Tag | Content |
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EnhancerAtlas ID | HS034-00853 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:33446570-33447510 |
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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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I032980 | chr1 | 33445638 | 33449040 |
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Enhancer Sequence | TGATGGAGGC AGGATTTGAA TCCAGATCTA AGTGACTTCA TAGTTTGTAA ATTTTTAACC 60 TCTGAACTTT GCCCTTCCAG TTGCAAGATG CTGATGCATT CCTGTATTTC CAGCTCTTCA 120 CACACAGGCA CTCATCGATA TTAGCACTGC CTAGAGAAGC CAGTGAGGTA AAGATCATTG 180 TCCCATTTTC CAGGTGAGAA AATTAAGGCC AGAGAGGGGA CTTGCTCAGT GTGGTCAGCT 240 GAGAAGTAGT GGCATTCCTT CTAGAATCCA GGTCTCCTTT CTTGCCTCTG GCAGCCTTCC 300 TCCTTCCTAT ACTTTCTGCC AACTGCTGAG GCTTCCGTCT CGAAACAAAT GACTCAAGGT 360 AAATCACTGG TTGGACTTCC CCTTTCTCAA AATACAGGAA GTCTGTGTTG TTTGCAGTCC 420 CTGTGGGTGA ACAGTTTCAG CTCAGTTACG AAGTAGGCTG GGCCACATAG AGGACTGGGT 480 CCTGCTGGGG CAGGGTTCCA GGCTACTGGG GCTGGCACCG CTGCATTTTT CCTTCCTAAG 540 AGTCATGTCA GTGTGTCTGT CAAGTCAGGC TTGACGTCTT ACCCCAAAAA GCCTGCTGTA 600 CTATTATGAA ATTTAGAAAA ATGAGCCCAA GAGGGAGGGG CCCTGTCAAT AATTAATAAT 660 AACAACTATT ATTTCATGTT TATGGCACAT TAACCTTCCT ACCAGGCACT GTGCTAAGTG 720 GCTGACACGT GAACCCATTT GAGCCCCGTA ACAGCCCTAG TAATAAGGTT CTATAGCTTT 780 GGAGCCAAAT AACACTAGAT ACAAATCACA GAAATGCCAC TTTCCAGCTG TGTGACATCA 840 GGGACATTAT TTACATTCAT TCAGTAAATA CTTTTGAGCA CTTACTATGT GCCATATTTC 900 AGTGAACAGA ACAAAGATCC CTGCTCTCTT GTGATGTTTA 940
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