Tag | Content |
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EnhancerAtlas ID | HS101-06243 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:118647340-118649600 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr10:118649090-118649111 | GGGGCATGAAGAGGGGAAGGA | + | 6.27 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I116887 | chr10 | 118647426 | 118649143 |
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Enhancer Sequence | AATGAAGGGG GAGAAATCAA GGTTTGGGTG TGAGTAGGTC TGGATGTCTC TCTTGCAACA 60 AAAACAACAG AACAAATGAT CAACTACTGA GCAAAAGTAA CCTGCATGAC CCGGTCACGG 120 GCACAAAACC TCAAACCCAA AGACCACACT GCTTTTTTCA CTTTCTGACC AGTACTGTAA 180 GATCTGTCCA AATGTTTAAA AACCACTCCC TCTGGCTACT GGGTTATATT ACCTATGTGT 240 GGCTCGGTCA TCATCCTAAG TGACAAACAC TATGTCTTCC TTGGAGGTGG TAAAAACAAA 300 AATAATCAGG AGCCTGGGGA CAGGCTGTGC TGTAGTGAGG ACAGATTCCT TTATTTTTGC 360 CTGATTATGG CACCATGACA TTGTCCATCT ACCTTGGCCA AGGAACTACT TCTCCAGACA 420 TCTGCCGCTA TGCTTTGGGA ATCAGAATGG GGTGTAGTTT CTCCAGTGGT ACCTGTTTTG 480 ACTCTCTCTG ACCCACACAA TATTTAAAAG CCTGTGATGG GAGAAGCAGA ACAACTATGA 540 GTAATATTAA GGATTGATCA GAGGAATCAG ACCTTAGGGA ATGAGAGGCA CTAGTCATGC 600 CGTCTGTGTA AATCTGCTGC TTCTGCGTCT GACACTGGGC CTGCAGTCAG CTGTTCTGAC 660 AGTTGGGAGG GAAGGCGGCT GTAAAGTGAC AGAGACTGGG GACAAACTAG AGCTGCACCT 720 ATCTCTCTCT CACAAGCACC AATCTTGATG ATGCAAGACA ATCTGCAGAA TAAGCAGGAG 780 CCTTCCCCAA GGAGCTGCAC ATGCACCTGC CCCAGGATTT GGAAAAGCTG GAGGAGGAGA 840 TGTGGGGAGC TGGAGAAACT GTGGGCCAGT CACTGCCACA TGCCAGTTAG GTGAGTCAGC 900 ACATCAGGAA TGTCATGCAC AAGCTATAAC AGAGCCTGCC CTACACGGAC CTTCCGAGGG 960 TTAAAAAAAA TTTTTTTAAG ACAACTACTT CACTTCCACC TTCTAAATCT CATGCAGATT 1020 TATCTGTCGG CAACTCTAAA CTGAAAACAA ACAGGTGAGG AGATTCTAGG AAATAAAGCT 1080 GCAGCCCAGC TAAGGTTCCA GGGAAAGTCC CATCCAAGTC TGCAGATTGA GTCACCAGTA 1140 CGAAGGTTTC ACCATCTTGG GCCTGGGCCC ACTCTTATGT AAGCCAGTCA AACTGCTTTC 1200 AGCATGCAAA GGAGGTAGTA TTTCTCTCAT TCTAGGTGAG CAACTTCCAT CAACCCATAC 1260 TAACCTTCAT CACTTCTGTA GAACTACCAT GGATGTTTCC ATGCTCGTGT GTGTCTGTAG 1320 GTGAAGGGGT GGTGCACAGA TCCTAGAAAA AGCTTTCTTC ATCAGCTCAG GGCTAAAAAT 1380 TTCCAGGAAG TGCTCTCTGG GCTCCACAGC AGCAATACAT GGATGTTGAT TGAACTGAAA 1440 ACTCATAAAC CTAGTATTGT CAGGCTGAAA TTGTCCTGGA ATTGTCTCAG TCCAAAGAAC 1500 GATCTCCCTG TCCTGAAGCA AGCTTCTTGA CTGCAGATTA ATCTATTATT AAGTCACTTA 1560 TAGGCTACAA TTTGAGAACC CCTTTGTTAT CACTGAACTA GGCGCAGTGG GCATTTTCTG 1620 AATCTAGGCA TGGAGGGAGA GTGACTGGTT TCTCAAGGAT AATGACCACT GCCTTAGAAT 1680 CCCAGTGGAA GGTGGAAAGG GACTAGGGCA ATCGTCTAGT CTGACCTGTC CTTTTACAGA 1740 TGAGGATGAT GGGGCATGAA GAGGGGAAGG AACTGGCCCG AAACCACACA GCTCATCAGT 1800 GGCAGAGTCA GAACAAGAGT CAGAAGCTCC TGTCTCCCTG TTTCTGCCTT TTCCATGACA 1860 GCATGCTGTT TCTCAAAGGC ATCTTCTCCT AGAAACAGGA GGCTACAGGC TAGTTTTTGG 1920 CATGTTTACT GATTTCATTC TTTCCGAATC CGTTTCCATC TCCATCTTCC AGATCTGTAA 1980 ATAAAGTCTA TCCCTTCAAG CTATCCCTTA GTTTTAATTT TTCCCCTGTG GTTTGTAGCT 2040 CCTCCTGGCT TGACATCACT AGGTCCACTC TTGGCTCCCA CGGGCAGCTG CCCAAGACTC 2100 CTTCTGGAAT GAGAGTCCTT TCTTTCTCCT AGGCCTCATT CTACCTTCAT TCCTATCGTA 2160 TGGGAAGAGC CACAGAGCCG CATCAGTGAT GGTGCCAAGA ACCCAAGTTC TCACTCTAGT 2220 AGTCATGGTG GCAGGTTCTA GAGGGTTAAA TATGAAGCTT 2260
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