Tag | Content |
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EnhancerAtlas ID | HS049-01770 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr12:49379000-49381570 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr12:49380532-49380542 | GCCCCGCCCC | + | 6.02 | MIXL1 | MA0662.1 | chr12:49380476-49380486 | TCTAATTAAC | + | 6.02 | ZNF143 | MA0088.2 | chr12:49381069-49381085 | GTCCCACAATGCCTCA | + | 6.18 | ZNF263 | MA0528.1 | chr12:49380375-49380396 | CCCCTCCCTTTTCCCTCCTCC | - | 7.65 | ZNF263 | MA0528.1 | chr12:49380995-49381016 | CCCTCCCTCCCCTCCTCTTCC | - | 7.69 |
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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 |
GH12I048987 | chr12 | 49380850 | 49380994 |
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Enhancer Sequence | TGTCATCAGG ACTGTGCTTG ATGCGCCACC TCTCACCACC TCTGATCTTC AGGTGCCAGG 60 GCGCTGGATA CACGTTGGCC TGAGCAAGTG AGGGAAAGAC TAGTCCTGAA ATATCCTGGG 120 GGGAGTGGAA AAGCTGAGAA GAAAGGCAGG CTGTGCACAG TCCCCAGGGG GTCAGCAAGC 180 CAGCACCACA CACACTCTGC CACACGCACC CTGGAAAAAC CCTGTCAGTG GGGCTGCAAA 240 TACCCTAGGG TCCAGCCTCC CCCAAAGCCT CCCCCCTCGC CCCAGGCTGG CTCAGTCCTC 300 CTCTCCAGCG CAGAGGGAGA AAAATAACAA AACGAGGAGA AAATAAGCTG TTTGGCTGTG 360 GTGTGAGCAG GAATATCCAT GCAGGGCTGC CCACCACTCA CCCTTACTCA CTCTTTCCAC 420 ACCCAGCCGG GGCGCCCAGC ATGAGACAGA CCACCCCCCT GCCCCCTCCC CCGTCTGGTC 480 TAAAAGCAGA CGCTGGTGAG CGAGCAGCAG GTTATAAATA TGCCCAGGGA ACTGCCGCCA 540 ACTCGCTCCC TTGTCATCCC CTGGGAGGGG CAGGGTGGGG TGGCTCCCAG GGAGGAGCCA 600 GGGCTGCCCT GTTCCCTGAG GCCCAGGAGG AAGTGGGGCT TCCTAGAGGC TACCATATTT 660 TCCCCCCTTT TCAAGGTGAA GGAACCACTG CCACTCCATT TTCCCTGAAC ATTTGCTCAT 720 CTCTTCAGAT ATGTGGTCCC TACCCTCCCT GGGCCCTGGC TGGAGGCTCG GAATGAAAGG 780 GCCCAAAGTA CTCTGTGTCA TGGCACAGCC CGCTGCTACT TCTCTTCTTC ACATGCATTT 840 GCTCTCAGCA AAACAGAAGT TCATTCATTC ATTCAACAAG CATTAACTGA AAGCCAGCTG 900 AATGCCAGAC CCTGTGCACA GGCCCACCTG TGTGCACAGT GTCTGCACAC ACAGGTGCAA 960 GCACACACAG CTGCCCCTAC TCCATGTGCT CACATCACCT CCAGCCCCCA CTAAGGACTT 1020 CCTGGCTTCA ACCTGCCAGC CTCATCAGGA AAGCAAAGCT TCAAGCTCCT GGTTGTGCCT 1080 CAGAGTAGGT TAGGGGGCAT GGGGTAGGGG GTGGCTGAGA ACAGGACCCC AAACACTTCT 1140 GCTTCCACTA CTTCCCCTGT AAATGAGGGG GTCCTTTCTC TCCTTCCTGC CCAATCATCC 1200 TCCCTAAGTA GGTGCCATGT GACGAAGAAA GAGCCATTCT TGGGATGCTG AGGGTACCTG 1260 TCCAGGCCAC CAGAGCCTCC CACCTCCCAG CAACTTGCCA ACTAGGTGCC AAGCTGGGGC 1320 AAGAGGGGGC ACTTCCACCC TGTGAAGCTC CCAGCTCTCC TCCCCCAGGG CTGAACCCCT 1380 CCCTTTTCCC TCCTCCCTAT TAATCCTCGG AAGTTAAGGG GCCGTCCCTG GCGGCCCCTC 1440 AGCCCTATCG TGGCCCCTCA CCCTCCTCGG CTGGCGTCTA ATTAACTCCT CCTGCCCCTG 1500 GTTTTGTATG CCCCCCTTAC CCCACCTTGT CGGCCCCGCC CCTCTGCTCG GCCAGCTCCC 1560 CCCCACGGAC ATTCCAGCCA GGCCGGGCCA GTGTGCCAGG GCAACCAGGG CCGGACCGAG 1620 GCCTAATCCT CCCGCCGCCT GGCCCGGCTG GGGGAGCCCC ACTCACCTCC CCACTCTCTG 1680 GGGGCTGCCC GGCTCTGCTG TGGCGGAGAC ACACAATCGG GACAAAGGCA CAGCCCCCAG 1740 GGGGCTAACT CAGCCTTCAC GCCCAGGTTG TGCGGCATTT GGGGAGTTTA ATGAATTGTC 1800 CATCACGCCT TTCAGGGCCC GCCCGTCAGC CTGGATTAAT CTTCGGAGCC CTGGTGGGGT 1860 AGGAGACACT AAGCCTGTAT TTATTACTCT CCCATTGTCA CTAATTGAGG TAATTATCTG 1920 TGACTCTGGC CTGGCCAACA ATGAGGCATT CACTCCTGGG ACCTCGATGG GCCTGGCTCC 1980 CACTCTCAGC ACCAGCCCTC CCTCCCCTCC TCTTCCAAAC CCGCCAAGGA CTACGATGGG 2040 CCCTGGAGCA TGTTGGGAAA GTGGACAGCG TCCCACAATG CCTCACCTCC CCACCGGCGT 2100 CTCCCATAGC CATCACTACA GAGCTGTCTC CTGGTCCCCC CAGAGAAGGT GAGAAAAGAA 2160 GGCAGCCTCT GCCAGGGGAT GGATTTGGCT GGCAGAGCCC TCAGGCCAGA GAGGGACCTG 2220 TTTCTGAGGA CTTTGGTTTT CTGGACTCTC CAACTCCTCA TCTCCAGATG CATGACACCA 2280 GGGTCTCACA AGGTGCTTTT GCAGATCCAT CCTCATGTCC CTATAGCCTC TAGGGTGTTA 2340 AGAGGCTCTA GCCTGTACCA GGCCTACTCT GGGGAGGTCC CTAAACCTAC CAGTGCTGGC 2400 AGAGTGGCTG TGGATGTGAT GGGAGATGTT AAGAGAGACA GCAGGAAAGG TTCTGTCAGG 2460 GGAAGAGCAA AAGGAGCCAA GTCAAGAAGG AGCAGTCAAG AGTCACAGCA TTCCCGGGGG 2520 TCACACTAAT GTGGCCATGC AGCAACTTCA GGGAGAAACT TGGATTTGGA 2570
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