Tag | Content |
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EnhancerAtlas ID | HS194-00069 |
Organism | Homo sapiens |
Tissue/cell | Urothelial_cell |
Coordinate | chr1:27175420-27176320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:27175994-27176005 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:27175994-27176005 | GGGTGACTCAG | + | 6.02 | ZBTB18 | MA0698.1 | chr1:27175584-27175597 | ATTCCAGATGTGT | + | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23384 | chr1:27174699-27178454 | Colon_Crypt_1 | SE_24351 | chr1:27174710-27177316 | Colon_Crypt_2 | SE_26621 | chr1:27173970-27186608 | Esophagus | SE_34025 | chr1:27175414-27176113 | HCC1954 | SE_34526 | chr1:27174651-27176664 | HCT-116 | SE_50491 | chr1:27174691-27177388 | Sigmoid_Colon | SE_53016 | chr1:27174654-27177272 | Small_Intestine | SE_57686 | chr1:27174839-27175963 | VACO_503 | SE_57686 | chr1:27176013-27177166 | VACO_503 | SE_64263 | chr1:27174693-27178982 | 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 |
GH01I026847 | chr1 | 27174110 | 27178056 |
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Enhancer Sequence | CCCTCAGCAT AACCAGGAGT GTTTTGGCTT CAGCTCAGGA TTGGTGGATT CCTTCCCCCA 60 GCTCTGAGGT GTGGGGCAGA CAGACAGGCT TTGAACCCTT CTCCCAGGCT TCAGCCCGGT 120 CCTCAAGAGG TCCAAGCTCC CAGGAAACAG ACTGGAACAA TAACATTCCA GATGTGTTTG 180 GGCCAGAAAG AATGAGTTAC TGTCCAGTGG CCCAGGGCCA GCTGTACTGA AAAACTTTGA 240 TCTGATTCCC AGAGTTGAGA GGGAAAAGCA TCTAGCAACA GAGGCGTTTA AGCTGATGAG 300 GTGCAGAGGA TGTCACCACT GGAAATGGCT CCTGACCCTA CAGCTGCCTG CAGTGGTTGT 360 TTTGTCCCCT CTCCCTGCTC TCCAGAGGCT GTGTAGTTCT GATGGGCACC CTGAGAGGGT 420 GTTGTAAGGG AAATAATGCA TGAGAGGGCC CAGGTGAGCT GAGCCACAGT GACTGTGCAT 480 AGTTCCCAGG GCAGTGAGCT CATCATGCCA GCTCAGTACT CCCTAAGCAA GAGAACAGCA 540 GGGAACACCC CCCCGTGACG GCATGCAGTG AAGGGGGTGA CTCAGTGGGC ACCATTCATC 600 CCCAAGGAGC TGCCCCGCCC ACGCCGTGCA AAGGGCACTG GCCTTGGCAT GAGGCCTGCA 660 ATGGGCTTGT GACCCACATT CCCACAAGGA CTTTCTTTAC CAGTCTGGGT GTGCCTCCAC 720 CCCCGGGGAC AGTGTGCAGG TGAGCTCAGC CCTTTGACCT GGCCTGTGAT GCTGGCTGGC 780 TGTGAACCCC ATTGCAGCTC AGCCCCTCCC TGGGCCGCTA GTCCTAGAGC AGGAGACGGG 840 TTGTTGACTG TTAGCATGTG GTTGGGATGG TAGACCAGGT GACAAGTATT TTTGTGAGTC 900
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