Tag | Content |
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EnhancerAtlas ID | HS122-00329 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr1:44014680-44017290 |
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) |
KLF5 | MA0599.1 | chr1:44016018-44016028 | GCCCCGCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:44015762-44015772 | GGGGCGGGGC | - | 6.02 | Myog | MA0500.1 | chr1:44017053-44017064 | GACAGCTGCAG | + | 6.62 | SP1 | MA0079.4 | chr1:44015760-44015775 | GAGGGGCGGGGCCTG | - | 6.22 | Tcf12 | MA0521.1 | chr1:44017053-44017064 | GACAGCTGCAG | + | 6.14 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | SE_04240 | chr1:44003988-44015177 | Brain_Anterior_Caudate | SE_04240 | chr1:44016899-44020669 | Brain_Anterior_Caudate | SE_05040 | chr1:44001099-44015486 | Brain_Cingulate_Gyrus | SE_05040 | chr1:44015834-44021066 | Brain_Cingulate_Gyrus | SE_05962 | chr1:44000439-44020958 | Brain_Hippocampus_Middle | SE_07193 | chr1:44003475-44015024 | Brain_Hippocampus_Middle_150 | SE_07193 | chr1:44016119-44020709 | Brain_Hippocampus_Middle_150 | SE_08033 | chr1:44003431-44015175 | Brain_Inferior_Temporal_Lobe | SE_08033 | chr1:44015878-44020741 | Brain_Inferior_Temporal_Lobe | SE_23218 | chr1:44005985-44017477 | Colon_Crypt_1 | SE_23829 | chr1:44013362-44015343 | Colon_Crypt_2 | SE_23829 | chr1:44015459-44017409 | Colon_Crypt_2 | SE_24870 | chr1:44012836-44017627 | Colon_Crypt_3 | SE_26649 | chr1:44010798-44020559 | Esophagus | SE_27645 | chr1:43995619-44017587 | Fetal_Intestine | SE_28595 | chr1:44005404-44017604 | Fetal_Intestine_Large | SE_31538 | chr1:44004919-44019003 | Gastric | SE_41575 | chr1:44001646-44015303 | LNCaP | SE_41575 | chr1:44015364-44020400 | LNCaP | SE_47657 | chr1:44013015-44015395 | Pancreas | SE_47657 | chr1:44015425-44018793 | Pancreas | SE_50363 | chr1:44005822-44020588 | Sigmoid_Colon | SE_52524 | chr1:44004832-44019377 | Small_Intestine | SE_56987 | chr1:44014752-44017377 | VACO_400 | SE_65452 | chr1:44004903-44018198 | Pancreatic_islets | SE_69138 | chr1:44014239-44017340 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 44015731 | 44016125 | chr1 | 44016660 | 44016751 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043539 | chr1 | 44005459 | 44020850 |
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Enhancer Sequence | CTTCCTCCCA CCCTGCATGG GCTTGGTGGC TCGAGAATGT TGCCGTCCAT ACCCCGGGAG 60 CTGTGCTGAA AGGGCTGTGC GGCCCCCGAC CACTGTGTGT GTCAGGGAGG GGGCACGCTC 120 TCGTGGGGTG TCAGGCCAGG TGGCAGTGGG TAACTGGCAG AAAGGCCCTC CTGGTGTGCT 180 CTGGTGGCAC CCTGTTGACC CAGTCTCAGA AGTTGTGTTC CGACCCTCAC TGAACACCAG 240 CTGTGGGTCA GGCACGGGGC AGAGTAGTTC AAGTAGCTTG GTTTGCTGCC TGCCTGGGGA 300 CCTGACACTG TGGGATCTGG TCAGTGCTGG GATGGGAAGC TCTGGGCACC