Tag | Content |
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EnhancerAtlas ID | HS082-29496 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr5:156942480-156945180 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Lhx3 | MA0135.1 | chr5:156943107-156943120 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr5:156943104-156943117 | GATTAATTAATTA | - | 7.34 | MSC | MA0665.1 | chr5:156943970-156943980 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr5:156943970-156943980 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr5:156943970-156943980 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr5:156943970-156943980 | AACAGCTGTT | - | 6.02 | POU6F1 | MA0628.1 | chr5:156943105-156943115 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr5:156943109-156943119 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr5:156943105-156943115 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr5:156943109-156943119 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_10243 | chr5:156942912-156944407 | CD19_Primary | SE_10863 | chr5:156909781-156978888 | CD20 | SE_14730 | chr5:156942857-156944779 | CD4_Memory_Primary_7pool | SE_25805 | chr5:156942317-156945425 | Duodenum_Smooth_Muscle | SE_27121 | chr5:156942543-156944778 | Esophagus | SE_30832 | chr5:156943004-156944357 | Fetal_Muscle | SE_36955 | chr5:156931578-156947133 | HSMMtube | SE_40934 | chr5:156942403-156945364 | Left_Ventricle | SE_42416 | chr5:156942579-156945185 | Lung | SE_46096 | chr5:156942484-156945222 | Osteoblasts | SE_48834 | chr5:156942561-156944752 | Right_Atrium | SE_50178 | chr5:156942538-156945172 | Sigmoid_Colon | SE_51718 | chr5:156942296-156945287 | Skeletal_Muscle_Myoblast | SE_52470 | chr5:156942669-156945189 | Small_Intestine | SE_53856 | chr5:156942391-156945002 | Spleen | SE_54595 | chr5:156941720-156945392 | Stomach_Smooth_Muscle | SE_63503 | chr5:156941760-156945350 | HSMM |
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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 |
GH05I157514 | chr5 | 156941546 | 156945274 |
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Enhancer Sequence | CCATAGTCTC TGCTACAACT CTTCAACTGT GCAGTGGTGG CTCAGAATAA TACAGACACC 60 TGTATATATA ATACAGAAGC CTGGATAATA CAGAAACCAA TGGGCCTGGC TGTGTTCCAG 120 TAAAATTTTG TTTGCAAAAA CACAGGATAG GCTGGATGTG ACCATGGGGT ATAGTTTGCA 180 GACCCCTGAT GTAAAGAAAG GACTGTCTCA AACTTACATT TTCTAGGGTG ACACAGTGAG 240 TACCACATGC AGCACCATCC TTTCCCAGCC ACTCTGCACT GTGCCAGCAT CATGGAAGTC 300 CTTTACAGGC CTGTGTTTAC AGTTATCCTG TCTACTCCTA CAACAGCCCA CCTTACTCTT 360 TATCCCCACC TGGATTCCGT TCCACCTGGG GAATGAATAA ACTGAGAACC ACCCTAGAAG 420 CTCCCACCTA GGCCCAGGGA GCGAGGAGCT GCCTGCTCAT TTTTACTGCT