Tag | Content |
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EnhancerAtlas ID | HS116-26765 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr5:1127330-1130170 |
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) |
HSF1 | MA0486.2 | chr5:1128622-1128635 | GAAGGTTCTAGAA | - | 7.12 | KLF14 | MA0740.1 | chr5:1128251-1128265 | GAGTGGGCGTGGCT | - | 6.51 | NR2C2 | MA0504.1 | chr5:1130056-1130071 | GAGGGTCAGGGGTCA | + | 6.47 | SP1 | MA0079.4 | chr5:1128252-1128267 | AGTGGGCGTGGCTGG | - | 6.32 | SP3 | MA0746.2 | chr5:1128252-1128265 | AGTGGGCGTGGCT | - | 6.54 | SP4 | MA0685.1 | chr5:1128250-1128267 | GGAGTGGGCGTGGCTGG | - | 6.73 | SP8 | MA0747.1 | chr5:1128252-1128264 | AGTGGGCGTGGC | - | 7.22 | SPI1 | MA0080.4 | chr5:1130129-1130143 | TGAAAGAGGAAGTT | + | 6.03 | SRF | MA0083.3 | chr5:1127433-1127449 | TGTCCTTATATGGACA | + | 6.55 | SRF | MA0083.3 | chr5:1127433-1127449 | TGTCCTTATATGGACA | - | 7.36 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_23448 | chr5:1127976-1132214 | Colon_Crypt_1 | SE_23989 | chr5:1128079-1132174 | Colon_Crypt_2 | SE_24840 | chr5:1128000-1128624 | Colon_Crypt_3 | SE_24840 | chr5:1128652-1132261 | Colon_Crypt_3 | SE_28283 | chr5:1129844-1132139 | Fetal_Intestine | SE_29290 | chr5:1129882-1132174 | Fetal_Intestine_Large | SE_31577 | chr5:1127256-1132504 | Gastric | SE_40750 | chr5:1126628-1130046 | Left_Ventricle | SE_41639 | chr5:1127343-1127787 | LNCaP | SE_41639 | chr5:1127884-1132182 | LNCaP | SE_42534 | chr5:1127296-1132332 | Lung | SE_47514 | chr5:1128007-1131783 | Pancreas | SE_48976 | chr5:1127774-1129305 | Right_Atrium | SE_49487 | chr5:1128081-1129127 | Right_Ventricle | SE_50482 | chr5:1127887-1132021 | Sigmoid_Colon | SE_52622 | chr5:1127966-1132104 | Small_Intestine | SE_53895 | chr5:1127979-1128693 | Spleen | SE_57916 | chr5:1128138-1128944 | VACO_9m | SE_61441 | chr5:1092795-1176993 | Toledo | SE_65274 | chr5:1127036-1132318 | Pancreatic_islets |
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| Number: 2 | ID | Chromosome | Start | End |
GH05I001128 | chr5 | 1127344 | 1127787 | GH05I001127 | chr5 | 1127966 | 1132045 |
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Enhancer Sequence | TGTTGACCAG GATAGTCTCG ATCTCTTGAC TTCGTGATCC ACCTGCCTTG GCCTCCCAAA 60 GTGCTGGGAT TACAGGCGTG AGCCACCACG CCTGGCCGAC TGATGTCCTT ATATGGACAG 120 CTTTGAGGCC ACAGAGGAGA GGCAAAAGGC AAGGGCCACA GAGATGGAGG CAGAGGCTGA 180 GGCGATGGGG CCACAGACCC AGGGATGCCT GGAGCCGCAG AAGTTGGAAG GGGCAGGAAG 240 GAGCCTCTTT TAGAGCCTCC GGAGGGCGTG CAGCCCTGCC CACACCTGGA CTTCAGATTT 300 CCTTTCTCCA CCACTGAGAA GGCAGATCTG TGAAGCCACA GTGTGTGGTG ATCACAGCAG 360 TCCGAGGAAA CTGATGGATA TACAAATACC ACAGATAACT CTGTGATAAC GATCTTGTAA 420 ATGGAGATAA AATAGACACA TTCTCCAAAA TCCATACAAA AAGAAACAGA AGCTCTGAAT 480 AGTACTATGT CTCATGAAGA AATTAAATCC TTGATTTAAC