Tag | Content |
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EnhancerAtlas ID | HS042-41667 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr6:168126560-168128200 | SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr6:168127538-168127549 | AAATCTCAGCA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAATTGCCT GTGGTCCTAC AAAGGAGACT CAGGACTTTG GGCCATTTGG TGGGTTCATG 60 CTCATGGCAG AGCTGCCCTT CCCCACCCTC TTTCACGTGC TGGTCAATGT AGCCCAGCTC 120 TGCTTCAGAT TGAAATGCTC ACCAGCATCA AATTTTCTCT ATCTTGGTAA ATTGTACTTT 180 GCTCTGTGTT CAGCTGGTCT CCAGGTAGGA GTGCCCTGAT AGAGAATTAG AGCCCTAAGA 240 CCACATTCTC ATTCCATGCC ACTGCTTGGG AACTGTACAA GTCTGCAAGA TAACATGGAA 300 ATGCAGCCCC TGGGTCGCAA TGCCAAGAGC CCTCTGAGAT GCTGTTTGAC GTTCCTCTTC 360 CAATCCGTTT GAAAGGACCT GTTCCGTACT GACACTGTAG GTTCCTGAGC CAGCGCGGAA 420 GGTTGCTCAG CCATTTAAAA TCTGTCTGTC TCGATAGGAA ATACAAAGAG AAAATGGAGG 480 GTGATTGGCA GAGCAAATTG GATCTTCACT TGCCAATTCT CTTCTCATTT GCAAATATGC 540 TAGTGAAAAG CCCAAAGCAG CCCTAAGCCA GTTTCATGAA TCCAGCACTC CTGCCTGACA 600 ATTAGAGGCC CTCATCTGAA AATACTAACA AAGGAGTTCA GGCTTCTCAG CTGTTCACTC 660 AGCTAGAATT TACCTTGAGT TCAAGAGAAG AAAATAAGTC CTGCTTTGGA AATGACAATT 720 TGAGAGAACG ACACCTTTCC AATTGTAACA AGACAGTGTT ATTGACCCGG TTTTTGATAT 780 TATTATTATC AAACATAATT TAAGGCTGAC CAAGAGTTCA GCTGAGGACA CGTCCTTGCT 840 AGGGTGGCTA AGTTTTCGTG TTTAGATAAT CTCTTAAAGT AATTTCTAGA ACATATTCTT 900 TAAGTAGGAT TGACTATAAA TCAACACTGA AAATGCTGAA ATAGAGTTGC GATGTGATAC 960 TAAGACCTAG ACATTCTGAA ATCTCAGCAT CTTTCCCAGC TGTGGCACCA GCAAGCCAGA 1020 CCCCAGGGGC CACCGGAATA CTGGGGAAGG GACAGTGGCA GGAGGCAGAG GAGGCTGTGG 1080 GAGGGAGATA AGGAGACAGA AATAGGTCCT CTTTCTTCCC TTTTTTGTCT CTTTCTTGCT 1140 GTCCTTTTTA AAGAAGAAAA GAAATGGAAA ACACTCACAA AGTGTTTCTC ATAAATCAGG 1200 TAGTAAAGTT CATTCACTTA TCCATAGCTC TGAGGTTCTG GAGACATGGC AGGAGCTAAC 1260 AGAGCTGATG TCTCTCAGGA CAGAATTAAA CCAGATGCAG AAGGCCAACA CAGGAGCGTT 1320 GTCCCCAATC CCAAGCTGTC CCTGCCATGA GGGCGCCCCA ACTTAGTCAT CCTTCCTCTG 1380 ACACCCACCC CCACTGCATT GGTACCTGAA GATGAAGCTC TTCAAAGAAG GTCTGGAAAA 1440 ACAGGCCTCT TGGTGTTTTC CACCCCACAC TCCAGGGTGG CTCTGGGGCC TTTCTCTGGT 1500 TTTGTTCTTC ATCTGAAACT GAAGGGCCAT AACCATGGAC TCTGGACTGC GCAATGCATG 1560 GAAACCTCAC GGTGATGGTG CCTTAACCAG CTTTGAACAT GAACTCGATG TAATACCTTT 1620 TATTCAGCTA TTAAAAATGA 1640
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