Tag | Content |
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EnhancerAtlas ID | HS012-01390 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr10:31421710-31424420 |
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) |
CREB3 | MA0638.1 | chr10:31422761-31422775 | GCGCCACGTCACCC | + | 6.07 | EWSR1-FLI1 | MA0149.1 | chr10:31421974-31421992 | ACATCCTCCCTCCCTTCC | - | 6.3 | EWSR1-FLI1 | MA0149.1 | chr10:31422196-31422214 | GGAAAGGAGGAAGGGAGG | + | 6.88 | EWSR1-FLI1 | MA0149.1 | chr10:31421982-31422000 | CCTCCCTTCCTCCCTCCC | - | 6.88 | EWSR1-FLI1 | MA0149.1 | chr10:31421978-31421996 | CCTCCCTCCCTTCCTCCC | - | 6.92 | EWSR1-FLI1 | MA0149.1 | chr10:31422192-31422210 | GAAAGGAAAGGAGGAAGG | + | 7.05 | EWSR1-FLI1 | MA0149.1 | chr10:31422204-31422222 | GGAAGGGAGGGAGGGAGG | + | 7.08 | LMX1B | MA0703.2 | chr10:31423921-31423932 | AATTTAATTAA | + | 6.32 | MEOX2 | MA0706.1 | chr10:31422236-31422246 | AGTAATTAAC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr10:31424180-31424195 | AAGTTCAAAAGTTCA | + | 6.19 | Nr2f6 | MA0677.1 | chr10:31423949-31423963 | CAGGTCAAAGGTCC | + | 6.05 | RARA | MA0729.1 | chr10:31424180-31424198 | AAGTTCAAAAGTTCATAT | + | 6.18 | Rxra | MA0512.2 | chr10:31424173-31424187 | AAGGTTAAAGTTCA | + | 6.18 | ZNF263 | MA0528.1 | chr10:31421974-31421995 | ACATCCTCCCTCCCTTCCTCC | - | 6.09 | ZNF263 | MA0528.1 | chr10:31422888-31422909 | CCCCTCCTCGCCCCCTCCCCC | - | 6.36 | ZNF263 | MA0528.1 | chr10:31422202-31422223 | GAGGAAGGGAGGGAGGGAGGA | + | 6.63 | ZNF263 | MA0528.1 | chr10:31421981-31422002 | CCCTCCCTTCCTCCCTCCCCA | - | 6.85 | ZNF263 | MA0528.1 | chr10:31422210-31422231 | GAGGGAGGGAGGAAAAGAGGG | + | 7.25 | ZNF263 | MA0528.1 | chr10:31422201-31422222 | GGAGGAAGGGAGGGAGGGAGG | + | 7.9 | ZNF263 | MA0528.1 | chr10:31422198-31422219 | AAAGGAGGAAGGGAGGGAGGG | + | 8.12 | ZNF263 | MA0528.1 | chr10:31421977-31421998 | TCCTCCCTCCCTTCCTCCCTC | - | 8.35 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_25423 | chr10:31420765-31433717 | DND41 | SE_30759 | chr10:31421649-31424498 | Fetal_Muscle | SE_39587 | chr10:31421494-31430224 | Jurkat | SE_66545 | chr10:31421494-31430224 | Jurkat |
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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 |
GH10I031132 | chr10 | 31421546 | 31427344 |
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Enhancer Sequence | CTCACGAAAC TTACAGTCCG GTGGGGAGGG TGAATTTTGC CCGGTTGTAC ATTTGATGAG 60 TATTACAAAA GAGAAGATGA AAGAGCTACA GGATCCTGTA ACTGGAGGAC CTGATCTGGC 120 CCAGGCACCA GGGAAGTGAC ATTTCACCTG AGGCCAGAGG AATAAGTGGG AGGGGAATGG 180 GCTGGGGGTG GGCTATGCAG GGAGACCTAT GTGGGCAAAG GGCCTTTCTC CTGGTAAGTT 240 TCTACTCACC CAGCCTCCAC CTGGACATCC TCCCTCCCTT CCTCCCTCCC CAGGAGCTGG 300 GCTGAGGGCC GCCCTACTGC TATCCATGGC ACTTGTCACC CAGAGCCCTG GTGAACTGTT 360 TGCTTGTATG CAGCACCCCT