Tag | Content |
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EnhancerAtlas ID | HS184-06973 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:129697960-129699100 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_27353 | chr11:129697541-129700314 | Esophagus | SE_27846 | chr11:129697695-129699850 | Fetal_Intestine | SE_28695 | chr11:129697699-129699937 | Fetal_Intestine_Large | SE_35121 | chr11:129697671-129700326 | HeLa | SE_36539 | chr11:129697544-129701852 | HMEC | SE_64293 | chr11:129697692-129702002 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I129826 | chr11 | 129696789 | 129700444 |
|
Enhancer Sequence | TATACAGCTG TCTACTAGAT TATAAACTCC TTGCAGATAA AACTATTCAT TTCATCATTA 60 TCCATTGTAT TATTTCCTTA GCACCCAGAA GAATCCTGTA TTTAATTGGC TCATATGGAA 120 AATTTTAGAA AGAGAGAGAC AGCAGGGCTG AGACTATCTT CTGCTCAGGA ACCAAAACGA 180 GCTGGGAGGT AACAGAATTC TTTTTCATAG TAATTGTATT CCATATCATG GTGAAATCGT 240 GCCAGAACAA GCTTCAGACT CTTTCTGGTC TTACTCCTTC TGACCGTGCT GTTCCCAAGA 300 ACCTCCCACA CAGGAAATAA CAATGATGGC AGTAGCTGTC AAATTCTAAA GACGGGGATA 360 GACTCTGGAC CTCCTCAGGC CCCTGAGCCC ACTGTAGAGC AGGGACGTGA CTTAGTTGAA 420 GTTCAGGACT GCGGCCACAG TCACACCACC TGTAAGCAAT GGAGGACTTT CAACACAGAA 480 CTCTCTGCTT CCCCTGCATT CTGTTACTAA GCAGCTCATA GAACGTGAAG AGGTATTAAC 540 CTTGTTATTT GCAGAGTTAC AAAAAGCTGA GTCAGGTAGG TTTGGCTGTA TTCCAAAGCA 600 AACCCAGACC AGAAGCCACC TGAGAGTTCC TGCCGGCAAG GACAAATTCA GAATGTAGAA 660 AAACGATGAA AATAAATATT CTATGATCAC CCTATAACCT ACTTCCTTAC TGACCAAACA 720 CACGTCTCAT TCCCATTAAC AAGTTATGCT CAGCCACTGC CCTCTCTAGG ATTATGTGAT 780 GTTAAACAGT AATTCTGCCC ATTTAGGGTC AGCTACTCAA AAGCAAAGAA CAGCAACTTT 840 AGGTCAAAAT ATGTTCTTCT AGGAGAGAAG CCTAAGTCTC TCCCCTATTA TTGCACGAAT 900 AGTGTACCAG CACCAGACTA GAGAGGAAGT TAACACTTAT TAAACATGTA TTCTAGTCAC 960 CTGCTAGACA TTTTCAGGTA AGCCTCACAG GATCCCTCCA AGGTGGTATT AATGTCCCTG 1020 TTTTAGAAGG AGGAGTACTG AGATTCACAG ACATTAGAGA ACTTGTCCAA GGTCTTACCA 1080 GTAAAAGTGG CAAAACCAGG ACTGAACTTA GGTCTGACAC TACATAGTTC ATATTCTATT 1140
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