| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10512 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:69234180-69236530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr11:69235505-69235520 | TAGTGACTCAGCAGA | + | 6.38 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_57195 | chr11:69235110-69235906 | VACO_400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I069419 | chr11 | 69233914 | 69236690 |
|
Enhancer Sequence | GCACAGCTCC GGGCATGGGT GCAGGGATCA CACTGGACAC ACCAGATTCA GACCCTTCCA 60
GAGCCCCTTC CCTGCTGCAG GGGGCAGAAA AGAACAGATA AGCGATGGTG CATAGTGGGG 120
CAGCAGCTAC CCCCAGACTT AAGAAGAGGA CCAGGACATT TTTCGGGTTT CTGGTCAATT 180
AAATGGAACG CCAAGCAGAG TCATGTTCTC AGCATCTATG TTTAACAAAT CTATACTTCA 240
AATGCACACC CTCTCTGCTG AAAGAACACA GTCCCATCGA AGTATTTTTG CCTGATGGGA 300
GGGATTAGAA TTTCCGTGGC AACATTACAT CACTTTAGAC CAAAGCGACA GTGTCTGGGA 360
AGACAGAGCT GGTTCTGCAC GTACCTCCGC TCCACAGTCA CGGACACTGA GGTGCTCAGG 420
GGTCGGCGCT CAGGATCACT GGGCAGCCGT ACGTGTCCCA GGCAGCGGGA GCCCCGGCAG 480
TGCCAGCTCC CACACCATCC GGCTGTGACA ACCTCAGGTC CTTGATGACA GGGAGCCTCT 540
GCCAAGACGG TCCGAAAATT GGGAAGGGGA CCCGCTCATC TTTGTGGGGT CCCCAAGAGC 600
TTCAGATAAG TTTGCTGAGC ACCGGCTTCC TGATCACATT TCACATTTGA CCAAACGATG 660
TTCCTCTGCA GCCTCCCTCC CTTGGTCCCC AAATTGGCAG CACTTTCTAG AAGCTAGATG 720
CAGAGGATGT CCTTTGTCAA GGGAAAAAGA AGTGTTTCCT TTGGGATAAA AGGACACACA 780
CACGAGTGTT TATGCACATG CAGATACGTC TGCCTCTCTC TATGGACATG TATAGAGATT 840
TGGTTGTTTA TGCATAAAAT ATCCCTGCAT GGATACCCAG GAAACTGGTA ATGTCAGTTG 900
CCTTTAGGGA GGAAAACTAG GGGTCTGGGA GTCTTAAGTA GGAGAATTTT TTAACCATAT 960
TTTATATTTT TTTAAATTGT TCTACTCTGA GAAAATTTGA AAGTGTATAA AAAGCAAGCT 1020
CTGAGCCCCT TGTCTTCAAC CCCGGGGCCT CTCTTGCCTG AAGTCCTGCC ATGAAGATGA 1080
ATCTCTGCCT GTACCCAGTT CCGTCAGGGT CCTGCTAAGG GGTGAGCAGA GGACACCACA 1140
CCGAGGGGCC ACCCATTGTC TCCCAACCTC GGTTCCCAGG ACTCCCGTCC CCACGGGCCC 1200
TCTAGACTCT GTGAGGCTGT GATTCTGGGC AGGGTGAAGC CGGACATGCC GCAGGGCCGA 1260
TGCCGGCCGT TGTGGAACCA GCCCTGGAAT CTCAAAAATG TCCTGTGGTC AGGCCTGAGC 1320
TTTGTTAGTG ACTCAGCAGA AAGCACCCAG CCCTGGCCCC GTGGCAGGTA GGCCAGCCCC 1380
AACCTGGGGT GCAGCCTCAG GCCTCCAGCG TCCAGAGCCC AGGCCTGTGG GGATGTGGGC 1440
CCAGTGGGTG AGTGGCCACT GTCCAGACCC TCTGTCTCAG CGAGGCATCA AAGGCTGGCA 1500
GAGTTGGCTG CTGGGGGAGC CCCTGGATGG GGCCAGAGCC CCGGCTCTGG GCTGAACTGT 1560
GTCCTGACCT GCTGACTGAC TTCCAAGGCC TCAGTTTCCC CATTCACAGG AGAAGACCAA 1620
CTGCATGTAA GCAGAAGCCT GACATTAGAA ATGCAGCTGT TCTGTGATGC AGGTGGCGTG 1680
CTTGTCAAAG GAGGTTGACA AGCCTCCCAG GCTGCGTGGC CACAGGCAGC CTCCATGCCC 1740
TGGAGCCCCA GTTTCTCCTC CATGAAATGA GGCTAATAAG ACTTCCTCCA GGCCGGGAAC 1800
CGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCAGGCATA TCACTTGAGG 1860
TCAGGAGTTC GAGACCAGCC TGGCCAACAT GGTGAAACCC CATCTCTACT AAAAATACAA 1920
AAATCAGCCA GACATGGTGG GACGCACCTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG 1980
GAGAATCGCT TGAACCCAGG AGGCAGAGGT TGCGGTGAGC CGAGATTGTG GCAGTGCACT 2040
CCAGCCTGGG TGACATAGTG AGACTCTGTC TCAAAAAAAA AAAAGACTCC CTCCAGTATC 2100
CGTGCTTGGG ATGATTAAAT GAGACAGTGC AGTCTTTAAG ACATCAGCTG CCGCCAGCAC 2160
CTTGAGGCTG CTGAATACCA CCTGTCCCAT CACTGACACG ATGCTTCCAC TCTGCTTATT 2220
TTCTTAAATA AATGTACTTT TACTGGCTAC TTGATAGCAC TGCCATATGT GGTGGATCAA 2280
CGTCACTTGC CATAAATAGA TTACACATTA AAAGTCACCC TTCACAATAG GGCTAAAACC 2340
CAGCCATCTG 2350
|
