GGACAAAACA TCATAGGAAG TGGGTTTTGT GGTGAGAGAC 600
AGTGAAGCAC TGAGCTGTGA ACCTCAGGGG GGGCCCCGAG CACTACAAAG CCCTTCTCCC 660
ACGCCTTCCT TCCAGTCTGG TGAGGCCAGA CCCAGGGATT CTCAGCCTGA GAGGCTTCCA 720
GCCTCTGGCC TCAAGCCCTT CTGGGGAGAC AACTCCCCTA AGCAATGCCC CTCGTGATAC 780
TCCACCTGTT CCACCCCCAG ACCTACTGGA CAGACCCAGA ACTGAGGAGA CTGGAGCTGA 840
GCATAGCTGT ACCGGTGAGC CCAGCCACAC ACTCATGTCC CCGCCGTGAC AGCCTTCCAA 900
CTTAGGTTCA ACACCCCACC 920
|