GACAACTCTC 480 TCTCTAGGCA GCAGCAGGGT CTTGCTCTCC CTATCTGTGT CTCCACTTTC TGCTCTGCAT 540 TCAGAGCCCC AAGGCTCTGT CTCTGCAGCA GGTTATAAAT CATGGTAAAG CAGCCCTCCC 600 CTTTCCTGCC TTCCCATCCT CTCAGATTAA TTAATTAATT GTCAAGAATA TATTTCTGTC 660 TGCAGAGGAT GGAGACAGGT GGAGAGGGGA TGATTCGTGA GCCTGTGAAC CCAGCCTGGC 720 CTGTTACACA CCCCCACCCC AGTCCCTCAA ATGAATCATT CAAAGCCTTC AGCGGAGGGG 780 TGTCCAGGAC TGAGAAATGA GCACGTTCCC TTATCCACCA CAGCTGCATG AATCACAGCC 840 CTGTTGGGAA CCCAGGGCTG TTGCTGAGAC ACTCTCCTTT GTAAGAGAAA GATGGCTCTA 900 GCTGACACCA GAGTCCTGGA GGCACCTTGA GTGGACACTT TTTCTCTGGA GGTGTGCTGT 960 GACTCTGGAG GTCAGGAGAT AGAAGATGCC TAATCCCTGC CTCCCACCAT GCTTCCCACT 1020 TCTCCAGCTG CTGGAGATTC ACACCCAGTG GGTTTGAAAG CCTGCACAGA GATTCCTCTG 1080 AGAACAATGC AAGGCCAAAG GGGAGAAACA CCCCACCTTT AAACAGAGCA GCTGGGCTCT 1140 ATATGCTTAA CTACTGGGGT TCCCAGGAAC TTCCATGTAA CCAAAGGATT CTGTAGCTGA 1200 AAAAAATGAC TCAAGACCAT TGTATCAGAT GATCACAGAT GCAGAACTTA AGTGGAAAAA 1260 TGTCCCAGAG TCAGAGGAGC TCAGTTTTCT TCCACCAGTC CTCCCACTAC GGGCAGTCAG 1320 GCAGGGCAGG CCAGAGTCAG TTATCTCCTC CCACGACTAT GGAGCCTCAG CTGGCTTTTA 1380 AACCAGCTTT GGATTTTGCT CCCCACACTA TTCCCCCATC CTATAGACAC ACTAGTCTTT 1440 GGAGAGGAAA CAGAAAACAT AGAACACACA CACACACACA CACACACACA AACAGCTGTT 1500 GGAAAAACCA ATATCAACAT CAGTTAAAAT AAATCTAAAC GCTTTTCAAA GCAGAGCACA 1560 ATGTTCCCTC GGCCCGGAAT GCCCTTCACC TCCACTCCTC TGCCCAGTTA ACTCCTCCTT 1620 GTCTTTTAAG ACAGCTTCAA GGGCCACCTC CTTCTGCTGC TAACATCCAG TGACTAACAC 1680 TCAAAGACCT TCTGGCCTGC AGCCTAGTGC TCTCCCCACC ACCAGGCCCT GCTGCCAGGA 1740 CACATGCTTT GGAAATGTGA CTAGGTACAG CTGCCTTAGA ATGAGCTCTT TGGGAAGATG 1800 GTAGCTAAAC TATGTGGATG GGATACAGAC AGACTGGAGT TGTGATGGGC TCTATCCTCA 1860 GGAGAGACCA AGGCCAGTGT CTGCCCTGCT CGAACACAGC GAGCGCTCAG CTCATAATGA 1920 CATCCAATGC ACAGAAGATG CACTTAGTAC TTATATGATG GAGTCACTAA ACAAAGTGAG 1980 AATTGGAGGT AACAGCTGGC TAATTTAGGC AAATATGGGC TCTGGGGCCT AAACTCACTC 2040 TTTAGGTGTC TGCTTCAATG TCAGGGAAGC TTTCCCTAAT TCCCAAAACC ATGTTGAATC 2100 CCCCATTATC TGCACTTTCA TCCCTCCTAA TGGTCCATCT TAGTGCTTAT CACACTTTGG 2160 ACCTACAGGT TTGTGTGCTG TTACTGCAAA CTCTGCGATG CCTGGGGAGG GTCTGTCTTC 2220 TTGAGATCTA TATATCCAGG TGCTTGGCAC ATAATAGAAA ATCAAGAGAT CACTGATGAA 2280 TAAATGAAAT ACATGATGAG CCAGGTGAGG GTTCCTCAAA TTCTTAGAAC CTGTCTGATT 2340 TGAGGAACAT GGAGTTAAAG GCTGAACTGC TATGCCTTTA GGTCAGTGGT TCTCAAACTT 2400 GACTGTGCAA CCCAATCGCC CAGAGGTCTT GTTAAAACAT GGATTTCTGG ACCCCACCCT 2460 GACAGTCTGG GATTCAGGAG GTCGGGGGCA GGGCCCGAGA ATTTGCATCT TACACAAGGG 2520 TGCTGCTGAT GCTGGTGCTC TGGGGACCAC ATTTTGGGGA CCATGGCTTT AGGTCATCAT 2580 TTGGCATCAA CATGATTATA AAAATGGACC CACACATGGG CAAGAATACA GTTTTCAGTC 2640 GGATGACTGG GAATATATTT ATCATCTTTG CAAAAAAAAA AGTTTTAGAA TTTCCATAGA 2700
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