Tag | Content |
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EnhancerAtlas ID | HS023-05437 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr12:10401140-10404210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Atoh1 | MA0461.2 | chr12:10403634-10403644 | AACATATGTT | + | 6.02 | Atoh1 | MA0461.2 | chr12:10403634-10403644 | AACATATGTT | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr12:10401143-10401161 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:10401147-10401165 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:10401151-10401169 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:10401155-10401173 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:10401159-10401177 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:10401163-10401181 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:10401167-10401185 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr12:10401175-10401193 | CCTTCCTTCCCTTCTTTT | - | 6.17 | EWSR1-FLI1 | MA0149.1 | chr12:10401171-10401189 | CCTTCCTTCCTTCCCTTC | - | 8.32 | IRF1 | MA0050.2 | chr12:10401196-10401217 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 | Nr2f6(var.2) | MA0728.1 | chr12:10401415-10401430 | TGAACTCCTGACCTC | - | 6.22 | RORA(var.2) | MA0072.1 | chr12:10403251-10403265 | TTGACCTAGATAAA | - | 6.36 | ZNF263 | MA0528.1 | chr12:10401143-10401164 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr12:10401147-10401168 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr12:10401151-10401172 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr12:10401155-10401176 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr12:10401159-10401180 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr12:10401163-10401184 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 10402360 | 10402995 | chr12 | 10403463 | 10403517 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I010249 | chr12 | 10401844 | 10403498 |
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Enhancer Sequence | CTTCCTTCCT TCCTTCCTTC CTTCCTTCCT TCCTTCCTTC CTTCCCTTCT TTTCTTCTTT 60 TCTTTCTTTT TTTTTTTTCA GAGTCTCTCT CTGTTGCCCA GGCTGGAGTG CAATGGCGTG 120 ATCTCGGCTC ACTGCAACCT CCGCCTCCTG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC 180 CAAGTAGCTG GGATTACAGG TGCCCGCCAC CACACCCGGC TACTTTTTGT ATTTTTAGTA 240 GAGATGGGGT TTCACCATGT TGTCTAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCA 300 CCCACCTCGG CCTCCCAATG TGTTGGGATT ACAGGCGTGA GCCACCATGC CTGGCCATAA 360 GTATACTTTC CGCTTGATGA TTGCACTTTT TGTTTTCTTT GAATCATATG CTTAGATAGA 420 ACATCATTAC CATTCTGTTA CAATGGAGAT TTTAACATGT TCACACTTGA AAATATCAAT 480 TTTGAATTCC ATTTGCATCT ATAATTATAT CAGGTTTAAA CTCACATACA ATAAACTATA 540 TACGACGGAT AATGTGTCCT CTATTATTCT ACCCATAAAC AAAGTAAATG TATTTCCAAA 600 CATGGAGTCA TTGGCATCAG CCAACCGGTG GGGGAGATTC TAAATTAGGC TTAACAGGGG 660 ACAGGGGAGT TGCTAACATC CCTTACAGTA AACTACTGAG