Tag | Content |
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EnhancerAtlas ID | HS095-12540 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr17:37229690-37231140 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
YY1 | MA0095.2 | chr17:37229874-37229886 | GCTGCCATCTTG | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH17I039074 | chr17 | 37230261 | 37230390 |
| Enhancer Sequence | ACTTGATTTG AATCAACTTG TTGCAAATCT AGACCATTGA AGATCAATTA TGGCTCAGTC 60 TGCACCTACC ACTGGTAGAC AAAAGGACAC AGTGCCGCCC ACTGCCAGTC CCTCCCAGAG 120 TGACTGAAGG TGGCCACACT GTGCCCACGC AGCCTCTCTC CCACTCACCA AGGGCTGGTT 180 CCCAGCTGCC ATCTTGCTGG GGCTCCATGT AATGCACATT GGCTCCTGAG TTAGTGGATC 240 ACATGAGAAC TCACACAGGA AGAAATGCAT GCAATGTTGA TCAAATGAGT GGTCATTTTC 300 TGTTGTTAGT TGTCACTTCT TGTGGCTATC AAGGTGTTCT GTTCTGTTGC TTATAAGATA 360 AGCCCTTCTG CACACAGTTG TTCTGGGTGA GTGCCTGTCT CTCTTTGCAA TCAAATGCAT 420 GGGCTTTGTG ACAGCTACTT GCCACTCAGA GGTCATCTGG TTCATTTAAG TGAGTAGCGT 480 TTGACTGCAA GTGAACGGCT CTTAAATCCA GGCCCCATGT CTCCCACTCC TCCTGCCCTG 540 CTGCTTTCTA CTTCTGCCTG CCCAGGCAGG CCCCTCTGGC TGGAGTGCTG GGTCCCTTCA 600 TTCAATCTCC CTGTTAGAGC CTGTACCCTC ATAGAATGTA TGGGAAAGAC TCTATCCCAC 660 ACCTGCCTCT GCAAGTCTCC CTGTGTGGGC TGTAACCACA CAGGCAGGAG AGTGACTCAA 720 ACTCTCCTGC CAAGATGCCT TGCAAGTTGG GCATGTGGGG GGAAGTCATC ATTAAAAATG 780 TTTTTTCTTA TAAACCAGGC ACAATGGCAT GTACCTGCAG CACTTAGTAG GTTGAGGTGG 840 GAGGATCCTT GAGCCCAGGA GTTCAAGTCC AGCCTAGGTA ACATAGCAAG ATCCTGTTCC 900 ACCCTCCAAA AAGTTTTTTC TCTTATAGAT GTAACTTCAG AATCTTTGCC ACCTCTTCCA 960 GGACTGGAAG GACATAGAGC CCTAACTGTC TTCACTTTTT ACTCTAATGA ATGTTTTCTG 1020 TTGGGAACCA CTACACAAAA CATGGAAATG AGACCCATTC CTTAGCTGGC AGGGGATGCA 1080 CACAGATAAT AAAACTGGCA AACAGAACTC GCTACCTCTG TAGGACAGAG GACCTACATG 1140 GTGGGCTGTA GGACAGCCCA GGGGGCTCAG TAATAACAAG TCAGGATTTA GGCTTGGCCC 1200 CCAAGTGCTG TGCCCTGGGC TCCCCACGCC ACCACAGACC CCCTTCTAGC CTCTGACACT 1260 GTGCCTCCAC CAGACACTGT CTGGCTAAAC CCTCTGGGTG GGGCAGGGTA TGTTTGCAGC 1320 ACCCCTCCCC GCCCTGGCCC AGTGCTGGGC TCAGAACATG CCCTCAGTAA GCCTAGGGGG 1380 TTAACTGGCA GTAACTAATC AGGGACTACC TCCTTGTAGG AGGAGCTTTC TTTGACTGGA 1440 AGGTTAACCC 1450
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