Tag | Content |
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EnhancerAtlas ID | HS118-10383 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:127839800-127842580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr2:127842205-127842216 | AGAGATAAGAA | - | 6.32 | Gata1 | MA0035.3 | chr2:127842205-127842216 | AGAGATAAGAA | - | 6.32 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_00572 | chr2:127838207-127846198 | Adipose_Nuclei | SE_00914 | chr2:127837091-127843980 | Adrenal_Gland | SE_03157 | chr2:127836518-127840699 | Brain_Angular_Gyrus | SE_03157 | chr2:127840812-127842608 | Brain_Angular_Gyrus | SE_03883 | chr2:127821506-127844236 | Brain_Anterior_Caudate | SE_04777 | chr2:127820278-127857314 | Brain_Cingulate_Gyrus | SE_05775 | chr2:127806116-127867885 | Brain_Hippocampus_Middle | SE_06689 | chr2:127821297-127857092 | Brain_Hippocampus_Middle_150 | SE_07740 | chr2:127821073-127849400 | Brain_Inferior_Temporal_Lobe | SE_08942 | chr2:127842192-127842509 | Brain_Mid_Frontal_Lobe | SE_19824 | chr2:127833985-127840684 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22831 | chr2:127831598-127840986 | CD8_primiary | SE_22831 | chr2:127841008-127845265 | CD8_primiary | SE_24390 | chr2:127837483-127840259 | Colon_Crypt_2 | SE_24390 | chr2:127841733-127843718 | Colon_Crypt_2 | SE_29563 | chr2:127836160-127857245 | Fetal_Muscle | SE_31713 | chr2:127837676-127844066 | Gastric | SE_36991 | chr2:127828440-127865759 | HSMMtube | SE_41757 | chr2:127839666-127840551 | LNCaP | SE_41757 | chr2:127841273-127843893 | LNCaP | SE_48048 | chr2:127806769-127857236 | Psoas_Muscle | SE_50749 | chr2:127836629-127840644 | Sigmoid_Colon | SE_50749 | chr2:127840740-127843883 | Sigmoid_Colon | SE_51095 | chr2:127817891-127857315 | Skeletal_Muscle | SE_54239 | chr2:127837127-127840577 | Spleen | SE_54239 | chr2:127840923-127843925 | Spleen |
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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: 1 | ID | Chromosome | Start | End |
GH02I127071 | chr2 | 127828680 | 127857094 |
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Enhancer Sequence | CTCCTCCTCC GTCGTCTCCC ACACACAGCT CGGGTCAGCC AAGCTGGGGA GCTGTGGATG 60 ATGACACAGG GCTGGCCTCG GGGATCTTTC CGCCCTCATG CTCCAGGGGC CCCTGCAGGG 120 GAGACAGAGG GCAGGATGGC CAGCTGAAGG CCTCCGTGGT CACAAGCTCT GAGGCCTTGC 180 AGGCACTCAG CTGGGGATAC CAGGGACATC GCAGGACAAG TCTGCACCGA GACCAGGGTT 240 GGCGTGGGCA GGCCATGGTG GGCGCCCAGG CAGGGGAAGG GGTACAAGGC CCTCTGCCTC 300 CCCTCTCCTG CCCCAAGATG CTGCCTGCTG TCTGACACAT CAGGCTGGGG TGGCAGTGGT 360 GAAAGGGGTA CAATGGGAGT CTTAAACCCC CAGGGGCAGA GGGAGCCAGT CTGAGGACAG 420 TCCCGCAGAT CCCATAGTCA CCTAGTTCCC CAGCACACAA CCCCTCCTCC AAGCCCATCT 480 CTCAAATGCG AGCTGTCCCT GCAACCAGAC ACACAGGACC