Tag | Content |
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EnhancerAtlas ID | HS190-00195 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr1:23445810-23446920 |
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) |
IRF1 | MA0050.2 | chr1:23445890-23445911 | TAACTGAAAGTGAAAGCAAGT | - | 8.14 | IRF2 | MA0051.1 | chr1:23445894-23445912 | TGAAAGTGAAAGCAAGTA | + | 6.58 |
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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 |
GH01I023118 | chr1 | 23445090 | 23447083 |
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Enhancer Sequence | GCACAATCAC AGCTCACTAT AACCTCGAAC TCCTGGGCTC GAGCAATCCT CCTGCCTCAG 60 CCTCCTGATT AGCTAGGACA TAACTGAAAG TGAAAGCAAG TATGACAACT CAGATCTTAG 120 TTTTAGCTTT AAAAATAACA AGCTATGGGT GTGACCTTAG GCAAACTGCT TCATTTCTCC 180 AGGCCTCATT AAGATATCTC TTACAACTTT TAAACAAAGT CTGGAGAGGA TGTTGAGAGG 240 AATCAAGTAA GAATAAGCCC TTCTGAAAAA CCCTAGGTTT ATCTCTAGTA TAGCACTTAT 300 CATTCTGTAT TATAATTGTC TACTTGTTAC TCTCCTGTAC CAAACCCCGA GCTCCTGAAA 360 GGCCAGAATT ATGTATTTCA TCTCTGAATC CAAGCATGTG CATAGAACGT GGCACACAGT 420 AACAGTTCAG TAAATGTTCA ATGGCCAAAC TACTGAAAAT TATAAGTGCC TATACTTACG 480 AAGACTCTTA TGTATAAATG GACTTATATA AACTTATAAG AAAGAATAAT TCATCTCCCT 540 CATGTACAAC CCTTTCAAAT AACATTAAAT AAAAGTATTT TTCTTATTAT CACCAGCTCA 600 AGTCCAGGTT TTGTTTTTTG TTGGTAGTTT TTTTTTTTTT TAAAGACAGA GTCGTGCTCT 660 GTCACCGAAG CTGGAGTGCG GTGGAGCAAT CGTGGCTTCC TGCAGTCTCA ACCCCCTGGA 720 CTCAAGCAAA TCCTCCCCGC TCAGCTCCCA GAGTAGCTGG GACTACAGGG ATGTGTCACC 780 ACAACAAGCT AAGTTTTGTA AGTTTTGTAG AGATGGGGTT TCACCATGTT GCCCAGGCTG 840 GTCTCAAACT CCAGAGCTCG AGCAATTCAC CCACCTCAGC CTCCCAAAAT GCTGGAATTA 900 TAGACATGAG ACACGGCACC AGCCTAGGAA GTCCAATTAT TGAATGCCCA GAATCATCTG 960 AAATTCAGGA TCCCTAGAAG ATATCCTGAC AAGGGCCTCA GAAGTGCATG CCTCCTACGC 1020 TCTAAATAAT ATACCTCCTA ATAAATAAAT AAACATATAT ATATGGAGAC AGGTCTCTCT 1080 GTCACCCAGG CAGGAGTGCA ATGGTGCAAT 1110
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