Tag | Content |
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EnhancerAtlas ID | HS193-14869 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr17:75381380-75383300 |
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) |
NR2C2 | MA0504.1 | chr17:75382536-75382551 | GCAGGTCAGAGGTCA | + | 7.23 | Nr2f6 | MA0677.1 | chr17:75382537-75382551 | CAGGTCAGAGGTCA | + | 6.67 | Rxra | MA0512.2 | chr17:75382537-75382551 | CAGGTCAGAGGTCA | + | 6.27 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00752 | chr17:75379427-75386768 | Adipose_Nuclei | SE_00855 | chr17:75381658-75386492 | Adrenal_Gland | SE_02895 | chr17:75381658-75382852 | Bladder | SE_02895 | chr17:75382962-75383465 | Bladder | SE_05840 | chr17:75381615-75389667 | Brain_Hippocampus_Middle | SE_14415 | chr17:75382058-75383438 | CD4_Memory_Primary_7pool | SE_17309 | chr17:75382056-75383624 | CD4p_CD25-_CD45RAp_Naive | SE_18261 | chr17:75382380-75383573 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19099 | chr17:75381541-75383434 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22389 | chr17:75382025-75383434 | CD8_primiary | SE_25342 | chr17:75382053-75383383 | DND41 | SE_26523 | chr17:75381117-75386501 | Esophagus | SE_31375 | chr17:75381198-75386381 | Gastric | SE_36938 | chr17:75378213-75383637 | HSMMtube | SE_40707 | chr17:75378294-75386541 | Left_Ventricle | SE_42146 | chr17:75378304-75383976 | Lung | SE_44144 | chr17:75379225-75383253 | NHDF-Ad | SE_44761 | chr17:75381422-75383184 | NHLF | SE_45597 | chr17:75381211-75383495 | Osteoblasts | SE_46677 | chr17:75381657-75382886 | Ovary | SE_47187 | chr17:75375489-75383559 | Panc1 | SE_48637 | chr17:75381118-75386461 | Right_Atrium | SE_50053 | chr17:75381639-75383963 | Sigmoid_Colon | SE_52347 | chr17:75381276-75383382 | Small_Intestine | SE_53286 | chr17:75378270-75383520 | Spleen | SE_54499 | chr17:75381684-75389681 | Stomach_Smooth_Muscle | SE_62213 | chr17:75358289-75491858 | Tonsil | SE_65344 | chr17:75381637-75382916 | Pancreatic_islets | SE_68672 | chr17:75381609-75383265 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 75381380 | 75381486 | chr17 | 75381771 | 75383179 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I077379 | chr17 | 75375109 | 75393825 |
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Enhancer Sequence | TTACAGACAC TCATATTTGT AGGATTTGAG AATCCTACAA GAGGAAAGCC TCCATTCGGA 60 GGCTGCTGGG GACTTGGAGT TGCCAGCTCA CATATTTTTT AGTAGAGACA GGGTTTCACC 120 ATGTTGACCA GGCTGGTCTC AAACTCCTGT CCTCAAGTGA TCCATCCATC TCGGCCTCCC 180 AAGGTTCCAG GATTACAGGC GTGAGCCACT GCGCCCGGCC ATGGGAGACC CCCTCTTAAA 240 ACAAGAATAA AAATAAAAAT AAATAAAAGT TTACTGTCAA AAAGAAAAAC ACATCACCCA 300 ACCTAATCTC CCCCTAGGAT TGAGAGATGA GGAAGCAGAG GCCGGAAAGT GTCACATTCC 360 CTGGTCGCTG GCAGTCAGGG GACCTGAGGC CTGGGCTGGT TTTCTCGTGC TCCAGGCCTG 420 GGGTGTCAGG TGGAGCCCCT GCTTTGCCCA AAGGTCTAGG TGCCTCTGCC AGCACTGCTT 480 GCTTCTGCAT TTTTGGCCAC AAGGAATGTG GGCCAAAGGC AGGGTCCTTG ACCTCTGCCC 540 AGGAGGGTGA AGTGGGCTGG TCCTCCTTGT CCCTGCTCCA AGGCCCCTGC GGCTGTGCCT 600 TTGGAAACTG CTGGCCCGAG CTAGTGTGCG GAGCTGGGAC AGACCTCACC GTGGCCCTCG 660 TGGGGTCATT CCATGTCCGG GCTGGAAGGG ATCTTTCGGT CCAGCCCTTC CTGTTCCTCA 720 TCAGGAAACT GAGACCAGAG AGGTCATCTG CCTGGCCCGG GGTGGGGTGT AGATGGCGCT 780 TGTGACTCCT GCATGCCACG TGCAGACAGT CCCTCAGCTG TGGGCTTCCC ACGCAAGCAG 840 CCATGCTGGG GATAACTTGG CTGAAACCTG CGATTTAATG AAGAGAAGAA TGACTCCTCC 900 TGCAGCCCTG TGCCCCACAG GCTCCCTCCT GCCCCCACCC CTCCTGCAGA GGGGCCTCAT 960 GCTGGTGGGT GGGTCCCTGT TGCTGCAATG GGCCCAGGCA GTTTCTGGGC AGTGGAGGCT 1020 TGGCTGTCTT CCTGCCCAAT GTCCCCTGTA GCCCACGCTG TCCGGGAAGG GCGGGGAAGC 1080 ACTCAGCCAC TGGGGACTTC ACAAGATGGG TATCTGGGAG ATGCTGATTG GCAGGCCAGG 1140 CTCCCGTGGC CCACAGGCAG GTCAGAGGTC ACAGTGCTGA GCTGGGCTGA GTTGGCAGCT 1200 CAGGGCAGTG GGGGTGGGGG TACCTTGCTC AGCCATGGGC CTCTCTGGCA CAAGGGTTTG 1260 GAGTTTACTG TAAACAACTC CTTCAGTTTT TCCTTCTCTC ATAGGCCACC AGCAGAATTG 1320 AGGGGCCCTC TGTTGATGAG GTGTGGCCTG GGAGGGGCTA GTTGTCTGTC CACCTGATCC 1380 TTGCGGACAG GTGACCACAG GCTTCCTGCC CCAGGGGGCT GGGGGAAAGA TCGGGGAGGC 1440 CTCTCTGGCT TCCCCACTTG GAAGGAAAAT ACGGGCATAG GGGAGACACT TTACAGGGAC 1500 ACATTTCAGC CAGTACCCTC TGGCTGTGCT GGGGGCACAG TGCCTGCCCT GCCCACAAGA 1560 GGGGTCAGTT CTCTCCAGGA TTTAACTTCA GCCTTCAGTG CAGGGCAGAT GAGCACTCAG 1620 AGGCCCAGAG GACTCATATC ACGAGAGAGA AGCTGTGACC ACACAGGCAC TGAAGGTTAA 1680 GCAGAAGAGT GGGACACACG GGTGACCTGA AAGTCCCAGG GTCAGTGTGG TTAGCCCCAG 1740 ATAGCTGGGG AGCTTTGGGT ACCAGGCTTA GCAGGGGAGG AGGGCCCCCG TGACAGTTTG 1800 CTGGGGCTGC TGCAACAAAG CCCCACGAAC TTTGGGGGCT GAAGATGGTT CTAGAGGCCA 1860 GAAGTCCAAA ATCAAGGTGT CGACCAGGCT GATCCTTTGG GGCCTCTGCG GGAGGCTCCG 1920
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