Tag | Content |
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EnhancerAtlas ID | HS101-39151 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr7:369450-371270 |
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) |
ESR2 | MA0258.2 | chr7:371028-371043 | GGGTCAGCGTGGCCT | + | 6.43 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_24141 | chr7:369546-369918 | Colon_Crypt_2 | SE_24141 | chr7:370018-371229 | Colon_Crypt_2 | SE_28128 | chr7:368992-371275 | Fetal_Intestine | SE_29038 | chr7:368980-371516 | Fetal_Intestine_Large | SE_31770 | chr7:369489-371372 | Gastric | SE_65801 | chr7:370052-371297 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I000329 | chr7 | 369138 | 371197 |
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Enhancer Sequence | TCCCGGGTTC ACACCATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGACT ACATGTTCCC 60 GCCACCACGC CCGGCTAATA TTTTGTATTT TTAGTAGAGA CGGAGTTTCA CCGTGTTAGC 120 CAGGATGGTC TCAATCTCCC AACCTCGTGA TCCACCCGTC TTGGCCTCCC AAAGTGCTGG 180 GATTACAGGC GTGAGCCACA GCGCCGGCCG GCAACTGGCA TTTTAACACA TAGAAAGACA 240 CCCAACCACA CTGGTAACAA GGAAACACAA ATTGAAACTA AATGGAGGTT CCATTTTATG 300 ACGGGTCAGA CTGGCAAAAA GCAAAATGCC AGGCAACCCT CAATGTTGAC AGACTTGTGG 360 GGAAGCAGGC GCTCTCGTAC ATAGCTGATG AAAGGACAAG TTAGCACAAC GTTTATGGCC 420 ACGAAGTTGG CAACATCAAT AAAAATGTAA ATGCATCTGC CCTTTGGCCC GGCAATTCTG 480 CTTATCCTAT AGATACCATT GCGCACAGGT GAGGCCGTCT ATGTGTGAAA TTACTCACTG 540 CAGCATTATT TACAATGGCC TAAAAGCCCG TTGATAAGAG GTTGTTATAT AAATCATAAT 600 AGATCCATAA AGTGAAACAC AACTGTAAGA AAAACGAGGA GGCTGGGCAC AGTGGCTCAC 660 ACCTGCAATC CCAGCACTTC GGGAGGCCTA GGCGGAACGC TGGGCAACAT GACGAGACAC 720 CGTCTCTACA AAAATAAATT AACCGGGCAT GGTGGTGTAC ACCTGTGCTC CCAGATACTC 780 AAGAGGCTGA GGCGGCAGGA TGGCTTCAGC CCAGGACGTT GAGGCTGCAG TGAGCTGTGA 840 CCGCATCACT GCACTCCAGC CTGGGCAAAA GAGAAAGACC CTGTCAAAAA ACAAAAAAAT 900 AAAAAGGAGT CCACTTTTGG CTTCCATCAA CCAGGTTGGA GAAAACAAAT GACCACATGT 960 GTCTCAATGT GTCAGAGAGT TACCAAGGCA GCCAGGACCT GAAGGCCCAA GACATTGTGG 1020 GGGAGGGAAA CGCGTTGAGG TGACCCGAAC TTCTGCACCC TTTGGGGCAA CCGCAAACTC 1080 ATAACTGGCA TGAGCAGAGA TGCTGAGAAG CTGAGCAGGG AGGTCTGCTG AGAATCCGAG 1140 AAGCTCAGAG GAGCTTTCAA CACTGTCGTG CCAGCAGGAA GACGAGAATC AGAGTGCAGG 1200 ACTGCTCACA CAGCCAGGGC TTGGAGAGAC AAGATCCCGG GGAGAGGAAA GGATCCCAAC 1260 AGTCCAGGGT GTCTGTTTGC AAGCAGCACA GGGTGAGCGC AGAGGGGCTG AGCAGAGGCT 1320 GCTAGGAATC TAAGCAGAAC TGCGGGAGCC CTGCAGTGCC GGAGAGGGAA AGACGGGCTC 1380 AGACCTGTCA TGCCAGAGGA TCCCTCGGAA GCACCTGAAG CTTTCATATG GACCCCTGAA 1440 GGACAACCTC TCCTCTCAAC TCTAGATTTA AATCCAAGAG GTTTCTTGAG CTTGAAGTCC 1500 AGCAGGCATC TCAGCCAGGA CATGCTCAGA ACAAACTCCC CATTGTCCTC CCTGCACTGC 1560 CCTTCCCCAC TCCCCACTGG GTCAGCGTGG CCTCATCCCT CTAGCTAGTT AGGCGAGACC 1620 CTGGGCTCAG CCCAGACTCT CCTTTCCTCT CATCCCCACG CTGAATCTGT CAGCAACTCT 1680 TGTTGGCTTC ACCTTCAAAA CATACCTGGA ATCAGACCCC TTCTCCCCAC TTCAGCACCA 1740 TCCTTTGGCC CAAGCAACCA TGTCCTCTCC CCCGTCCCCC GGCACTAGTA CCCAAGCCAC 1800 CATTTCCTTC TTTCTGCATT 1820
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