Tag | Content |
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EnhancerAtlas ID | HS076-11035 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr11:72475220-72476090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr11:72476072-72476086 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_23353 | chr11:72475053-72476107 | Colon_Crypt_1 | SE_24028 | chr11:72475154-72475671 | Colon_Crypt_2 | SE_24028 | chr11:72475763-72476072 | Colon_Crypt_2 | SE_27728 | chr11:72474085-72476882 | Fetal_Intestine | SE_28682 | chr11:72474063-72478898 | Fetal_Intestine_Large | SE_31502 | chr11:72475068-72476122 | Gastric | SE_65258 | chr11:72474689-72481022 | Pancreatic_islets |
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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 |
GH11I072762 | chr11 | 72473538 | 72479175 |
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Enhancer Sequence | TTCCCTAGCC AGGCTCAGTG CTCCCAGGGC CCAGCTGCAA AGCAGCTGAA TGCACACTGG 60 GAAGGGGCCC ATGCTGCCCC ATCCTCCTTC CAGAGGCTCC CAGAGCAGGG CTGTTGAGGC 120 TCCAGAGGCC AAAGACCCAC CTCTGGGACA GAGGACAGTG GCCGGAGCAT GCAGAGCCAC 180 GAGACAGACC AGTTGCTCAG CGTAAACTCT GAGTAGCACT TTATCTCATA AAGAGAAACT 240 TCAAAGGTTT CCCAGGCTAG TGGCAGACTC TTGTGGAGGA AGGCCTCTGC CCAGAGAGTA 300 AGAACCTTTG CTGTGGCAGC GCAGGTGAAG AAACTGAGGC AGGCCGGGTC GTGGGGGTCA 360 GGTAAGTGTC CACAGGCCTC CCTAGCCTGG CCTGGCTCGT GCCCTTTCCA TAGCCCCCAG 420 CAGGCAGCAC TGCTGCGCTA AGCAGAAGAA ATTACACCCA TCTTTGTTCC TGCGGGCGGC 480 GGTGGCCACG CCCCAAAGGT GTAATTCTAA GAGGCTTGGG GAGGGACAGG TGGCGGGGTA 540 GGGCTGAGTC TCTGGAGAGC ACCAGGTGGG CGGGCCGGTA CCAGGAACCC CCAGCTATTA 600 GGCCCTGGCT GAGTGAGTGT CCACACCAGA TGTTGCCGTC AGGTGTTGCC TGGTAGGCCA 660 TCTTGGCTGC CCCCGGAGAA ACTCCCCCTG GAAACAGGAA CCCAAGGGGT GTTGCTCCAC 720 CAAGGAGCCA TGCTGGGCTT GAGTACGTTT AAAGCCTGGT GACAGCAGGG ACCCCGACAT 780 GCAGTGGTAT TACATTTGAG AAAACAGGCC AGCCAGGTGC GGTGGCTCAC TCCTGTAATC 840 CTAGCACTTC GGGAGGCCGA GGCGGGCAGA 870
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