| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08617 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:102501060-102503720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr11:102503126-102503138 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr11:102503126-102503138 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr11:102503124-102503139 | AAACTAAAAATAGAT | + | 6.73 | | ZNF740 | MA0753.2 | chr11:102502329-102502342 | CCACCCCCCCCAC | + | 7.52 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I102629 | chr11 | 102500378 | 102502299 |
|
Enhancer Sequence | AGGGCAGAAG AGGGAAAGCC CATCTCTGCC TGGGCAGCTG AGAATGAGAG TAAAATGGAG 60
GAAAGTAGGG GCCAGGGCAG ACTTTCCATG GGGATGGGGC TTTAGTTGAG GGCTGATTGC 120
TAATGGAATT AGAAGTCACC TGCAAGAAGG GTGCAGTGAG AAGGAAGGAG AGTGACAGGT 180
AGTGGGAAGG GGGAAATTCC AAGCAGATGA GGCGATGAGG TAAGGAGATG TTAAAGAAGA 240
GCATCTCTTC TAAGAAACTG AAGATATTTC TATGTACAAG GCAGTTTGGG GGCAGCCAAC 300
AGGAGGTGGG CAGAAAAGAA AGGCAGAGAC CGGTCTGTTG GAGGACGCCT CTCACCCACA 360
GTTCCAGGTA CTGACACAGA AAAGCAGAGG CCAGGAGTCA TTTGCCGGGT GAACCTTGGT 420
CAAAGGGAAA GCCAGAGAGC AATTTCTAGC ACAAGCTGCA GATCCAAAGG GCAGGACTGA 480
CATGAGGCTC CAGGGTGCAG AGCTGGAATA TGGTTGGCAA AACAGAGAAG GCAGAAGATG 540
GGCAGAATGG CATGGAACAA ATCCGGAGCA GCCACAGTGC AGCAAAGGCT TGGAGGGCTT 600
GTGGGGTTTT ATTTAAAGGG CCTGGAGAGG AGTGTGCTGG GCAACGTCAC AGGCATCTTG 660
TGTGCCAGGC TAAGGCATCT AGACATTAAT GGTTTGTGAT GGGAAACCAC TGGAGAGTTT 720
CTTCCCCAGC AATGACATGA TGAGGTTTGC ATTTACAGGA AGATTGCTCT GAAAGGAGCA 780
TGCGGGATGG ATCGGAGGGG AGTGAGGATG GAGGCTGCCG GGGGCACCAA GGGGAGGGTT 840
ATAGGAGGTC CAGTCACAAG GCTTACCGTT ATGTTTATCT TAGGTCATGA ACTGTGAGAG 900
ACGAGCTGTC AGTATAAAGA GCATTTTGTT TATTCTTGTA AAATCTCTGG CATATATTGC 960
AATGATCACC AATGTGAGCT TTTGAGATTG GATAGTAAAT GTGTTTACAG CTGCCTGTGT 1020
AGAGGGCGGG ATGTCAAAAG TCCCATTAGA GCACATTCCA CTTGCCCAGT CATTTTAGTG 1080
AGTCAATTTG CTAAATTATA GACTTATTTC AGCATACAAA TCAGCAATTC TGGAAGCTGA 1140
TAGTTTGCCT GGCAGCTTCT TTTGAACATC TCCATTTTTT CTTAGAGTGT TGTCTACAGG 1200
TAAAATCAAT TTAACTATTT TGAAAGATCT ACCTTATCCC CAGTGCTATC GTCTGAATGT 1260
TTGTGTTGCC CACCCCCCCC ACCCAAATTC ATATGTTGAA ATTCTCGCTC CCAAGGTGAT 1320
AGCACTAGTA GGTGGGGCCT TTGGGGTGTG ATTAGGCTAT GAGGCTGCAG CCCTCGTGAT 1380
TGGAATAAGT GTCCTTATTA AAGATGCTCC GGGGAGCTGC CTTGCCCCCT CCAGCAAGTA 1440
AGGACACAGC AGAAAGGCAC CGTCTATGTA TCAGGGAAAG CTTCCTTGAT CTTGGGTGTT 1500
CCAGGCTCCA TAACTGTGAG AAATAAATTT TTGTTGTTTA TAGGCCACCT AGTTTATGGT 1560
ATTTTGTTAT AGCGACCCAA ATAAACTAAG ACAAACCTGG AGCATATTGT GGTGCCAGGT 1620
AGTAAAATGA TGAAGGAATG TTTAAAGGAC ACGATCCAGC TTGTTGGAGC CCCCTCTGGG 1680
TTAATCTAAG ACACTTTGAG CATCAAAATC CATAATGATA GTAATGGATT GTGGTCCATT 1740
GAATGAAATA AAAACTCATG AGTCTGTACT GATATAAACA AGCAATAATG GGGAGAAGAG 1800
AAAGCACTTC CTTATGGTAA AAAGGTAACA TAAATACATG TAGAAAGAAT GATGGCTTTA 1860
GAAAATATGC ATTTGGTCAA CAGGGAAGTG CAAACCAAAA CCACAGTGAG ATATCATCTT 1920
ACCCCAGTAA AAATGGCTGT TATCAGAAAG ACAAAAAATA GCAGATGCTT GTGAGGATGC 1980
AGAGAAAGAG ATGCGCTAAT ACACTGTTGG TGGAAATGTA ATTTGGTATG GCCACTATGG 2040
AAAACAGTAT GAATGTTTCT CAAAAAACTA AAAATAGATC TGCCATGTGA TCCAGCAATC 2100
CCACTGCTGG GTAAATATCC AAAAGAAAGG AAATTCATAT GTTAAAGGGG TTACTTCATG 2160
TCCATGTGTA TTGTGACTAT TCACAATAGC CAAGATACGG AATCAACCAA CGTGTCCATC 2220
AATGGATGAA TGGATAAAGG AATGCGGCAT ATATACACAA TGGAATACTA TTCAAGCGTA 2280
AAAAAGAATG AAATCCTGTC ATTTGCCACA ACGTGGATGG AACTGGATGG AGGTTGTTAC 2340
GTTAAGTGAA ATGAACCAGG CACAGAAAGA CAAATATGAC CTGTTCTCAC TCCATAAGTC 2400
GGAGCTAAAA AAAGTTAATC TCACAGAGGC AGAGATATAT GCTCTGGAGG ACATTATGCT 2460
AAGTGAAATA AGGCAGTCAC AGAACAAATA CTGCATGATT CCACTTATTA ATACATGGAA 2520
TACTTAAAAT AGTTAAACTC AGCCAGGCAT GGTGGCTCAG GCCTGTAATC CCAGCACTGT 2580
GGGAGGCCGA AGTGGGAGGA TCACTTGAGG TCAGGAGTTT GAGACTGGCC TGGCCAACAT 2640
GATGAAACCC TGTCTCTAAT 2660
|
