Tag | Content |
---|
EnhancerAtlas ID | HS034-29833 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr8:131057750-131059220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr8:131058105-131058116 | GAGCCATAAAA | + | 6.14 |
|
| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_00708 | chr8:131057605-131059064 | Adipose_Nuclei | SE_58319 | chr8:130983513-131114285 | Ly1 | SE_58914 | chr8:130970257-131059501 | Ly3 | SE_59893 | chr8:131020352-131075191 | Ly4 |
|
| 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 |
GH08I130045 | chr8 | 131057569 | 131059297 |
|
Enhancer Sequence | TACTGTTGCA AACAGGACTG CTACGGACAT TCTAGTGCAT GTCTTTGGCC AATGTATGTC 60 ACATTTCCAC TCAAGAATCT ATGGGTCACA GAACACGAGT ATGTCCAGCT TGAGTAGATA 120 TGTAGCCGAC TTCACTTTGA CTCTATTCCT GTTCTCTGCC TCCTATCCCA TGCCCTTAAC 180 TTCCCTTTCC TTGCAAGCAA GCAGGGTCAC CACCCTGGCA TCTTCCACTC TGGGGCAGAC 240 CAGACAGGGC CTGGGTTTTG CGTGGGAAAG TAAACCCCAG GCCACTGGGA CTAGTTGGTG 300 GGTAACCCTG GAGGCACCGC TGTTCCTTCA TCTTCAGAGC TCACTTAGGG TGGCAGAGCC 360 ATAAAAGGAG CTTCAGATAG GGAAGTAGCT GGTAACCGGA GGTGGAGCCA GCCAGGGTAG 420 TCTCGGTGTC TGACGTTTCT AAGTGCTTCC AGCTGAGCAG GAACCAGGCT TGCACATTCA 480 GACAATGTAT TCCTGTGAAT CTGTTCAGCG GCTTAATGCA CCATAAAAAG AGGTCCATTG 540 TCAAGCAGCC TGTTTCCCGG GTGGGAGTCA GCAATATGCA GCGTAAGTGG GTAGAGCCAC 600 TGTGGCTCAG AGGCTCCCCG GCTTTGGCCC TCGGTTGGGG GCGGGTGCTG CCCATGCTTT 660 TGAAAGGAGA GCAGCTAATG TGACTCCCTG GACTCCGCCC CTTTCAACAG CGGGCGCTCT 720 GCTCGTTATT TTTGACCGGT TTCATGTGCT CACTCGTTCA AGAAATACTC TTGTGATCAC 780 CAACTGCAGG TCAAGCATGG AGGAGGTTTA TGTCTCTAAT TTATCACTTG TCACCGGGGA 840 AGGTGAGGAG TTTTCAAAGT TCTAGTCATT TTATTATTCT ATTTTGCACA TGGTGGTCAG 900 TGTGCAAGTT CTCATCATTT TTGAAGTGGT GAGTGCTGAG GATTAGTATT CTGTGCTACT 960 TTGTGTTAGG CACTAGGACA AGCATGTTAC ATGTACCGTC ACATCAGTGA TGTCATTTAT 1020 CACACCAATT CTATGATACT AAGACTACCA TTATCCCATT TGGGCAAAGG AAAAATGCTG 1080 AGGCTTGAAG AGGTTAAGGC TCAGCACATT GTTTTCTGAT TTCAAAGTCC AGACTCTTAC 1140 CCTCCCCTGA TCCTATCCCT CTGGACCCAG GTAACAAATG GCTGTGGCTG GCCCAGCCAG 1200 GCTACCAAGC TGCCACCCTT AGGGATGAAC AGAAGCTGTG CTGCAGGTGA TGAAAGTCCC 1260 AGGCCCTGCA TCCAGTTCAC ACTGCACGGA GAAGCCAGTG GCTACGCATG GACAGTGTGT 1320 GTCTGGCTTT ATAGAGATGG TCACACAGCA TTGGGCGGGT CACTGAGCAC TGTTCCACCT 1380 TCCAGCCCAC AGACTCCCAA GCTGTGTCAC ATCTAATGGA ACTTGAGGCT CAGAGCTCAG 1440 TCCATGTGCC TGAGGTTAGA GATGGCTGTT 1470
|