Tag | Content |
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EnhancerAtlas ID | HS180-38118 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr5:1128140-1131950 |
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 | chr5:1130320-1130333 | GAATCTTCCAGAA | - | 6.09 | HSF1 | MA0486.2 | chr5:1128622-1128635 | GAAGGTTCTAGAA | - | 7.12 | KLF14 | MA0740.1 | chr5:1128251-1128265 | GAGTGGGCGTGGCT | - | 6.51 | KLF16 | MA0741.1 | chr5:1130559-1130570 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr5:1130559-1130569 | GCCCCGCCCC | + | 6.02 | NR2C2 | MA0504.1 | chr5:1130056-1130071 | GAGGGTCAGGGGTCA | + | 6.47 | RREB1 | MA0073.1 | chr5:1130883-1130903 | GGTGGGCGGGTGGTGGGAGG | - | 6.07 | SP1 | MA0079.4 | chr5:1128252-1128267 | AGTGGGCGTGGCTGG | - | 6.32 | SP1 | MA0079.4 | chr5:1130556-1130571 | AAAGCCCCGCCCCCA | + | 6.51 | SP2 | MA0516.2 | chr5:1130555-1130572 | GAAAGCCCCGCCCCCAC | + | 6.39 | SP3 | MA0746.2 | chr5:1128252-1128265 | AGTGGGCGTGGCT | - | 6.54 | SP4 | MA0685.1 | chr5:1130556-1130573 | AAAGCCCCGCCCCCACC | + | 6.71 | 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 |
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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 | chr5:1127884-1132182 | 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_57916 | chr5:1130439-1131776 | VACO_9m | SE_61441 | chr5:1092795-1176993 | Toledo | SE_65274 | chr5:1127036-1132318 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 1130800 | 1131471 | chr5 | 1129600 | 1130521 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I001127 | chr5 | 1127966 | 1132045 |
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Enhancer Sequence | CTCTGGTTAT TCCAGAAGCA GTGAATGTAG GATGTGTGTC ATTTAGCTTC TCACGCCATG 60 CACTGGGGCA AGTTCACTGA GGAAACAGAT CTCATCCTTA AGGCAGGCTG GGAGTGGGCG 120 TGGCTGGGAG GTGGGTGCCT GAGGAACACT CTCGCCCCTT CCCCTGCACC TGTGGTCTCA 180 ACCTGGCGGG AAGTCCGCTC CAGCTCCTGT GGGACCAGGG TTGCTGGATC CAAGTTGCCA 240 GGTAAACTCC CGCTGATCTG CAGCACAAGA GCCAAATCCC AGGACGAGCT CTCACGGAGC 300 AGTCAGGCCC AGTGGAAACT GGTGGCCTCG CTCCAGGAAA TGAAGCCAGA CTCAGACAAA 360 CAAAAGCCAC CAGCAATGCA TGGAGGCAGG ATGGGACATC TCACGCGGAC CCAGTGACCC 420 TGGAGCATGC CTGGGTACAG ATGGAGCCCC CAACAGGGGT TTCCTTCCTC ATGTGGTTGA 480 TGGAAGGTTC TAGAATTCAT CTTCTCATAG GGAGGAAAAG TGCTGCCCAG CCCCCAACAC 540 TCTGAGACCT CTGGGGCTCA GTAAATATTT GATAAACAAC AGGCTCAGCA GGTGCGGTGG 600 CTAGTGAGAC TGGTACAGAC CAGGTGGCCC ATGGGTATTG GGTCTGCCCT GTGACCACCA 660 GTCCTGACAG GCTGCAGCGG AGCATGTGTG CACGTGTGTG CATGTATGTG TGCGTGTGTG 720 TGTGCATGCG TGCACACCAA TGGGAGTGGC CCCAAGTGCC TGCCTGGTCT CTACACGGCT 780 TCCAGCCTTT TCCTAGAATG GATCACATGT TTGCATACAC ACATATGTGC ACACACATGC 840 AGAAACCAGA CCCACTCCCA CCATCCACCC ACACAAGCTG GACCCTCAGT CACGCGGCTC 900 CCTGCCACGT GCTCCATCCC CATGTGCGTC CAACACACCT GCCAGCTCTG CTTTCAGCTT 960 TCCCTGATGG CCAAGCATAC CCCGCTGCCC CTGCAAGGCT TGGGAGCACT CCTGGGATCC 1020 CCTGCAAGGC TTGGGAGCAC CCCTGGGATC CCAAGTCTGA TGGCCTCTAG AAGTCCCTCT 1080 CCTCAAACCT CGGTCACAGC TGCTGCCTAG GGCCTGCCAG GCCAGGGGGA CAGCCACGTC 1140 TCTCCTAGAC ACACGAGGAC ACCCCTCCAA GAGGCCTCCC TCAGCCAGCC GCCACTGCTG 1200 CCGGCCCCTC TGTGCATCCC CAAGGGCTGA