Tag | Content |
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EnhancerAtlas ID | HS105-47091 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:202724500-202725900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:202725453-202725472 | TGACCACCAGGTGGAAGCA | + | 7.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_46387 | chr2:202722074-202726199 | Osteoblasts |
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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 |
GH02I201858 | chr2 | 202723007 | 202725783 |
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Enhancer Sequence | TTTCTGATTT TTCTTTCTCA AATTCCCTTT AAATAGATGT TCCAATGGCA ATACAGAGCT 60 GATAAGATCA TACCTTAGAA ATCAGTTTGC TACAGAATCA TGTAGAGCTT TTAAGAGAAT 120 CAACTAAATA TTTAGACATT TCTCAACTAA AGTAAACGGA GGCCTTACTC CTCTGGAGGT 180 TGTCCAGTCA CCATCTCATT AGATGCAAAG ATCCTGCGAT AAAGAGAAAC TTTTTTTCTT 240 GCCTACATGA TTGCAGCCCA GTTGTGGTTT TTAATGTGTC ATTGATTGTT TCATCCAACT 300 CCTTTTGCTC CACTGAAAGG GTCTGTCATA GCTCTGTTTG CTTCCTTAAA CACGGTTTTT 360 GAAAGCGCTC ACGCTGTGTG AGCTCAAATC CTAGCATTAA TGTACTGCTG GGTTCATTTC 420 ACCAAACTCA AAAGCGCTGA GTTTAAATCC CTCTCAATTC CATTTGAGGC ACCAGAAGAC 480 TTTATCCTTC TCCACTAATG GTTCCAAGTT TACATCTAGA TACTGGGGGT CAAGGACAGG 540 AGAGGATTTA GAAATAACAG TGCATGACAT TAGTCAATGC ATTTGCCAAA TTGGCAATTA 600 GTTCCTGATG TGCGTGCAAA GCATTTTATT CCTGTCTCTT TGATGCTTGT TCCCATAAAG 660 AAGGGAATAG GGTCCACAGA GGCCTTCAAA CTTTTAAAGA AATATCTGCT GAAAATCATG 720 CCTGATTTGT GACATGAGCT CAGCCGCAGG GAAGCATCCG GGATTATCCT GGTTATTTTA 780 GTCCTAGGAA AGAACACTGC ACGTGGGAAG TTTTTCCACT AGAAGAACGT AATGAAAATC 840 AAAAGGCAGG AAAGCGGTAC TAAAAGCCCT GCAGGGACCA GAATCAGATG TACCATAAGC 900 GACAGGCCAA GGGATGCCCA GTTGTTTTTC AGTATGCTTG CTTTATCAAC TTCTGACCAC 960 CAGGTGGAAG CAAGAAACAG CATGGATGGC ATACTGACAT CGGACAGCAT CGTACTGCAG 1020 CAATGCAGCC TTGTTCTAGG AATGTCTCAT TTTGACCTTA AATCCAGTGT GAGAGCTTCA 1080 CTGCGTCTGA AACCACTATG AGACAGAAGA TGATTAAAAT GATCCTTGTC CCCACTGGGA 1140 TGATAAAGAG CTATTCTGCT TTGGGCTCAA TGAGTTCTGA GCAAGTCTCT GTGTTTGCTG 1200 TGAGCACAAG CTAAGGTCTG CATCTGGGTC GGCATCAGCT TGGTTGTATG AGCTATTAGC 1260 CAAGGGAGTT ATTCAGTGGG TTGAACTAAG GGGAAAGATA TTGATAAAAG AGGCTTTAAC 1320 TGCAGGCATC AATTCATATG GAACTGTAAG TCCAAGCTCC CCCTTTTACT ATCTGGGGTA 1380 ACTTGAGGAA GTTACTTATT 1400
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