Tag | Content |
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EnhancerAtlas ID | HS095-19345 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr21:47832910-47834230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr21:47834124-47834139 | TGAACTCTTGACCTT | - | 7.36 | PLAG1 | MA0163.1 | chr21:47833576-47833590 | CCCCCGTGGGCCTC | - | 7.01 | RARA | MA0729.1 | chr21:47834121-47834139 | TCTTGAACTCTTGACCTT | - | 6.24 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68992 | chr21:47830338-47833703 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 47833104 | 47833244 | chr21 | 47833336 | 47833655 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I046410 | chr21 | 47830339 | 47833703 |
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Enhancer Sequence | GGGGAGGGGG GAAGGCGCGA GGTCCCCCCG GGAGAGGCTG GACACGCGGC AGCAAGGTGT 60 GGGGAGCGGG GAAGGCACGA GGCCCACCCG GGAGAGGCTG GACACGCGGC AGCAAGGTGT 120 GGGGAGCGGG GAAGGCACGA GGCCCACCCG GGAGAGGCTG GACACGCGGC AGCAAGGTGT 180 GGGGAGCGGG GAAGGCACGA GGCCCACCCG GGAGAGGCTG GACACGCAGC AGCAAGGTGT 240 GGGGAGGGGG AAGGCGTGAG GCCCCCCTGG GAGAGGCTGG ACACGCGGCA GCAAGGTGTG 300 GGGAACGGGG AAGGCACGAG GCCCACCCGG GAGAGGCTGG ACACGCGGCA GCAAGGTGTG 360 GGGAGGGGGG AAGGCGTGAG GCCCCCCTGG GAGAGGCTGG GTGCAGAACA TGTGGGTCTT 420 GCCCTGGGCA GAGGCGGGTA TTCTGCTGAG GTGAGGAGCA CAGTCCGTGC CTGCAGTGAC 480 ATGTTCTCTG AATCCTTTCT GTTCTGTAAC GAGCTGTCCA TAACTGTTGT GAAATTTCGT 540 ACGTGCTTCA TTTAAGCCAC TCTGTAGAAA CAATCAGTTG GGTTTTTTTC TTGTAATTGA 600 TCCAAATGGA TTTAACTGTG CTCGAGGGTT AGTCCTGGTT TGTCTTTTCA TGGGAGGACC 660 ACATCGCCCC CGTGGGCCTC ACCTCAGCTC AGGACTTTGA TGGCCAGCGT CTGTTTTACT 720 TTGAAAGGCC TCAGATTTAT TCTTGTAATC TGTTCACCTC ACTCCATATT GTCACTTGAA 780 AAAAAGCTGG CACTTCTTTT CCCCGGGGAA GGAGGTTGCA CCTTGACCAT CTCAAATTGT 840 AGCAGGGTGG AGATTTAGCG AGAAAAGCGG GTGCTGGTGC TTCTCCCACC CAGTGCACCA 900 GGGGCAGGTC CCCAGTGCCC CTAGGAAACA CCTGCGCAGG AGCTGCCCTC TCCTCAGGCC 960 GCATCAGGTG CAGATGGCAC CTTTATTTTT TTTCTCTCTT TTTTTTTTTT TTTGAGACAG 1020 AGTCTTGCTC TGTCGCCCAG GCTGGAGTGC AGTGGCACGA TCTCAGCTCA CTGCAACCTC 1080 TGCCTCCCGA GTTCAAGTGA TTCTGCAGCC TCAGCCTCCC GAGTAGCTGG GACTGCAGGC 1140 ATGCGCCACC ACACCCAGCT GATTTTTGTA TTTTTAGTAG AGACGGGGTT TCACCATGTT 1200 GGCCAGGCTG GTCTTGAACT CTTGACCTTA GGTGATCCAC CCTCCTCAGC CTCCCGAAGT 1260 GCTGGGATTA CAGGCGTGAG CCACCACGCC CAGCCTTAGA TGGCACCTTT TGATGCACTG 1320
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