Tag | Content |
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EnhancerAtlas ID | HS034-06462 | Organism | Homo sapiens | Tissue/cell | ECC-1 | Coordinate | chr12:19935980-19937380 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:19936254-19936272 | GGAAGAAAGGAAGGGAAC | + | 6.42 | KLF4 | MA0039.3 | chr12:19936941-19936952 | ACAGGGTGTGG | - | 6.14 | Klf1 | MA0493.1 | chr12:19936943-19936954 | AGGGTGTGGCT | - | 6.02 | NFKB1 | MA0105.4 | chr12:19937225-19937238 | AGGGGAATCACCT | - | 6.22 | NFKB1 | MA0105.4 | chr12:19937225-19937238 | AGGGGAATCACCT | + | 6.5 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATCATCGTAC CATAAAGACA CATGTAAATG TTCATTGCAG CACTGTTCAC AATAGCAAAG 60 ACACAGAGTC AACCTAAAAG CTCATCAATA ACACGCTGGA TAAAGAAAAT GTGGTACATA 120 TACATCAGCG AATACTATGC AGCTGTAGAA AAGAATGAGA TCATGTCTTT TGTGGGAGTT 180 GGAGTCCATT ATCCTTAGTA AATTAACACA GCAACAGAAA ACCAAATACC ACATGTTTTC 240 ACTTAGAAGT GGGAGGTAAA TGATGAGAAC TCACGGAAGA AAGGAAGGGA ACAACACACT 300 GGGGCCTACT TGAGGGTGGA ATGTGGGAGG AGAAAGAGGA GCAGAATAAA CAACTATTGG 360 GTACTAGGCT TAGTACCTGG GTGATGAAAT AATCAGTGCA ACAAACCTCC GTGACATAAC 420 AATCCTGCAC ATGTACCCGT GCGCCTAAAA TAAAAGTTAT TTTTTAAAAA AACACGGAAC 480 CCTTCCCCCC GCCCCCCGCC CGATCCCCCG ACCCCCCGGC CAGAAACAAA ACCAGTCTGG 540 CCTCTTTTCT GTGGGAGAGC TACGCTGTGC AGGTGCTCTG TGCCACTTCC TAATCGCTGC 600 TTGCTCTCCA GTGCATGAAT GCTACAGCAG CGGGGGCTGC AAGACAGCAA CAATGGCAGC 660 TGGCCTCTTC CTCTGGGAGC TCCGACCCAG GGAAGTGCAA AGCTGCTACC GGCCTGGGAG 720 CCCTGGTGTG GGGGTGTTTG CAGTCCAGGG CGTGTGTGCG GGGGGCGCGG GGGTCTTGCC 780 CCGTGAGGAG GAGCAGGATT GGGGAACTAT GTAAAAAATA CTCTGGCCGC TTTTCCGTGG 840 AATGGCTGCG CTGTGCAGAT CAGCGGCGGG GCCTGTCAGA CAGCAAAACT GGCAGCTGGC 900 GTCTCCTTCT GGGAGATTTG TCCCAGGGAA GTGCAGAGCT GCTACAGGCC TGAGAGTCCA 960 GACAGGGTGT GGCTGGAGAC CCAGGCCAGT GGGCCTTACG CTGTTAAATG CAGGGGAGGC 1020 GAGGTCTGCA TTTGCTTCTC AGTGTCTAGA TTAGGCTCTG TTCTTGGGGG AGTGCATGGG 1080 GATCTTGACT TTCTCTGCTG CCCCAGCTGC AGCTGCTAAT GCAGGGATGC CTGGGGATTC 1140 CAGGCTTCCA GGACTCTATG TGTGGCGTGT GCCTGAGTCG GGGCTATGGC CAGGCTCCAC 1200 GTAGTTCTCC ATGTCAGACT GGAGGTCCCA GTGAGGTGGG CTCACAGGGG AATCACCTGA 1260 GCCCAGGCTG CAGAAGTGTG AGTCCCCACG GACTCTCACT CACTATCCTC CCCGCCTCTC 1320 CCGTGAAGGG AAGAAGCTCC CCCTGACTCC ATGCCACTCT CGGGTGTGAA GTTGTCCTGT 1380 CTCACTCCTC TCCGTTCTCC 1400
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