Tag | Content |
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EnhancerAtlas ID | HS073-05966 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr17:18894700-18896920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr17:18895252-18895263 | GCAGGGTGTGG | - | 6.62 | MSC | MA0665.1 | chr17:18896261-18896271 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr17:18896261-18896271 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr17:18896261-18896271 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr17:18896261-18896271 | AACAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23200 | chr17:18896005-18898165 | Colon_Crypt_1 | SE_23774 | chr17:18896053-18896631 | Colon_Crypt_2 | SE_23774 | chr17:18896672-18898105 | Colon_Crypt_2 | SE_24766 | chr17:18894655-18897891 | Colon_Crypt_3 | SE_26604 | chr17:18891559-18898201 | Esophagus | SE_27747 | chr17:18890621-18894968 | Fetal_Intestine | SE_28726 | chr17:18896591-18898838 | Fetal_Intestine_Large | SE_31857 | chr17:18895870-18896499 | Gastric | SE_33437 | chr17:18881926-18898915 | H2171 | SE_66943 | chr17:18881926-18898915 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I018992 | chr17 | 18896114 | 18898615 |
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Enhancer Sequence | TTCTATCCAG TTCACACATT GTCAGAGCTG GCCCAAGTCA AGAAAAGTAC CAGATGCTTC 60 ACGTAGCCCC AAGCCCACAC GTCCTCTCAG AGGTCCTGGG CAGGGCAAGG GCTGTGGAAA 120 TGAGAGGGGA GGCTGACTCC AAAGACCAGC TCTACCTGCT GTTATGTCAG GGGCCACACT 180 GGGCAGGAGG CGGGTGGCCT GGGTCCCATC ACTGAGCTTG TTCCGCTCCT GAGGCAGGAA 240 CCAGCCATGT CCATGTGAGC AGCTGGCACA GGGGCAGGCA TGGCAGGCGG GCACGTGTGT 300 GTCCTGCACC CCAGGTACCG TTGTCAAAGC CGACGGGCAG CTCCCAGCCC AGCAGCCTGG 360 AATCTGCGCA GGCCACACAG CCCAGCTCCC AAGTGAAGGA GGGAGCCCAG TGGTCCCTGT 420 GCATCTTACT GATGGACAGG CCTCTGCTGG GCGGCCTTGA GGCCTCGAAG ATGCAGCTGC 480 AGAACCCAGG AGGCCCAATG CCCAAGACAA CCATCTGACT CCTGCCAGGG TGTGGGAGGA 540 TGGCCCAAGA TGGCAGGGTG TGGGAGGATG GCCATGCCTG GGGGGCAGAG GCAGGCAGGC 600 TGCACTGGAG GGAAACACCA GCAGGGATGT GGGCACTCCT CCAGTGAGCC AACAGCGAGC 660 CTGCGCCTGC CCCAGCCCAG GCCTCTCCCT GGGGGCTCCT GGTGCCCAAA CACCTCCGGC 720 ATGTCTGTCC AGGGGTGTCC ATATGCACAA GCCCTCCAGC GCCCCGCCCG ATGAGCACCT 780 CCTCCCATGC TGTACCCTCC CTGCCCAGTG GATCCGCCGG CCTTCTCCAC CCTGCCTTCT 840 GCCTGTGTCT CGAATCCCCC ACCTCCCTCT GTGTCCTTGG GACAGGGGGA CATCCGCCTC 900 CATGTGAGAG ATGCAGAAAC TGCAGCTGGG AGAGGGGAGG GCACTGGTCC AAGGTGGTGC 960 TGCATGGGGA TCCCCAGTGC CCTGCCAGGA GCACCTCCAA CACCTGGGCA GTGACCGGAG 1020 CAGCTTGAGC TGGGATGCAG GGGTGACAGC ATCTCACACA AAGGAGAACC CCACCTGTGG 1080 CCACTGCCCC CCAGCAGACA CGGCCTGAAG CCACGTAACA CTGGCTGCTG GCGTTGGGGG 1140 TGGGACAGGG CTTTAGGTCA CAGAGGCAGG GAGCACAGGC GTGGGCCTCC TCAATCTCCC 1200 TCAGCCCCAG CCAGAGCCCC CTGAGCAAGG GTGGAGCGGG CGGAGTCGGT CCAGCACCGG 1260 CGCCCAAGCT CTAGGCTGGG CTTTGGGTGA GCCACACCTG CGTTCCAGGT CTCAGTTTCT 1320 TCACCTGTCA AAGGAGAAGG TGGACAAGAT GTCCAAGGCC CTTCGTCTCT GATGTCCCTG 1380 CCGAGGGACC CCAACTCCTG TTCCCTGCCT GGTGCCGGGC AGGGCCTGTC TGGGCGGCTA 1440 ACACATCTCA TTGCGCCCAC AGGTCTGGGA GAGGAAGTGC TGGTGGCCGC CCTCTCCCTG 1500 CCTCCCCACA CAGCTCCTGC CTCACAGGTG CCAACAACAG CCTGTGGCTC CTGACACCCA 1560 CAACAGCTGT TTCCTAGCCT TCCTGTGACC ACAGAACCAC TCTTGAAGCA GAAGTGCCCT 1620 CGCAGGACGA GTAGGTAGAA CAGGTCTCCA CAGAGGTGCC TGGGGAGGAG GGGTGGGGCG 1680 AGACGGGCTG GCCTGGTTCC GAGCATGGTG GGAAACCACG GGTGCACAGG CCCAGCCTCT 1740 GCAGCAGCAC CTCTTCAGGG GGGCCCTAAA CCAACGCATC CTGACCCCTC TCCCCGACGC 1800 TTCCTGATCC CTCTCCCCGA CGCGTCCTGC CTCAAGCCAC TGTGTCTCCT ACATGTTGTT 1860 CTCCTTGCCA CCTGCCCATT TTGCATCTGC TCGGACAACT ACCTTTTTTC AAATCCCAAC 1920 TCCAGTGCAG CCCCAGCCTC CCCTGTCGTC ACTCTGGCCT GTCTGGGTTG AGCGTGTATC 1980 ACTTGCGTAT TTCTTCTCAG GCACAGCAAT GGAGTCTCCC AAGGACTGAG TCGCAAGACT 2040 CGGGTAAGAG GGGACAGTTT CCAACCTGCA CGTGACAAGC CTTACACTCA CCTCACCCTC 2100 CTAGGCCTCA GAGATCCCTA GAGGCGGCTC AGAGAGAGGA GAGAGGCGGC CATATTCTCT 2160 CTCCTCACTA TGCTCCAGGC AGGTGGAGGA CAGATACCCT CAAGCCTGCC CCAGAACCTG 2220
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