Tag | Content |
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EnhancerAtlas ID | HS087-14844 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr3:112994440-112995850 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_25960 | chr3:112993394-112996406 | Duodenum_Smooth_Muscle | SE_26961 | chr3:112994449-112996268 | Esophagus | SE_30079 | chr3:112993387-112996620 | Fetal_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I113274 | chr3 | 112993226 | 112997112 |
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Enhancer Sequence | TTTTAAAAAT TGTATGTGAT AAAAGCATAT ACATGCTGAT TTTGCTTATA AAAATGCTAT 60 GTGCACTTGA TGGAAAGCAT ATGAATGTGG AATTAAAAGT CTTTCTCCAC TCCTCCCCAC 120 CTCCACAAAC AAGCAAGAAA ACAGAACCAA CCCTGCACAG TGGAGAGCGC TAGCTGTGCG 180 GAAGCTGTTT CCCTGCCTTG GAGCCCTGGC CCCTGACTCC TTCTATTCTG TTTTTTTCCC 240 CTTACATGCT CTCCTAGAAG TCCTTGGGTC AGGACAAGTC CACAGAGACC CTGGGGTTGT 300 CAGAAAGACA CCTAAGGCAG AGCACCCCCT ATGCTCCCTC TGCTGCCTCC CCAGAGGCAG 360 GGGGACGGGG CGAGCAGTTT CTCATTAGCC CTCCACCTGC TGGCCTCTTC ATAGGCAGCC 420 AGCAAAGCGG GTGAATGAGT TTTTAACAAA AAGCAGCATT GTTCACATGT TGTAGGGCAG 480 GGCTGGTCCT AATCCTATTT CCCCATGTAA CTGGACACCT CCATCTCAGA GTTGTAGACA 540 AAGATCAGGG CAGGCCAAAC GCCCATGGTT CCCAGGAGAC AAAACCCAGC ATGAGAGCAA 600 GACTAATATT TTTCAGGCCA ATAGGTGGCC GTGAAGCAGC CTCGCAGAAG AGGCAGATTG 660 GCAAAGGCCA TGCCGTGGTG ATCCGGAAAT GCCAGGCTCA GGCCGCATTC ACCCCCTCAG 720 TGTGTGTGAC AGTGACTAAT TACCCTTCTA TTTCTTATTT TCATTTCTGG GCCCAGTGGA 780 AGTGTGAGGC CAGTGCTGGG AGGGCAGGGT ACATGGGGCG CAGGGGAAGT GAGAGTCCGG 840 ACAGGCCCCT GCTGCGTCTG GCTTCTCTCA GGCTCCAGCC TGGGGTCTCC TCAGCCTGGG 900 GTTGCCAAGG CAGAAGTTCT GGCTTGAAAG CAGTTCCTCT CTTACGGAAC TAACAAGTCT 960 TAAAGATCAC CCGAGAAAGA ATTTGAAATC GAAAGTCAGC ATTCGGGCTG TGTTTTTTCA 1020 TCCCCCTTCT CTTGCTGGGG ATTGGGAATC ATTCAGCTAA TTTTCACTGT TTCACATCCA 1080 TGAAGCAAGT TTCATTTCCT GGTGCATCTG CAGACCCTGG GCTACTGTGT TTGGGTTTCC 1140 AGCACCACTG GGGAGTCTCA GTTTGTAAAA ACGTCTCCCC TTGGAACAAA TCCTGGAAGC 1200 CTGACAATGA GCCCAGACCA TTCCTGTGCC TTGAATGGTA GGTTTTGTTC GACTTTGGAA 1260 TATTCTGCTC AGAGAGAAGA GCTTTTCCTT ACAGCTGTTT TCTTCCTTCA GCAAACCACA 1320 ACTTGAGGCT CCAGCAGGTT CTCTGGGGTG TAGAGTTGGC AGTAAAGTCT GTTGTCCCGA 1380 AAGGTGGCGC GGCAAAGATG AGCAGCCTCT 1410
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