| Tag | Content |
|---|
EnhancerAtlas ID | HS024-00414 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:27321100-27322470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Six3 | MA0631.1 | chr1:27321807-27321824 | CCAGGTGATACCCTTTA | - | 6.36 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_26796 | chr1:27320100-27322233 | Esophagus | | SE_26796 | chr1:27322265-27329040 | Esophagus | | SE_31795 | chr1:27319283-27327051 | Gastric | | SE_34461 | chr1:27319108-27326655 | HCT-116 | | SE_36077 | chr1:27320120-27329970 | HMEC | | SE_47963 | chr1:27320102-27321641 | Pancreas | | SE_49333 | chr1:27319936-27322236 | Right_Atrium | | SE_49333 | chr1:27322274-27323394 | Right_Atrium | | SE_65116 | chr1:27320938-27323497 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGGTGCGGT CTTAGCGGCT GGTGCGTTCG AGGGTCGGTC ATGGCGTGTG GGGGGCTGGT 60
CCAGGGCCCG GGAACTCCCT TCCCTGGAGC TTCTGGCGTC TGCTGGGTCC CTAGTAAAGC 120
TGCCACTTTC TGTTGCCGCC TCTCCCGACC ATCTGGAGAG TGAGAGGTGG TAGCATCAAG 180
TCTCCATTAT AAGAGTTGGA CTCTTGAGGG GGCTCAGATC CCAGGAACGG GTTGGCGGCA 240
AACTTTTACC ACTTGGAACC TGCCGCACGG ATGCAGCACC CCCCATCCTC ACCCCCACTT 300
GCGTGGCCTT TCCCGGGCCC CTCGGAGCTG TGAGCAGTCT TGCCCTTGAG GATGCTGCTT 360
CCTGGCGCCG CCCAGCTCCG TGCCTTCGGG AGGACAGAAT AATGAGGCCC CAGGATGGGG 420
TGGAGGCTGG CACAGGGCTG TACCACTGAA TTCCCCCTCT AGGCCTGTTT CACCTTTGGG 480
GAGACGGAAT CCCAGAGAGG TTTAGGATTT GTTCTCTTCA TACTTAGGCC CTTCTTCTTC 540
TAGGAGACAG CTTTTCTTAT GCCGTCATGC AGGTTCGCAA AAATTACAGC CTGACTCACA 600
TAACCAGGAC AGGATGTCTG GCACCTGCTC ACCCAGGGAT CCTTACATAG CAGAACCTAG 660
AGGCTTAACT CCCAACCTGT TACTAAGATG GCTCGGCCAG GTTGGAACCA GGTGATACCC 720
TTTAACAGGC CCCAAGGGGG CAGGTGTGGT ATCAGCTTCC AGAAAGGGGG GCCTTAAAGA 780
GCCAGATCTG AGGTGAGATC TGCTTCTCTT CCTGTCCAGA TGCCCTTCAG TCTCCCATTC 840
CTCTGTCCCC ACTGTGAATG ACCTGGCTAC CACATTGCTG CTCACCAGCT GAGTTAATTT 900
CACTCTCACT TATCAGTCTG CGAAGTGGAT CTCTTAACCT CCCAGAGGGG CTGTGGTGAC 960
GTTAACCCAG GGCAGAGGTC CTTCTTCTTC CTCACTAAAT CATGGAAAGA TAATTTTTTT 1020
GTTGTTGTTG TTTGTTTTGA GACAGTGTTT CGCTCTTGTT GCCCAGGCTG AAGTGCAATG 1080
GTGCGATCTT GGCTCACTGC AACCTCCACC TCCCGGATTC AAGCGATTCT CCTGCCTCAG 1140
CCTCCCAAGT AGCTGGGATT ACAGGCATGT GCCACTATGC CCATCTCATT TTGTATTTTT 1200
GGTAGAGACC GGGTTTCTCC ATGTTGGTCA GGCTGTTCTT GAACTCCCGA CCTCCGGTGA 1260
TCTGTCCGCT TCGGCCTCCC AAAGTGTTGG GATTACAGGT GTGAGCCACT GCACCTGGCT 1320
GATAATGTAT TATTTTAACT CACACCTGGA AACAGGCACT GCTTTTGCTG 1370
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