| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23351 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:13041560-13044360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:13043065-13043080 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_40479 | chr19:13042365-13042943 | K562 | | SE_40479 | chr19:13043191-13045483 | K562 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I012931 | chr19 | 13042366 | 13042943 |
|
Enhancer Sequence | GACCTAGAGG GAAATGTGGG GAGGGTGTCC AGGCAGGGGT GAGGCTCAGA GCCAGGCACC 60
CCCTTTCTGC AGCGCTGGGT CCCAGGTTGA AAGCACAGCC CTTAAAGCTA GGTTCACATC 120
CCAGCTATAC AACTTTACAG CCAAGTGGTC TCAAGGGAAA GACTTCCCCT TGCTGTGTCT 180
CCATTTCCCT TATGTAACAC AGGGGTAGTA ATAATGATAG TTTACACCTC CCAGGGTAAA 240
GTACACCACT AAAGATGTTA CCTGGCAGAA GACAAATTCT GTCGGTTTTG AACCTGTGAC 300
AGATTTTAAT GTGAAAAATT AGGTGAACTG ATATGTCTCC ACATTTTTTT GTTTGTTTTT 360
GTTTTCTTTG AAAGGGGGTC TCACCCTGTC ACTAGGCTGG GTGCAGTGGT GTGATCATAG 420
CTCACTGCAG CCTAGACCTC CTGGGCTCAA GCGATCCTTC CGCCAGTCCC GAGTAGCTGG 480
GACTACAGGC ATGTGCCGCC ACACCTGGTT AATTTTTAAA TTACTTTTTT TTTTTGAGAC 540
GGAGTCTTGC ACTGTCGCTC AGGCTAGAGT GCAATGGTGC GATCTCGGTT CACTGCAACC 600
TCTGCCTCCC GGGTTCAAAT GATTCTCCTG CCTCAGCCTC CCGAGTAGCT CGGATTACAG 660
GTGCCCACCA CCACCCCCAG CTAATTTTTG TATTTTTAGT AGAGATGGGG TTTCACCATG 720
TTGGCCAGGC TGGTCTCAAA CTCCTGACCT CGTAATCGGC CGACTCCGCC TCCCAAAGTG 780
CTAGGATTAC AGGCGTGAGC CGCCGTGCCC GGCCCTTTAA ATTACTTTTT AAAGACAGGG 840
TGTTGTTATG TTGTCCAGGC TGGTCTCAAA CTCCTGGCCT CAAGTGATTC TCCTTCCTCA 900
GCCTCCCAAA GTGCTGGCAT AATGGGCATG AGCCACCATA CCCAGCCTGT CTCCATGTTT 960
AAATGTTCAC ATGTCAGTGC CCAGAATGTC AGAGACGGGC CCTGGAGGTC CACATTACAA 1020
ACAAAAACTG AGGTTCCAGG TCCAGAGTCA TGAAGACAAG GACAACAAGG GTAAGTAGAG 1080
TGCACAGGGC CTGGCTCCCA CTTCATTCTA ATCCCAACTC TGCCCTTCAC TTACTGTGTG 1140
ACCTCAGGAA AGTTGCTTAA CCTCTCAGTG ACTCTTCTCA TCCATAAGAG AAAGGTGTGA 1200
TGGGTTCTAC CTCAGATGAT TTTAAGGAGT AGCTAAATTA ATACTCAGAA AGAATATATA 1260
GTGCCTACCA CGTGACAAAC ACTGCATAAA TTTTTTTTTT TTTTTTTTTT GAGACGGAGT 1320
CTCGCTCTGT CGCCCAGGCT GGAGTGCGAT CTCGGCTCAC TGCAACCTCC ACCTCCCGAT 1380
TCAAACAATT CTCTGCCTCA GCCTCCCAAG TAGCTGGGAT TACGGGTGCC CACCAACACG 1440
CCTGGCTAAT TTTTTTTTGT ATTTTTAGTA GAGACAGGGT TTCATCATCT TGGCCAGGCT 1500
GGTCTTGAAC TCCTGACCTC GTGATCCACC CGCCTTGGTC TCCCAAAGTG CTGGGATTAC 1560
AGGTGTGACC ACTGCACCCG GCATAAATTC TAATTACTAT AATTATTTTT ATGGCTATTA 1620
CTGTCATTAG ATTGAACCTC ACCTCCTTAT ATTATTTAAC CCTCTGTGAC GTATACAAAT 1680
GTCAGATCAT ATTGGTCAAG GCACTGTCAC CCCACACAAC ACAGCTGCCA TCTCTCCTCT 1740
GCATTGAGGA CTATGGGCTC TGCAGCCTGA GTGCCTAATT TCAAATCTGG GCTCATCGGC 1800
CTCTTCTATT CACACTGATT ATGTTACTGA CCATCAGTTG TCACATCTGC AAAATGGGAA 1860
TAACATGGCC ATCAGCCAGG ATTATGGAAT GGATTGGACA AACAAGCTGA GACCAAAGTG 1920
GGGCACAGAA CATGAGCTCT ACGGATAAAC AGCCCAGATC CTGGCCCCAT GGATCTAGCC 1980
TTCTGGGTGG CCCACGGGCC CCTCAGCATC CTACGCCTGT GACTCTGTCA CTGTCCACTT 2040
GCCCAAGTCA GAAGGCTGGA CTTCATCTGT GCGCCCCCTG CCTTGTCCTG AATCCCACGC 2100
CTTCCCCACC TCCCCCAAGC TTCCTTCCCA TAGCCAGACA TCATGCCCTC CAGCTTGGGG 2160
AAGTGCCAGC TTCTTCTTTC ATCCCTTCAC CTCCAGTCCT GTCCATGCCA ATTCTTCCCA 2220
AAGGTGATGT GGATAGCACA CTCATCTGAC CGGCTCTAGC TCCTGCTATC GCTTCCCAGT 2280
TCCCTCATGA GGTAAAGACC TAAGAGGCTT TGCAATTACA GCTATGCTGG TCTCCCTTGC 2340
CGCCTGCCAT CCCCCAAGAT CCCGGCCACT GATCTCTAAA GTGCTATCAC TTTCCTCAAC 2400
AGAGAACAGA CTCAGCCGTC ACCTGCACCA GGCCGCTCTC CCTGACCCCC AAGGCTGGGT 2460
CAGCTGTCAC AGCTGGGTCC CCTGTTTTCC CCCATCACTC TGGTTCTTGA AGCACCTTCC 2520
TATTACGTCG CAACCTGCGT GAGGGCAGCA ACCGCGACTT CCTCGTCCAT CATCGTACCC 2580
TCTACCCACG CTGACCGTGC CTCAATAAAC GTTTATTGCA TGAGGAACAT CCGTGCGTCT 2640
GGGCCCTCAC TCGTCCCACT TCCCGCCCGC ACATCCCGGA GTGGACACAT ATACAGCTAC 2700
CCCAAACTAG GCCTGAGGGA ATTTGGCTTG GACGTAGAGC GCCCGTGGCA AGGGGACTGT 2760
AGGTGCAAGG GCAAGGCGGT CCGGCATCAC GGGCCCGGCT 2800
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