Tag | Content |
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EnhancerAtlas ID | HS116-14398 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr17:16981390-16984000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF13 | MA0657.1 | chr17:16982440-16982458 | CAGAAGTGGGCGTGTTTG | - | 6.07 | KLF14 | MA0740.1 | chr17:16982443-16982457 | AAGTGGGCGTGTTT | - | 6.05 | SP8 | MA0747.1 | chr17:16982444-16982456 | AGTGGGCGTGTT | - | 6.07 | ZNF263 | MA0528.1 | chr17:16981928-16981949 | TTCTTCCTCCTCCCCACCTCC | - | 6.04 | ZNF263 | MA0528.1 | chr17:16983563-16983584 | GGAGGAGGCAGAGGCTGGAGA | + | 6.42 | ZNF263 | MA0528.1 | chr17:16981607-16981628 | AGAGGAAGAAGTGAGGGAGGA | + | 6.61 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_03884 | chr17:16980412-16986734 | Brain_Anterior_Caudate | SE_04928 | chr17:16982213-16984039 | Brain_Cingulate_Gyrus | SE_05858 | chr17:16982337-16985585 | Brain_Hippocampus_Middle | SE_07879 | chr17:16982274-16985370 | Brain_Inferior_Temporal_Lobe | SE_23653 | chr17:16980973-16982502 | Colon_Crypt_1 | SE_23653 | chr17:16983058-16983968 | Colon_Crypt_1 | SE_23958 | chr17:16981090-16982048 | Colon_Crypt_2 | SE_23958 | chr17:16982052-16982506 | Colon_Crypt_2 | SE_23958 | chr17:16983561-16983874 | Colon_Crypt_2 | SE_27670 | chr17:16980514-16984115 | Fetal_Intestine | SE_31426 | chr17:16981072-16982899 | Gastric | SE_31426 | chr17:16982914-16985561 | Gastric | SE_41792 | chr17:16981074-16982066 | LNCaP | SE_41792 | chr17:16982613-16983933 | LNCaP | SE_42192 | chr17:16980979-16984288 | Lung | SE_47491 | chr17:16981080-16981955 | Pancreas | SE_48203 | chr17:16980429-16983971 | Psoas_Muscle | SE_48857 | chr17:16982571-16984063 | Right_Atrium | SE_52535 | chr17:16980394-16985649 | Small_Intestine | SE_65457 | chr17:16981017-16981925 | Pancreatic_islets | SE_65457 | chr17:16982981-16984041 | Pancreatic_islets |
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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 |
GH17I017077 | chr17 | 16980692 | 16984386 |
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Enhancer Sequence | GTAAGTGTTA TCCTTGCCCA CTCCCTGTCC CCAGCCTTCA CCAAGTCCCT CCATTACAGT 60 GCCCTTGCGT TGTCATGTGA GAGCACAGCA GCCATGTGCT CCTGCTTGTG TCTGTTTGGG 120 AGTGTGGAAT GTTTTGAAGA ACTTGTGGCA CCTGCTGGAG ACAGCTTTAA AAACCCAGAC 180 CTTTGGTTTG AAACATCATC TTCTGTGGTC TTGAGTGAGA GGAAGAAGTG AGGGAGGAAG 240 TCATTTCTGT TGAAGGCTAA TAGTGTGGAC TTCACTGGAG CACTCCTGGT TAGGGGAAAG 300 CAAGGGCAAA GTCCTGGATC ACGTGTGCAG GCTGTGGACC TGTGGGCGTG GGGCAGGGGC 360 TGGCCCTGGG GCTGGCACAT GTGCTCACGC ACCTAGTCCT GGGGTTGCCT GTCAATTCTG 420 CGACTGTAAT TGGTTTTGCT TGTCTCATTT