Tag | Content |
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EnhancerAtlas ID | HS070-00034 |
Organism | Homo sapiens |
Tissue/cell | GM19099 |
Coordinate | chr1:33446270-33447410 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1B | MA0153.2 | chr1:33447214-33447227 | GTCAATAATTAAT | + | 6.15 | HNF4G | MA0484.1 | chr1:33446632-33446647 | TGAACTTTGCCCTTC | - | 6.55 | Hnf4a | MA0114.3 | chr1:33446630-33446646 | TCTGAACTTTGCCCTT | - | 6.2 | SPIC | MA0687.1 | chr1:33446943-33446957 | GACTTCCCCTTTCT | - | 6.23 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_00738 | chr1:33446017-33448135 | Adipose_Nuclei | SE_09317 | chr1:33445189-33451590 | CD14 | SE_19095 | chr1:33445525-33448625 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19886 | chr1:33445608-33451741 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23323 | chr1:33446275-33447541 | Colon_Crypt_1 | SE_32111 | chr1:33446363-33447930 | Gastric | SE_35956 | chr1:33445965-33447936 | HMEC | SE_38650 | chr1:33445932-33449345 | HUVEC | SE_42882 | chr1:33445704-33448313 | Lung | SE_46598 | chr1:33446110-33447747 | Osteoblasts | SE_53906 | chr1:33445858-33447937 | Spleen | SE_64575 | chr1:33446164-33447985 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I032980 | chr1 | 33445638 | 33449040 |
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Enhancer Sequence | CAGAGTGAGA CTCTGTCTCA AAAAATAAAA AAAAAGAAAT ACTCTCAGCA GGGGTTTGTC 60 CTGGGCACTG GCATCACACA GAGAGGAAGT GAGAGCTCAT CCAGGATTAA AAACAAGAAT 120 CACCATTTCT GAAGGATTCC TCTGAGCCCA GTTCCTTGTT CCTTCATAGC CATTGATATG 180 CATATCTCAT TTAATCCTCA AAATCAGTTT AGGAGAAAAA TTATTTCACA GCTGAGGAAA 240 CCAAAGATCC TGAGACTTAG AGAGGTTACA TTACTTGCCC AGGGACACAC AGCTAGAAAG 300 TGATGGAGGC AGGATTTGAA TCCAGATCTA AGTGACTTCA TAGTTTGTAA ATTTTTAACC 360 TCTGAACTTT GCCCTTCCAG TTGCAAGATG CTGATGCATT CCTGTATTTC CAGCTCTTCA 420 CACACAGGCA CTCATCGATA TTAGCACTGC CTAGAGAAGC CAGTGAGGTA AAGATCATTG 480 TCCCATTTTC CAGGTGAGAA AATTAAGGCC AGAGAGGGGA CTTGCTCAGT GTGGTCAGCT 540 GAGAAGTAGT GGCATTCCTT CTAGAATCCA GGTCTCCTTT CTTGCCTCTG GCAGCCTTCC 600 TCCTTCCTAT ACTTTCTGCC AACTGCTGAG GCTTCCGTCT CGAAACAAAT GACTCAAGGT 660 AAATCACTGG TTGGACTTCC CCTTTCTCAA AATACAGGAA GTCTGTGTTG TTTGCAGTCC 720 CTGTGGGTGA ACAGTTTCAG CTCAGTTACG AAGTAGGCTG GGCCACATAG AGGACTGGGT 780 CCTGCTGGGG CAGGGTTCCA GGCTACTGGG GCTGGCACCG CTGCATTTTT CCTTCCTAAG 840 AGTCATGTCA GTGTGTCTGT CAAGTCAGGC TTGACGTCTT ACCCCAAAAA GCCTGCTGTA 900 CTATTATGAA ATTTAGAAAA ATGAGCCCAA GAGGGAGGGG CCCTGTCAAT AATTAATAAT 960 AACAACTATT ATTTCATGTT TATGGCACAT TAACCTTCCT ACCAGGCACT GTGCTAAGTG 1020 GCTGACACGT GAACCCATTT GAGCCCCGTA ACAGCCCTAG TAATAAGGTT CTATAGCTTT 1080 GGAGCCAAAT AACACTAGAT ACAAATCACA GAAATGCCAC TTTCCAGCTG TGTGACATCA 1140
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