Tag | Content |
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EnhancerAtlas ID | HS095-25969 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr6:35364430-35365270 |
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 |
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Enhancer Sequence | TCCCGTCTTT ACTAAAAATA CAAAAAATTA GCTGGGCGTG GTAGCATGCG CCTGTAGTCC 60 CAGCTACTCA GGAGACTGAG GCAGGAGAAT CGCTTTAACC CAGGAGGCAG AGGTTGCAGT 120 GAGCCGAGAT TGCACCACTG CACTCCAACC TGGGCAACAG AGTGAGACTC TGTCTCAATA 180 AAGAAAAAAA TGAGACAGGG TCTTTCTGTG TTGCCCAGGG TGGTCTGGAA CTCCTGGGCT 240 CAAGCAATCC TCCCATCTCA ACCTCCCTGC CCAGCTGCTG TGCCCAGCAG TATTTTCTAT 300 AATTAGCATA GTGTACTTTT CAGATTATCT TGAAGACCCA GCTCTCCTTG ACCTTGAACC 360 TTCCCTGAGG CCTCCAGAGG CAATTTCCTC CTCAGGACTC AGCTGCCCTT CACTCTTCCC 420 TCGTGCACAG CCTGTCCTGT GAGTAGGTGC AGGTACTGAC TGGTCTTATC TTTCGCCCTG 480 AAAATATAAA CGTTTTAAAG GCACCTGAGG ATTTGTCAGC ACCTCCCCAC CCCCACCCTG 540 GGTCTGACCT AGGACTCTGA GTCAGGGAGG CCTCCCTCCA CTGAGTAATA GTAGCCTTGG 600 GATCTGCTCA GCAAGAGGAT TGTATAGTTT AAGGGAGGAA GAAGCACCAG TGCTGCCTCC 660 CCATGGGAAA AATGAAGCCC CCCCTCCCGC AACCACCACC ACCACAGAAC CACCAACCCC 720 AACGTCACTT GGCAGATTAG CAAAAGAACT AGCCAGACGC TGCTAGGCCC CTCAGGCTTC 780 TAGATTCGCT CTCCACCACA TTTCTACCAA TTTATGCTCA TCTTGATAAG CTCCTCCTTT 840
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