Tag | Content |
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EnhancerAtlas ID | HS106-01237 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr2:85482440-85483930 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr2:85483818-85483829 | ATATTTACATA | - | 6.62 | TFAP2C | MA0524.2 | chr2:85482641-85482653 | AGCCCCAGGGCA | + | 6.11 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_30140 | chr2:85481584-85483979 | Fetal_Muscle | SE_32959 | chr2:85481675-85483962 | H1 | SE_37756 | chr2:85482637-85487486 | HSMMtube | SE_68755 | chr2:85480692-85483989 | H9 |
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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 |
GH02I085254 | chr2 | 85481196 | 85487497 |
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Enhancer Sequence | AGAAGGACCA TTCCCATACC TCACAGTCCA GCTGTCTCCC CATTCCCTCC CCCCTACATG 60 CTGTTGTGTT TCCAAGTTCA TGCCTGTGTG CACACCTGCA CACAAGGGAA TAGGAAAATG 120 GCTTTGATGT ATGGAATCAT GTCTACAAGC TGCTTCAGTC AGGGGCCCTT CTTGCTGAGA 180 GACCAGGCAG CTTTCCCAGG GAGCCCCAGG GCAGGGGCCT GAGGCACCTG CTTCCTGTTC 240 TGTCCCCTGA GAGCTCCGCT TTGCCGGGAG AAAGGAGAAG CCTAAACAGG GTGGGCTGGG 300 TCTGCGAGGC CTGCCTAAGG CTGCCCTCTG CCTTCCCAGC CCTTCAGTCC CTGATCCTTT 360 CGGGCCCCTC CTAGGCCAGA ATGTCCCAGA TTAGATGGGG TGGGGAGGAT GTCTTCTGGT 420 TGCTGTAGGC CTGCATTAGG GGAGTATCCT CTCTGGTCCC ACGTGGGGCA GGTGCCCAGA 480 GCCAGGAATG AGCCGCCTGT GGTGATTCCT GTGTGTCTGG AGTCCAGGAG TCCCTTGCAC 540 TGTTGGCCAG TGGTCACTGT GCGGTGATTG ACTGGGCTCA GTGTCTGTAG CTTTTGTCTG 600 AGCCCCTTGC ACCCCTCCCC GGGGATGATT GTCTGAGTTG GTGGATGTTA ATCTGCAGCC 660 CCTGAGAAGC TGCCTGGCAA ATGGGAGGTT AATGTGCAAA CAGCGGGGAG CATTGTCCAT 720 GTGTGAGGCT GGACAGCAAG TGGGAGGGAA ATAGTTAAAA ATCCTATTCA TGGCTCAGGA 780 GGGGAGGAGG GGTGGGCGCA GGAGCAGGCC CGGCCTTGTG CTAATCTTGC TGGAATGTAA 840 CTAGTTCGGG CAGTTTCTGG CTTCGATGTG CTTTGGGGCC GGTTGGCGTC CCCCCCGCCC 900 CAACCCAGTA CATCGATGGT GCGTCCGCGC GCCGAAGGCT GCTCTTTGTG TTCTCTGCAG 960 CCACAGCTTA GAAGCGTCCG AGTCAGACCG CTTTCAGTTG TAAGGATGGG GAGGGAGGAA 1020 GCTCAGCGAG GCAGTTGTGT TATCCAAATC CACAGGCTCT TTCTCTGTTG GAGGATTTGG 1080 GTGGGGGAAG GGAATGGGCA GAAGAGAATG TTCAAGGAGA AAGACCCTAA ACCTGTTGGG 1140 TCAGGCTGCT CAGCTGCCTA GAGGCCTGGG AATGCCTAGG GGGAAGCCCC TGCTTCCGGA 1200 CACACAATCA ATTACATATA ACAGTGGGGC CTTGTGTGTG TAGGCGGGAC ACTGGGAGGG 1260 GTCGGCTCAC AGCTCATGTT TTAATGCTTT ACAAGGAGAG TGTGTTCATG CATTGCTTCT 1320 GCAACTTATA ATCAATTTAA AACATTCTAC ATCTTGATCT AGGCTGGTGG TTACATTGAT 1380 ATTTACATAT TGGGCCAGGT TTGGTGGCTC ATGCCTGTAA TTTGGGAGGC CGAGGTGGGT 1440 GGATCACCTG AGGTGTCAGG AGTTCGAGAC CAGCCTGGCC AACATGGCGA 1490
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