| Tag | Content |
|---|
EnhancerAtlas ID | HS148-02951 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr11:13281910-13284170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LHX6 | MA0658.1 | chr11:13283473-13283483 | GCTAATTAGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_36180 | chr11:13279937-13285048 | HMEC | | SE_64753 | chr11:13279910-13285129 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I013258 | chr11 | 13280212 | 13285064 |
|
Enhancer Sequence | TCCCTGGGGA GCCCACAGTC TAATGGGGAA GATCAAGAGC ATGGACCGAT CCCATACAAG 60
GTAATAGCTG CTAGAAGAGA GGCACGCATC TAGTGCCATG CAAACACAGA TCAGGGAGCA 120
ACGAACTCAG CAGGGGTGGG AACAGGACCC AGGAGCACTC CTGCAAAAAG AGGTGAGATG 180
TGGGGGGGCG CACTGCAGGG CTGAGCAGGA GGCAGTCAGT AGGCGATGGG ATTCCAGGTA 240
GAAGAAACAG CATGAATAAA GAAAGCAGAG CTAAAAGTAC ACAATGTTTT CAGGAAATAA 300
TGAGCAGGCA AATGTGGTTA GAAGCTCAGG GAGTGGCTGG TAATGAATCT GAAAGTTAGG 360
CAGAAAGTCA AGGAGTGAAG GGCCTTGGAT GGCCTATGAA GAATTTTGGA ATTTCTGTAG 420
GTGTGTATTC AGGGAGGGTT CCCTCAAAGG CTTTCAGGAG AGGAGGTGAT CTGAGAGCTG 480
CGTTTAGAAA GATGACTGAC TACTGCGTGA CAGATGGACA GAGGGGCAAG TCAGGGCAAG 540
CAGATGAGAC AGGATTCTTG TTTAGGACAC TGTTCCTCCT CCACCCCACC CTCACCTCAG 600
CCTGGCCTCT GTACACGAAT AGGTCTAATG GCGGATCGAG AAAAACACCA GTCAGCTTCC 660
GCTCTTCCTC CATGGCAGGG CCGACCTCGG CACATCCACA CTGCGGTTTT CTCTTGGAAG 720
GAAGGATCAG GCTAGCGGGG CAGTGTCCTC ATGAGGCCTC GTGCACACCC CTAAATCCTC 780
CGTTAGGAGA TGCCTGTAGG CCTGTAGCAG CCGCAGACAG AGCTGAGCCC TGGCTTCAGA 840
CTCTTCCCTA GAAGGAGCAA TGAGGAAGTT TATCCTCTAC CTTCCCAGGA GAGTATCTGC 900
TTGATGCTGG GTTATCTCCT AAACTGAATT TTGATTACTT TGTATTTAAG TTTAGGAACG 960
TCTCTGTCAT TTGGGAACTG CTTTTCTGGC TGCAGCTCAA CAGTGGCGAA CATGGACACT 1020
GGGAACAGGC CCAGAGTCCT GAAATGATTA ATATCCTGTG TTGTGGGACG TCCAAACGCA 1080
TGGATAGCCA AAGCATTTAG AGAGCCAGGC TAGGCAGTGC AGTGTGATGG CAGACAAGTC 1140
CCTTGAGTTA TACGGGGGGA AAGATGCTAC AATTCCATAC ACTAAATCAA TGAAATTGAA 1200
TAAAGGTTCT GAACCAAACC TCCCTGTGGA CATTGACTTT CGGGAAATGG CTCGGGGCTG 1260
GTTGGTCTGC AGAGCTCTGG CACGGCTTCT CCAGGGAGAC TCAGCCGATC CCAGGTTTAC 1320
CATCTTACAC TCTAGACCTG ATCCCTCACT TTGACCAGTG GCAGCCCTGA TCTCCTGACT 1380
GCCACAGATC AATTGCTTTG TTTATCTTAT TGTCAGCCTG TTTTGGAAAC ACTCTCCTAG 1440
ACTCCTTTCT GACTCATAGG TTAAGGAGCG TGAGTAATTC TTCTGGAACT CACTTGGAAC 1500
AGGAGGGAAC CCTTCCCATT TGATTTCCGG TCCTAAAAAA AGACAAGATA GTTCACACAG 1560
GATGCTAATT AGTTTTCCTA TTCAACAGTT AGCGTGGCCT AGTCCTGTTT GGAAAGCTGC 1620
CTTTTGTGCT GCAGGGTTTA GAAATTTGAA TACCTCCAGC TTTTATTCAG AATTTATAAA 1680
ATGACACCAG AATATCGTTT TGTTGTGATT AGTTTTGCTG CTAAAACTAG GGTTTTTGGT 1740
TTTGTTTTGT TTTTTTACAG AGAAAACCCA AATGATTTCT CTTATGAGAC ATAAAAATGA 1800
GGAGAAATGA ACAACCAGAT TTCTCTTCTA CATTGTTCTC GTTTTATTGT TCGTGGATGA 1860
AGGTAAACTC TCATTGTCCT CCTGCTGTAT TTTTTGGCCT GTCCTTCTAA GCAGTGATGT 1920
AAACTCATGA AAGCTTTCAC TCCAAATGGG TGTGACTCTC TTTGTAGCCA GAATGGTTTG 1980
GCGTTCACTT TCTATAGCAG AAATGGTAAG AAAGTGGCTT TATATTCTTC TGTTTCTAAA 2040
CTGGCTTAAG AGAGGACCAG CCCCTTTGTA GAAGTCAGAT ACCTGAGAGC TTTTCAGGTT 2100
GCCTATAGGA AGTATTCTAG CTCTGCTGGG GGAAAAACCA CGGAGCGCAA GTTCAAACTC 2160
TCACCTTAGG GGCAGGGTTA CAGGGAGCTT TAACTTTCTA CTTTATGCAG TTTTGTACAG 2220
TTTGCATTTT TCACAATGAA TGTGGAAGAC AGGACGAAAA 2260
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