| Tag | Content |
|---|
EnhancerAtlas ID | HS091-31035 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr20:42159530-42161410 |
Target genes | |
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 | chr20:42160137-42160152 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I043530 | chr20 | 42158846 | 42160370 |
|
Enhancer Sequence | TGAGTGCCCC TGAGTGAGAG TGGATGTCAC TCCCATGTGC CAGAGTTCAC TGCAGCTGGC 60
CCAGGGTATC TGACTCATCA GAAGGGAGCT CATGTGCTGG TTCTCTCAGC TTTGTTCTGA 120
TCTCTCATAT CAGATGGGAG GGGTACAGCT GGGCAGGGTC CAGGGCCAGA GATGGGAAGC 180
TGGTTATAGG TTTTTCCCGA CTTCCCTCCC TCCTTTGCTA CTGCAGATAC CCTGTCCTCA 240
CATCCCCTTG GAGCCCCTGG CCCACTACCC TAGTCTGAGC ACTGAGATGT CATTGCTCAT 300
ATATTCTTGC TTTGGCTTGC TCTGCAGTTC TTTGGTGTAA GGTCAATGCC TCTATTCTGG 360
GAGCTTCTTT TTCTTTCCTT TTGCCCAACA TTGAGACTCT TCCATTTATT TCCAACAATT 420
CATCCCTTGT CCTTTCCTCT GTTCAGGGCA GCTGGCAGCT TATCCAGCAG TTAAAGTATC 480
TCATAATCCC AACCAAAAGG CCTAAGAGAT ACAGGGAGCC TCCATTAAAA ATATCATACT 540
GGACCAGGTG TGGCGGCTCA TGCCTGTAAT CCCAGCACTT TGGGAGGCTG AGGCGGGTGG 600
ATCACCTGAG GTCAGGAGTT CAAGACTAGC CTGGGCAACA TGGTGAAACC CCCATCTCTA 660
CTAAAAATAT AAAAAATTAG CTGGGCGTGG TGGTGGGTGT CTGTAATCCC AGTTACTCAG 720
GATGCTGAGG CAGGAGAATC GCTTGAACCT GGGGGGCGGA AGTTGCAGTG AGCCAAGATC 780
ACGCCATTGC ACTCCGGTCT CAGCAACAAG AACGAAACTC CGTCTCAAAA AAAAGAAGTA 840
TGTATCAGTC TTACTGGCTG GGTGCGGTGG CTCACACCTG TAATTCCAGT ACTTTGGGAG 900
GCTGAGGCGG GAGGATCACT TGAGCCCAGG AGTTTGAGAC CAGCGTAGGC AACATAGTGA 960
GACCCCATCT GTACAAAAAA TGTCATTAAA TTATTAGCTG GGCATGGTGC ATGTGCCTGT 1020
AGTCCTAGAT ACCACAGTAG CTAGCTGAGC TGGGAGGATT GTTTGAGCCC AGGAATTCAA 1080
GGCTACAGCA AGCTATGATT GTACCACTGT ACCCCAGCCT GGGCGACAGA GTGAGACCCT 1140
GTGTCTAAAG AAAAAAAACC ATATTGAATG TCTAGAGTTT CCCTGGGCCC AGGACTCCAC 1200
CATGCTCTTC AGGCAGAGAC AGTTACTCCC CTACCCCAGT CCAGCCCCAG AGTTCATACT 1260
TGCAAGTTCC CAGGTGACAG GTGGGGTCCT GCCTGCTGTT GTGACAACGA ATGCCGACTT 1320
TTAATTCAAA CTATTTAAAT ACTGGCCCCG CCGTTGACTA GCATTGTGTT CTGGGCCAAG 1380
TGATTTAACT TCTTAAATGG GAATAGGGTT GTTGTAAAGG TCCAAGGAGG TGATGTCTTT 1440
TGAAGCTTAC ATGGCAGGTA CTCAGTTTAT ACTGGTTCCC TGTCTGCCTC TATGCCATAG 1500
ATGTCCGCTG TTTCTTCCCA GCCACCCCAC TGTTGCCACA ACTGCCTCAG GACAAGCTGG 1560
GAAGGGCTTG TCTGGGTAGG GAAGATTTAT ACTTGGTTCA CCAGGTTCTT TGGGCGAACG 1620
CATAGCCTCC TTCCAGGCAC TTACCTTCTG ACACAAGCCA GGCCTCTGAG TGCACCTTGG 1680
AGGCCAGAGG TTCCTGAGTG CCTCAGGGCT CAGGTTATGA TTCTGCCCTG GAGGGCCCTC 1740
TTTCCCAGCT TATTTCTCCT TCCTTTCTCA CTGCCCACAC CCCAGGCTTT CCTAGAGAAC 1800
CTATTCCTTT GTTTGCCAAT GGGCTCTGGG CTGGTCTTAG CCAGCTTGGC CCTGGCCGTG 1860
GCAGCTCCTT TTTTTCCCCT 1880
|
