Tag | Content |
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EnhancerAtlas ID | HS024-13314 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr5:149988890-149990230 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr5:149990197-149990207 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr5:149990197-149990207 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr5:149990197-149990207 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr5:149990197-149990207 | AACAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00123 | chr5:149988443-149996761 | Adipose_Nuclei | SE_01549 | chr5:149989048-149990225 | Aorta | SE_06402 | chr5:149988927-149990383 | Brain_Hippocampus_Middle | SE_08263 | chr5:149988978-149990399 | Brain_Inferior_Temporal_Lobe | SE_23666 | chr5:149989078-149990282 | Colon_Crypt_1 | SE_26296 | chr5:149989147-149992534 | Duodenum_Smooth_Muscle | SE_27146 | chr5:149989116-149990290 | Esophagus | SE_27995 | chr5:149988076-149994045 | Fetal_Intestine | SE_29147 | chr5:149988185-149993250 | Fetal_Intestine_Large | SE_29818 | chr5:149989311-149990661 | Fetal_Muscle | SE_31661 | chr5:149989262-149990270 | Gastric | SE_40596 | chr5:149989004-149997010 | Left_Ventricle | SE_42134 | chr5:149988999-149990374 | Lung | SE_46676 | chr5:149989319-149989558 | Ovary | SE_46676 | chr5:149989564-149990152 | Ovary | SE_48061 | chr5:149987456-149990272 | Psoas_Muscle | SE_48556 | chr5:149989028-149990362 | Right_Atrium | SE_49445 | chr5:149989259-149989610 | Right_Ventricle | SE_49445 | chr5:149989611-149990165 | Right_Ventricle | SE_50806 | chr5:149989183-149990245 | Sigmoid_Colon | SE_51080 | chr5:149987244-149996627 | Skeletal_Muscle | SE_52506 | chr5:149989033-149990362 | Small_Intestine | SE_54988 | chr5:149989204-149992386 | Stomach_Smooth_Muscle | SE_65294 | chr5:149989219-149990181 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 149989391 | 149990000 | chr5 | 149989582 | 149989693 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I150608 | chr5 | 149988419 | 149996410 |
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Enhancer Sequence | TTGTCGCCCA GGCTGGAGTG CAATGGCTCT ATCTCGGCTC ACTGCAACCT CCACCTGCCG 60 GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGATTACAGG CATGCACCAC 120 CACGCCCAGC TAATTTTTGT ATTTTTAGTA GAAATGGGGT TTCACCATGT TGGCCAGGCT 180 GGTCTCGAAC TCCTGACCTC AGGTGATCTG CCCACCTCGC CCTCCCAAAA TGCTGGGATT 240 ATCGGCGTGA GCCATCATGC CTGGCTGGTT AGGCATTTTC TGAATTTTTA GTCCTTGAAC 300 CCTTTCTGCA ATGCAATATT TGGGAGCCCC AATGTATGCA ACAGATAAAA AGCAGTATGT 360 TATCAGCATA AGTTTACTAT AGAAACCGAA ATCATAGTAT CCGTCTCAGT CTCTTGTTTA 420 AACTGGGGGA CAGGGTGAGG GGGCACTGTG AATGTGGCGG GGGGGGGCAG TGTGGAGCAG 480 TCTCAGAGCC AGGGCCCTGT GTGCCAGCCC TCTCCCCATC TGCTGACTGC GTAGCCTTGG 540 GCAAGTCCCT CCCCATCTGA GCCCCCATTT TCTGGTGTGG CCAAGGGAGA CTGGACTTTG 600 TGCAGAGTGG CCTCTGCCCT GCCACACCCC TGCCTGACCT CAGCCAGTCT CAGCCCCGTA 660 TTTATAGCCA TGACTTCAGT CTCCCCAGTT CCTCTGAAGC TGGTTCCCTG GCCCATGTAT 720 TTATAAACCC AGCAGGGCAG AAATAGATGT GACGTACTGG GGACTTGGCT GGTTCTGTGA 780 GCAGGCTGGC TTCAGTGAGT CCACTTGGAA CAGGCTTGAG TGCCCCAGCA TCCTGGGTGC 840 TGAGTTCCAC AGGCAGTCTA AAGCTGGAAG AGCATTTTGA GACCCCAGGC CCAGGCTTGT 900 CATTGTGCAG GGAGGTCACC AAAGCCCAAG AGTGGAGGCA TGTGGCCACA GTCACAGGCA 960 CGGCAGAGCC AGAGCCAGAA CAAAGGACTC TGTGCTGTGT GAAATGGCCT CTCCCCAGAC 1020 CCTCAGAAAA CCTCCAGTGA CCACGCCAGG CCACAGACAC CGGTCAGGTT CCAGCTTGGT 1080 CATTTTCCTG CTCTGGGATC ATGGGCACAG ACTCACCCTC TGTGAGCCTC TGCTTCCTCA 1140 ATCTGTTAAC TGAGGGATAA CAGTAGGTGC CTGCCTCATA ATGTTATTGT GAGGAAGAAA 1200 CAAGAAACAA GATTGATACA GTGCCCAGCA CATGCTCAAT ATTCAATACG TGGTAGCTCT 1260 TGTAATGCCC TCAGTCACCA CTTCACAAAA ACAATAATTA TAATAACAAC AGCTGTTTCT 1320 ATTGAGCATG TACACAGGTT 1340
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