Tag | Content |
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EnhancerAtlas ID | HS146-13086 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr6:158477330-158480280 |
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 | CTCTCTCTCC TCACAAGCAC CCCAGAGGCT GCCTTGCCCC TTGGAAAGCA TTCCTAAATC 60 TAGGGGTACA CTTAGATCTC TTCTGCAAAT CACAGGACAA GCTGCTGAAA GGGTGAGTCT 120 TTCTACAGGC AGCTACTGTG TCCAGGAAGT CTCTTCTGTA ATGCTTCTTA CCCACGACAC 180 TGGGCTGGAG GCAGGAGCCC TCCCGTTCCC TTGCAGGTGC TGCTGCTCTC ATGTTCATTG 240 CTGACTATGT TCCCCTCATT CGAGATAACG TTTGGAAATA AGGTGACATG TCTGCCTAGT 300 GGCCGCAGTG GGGCACCATG AGGGTCCCCC TGAAAGCAGG CTGCCCAGGT CCTCGATGGT 360 GTCCCTGGAC TGGCATGTGC ATTGTCCTGG GTGCTTCCCA ATTCTCTTCT CTGGGACATC 420 ACTGCGCTCT CAAGAGTCGT GCGGTTCTCT GATGGATTTG GTTGAGAGTA AATCCTTTCT 480 TTCCCCCGCA AAACCTTCAC ACAGATAGTT TTTCTTCCCA GAGGATGCTT GTTTTCCTTT 540 GCCTGAGCTG CATGGGTGCC CCTGTTAGCC GAGGCGGTCT CTTGTCACTT TGCTGTATGT 600 GCTCCATATC TGAGGAGGGC TGTTTGCAGC AGGACTTTGG CTGCAGCTGC TTGAGTGGGG 660 TCTTGTCATC TCTGTGTGGT GATGAGTCTC GGTGGAAGGG CTAACCTTTC ACAGGGCGGT 720 GCCTCAGTCT CTCCTCACAG GACAGTGAAC CCCTTCTCCT TCCCCGCCCC GCTCTGCGGG 780 CGGCTGCTGT GCACATCAGG GTGTGCTGAA CTCTTGGTCC CTCCCTGAAG ATGAGAAGGA 840 TGCTTCCAAA TAGAAATCTG ATTCCTCAGT ATCCCGAAAA ACTCCTGTTT TCCAAGTAGC 900 TTCCTATGAC AGTAACCCGT AGGCAGGGGA AGTGAAAAAA AGGCCTCAAT GCTCAGGGTG 960 ACCCAGGAAG AAGCCCGTAT GATGCCGACC TTGCTGCTGG TGCCAGCGTC CCCTTACACC 1020 CTGGGTGCCA GCGCTCCCTT ACGCCCTGGG TGCCAGCGTC CCCTTACCTG GGTCGGCAGG 1080 GCCTCTCAGC TCACCAATAA CGAGCATTTT ACAATAAAGG GAAAGAAAGA GGAACCACGT 1140 CCCACACACC AAGCACTGTC CTTGTCACTT TCACTCGTCT TTTTAGTCCT CCTCGCCATT 1200 CTCCGCAGGA GGGGAAGTAG CCCTGCTTTA TAGATGAAGG AGCCAGCTCA GAAGGGATGA 1260 ATCATTTGAT CAGGGGAGTT TGGGGTTGGG ACAGCATAGA GTAATGATGA GGAATAGTGA 1320 GTAATAATGA GTAATAACAG TTTCCTTCTG GCCCTGGGCT TTGGAACCAG TTGAGAAGAA 1380 GGGGCAGGAA TGAGACAGGA AGAGATCAGA AATGGGCCTT GTTTCCGATG AGCCACATTG 1440 TGGGATGTGG CTTGGATGTG TGGCCACGGT GGGCTCCCTC ACCAGGGGCA GAGCCTGCAC 1500 GTGTCAGAGC CAGGCCTGGG ATGCACCTTC TCTGGGCAGA CCGACCCAAA AGAAAGCCCA 1560 CAAGGGCTGA AGCCACACAC AGCCCGCCCC AGGGCTGCCT GGAGCTGCAC GTGGAGACGG 1620 GAGCCCGGGA GGGTGCTCAC CCTTAACTTA GGCCAGGGAG TCAGCAGGCA AGCCTAACTT 1680 CAAACTACCC ACTTCAAAAT CCATAGTCTT TCTACTACTG TCCCTTAAAG TTAGTAAGAG 1740 AATGTTTTCT CTTACTGCAT AAGAAAAAAA ATGATTTTTT TCATGATCAT TATTAGCTCT 1800 TTAAAAAATT CCGCTCATAA ACGTGTCATT ACAGAAATTT GGAAAAGAGA AAGATGTTTA 1860 AAGAAGAAAA GAACTTGAAT CATATAAAAT TCTACCACTT TTGACATCAT GTGTTTTTTT 1920 CCAGTGTTTT TTCTATATTT AGGCATAAAG ATTGCACCAT TAAACGATAA TTTGACATCT 1980 GCTTTTTGCA TTGTATCATT TCCCTATGTT TTGTTTAAGG CACTACATTT CAACATGTTT 2040 AAATTTGAAA TGTAAGGTTA CTTTTAAAAA GCTGGTGATC AAGAATAAAT ATTGGAATCT 2100 CTCCCTAATA TTTCAACATA CATATTTAGA AAGTAGCTTC CAATACAAGG AATGTTTTCC 2160 AAAGCCTGCA AGTTTTGTTG TATCTCCTTG TTGTGGTTTA GCATAATGCA ATATAGCACT 2220 TAGATTGAAA ACAGGATGCT GAGTTGAGAG CTCTCCTGCC AGTTGTTCTA GTTTTGAGAA 2280 GGGTGGGTAC CAAGCAAAAT AAGAGATTCA TTTCACACAT GTGCACATTG CATGTGTAAG 2340 ACTCTAGCCC AGGCACGGTG GCTTATGCCT GTAATCCCAA CACTTTGGGA CGCTGAGGTG 2400 GGAAGATTGC TTGAAGCCAG GAGTTCGAGA CCAGCCTGGA CAACATAGCA AGACCCTGTC 2460 TCTATGAAAA ATAAATAAGT AAAAATTAGC CAGATGTGGT GGCATGTACC TGTAGTCCCT 2520 ATTACTTGAG AGGCTGAGTT GGGAGGATTG CTTGAGCCCA GGAGTTTGAG GCAGCAGTGA 2580 GCTATGATCG TGCCACTGCA CTCTAGCCTG GACAACAGAC TGAGATCCTG TCTCAAAAAC 2640 AAAATTCTCT TGATGAAAGT TCAGGTTAGG TGTTCTAGAT ATAATGGGAG GTGCTTTATA 2700 GAAAGTGCAG CATATCCTTT GTCTGATTCC AAACAAATGT AGAAGTCTAC GCTAGCTAGT 2760 AGTAATGGCA GCTGGGAGGT GCAGGTTCTC TCCACCCAGG CTCATTTTCC ACGATTTGGG 2820 TCATGGGGGA CAGCTGGTCC TGGACTGTGG CACTAAGAAA GCATGACTCC TGCCCCGTCT 2880 TCCCTTGAGG GGCAGAACAG GGCAGAGTCT GCACCTGTGC CCGTGCCCAG CATCACGCCC 2940 ACCCCGCTGC 2950
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