Tag | Content |
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EnhancerAtlas ID | HS109-01878 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr1:208026150-208027160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:208026877-208026888 | AACAGCTGCAG | + | 6.02 | Tcf12 | MA0521.1 | chr1:208026877-208026888 | AACAGCTGCAG | + | 6.62 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_01610 | chr1:208022251-208026688 | Aorta | SE_03907 | chr1:208025443-208026819 | Brain_Anterior_Caudate | SE_09440 | chr1:208020638-208026948 | CD14 | SE_25552 | chr1:208026162-208027148 | DND41 | SE_25829 | chr1:208025792-208027181 | Duodenum_Smooth_Muscle | SE_42138 | chr1:208021104-208027882 | Lung | SE_48593 | chr1:208025677-208027183 | Right_Atrium | SE_52485 | chr1:208025802-208027153 | Small_Intestine | SE_53314 | chr1:208020267-208027245 | Spleen | SE_65312 | chr1:208025577-208027381 | 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 |
chr1 | 208026738 | 208027051 | chr1 | 208026221 | 208027133 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I207846 | chr1 | 208020137 | 208027145 |
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Enhancer Sequence | ATAAGAGATC CCACCCACCT AGTCCCAGAG CCTGTGGCTC CTGCCAGAAA GCCACTGACC 60 CCCATGATTC CCTAAACCCC AAAAGAGCCA GGAAAAACCC AGCTCTGCCC ACAAGGGAGT 120 CCAGAGCAGC TGGCCACCCA ACAAGCTGTA AGCCTCTTAC AGATTAAAGG TCCTAATTTA 180 AACCTCTATT TGAGGTACGA CAAGTGGGTC AACACTCTGC AGGTCGGTCA GTGCAGCTGG 240 TGGAAGGAGA GGCAACTATG ACCCAAGAAA GGCTCTTCTT CTTCGGGGGG AAAGATGGAG 300 CCAGAGAATC ACAGATCTAA GTGGAATCAC TGAGGTGACA GGAAGTTCAT TCTGATGCAC 360 CACGAATCCT ACCCCCACCC TGCCCCCAGA TCGCCGGGAC TCCACCCTCC CTAGGCAACG 420 AACCTGAGAA ACAGAGAATA TAAGGACAAA ACCACAGTCG GGATGGCCTT CCTCTTCCTG 480 CTATGGCTTT GGTATGTGGG GAAGAAGGAA ATTTGCTGCT AAAAGATAAA ATTTTTTTAA 540 AGCGAAGAGA CAGTTAATAA AGCCAGGAAC CAAGAGAAGA GGGAAGGGGC TGGATATGCT 600 GCTGCATTCT AGGGAATCAT ACCCTGGTGA GAAGACAGGG AAGGTGACCT TTGCTCCTAA 660 ACCTGGCTGA GGTTTTCCTG ATCTTTCTCC CTAGCTCCTC CGCAGCAGGA AACACCAGGC 720 ATGGGTGAAC AGCTGCAGAC AAGCCTAGGA TCATGCTGTC AGAAGCTGAC TCTGGCTGCT 780 CTTTAAAAAG AGCCCTCTCA CCACATCTGT CTCCATAGAG ATGGCCTCTG GGGAAGTGGC 840 TGGAACCCAC TGTCTACACT AAGAGCAGAG AAATCCTTCC AGGACAATGT TTCTCAAATT 900 TTCTGGACCC TGATTCATAG TAGGAAATCA ATGTTATGCA GTAGCCCAAC ACAGGCATAT 960 ATGTGCACTT ATCTATATGT ATCACTCTCT CTATATATAT AACTGAAACA 1010
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