Tag | Content |
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EnhancerAtlas ID | HS034-01068 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:44014040-44017340 |
SNPs | Number: 2 | 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: 28 | ID | Coordinate | Tissue/cell |
SE_00616 | chr1:44009256-44025211 | Adipose_Nuclei | SE_03403 | chr1:44013988-44014536 | Brain_Angular_Gyrus | 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: 3 | Chromosome | Start | End |
chr1 | 44015731 | 44016125 | chr1 | 44016660 | 44016751 | chr1 | 44014536 | 44014607 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I043539 | chr1 | 44005459 | 44020850 |
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Enhancer Sequence | GGAGCTGGGA GTGTGTCTGT TGTGTCATTT CCCTCCTCCC CAGAGCCTGT GGAGCACACA 60 GGGTCTGTTG TCTGTCGTCA TGCTCTCCCC CTCGTTCTAT GGGTGGCCTG TCTAGACTCT 120 GCTCCCTGTG GGACTTCCCG CAGATTCCGT TGCTTTCTCT CTCTGGGCCT GTTTTCCTAT 180 TGCACAATGG GGATAATCAC TCCTACCTGG AAAGGTTAAC TGAGGTCACA TGGATGAGGT 240 GCCTGGAACC TAGTATGTAT TCCCCTTATC TGAGGCCATG ACCTGGGGCT CTTGCTCTGT 300 CCCTGGGAAC CAGGCTTGTC TCTGAGTGGG CTCCAGGGGG GTACCAGGAA CAGTCACAGG 360 AGCTCACTGA GTCCCAGCTT AAGCTGCTCA GACCCAGGGA TATCTGTCTC TCCAGAAGCT 420 CCCTGCCCTG CCTTCGCCGG CCCTCATGGC CCTGCCTCCG TGTGTACATG TGTATGTGTA 480 TTCCATGGGA AAGGCACAAA ATAGCAGTCA GTCTCTCCAT AGAAGAGCCT TGATGGTGGC 540 CCAGTTTGAC TCTCCCTGGG GCTGGACCCC TACAGCCTCC CTGGGAGGTG GTTGCAGCCC 600 CCTTCCTCCA GCCAGTTCCA CTTACTCCTT TCTTAGGCCA CTTCCTCCCA CCCTGCATGG 660 GCTTGGTGGC TCGAGAATGT TGCCGTCCAT ACCCCGGGAG CTGTGCTGAA AGGGCTGTGC 720 GGCCCCCGAC CACTGTGTGT GTCAGGGAGG GGGCACGCTC TCGTGGGGTG TCAGGCCAGG 780 TGGCAGTGGG TAACTGGCAG AAAGGCCCTC CTGGTGTGCT CTGGTGGCAC CCTGTTGACC 840 CAGTCTCAGA AGTTGTGTTC CGACCCTCAC TGAACACCAG CTGTGGGTCA GGCACGGGGC 900 AGAGTAGTTC AAGTAGCTTG GTTTGCTGCC TGCCTGGGGA CCTGACACTG TGGGATCTGG 960 TCAGTGCTGG GATGGGAAGC TCTGGGCACC TCAGGCCATG GGACACAGAG CAGGCTCCTA 1020 CAGCAGCTTG GCTGGGTGGG ACATGAGAGA GGGGCTGGGC TGGGCACACT CAAAGGCAGG 1080 GAGGAGTCTG AGGGCCTGGC CTGTCAGGGT GGCCTAGGTG GTGGGTCCAA GCTGTGTGCT 1140 CTGCACAGTG CTAGGCCTGT ACTATAGTAG GTGCTCAAAA AATACTTGTT GAAAGAGTAA 1200 AGAAGCCGGG TGTGGTGGCT CATACCCGTA ATCCCAACAC TTTGGGAGGC CAAGGCAGGT 1260 GGATCGCCAG AGCTCAGGAG TTTGAGACCA GCCTGGCAAT GTGGTGAAAC CCTGTCTTTA 1320 CCAAAAATAC AAAAAATTAG CCAGGCATGG TGGTGTGCAC CTGTGGTCCC