CACCACATGA AGAGCATCTC AAGGGCTAGG AGTCTCGTTT 420 CTTGTATCCC TGGTCCACCG CCTGATCTCC AGCACACATG AGGTATCCAT CAAAATGTTA 480 GCGAAAGGAA AGGAGGAAGG GAGGGAGGGA GGAAAAGAGG GAACAAAGTA ATTAACGAAT 540 CCCTAGCTGC AGGCACAGGT TGATTCTCTG CAATGTCTCC TTTTCTGTCA CAGAGAAAAA 600 GAGCACAGTT AGAGTTCACA GGGACCGCGC CCTGCCACAC ATTAATTTAT TCTCCAAACA 660 TTTGTGGAAG TTGCTAGAGA CACAGATGCA ACGTGTTTTC AGGGAGCTTA TGATCTAGCA 720 GTGGAAGCGC AACAGAAGTG CAATTCTTTC ATCCTTTTGC CCACATAAAG CAGGCAAGGC 780 ACGACGAATT TTGATGTCAA CTGCCCAGGC AGGACTTTGT CCCAGCCCAG CGACCCTCAC 840 GAGGCCAAGG GCAGAGATGA TAGTTGTAAT ATACTCTTCT GTCCATTTCC TTGATATTCT 900 CCTCAAGGGG TGGGGGGCGC CTGAAATCCA TCTGCCCCGG GGAGAAGGGC CTCGTGGGCC 960 AGCGCAGCTT GCTCCTCTGC AGACCCAGAA GCATTTGTGC GTCCCGGGCG TGGCAGGCCC 1020 GGCGCCCACT CCGCCCTCCC GCCCCTCCCC CGCGCCACGT CACCCGGGTC ACGTGAGTGA 1080 CCAGGCTCCT CACCCCAACC CCCCTCCCTA CTCCCGCCAG ACTCAGCTGC TCTCCCCGGG 1140 AGCTGGGGAG CCGGGGGCGG GCAGCCGCGT CTGTCCTGCC CCTCCTCGCC CCCTCCCCCG 1200 CAGCCTGAGG AGGGCGTTAA GCAAGGGGCT TCGGAGAAAT TAGAACCAGC GTTCTAAATT 1260 AAGGGGAGCA GATGTCCTTG TTTTGCTCGC GAGGCCTGGG TGGCCTGCTG TTCAGACAGA 1320 AATCGTTGAG GCGCTGACCT TCCGGGACTG CTGTCAATCT CCGCGTGCAG ATGGCCAGCC 1380 CGGAGCCTCG CCGCTCCCCT GCATTGGAAA TGCGGCAGCC GGGGGTGCCG GCAGCTTGAG 1440 AGAAAAGTCT GCGTGGAGGG GGGGTGGGGG GGATGAGGGG AGGCCCGGGG AGACAGAGGG 1500 CAGGAGAAAA AGGCCGGCCC CGCTCACAAT GGAGCCCCTG TGGCGGCCCC TCCGAGACAA 1560 TGCGGTCCCC CGGGACCCGC GGTGGGTTGC GCCAGGCCAG TCCGCGCTCC AGCTGCCTCT 1620 TCAGAACAAG GCAGTGCAAA TGTGCCCACT TGATTCTAAA TCCTCTTAGG CGCTGTCCAT 1680 GTGAACAAGG AAAGGGGTGG CCCTACGATC CTTTACAATC GGAGGCCTGG GGAGGCCTGG 1740 GAGCCCTGGA GCTCCGGAAA ATGTCTGCAC CACGCATGCA AATGGGTCAT TTCGCTTGGA 1800 GAGAGGCATC TGGCGACATC GGCAGAAAGG CTCTCTGCCC GGTAGACGGT GAACAAAACC 1860 CACAAAACCA GCCAGCCAAC AGCGTGCACT AAACACCCCT CTCTGGCCCT TCAATGCCAC 1920 CCGGAGTCCT GAAACATTTT CAGGTTGTTT CCCCTGGAGA GACGTCCCAT GAAATGTTCA 1980 GAAAAGCCAG CTGAGCTGTG CAAAGTCATT AGTCACCCAG GTATTTACAC TGTTTTTCCT 2040 ATTTCCTTTC TCTTTTGGCC TCTGTGGTCA GTGGTATAAA ATTCCTAGGA ACTCCCACCT 2100 AAACACCAGC TTCCTGTTTA TTCTTGCAGT GGCTTTAATG TTTCGCTGTT AAAAGCGGTT 2160 GACCAAGACA CTGAAACAAT CAGTAGAGGT TCGCAGGTGA ATGGAAAAAA AAATTTAATT 2220 AAAAAATATA TCTACTGCTC AGGTCAAAGG TCCAGGTTCA TTTTTACTGC TTATGTCAGA 2280 ATCGCAAAGG GGAAAAGGTA AAATTAAAAT GTAACTTAAT GCCTAAGATC TTGGTTCAGT 2340 TTCATTTGGC CCCTGTGTCT ACATGAACCT ATAAAATACG ATACACTAAA GTATGAATGT 2400 TTTCATTTCT AGCAGTGGAA GGCCTTTTTT TTTTCAATGT GGCATGACGT TCTTTTGTTA 2460 GAGAAGGTTA AAGTTCAAAA GTTCATATAT TAGCACAATC TGTGTGCTCC TGCGTGTGCC 2520 TTACACCTCG CTATGCCTGT TCCGCCTTAA TTTCCTGCAG CAAAACCTTG CATTTACAGA 2580 GCCATCAGAA TTGCAGCCTC CCTGGCCTGG AAAAGAACCC TCGAAGTCAC CTCATTCAAC 2640 CCTTTTCCAA TACTGAATTC CCTGTATGGC CCCTAGGGAG TGTTAGTGAT GGGACCCTTT 2700 CTACCTCAGA 2710
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