Tag | Content |
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EnhancerAtlas ID | HS187-10155 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:18895910-18897100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
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: 11 | 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 | chr17:18896858-18898757 | Fetal_Intestine | SE_28726 | chr17:18896591-18898838 | Fetal_Intestine_Large | SE_31857 | chr17:18895870-18896499 | Gastric | SE_33437 | chr17:18881926-18898915 | H2171 | SE_49309 | chr17:18896706-18898244 | Right_Atrium | 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 | CCAGAGCCCC CTGAGCAAGG GTGGAGCGGG CGGAGTCGGT CCAGCACCGG CGCCCAAGCT 60 CTAGGCTGGG CTTTGGGTGA GCCACACCTG CGTTCCAGGT CTCAGTTTCT TCACCTGTCA 120 AAGGAGAAGG TGGACAAGAT GTCCAAGGCC CTTCGTCTCT GATGTCCCTG CCGAGGGACC 180 CCAACTCCTG TTCCCTGCCT GGTGCCGGGC AGGGCCTGTC TGGGCGGCTA ACACATCTCA 240 TTGCGCCCAC AGGTCTGGGA GAGGAAGTGC TGGTGGCCGC CCTCTCCCTG CCTCCCCACA 300 CAGCTCCTGC CTCACAGGTG CCAACAACAG CCTGTGGCTC CTGACACCCA CAACAGCTGT 360 TTCCTAGCCT TCCTGTGACC ACAGAACCAC TCTTGAAGCA GAAGTGCCCT CGCAGGACGA 420 GTAGGTAGAA CAGGTCTCCA CAGAGGTGCC TGGGGAGGAG GGGTGGGGCG AGACGGGCTG 480 GCCTGGTTCC GAGCATGGTG GGAAACCACG GGTGCACAGG CCCAGCCTCT GCAGCAGCAC 540 CTCTTCAGGG GGGCCCTAAA CCAACGCATC CTGACCCCTC TCCCCGACGC TTCCTGATCC 600 CTCTCCCCGA CGCGTCCTGC CTCAAGCCAC TGTGTCTCCT ACATGTTGTT CTCCTTGCCA 660 CCTGCCCATT TTGCATCTGC TCGGACAACT ACCTTTTTTC AAATCCCAAC TCCAGTGCAG 720 CCCCAGCCTC CCCTGTCGTC ACTCTGGCCT GTCTGGGTTG AGCGTGTATC ACTTGCGTAT 780 TTCTTCTCAG GCACAGCAAT GGAGTCTCCC AAGGACTGAG TCGCAAGACT CGGGTAAGAG 840 GGGACAGTTT CCAACCTGCA CGTGACAAGC CTTACACTCA CCTCACCCTC CTAGGCCTCA 900 GAGATCCCTA GAGGCGGCTC AGAGAGAGGA GAGAGGCGGC CATATTCTCT CTCCTCACTA 960 TGCTCCAGGC AGGTGGAGGA CAGATACCCT CAAGCCTGCC CCAGAACCTG GAGCCCTGAA 1020 GCAGCCACAG ACACTGCACA CACTGCAGAC AAGTCCCTAG GCCTCTCTGG GCCTCACTTT 1080 CCCACCTGAG AAGTGCCGGG GGTGGACAGA GTCTCTCATC TTGGGGTTCG TTATTCTCCA 1140 GGTCTGATGG CAGATGCCCA GACAGTGGCA GTGTGGGCTC TGCACCCGCT 1190
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