AGCTACTCGG 1380 GAGGCTGAGG TGGGAGGATT GCTTGAGCCT AGGAGGTGGA GGCGGAGGTT ACAGTGAGCT 1440 GAGATTGTGC CACTTGTACT CCAACCTGGG TGACAAAGTG AGACCCCCCT CTCAAAAAAA 1500 AAAAAGACTA AAGAAAAGTG AGCCTGAGAG CTTAGGAGGA GCACATTTCA GAGGGGAACG 1560 GAGAGAGGAA CATCAGGCCC GTTGGTAGCT GAGGAGAGGT GCGGTTAGAT CTGTGCTCCC 1620 CAAAGATCCT CTGCTGAACA TAAGGGGCAA CGCCTTGTCT CCTGTGCTGT GTCCTGCGGG 1680 TGGAGGTGGA TTGGAGGGAA GCGGAGGGCG AGGCCTGGTT GAGGGGCGGG GCCTGCCTGT 1740 CTGGTCCCCC GGGCTGCCTT GGGCCAGCTT GGCCTAGTCT GTTGGGTGGG CGGGCAGGGT 1800 GCAGGCTCCT CTCCAGCCTC CAAGGGAGGG GAGTTGTTCT GCCTCCTCGA TAGCCCCAGG 1860 CCTTGGGCAC AGCCCAGCCT CCCACGGCTC TTGGGCCCTC CTCCTTCCAG GCCGCCGGTG 1920 ACCCACACCT GGCTCTCCTC CCCGGCGTCT CCTCTCCGCT TCTTTGTTTG GAGCGGAGGC 1980 CCCGCCCCAC CCCGCCCCCA GGCGCACTCG CCCGGCCATT CCGGTTCAGC CGGTTCCAGC 2040 CCCCAGTTTC TGCCGCTGCA GGTCCCGGCA GGAGCTGGAG GGGCACTTTC TCCCTGGGTT 2100 TCTCTTCCCT GGTGCAGCAG GGGCCGCGGT CCTCATCCTC CTGGTTCCTC AGTTCGGTCC 2160 TTCTTTCATT CTCCACCCCT GGGTGCCAGG AACTGGGTCA GACACTGGGA CAGGAATCCA 2220 GACAGGCATG CTATCTGCCC TGCCCAGGGT TATGTTCTAG GAGGGGAAGC AGCCATTAAT 2280 CAAACACCAA AAATGTGGAA AAGTAATAAT CTCACACGTG TGCATAATAA ACTGTGAGTG 2340 AAAGTTATAA GCTCGGCAGG TAGGTAATAA GCTAGGAGCA GTGCTGTGGG AGGCAAGGGA 2400 GTTACCCGGG AGTTTCAAAC TAGGAACTGA GCTCATAGGT TGGGGGCAGG GGGACTGGAG 2460 AAGGCAGTGA TACTTAAATG GAGAGCAGAA GGATGAATGG AAGTTAGAGT GTATGGCGGA 2520 GGTTGGCAGA AGCAGCAGCT TATGCAAAGG CCCTGTGGCT GCAGGGAACA TGACGTTGCT 2580 CTTTAGAGGA GCCAAAGCTG GGGCTCTGGG GAGAGCAGCT GGGTCAGACC CCGCGGCTTT 2640 GTCTGCCATA ACAGGTGTTT GGAGAGTGAT TCGGCAGGTC TTTGGAGGGT TTTGATAGGG 2700 CGGGGTGTCG GGGGAGGCTG TCAGCTCACT CTGGACACTG AGTAGAGAAC AGACGGGAGG 2760 CGTGGGGCAG GCCTGGAGGC AGGGGCTTCC GCGTGTTAGG CCAGTGGAGT GCCAGTCAAG 2820 GGAAGGTGGT ATCTGGACTA GGGTGTGGCA GCGCAGGTGG AGAACCCTGA GCTGCTTTGT 2880 GGAGGGCTTC AAGTGTGGGG GAAGAGTGCA CGGTATGGGG GTGGGGGACA GGAGACACCC 2940 CCAGTGGAGC CTGAGCAGGA GAGTCGTGTC TGAGAGGGTC TGTCTGGAAG GCGCAACAGA 3000 GGCCAACTTT GCAGACAGCT GCAGTCGGGA GAGCCTGGAG CCTCCTTCAA AGGGCATTCA 3060 GGGGAAGGGC AAGGCACGCT GGGGGGTTCT GGACCTTCTG TGGTGTCTTC TTGTCTTTCT 3120 GGTCCCTACA GCCTCCCTGA GCTGGCTGCC CGAGCCTGCC CTAGGCACTC TAAGAACATA 3180 GTCAGTCCCA AGGTCTCCCT CCAGGGAAGG CCGTAGGTGA GCTTAGGAGT GAGAAGGCTG 3240 GATCAAAGCC TGGCTCCATG CCTGCATCCC TCTGACTTGC CAGTCATTTC ACCCTCCGAG 3300
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