Tag | Content |
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EnhancerAtlas ID | HS087-02422 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr1:226369410-226370710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr1:226370400-226370410 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:226370400-226370410 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:226370400-226370410 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_11118 | chr1:226367565-226371348 | CD20 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 226370122 | 226370365 | chr1 | 226369578 | 226369655 | chr1 | 226369500 | 226369600 | chr1 | 226369600 | 226369755 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226181 | chr1 | 226369044 | 226371316 |
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Enhancer Sequence | TGAAATCTTA AATTAATGTA AACAATCTAC CAGCTTAATG TAATACAGTA ATAAAGTATT 60 AGAGAAGGAA AAGTCCACCC CAAAGAACTC TAAAAACCAA AATACAATTC CCCAGGTCAA 120 CTCCATCCAA GAAGTATAAA GGTCATAATA AAATGAACCC ACTGGATTCC TGTGGGTCCT 180 TAACCCATGG AGATAAGAAA ACCTAGCTTA ACATTGTTAA AATAGAACTG GGCAACTCTG 240 GCCGGGCGTG GTAGCTCATG CCTGTAATCC CAGCACTTTG AGAGGCCAAG GCGGGTGAAT 300 CGCTTGAGCT CAGGAGCTAA AGACCAGCTG GGCAACAAAG CAAGACCTCT GTCTCTACAA 360 AAAATACAAA AATTAGCCGG GCATGGTGGC TCGTGCCTGT GGTCCCAGTC ACACAGGAGG 420 ATGAGGTGGG AGGATGGCTT GAGCCTGGGA GGCATAGGGG GCAGTGAGCC AAGATCGCAC 480 TACTGCCCTC TAGCCTGCAT AACAAAACCA GACTGTCTAA AAAAAAAAAA AGAATTGAGC 540 AACTTTGCTC CTCCCTTTAA AAACCTCCAG TGGTTCCTCA TCTTCTAATT TACTGACAAA 600 AAGGCCGAAC TATTAATACT TACATGGCCA GGCGCGGTGG TTCACGCCTG TAATCCCAGC 660 GCTTTGGAAG GCCGAGGCGG GGAGATCATT TGGGGTCAGT CCAAGACCAG ACTGGCCAAC 720 ATGGTGAAAC CCCATCTCTA TTAATAATAC AAAAATTAGC TGGGTGTGGT GGCACAAGCC 780 TGTAAGCTCA GCTACTCACG AGGCTGAGGC AGGAGAATCA CATGAACCCA GGAGGCAGAG 840 GTTGCAGGGA GTGGAGATCA TGCCACTGCA TTCCAGCCTG GGTGACATAG CAAGACTCCG 900 TCTCAGAAAA AAAAAATGAC AATGGCATGC AAGTCCTTCC AAGAATTGAA CTCAGTTACC 960 TTCCCAGCTC TCTCCATCAA ACTGCTTTCT ATTTTCCATT TTGCAAACAG ACATGCTTTG 1020 ACTTCTCATG GCTTTCATGG CTCTTGGCCT TCCCCCCTCT GGAATGGCAT CTGCTCCCTC 1080 AGTCCTCCAC ACTGTACTGC AGTTGTCACT GGGTCCTTAA CTCCTCTTTT GGACTCTAAG 1140 CAAAAGATAA CGTACTATTC ATTTATAGTT GTAACCTAAT ATAAAACTAT CCATACTGAA 1200 AAGTCAATAA TGTCTGAAAT TTAGATGGTA AAATGCTAAC TTACATTTAC CCACATCTTC 1260 ATCTATTTTA CTTTTACTGT CATAAAAAAT TAAGAATAGT 1300
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