Tag | Content |
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EnhancerAtlas ID | HS060-16824 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:6087850-6088510 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF9 | MA0653.1 | chr19:6088254-6088269 | AGTTTCACTTTTGTT | - | 6.15 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_00353 | chr19:6086422-6089418 | Adipose_Nuclei | SE_01604 | chr19:6086520-6088344 | Aorta | SE_09597 | chr19:6086512-6089461 | CD14 | SE_24492 | chr19:6087023-6088416 | Colon_Crypt_2 | SE_24492 | chr19:6088420-6088662 | Colon_Crypt_2 | SE_25797 | chr19:6086002-6089696 | Duodenum_Smooth_Muscle | SE_26679 | chr19:6086617-6088822 | Esophagus | SE_29788 | chr19:6087109-6088207 | Fetal_Muscle | SE_33560 | chr19:6086131-6102160 | H2171 | SE_35921 | chr19:6086278-6089174 | HMEC | SE_37314 | chr19:6086485-6089390 | HSMMtube | SE_38527 | chr19:6085789-6089897 | HUVEC | SE_42288 | chr19:6086810-6088691 | Lung | SE_44165 | chr19:6086035-6090064 | NHDF-Ad | SE_44879 | chr19:6087624-6088603 | NHLF | SE_52794 | chr19:6086935-6088469 | Small_Intestine | SE_54507 | chr19:6086291-6095033 | Stomach_Smooth_Muscle | SE_64265 | chr19:6086123-6089311 | NHEK | SE_65533 | chr19:6086694-6088961 | 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 |
GH19I006085 | chr19 | 6085948 | 6089661 |
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Enhancer Sequence | GGACAGCGTG TTTTGATACG AAGGTGATGG GTTACAGGTG CTGGGTTTCT CCACATGGGC 60 AGTTTCTCCC CAGGAGTCTC ACTCCTTACA TCATCATCTA GAGCAGTAAT TAATTTCAGA 120 AACCACTCCT GGCTGCCATA AGCTGCACAC CCACTTCCAG AACTGGCTTA ACCCGCCAGG 180 AAGCCACAGT CCTCAAGGGA CAGTCACCCA GAGCTGCATG TTGGTGAGTC AGAGACGAGA 240 ACAAAGAGGA AGCAATGACC CCTGAACACA GAGCCCTTCC CAGCCCAGAG TGCTGCTCTA 300 AGCCTAACCC AGGCTGGCCA GGGCCTGAAA GACAAAGAAG AATGCCACAG AGAAGGGCCA 360 GGGCACTACA GCTTTTTTTT TTTTTTTTTT TTTTTTTGAG ACGGAGTTTC ACTTTTGTTG 420 CCCAGGCTGG ACAGCAGTGG CGTGATCTCG GCTCACTGCA ACCTCCGCCT CCCGCGATTC 480 TCCTGCCTCA GCCTCCTGAG TGGCTAGTAT TACAGGCATG TGCCACCATG CCCCGCTAAT 540 TCTGTATTTT TAGTAGAGAT GGGGTTTCTC CCTGTTGGTC AGACTGGTCT CGAACTCTCG 600 ACCTCAGGTG ATCCACCCGC CTCAGCCTCC CAAAGTGCTG GGATTCCAGG CTTGAGTCAC 660
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