Tag | Content |
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EnhancerAtlas ID | HS044-10724 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:139080110-139081440 |
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) |
EN2 | MA0642.1 | chr5:139081161-139081171 | GCTAATTGGG | - | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_25255 | chr5:139080689-139081326 | Colon_Crypt_3 | SE_27739 | chr5:139079784-139081582 | Fetal_Intestine | SE_28684 | chr5:139079776-139081784 | Fetal_Intestine_Large | SE_33374 | chr5:139080779-139081372 | H1 | SE_40547 | chr5:139079989-139080783 | K562 | SE_47460 | chr5:139080822-139081271 | Pancreas | SE_58504 | chr5:139012442-139092243 | Ly1 | SE_59951 | chr5:139067745-139092302 | Ly4 | SE_65250 | chr5:139080266-139081646 | Pancreatic_islets | SE_68692 | chr5:139080032-139081559 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I139683 | chr5 | 139062979 | 139081910 |
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Enhancer Sequence | AAATTACTGG GAAGAAGTAG GGGTTCTCTG ATCTGGTAGT GTGGGAATCT GGGGCCACCT 60 ACCTTTTGAG GAGAGCTACC CATGAATGAA GCCAGCAAAG GGATACTGAC CCTTTTAAAC 120 TTGAAGCCAA ACACTCTTCT ACTTGAGCCT TAGAACGAGC CAGTAGGGTC CAATTTTGCT 180 TAAGCCAGTG TGTGTTGGCT TTTTGTCATT TGCAGCCTGA AGGTCTGACC AGATAGTGCA 240 TGCCTTGCCC ATTTCACCTT CAAGCCTTTG TCCATGCACT TCTCCTCTGC CTGGAATCGG 300 AGAGCCTTCC TCTTGCCCTC TCCTGACCAG CCATGCCTGT GTTTTGAGGC CCAGCTACTC 360 TCCTCCAGGG CGCTGGCTTC CATGCGGTAC CCTCCTCTTT TGGCCCCACC CTCCTGGAGA 420 GTTACCTGGA ATTCTGACCC CCAGCTTGGT GCTCAGTGTC TATGCCTACA ACTGCTGTGT 480 TAATTTCCCT TTCTGGGGGC TTGTATCACA CAGCCCCAAA GTAGGTTGTA AATTCTTGAG 540 TGGCATGAGC TGAGTCCCCT CCTACAGAGA GGGGTGATAA AGTACAGTGG TTAGAAGCTT 600 GGCTTTGGCG TCAGGTAGTC TCAGCTCAAA TTCTAGCCCA TCGGTGTGAC CTTTGGACCA 660 GTCTCTCCTT TTCTGAGTTT CCTGTCGGTC CACCCCCCCC AGTGCCGAGG GCGCCACTGT 720 GAAGCATTCA CAAACATACT CTCTGCCCTC AGAGGAGCTA AGGATGGAAG TTGGGGCAGT 780 GGCCCCAACC GGGAGCAGCC AATCAGGAGG CTGAGGTGGT CCTTCCCAGC CTGCCAGCAC 840 TCGGCTCTTG GGGGAAGAAC CCCCTCCACC CTCACACACT TCCTTCCAAG GCGCTAGGGG 900 ACCTTGGTCG GGGGAGGTCT GGTCGTCCCC TCCCCCTTCC GCCCCTTCCT GTCGTCCCTT 960 CGAGCTGGCG CTGCTCTGAG TTAATCTCCT TGCCCGTCAG GGGGTGACAG GAGGTGTCTG 1020 TCATTCGAAG CTGAGGCCGT CAGCCTTGCC GGCTAATTGG GGCGCGGGCA CCAGGAGCAC 1080 GGGAAATGGC CGGAGGGAAG GAGAGGGAAT GAGAGGGGAA GCCACCCTCA CCTCCTACCC 1140 ACCAGCTTGG GGCTGATCCA CATGGCTACT TAGGGGAGGG AGAAAGGAGG AAGGGACTGT 1200 GGGATGGGAA CTTTGTGACC TTGGGCATTG CTGTTCCTCT CTGGGCTTCA TATTATCATT 1260 CATAGTGATA ACAGCAAGCC TTTAATGAGC AATTACCGTG TAAATCAAGC ACACCTGATG 1320 AAAACCTCTG 1330
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