Tag | Content |
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EnhancerAtlas ID | HS012-17409 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr20:48982920-48984010 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr20:48983073-48983091 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:48983077-48983095 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:48983081-48983099 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr20:48983061-48983079 | CCTCCCTCCCTCCCTTCC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr20:48983043-48983061 | CCCTCCCTCCCTCCTTCC | - | 7.12 | EWSR1-FLI1 | MA0149.1 | chr20:48983085-48983103 | CCTTCCTTCCTTCCTTTT | - | 7.95 | EWSR1-FLI1 | MA0149.1 | chr20:48983065-48983083 | CCTCCCTCCCTTCCTTCC | - | 8.13 | EWSR1-FLI1 | MA0149.1 | chr20:48983069-48983087 | CCTCCCTTCCTTCCTTCC | - | 9.42 | IRF1 | MA0050.2 | chr20:48983319-48983340 | ACACAGTTTCATTTTCACCTT | + | 6.64 | Stat6 | MA0520.1 | chr20:48983524-48983539 | GTTTTCCAGAGAAAA | + | 6.07 | ZNF263 | MA0528.1 | chr20:48983056-48983077 | CTTCCCCTCCCTCCCTCCCTT | - | 6.14 | ZNF263 | MA0528.1 | chr20:48983081-48983102 | CCTTCCTTCCTTCCTTCCTTT | - | 6.16 | ZNF263 | MA0528.1 | chr20:48983043-48983064 | CCCTCCCTCCCTCCTTCCCCT | - | 6.46 | ZNF263 | MA0528.1 | chr20:48983042-48983063 | TCCCTCCCTCCCTCCTTCCCC | - | 6.61 | ZNF263 | MA0528.1 | chr20:48983069-48983090 | CCTCCCTTCCTTCCTTCCTTC | - | 6.76 | ZNF263 | MA0528.1 | chr20:48983073-48983094 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr20:48983077-48983098 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr20:48983039-48983060 | GTCTCCCTCCCTCCCTCCTTC | - | 7.12 | ZNF263 | MA0528.1 | chr20:48983065-48983086 | CCTCCCTCCCTTCCTTCCTTC | - | 7.19 | ZNF263 | MA0528.1 | chr20:48983061-48983082 | CCTCCCTCCCTCCCTTCCTTC | - | 7.38 | ZNF263 | MA0528.1 | chr20:48983052-48983073 | CCTCCTTCCCCTCCCTCCCTC | - | 7.65 | ZNF263 | MA0528.1 | chr20:48983048-48983069 | CCTCCCTCCTTCCCCTCCCTC | - | 7.73 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_28491 | chr20:48982335-48987321 | Fetal_Intestine | SE_31629 | chr20:48983043-48983874 | Gastric | SE_33764 | chr20:48982789-48984100 | HCC1954 | SE_52401 | chr20:48982681-48987083 | Small_Intestine | SE_53316 | chr20:48982599-48984069 | Spleen | SE_56118 | chr20:48982851-48984157 | u87 |
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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 |
GH20I050365 | chr20 | 48982431 | 48987174 |
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Enhancer Sequence | TCGCCTGCCA GAATAGTGGG TTTTTAATAC GGTGTTTACC TCTTCTTATT GTTTTGCAAG 60 AACTCTTTGT ATATTAAGGA TAGTAATTCT TTCTAAGAGT CTTATAATTG ACTATAAAAG 120 TCTCCCTCCC TCCCTCCTTC CCCTCCCTCC CTCCCTTCCT TCCTTCCTTC CTTCCTTCCT 180 TTTGTTCCCT TCTGCTTTCT AAGGATATGC CTGGTGTTTG GCAAGCATTG CATGAATTAC 240 ATTAGGAAAT AACTTTTGTA ACAAACCCAT TTAACAACCA TTCTTTGTTC CCCGCCTCCT 300 GATAATGCTC AGAGCCACAG CAACAGCCTT TGCCCAACTC CATGTCATTA ACCCTTGATC 360 TTTTCCTGCT GAATAGCAGA TTGCTTTCCG GGGCTGGCAA CACAGTTTCA TTTTCACCTT 420 CCTGCTGATG GAACTGCCCT GGCTCTGTGC CAGATGGCTG TTTACATAAG AAATGATTTG 480 ATTATATTGC ACAGCCAATG GCAGCCTTTC TCAGAATAAA GAAGCCAGAA ACATATAATC 540 AAAGCCATTA ACTGTGTACA AAGAAACGCA GCCCACTCTA AATTTCCCAC CAACCATAAT 600 CACAGTTTTC CAGAGAAAAA TAAGAACAGG GTTATGGTTC CCTACTAAAA ACGTGTTAGG 660 GGAAAGACTT TTAAAAGGAA ATTGTGGTAT AGCTCAGTTG CACTCTCAGA TCAACCCTTG 720 AGCCTTGACT CCAATCCCAG CTCTGTAACT CACTGTCCTT GTGACCTTGG AAAAGTCGTT 780 TACTGCCAAA AGCCTCCGTT TCTTTATTGT AAAATGGCTA TAATAGTAAT ATCAACCTCA 840 GAGGTTTACG AGAGGATTAA GTGAGATAGT GCATAAGAAC ACTTTCTCAG TCAGAATGTT 900 TTCAGCCGCA AGGAGCAGAA CACTTGACTA AAGGAGGGAA AAAAAAGCTA GAGGACTTAT 960 AATTTTATTT AACAGGGTTG TTTCATTTGG AGGCATAAAG ATGTAACCAG TGATTCACAT 1020 TCTTTTCTTC TTCCTGCTAT GCCATTCTCA GCAATTTATG GACATGTCTC CTCATGGTTT 1080 CAAGACAGCT 1090
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