Tag | Content |
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EnhancerAtlas ID | HS059-32220 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr3:56726550-56728100 |
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) |
GATA2 | MA0036.3 | chr3:56727785-56727796 | AAAGATAAGAA | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 56726951 | 56727634 | chr3 | 56727841 | 56728091 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I056692 | chr3 | 56726629 | 56730144 |
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Enhancer Sequence | GAGAACCTTT GTGTCCACAC TCTGTATCTA GCTAATCTAG TGGGGACGTG GAGGACCTCT 60 GTGTCTAGCT CAGGGATTGT AAACGCACCA GTCAGCGCCC TGTCAAAACA GACCACTTGG 120 CTCTACCAAT CAGCAGGATG TGGGTGGGGC CAGATAAGAG AATAAAAGCA GGCTGCCCTA 180 GCCAGCAGTG GCAACCTACT CGGGTCCCCT TCCACACTGT GGAAGCTTTG TTCTTTCGCT 240 CTGCAATAAA TCTTGCTACT GCTCACTCTT TGGGTCCACA CTGCTTTTAT GAGCTGTAAC 300 ACTCACTGCG AAGGTCTGCA GCTTCACTCC TGAGCCAGCG AGACCATGAA CCCACCAGAA 360 GGAAAAAACT CCGAACACAG CCGAACATCA GAAGGAACAA ACTCCAGACG TGCCACCTCA 420 AGAGATGTAA CACTCACCGC AAGGGTCCGC GGCTTCATTC TTGAAGTCAG TGAGACCAAG 480 AACCCACCAA TTCCGGACAC ACTAGGGAAG CCTGAAAAAG ACCCTCTTAA TTTGGCAAGA 540 AACCATGTTG AAGTTGATTC CTGGTTAATG ACTGGAAGAA AAACTTCCAT GCAATGAGGA 600 GAAGCAACAA AAGGGAGAAA TTCAATTGAA AAAAAGAATA TAGTTAGCAA TGAACAAGAA 660 GCAAGTGTCC TCTCACCAAC ACAGCTGACT CTGGTAACCA CAAACCTCAG CTAAACCCAG 720 AAGTCAAGAG CTGTCACTTA AGTTTTGTTT CATTTCTGAG TGAAACCCTT CTAAGACTTT 780 ATTACATGCA ATGCCATGGA TTAATGTCAT AGACATAATG TTAAATGAAA GACGTACTGT 840 ATGATCCCAT TTACATGATG TTCAAGGACA GACAAAAATA ATCTATGGTA ATAAAAGAAT 900 TGTGGTTCCC TTGTGGGGGT GAAGATGTAC TGTATGATCC CATTTACATG ACGTTCAAGG 960 ACAGACAAAA ATAATCTATG GTAGTAAAGG AATTGTGGTT CCCTTTTTGG AGTGGGGGTG 1020 GTAGGTAATT GACTCAAAGG GGACATGAAG GAACTTTCTG GAATGATGGA AATGCTCTGT 1080 ATCTTGATCT GGGTGGTAGT TATACAGACA GGGGCATACA CATATAAGTA TTCATTGAAC 1140 TGTATGCATA GAGTTGCATT TTATTCTGTG ATGTTATTCT TCAATTAAAT AAACAAAAAC 1200 AAAACTTTTC TATGGATTCT CATTATTCCA GGGACAAAGA TAAGAATTCT TCATGTGGGC 1260 AATGGACCCT TACTGATTCT GACCTTTGCC TGCCTTTCCA TCTTGCACTT CACTTCCCTA 1320 AGCTCCTCCT TGGTTCTTCC TATGTCTGGC ACACTTGCCA AACTCCCTGG CCATGCAATC 1380 AACCTCAGCA CATGATATGT TTCCTGTGTG GGATGTTATT CTTCCCCGTG CCACCCTCTT 1440 CTCCAGTTCC AGTAAGCTAC TGCACTTCCT TTGGCTGAAG CTTCACTTCC CTGTGTGAAC 1500 TTCTTTCATA ATCGGCCCCC CATTCTAGGT CGAGTTCCCC ATTGGATGCT 1550
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