Tag | Content |
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EnhancerAtlas ID | HS050-04872 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:178533140-178534280 |
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) |
HNF4G | MA0484.1 | chr1:178533742-178533757 | CAAGACCAAAGTCCA | + | 6.37 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_10954 | chr1:178529343-178538472 | CD20 | SE_58337 | chr1:178530312-178588990 | Ly1 | SE_59705 | chr1:178531640-178578875 | Ly4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 178533812 | 178533910 | chr1 | 178533979 | 178534243 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I178560 | chr1 | 178529344 | 178538472 |
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Enhancer Sequence | ACTGTACTCC AGCCTGGGTG ACAGAATGAA ACTCCATATC AAAAAAAAAA AAAAGAAAAA 60 AAGTCCTCCT TCACATCTTT TAAATCATTC CTCTTTTAAT TCAGATTCAA ATTCATTTCT 120 TCTGGTCTGG CTCAAGTTGA GTCCTTGTCA GTGTCCCAAA TTTTGAGCCA CAAAATCCAG 180 AGTTGTAGAA AAAGGAGTAG CTGGGGAAGG GAAAAGTCTG TGACCACAGT CAATGGAAAT 240 TGTGGACCAA GCATTTCTAG AAAATGAATT ACACTGTTAC AGAGGCTTGG ACTGCAGCCA 300 TAGGAAGGGA GCTATTGTTC TGCAGAAAAG TTCGTGAACA ATTCCCACTT GGCAAAATGA 360 ATGAGAAGGA AAATCAGAAA TACCTGAGTC TTCCAGTGGT GTAATTTCTA ATGCTGATTG 420 ACACCAATCT GAAGCAACCG AGAATACTGA CAGCAAGGTG GAACAAAAAT GCCATTCACC 480 ATGAGCCCAA ATGGGTACTG AAGCTGCTAA GCACAGTTTA ATCTCCTCAG CCCTGTCCGG 540 TTGCACATAT AAATCTGCCT TCTGTCTCTA TATGTGCCAA GGGGCACTTT CATCTTTGAC 600 AACAAGACCA AAGTCCATGC CTATTTTCTC AGCAAGGATC TCCCTGTTTG TGTTAAATCA 660 GTCCCGTGTT GTTAAGCTAA GGGCATTCTG TGTAGAAACA TCTCAGGCAT TAAAATTTGT 720 AAAAACCTAA CTAGTGTCTG CCCCCTTGCA GGGCCCTGTC TGTAGAAGTA ACTAGGTCTT 780 ATTTATTTAT TTATTTTTAA AGAAGTATCA TTAGGAAACT TTCATTTTTA TCAGCTACCA 840 TTTAGATCTC AGGACACATT TTACTTCTCA TTTCATTTGA CATATGAGAA AAATGTTGCA 900 TGCCAATTGA GCTGTAAGGT GAACTTGACT GTGATAATGG GACACAGCTC AGCAAAGACA 960 GCAAGGTCAG CTGACTGGTG TTCTGTTTTC TGTACGCATA TCCACTGACC TGGTTCGGGA 1020 TCACCTCTTT GTTCTGCAAA GGACTATCAG ATTATCACCA GGGTGGTCCA AGAGCATCTT 1080 CTGTACAATT AACTGGTAAG GACACTAACA AATGTATGTG GAATGAATGG ATTCAAAGGG 1140
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