Tag | Content |
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EnhancerAtlas ID | HS187-13011 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:28356670-28359290 |
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 | chr2:28357876-28357897 | TCTAAGTTTCAGTTTCATCTA | + | 6.37 | IRF8 | MA0652.1 | chr2:28357880-28357894 | AGTTTCAGTTTCAT | - | 6.74 | IRF9 | MA0653.1 | chr2:28357880-28357895 | AGTTTCAGTTTCATC | - | 6.04 | TP63 | MA0525.2 | chr2:28357732-28357750 | GGCAAGTTGTGACTTGTG | + | 6.21 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 28357147 | 28358000 | chr2 | 28357100 | 28357758 |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I028133 | chr2 | 28356741 | 28357822 | GH02I028137 | chr2 | 28359268 | 28359467 |
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Enhancer Sequence | ATCCTGACAA AAGAGAACAT CAGTCAGATT CATTGGTAGA AGACTCTGAG ATGTGTTCTA 60 ATTTGATGAA GCTCTGAAAT GTGATCCCAC TTCTGAAGTC TGTTTGCCCA GGGTCGTGGA 120 ATAGTTGTCT GGTGTCCCTG GCAGCCCTGC CGCACGTGGC TGCACGCCCT TACGATGCTT 180 AGATGCATAT TGTTTACCGG TCTCCCACTG CGCATTTCTA TGACTTGCAG AGTAAATGCT 240 TCTGAGAAGA ACTTTGTGTT CTTGCACAAG GGACATTTAT GAAATAAACA TATTTCTGGC 300 CCTATACATT TGTCTTCCAA GGAACCAAAA CCAATCCGTT GAATTAGACA CGAGTAAGTT 360 CTGTTAATTA AAAAAAAAAA AAAGTCAATG GTGAGTTATG CAAAAAAAAA AAAAAAAAGC 420 TAGTAGTCAA TGATGCAAAT TAGATTTTGG TTGAATATTA GAAAAGGGGA AAAAATAGTT 480 TCTAAACCAG TTGCTTTTTT TTCCCCTGGC AGAAAAGCTG TGAGTTTTAA GGTTACATCA 540 TCAGAGCTGG CGTGAAACAT GCTCTACCTT TCCCTCTTCC CCAGACTGTT GGCAGTTGTT 600 GTAGTGAACC CAAAGGTTAA ATGGGCATGA GAGTCTGCAT AGCACTCTTC CACGAAAGGT 660 GTGGGCCCTT TTCTTGGCTT GAGCCACTTT GTGGGAGTGG TTTAAAGACA ACCAGCTTCC 720 TCATTCCCTG TGCTGTTCCC ACTCTGTGCA TAAAAAGAGG ACTTCAGCCC TGAGGCAGAC 780 CAGGTGGCAT CTTTCACAAG TACAGAATTT GTTTTTAGAA CTTTTTGTTA AGTTACATCT 840 GCCTTGGAAA TGAGTACTCA AAACTTCCCA GCCCACGAAC GCTCACTATT ATTGAGGCCT 900 GTGTACCTGC AATATGCATG TTTGTTCTTT CAGGCAACAG AAACCCAATG AGAATCAACC 960 ACATGTGAGG CCCTTTGCTA GGTGCTTCAG AGGCTGTCAG CATAAATGAA ATGTGGCTCA 1020 TCTCCTTAAT TTCCTCAAAG TAAGAGGGAT CAGAACAAAT ATGGCAAGTT GTGACTTGTG 1080 GATTAATAGA AAAGGCATAT TAATACATGG CATCAGAAGC CCCCTGTTCC TTCACTTATT 1140 GGCTGGCAAT CTTGGCTTAA GTTAACGTTT TTGAGCTTCA TTTCATCTTC TGTGAAGAGG 1200 AATAAATCTA AGTTTCAGTT TCATCTACTC CAAGTGGGGA GGTAGATGAG AAAGGCCCTA 1260 CTGTAGTGCT TGGCCCATGG TTGATGCTTA GTTAGTGCTC CTTGAGAAAA TACTTATTAA 1320 GTGCTATAAG AGTTCAAGAG AGTGGGAGAT CACATTTCCA TTTGACTTGG TGGAGAAGGA 1380 GCTTTGGAAG ATTATGGAAA GCCTGGCTTT TCTAGAGATT AAATATGCAA TACTGTAACA 1440 ATAACAGATA TGTATTTGTT CAGTACTTTA AAATATTCAA ACTGCTTTTC ACTTTACCAT 1500 CCCATCTGAT CCTCATGATA GTATGTCTAT CATGTGTTTT ATAATATAGC TTTTTTCTTC 1560 CATAACTTGG AGTTTTTAGA TCCTTCCTTG TCTCCTTCAC TGCTACTCCT TCCTTTTTTC 1620 AACCCATTAA ATTATGCTAA ATTGTGCTTC CTGTGATAAC ATCCCTAGAC ACTTTTGTGG 1680 CATTGCCTGT TTGTGGATGA CACCCAGATC CCCATTTCTA ATCTCAGCAT TTCTCCCTGC 1740 TTACAGATCT GCTTCTCTAA CCACTAGATA GACATGTCTA TCTGTGTGTT CAGTTGACAC 1800 CTCAAATTTA AAGGGCCTGA AACTAAACTC ATCATTCCCC CAATAAGCTA ATGTTTCTTC 1860 TTTACAGCCT GTTTTTATTC ATGACACTCT TGTCTTCTTG GTGCCCAGGT GGTACATCTT 1920 AAAGGCATTG ACCATACCTC ATGCCCCTAT TAGCCAGCCA GTTGTTTTGG ACTAAAAACC 1980 CACTCTCCAC AATGTCTCTG AGTCTTGTCA TGCCTACTAT CATTACCTAG TTCAGTCTTC 2040 CAGTTGCCAT GGGTCCTGAG GGGCTCTTAA CTTCTAGTTC CTTCCTATTT CAGTTTATCC 2100 ATGTGGAACT GTCACTGTCC TTTGAAGTAA ATTCCAGTCC TGTAATGTCC TTGCTGAGAA 2160 GCTTCAATGC CTCTCTGTTG CCAAGCGAAG TAAATGCACA GCTCTCCATC TGGCATTCAG 2220 ATTCCGTGTT ACAGTCCTGT TCACTTTTCC ACCCTAGGCT GGACTCTACG TGTATCCTGT 2280 TGTCCAGCCA AGCAGAATTT TGTGATTTCC CGAACACATC TTGTATTTTT TTCACTTCCA 2340 TACCTTGCTC AGGCTGCTCC TTAGACCAGA ACATTGAGTT TATTTACCTC CCCCACAGGG 2400 TCCGTTAAAG TCCTGCCCAT GTTCTTAGAT CTTCTCAATC ATCACCTCCT CCATGGAACA 2460 TTTCCTGACC GCCACTGCCT GCCTCCACAA TGGCACCACA CTTTTTCCCT GTGTTTATGC 2520 CTCCTTTGTC ATATTGCCTC CCTGGACTCT AAACTCTTTA AGGCCTGGGC CTCTTTTCCA 2580 TCAGTTGAGG GCTGGTGAGC CACAGCCCCT CTGGCCAGGC 2620
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