Tag | Content |
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EnhancerAtlas ID | HS197-08552 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr17:1008970-1012170 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:1011959-1011978 | TGGCCTGGAGGGGGCGGCC | + | 6.03 | Myod1 | MA0499.1 | chr17:1012029-1012042 | GGGAACAGCTGCC | - | 6.24 | RFX5 | MA0510.2 | chr17:1011845-1011861 | GGTTGCCGTGGAAACG | + | 6.04 | RFX5 | MA0510.2 | chr17:1011845-1011861 | GGTTGCCGTGGAAACG | - | 6.08 | ZNF263 | MA0528.1 | chr17:1008996-1009017 | GGGGGAGGCTGAGGTGGGAGG | + | 6.15 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_01841 | chr17:1008630-1009856 | Aorta | SE_01841 | chr17:1009947-1016747 | Aorta | SE_09651 | chr17:1010674-1016704 | CD14 | SE_23220 | chr17:1009979-1016517 | Colon_Crypt_1 | SE_23794 | chr17:1010011-1015748 | Colon_Crypt_2 | SE_24832 | chr17:1009980-1016127 | Colon_Crypt_3 | SE_26634 | chr17:1009963-1015451 | Esophagus | SE_28034 | chr17:1010292-1016009 | Fetal_Intestine | SE_29195 | chr17:1010053-1015863 | Fetal_Intestine_Large | SE_31579 | chr17:1009291-1009789 | Gastric | SE_31579 | chr17:1010605-1015798 | Gastric | SE_40640 | chr17:1005961-1009914 | Left_Ventricle | SE_40640 | chr17:1009930-1016538 | Left_Ventricle | SE_42145 | chr17:1006133-1009883 | Lung | SE_42145 | chr17:1009966-1016536 | Lung | SE_49097 | chr17:1009137-1009888 | Right_Atrium | SE_49097 | chr17:1009982-1015834 | Right_Atrium | SE_49495 | chr17:1010034-1015614 | Right_Ventricle | SE_50313 | chr17:1009951-1016659 | Sigmoid_Colon | SE_52631 | chr17:1009961-1015957 | Small_Intestine | SE_54272 | chr17:1011198-1015848 | Spleen | SE_57155 | chr17:1010616-1015728 | VACO_400 | SE_57710 | chr17:1011111-1013762 | VACO_503 | SE_65254 | chr17:1009753-1017402 | 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: 2 | ID | Chromosome | Start | End |
GH17I001105 | chr17 | 1009181 | 1009330 | GH17I001107 | chr17 | 1009513 | 1009734 |
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Enhancer Sequence | AACGTGGTGG CATGTGCCTG TAGTGAGGGG GAGGCTGAGG TGGGAGGACT GATTGAGTCT 60 GGGAGGTGGA GGCCACAGAG AGCCATGATT GTGCCATCGC ACTCCAGCCT GGGTGACAGA 120 GTGAGACTCT GTCTCAAAAG AAAAAAAAAA ATGGCACAGA ATGATACCTA AAGGGTTAAT 180 CTGCATTACA AAAGGGTTTT TATTCCTGAC AAATAAGTTC CTTAAAATAG CACCTTCTAC 240 AACGCCCCCG TCACAACCCT ACCTATCTTT AAATAGAATG GCATGAAACA TTTTTGGCAA 300 GTGTAAGCCA TTTTACAAAT GCAACATGAC GCTGCTATCA GTATTTTATT TGCATTACCA 360 GTTTTACAGA TCAATAACTC TTCAAAGGTA AGTCTGGGCT GAGATATGCA GCAAACTCCA 420 GCTATAGCTT TGGAGAAAAC TGCAGCCAAC TTTACCTCTG CCCCCCAGGA AGATGAAGCG 480 TCTTGGAAAT GACACTGGAA ACAGGATTGA TTTATGGGCC TGGCACTTGG GCACATGCTC 540 ACAACGCAAC TGCTGCTTAA GGTAAGTACC CCTAAAGTAA AGTAATAGCA AAGAGAATTG 600 CCTTGGATTC CTACTAGCTG CCAGGGAAGG GTGTGCCAAG AACCTCTGCA GCCCAGGACA 660 GGAGTGTATC ATCCAGAAAT GACCCTTGGC CTGCACACAC ACACACATGC ACGCATCCAG 720 GCCATCCCCA ACTCCACTAG AAGTGGTCCC TTCTCCCCTG AATTTGGTGC CCTTTTATCA 780 GTACTCTTCT