GCTGTTGCAG GGTACAACGC CTCCTGGCTC 1260 CAAGTGAAAG TCGGAGGTGG GCAGGACGTT CAGGTAACAC CCCCACCTCC GAAGTCCAGT 1320 CTCACAGAGC CTTAGCAGCC ACCCAAGGCA AGGAGGTGGC CATGGGCCAC CAGGAGTGTC 1380 CCGAGCATCC CAGGCCCACA AGGGCCAGAG AAAGTTCCGG GCTTCCCCTA GCGTAAGGGA 1440 CAGAACCAGG CGCCCTCCCC TCCTGGCCCC CTCAGCTTTC CTGTGACGCC CAGGACCAGG 1500 ACCAGGACCA GGGAAACCAC AGCGTCCCAG GCGACAGGGT GGAGGGCGGC TCCAGGAGCC 1560 CAGCTGGGGC ATCGGCCAAC CCCCGAGAGA CACACTTGCT CAGGCATCCC TGGCAAGGTT 1620 TCCAAAGCCC TCACGCGGAT GAACACGGGA ACACCTGGGG CACCCACTGT TTCACGGAAA 1680 AAGTCACAGG GGTCACCCTG ATGGGATGTA ATTTCTGGAT ATGATTAAAC AGGAAGAAAA 1740 GATCCCGGCT GAGATTACCG TTCAGAAGCA CCTTGGAGCC GGGCTCTCGA CACTGCTGAC 1800 CCGAAACCTG GTGATTCAAG AGGAAAAGAA CGCCCTGCTG CCGTCAGAGC TGGAAACTGC 1860 ACAGCCCATT GTGTCCTGGG CGTGAAGCCA TCACCTGACT CCCAGGTGAG GAGCCAGAGG 1920 GTCAGGGGTC AGAGCTCAAG GGACGCCCTG GCCAGCTGGG GCAGTCAAAG CTACCTCTGC 1980 TTCTTCCCCT GAAAGAGGAA GTTTAGATAC CCAAGAAGTT TTGATATCTC CTCCACGACT 2040 TTACTTCTGG ATGTGGTTCA GAAAAATCTG CGGAAAATCA CCCAGAATTG CACCCGTTTG 2100 GTTTACAGGA GTATTAGCTG TGGGGGCCCC TTTTCCACCA CCCCCATCAA GCAGCCTCCC 2160 GGGCAGCCCA GGACCCTCCA GAATCTTCCA GAAGCCGCAC CACTCGCTTC AGTCGTAACC 2220 TGCAGGACCC CACCGGGCGA GGCTGGCTGG GAGGAGGCAC TCTCAGGACA AGGGACCTGG 2280 GCAGGCACCT CCTGTCTCCG CTCAACACCC AGCGAGGACA GGAGGACCCA GGGTGCACCT 2340 GCATCTGCGT CTGGGCAGAG GAGCAAAGAC CTGGCCTTCC CAGAGCTTGA GCTGTGGGAG 2400 GAAGAGAGGC TGAATGAAAG CCCCGCCCCC ACCCCACCCC AGGAGAGGCC ACCTGGGGCC 2460 TCCCACAGCC CTGCCCACGG CTGCACACGC GTGTCCCCTC ACCTCCTTAG CCAGGGCGGC 2520 TGCCCGCGCA GGTCCCCTCA CCTCCTTAGC CAGGGCGGCT GCCCGCGCAG GTCCCCTCAC 2580 CTCCTTAGCC AGGGTGGGGG CAGCAGGGAG GGAGGGCGTG CTGCATTCTT CCCTGGGCCT 2640 GCAGGTGCAC CTGTGCCTGC CCAGAGGGAG CAGCGGGAGC TTCCAGCAGA CACACCTGGA 2700 CAGGTGCACA GAGCTCCTGC CAGGGAAACC CAGCACAGAC GCAGGTGGGC GGGTGGTGGG 2760 AGGGTGGCAG AAGCGGAAAG AGGAGGAGGC TGAGCTCAGC ACAGCCCATG CAGTCTCCTT 2820 CCGGCCAAGG GGAGCGGCTG GGCCAGTCTG AGCCGGGAGG CAGCTCAGGG AGTAAGCCCT 2880 GGGGACAACA TTGGAGTAGC ACAGGGTTCC CTGACAGAAC CTCACGTCGG AGGGTGGTCT 2940 GAGGGCTGCT GGGGGCCCAC CTAGGAGATG GGGTCCCAGG ACACAGAACA GGGAGGGGGT 3000 GGTGTTTCCA GGGTGAGGCC TGGGGGAGGG TAGCAAGGCC TGGACTAGGA GATGGAGGCC 3060 TAATCAAAGC AAAACAGAGA CTCAGAGCTC AGCGCCTGTA TTCGCAGGGA CACACAGGGA 3120 CTCACAGGGA CGTCCCGGAT CGCTAGGGGA CTCACGGGGA CACGTGGGGA CACGCTCGGA 3180 CTCACGGGGA CTTGCAGGGG CCCATGGGGA TGTGCAGGGA CACCGTCCCT CCCGGCCGTC 3240 CTGCTCCTTG CCAAGAGTCA CCCAGAGGCT GGGGCCTGGC ACCACTTGCA GACAGGGGCA 3300 TTCCTGGGCC CCTCCTTTTG GCACCTCAGC CTCAGCAGCT GCTGAAGGGT GTGGGGGAGG 3360 GAGCCGGTAT TGGTGCAACA GGCAGATGGT TCCAGAAACT CAGGATTCTA CACAATCCTA 3420 GCACCTGAGG CACAGTCCTG CACGGCCGCC ACGCTGTCGG AAGCAGGCAC CGGCCCTGGT 3480 GGTCAACACA AGCCCTGAGG ACCTCCCAGA GGGCATGCTC CGGGCAACCT GCCAGGACCA 3540 CCTCTCCTGC CTGGTGTTGG GGGCCTCACC TGACCTCTCC GGGTCCCTAA CCAGGCGCTA 3600 GGGCTGCCTC CCTTGGGGCC CCCAGAATCC ACCCTGGAAC GGCTGCTGGG ACTGAGACCC 3660 TGAGTCAGGC CAATCCCCAG AGCCTTGCCT AGCCATGGCT TGTCTGGGGT GGGTTCCCAG 3720 ATCCTCGTCC AGGACACGGG AAAGGGGCTC CTTTTGTGGC CTGTGCTGTG GAAGGGCTCA 3780 GTAAGCAAGG TGATCCTCCT GGGAGGTAGG 3810
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