Tag | Content |
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EnhancerAtlas ID | HS006-01463 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr1:68152270-68153340 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:68152653-68152665 | GCTAAAAATAGA | + | 6.92 | MEF2B | MA0660.1 | chr1:68152653-68152665 | GCTAAAAATAGA | + | 6.44 | MEF2C | MA0497.1 | chr1:68152651-68152666 | GAGCTAAAAATAGAA | + | 8.42 | TP53 | MA0106.3 | chr1:68152458-68152476 | AACATGTCTAAGCATGCT | + | 6.87 | TP53 | MA0106.3 | chr1:68152458-68152476 | AACATGTCTAAGCATGCT | - | 6.98 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_02387 | chr1:68150798-68153933 | Astrocytes | SE_25144 | chr1:68149698-68153190 | Colon_Crypt_3 | SE_27725 | chr1:68148478-68155923 | Fetal_Intestine | SE_29142 | chr1:68148266-68155916 | Fetal_Intestine_Large | SE_36223 | chr1:68147605-68155969 | HMEC | SE_38054 | chr1:68147777-68153961 | HUVEC | SE_40089 | chr1:68150789-68153949 | K562 | SE_41280 | chr1:68149853-68153764 | Left_Ventricle | SE_45351 | chr1:68150793-68155051 | NHLF | SE_64600 | chr1:68150860-68155989 | NHEK |
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Enhancer Sequence | GTAAGGGACT GGGGGACTGC AGCCTGCAGG GTAGAGCCCC GGAAGGACGG GAGTCAGGGC 60 TGGGTTGCCT GATTGTGGAT CTGTGGTAGG TGGGGGTCAG GAGGGTGGCT GCCTTTGTCC 120 GACTAGAGTG TGGCTGGACT TTCAGCCGAG ATGTGCTAGT TTCATCACCA GGATTTTCTG 180 TGGTACAGAA CATGTCTAAG CATGCTGGGG ACTGCCAGCA GCGGAAGAGA TCCCTGTGAG 240 TCAGCAGTCA GCCCAGCTAC TCCCTACCTA CATCTGCACT GCCTCCCGTG ACTAATTCCT 300 TTAGCAGGGC AGATTAGATA AAGCCAAATG AATTCCTGGC TCACCCCTCA TTAAGGAGTC 360 AGCTTCATTC TCTGCCAGTC AGAGCTAAAA ATAGAAATTG TGTAGGAGAC AAACCTTGTT 420 AATTCCCTAG AAATACATTA AGAGGATAGA GTGGAATTTT TTTTCTCTGC AATCTTGCAT 480 TTTTTTAATG GCTCTTTTTT TTTTTCCTGA TAAAAACCTT TGGTAGGTAG GGAAGTTATG 540 TTTTCAGGGG TAAATGTGCT ACTTTTGTCT TCTAAATTTT GCTCTTTTTT GACTGGTCTA 600 GTCAAGTGAC AGCCCGATTA TTTTGCTACT CCTTAAAAGT ACTATTCTGT CTCTTGGAGT 660 ATGGTTGATG GCAATTCCAG TTAACTGCTG TGCAGCTCTC ATCTCATTGT GCACACAGCA 720 TGGAAATCTT TCTCAAAACT GTTTCACTCA GGTCAGGGTA ACAAGTTTGG TAGAGCAAAC 780 CGGTGAATGA TACTCTCATG CAAAACTGAA CAGATATGCA AACATATGTA TGTGGTTCAG 840 CTTGGGTTGC ATGGGTTCAG ACTTTGCAAT GTGTAGTTTA ATAGGTAATT ACCCTTAACG 900 CTTTTGCAGG GAACCCAACT ACCTTGAAGA AACTTTAATT TTTTTGTGCT TCTAATTTGT 960 CTCCATGTCA CATAGCCAAA ATATAGAATG TTCAAGTGTT TTCTCCTCAA AAGTATAATT 1020 ACTAGAATAT ACTGGTTTTT AAAATAAGTT TATTTTTATA AATTTGTTTC 1070
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