| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08776 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:116611750-116614980 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr11:116612449-116612459 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr11:116612449-116612459 | GGCACGTGCC | - | 6.02 | | MYC | MA0147.3 | chr11:116613008-116613020 | GCCCACGTGCCC | + | 6.44 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I116742 | chr11 | 116613516 | 116613916 |
|
Enhancer Sequence | AATTTGATGG GGACACAGTG ACCAGGGTAA AGTGCCCAAG CTCTCTGTCA ACAAGTAATC 60
AGCATGAAGG TCCTATAACT TCAGGATGTA TGGGGGAAAA CAAGGAAGAG TTTATCCTGC 120
TGGGATATCC CAACCCCCCT TTTCTTGGGA GACCCAGAAA TGTGGCTCTC CCTAATCTAC 180
AACCATTCAC AGACTGATCT CTCCCTGACA ACAGAGGTAA TGTAAGTACG CACTGAACAT 240
ACACGTTTGA CACACAGTAA GTACTTAATG AAAGAGAGCA ATTAAAACAA TAATTTTTTT 300
CCCAGACAGG CATTCCTCTC TTCCCAGAGG TCTTGTCTAC CACCTCCCAA GCCCCTGGCA 360
AAAAGAGACA AGGGGCCAGG CGCAGTGGCT CACGCCTATA ATCCCAACAC TTTGGGAGGC 420
AAGGTGGGCG GATCACCTGA GATCAGGAGT TTGAGACCAG CCTGACCAAC ATGGTGAAAC 480
CCGGTCTCTA CTGAAAATAC AAAAATCAGC TGGGTGTGGT GGCGCACATC TGTAATCCCA 540
GCTACTGGGG AGGCTGAGGC AGAAGAATTG CCTGAACCCA GGAGGCAGAG GTTACAGTGA 600
GCTGAGATCG CGCCACTGTA CTCCAGCCTG GGTGACAGAA TGAAACTGTC TCAAAACACA 660
CACACACACA CACACACACA CACACACACA CGAGTCAAGG GCACGTGCCC CTCTAACACA 720
CTTGGTTAGG ATCTTCAAAG CCGAGTTCCA AACTGAAACT ACCAGCAAGC AGTTCTTCCA 780
GGACTGGGGA ACTCAGCTTC AAGTACACTA GGACCTCCTT GCAGAGGCTA TGAGAACCCC 840
TGGTAAGAAC TGCTCTGGAC AGGAAACAGT CCCTTGGACT GCCCCCTCAC CTCTTACCTT 900
GCTACTGGAG TGAAGATAGG TGGGGGTGAC AACTGCAGGG AGAGGAATCT GTTGTTTAAA 960
TTCTGACTCT TTCCCAACTC AGAGCGATTT TGAGCAAGTT AACCTCTCTG CACAATTGCT 1020
TCCTCTCCTA CTAAAAGGAA AATAAAGAAA ACAGGCCCTG TTTACTAAGC ACTAGAGATT 1080
GCATTTTTAC GTGTGACAGG ATAAAGTCAC ACACTTTGTA ATTCCTTAGC TGACAGAGGG 1140
CGCTGGATGT GATATGCGGA GGGAAAGACT GACTCCTTTT TCAGCAGACT GCTCTCTGTC 1200
CCCTCCCAAG GGGGTGGGTT CACAGGTACT GCCTGAGTAT CAACCTACCA CCAAGATCGC 1260
CCACGTGCCC TTGTTTTCTG AAAGGGTGAA GCTGTATAAG GCCAAGATCA ACACCATCAA 1320
GTTTGAATCA TTCAGGAGAG ATAAAGGAGA GACTGAGTCA TTCCAGTCTA TTACTACGTC 1380
TATTACTACT ATTATATTCT ATCTGAGCCA GAGTGTCTGC TCAGTGATTC TTCTTTTTTG 1440
