Tag | Content |
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EnhancerAtlas ID | HS108-00403 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:12269280-12270450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr1:12269727-12269742 | TGACCTCTGACCTCC | - | 8.03 | Nr2f6 | MA0677.1 | chr1:12269727-12269741 | TGACCTCTGACCTC | - | 7.42 | Rxra | MA0512.2 | chr1:12269727-12269741 | TGACCTCTGACCTC | - | 6.88 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09154 | chr1:12267985-12269870 | CD14 | SE_18389 | chr1:12267917-12271730 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19117 | chr1:12267993-12269825 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19117 | chr1:12270287-12271189 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22347 | chr1:12268147-12270077 | CD8_primiary | SE_22347 | chr1:12270206-12271340 | CD8_primiary | SE_53313 | chr1:12269042-12269873 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I012208 | chr1 | 12268374 | 12269969 | GH01I012210 | chr1 | 12270127 | 12271427 |
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Enhancer Sequence | GTCGACCCCT GGCTCTGCCT GGGGTCTGGG CTTGGGTTTG TCCATGCTCC TACTTGTCTG 60 CCACCCCTGT GTAAGGGGAG ATGGCGTCAC GGTCCCTGGA GTCTGGCTGG CCCCTGTTGT 120 GACTGGACCA CAGAGGGACC CCTGTTACAG CCGCCCCCTC AAGCCTGTGA ACCATAAGAG 180 AACTTCCTGC TCGGGACCAC ACAGCTGGCT GGGTTCCAAG TGTGCCCTGG TCTCATGCCT 240 TCATCCTCCA GGTCTCCTGG GCCTGCTCTC AGGACCGGGA TGGGGTCTCT GCAGATCCCT 300 AGCAGCCTAG GCAGCCAGGC TCTGCCCTCC TGGGGACCCC ACTCGGGGAG AGTGGTTGCC 360 CCTGGGATAC TCAGACCAGT ACAGGGTTTT GGGGGCCCAG AGGACATCCC TGGGCCCAGG 420 TAGGAGGTTA GAACAGGGTT CTGGAGATGA CCTCTGACCT CCTCCTGAGG GATGAGCAGC 480 AGTTTTCCAG AACAAAGGAT TGCAGGGAAC TGTCAGGCAA AAGGAGTTCT GAGTTTAAAG 540 GCCTTAGCCT GGCCAGCATG GTGAAACCCC ATCTCTACCA AAAATACAAA AAATTAGCTG 600 GGCATGACGG TATGCACCTA TAATCCCAGC TAGTCAGGAG GCCGAGGCAC GAGAATTGCT 660 TGAATCAAGG CAACAGAGGT TGCAGTGAGC TGAGATCGGG CCACTGCACT CCAGCCTGGG 720 TGACAGAGTA AGAGTCTGTC TCCAAATAAA ATAAATAAAT AAAATCAATT AATTAGAAGA 780 AAGCCTTGGA GGGGAGAGAG ACCTTGGCCT GTGTATTGGT TCCACTGACC CCCTGGGTCA 840 CCATCGTCAC TCCAGCTCCT GTGACTCCCT CAGTGGGACC ATTTTCATTC TTGGTGATTA 900 TAGGATCTGT GATTGATGGA ACGCCCCGCC TCCTGGCTTC TCGCCCTCCT CTCCTCCATG 960 GTCCTGTCCT CCAGCCTGTC TCAGTCACTC AACCCTTGAC CAAGGCTCCC CACACTTATT 1020 CCATAAAGAG CCAGGGAGCA AATTTATTTT AATTTTTTGA GACAAGGTCT CACTCTGTTA 1080 CCCAAGCTGA AATGTGATCG TGGCTCACTG CAGCCCTGAC CTCCAGTCGC AGCCTCTTGA 1140 GCAGCTAGGA CTACAGGCAT GGACCACTAT 1170
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