Tag | Content |
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EnhancerAtlas ID | HS180-00512 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:16275430-16277690 |
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) |
MITF | MA0620.2 | chr1:16276939-16276957 | AAAGGTCACGTGAGCACA | + | 6.13 | MITF | MA0620.2 | chr1:16276939-16276957 | AAAGGTCACGTGAGCACA | - | 6.13 | MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr1:16276484-16276494 | AACAGCTGTT | - | 6.02 | RREB1 | MA0073.1 | chr1:16277529-16277549 | CCACATACCACCACCCGCCA | + | 6.33 | SP1 | MA0079.4 | chr1:16276264-16276279 | GAAGCCACGCCCCTC | + | 6.67 | SP4 | MA0685.1 | chr1:16276264-16276281 | GAAGCCACGCCCCTCAC | + | 6.35 | TFAP2C | MA0524.2 | chr1:16277366-16277378 | TGCCCTGGGGCT | - | 6.11 | ZNF263 | MA0528.1 | chr1:16276035-16276056 | TTCTCTGCCTACTCCTCCTCT | - | 6.37 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_01097 | chr1:16275403-16279590 | Adrenal_Gland | SE_01987 | chr1:16272432-16279631 | Aorta | SE_02709 | chr1:16274610-16280662 | Astrocytes | SE_03452 | chr1:16275260-16277700 | Brain_Angular_Gyrus | SE_04408 | chr1:16274061-16278759 | Brain_Anterior_Caudate | SE_05249 | chr1:16273948-16279656 | Brain_Cingulate_Gyrus | SE_06124 | chr1:16270812-16279644 | Brain_Hippocampus_Middle | SE_07342 | chr1:16272948-16278751 | Brain_Hippocampus_Middle_150 | SE_08131 | chr1:16272535-16279679 | Brain_Inferior_Temporal_Lobe | SE_18522 | chr1:16273733-16281386 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19255 | chr1:16273419-16281362 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_27189 | chr1:16274173-16281550 | Esophagus | SE_36664 | chr1:16274460-16277822 | HMEC | SE_38820 | chr1:16274752-16281466 | HUVEC | SE_40080 | chr1:16274659-16281418 | K562 | SE_45001 | chr1:16274543-16280813 | NHLF | SE_45986 | chr1:16274066-16281079 | Osteoblasts | SE_47059 | chr1:16275327-16277770 | Ovary | SE_55849 | chr1:16274274-16283539 | u87 | SE_61132 | chr1:16274043-16303645 | HBL1 | SE_64852 | chr1:16274416-16281190 | NHEK | SE_67570 | chr1:16274274-16283539 | u87 |
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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 |
GH01I015947 | chr1 | 16274011 | 16281336 |
