Tag | Content |
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EnhancerAtlas ID | HS095-16343 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr2:65294610-65296530 |
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) |
HNF4G | MA0484.1 | chr2:65296253-65296268 | TGGACTTTGGACCTG | - | 6.67 | Hnf4a | MA0114.3 | chr2:65296251-65296267 | ATTGGACTTTGGACCT | - | 6.18 | MEF2A | MA0052.3 | chr2:65295795-65295807 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr2:65295795-65295807 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr2:65295793-65295808 | CTACTAAAAATAGAA | + | 6.57 | TP53 | MA0106.3 | chr2:65296063-65296081 | GGCATGCCCTGACTTGCT | + | 6.28 | ZNF263 | MA0528.1 | chr2:65295301-65295322 | ACCTCCCCTTCCACATCCTCC | - | 6.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_00295 | chr2:65294777-65298905 | Adipose_Nuclei |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 65294777 | 65294891 | chr2 | 65294927 | 65295019 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I065068 | chr2 | 65295161 | 65299008 |
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Enhancer Sequence | TGTGGGAGTA TCTAGTAGTA AATATTTTGT TTGATTTGTA TTTAAAAATG GGCTGCTTTT 60 TCTCCCATTT GGCTCCTTTG TCCTTCCTTG TAAGGTGACC TGTTACACTG ATTCTGTCCA 120 TGCCTCCCCA TGACACTAAT GACAACAGCC AACACTTAGT GTCCATACCA TGCCAGGCAC 180 TGTCATAGAT GTTCTGCCTG CCCTGGCTCA TTTTGGCAAA GGAATGGGGG ACAAGGGCGG 240 AGAGAGACTT ACATCTGCTG TGCATTTTAC ATTTGAGCTG TATATTACCT TTCAAAAATA 300 ATTTTCTGAT TAGTTCCTGC CCCACCTGGT GGTTGTGGGA ACTAGACGAG CGTCCGTGCG 360 AAGGGCATGC TCTTCTCCAG GGTCACTTCT GAATCAGGCT GGAGCCTGGC ATGCCCCATC 420 AGGCAGAGTA GGGAAGGGCC CTCTTGGATT CCAGTGCAAG GCGTCCTCAG TGTGTGCAGT 480 GCCCATCTAG GTGGTATTTC CCAGCGTGTG AGCTGAGTAA GATGAGCCCG CAGCCATTCC 540 CCCTTTGCAG GCTCTCCACC AGCATCTCCT CTTACCATCT GTTTGCCTCC TGACTAAGGA 600 AACAAGGCCA TTTCTGCCCA CATTTAAGCT TTGAGGTTGG CCCAGTGCAC TCCGGGTGGC 660 TGCCGACATC CTGGGCATTC ACGGTTCCGT TACCTCCCCT TCCACATCCT CCCAGCATTG 720 GTCTTCCTCC TGTTGGCTTT TTGGCCCCCT ACCCCATCCC ACCAGGGCTC TCAGCATCAA 780 CTTTTGCTGG CATGCTTAGG CTGAGGGTGA TGTCCCTCTG TTGTTCCTGA ACCTCTTTGT 840 GTTGGAATGG TCCTGTTTGC AGATTCAGCT CCCAAATCAT CATCCTTCCC TGAGTGCTCG 900 GCCTGTGCTC CCTCGCCTGC CTGCCTGCTG ATTGGCTCTT GCTCTCATGT GCACACATGC 960 TGTGTTACAC TTACCCTACC ACTGTTACCC ACCAGCTTTC CACAGCTTCC CTCCATCACC 1020 ACGTGCAGCA TAACCCAGGC CAGCCTGAGG AGAGTTGCTG ATCTCTTTCT CTTTGGTCAC 1080 TGGCCATCCT TGGAACAAGT AGCTCTCACC TGTTCCACAG GCTGGATGTG GTTTCTGTGC 1140 TTTGAGAGGG TCCCAGCCTG GGCAACATGG TGAAACCCTG TCTCTACTAA AAATAGAAAA 1200 ATTAGCCAGG CGTGGTGGCA TGTGCCTGTA GTCCCAGCTA CTCAGGAGGC TGAGGTGGGA 1260 GGATCACCTG AGCCCAGGGA GGTCGAGGCT GCAGTGAGCT GAGATCATGC CACTGCACTC 1320 CAGCCTGGGT GACAGAGTAA GACCCTGTCT CAGAAAAAAG AAAAAAAGAA AAGAAAAGAG 1380 AGGGTCCTGC CTCCTCTGCC AGGCAGAGCC AAGCATCTTG GAGGGCATTC TTCCAGTGCC 1440 CAGCTGAGGC CTGGGCATGC CCTGACTTGC TGTTCTCTAG GATAGAACAG TCAGAGCCAG 1500 GCCTGAGTTG CTTGCTGAGG GGACCGTTAC GACAACAGAA CCACTATGGG CCTGTGCACA 1560 GGAAGGGTCC CACCAGGCCT CTTACCCAGT GGGGTTGGGC TAAAAGGGCA AAAAGGTGAC 1620 TTAGGCAGGA CCCCAGCCTT GATTGGACTT TGGACCTGTG TTGACCCTCT TGGGTTTCTG 1680 CTGGTGGGGA TGGCACCATC CACCATGAAA GCAGAGGGGA AATGGTGTGC TTCTGTGTCC 1740 CCTTTGGAAA GGTCTGGGGC CAGGGAAAAG CCGGAACTCG GTGCTCCTCT GAGGAAGTAG 1800 TCACCATTTG TTTCCTTTTT TCTTTGACCA AAAATATGTT TGCCTTAATT GTTAAAGAGC 1860 AAGACTTCCT GAACACAGAT GTAGAAGATT TATATTTTTC TCTCCCTTCC CCTGTTTTGT 1920
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