Tag | Content |
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EnhancerAtlas ID | HS048-33074 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:161125180-161126890 |
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) |
ZNF263 | MA0528.1 | chr6:161125844-161125865 | TCCACCTCCCTGTCCTGCCCC | - | 6 |
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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 |
GH06I160703 | chr6 | 161124781 | 161126782 |
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Enhancer Sequence | TTTGTTTGAT GTTTCCTTGC CAGCAAATAA GCCCTATCAA ATCCTATTGC CATATGAGTC 60 CTAGAGGTGA ATAAGAGAAG AAAAAATGGG GGAAAATTAT TTCAAACTGA AAAGAGAAAA 120 GTTTGATTCT GTTTTGGGAT ATTTCCTAGG GACATGAGCT GGGGAGGGGA TCTCAGCAGC 180 GATGCGCTAT GAAGCATAGT AACATAACAC AGAGAACTTA ATTGAAGGGG GAAATAAATG 240 GAAGTTTTCT TTTTTTGAAT ATCAGTTGTA GCCTGCTCTG CTATACTTCA AAAAAACTCT 300 TCAGAAAGTT TAACTGAACT CACTGTAGGA CACACTTTGT GGATTTATTG TGTGTTTTGA 360 AGTCACACTG TGAGCTATAT AGAATTAACC AAAACACAAC TCTTCTTGAA AATGAGAGTT 420 CAAGTTGGCA GAAAGTGCGG GGTAAAGACA TGGATATGGG CCTAAAGCAT CTATTTCTTT 480 GTGATCTTTT GATATATCTC TCAAGTGCTT TTTAGTGGAT TAGCTTTAGA ATGCATCAGC 540 CAACTCCTGC TCAATAATCC ATTTTTCCAG CCCGGAATGT CTTAAATTGA GGAAGGACAA 600 AGTCCCAGAG GTGGGGAGCA GGGGGACTTT GGCCGAGGAC TTTGCATGAA TCGATGAGCA 660 TGCATCCACC TCCCTGTCCT GCCCCTTGTG CTCTGTGTAC CCTCAGGAGG TCAGGACAGG 720 CCTTTCTGAG AATGAAAATC TGTTCATTTG CTTTCCTACT GGATACTTGT CATCAGCATA 780 CAAACCAATG CGCTCTGCAG TGTGTCATCT TTCAGAACCT CCCCTGACCG CATGTTCCCT 840 GGAGGGCTCG CTGTCTTCAG AGCCAGGCTT GTCTCCTGCT GCAGCCTCCA CTGCTCTCCT 900 AGTCACTCTG TAACCCACCC CCTCTGCCTG CGGCCCCCAC CACGCCCCTC AAAGTGGTCA 960 AGGTTGTCCT GTTGTCTAAT TCCATGGAGC TTGCCTGTCT TCATTTTATT AGCCTCTTTT 1020 GGCCTCTCAC CCTTGTGCAA ATCACTAGCA TTCTGTGCCA AGGACGGAGC TGGCATCTCC 1080 AGGCTTGGAA TAGAGCTACC AAAGCTCAGC CAGATGTCTG GAAGAGCCTC AGGACAAGGG 1140 GACACCCTGT AGCCTTGTGG TGGGAGCACA GCTGAGGCCC CCTTGGCCAC CCTCTGCCAC 1200 GACCAGGCAG AAAGCAGCTT TCGGACAGAT TCGTTGTCTC AGATTTGATC TCAAAGAAAA 1260 ACCAAGACCA GTATTTGTCC CAGGTCCTGC TTTTTTACAA TTTCCTCCGA AATCCAGATA 1320 CCTGTCAACA CCTTGGAAAA ACTGACTTCT CCCCAATTAG TAGTGTTGTG TGACTGTCAT 1380 AAGCCCAGTA CAAAAATGGC CTTCTTTGTT GGGGAGCTTC TTACCCTCCA GTGTTTTGCC 1440 CAATTTTTGT CCAAGGTGGC AACATAATTT AGTTCAGTTC TTGTTTATTT CCACCATCAT 1500 CTATGCACCA AAATTTATGT TTCTCAAGGA GGGACCATTC AGAGGATGCT TCCCACCGGT 1560 TCAAGTGACA GTGCCAGAAC CAAAGCGCAT ATTGTAGGAA ATCAAACAAT GGCCTCCAAG 1620 TTCCATTTCT ACCCAGGGAT GAACAAATCA ACATCAATCT TGGTAACACA ACTGCCACTG 1680 ATGGTGCCTT ACTCTTCTCT CATGACATGG 1710
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