Tag | Content |
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EnhancerAtlas ID | HS187-15440 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr20:48982980-48983880 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I050365 | chr20 | 48982431 | 48987174 |
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Enhancer Sequence | AACTCTTTGT ATATTAAGGA TAGTAATTCT TTCTAAGAGT CTTATAATTG ACTATAAAAG 60 TCTCCCTCCC TCCCTCCTTC CCCTCCCTCC CTCCCTTCCT TCCTTCCTTC CTTCCTTCCT 120 TTTGTTCCCT TCTGCTTTCT AAGGATATGC CTGGTGTTTG GCAAGCATTG CATGAATTAC 180 ATTAGGAAAT AACTTTTGTA ACAAACCCAT TTAACAACCA TTCTTTGTTC CCCGCCTCCT 240 GATAATGCTC AGAGCCACAG CAACAGCCTT TGCCCAACTC CATGTCATTA ACCCTTGATC 300 TTTTCCTGCT GAATAGCAGA TTGCTTTCCG GGGCTGGCAA CACAGTTTCA TTTTCACCTT 360 CCTGCTGATG GAACTGCCCT GGCTCTGTGC CAGATGGCTG TTTACATAAG AAATGATTTG 420 ATTATATTGC ACAGCCAATG GCAGCCTTTC TCAGAATAAA GAAGCCAGAA ACATATAATC 480 AAAGCCATTA ACTGTGTACA AAGAAACGCA GCCCACTCTA AATTTCCCAC CAACCATAAT 540 CACAGTTTTC CAGAGAAAAA TAAGAACAGG GTTATGGTTC CCTACTAAAA ACGTGTTAGG 600 GGAAAGACTT TTAAAAGGAA ATTGTGGTAT AGCTCAGTTG CACTCTCAGA TCAACCCTTG 660 AGCCTTGACT CCAATCCCAG CTCTGTAACT CACTGTCCTT GTGACCTTGG AAAAGTCGTT 720 TACTGCCAAA AGCCTCCGTT TCTTTATTGT AAAATGGCTA TAATAGTAAT ATCAACCTCA 780 GAGGTTTACG AGAGGATTAA GTGAGATAGT GCATAAGAAC ACTTTCTCAG TCAGAATGTT 840 TTCAGCCGCA AGGAGCAGAA CACTTGACTA AAGGAGGGAA AAAAAAGCTA GAGGACTTAT 900
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