GCAGTCCTTG ATTCTGCCAC 720 ATTATGAGGA TTTTATACAT AAGGTATTTC ATGAAAGAAA GAGAAATAGT AAAACTGCAC 780 CAAAGGAGAA ACAGTATTGA ATTGCAAACA AAGAAGACAG AAGAAACAAT AACAACAGTT 840 AACAATGCTT TCTCATTCAA TCCCTAGAAA AACCTTGTGA TGAGGATACT TTTATCCCCT 900 TCATTTTACA GATGTGGAAA AAGTAGATTA GGGAATTCAA CTGGACCAAA GTTATAAATA 960 TAGTAAGTGA CACAACTCAA ACTAATATCT TGCCTTCTCT GGTATCAAAC TTGTGCCCTT 1020 ATCATATATC AAAATGCTTC CAAGAAAATT AAATATACGG TTTGCAACCA GTGGAGAAAC 1080 TCTTGGGGAA ATCGTCAATT TTTTAAAAAA GAATTTATTG AGAAGCATCC TTGAAACAAC 1140 TTGAAAAAAG AGTAAGAAAT TATTTCATAC TTAATTTTCT ACAAAGAACA AAATAATGAA 1200 TCTCACATTT ATCACACATA TGCAGTGAGA AGGACTCCTG GAGGCTGTAG CAGTCAGTGC 1260 CTTTCACACA GGAAGGGACC CTTACTCTGA GCTCTGCTAA GCAGAAGGGT GGTAGTGTCC 1320 CATGGTGGCT CGTAATGCAT TTCTTGACCC AATGACTTCC TTTGTGGTTT CATCAGAGTT 1380 CGCAGGAGCT GCCATCACTC TAGCTTTATG GTTTTCAACT CTAACAAAGT GAGGAGTATA 1440 GTAGTCCTTT TGTTTTCTCG AAGACCATTA GGATCACTTG TTGTACATAC GTTGTCCGTC 1500 ATGCTCAGAT TTCCTAGGAA TTCAACTTCT GTCCTGAGTC TCTGCCTTTA TTTCTATCCT 1560 GGTGCGTTAG GCTGTCAACC TAGAAGGAAA CATTTACATC CCCTCAACCA CTCTCTCTCT 1620 TAAGTCCTTA CCATTTCCCA AGGTGGTGAT AACGTTTTGC TTTTTTTTTT TTTTTTTTTT 1680 TTTTTTAGGG GGGCTGTTAT GAGTGCTGGA AACCAAGAAA GGATGAGCAA AGAAAAAAGT 1740 TCCCCTGAGT CATTTGGCCC CAAACATTTT AGCATACCCA AAGGCGCCAG AGCCCTTTCA 1800 GTAACATGTA TTATTCCTGT TAAAGATCCT TCCCCTTGGT TTGGGTTCTG TAGCTAGACA 1860 AAGAGAAGGT TAAGAACATC TGCTTCTGTG TCACATTGTT CCAAACTTTT CTTTTCTTTT 1920 CTTTTCTTTT TTTGAGACGG GGTCTCACTC TGTTGCCCAG GCTGGAGTGC AGTGGCAAAA 1980 TCTCCCGCTC ACTGCAACCT CTGCCTCCTG GGTTCAACTG ATTCTCCTAC CTCAGCCTCC 2040 AGAGCAGCTG GGACTACAGG CTCCCGCCAC CATGCCAGGC TAATTTTTGT ATTTGTCCCA 2100 AAGTTTTCTG CTTGACCTAG ATAAAACTTG GGTATTAATT TATCAGTTAC CTTTTAAACA 2160 CATTTTAAAA TTTACATTTG CAACACCCCT TTGATTATTA ACTTCCATTA TATGTTGAGG 2220 CAAGTCAGTA CGAAGTGGTT TCAAAGTCAC ATAATACTTT AAAAATGGAT AGCGTATTAA 2280 GGTAATATAA AGGGTCTTGG GTCTGTGAAG CTAGAGAAGA TCCAGACCAG GAGAAAGTCT 2340 CAGGTATTTA AGAGCATGTT TTCTGGTTAA GGAAAGGATA ATTGAAAGCA GCCGCAAGTG 2400 CCATGTTTCG TTCATTTACC ATCATTATCA ACGACTTATT TAATGTAGTC ATAATTTTGT 2460 AATCGGGATT TCTGAAGTTC CATAAACTGG AGCTAACATA TGTTGCCTCA CTAGCATTAA 2520 CTACAGATGT TAACATACTA ACCTTTCACT CTGGAGTTTG GGACAGTGAG TGATTATTTG 2580 TTATTATACT ATTTTCTTTT TGAGATGGGG TCTCACTCTG TTGCCCAGGC TGGAGTGCAG 2640 TGGTGCGATC CTGGCTTACT GCAACCTCCG CCTCCCAGGT TCAAGCAATT CTCCTGCCTT 2700 GGCCTCCCGA GTAGCTGCGA TTACAGGCAA GCACCACCAA GCCGGGCTAG TTTTTGTATT 2760 TTTAGTAGAG ATAGGGCTTC ACCATGTTGT CCAGGCTGGT CTCAAACTCC TGACCTCAGG 2820 TAATCCTCCG GTCTTAGCCT CCTAAAGTGC TGGGATTACA GGTATGAGCC ACCATGCCCA 2880 GCCCTTTTAT GCTATTTCTT TGGCAAACAC AAAAAGGAAT GGTCTGGTCC AGTGGTCCCC 2940 AAACTTTTTG GCCCCAGGGA CCGGTTTCAT GAAAGATAAT TTTTCTATGG ATGGGAGCAA 3000 GAGGGGGATG GTTTGGGATG GTTCAAGTGC GTTACATTTA TTGTGCACTT TATTTCTATT 3060 ATTATTACAT 3070
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