Tag | Content |
---|
EnhancerAtlas ID | HS197-06870 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr14:100893920-100896250 |
Target genes | |
| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_23539 | chr14:100895511-100896725 | Colon_Crypt_1 | SE_33398 | chr14:100880989-100894517 | H2171 | SE_34657 | chr14:100893938-100895784 | HeLa | SE_65652 | chr14:100892783-100897421 | Pancreatic_islets | SE_66879 | chr14:100880989-100894517 | H2171 |
|
| Number: 2 | ID | Chromosome | Start | End |
GH14I100428 | chr14 | 100895201 | 100895350 | GH14I100429 | chr14 | 100895669 | 100896442 |
|
Enhancer Sequence | GCAGGAGCCG GGGGTGACGT GTGGGTGAAG GATGTGCTGT GGGGTCCCGT CATCACTTGC 60 TTTATTAAGC TGGTTGTATC ACTTGACATC TTTCACCACT GAAGGAAATA GAGCTTGTTT 120 TAAGGTACAA ATTCAGGGGT GTCTGGGCTG TGAGAGAAAT AGCTTCTGGC AGGAGTGCTG 180 GGTTGATGGG CACCTTTGCC ACCACCCCAC CCATTGCCCA GGCAGGGACA GGAGGCCAGA 240 GCTGGGGAGG GGCTGGAGCC CTGGCCTCCT GGCTCTCAGT GGCTCTCAGT GTCAGGAGAT 300 GACTCCCTCT GCACCCCTGC TGTTTCTCCT GGTGATGTGG TGCTGGAGTG GGTTTCTCTG 360 GCCAGGACAG CCAGTGGAGG CCTTGCAGCG ACTGCCGTGC CCTCAGGCTG AGGCTCCTTC 420 TACGAGGCTG GAAGCCTTTT CCTCCTGAGA CCCTAACACG CTCCCTTTCC TTTCCTTTTT 480 GAGGGAAGCC AGGTTCCCTG CAGCAGGGCC TCATCACAGT TCCCCCTGGA GCATTCACGC 540 AAGGTCACTT TTCCCATCTG AGGAAACGTT TGTCGTGTGC TCCGACCGAA GCGTTGGCAC 600 TGACCCGTCT AGAATTCTGT GTGCGGAGTG GAGGTGAGAT GCTGAGGCTG TGCCTCAGCC 660 TATCTTGGGT CCCCCTCTGC CTACAGGCAG TGAGTGTGGC CTGGGAGGCA GGTGGCCCTG 720 TGGGGTGACT GAGCTGGGCG TTGTCCTTTC CTCTTCCTGG TGTGTGTAGC GAGCCTGGTC 780 AGAGCATGGC GTCTGGAGTC AGGCGGCCTG GCTACGGGTC TTGGGTCTGC CACTCACCAG 840 CCTGGTGTGG GCAGCCATTT TAGCCTTTCT GGGCCTCAGC GTCCTCCTCT GTGGATGGGG 900 GACAGTGCCT GAGCGCCGGG GGCTGCACAT GGTGCCTGTC TCTCTGCGTT CTTAGTGGAG 960 GTGGCCCCTG TGGTGGTCCC TGTTGATGCC GACCTGCTAG CCTGCTCCAT GCTGTCCAGG 1020 AGAGTACTGG GGCCTTGCCA GCGGAGCCCC CTCTTCCCTG GTCTTATCCC TCGGAGGTGC 1080 TCTGCTGAGA GCTGCCCCTG TGAGGAGCCA TTTCACTTCT TTCTTCAAGT GGATGTATTT 1140 TTGAACATTT GATACCTTCT TTCAAAAGTG CTGTACCTTC GCTTTTATTC TACTTTGAAT 1200 GTAATTTAGT TGCACATTCA TATTTAAAAT CTCATATGAA TTAATTTCAT GAAATTGGTT 1260 TGTTTTTCTT CTTCCATTTC ATGAAGCAAT ATCACTCAAG CTCCTCTTGC GTCTTTGGCA 1320 CCAGAGGCGT CATCCCCCGA GCCACTCTGA GTCATCTAAT ATGGTTTCCC GAGCGTGTCA 1380 GCTTCACTTC ACATAAGTCA TTTCAGATCC TGCACTTATT GAATCAGTGC ATACTGCTGT 1440 CACTGGGAAG TTTCCACTGT GCCGTAGATA CTCGTTTGTA ACATTTTAGA ACATTTTCTT 1500 CCATTTGGCA CTTTGTGTTT TGTCCCCCGG GTTTTGATCT AGGCTGCAGA ACAGGACCTG 1560 TCCTGACTCC GTGCTCAAAG TGCTGAGTGA CCCTGTGCTC CACTGAAGTT GCTCCATCCA 1620 CCTTCTAGAA CTCTGACGCC AGCTTGTCAT CAGCTTCTCG TTTCCTTGGG AGATGGGGTG 1680 GTGCAGCAGA GGCCAGCCTG CCGTGGGGAG GTGGGCTGTG TGTGCTCCCA TCCCTATGAG 1740 GCTAACAGGA GACTTACCTA TAAGCAGGCA TGCAGGACCT GGAGTGAAAG AAAGAGGAGA 1800 AGAAGTTGCC TCCTTGGGCC AAGGGGCTAA GGTGGCTCAG GATATGTCTG TTCATCTTAT 1860 ATCGGAGCCC ACTGTTCATC TGCCCTGAGG CCTTTAATCA CCAAGACCCC AGTGGCTGGG 1920 GGAAGGCCTA GGCAGTCCTA TACATACAGC TTCTGAGAAC GTCAGAAAAT CAAGGATTCA 1980 ACCCCATAAT ATAGGTGACA CTGCTTGTCT TAGTCTGCTT GGACTGCCAT AACAAAATAC 2040 CCTAGACTGA GTGGCCCACA CAATAGATAG TTTATATTCT CCCAGTTCTG TAGACTGGAA 2100 GTCCAAGGTC CAGGATCAGC CAGCAGCATT GGTGTCAGGT GTGGGCTTTC CCCTTGGGTT 2160 GCACACAGCC ACCTTCTCCA CTATGTGCAC ACATGGCCTT TCCTTGGTGT GTGCGTGCTG 2220 CTGGGGTGGG GCGGTGGGGG CAGGGAATTG GGGCAGGGAG AGAGAGGGCT CTTATGTCTC 2280 TTCCTGTAAA GATAGTAATC CTGTTGAATC AGGGCCTAAC TTATATGACC 2330
|