Tag | Content |
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EnhancerAtlas ID | HS095-12842 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr17:48057360-48059090 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf12 | MA0742.1 | chr17:48058227-48058242 | GGCCACGCCCTTTCC | + | 6.73 | Znf423 | MA0116.1 | chr17:48057535-48057550 | GGCACCCTAGGGGGC | + | 6.27 | Znf423 | MA0116.1 | chr17:48057535-48057550 | GGCACCCTAGGGGGC | - | 6.43 | Znf423 | MA0116.1 | chr17:48057536-48057551 | GCACCCTAGGGGGCA | + | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 48058093 | 48058551 | chr17 | 48057675 | 48057818 | chr17 | 48057528 | 48057889 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I049980 | chr17 | 48057741 | 48058410 |
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Enhancer Sequence | CCAGAGTGGG CTAATGTGTG TCTACCACCA CTCTCCACTC TAGTCTGGGG CTTTGTAAAG 60 GCAGACCCTG CCTCTACCAT CAGACTGAGC TCCCCTGTGC CTCAGATGGG ATGCATCCTA 120 CAGCTGGCTC TTCCCAGCCC CCCAGTTTGA TGATGCTGAG GTACTCAGCC CCACTGGCAC 180 CCTAGGGGGC ATGTCTGGCC AGCTCAGGAA GGGGAAAGGA GTCGGCCCCA AGCTTCCTCC 240 AAACATCAAG CTTTCTGATT CAGTGTCTCA CAGTGCCAGG CCTTCAGCCT CTCTGACCCA 300 AAACTGGAGA GATGACTTCA TTTCCAGGGG AGGGTGCCAC TCTCTGTGGA GGGCATGTGG 360 AAGAGATTCC TCTCAGCTCT GTATGAACCA TTCCTTTCAG AGTTTAGTTG CTTGGGGTTA 420 AGCCTGAAGA AGATCATTTT GCCGCTGCAT GAGACTTCAC TCAGGTCTGT GGCCCCCATT 480 CTCTCACCCT CCCCATCTCC AGCTGATGTA ACGTAGAGCC CACATCATGA GGTTGGAGCA 540 CCCACCTGGA TCATCCCACT TTGATCACGA GGTTCCCTGG GCATCTCCTC CACCTACAAG 600 CCCACCCCAT GATTATCTTC TCTGTCCTGG TTTGCACCTT AACCTGATCC ATTAAGACTT 660 GCACTCTTTC TTCAGACTGG GGGTTGCCAG AGAGCGCTTC ATGGGCCTCC CCTCTTGGAC 720 TGGGGACTCC TGGGCACCCT GGCTTCTTCC TCTGCCTGCT CACCCCTCCC TCAACCCTGA 780 TGCTCCCACT CTCTTTGGGG TGGAGAGGCT CAGCACATGG GGTTGGGTAG AGGCCTAAGA 840 GGGGATGGGG CCACGTGGTA CTTGCCAGGC CACGCCCTTT CCACTGCCTG CCTTGCCTGC 900 CAGAGAGCCA CAAGACCACT CCTCTCGGGC TGGACCCAGG AGCTGCTTTC TCTGTCTCTG 960 CAAGCTCGGG CCTGCTGCAA ACTCCTCCTC CCAGCCCTGG AGCCGCCGGG AATTCTTTGC 1020 TCCAACAGAT CCTGGGGGAA GCCAGACTGC AGGAGGCTCC TGACATGCCT CTACCCAGCT 1080 CCTGTCACAT TCCCCAAGCC CAGGGGGATC AGCTGGATCC ACCAATGCAG GCTTCTTCCA 1140 CCCCTTGTGA CCCAGGTCTT TGCCTTACCG CCTCAAATCC TCCTACCCAC CTTTCTAAAC 1200 CGTGAATTCT GTCTTGGGAC TCACCTCTGA CTTTGGATCC CTCCCACTCC CAGCCCCTTG 1260 GCAGCCCTAC CCGAGCAATA ATTGTTATCC CCCCAGCTCC CTTGGAATAA CATTTACCTC 1320 CTTCTCCATA CAGCCTTTAT AAAGTCTTCA TGGATTTGCA CTCTGAGATG CAGGCACTCA 1380 GTCGAGAGGC CTTGGGCAAG TCACTTCACA TCTCTGGGTC TTTATTTCTT CACCTATGCA 1440 GTAGGGCCAA TGATCAAATG ATGCCTCCAA AGGTCATGGA GACAAGGAGA GTGCACCCCT 1500 AGTAAGTTGT GAAAAATACC AGGTATGCTA GGAGATATGG TGGCTTATTC CTTCACCCTG 1560 GCTAGACCAA CTTGGTGCTG GAAGTGTCTC TCTTTCCATC CCCTAACTTC TTCTCTGACC 1620 CACCAGTTCA CCATATAATG GAGAATAGTA TAGTTCTACC CCCAGGAACA CAAAATAACA 1680 AAGAGCCAGA TTCCTGATTC AAGTCCAACT CGATGACCTT GGGCAAGTTT 1730
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