Tag | Content |
---|
EnhancerAtlas ID | HS105-35927 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:75381130-75383920 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | Zfx | MA0146.2 | chr17:75383297-75383311 | CCGGCCCAGGCCTC | + | 6.38 |
|
| Number of super-enhancer constituents: 30 | 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 | SE_68672 | chr17:75383506-75386490 | H9 |
|
| 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I077379 | chr17 | 75375109 | 75393825 |
|
Enhancer Sequence | TTTTAAAGTT CATGGGCTCG TGCCCGTAAT CCCAACACTC TGGGAGGCTG AGGCAGGAGG 60 ATTCCTTAAG CCCAGGAGTT TGAGACCAGC CTGGGCAACA TAGGGAGACC CCCACCTTTT 120 TTTTTTTTTT TTTTTGACAG AGTTTCACTG TGTCCCAGGC TGAAGTGGCG GTGGCACGTT 180 CTTGGTTCAC TGCAACCTCT GCCTCCCAGG TTCAGGTGAT TCTCATGCCT CAGCCTCCTG 240 AGTAGCTGGA TTACAGACAC TCATATTTGT AGGATTTGAG AATCCTACAA GAGGAAAGCC 300 TCCATTCGGA GGCTGCTGGG GACTTGGAGT TGCCAGCTCA CATATTTTTT AGTAGAGACA 360 GGGTTTCACC ATGTTGACCA GGCTGGTCTC AAACTCCTGT CCTCAAGTGA TCCATCCATC 420 TCGGCCTCCC AAGGTTCCAG GATTACAGGC GTGAGCCACT GCGCCCGGCC ATGGGAGACC 480 CCCTCTTAAA ACAAGAATAA AAATAAAAAT AAATAAAAGT TTACTGTCAA AAAGAAAAAC 540 ACATCACCCA ACCTAATCTC CCCCTAGGAT TGAGAGATGA GGAAGCAGAG GCCGGAAAGT 600 GTCACATTCC CTGGTCGCTG GCAGTCAGGG GACCTGAGGC CTGGGCTGGT TTTCTCGTGC 660 TCCAGGCCTG GGGTGTCAGG TGGAGCCCCT GCTTTGCCCA AAGGTCTAGG TGCCTCTGCC 720 AGCACTGCTT GCTTCTGCAT TTTTGGCCAC AAGGAATGTG GGCCAAAGGC AGGGTCCTTG 780 ACCTCTGCCC AGGAGGGTGA AGTGGGCTGG TCCTCCTTGT CCCTGCTCCA AGGCCCCTGC 840 GGCTGTGCCT TTGGAAACTG CTGGCCCGAG CTAGTGTGCG GAGCTGGGAC AGACCTCACC 900 GTGGCCCTCG TGGGGTCATT CCATGTCCGG GCTGGAAGGG ATCTTTCGGT CCAGCCCTTC 960 CTGTTCCTCA TCAGGAAACT GAGACCAGAG AGGTCATCTG CCTGGCCCGG GGTGGGGTGT 1020 AGATGGCGCT TGTGACTCCT GCATGCCACG TGCAGACAGT CCCTCAGCTG TGGGCTTCCC 1080 ACGCAAGCAG CCATGCTGGG GATAACTTGG CTGAAACCTG CGATTTAATG AAGAGAAGAA 1140 TGACTCCTCC TGCAGCCCTG TGCCCCACAG GCTCCCTCCT GCCCCCACCC CTCCTGCAGA 1200 GGGGCCTCAT GCTGGTGGGT GGGTCCCTGT TGCTGCAATG GGCCCAGGCA GTTTCTGGGC 1260 AGTGGAGGCT TGGCTGTCTT CCTGCCCAAT GTCCCCTGTA GCCCACGCTG TCCGGGAAGG 1320 GCGGGGAAGC ACTCAGCCAC TGGGGACTTC ACAAGATGGG TATCTGGGAG ATGCTGATTG 1380 GCAGGCCAGG CTCCCGTGGC CCACAGGCAG GTCAGAGGTC ACAGTGCTGA GCTGGGCTGA 1440 GTTGGCAGCT CAGGGCAGTG GGGGTGGGGG TACCTTGCTC AGCCATGGGC CTCTCTGGCA 1500 CAAGGGTTTG GAGTTTACTG TAAACAACTC CTTCAGTTTT TCCTTCTCTC ATAGGCCACC 1560 AGCAGAATTG AGGGGCCCTC TGTTGATGAG GTGTGGCCTG GGAGGGGCTA GTTGTCTGTC 1620 CACCTGATCC TTGCGGACAG GTGACCACAG GCTTCCTGCC CCAGGGGGCT GGGGGAAAGA 1680 TCGGGGAGGC CTCTCTGGCT TCCCCACTTG GAAGGAAAAT ACGGGCATAG GGGAGACACT 1740 TTACAGGGAC ACATTTCAGC CAGTACCCTC TGGCTGTGCT GGGGGCACAG TGCCTGCCCT 1800 GCCCACAAGA GGGGTCAGTT CTCTCCAGGA TTTAACTTCA GCCTTCAGTG CAGGGCAGAT 1860 GAGCACTCAG AGGCCCAGAG GACTCATATC ACGAGAGAGA AGCTGTGACC ACACAGGCAC 1920 TGAAGGTTAA GCAGAAGAGT GGGACACACG GGTGACCTGA AAGTCCCAGG GTCAGTGTGG 1980 TTAGCCCCAG ATAGCTGGGG AGCTTTGGGT ACCAGGCTTA GCAGGGGAGG AGGGCCCCCG 2040 TGACAGTTTG CTGGGGCTGC TGCAACAAAG CCCCACGAAC TTTGGGGGCT GAAGATGGTT 2100 CTAGAGGCCA GAAGTCCAAA ATCAAGGTGT CGACCAGGCT GATCCTTTGG GGCCTCTGCG 2160 GGAGGCTCCG GCCCAGGCCT CTCTCCCAGC TTCTGGTGGC TCCCGGGTGC TCCTGGGCAT 2220 GTAGATGCGT CACGCCACTC CCTGCTCCGT CTTCACATGG CCTTTTCTCT GTGTCTCTGT 2280 GTCTCGTAAG GATGCTTGTC ATTGCATTTA GAGCCCACCC TAAATCCAGG ATACTCTCCT 2340 CTTGAGATCC TTTATTGCAT CTGCAAAGAC CCTATTCCAA CTCCTGTCAC ATTCACAGGT 2400 CCGAGGGCTA GGGCTCTGGC ATGTCTTTTG GGGGTCACTA TTCAGTCCAC TGCGGCAGCT 2460 GATCTTAGGG GAAGCAGAAT GTTCTAAGCT TGGGGTGAGC GGAGGGAACG CTGCTGGGTG 2520 GGGAGTGGGA GACCAGGCTC GGAGACACCG CGGATCTCCT CTGTCTGATG AGGGCGTGAT 2580 GAGGTTCTCA TCTCAGGTCC TCTGAATGGC GGCTGCTTCT GAGGAGACCC TTTCCCCTGG 2640 ATCTGCCCCT CCAGAAACCT CCACTTAGGT CCAGGTCCCA AGGTGGATGG TAAGAGGCGG 2700 CTGTCCCTGC CACACTTGAT GGGTGAGTGT GTGAACGGGG CTGGGAGCAG GACACTTGTC 2760 ACTTCTGTGG ACAGATTCCA GAGGCTCATG 2790
|