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Enhancer Sequence | GGTCTTTAAG AAAACTTTCC TATTTTCTCA TTCTCTCATG GACAGGTGAA GACAAGACGG 60 TGTTTCATCA GCCAGTGTTG CAGAACTCGG CCCCTCTCAG GCTCTGCACG TACCCCATCC 120 CCCGACAAAG CCTAGCTCTC CCTCTCTTTC TGATTCATGG GAACTACCTA GAGTTGCGGA 180 GTCTTCTGAC TCCAGAAACC TGTGTCCTGG TGGCCATCCC AGGAGAAACA ACTTTGATCC 240 TGACCCCAAG AGCTGCTGAC CTGGCCACAA CTTCTCTGTC AAGGGCCTCA CTTAATGCCT 300 GGAAATCCCA CAAGTGAAAA TGCTCAGGAA AATTCCATGG CCCAGTGCCG AGCAGTCTTG 360 AACCGCACAA GCCGTGACTA AGTAACTATC TAAAACAGCT CTCCCTCCCG CCCCAACACC 420 ACCCAGAGTG GGCGTCAACA TCAGCAATTG TCTAGGGAAA ATAAGCGGGC CCTCTTTTCT 480 AGAAAGAACC CATTTCAGAA TGTTTGAAGA GAAAAATCAA CACCCACTGT CTGGGGCCAC 540 ATTAGACAGA TTCAACTGGG CACGGCTGTC ACGCCCTGGC CCAGGATCTG CTAAGGGGTA 600 GTGAGTTCTC TGCCTACTCC TCCTCTTCTC TGAGGCCTGA GTCTGCACGG GGCTGGCTCC 660 CCGGCTTCTG GGCAGGTGAG AGGGACACTT TGGGGCTCTC CGCCCCCAGT TTCGGCAGCT 720 CTGCCCCGGC TCAGGCACTC CCCTGTGACA TCAGCATCTT GGGGGGTGAA TCACTGCCGC 780 AGCTCTGAAG CTGCTGTGGC CATGCATGGC TGTCGGGCTG TGATGAGTCC GGAGGAAGCC 840 ACGCCCCTCA CACCAGCACA GGTCGGCCTT GAAGGGCGCC AAGGCCTCCC ACCACGTGAT 900 GTCTGGAAAC TTTTCACAAG TGGGGGTATC TGCTGAGCGG GGGGAAGTGA CGCAACAAAT 960 AACGGGGAGC ATGGCAGTGG CAACAGGCAT GAGCCACAGC GCACCAGCCT CCGAGCCACA 1020 AGTTCAGCGT TGCTGCTGCT GCCAGAGGCC CAGAAACAGC TGTTCCCTCC CCCTACACAT 1080 CCCCGCGCAG GCTTTGGCTC TCTCAATGAC ATTCCTAAAT GGCTGTGGCT AGAGCCCTAA 1140 GTGTAAGCAC TGGAGAGCCA GGGCCAGCCC CGAAATCAGG AGGTAAGGCC CTGGGGCAGC 1200 TGGCCCCGCA CCAAGTGCAC CAAGTGGCTG GCAGCAGCAC ACGGCCACCT GGAGCAAAGC 1260 ACAGAGGCCT TTCTCTCCTG TCCTCAGTCC CTGGAAGCAG CAGGTTCCTA TCTGTGACCT 1320 GAAGGAACGC AAGGGAGAAT CGTGGCTGCG CTGCTCCTAT GCACTGGACA TGGGGAGGCA 1380 CCAATGTCCA GCTTGTGGAT CAAGACCTGA AGGGCACAAA GGGCAAGGTG GGTGCAGAAG 1440 GAACCAAAGG CAGGGGCGAG GTGGGCCCAG GCCACGGCAA CCCTAGAGCT GTCTTCTCCT 1500 GGCTGTGGAA AAGGTCACGT GAGCACACAG GTGTGTGGGT GGCAAGCCCT GGGCCTCAAT 1560 TGCTAGTCAC CCCCTACATA CCCAGGAGCC CCAAGTGCAG AAGAGGGGAA TACCAGGGCC 1620 CACACAGGGC AAAATCCTCA ACTGGCTTCA GAAGCAGCCC ATCTGGAACT TGCAAGTGAG 1680 GCCCAACCCT TCTCTCCAGG CTGTGTGCCT GGCTTCCTCA CCTTCCCCAG GAGCCAACCC 1740 GAAACTTGAG CCACCCAGGT GCTAAAACAA CCTGGGGAGC ATCAGCTGAA CCCCCAGAGG 1800 TACAAAGAAC CCTCTAGCAG GAAAACCATC TGACTTGCCG GGAAGAGACA TGTGAGGAGA 1860 CTCCTAGCCA AGGGGAGGGA CAGGATCAAT CCCCTTGTGT GGGCCCAAGG CTGGGATGAG 1920 CCTCCCTGTG GCCATGTGCC CTGGGGCTTC CTGGCAAGCG CAGCCCCGCC CAGCCATACA 1980 GCTGTCCTGG GACTGGATGG ATGGATGGAT GGGTAAGCTA GATAGATTAG ATAAGACACA 2040 TTCGCTAGAT AATAAAATAG TAAAGGCCCC AAGGACAGGG TGGGTGGTGG CCCAGCCCCC 2100 CACATACCAC CACCCGCCAA GAGAGCAGCT GTGTGCCCAT GAGCAACATT TTCCACCGTG 2160 CTGACTGCAC TTTTCCAATG CAAGATGCCC GCCCAGAAGT GGGCTCCTCC CACACACGGG 2220 TGTTAGGAGG AGAAACAGAG GCGTCTATAA TCCTCTGAGG 2260
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