TTTGCCCCCC TCCTGCACAT 540 AAAACCTTCA GGGCCACACA GACTCACTGG TAAACTTTTC CAAACACTGA AGGAAGAAAT 600 AATACCAGTT ACATTGAAGT CTTTCAGAGA ATTTTAAAAA AGAAGTAATT TTGCACATCT 660 CCTGTTATCA AATTAGCACT TGTCATCAAG GAAGGGAAGA TAAAGCACGA GGAGATGCCC 720 ACACCCCAGG AAAGTGTCCC AAGAGTGGCT CAGATTCTCC AGGGCTGCGA CGTCCTGGTT 780 TTCATCTGGG GGTGGTGACA GGCGCGTGAT CTCTGGTTAT TCCAGAAGCA GTGAATGTAG 840 GATGTGTGTC ATTTAGCTTC TCACGCCATG CACTGGGGCA AGTTCACTGA GGAAACAGAT 900 CTCATCCTTA AGGCAGGCTG GGAGTGGGCG TGGCTGGGAG GTGGGTGCCT GAGGAACACT 960 CTCGCCCCTT CCCCTGCACC TGTGGTCTCA ACCTGGCGGG AAGTCCGCTC CAGCTCCTGT 1020 GGGACCAGGG TTGCTGGATC CAAGTTGCCA GGTAAACTCC CGCTGATCTG CAGCACAAGA 1080 GCCAAATCCC AGGACGAGCT CTCACGGAGC AGTCAGGCCC AGTGGAAACT GGTGGCCTCG 1140 CTCCAGGAAA TGAAGCCAGA CTCAGACAAA CAAAAGCCAC CAGCAATGCA TGGAGGCAGG 1200 ATGGGACATC TCACGCGGAC CCAGTGACCC TGGAGCATGC CTGGGTACAG ATGGAGCCCC 1260 CAACAGGGGT TTCCTTCCTC ATGTGGTTGA TGGAAGGTTC TAGAATTCAT CTTCTCATAG 1320 GGAGGAAAAG TGCTGCCCAG CCCCCAACAC TCTGAGACCT CTGGGGCTCA GTAAATATTT 1380 GATAAACAAC AGGCTCAGCA GGTGCGGTGG CTAGTGAGAC TGGTACAGAC CAGGTGGCCC 1440 ATGGGTATTG GGTCTGCCCT GTGACCACCA GTCCTGACAG GCTGCAGCGG AGCATGTGTG 1500 CACGTGTGTG CATGTATGTG TGCGTGTGTG TGTGCATGCG TGCACACCAA TGGGAGTGGC 1560 CCCAAGTGCC TGCCTGGTCT CTACACGGCT TCCAGCCTTT TCCTAGAATG GATCACATGT 1620 TTGCATACAC ACATATGTGC ACACACATGC AGAAACCAGA CCCACTCCCA CCATCCACCC 1680 ACACAAGCTG GACCCTCAGT CACGCGGCTC CCTGCCACGT GCTCCATCCC CATGTGCGTC 1740 CAACACACCT GCCAGCTCTG CTTTCAGCTT TCCCTGATGG CCAAGCATAC CCCGCTGCCC 1800 CTGCAAGGCT TGGGAGCACT CCTGGGATCC CCTGCAAGGC TTGGGAGCAC CCCTGGGATC 1860 CCAAGTCTGA TGGCCTCTAG AAGTCCCTCT CCTCAAACCT CGGTCACAGC TGCTGCCTAG 1920 GGCCTGCCAG GCCAGGGGGA CAGCCACGTC TCTCCTAGAC ACACGAGGAC ACCCCTCCAA 1980 GAGGCCTCCC TCAGCCAGCC GCCACTGCTG CCGGCCCCTC TGTGCATCCC CAAGGGCTGA 2040 GCTGTTGCAG GGTACAACGC CTCCTGGCTC CAAGTGAAAG TCGGAGGTGG GCAGGACGTT 2100 CAGGTAACAC CCCCACCTCC GAAGTCCAGT CTCACAGAGC CTTAGCAGCC ACCCAAGGCA 2160 AGGAGGTGGC CATGGGCCAC CAGGAGTGTC CCGAGCATCC CAGGCCCACA AGGGCCAGAG 2220 AAAGTTCCGG GCTTCCCCTA GCGTAAGGGA CAGAACCAGG CGCCCTCCCC TCCTGGCCCC 2280 CTCAGCTTTC CTGTGACGCC CAGGACCAGG ACCAGGACCA GGGAAACCAC AGCGTCCCAG 2340 GCGACAGGGT GGAGGGCGGC TCCAGGAGCC CAGCTGGGGC ATCGGCCAAC CCCCGAGAGA 2400 CACACTTGCT CAGGCATCCC TGGCAAGGTT TCCAAAGCCC TCACGCGGAT GAACACGGGA 2460 ACACCTGGGG CACCCACTGT TTCACGGAAA AAGTCACAGG GGTCACCCTG ATGGGATGTA 2520 ATTTCTGGAT ATGATTAAAC AGGAAGAAAA GATCCCGGCT GAGATTACCG TTCAGAAGCA 2580 CCTTGGAGCC GGGCTCTCGA CACTGCTGAC CCGAAACCTG GTGATTCAAG AGGAAAAGAA 2640 CGCCCTGCTG CCGTCAGAGC TGGAAACTGC ACAGCCCATT GTGTCCTGGG CGTGAAGCCA 2700 TCACCTGACT CCCAGGTGAG GAGCCAGAGG GTCAGGGGTC AGAGCTCAAG GGACGCCCTG 2760 GCCAGCTGGG GCAGTCAAAG CTACCTCTGC TTCTTCCCCT GAAAGAGGAA GTTTAGATAC 2820 CCAAGAAGTT TTGATATCTC 2840
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