Tag | Content |
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EnhancerAtlas ID | HS108-26701 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:30216890-30218320 |
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) |
CEBPA | MA0102.3 | chr22:30217678-30217689 | ATTGCATAATA | + | 6.02 | EWSR1-FLI1 | MA0149.1 | chr22:30216921-30216939 | GGAAAGAATAAAGGAAAG | + | 6.12 | Gata1 | MA0035.3 | chr22:30217475-30217486 | TCCTTATCTGT | + | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_00294 | chr22:30216653-30218957 | Adipose_Nuclei | SE_27345 | chr22:30216755-30218495 | Esophagus | SE_31847 | chr22:30216749-30218515 | Gastric | SE_34183 | chr22:30216878-30218402 | HCC1954 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr22 | 30218081 | 30218319 | chr22 | 30217042 | 30217978 | chr22 | 30216935 | 30217016 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I029820 | chr22 | 30216542 | 30218948 |
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Enhancer Sequence | ATCTCAATAC ACAAAAAAAA AAAAAAAAAA AGGAAAGAAT AAAGGAAAGT GACCATTATA 60 AGGGATAACT CAGTTTTGTA ACTAGGTATT TCGAAGACTG TGTCCTACAG TCTCCAGGTG 120 AGGAGAGCTG GCAAGGGCGT CCAGGGTGAG CACCCCTCTG TGCCAGGCCC AGCTCCATGA 180 GCTACAATTC AAAGAGGAAT TCACTGGGGC GCTCCCTCTG TAACGTCCCA CAGTGCTTCT 240 GTTTCTCTTT TTTTCTTATT TTTTTGTGTG TGTGTGCGTA TAAAGAGGAA CCTCTAAAAA 300 AAACTGCTTG TTTTTGATCA AACCTTCTCC CCTCTGCCTG CTAATGGGAT CCAACGGCTA 360 ATGTCCGTTC CTTTTGCAAC CCAGAAGAGC CCTCTCTGAA CTCTGTCCCT ACCTGCTCTC 420 AGCAACAATG CAAATCATGA CATTTTTGAC ACAGTGCCAT CATCCCTGAA GCAGGGAGTT 480 GCAGAGCAAG AGCTTGAGAG TCAGGTCTAC GTTTACACAC GTCCCAGCTG GGCCACTTAT 540 TAGTCATATC CTCTCAGGCA AGTCCCCTAC ATTTTAACCT CAGTTTCCTT ATCTGTAAGT 600 GGGGATGATG ACAGCACTTA TCTCACAGGG CTGCTGTGAG GATCCAATTG ACATAACATA 660 TGTGGAGTGC TTGGCAGAAT GCCAGGTCCC CGGAACACTC TCCAATAAAG GTTAGCTTAG 720 TTATCACTGC TGTTCTTACA TTCGTCGCCA AAGGAAACTT CCCCATTCCT ATGTCTGATG 780 CATGGCCAAT TGCATAATAC TAATACACTC CCAAGGCAGA ATGGTGGCTT ACACTGTAAT 840 CTCAGCTGTT CAGGAAGCTA AAGCAGGAGG ATGACTTGAG GCCAGGAGTT CAAGACCAGC 900 TGGAACAACA TAGTGAGACC CCATCTACTA AAAAAAATTT TTTTTTAATT CGCCAGGCAT 960 GGTGGTGTGC ACCTGTAGTC CCAGGTACCT GGGAGGCTGA GTTGGGGGGA TAGCTTTACT 1020 CCAGGAATGT GAAGCTGCAG TGAAATATGA TTGCGCCACT GCACTCTTGC CTGAGTGACA 1080 GAGCAAGGCT TTGTCTTTTT TCTTTTTTTT TGAGATGGAG TCTTGCTCCA TCTCAAACAC 1140 TGCAACTTCT GCCTCCCAGG TTCAAGTGAT TCTCCTGAAA AAAAACAAAA ACAAAAAATT 1200 TCCAGATCCC TGGGGAACTG TCTGGTACAC AGTTTTATTT CCACCTCCCT AGGTAGTGTC 1260 ACTACCTAGT CATTTTGAGG TGACACTCAT ATATCTGTTA AGCAATTTCC CAAGACTCCC 1320 TGCCCCTATC GCCCTGAGTC CCTGGGCACT GTCAAAGCGC TGGCCTTTGC AACCTTTAGT 1380 TTGGCATGTG GGGGCCATCT TGGTGCATCC TCCCAGTCCT GCATCCTACA 1430
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