Tag | Content |
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EnhancerAtlas ID | HS037-18839 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr2:18073650-18075200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr2:18074431-18074446 | TCTGCTGAGTCATGC | - | 7.23 | Nfe2l2 | MA0150.2 | chr2:18074433-18074448 | TGCTGAGTCATGCAG | - | 7.41 | RREB1 | MA0073.1 | chr2:18074962-18074982 | TGGGGGTGTGTGTTTGGGGG | - | 7.97 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 18074112 | 18074343 | chr2 | 18074367 | 18074908 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I017892 | chr2 | 18073975 | 18074891 |
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Enhancer Sequence | GTCCCTCCCT GTTTAGCTTA ATAACTAACT TCCCAAATTC TTTTTCAGGT AACTCAGGGA 60 TTTTGTCTTG GTTTGGACCC ATTGCTGGTG AACTAGTGTG ATTTTTTGGG GGGTGTTGAA 120 GAGCCTTGTT TTGTTATAGT ACCAGAGTTG ATTTTCTGGT TCCTTCTCCT TTGGGTAGGC 180 TCTGTCAGAG GGAAGGTCTA GGGCTGAAGG CTGTTGTTCA GATTCTTTTG TCCCACTGGG 240 TGTTCCCTTG ATGTAGTACT CTCCCCCTTT TCCTATGAAT GTGGCTTCCT GTGAGCTGAA 300 CTGCAGTGAT TGTTGTCTCT TTTCTGGGTC TAGCCACCCA GCGAGTCTGC CCAGCTCTGG 360 GCTGGTCCTG GGGGTTGCCT GCACAGAGTT CTGTGATATG AACTGTCTAT GGGTCTCTCA 420 GCCGTGGATA CCAGTGCCTG TTGCAGTGGA GGTAGCGGAG GGTGCAATGG ACTCCATGAG 480 GATCCTTAGC TTTGGTGGTT TAATGCTCTA TTTTTTTACT GGTTGGCCGC CTGCCAGGAG 540 GCGGCACTTT CAGCTGTGCT AGTATGGGGA GGAACCAGCA GTGGGTGGGG CCCTAGAACT 600 CTCAAGATTA TATGCCCTTT GTCTTCCATT ACCAAGGTGG ATAGGAAAGG ACCATCAGGT 660 GGGGGTAGGG CCAGGCACAT GTGTCTGAGC TCAGACTCTC CTTGGGTGGG TCTTGCTGTG 720 GCTGCTGTGG GGGATGGAGG TGAGATTCCC AGGTCACTGG AGTTGTGTAC CTATGGCTGC 780 CTCTGCTGAG TCATGCAGGT TTTCAGTTAA GTGGGGGAAA GCTGGCAGTC ACTGGCCTCA 840 CCCAGTTCCC ATGCAAACTG AAGGGCCGGT CCCACTCCCA CCCTGTCCCC TCCTACAGCC 900 TGGAGTCTGT TTCCAGGTGG AGAGTGAGAG GGTCTTGAAA ACTTGCCCGA GGCCATCTGC 960 CTCCCAGCTG AGAAAGAAAG GGCTTTAATT CTTCCTGGCC TGTGAAGTCT GCATGCCGGA 1020 TTAGGATTCG CAACCTCTCC TGAGTTCTGG CCAGGGGGCT TCTCGCCCCG TTCAAATTGT 1080 TACAGAGTTT GCCTAGAGAA TTCCTTCTCC TTGTTGAATT TTACCCCCTG CATCTCTGGG 1140 CACCCTCATG ATGGATCCCC GTGGTGCCAG GCAGGAATGG ACTGCTTGGG GACCCAGTGA 1200 GCTCCCAGGG CTTTTCTGCT GCTTCCTCTG TATTTCGCTC GGCTCTCTAA CTTGACTCAG 1260 CTCCAGGTAA AGTTGGAAAC TTCTCCTGCA AACAGACCTT CAGCTTCTCC ACTGGGGGTG 1320 TGTGTTTGGG GGAGGAGGGT CTACCTTTCC CACTTCCGCA GTTGGGGCAC TCACAGTATT 1380 TGTGGGTCTC CTGGGTCCTG CAGGAGCAGT CCGCTTCCTT CAGAGGGTCT GTGGTCCTCT 1440 CAGTATTTCT GATTTGTTCT TGCAGCCAAT CTGAAGCTAA AATTCACAAT GCGAGCCTCC 1500 ACATGCCGGA GCTGCAATCT AGTCCTTCCT CCCCTCTGCC ATGATCCCAG 1550
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