Tag | Content |
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EnhancerAtlas ID | HS136-00215 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:23158130-23159490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:23159451-23159464 | GAATGTTCTGGAA | - | 6.62 | TBX21 | MA0690.1 | chr1:23158262-23158272 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:23158262-23158273 | AAGGTGTGAAA | + | 6.62 |
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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 |
GH01I022824 | chr1 | 23151232 | 23159621 |
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Enhancer Sequence | ACACCATGCC ACACTGTGCT GGCAGAGATA GCAAGAGTTG TTGGAGATGA TTATAAGGGG 60 AGGGCCAAAA TGATCGTGGG AATCCAATCC CCGTGGCAGT AGGTGGGAGA TGCTGACCTG 120 GGCTTCCTCA GAAAGGTGTG AAATGTTGAC ACCCTCCCCT TGGGCTCTTC AAGGGCTCAA 180 GAGGGGCTGT GTTAGGCTGG GCTGGAAACA GAGGGCTGAC CATCATGGGT TCCAGAGGGA 240 GCTATCCACC CCCCTACCTA GCCAGAGGCA GCCAGGATTC CATTAACCTG ATTCTCTGCC 300 CCACATAAAC CTGCAAAGGG AGCCCCTGGA GGGAGGGGTA CTGGGGAGAG GAAGAATTGG 360 GCTTCCCCAG GCCCCAAATG GAGCAGCCAG TGGTGCTAGT TTCCTCTCTT GCAGTCCAGG 420 AGGACCTTCG AGGCCCCTGG CTGTTTGAGC GGGGAATAGG GAGAGCGATG GAGAGCCAGA 480 AAGTAGGGAC AAGAGACTCC AGGCTGGGGT GCAACAGCAG GAATAGCAGG AACAGGGTGC 540 ACGTCATCAG AACAATGGGT CCTGAGTCAC TCTGTGCCTG CCCAGCCCTG CATGGCCCTG 600 GGTGAGTCAT GTCACTTCTC TGAGCTGTGG GTTCTTCCTC AATAGTAAGG GCAAACCAAT 660 GCCACCTCTC AGTGTTGCTG GGCTGATTCA CAATACCGGG CCTCAAGAAA TGGTGGCTGT 720 TGCCAATGCT ATAATTTTAC AATCTTGACC CCATGTATCC CTTCTCAGCT TGCAAGCCAC 780 ATTCATCCTT TTTCTCCTTG GAGCCTCACA ATACTTCTGC AAGGTGTCCA GGATTCTTAC 840 CAGAGAGGTT AAGGGACTTG TTCAGAATCA CACAGCTTCT AACCCTTGGC CTGGGATGCA 900 CCCCTAGTGA TTGTCATGGA GTGGGCCATC CCAGCCAGGC TACGCCACTC TTCTTCAGTC 960 TGGGTGGTTG CTATTCCTCT GCCATGATTC ACGTCAGATG CCTCTTCCTC CAGGAATCCC 1020 TCCCTGACCA CACAAGAGCC TGGTTAGTAC AACTCTCTGC TTTCCCACAA CCTTTGAGAC 1080 ATTTATCAGA GTGTTTATCA GCAGTCATCA CAACCGTTAG GTGCTCCCAC CTAAGACTTT 1140 GAGGGTTCAG CCAATACTTT ATAATAGAAG AAGAGGGGGT ACAATAAATA TTTTGTTAAT 1200 GACTACAGCA CCTGTACAAA GGGACAGATA GGTGTCCACA GACTCACATG TATAAGTAAC 1260 AGTCATGCAT GCACAGCCAT GCACATGTGG CTTAGTGAAT ACACATGTAT ACAGACAGGG 1320 AGAATGTTCT GGAACATGAA TTGTGCTCAT GTGGATGCCC 1360
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