TCAGGCCATG 360 GGACACAGAG CAGGCTCCTA CAGCAGCTTG GCTGGGTGGG ACATGAGAGA GGGGCTGGGC 420 TGGGCACACT CAAAGGCAGG GAGGAGTCTG AGGGCCTGGC CTGTCAGGGT GGCCTAGGTG 480 GTGGGTCCAA GCTGTGTGCT CTGCACAGTG CTAGGCCTGT ACTATAGTAG GTGCTCAAAA 540 AATACTTGTT GAAAGAGTAA AGAAGCCGGG TGTGGTGGCT CATACCCGTA ATCCCAACAC 600 TTTGGGAGGC CAAGGCAGGT GGATCGCCAG AGCTCAGGAG TTTGAGACCA GCCTGGCAAT 660 GTGGTGAAAC CCTGTCTTTA CCAAAAATAC AAAAAATTAG CCAGGCATGG TGGTGTGCAC 720 CTGTGGTCCC AGCTACTCGG GAGGCTGAGG TGGGAGGATT GCTTGAGCCT AGGAGGTGGA 780 GGCGGAGGTT ACAGTGAGCT GAGATTGTGC CACTTGTACT CCAACCTGGG TGACAAAGTG 840 AGACCCCCCT CTCAAAAAAA AAAAAGACTA AAGAAAAGTG AGCCTGAGAG CTTAGGAGGA 900 GCACATTTCA GAGGGGAACG GAGAGAGGAA CATCAGGCCC GTTGGTAGCT GAGGAGAGGT 960 GCGGTTAGAT CTGTGCTCCC CAAAGATCCT CTGCTGAACA TAAGGGGCAA CGCCTTGTCT 1020 CCTGTGCTGT GTCCTGCGGG TGGAGGTGGA TTGGAGGGAA GCGGAGGGCG AGGCCTGGTT 1080 GAGGGGCGGG GCCTGCCTGT CTGGTCCCCC GGGCTGCCTT GGGCCAGCTT GGCCTAGTCT 1140 GTTGGGTGGG CGGGCAGGGT GCAGGCTCCT CTCCAGCCTC CAAGGGAGGG GAGTTGTTCT 1200 GCCTCCTCGA TAGCCCCAGG CCTTGGGCAC AGCCCAGCCT CCCACGGCTC TTGGGCCCTC 1260 CTCCTTCCAG GCCGCCGGTG ACCCACACCT GGCTCTCCTC CCCGGCGTCT CCTCTCCGCT 1320 TCTTTGTTTG GAGCGGAGGC CCCGCCCCAC CCCGCCCCCA GGCGCACTCG CCCGGCCATT 1380 CCGGTTCAGC CGGTTCCAGC CCCCAGTTTC TGCCGCTGCA GGTCCCGGCA GGAGCTGGAG 1440 GGGCACTTTC TCCCTGGGTT TCTCTTCCCT GGTGCAGCAG GGGCCGCGGT CCTCATCCTC 1500 CTGGTTCCTC AGTTCGGTCC TTCTTTCATT CTCCACCCCT GGGTGCCAGG AACTGGGTCA 1560 GACACTGGGA CAGGAATCCA GACAGGCATG CTATCTGCCC TGCCCAGGGT TATGTTCTAG 1620 GAGGGGAAGC AGCCATTAAT CAAACACCAA AAATGTGGAA AAGTAATAAT CTCACACGTG 1680 TGCATAATAA ACTGTGAGTG AAAGTTATAA GCTCGGCAGG TAGGTAATAA GCTAGGAGCA 1740 GTGCTGTGGG AGGCAAGGGA GTTACCCGGG AGTTTCAAAC TAGGAACTGA GCTCATAGGT 1800 TGGGGGCAGG GGGACTGGAG AAGGCAGTGA TACTTAAATG GAGAGCAGAA GGATGAATGG 1860 AAGTTAGAGT GTATGGCGGA GGTTGGCAGA AGCAGCAGCT TATGCAAAGG CCCTGTGGCT 1920 GCAGGGAACA TGACGTTGCT CTTTAGAGGA GCCAAAGCTG GGGCTCTGGG GAGAGCAGCT 1980 GGGTCAGACC CCGCGGCTTT GTCTGCCATA ACAGGTGTTT GGAGAGTGAT TCGGCAGGTC 2040 TTTGGAGGGT TTTGATAGGG CGGGGTGTCG GGGGAGGCTG TCAGCTCACT CTGGACACTG 2100 AGTAGAGAAC AGACGGGAGG CGTGGGGCAG GCCTGGAGGC AGGGGCTTCC GCGTGTTAGG 2160 CCAGTGGAGT GCCAGTCAAG GGAAGGTGGT ATCTGGACTA GGGTGTGGCA GCGCAGGTGG 2220 AGAACCCTGA GCTGCTTTGT GGAGGGCTTC AAGTGTGGGG GAAGAGTGCA CGGTATGGGG 2280 GTGGGGGACA GGAGACACCC CCAGTGGAGC CTGAGCAGGA GAGTCGTGTC TGAGAGGGTC 2340 TGTCTGGAAG GCGCAACAGA GGCCAACTTT GCAGACAGCT GCAGTCGGGA GAGCCTGGAG 2400 CCTCCTTCAA AGGGCATTCA GGGGAAGGGC AAGGCACGCT GGGGGGTTCT GGACCTTCTG 2460 TGGTGTCTTC TTGTCTTTCT GGTCCCTACA GCCTCCCTGA GCTGGCTGCC CGAGCCTGCC 2520 CTAGGCACTC TAAGAACATA GTCAGTCCCA AGGTCTCCCT CCAGGGAAGG CCGTAGGTGA 2580 GCTTAGGAGT GAGAAGGCTG GATCAAAGCC 2610
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