Tag | Content |
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EnhancerAtlas ID | HS187-03989 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr10:135213710-135215030 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr10:135214608-135214623 | GAGGCAGGCTGACCT | - | 6 | IRF1 | MA0050.2 | chr10:135214802-135214823 | TGACTGAAAGTGAAACAAATT | - | 6.46 | IRF1 | MA0050.2 | chr10:135214841-135214862 | TCTGGCTTTTAGTTTCCATTT | + | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr10 | 135214200 | 135214600 | chr10 | 135214264 | 135214898 | chr10 | 135213742 | 135213886 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I133400 | chr10 | 135213952 | 135215403 |
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Enhancer Sequence | AGAAAAGAAA AAAAATCCCT TTGATCCAGA GAATACAAAG CGTGTGAAGT AGACGGGGCT 60 GGATTATCAG GCAGGGAGGC TGCAAGGCCA TTCCTCCATG GCGTCCGCCT TGCCTTTGCT 120 GGAGGGTTCC TGGACTCCGG AGTCGCAGGC GCTCCTTTCC TCCCTCTGTG CCTGTTCTCA 180 GACTCTGATT CAAAGCAGGA GCCCCGAGCA CCCTTCACTG CCCCGTGGGC TCTTTTCCTT 240 AAGTATTTTC AAGTTTAATT CAAGTCCTTG TTGGCTTCAT TTTTCATATT AATAAGGCAT 300 TTATTAACAA ACCCATTCAT GATGTGCAAA TCTGAAGGCT TTAAACTACG GTGAACTGTT 360 ATTTTACAGA GAGGGTGTTT TTGGTGCTAA TTGGAGCATT GTTACAGTCA TTTATTCTTT 420 TAAGTTTATT TTTAAGCGTA TTATTTTTTA TCAGTGGTAT TAAGTGCATT TATAGGGTTA 480 TGCAGCCAGC ACCACTATTT TCAAATATTT TGGTTACCTG AAAATGAAAC TCTGTAAATA 540 CAAAGAGTCA CTCCCCCAGC CTCCTACACC CCTCGTTCCA CTTTCTGTCT GTGAATTCGA 600 TGACTGTAAC TGCCTCCTCC AAGTGGACTC ACAGTACTTG GCCTTTTGTG ACTGGCTGAT 660 GTCACCGATC GTGATGTCCT CAAGGTTCGT CTGTGTTGTC CTGAGTGTCA GAATTTTATT 720 CCTTTTTAAG GCTGATCACC CCGTTGTGTG TACAGACCAC ATCCTGTCTT GTCCATTCAT 780 CTGGATGGAC ACTTGTGTTT TTTATTCTTG GGTTGTTTGT CCACAGTGGA GTGGCCTCCT 840 TGGGACACAC CCTGAGCTGG GTCCTAGAGC AGCCAGTCGC CTGTGGACAG TGCTGTGGGA 900 GGCAGGCTGA CCTTGGGGTG CAGGGGTGGG TCCAGGAGGG AGGTGGGGGA CTGCGTGGAA 960 GGAGCAGCTC AGGTCTGACC TCCGCAGTCT GACAGTGCCT TTCCAGTCCT GGGGAGTTAG 1020 GTTCTGGTGC ATTTGTTGAA GAATCTCAGT CTCTGTGTGG CTTGGAAAGT GCCCTTGCTG 1080 TGAGCTGGTT TGTGACTGAA AGTGAAACAA ATTATAGCCT TGGGAAGCTC ATCTGGCTTT 1140 TAGTTTCCAT TTTGGCCAGA TATGTTTGTT ACATAGTCTC CCTGCTTGGC TGGTAAGTTG 1200 TGTTTGTTAC ATAGTCTCCC TGCTTGGCTG GTCAGATGTG TTTGTTACAT ACGTCTCCCT 1260 ACTTGTTCTG CAGCTTCTGT GTTTAGTATA CATTTGAGCC TCCTTTTCTC CTTTTCCTAC 1320
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