Tag | Content |
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EnhancerAtlas ID | HS136-17650 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr6:158477500-158480280 |
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) |
PRDM1 | MA0508.2 | chr6:158478494-158478504 | TCACTTTCAC | + | 6.02 | Znf423 | MA0116.1 | chr6:158478344-158478359 | TACACCCTGGGTGCC | - | 6.19 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_01353 | chr6:158478003-158479062 | Adrenal_Gland | SE_01612 | chr6:158477647-158479067 | Aorta | SE_01612 | chr6:158479817-158480748 | Aorta | SE_02260 | chr6:158476787-158479406 | Astrocytes | SE_04807 | chr6:158476841-158479168 | Brain_Cingulate_Gyrus | SE_04807 | chr6:158479750-158483023 | Brain_Cingulate_Gyrus | SE_05791 | chr6:158477032-158479294 | Brain_Hippocampus_Middle | SE_05791 | chr6:158479506-158483753 | Brain_Hippocampus_Middle | SE_06699 | chr6:158476876-158479129 | Brain_Hippocampus_Middle_150 | SE_06699 | chr6:158479845-158483538 | Brain_Hippocampus_Middle_150 | SE_07755 | chr6:158476970-158479146 | Brain_Inferior_Temporal_Lobe | SE_29930 | chr6:158478016-158479841 | Fetal_Muscle | SE_34547 | chr6:158477878-158479401 | HCT-116 | SE_34547 | chr6:158479766-158480414 | HCT-116 | SE_37125 | chr6:158477649-158479251 | HSMMtube | SE_37951 | chr6:158476913-158484134 | HUVEC | SE_38898 | chr6:158477261-158479873 | IMR90 | SE_40902 | chr6:158477971-158479093 | Left_Ventricle | SE_42660 | chr6:158478097-158479162 | Lung | SE_44330 | chr6:158476577-158480724 | NHDF-Ad | SE_44789 | chr6:158477249-158483106 | NHLF | SE_45571 | chr6:158475271-158484548 | Osteoblasts | SE_47213 | chr6:158476595-158479517 | Panc1 | SE_55691 | chr6:158475095-158484350 | u87 | SE_65268 | chr6:158477465-158479164 | Pancreatic_islets | SE_65268 | chr6:158479828-158483514 | Pancreatic_islets | SE_67484 | chr6:158475095-158484350 | u87 |
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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 |
GH06I158055 | chr6 | 158476791 | 158483822 |
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Enhancer Sequence | CCCACGACAC TGGGCTGGAG GCAGGAGCCC TCCCGTTCCC TTGCAGGTGC TGCTGCTCTC 60 ATGTTCATTG CTGACTATGT TCCCCTCATT CGAGATAACG TTTGGAAATA AGGTGACATG 120 TCTGCCTAGT GGCCGCAGTG GGGCACCATG AGGGTCCCCC TGAAAGCAGG CTGCCCAGGT 180 CCTCGATGGT GTCCCTGGAC TGGCATGTGC ATTGTCCTGG GTGCTTCCCA ATTCTCTTCT 240 CTGGGACATC ACTGCGCTCT CAAGAGTCGT GCGGTTCTCT GATGGATTTG GTTGAGAGTA 300 AATCCTTTCT TTCCCCCGCA AAACCTTCAC ACAGATAGTT TTTCTTCCCA GAGGATGCTT 360 GTTTTCCTTT GCCTGAGCTG CATGGGTGCC CCTGTTAGCC GAGGCGGTCT CTTGTCACTT 420 TGCTGTATGT GCTCCATATC TGAGGAGGGC TGTTTGCAGC AGGACTTTGG CTGCAGCTGC 480 TTGAGTGGGG TCTTGTCATC TCTGTGTGGT GATGAGTCTC GGTGGAAGGG