Tag | Content |
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EnhancerAtlas ID | HS108-38761 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr8:11754200-11755670 |
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) |
IRF1 | MA0050.2 | chr8:11754639-11754660 | TTTTTCTTTCTCTTTCTGTCC | + | 6.59 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09230 | chr8:11752974-11756738 | CD14 | SE_26133 | chr8:11753966-11756300 | Duodenum_Smooth_Muscle | SE_26664 | chr8:11754373-11755368 | Esophagus | SE_28772 | chr8:11753187-11756743 | Fetal_Intestine_Large | SE_42363 | chr8:11754182-11756283 | Lung | SE_46238 | chr8:11754152-11755841 | Osteoblasts | SE_49106 | chr8:11754216-11755643 | Right_Atrium | SE_50500 | chr8:11754129-11756424 | Sigmoid_Colon | SE_52567 | chr8:11754004-11756317 | Small_Intestine | SE_54194 | chr8:11753967-11756413 | Spleen | SE_56280 | chr8:11754449-11755859 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr8 | 11754568 | 11755261 | chr8 | 11754378 | 11755121 | chr8 | 11754453 | 11755446 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I011895 | chr8 | 11753368 | 11756709 |
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Enhancer Sequence | CCAGCCTGGG CGAAAGAGTG AAACTTTGTC TCAAAAAAAA AAAAAAAAAA GGGTAGGGGG 60 GCTCACTGAC ATTGGTATGA AGCCATGAAG GGCAGTGTTC AGTCCAATAT ATGTCGATCC 120 CATGCTCACA CAGATCCCTT TCTGCTTGTG GAAGTTGGTT AATTTTTCTG GTTATGATAC 180 TGAATGTTGC TACATTTTCC TTGATAGTAT AGTATCATCT GGTTGATGAT TTTGCATCTT 240 AGCATTATAC TCCCCTTCTC CCAGCAGCCA GTGCCTCTCC AGTCTTCCTC AGCCACACCG 300 GGGCTCACTG CAACCTCCGC TCAGCTGGCC CAGATGCAGC CATCTTTCAA GAAATCCAGA 360 TCTTGAGGCA AAATTTCAGA GAGCAAAACT TTCACAGGGA CTTTCAGGCA TAATTTGACC 420 AGGTCATTCG ACCAGGTTGT TTTTCTTTCT CTTTCTGTCC CCCTATCTGC GTGGTTCTTG 480 GCCTGCTGTC AGGGCATGAT TTAAGAGGGT TGTTTGCTTA CCTTGAGTGG ACGCCCCCAC 540 AGGCCAGTTC CCTCCCCAGA AGGACTTGAG GGCAGGGTGC AGGGGGGCGG GGGGAGCTGC 600 CGAACCATGG ATGTCAGACC TGTCCACGCA CAGGCAAAGA GAGGGCACAA ACTTGACAAC 660 ACAGCGAAAC TCCACTTGTT TCTTCACAAG TCTTTAGAAA GGAGCTTTCA TTTCTGTAGT 720 TTTGCTTCCT CTCTGAATCT TTGGCCTGCA CAGTGACCTC AGTGTCTCCT GACCACGGAA 780 TCACATGCCC GTATCTACTT TGGAGTTTGA GCTTTTCAAA ACTGCAACTC TTTGCCAATA 840 GCTGGTTTGT GGGCCTGGTG TCAGCAGTGG GGAACAGTCT TCCTGCCACT TTCCATTCAT 900 GTCTACGTGA CTCCAACCTA AAATAGATTT TTGGGGGAGC CCTTGATTGT AACCTTCAAC 960 AAAGGAAGTC ATGCTAGGCA GATTCTCCTG AGACAGGTCC TTACGTGCTA GTAAGAGCCT 1020 TTGGTGAGTA CTTTAGGATT TACAAAGCCT CTCCAAAGAC AGACTTTGAT TTGATCCCCA 1080 CAGCAATCTC ATGGGAGGTG TTTCAAGTCC ATTTTACAGA TGAGAAAATC TGCCACTGAG 1140 TGGGAGAATG GTGGGGTGGG AAGCGTGGTT GAAGAAGAGA AACAGCATTT ATTACCTTTC 1200 TGGGCCTAAC ACTGCGCTGT TCGCTTTATA TATGTTTGAT CCTTTAACAC ACTTGTGAAG 1260 CCAGTAGTAT TTTCACACTA TTGTCTTTTT TAGGTGAGTT CACTGAGGCT CAGACAGGCA 1320 CAGCAGTAAG TGGAAGCACA GGAACTGAAA CACATCTCTG CTATCTCATG GTTTGTGCTT 1380 TTGCCCATCA CTGCTTATCC CAGTTATCTT TTGCTGAGAA GCAGTTTACT TCCAAACTTA 1440 GTGGTTTAAG ACAACAGTCA TTTATGATCT 1470
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