CACAGTCTTT TTTTTTTTTT TTTTTTTGAG ACTGAGTCTC ACCCTGTCGC 840 CCAGGCTGGA ATGCAGTGGC ATGATCTTGG CTCGCTGCAA CCTCTGCCTC CCAGGTTCAA 900 GCGATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGGATTAC AGACGCCCAC CACTACGCCC 960 GGCTAATTTT TGTATTTTTA GTAGAGATGT GGTTTCACTA TATTGGTCAG GCTGATCTCG 1020 AACTCCTGAC CTCAGGTGAT CCGCCCACCT CAGCCTCCCA AAGTGCTGGG AATACAGGCG 1080 TGTGCCACCG CATCTGGCCC ACCCTGCCTA CTTCCGTACT CTATTCCTAC TCCCTGTACC 1140 TGCCCCTTGC TCTGAACGCC TTGTGAGGGA AGATCACGCC TTGTTCCTCT TGTCATCTCT 1200 ACAGTGCCAG GCAGGGTGCT CTGAAGAGCA CCTAACCTGA GAGTGTTTGT TGAATGAATC 1260 CAGGAGCTTT CTTCCCACCG CTCTGTGGCC ACCTGCTTGT CTTCTCCCTC TGAGGCCAAT 1320 GCCGGTAGAG GAGGGAGGAA TTCTAGAGGT GTTCAGGATG GAGCAGGGAG CCTGGAACTC 1380 CCCGGCATTC GAGAAAGGTC TCCTTCCCCC ATGCTGGCAG CAAAGTAGAG GGGAAGACAC 1440 CATCCCGGTG CTCACGGGGA CCCAGGAGGA GCAGCGTTTT CAGGTGTGAC ACGTGCTCAG 1500 GCTCTCTTGG CATCCGTGGG CCACCGCCGT ACACAGCAGG ACACCTCTGA GATGGAGCGA 1560 GGCTGGGAAC CTGGTGCACC CTTCGTGGGC CCCAGCGGGC CTCACACATT GTGCAGACTC 1620 TCACAGGCAC CAGCCCCACA CCAAGCACTG TGCAGTGTTC AGCAATGAAT ATGACATGGT 1680 CCTGGTCCTC CAGGAGAATG GGATATAATT GCGGAGGCAA ATGTCTAGAG TTCTGAGCAT 1740 CTGAGCAGAA TGAAATACGG GCTTAGCTGA GGCATACGCC GGGGTCCAGC AGAAGGGGAG 1800 GTCCAGGAGG CAGCCTCTGA GTGGGCCCAC ATCTGTGCTG GGGGCTTCCC AGAGGAGGCC 1860 CATGAGGGCC ACACACCTCC CATCCCAGCA TTGCTACTCC CAGCCTGACT CCTGGCTCAG 1920 GAGCAGACTT TCCCACCCTG TTCCTAGTGG GGAGGCTGGT CAGACCCTAA GTGCAGAGGC 1980 CTCCCTGAGC CCACGGGGAG ACGTGACTTA CCCCCACGGC CCTACGCCAG CACCAGATCA 2040 GAGAAGACAG GGTGGGGTGC CAGCCACTGC CAGCCTCCCT ACAGCTCCAC TCCCCACCCA 2100 GGCCTGCAGC CACCGCTCCA CCCATACTCA CACATCAGCC ATCTCCCGTG GTTCTGCATC 2160 TATTTTTACC TCCATTGGCT CCTCCTCAGA GCCACACTGT AGAGTGGGTG GGGCAGGACT 2220 GTGATCCCCA TCTTCTGTGA GGGGCAGGGA GGCCCAGAGA GGTTCAGGGA CAGCCTCCCG 2280 TCCCCAGCAA TGCTGGCTGC ACATGCCTTC TAGGCCCCGC CGATGGGCAC TCGGTTAGGC 2340 AGCCTCGCCT AGCAGTCTGC AAACTCCCCG AAACGCATCC TCACTGGGCC TCCCTTCTCG 2400 ACACAGAACC AGAGAGCAGC TGAGCAAAAG GCTGAGGTGG AAGCTCTGAG AGGTGTGTCC 2460 AGGAGAGAAA AAGGAAGACC GCTGTGGTGT GCCGGGCCAG ACTCACAGAG CCGGCGTGGT 2520 TCCGGGGCCG CCCCGCTCCT CAAGGGATTC TGGCCACCAC TGCCCTCCAG TTCCACCGGG 2580 AGCCAACCTC TCCTACAGGA CGGGTCACTG CTGCAGAGAA CGCCGTCAGC CCCAGAGCGG 2640 GTGGGCCAGG GCCCAGCAGA TGCTCCCTGC CTGTCCCGCC TCGGGAAGGG CACCTGCCCA 2700 CCTGGCTGCA GCCTCCAAGC CAGCTGTTCC CTCCCCCCTT CAGCTGACCC AGTGCTTTTC 2760 CTTCAAGGAA GCTCAGTGAC CTCTGGCTCT TGCCCTTTGC AAACACCCTC TTGCCTCAGC 2820 TCGGAGACAC CAAGTCCCTG TCTCCTGGCT GGGAAGAGGG TGGCCCCTCT CTTGCGGTTG 2880 CCGTGGAAAC GGGGGATTCC TGCCCACCCG CTCCAGGGAG GCGGCGAGGC TCGGGCTGAC 2940 AGGCGCGCCA GGTGACTCCT GGCACAGCCG CCGGAGCCCT GAGCTGGGCT GGCCTGGAGG 3000 GGGCGGCCAC CACTGCCCCG AGGACACCGG TCGGGGAGGC AGGCCCGCCC CTCTCCCCCG 3060 GGAACAGCTG CCGGGGCCGG GACCCTCCGC CGAGGGCTTC CACCCGGCCG CGCGCTCTGC 3120 GCCCGCATCA GCCATTTCTC CCGCGCACCT TCGGCAGCGC CGGCCCGGCC CCCCCCAGCG 3180 CCCAGGGCGT GTCACGCTCC 3200
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