Tag | Content |
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EnhancerAtlas ID | HS146-06426 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr17:39703770-39705750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:39705664-39705683 | TGGCCACAAGGGGCCGCTG | + | 6.17 | FOSL1 | MA0477.1 | chr17:39704340-39704351 | AGTGACTCATC | + | 6.02 | JUND | MA0491.1 | chr17:39704340-39704351 | AGTGACTCATC | + | 6.32 | Zfx | MA0146.2 | chr17:39704284-39704298 | CAGGCCTGGCCCGG | - | 6.23 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_25240 | chr17:39703505-39707319 | Colon_Crypt_3 | SE_34320 | chr17:39701952-39706192 | HCT-116 | SE_35061 | chr17:39703049-39706486 | HeLa | SE_36117 | chr17:39702860-39706091 | HMEC | SE_47260 | chr17:39702300-39707539 | Panc1 | SE_52581 | chr17:39703339-39706904 | Small_Intestine | SE_56788 | chr17:39703186-39706477 | VACO_400 | SE_57935 | chr17:39703220-39705718 | VACO_9m |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I041546 | chr17 | 39702965 | 39706888 |
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Enhancer Sequence | ATCCCTCCGC TTCCCACTGC TCTGCTCTGG GCTGTCTGAT CCCTGCTGCT CCTGTCCACA 60 CCTCCAGAAA TAGTTCCCTT TCTACACTCG GTCAACCCTG AGAGTCCGTC ATATTCTGTG 120 GGGCCCCTGG TGGATGCAGA TGTGGCTGAT CATCTACGTG GACAGCCAGG TGCAACACGC 180 CTGGTAGATG TGTGAACACT GCTTCGGTCT GTCTGTCTTA GATGATGGCT GGCTGGGAGG 240 GGCACTCCCC ATCCCCAGCA CACAGGCAGG AAGAAGGGCG TTGGCACTGA CCAGGAGAGG 300 CTGTGAGCAG GACAAAAAAG CAGCCAGACC CTCACCCCGT CTCTCCCCAC ACAGACCCAC 360 ATGCTGACAG GTCCCAGGAC ACATTTCTCC TGCCCACCCT CACCCCTAGG GAGCTCCGGG 420 CAGCGCAGAG GCTGGGCAAG TGGGACTGGC AGGGTGCCAT GCCTTGGTCC CAGAGGGCTG 480 CCTCCCTTCC TGGTAGGTCT GTGCCTGGTG CTGCCAGGCC TGGCCCGGCC TCCACACTCC 540 TTCCCCTTCA CACCACAATC TGAGCTGGCG AGTGACTCAT CCCACCATCC TCCTACGTGC 600 CCCGTCCCTG ACTCCACCAA ACTTGGCCTC TCTTGGCTCC ATCTCTGCAC TGGCTCACAG 660 CAGCAAAAGC ATGTCCACCC CCACGCCCTG CACCGCAGAC TAAGGCAGCT CACTGCACCT 720 CAACGAGGAA GAGCCAGGCT CTGACATTCC CAGCTTGGAT CTCCAAGGAG GTGGCTGTAC 780 TGACACGTGG ACAGAGCCCC ATGGCCCCCA CACTGACACA CTGGATCAGG CAACTCTGCT 840 GTCTCTTGAC ATCCATGATG TCCACTCCTT ACAACAACCT TCCAAGGGTT ACTGCCCATT 900 TTACAGATGA GGAAACTGAG GCTCGGGGAG GTTACATGAC ATGGCAGGTG GTAGTGGAGC 960 TGACTCCAAA GGCTCCTGCC TTCCTCTATA GCATCTCCCC CTCTACCCTG AGCCAAACTC 1020 CGGGAAGCCA TGAGTTGTGT AGGAAAGGGC TTGGGCACTG ACTTGGCGGT CCAAAGCCCT 1080 GAGGCCAGGC TCCGCCTTTC ATCAGCTGGC TGACTTCGGG CAAGCCCTCG GCCTCTGTGA 1140 AACTGTTTTC CAGTCCATAA CAGGAACAGG GATCCTGCCC TGCCCACCTC ACCGGGCATT 1200 CAGAGGCTCA GAGAGAAGAA GCAGCGTCTG CAAAGTGAAG TCTGGGGAAG GTGGTTGTGG 1260 GGTGCCTCAG CAGCCCGCCA CCGGAGCCCG GAGAGAGGCG GTGATGTCCG CTTTGGAGCC 1320 AACCTCGGCT CTGGACAGGG CAGGCTGCCG GCCACAAGGC CCCGTCTTTG CAAGCTCCCC 1380 AGGCGGGGTG CAGCTTCCTT TGTCCCTAGG CGGGGTGCAG CTTCCTTTGT CCTCAGACTG 1440 AACATCTCCC TCCGCCACCG GTGCGGGAGG AGCCCAGGAC CTCGCCAACT CGGCTTCACA 1500 GCGCCTCCTG GGGGCCGCGA GGGGACTCGC CAACCTGCCT GCAGGCGGGC TCCCTCCTAC 1560 CGCCTCCCTC TGCACCCCTG ACCCTGCTCA GTGCTGTGTG AGAGGAACGG TCAGAGGGAG 1620 CCTGTCTGGG CAAAGGCAGG CCCCACACTC CAGGCTGCTC CCTGGCCTCC CTACAGCAAC 1680 AAAGGGACGT TGAGCTGAGA GCAATACAAG AGAAAGAGCC CTAGGAGGGC TGGAAGTCCA 1740 AATGCCTGCA TTCTACCTTT GTGGCCCTGG GCATGTGTCT TCCCCTCTCT GGGCCACAAA 1800 AGAGTGGAGG AGGCCACCTC TCTAAGGAAA GAGAGCTCCC CGCCCAGCGC TAAAACTGTG 1860 GTTTCTCTGA CGCTCAATTT CCTGGCGTGT AACATGGCCA CAAGGGGCCG CTGCAGCCAC 1920 AGCTGTGAAG GAAACAGTTC ACACCGTGCT ATATCGTTCA TGGATAGTTC ATGGGGTTTT 1980
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