Tag | Content |
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EnhancerAtlas ID | HS047-28886 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr6:35364440-35365270 |
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) |
Esrra | MA0592.2 | chr6:35364777-35364788 | TTGACCTTGAA | - | 6.14 | Nr5a2 | MA0505.1 | chr6:35364776-35364791 | CTTGACCTTGAACCT | - | 6.42 | RREB1 | MA0073.1 | chr6:35365115-35365135 | CCCGCAACCACCACCACCAC | + | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_36118 | chr6:35364441-35366616 | HMEC | SE_45701 | chr6:35364445-35366574 | Osteoblasts | SE_64384 | chr6:35364396-35366580 | NHEK |
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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 |
GH06I035396 | chr6 | 35364378 | 35366479 |
|
Enhancer Sequence | ACTAAAAATA CAAAAAATTA GCTGGGCGTG GTAGCATGCG CCTGTAGTCC CAGCTACTCA 60 GGAGACTGAG GCAGGAGAAT CGCTTTAACC CAGGAGGCAG AGGTTGCAGT GAGCCGAGAT 120 TGCACCACTG CACTCCAACC TGGGCAACAG AGTGAGACTC TGTCTCAATA AAGAAAAAAA 180 TGAGACAGGG TCTTTCTGTG TTGCCCAGGG TGGTCTGGAA CTCCTGGGCT CAAGCAATCC 240 TCCCATCTCA ACCTCCCTGC CCAGCTGCTG TGCCCAGCAG TATTTTCTAT AATTAGCATA 300 GTGTACTTTT CAGATTATCT TGAAGACCCA GCTCTCCTTG ACCTTGAACC TTCCCTGAGG 360 CCTCCAGAGG CAATTTCCTC CTCAGGACTC AGCTGCCCTT CACTCTTCCC TCGTGCACAG 420 CCTGTCCTGT GAGTAGGTGC AGGTACTGAC TGGTCTTATC TTTCGCCCTG AAAATATAAA 480 CGTTTTAAAG GCACCTGAGG ATTTGTCAGC ACCTCCCCAC CCCCACCCTG GGTCTGACCT 540 AGGACTCTGA GTCAGGGAGG CCTCCCTCCA CTGAGTAATA GTAGCCTTGG GATCTGCTCA 600 GCAAGAGGAT TGTATAGTTT AAGGGAGGAA GAAGCACCAG TGCTGCCTCC CCATGGGAAA 660 AATGAAGCCC CCCCTCCCGC AACCACCACC ACCACAGAAC CACCAACCCC AACGTCACTT 720 GGCAGATTAG CAAAAGAACT AGCCAGACGC TGCTAGGCCC CTCAGGCTTC TAGATTCGCT 780 CTCCACCACA TTTCTACCAA TTTATGCTCA TCTTGATAAG CTCCTCCTTT 830
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