Tag | Content |
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EnhancerAtlas ID | HS176-24629 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr21:35917310-35918450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr21:35917721-35917735 | GAAATGAGGAAGTG | + | 6.22 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_02750 | chr21:35916566-35918720 | Astrocytes | SE_09811 | chr21:35914742-35920153 | CD14 | SE_29460 | chr21:35915039-35918724 | Fetal_Intestine_Large | SE_41006 | chr21:35915863-35918362 | Left_Ventricle | SE_46107 | chr21:35915787-35919758 | Osteoblasts | SE_56471 | chr21:35916179-35919116 | u87 | SE_67780 | chr21:35916179-35919116 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I034543 | chr21 | 35915834 | 35919761 |
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Enhancer Sequence | TTTACTCCTC ACCATCAGTG GAGCGAGAGC CTCTGGGACC ACGTCTCCCG AGTCCCATGC 60 CTGCCATCAT GGTGCGGGCT GGACCAGCCT TCTTAGTGGG ATATGTTCCC CATAGAAAGT 120 AAACCAAGAG GCAAAAGCAA AGCAAAGCTA CGAAAGCAGG CTCAGTGCCC CCGCCCCTTG 180 TTTCAGTGTC ACCTCAAGTT TGCTTCTTGC TCTCAGAGGG AGATCACAGC ATTGCACAAC 240 GGGCAGTGTT GACTATTTGC TGGCCCTTGT CACCCACCCT TCCAAAACTC GGGCAGAGGA 300 CAATCTGAAC ACCAGTGTGA CAGTTTCTAA CAAAAGGCTT TGCTAGTACA GTGCCTGAGT 360 GTGGGTGTCC ACTGAAAACT AATTTCAGCC CTGACTAAGA AAGGCATCTC AGAAATGAGG 420 AAGTGTATTT TGGGCTCCTG TGGTTTCTGA TGAAAAATGC TGCAATGTGG GGCATGGGTG 480 AAAGGGAAAC ACTGAGAAAA TAGATGTGAC CCCCAGTATG CTTCCTTGAA GAAGTGGGGG 540 GCTGGCCAGG CCAGGCACAA AGATCCTTTG TGTTCCCTGA GCCTGTGACT TCTCCCGCTG 600 TTTCTCAGCA GTTACACTAA CGACATTGTG GAGGAAACAG CTTCTCCTTG CATGGCCCTG 660 CCCCTTGCAC TCTAGACTGT TTAGCCTCCC TGCTGGTCAG TCCCCTCTCC CTACAAATGC 720 CAGCAGCTTT CCCCCAGTCC TTGCTGCAAC CACAAAGTCT CGCAAGGATT TTCAAATGCC 780 ACTGGGAGGA TAGCGGTGCC ACCCATGGAG AATAATGACC CCAGGCCCTA AAATGAAACA 840 GGTTGCTCTA ACATTCGAAG AATAGCCCCA GCACACCAAA TGCATTCACT TAATTTCTTG 900 TTCAACAGAA AAGAATGACC TCTTTTAATA CAGAGCTGCT TTGAAACATG TCATTTCAAA 960 CAGGTCCTAA GAAGATCCTG ATATTTGTCT GTATCTTAAC TGGATCTCTG TGGGTTGAAA 1020 AACGCTCATA GAAATGTTGA AGGACATCAG TCAATCTTTA ATAAGATGAG ATTTCTCAGA 1080 GATACAACAT GCTGTTTGAC CATCTGAAGG ATGCTAAAAG AAAGTGATTT ACTGAAATAA 1140
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