GAGCTTGGCT TAGTTTTCCG AGCTGACTTC 480 AGAGGCCTCC TGGTCACAAG GTCATCGTTC TTCTGGTCAC TAAACCAGGC AGACAGGCTT 540 CTTCCTCCTC CCCACCTCCC TGGTTTTCCA GTTGCTTCCT GGGCTGGATG AGTGTTTGCT 600 GCTGTTGCCC CAGAGGCCAA ACCTGAAAAT CAACTAGGTG GAATTTCTGG CTTTTCTTTT 660 TCCACCCATT TTATCTCCTG ACTTTTTCTC TAAAGGAGAT TAGTCTCTCC TAATTAATCT 720 AAAGTAGGAC TGCATTCCAA ACTTTGTAAA GGGTTGAAGA TGCGAGATTT GATCGCCTTT 780 TCCAGTTCCA CTTGGTGGGT GAATGTTTGT GTGCCCATAT GTGCAGCATT TTAAAATTGG 840 GACTGTCCTG GAAAGCCTAG TCTCACTATG TAAAATAGGC AGCCCCTGCC TATCCTACCC 900 AGAGTTTGTT TCTTTGCTGC AGGGGCGAGA CAGACTCTGG AAGTATGAGT GGAGATAACT 960 GTCCCTAGAG GTACCTTCCA GACTGCGGCA GGGGGTGGCG GGGGTGCCTG GGATTTTTGG 1020 GTGGTCATTA CAGCTCACAT GTGCAAAGGT CAGAAGTGGG CGTGTTTGTA CTCGAGTCCT 1080 AACCTTTGTG ATGTGATATG TTTTCTACTT TTGTTTCTGG GGTGAATTAA GAGGATGGTA 1140 CCATAATCCT GTATCAACTG TCACCTCACT GGTTCCTACT TAAAAAGAAT TGTCTTCCTT 1200 TTCATTCTTT CCGGTGAGCA TATTTGTACA TCATGATTAG AGCATAGGGG GTTTTTGCTA 1260 TGGGAACGTC TGTGCTCCAG GGTAGTGTAC TGGAGGTGAG CACCGATTGT GGACTTGGCT 1320 GGAAGTAGGA GCAGGGAGAC AAAGCATTTG GACACTCCGT TCCTTTGAGG CAAGAAAGCA 1380 GACCTGGAGG ATTAGACTTC ACACTTCGTG TTCTCCTGGC TTAGCCCTTA CACAGGGAGT 1440 AGCCCTGGGG TCAGAGCTGG GCTCCTGCAG CTGTGAGGTT TATCTTGCCT CCCTGTGGCT 1500 GACTGACTGG CTGAGTCCTG CAATTGACTT AACAGTATCA GAGGAGCCTC AAGAGGTCAC 1560 TGGATTACAT TCAGGCTGGG CTGGGTCATG AACCATCCCA AAAAAACAAA GTTCCCTGCA 1620 CTGTTTCCTT GGGGACTGAT AATTTCAGTC AGGAAATCTT TCTTTAGGTC TAACTAAAGT 1680 CCAGCAAAAT CCATTATTCC CTCTGGCTCA GTTGCACAAG CACAAAGAGG GTAGCTTCTG 1740 GGGACGCCTT GGTGCTGGCA CAAGTGCAGA GCACATGCTG CCTCCCAGGC ACGGCTTCTG 1800 GATAATTGAG GCCGCTTAGC CAGGAGCACC GACACTTCAC AGTGCACTGT GGTCTCCCAG 1860 CAACCTGGAT ATGAGTTGCG TATTATTTCA TGGAGTGCTC AGGCAGAGGT GGGACTGTGC 1920 CAGGGATGTG GGGAAAGAAA GAAGTCCCAG GGAAAACTTG GACTGAGAGA GGGCATGGGG 1980 GCAGGCCCAG AGCTGGGAGT TTTGGGCCAC GGGCTGCTTT CTGGCAGATG ACCTGGGAGC 2040 TGGAGAAACT GACCCAGTGA GCCCATCAGT AAATACTGCT TTGCCCAGCC GAGGCTGTGG 2100 AGGGGTTTCC CTGTTGTATC AGGAAGGTCA CAGGGGAAGG TTGCAAGGAG GCACTTAGGG 2160 TAGAAGCCAG GTGGGAGGAG GCAGAGGCTG GAGAGATTTC TCTAGCACCC AGTGCTCTGC 2220 ATCAGGGTTT GCTCCTCAGA GCCACTCCCC AGAGTGAGCA GACAGCCTGT AGCCCAGGAG 2280 CTCCAGCTTA ACGGTCAACC GCCCTGAGCT GAGAGTCCCA CCCCAAACAG GCTGGCAGGA 2340 TCCTGAGACC TGGAGCAGGA AAACTCCATT TCAGATAGGC TTATGTGTGG GTAAACTCCA 2400 GCCAAGCTGG AAGCTTCCTT TGTGAGTGCC TGGAAATAGA CCAGTGGTCC TCAGCGTCAT 2460 GCCTCCCAGG GCCACTGGCC ATGTCTGGAG TCATCCTTGA TTGTCACACC TGGGGCAGGA 2520 ATGCTGCTGG CATCTAGTGG GTGGAGGCCA GGGATGCTAC TGAATCTCCT TCACAGAACA 2580 GCCCCCAGAA CAAGGAAGGC TCCAGCCCAA 2610
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