CTAACCTTTC 540 ACAGGGCGGT GCCTCAGTCT CTCCTCACAG GACAGTGAAC CCCTTCTCCT TCCCCGCCCC 600 GCTCTGCGGG CGGCTGCTGT GCACATCAGG GTGTGCTGAA CTCTTGGTCC CTCCCTGAAG 660 ATGAGAAGGA TGCTTCCAAA TAGAAATCTG ATTCCTCAGT ATCCCGAAAA ACTCCTGTTT 720 TCCAAGTAGC TTCCTATGAC AGTAACCCGT AGGCAGGGGA AGTGAAAAAA AGGCCTCAAT 780 GCTCAGGGTG ACCCAGGAAG AAGCCCGTAT GATGCCGACC TTGCTGCTGG TGCCAGCGTC 840 CCCTTACACC CTGGGTGCCA GCGCTCCCTT ACGCCCTGGG TGCCAGCGTC CCCTTACCTG 900 GGTCGGCAGG GCCTCTCAGC TCACCAATAA CGAGCATTTT ACAATAAAGG GAAAGAAAGA 960 GGAACCACGT CCCACACACC AAGCACTGTC CTTGTCACTT TCACTCGTCT TTTTAGTCCT 1020 CCTCGCCATT CTCCGCAGGA GGGGAAGTAG CCCTGCTTTA TAGATGAAGG AGCCAGCTCA 1080 GAAGGGATGA ATCATTTGAT CAGGGGAGTT TGGGGTTGGG ACAGCATAGA GTAATGATGA 1140 GGAATAGTGA GTAATAATGA GTAATAACAG TTTCCTTCTG GCCCTGGGCT TTGGAACCAG 1200 TTGAGAAGAA GGGGCAGGAA TGAGACAGGA AGAGATCAGA AATGGGCCTT GTTTCCGATG 1260 AGCCACATTG TGGGATGTGG CTTGGATGTG TGGCCACGGT GGGCTCCCTC ACCAGGGGCA 1320 GAGCCTGCAC GTGTCAGAGC CAGGCCTGGG ATGCACCTTC TCTGGGCAGA CCGACCCAAA 1380 AGAAAGCCCA CAAGGGCTGA AGCCACACAC AGCCCGCCCC AGGGCTGCCT GGAGCTGCAC 1440 GTGGAGACGG GAGCCCGGGA GGGTGCTCAC CCTTAACTTA GGCCAGGGAG TCAGCAGGCA 1500 AGCCTAACTT CAAACTACCC ACTTCAAAAT CCATAGTCTT TCTACTACTG TCCCTTAAAG 1560 TTAGTAAGAG AATGTTTTCT CTTACTGCAT AAGAAAAAAA ATGATTTTTT TCATGATCAT 1620 TATTAGCTCT TTAAAAAATT CCGCTCATAA ACGTGTCATT ACAGAAATTT GGAAAAGAGA 1680 AAGATGTTTA AAGAAGAAAA GAACTTGAAT CATATAAAAT TCTACCACTT TTGACATCAT 1740 GTGTTTTTTT CCAGTGTTTT TTCTATATTT AGGCATAAAG ATTGCACCAT TAAACGATAA 1800 TTTGACATCT GCTTTTTGCA TTGTATCATT TCCCTATGTT TTGTTTAAGG CACTACATTT 1860 CAACATGTTT AAATTTGAAA TGTAAGGTTA CTTTTAAAAA GCTGGTGATC AAGAATAAAT 1920 ATTGGAATCT CTCCCTAATA TTTCAACATA CATATTTAGA AAGTAGCTTC CAATACAAGG 1980 AATGTTTTCC AAAGCCTGCA AGTTTTGTTG TATCTCCTTG TTGTGGTTTA GCATAATGCA 2040 ATATAGCACT TAGATTGAAA ACAGGATGCT GAGTTGAGAG CTCTCCTGCC AGTTGTTCTA 2100 GTTTTGAGAA GGGTGGGTAC CAAGCAAAAT AAGAGATTCA TTTCACACAT GTGCACATTG 2160 CATGTGTAAG ACTCTAGCCC AGGCACGGTG GCTTATGCCT GTAATCCCAA CACTTTGGGA 2220 CGCTGAGGTG GGAAGATTGC TTGAAGCCAG GAGTTCGAGA CCAGCCTGGA CAACATAGCA 2280 AGACCCTGTC TCTATGAAAA ATAAATAAGT AAAAATTAGC CAGATGTGGT GGCATGTACC 2340 TGTAGTCCCT ATTACTTGAG AGGCTGAGTT GGGAGGATTG CTTGAGCCCA GGAGTTTGAG 2400 GCAGCAGTGA GCTATGATCG TGCCACTGCA CTCTAGCCTG GACAACAGAC TGAGATCCTG 2460 TCTCAAAAAC AAAATTCTCT TGATGAAAGT TCAGGTTAGG TGTTCTAGAT ATAATGGGAG 2520 GTGCTTTATA GAAAGTGCAG CATATCCTTT GTCTGATTCC AAACAAATGT AGAAGTCTAC 2580 GCTAGCTAGT AGTAATGGCA GCTGGGAGGT GCAGGTTCTC TCCACCCAGG CTCATTTTCC 2640 ACGATTTGGG TCATGGGGGA CAGCTGGTCC TGGACTGTGG CACTAAGAAA GCATGACTCC 2700 TGCCCCGTCT TCCCTTGAGG GGCAGAACAG GGCAGAGTCT GCACCTGTGC CCGTGCCCAG 2760 CATCACGCCC ACCCCGCTGC 2780
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