Tag | Content |
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EnhancerAtlas ID | HS094-07341 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr11:67913460-67914950 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF5 | MA0136.2 | chr11:67913694-67913705 | ACCAGGAAGTA | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr11:67913579-67913594 | TGAACTCCTGACCTC | - | 6.22 | RARA(var.2) | MA0730.1 | chr11:67914025-67914042 | TGACTTCAGGGTGACCT | - | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_06593 | chr11:67913517-67915261 | Brain_Hippocampus_Middle | SE_23262 | chr11:67913531-67915399 | Colon_Crypt_1 | SE_27927 | chr11:67912746-67915438 | Fetal_Intestine | SE_31508 | chr11:67912040-67918103 | Gastric | SE_35342 | chr11:67911985-67915436 | HepG2 | SE_42889 | chr11:67912022-67915452 | Lung | SE_47694 | chr11:67913554-67915179 | Pancreas |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I068144 | chr11 | 67912141 | 67916582 |
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Enhancer Sequence | GTGATTCTCC TGCCTCAGCC TCCCAAGTAG CTGGGATTAC AGGTGCCCAC CACCACACTC 60 AGCAAATTTT TTGTATTTTT AGTAGAGACG GGGTTTTGCC ATGTTGGGCA GGCTGGTCTT 120 GAACTCCTGA CCTCAGGTGA TCCGCCCGCC TTGGGAGGCT GGGTTTTTGA GCTTTGTGCT 180 GTTGGGGCCC AGCCCTCAGG GCCGCGTGGG AACCCCCGGG GCGGGGTGTT CTATACCAGG 240 AAGTAGGCAG AGGGCCAGCC CGAGGACAGT TCGTTTCTTG CCAGTCCCCT GACCTCTCTT 300 GGCACACAGC CTGTGGCAGC AGCAGGTTGA AGCCAGACGC TGCTCAGACC TCACACCACG 360 TCGTTTGCCC AACCCAGAGA AAGCTCTGTC CCCGGCTTCT GGCTCCTTCT CTGCCAGGAC 420 TCACTGGGTG TGATGAGTTG GTCTTGGGGC ACTGTCTGGG CACAGCCTGT TTGCCCAACA 480 TGGCCTCCTG GGCTCCATGC TTCCGCAGGT GGGAGGGGTC TGGACTGGCC CAGGGGCTCT 540 GACAGCGGCT GGCAACCTGA GGTTTTGACT TCAGGGTGAC CTGAATCCTG CCGCATTATG 600 GAGGCTGGAG TCTCTGGGGG CTGCTTTCCC AGAGAAGAAG CTCCTTCCCC ATCAGCCTGA 660 CATTGGCTCC AAGGACTCCA TGTGGCTGGA GGGCTCAGGG CTAAGGGGAG GGAAGCCCCG 720 GGATGGCAGT GAGGGGTGAG GGAAGATTTG GGAGGTGACA TCTACAAAGA GACCTGAGCG 780 GGTGGGGCAA AGAGGGGGTC CCAGGCAGAG GGAGAAGCAA GTGCAAAGAC CTTCATAACC 840 CAGGGGAGCG CTGAGACCAC CGACCAGCAG CACCCCCACT TCTTCAAGCC ACCACTCCTC 900 AGGGCCTCCC AGGGGTCCCC AGCCTGGAGC ACCCCATGTG GTAGAGCTGG TAGGCTGGGG 960 GACACTGGGG ACTGCTGTCC CACTTGGAGC CTCGGGCTAC TCCGCCCAGG AGCAGCGATG 1020 TGGAACCTTG TTGGATTTTC ATGTTCCCAA ACATCCAGGA GACACACAGT TGTGAGTTTC 1080 CAGCCAGGCG ATCTCTAAGG CCAGAGCAGC CCTTGTGGGT GTCAGTGAGG AAGGGCAGAA 1140 AGACTCTGGC CTCAAGCTCA GCTCCCTGCT GCAGGGAGTT GAACGCCCCT TTGGTGAGTG 1200 GCTCTAGCTA AACAAACACG TGTTATCATC TGTCAATAGC GGCCACCTCC TTGCTGGCTG 1260 GGCTGCTGCT GGCTCAAAGC CCAGAGCAGC CCTTCCGGGG CACTGCCTGC CACAGCCAAC 1320 AGTCAGGGAA GGGCAGCTAC TGCCCTGGGT TCAAGCCCGG GCTACCCCTG CTCCTGCTCA 1380 CTGTGTGTCC CCAAGCAAGT CACTGTCCCT GCCTCTCTGT ACAGTGGGAG GCCTGGATCT 1440 CTCTGCTCTG GGAAGACACC CAGCCCTGGA ATGGTTGGGC CACACTTGGG 1490
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