CCTCTCCCGG CTGCTGCTCA 540 CACCTCCCCA TCCCCACTCC GACAGTGGAG CCACCTAAGC CTGCTCCCCA CCTCTGGGTG 600 GAGAGTCTCG GTGGCCTCCA ACAATCTAGG TGCCATGCAG GAGGCCACAG CAGCCCTGAC 660 GAGAGAGCAG AGGGAGGAAA AGAGGTTCTA AGCCCACCAC TCACCTCCAC ATTTCATGTG 720 GCCCTCTCAC CTCCTTATTT TCAAAGTATA AACCTCAAAG AAAGTGGAAA GGATACTACA 780 GGGACTATCA TCTACCCTTC ACCCAGATTC ACCAATCAAC TGTTACCACT TGGCCACACT 840 CATTTGCTTT TTTCTTTTTT TTTTTTTCTT TTTTTTTGCT TTTCTCTTTT CTTGCTATGT 900 CGTCCAAGCT AGAGTACATG GCGCAATCAT GGCTCACAGT AGCCTAGACT TTCTGAGCTT 960 AAACGATCCG CCCACCTCAG CGTCCCGAGT AGCTGGGACT ACAGGCCACT GCACCTAGCT 1020 AGTATTTTTA CTTTTTGTAG AGACAGGGCC TCGCTATGTT GCCCAGTTTT GTCTGGAACT 1080 CCTAGCCTCA AGTGATCCTC CCACCTCAGC ACCCTCAAGG TGCTGGGATT GCAGGTACAA 1140 GCCACCGTGC CCAGTCACTT TTCTCTATAT ATAAACCGTT CCTGCATTTG TATGTTTGCC 1200 CAGCCAACAG AAGGTAAGCA GCAGAAGGGT CACTGGGATG ACCTTCGCTC CACAATACTT 1260 CACCCCTAAA TACTCCAACA GATTTCCTAA GAACAAGAAC ATGCTCCAAA ATGCCCATGA 1320 TACCATAAGC ACCCCCAATA CATCCAAAAT GTATTTTAAA ATACCATCTA CCACACGGTC 1380 CGCATTCAAA TATCCTTGGG TGCCCCCCAA ATGCCCTTTA TGTCTGGGTC TAGGATCCAA 1440 CTGTGGTTCA CATATTGCTT CTGATTGTCG GGTCTCTTGT TCCTTTAGTC CAGAATATTC 1500 CCCGTATGCC TATTTATCAA TGTTATCCAT TTTTTTTCTT TCGTGATACT GGTATCTTTT 1560 TAAGAGTGCA AACCAATCAC TTGGAGAATG CCCCACACTC TGGATCCATC TGATTGTTTC 1620 CTTGTGAGGA AGTTCAGGTT AAAGGCTGCT TTGGCAAGAG TCCTGCAGAG GGAGGCTGAG 1680 CCTTCCCACC GCACCACAGC TGTGTTAGGC TTGACCGCCG GGTCTGAGTC GTGTTTGCCA 1740 GATCTCTTGG AAAGGAAGGT CACTTTTCTC TTAGTCATCT GCAGGACAAT CACGGTCACT 1800 GTGGCAAGGC AAAAAGTTGT TGAAATTTTT GCACAGTGCC TTTACTATCC ATCATTCTTT 1860 GCTATTCAGT GTGAGGTCTG TGGGCAGCTG CATGACAGTC TTCCAAGAGC CTGGAGGAGA 1920 AAAAAAACTG CAGACCTGCT GAACCAGAGT GTTCCCTTTA ACAAGTCCCC CTGGCGCACC 1980 GTATGCGCAG TGAAGTCTGA GAAGCACTGC AATAGCATCT TGGCTGGAAC CCGCTGTTAC 2040 CCAATCTCCT CCACGTGACC CGGCATTCCA CAAACACGAG CCTCCCCTGG TCTTGCCTTT 2100 GCGAGGAGGG TGGTGAGGAT ATCGTGAGTC CTTCGTTTTG CGTTCGTGAT TCATTTTGAT 2160 GCTCAAACAT CCCAAGTGCG ACCAGTGGGA GGTTTCGGAC ACGTCCTCAT TCATCTCCAG 2220 GCGCTTCCTT ACTTTCTGGC ACTAGCAGAT TCTCCAGGCT CAGCCTGCAC TGTCCCTGCC 2280 CCAGCCCTGG CATCAGCCAT TTCTCCAAGG AACCCTGATT TCCTTCGGTG GAGAGGCATG 2340 CTCATTGCTC TTAGGCATTT CAGCGTTCCC TCATGCTCAG AGCCGCAGAT TATTACCCCT 2400 GCTTTAGAGA TAAGAAAGGA AAGGCTGCGG CACTGAAGGA TTTGGCTCTG CAGCGAAGAA 2460 GCGACCGAGC TCAGATTCTG TGGCTTTGTG GTGGTGGTGA ACAAGCATCA TCACTCAGGT 2520 CTGTCTGCTT CAAGAAGTGA GAAAGGAGAC AGACCCATGG CCTAGCAGCT GCCCTCTGAG 2580 CCCATTGCAG TGTTCCTTAG GAGGCCACAC TGACTGTGGG CTGTGGCACC TGCCCCAGGC 2640 TGGTGACTGC ACAAGGGGCA GCTTCCTGGT CTCATCCAGC CCAGGGAAAC TCTCTTCCTC 2700 CTCAGAACCC AGTGAAGTCA CACGTACAGA GGCGTCTTCA GAGCAGCAGT GCTTAACCCA 2760 GAAGCTAGCA GTCTCCTGGT 2780
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