TTGTTTTTAC ATTTTTTAAA TTTTATTTAT TTCATTGAGA TGGGGTCTCA TTGTCCAGGC 1500
TGGTCCTGAA CTCCTGTGCT TAAGTGATCC TCCCACTTGA CCTCTTGAGT AGCTGGAATT 1560
ACAGGAATGC ACTACCATTC CCGGCCTGTT TTAATATTTT TAAATTCAGA TATAATTATC 1620
ATACCATAAA GTTCACCCTT TTAAAATGTA CAATTCAGAG GTTTTTCACA TTGCTCATGG 1680
CTTCTTAAGT CTAAACTTGA AAGTGGAGGA GGCGCAAGAA AGGAGATTTG ATTAAAAGGA 1740
AAAAAAAAAT CTTCCACGTA GAGAAAGGTT TCCAAAGCCC AAGTAAGGGA GATTCTGGTC 1800
AAAACCTAAA TACTAGGTCT CTCTCTTGAA AATCTTTTCC ATATTGGAAA CAGGATTATG 1860
TTCTAGATCT AAGGCCTACT ATTATTAAGT GTGTATAGAC CCAGGGCTCC GCTTTCGCCA 1920
GTCTAGAAAA GGCATATCAC ACTGCCCTCT AGTAGACAGC CTAGGAAATG ACAGTCAGCT 1980
AGGGACTGGA CAGGCTTGCG ATCTCTGCCC TACAAGATGT GCTGTGTTCT CACACTTACA 2040
GGCAGAGAAA TTGGAGGGGG TGGAGTTTTT AAATGTTCAC TAATGCCTAC TAAATAAACA 2100
TAGAGCTCAC CTGAAACAGA ATCTAACTGC TTTCCCTACA CCTTAATCTC TGCTTAAAAA 2160
TAAATAATAC ATTCCTGCGC ATGCCTGTAA TCTCAGCTAC TCGGAAGACT GAGGCAGAAT 2220
TGCTTGAACC CAGGAGGTGG AGGTCGCAGT GAGCCGAGAT CGTGCCACTG CACTCCAGCC 2280
TAAGCGACAG AGCGAGACTC GGTCTCAAAA AAATAAAAAA TGAATAAATA AATAAATAAT 2340
ACATTCCTTT GTTAAGGGAA AAAAAGTGAT TTCAGATTTC TAAAGCCTCT GAGCCTCTTA 2400
AGAGTGAGGT GTTCCTAAGA AACAGCGTGA GGGTCCCACA AAAATGAAGT TAAAACCCGA 2460
ACCCATACAG AAACAAAACC TAGCTGTGCA GAAGGGGTGT GACAATGAGC TAGGAGTTGA 2520
ATGCCTCCTC TGCCACCTTG GGAAGGCGAG ACAGTAGGAT CACAGCCCAC AAGTTTCAAG 2580
CATGCCATAG CACTCCAGCC TGGGCAACAC AGCAAGATCT GAGCTGTAAA AATAAATAAA 2640
GTACTTCCAT CTCATAAATG CTGATTCTCG ACACAATTCC AGTTTACATT TTATCTCCCT 2700
ACCTAAGCCC TTCTCTGACA ATCACTGGCC AGAGTTAGGG AAGAGACATC CCTAACTTGG 2760
TAGTGACCCC AACTGATACT CCCTTCGGGA TTTTCAGGTC TCAAAACTAT TTAAAAATCT 2820
ATGTATGTCT CAAATGGCTG GGGGATGGAC AGCCTTTCTT TACAAGTCTG AGAAGTATAT 2880
AATGTGGCAA AGATAATATG TTATGTGTCC AACAACATCC ATTTATCCCT TCTTCCTGAT 2940
GCATATTATA TGCCTCGGGC TCCTTTGCAT TAAGAGGGAG CCTTGTGACT AGGTTCTTAC 3000
CAACAGAATA TGAGTAGAAG TGTGTGCCGC TTCTAGAGCT AGCCGGTAAC ATCTGCCAAG 3060
CAATCCTTCA CGTTCTGCTC AACTCACTAA AATGGTAATG CCCAACACAA CCTTGGAAGC 3120
CATAGTGAAG CTGGCATCAG CCTGATCCCT AAACAACTTC ATAGAGTATC TCACTCCTAC 3180
TTTCTCAACC TGAAACGACC TGCATGTTAC ACGAGTGAGC AGGGGGGAAA 3230
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