Tag | Content |
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EnhancerAtlas ID | HS118-08105 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr17:44019070-44021300 |
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) |
EWSR1-FLI1 | MA0149.1 | chr17:44019071-44019089 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019075-44019093 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019079-44019097 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019083-44019101 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019087-44019105 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019091-44019109 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019095-44019113 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019099-44019117 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019103-44019121 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr17:44019107-44019125 | CCTTCCTTCCTTCCTGGT | - | 6.47 | INSM1 | MA0155.1 | chr17:44020358-44020370 | TGTCTGGGGGCA | + | 6.44 | ZNF263 | MA0528.1 | chr17:44020918-44020939 | TTTTCTTCCTAATCCTCCTCT | - | 6.39 | ZNF263 | MA0528.1 | chr17:44019071-44019092 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr17:44019075-44019096 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr17:44019079-44019100 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr17:44019083-44019104 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr17:44019087-44019108 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr17:44019091-44019112 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr17:44019095-44019116 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr17:44019099-44019120 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_03683 | chr17:44016721-44019722 | Brain_Angular_Gyrus | SE_03683 | chr17:44019858-44022888 | Brain_Angular_Gyrus | SE_05693 | chr17:44016402-44028022 | Brain_Cingulate_Gyrus | SE_07407 | chr17:44016244-44028031 | Brain_Hippocampus_Middle_150 | SE_68134 | chr17:43999844-44033224 | TC32 | SE_68411 | chr17:43970687-44036061 | TC71 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 44019661 | 44020036 | chr17 | 44020258 | 44020408 | chr17 | 44019596 | 44020069 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I045941 | chr17 | 44019181 | 44020092 |
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Enhancer Sequence | GCCTTCCTTC CTTCCTTCCT TCCTTCCTTC CTTCCTTCCT TCCTTCCTTC CTGGTATGTG 60 ACTAATTTCT GTTTCAGGAC ATAAATGTTG TCCAGGCTGT TCTTTGGTCT TTCTGTTGGA 120 TAATGGACAT TTGGCATTGA GAGAGGCTGC TTTTTCTGAA ATCATGTTCT TGGGGCCCAG 180 AACCTAGGTG TGTGCTTCTG ACTTTGTTTT CTTCCTGATC CAAATTCTGA TATGTCCATT 240 TAAATTGATC TAGACCCACA GGGCACTGTG GGACAGATCC TCAGTGGAAC ATGACTCTGT 300 AACGAGAGCA TTTTGTTTTG TCAAAATGAG AACATATTAT TGCCTTTCAT CTGATTGTAA 360 ACATAATACA TGTTTATAAA ACAGTATAAT GAGACAAAAA TGTAGACACT AATAAGGGAA 420 AATCTCCCTA ATTGTATTTC TCTTCACAGA GAAAGCCCCT GTTGGGCATA TATACTCTAG 480 TTTGTTTATT TGTTTGACTA CACATATATG TATTCTTTTC TTATGTATAA AAATTCTGAA 540 CATGCACATT TCTGCAACTA CTGTTTTCAC TTGATGATGC ATGGACCTCT CTAGAGTGTA 600 CGTTTCTTCT TCCTTACAAA GCAGTTGGCT TCGCCCAGGG TGCACCAGGA CACGGTTTTG 660 GCTCTGTCCC CAGGGTGTCA CGGGACCAGG GGATGATCTC ACAGGGTCTG CCATCTGCCC 720 TGCCTGGCCG GAGGCTGCAT CGAGAGGGCC AAGGGGCACC ACGTGTCGTG GGTACTGTCA 780 AACAAGAGCC TTCAGAGCCT TCCACAGTCT TTCTTTTGCT TCCCAGCATT GCTTCCCCGC 840 TGGTGGACTC TGAATCTAGA ACTAGCTCCA GGCGCCTCTC CAAATTCAGA CGGGAGCTGG 900 GGCACTATTA TAATGCAAAT CTAGGCAAAG CCCTCCCAAT ACCAGGATCC AGAATGGGGT 960 GGGGCCCTTT GCCCTGAAAA GCTGTTTAGT TTGAAAATAC AAACAGGAGA CAGAAAAGTT 1020 TGGCTAAATT AATGGATAAA GTTTTAACGA TGGTAACCAT AGTAGGGTTC ATCGACAGCC 1080 AGCGATGGTT CTGAACACTT GACATGTATT AACTCACCTA ATCCCCACAT TTTACAGACA 1140 ATGCAAAGGA GGCTCTGGGA GGTTGAGTGA CTTGCCCCAA AGTCGCACAG CTCCTAAGTG 1200 AAGGATTCGG AGTGGACTCC AGGCAGCCTG GTCTGACTCC CTGCACTGCG CTGTGCTTAT 1260 CTCTGGCCCC AATGCCGCCA TGCAGAAGTG TCTGGGGGCA CTTTGTCTCT GTCAGACAGA 1320 ATTCGGAGAT GTGTATGCTT GCCCTGGTAT GGCACTTCTC TTTTTTTGAG ACAGAATCTC 1380 ACTCTGTCAC CCTGGCTGGA GTGCAGTGGC ATGATCTCAG CTCACTGCAA CCTCCGCCTC 1440 CCAGGTTCAA GCAATTCTTG TGCCTCAGCC TCCCAAGTAG CTGGGATTAT AGATGTGCAC 1500 CATCGTGCCT AGCTAAATTT TTGTACTTTT AGTAAAGATG TTGTTTTGCT GTGTTGGCCA 1560 AGCTGATCTC GAACTTTTGG CCTCAAGTGA TCTGCCTACC TCAGCCTCCC AAAGTGCTGG 1620 GATTACAGGC ATGAGCCACC ATGCCTGGCA GTGTGGCACT TCTTACGTGT GTTCAGCGGA 1680 CACTGTTTAT CTTCTGTCCC TCCAAGACGG TGCTGAGCTC AGGTCGTTCA TTACTGGCAG 1740 ACAACTGCTG ATTTCCAACA GAATTGCCAT CCTCTTCTCC CCTGCGACTT TCAGAGTGTG 1800 ACCTCAGACT CAAAAATTAG AAGTGAAAAC ATCTTAAAAA CTATCACCTT TTCTTCCTAA 1860 TCCTCCTCTC CCCTCCCTGT CTTCCTTGTT GTCCCCATCT AATGAACTAT CATGGCAAAA 1920 AGAGCCCATT TCTGGTCATT TTCTGTGGCC TTTCAAACTC CCACCTACCC CACTGCTCCT 1980 GGGTGCATTA CCCGAAAGCT GAGACTTCAG TGCAGAAAGT GCCAGGCCCT CTGTCCCCCC 2040 AGATCGCCTT CCTTGTCTTC CCTGTGCTTG CCTGTCACAT TGTGTGGGTT CCAGCGCTGG 2100 AAGGAATGAG GAACAGATTC TCTGGTTCTC CTTTTGAAGT TTACCTTCGC TCCACCACTT 2160 CTGAGACCTT CCCGGAAGTT GCCCCTTGTT TCTCTCCTCT CCAGGGCTGC CCCAGAGCTG 2220 CCTCTCACCT 2230
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