Tag | Content |
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EnhancerAtlas ID | HS182-14904 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr22:30183260-30184590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:30184518-30184536 | CCTGCCTTCCTGTCCTCC | - | 6.04 | EWSR1-FLI1 | MA0149.1 | chr22:30184514-30184532 | CCATCCTGCCTTCCTGTC | - | 6.16 | Gata1 | MA0035.3 | chr22:30184275-30184286 | TCCTTATCTGT | + | 6.14 | Myod1 | MA0499.1 | chr22:30184540-30184553 | GGCAGCTGTCCCT | + | 6.48 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27345 | chr22:30182911-30184477 | Esophagus | SE_31847 | chr22:30182746-30184651 | Gastric | SE_34183 | chr22:30182849-30184241 | HCC1954 |
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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 |
GH22I029786 | chr22 | 30182837 | 30184246 |
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Enhancer Sequence | TGACCTGGCA CTACATTCTG AAAAATTTGA AAAACTGACT CCTTCTCAAA TACTTTAAAC 60 CAGGATTTTC ACATGAGGCC TGAACACCAG TCCAGGTGGG TGGGAGGTAT AGATGACTAA 120 GAGAATGTGA GAGGGGCCGT GTGAACAGGA ACAGGTAAGA CCAGTAAATC CTGGGAACTC 180 CCAACTCACC TTGCCTTGCT CCAGGGACAA GCACTGGACC TGAGGAGTTT AGGGAGGTCC 240 CTGGCAAATG CCTCCAGGAG GAAACAGAGT CTTCCTGCTG CCTGTCAGGA CGGCTGACCC 300 TGGGCCTGAT CTCAGCTAAT TCAGCAGCTC AGGGGGAGGA CACCACCCCC GTATCTGCTC 360 TGCATCTCAA ATACACCAAG AGGGCTGGCC AGGCAGAGGG ATTGCTATTG ATTTTCACTT 420 GTGCGGGCTG ACCTAACAAA ACCAATCCAT CAAGTGCCTG TCTGCCTCTG CTTCAGACTC 480 TCATCCTAAG CACGTGCAAA TAAATTGCAC CAGCATCCAG GGTGATTTGT CAAGGTCCAG 540 CCAGGCATGG GCCCTGGCTT CCACTGATAG GATGGGGCTC CAGGCTAGGC TGGGCTAGGG 600 TCAGCCCAGT CAATGCCCCG CTGTTGACTC GCCATTGAGT GACAACACGC AGTGTGGCCT 660 GGCATCTGCT GCCACGCTAG GAACTGGTTG GCCATGCCTG GGAAGGGGCT TTGAGGAAAC 720 AGGCCCAAGT CCCACTCACT TTGACAGGGC TTGGCAGCGA CATTCTCACT TGTTTCTTAA 780 GGTTTCTGTC CGAACTCTAG ATTTGGGGGG ATTTATTACA ATGTAGATAC AACCATGAGG 840 TGCTGAGTTT GGGTACTGCC TCTGCCACTG GCTGAATGTC CTTGGGCCAG TTGTGAGATG 900 GAGATGACAC CACCTACAGG GGTCTAGAAC CCTGTAAAGG CCAGGGTCCA ATCCCTGTTC 960 TGCCACTTCC TAGCTGTGGC CGGGGCAGGT GCCTTCAGCC CTCGGTGCCT CATTTTCCTT 1020 ATCTGTACTA CCGGGCTGAA AATGGTACCT ACCTCTTACA GTGGAGCTGT CATAACTGAA 1080 TGAGAAAATG CAAAGGACCA CAGGGGCTCA CCCCACCCAG CCCTTCATTC CACTAGCAAG 1140 GACTGGAGGC TCAGAGAAGG GGGTGATGTT CTGGGGTCAC ACAGCAAGGC AGAGCAGCAT 1200 CAGAGGGGTT ACAGGAGCCA CAAGCAGGAG AGGATGACGG AGAGAGTACA GTGACCATCC 1260 TGCCTTCCTG TCCTCCAGCT GGCAGCTGTC CCTGAAGAAT GAGACACAGG GAATGTGGGT 1320 CATGGACATA 1330
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