| Tag | Content |
|---|
EnhancerAtlas ID | HS146-15327 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr9:119310910-119313260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr9:119312714-119312725 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr9:119312714-119312725 | CATGAGTCACC | - | 6.02 | | ZNF263 | MA0528.1 | chr9:119311475-119311496 | GGAGGAGGAGGAAGCTGAAAA | + | 7.02 | | ZNF263 | MA0528.1 | chr9:119311469-119311490 | AGAGGAGGAGGAGGAGGAAGC | + | 8.13 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_56096 | chr9:119303186-119315382 | u87 | | SE_67783 | chr9:119303186-119315382 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I116546 | chr9 | 119308612 | 119313943 |
|
Enhancer Sequence | TCGGCTAATT TTTGGTACTT TTAGTAGATA TGGGGTTTCA CCATGTTGGC CAGGTTGGTC 60
TCGAACTCCT GACCTCAGGT GATCCACCGG CCTCAGCCTC CCAAAGTGCT GGGATTATAG 120
GTGTTAGCCA CTGTGCCCGG CCTGGGGAAG GTTTTAAAAA TGAACACCTG TGCCCCATCC 180
CCATAAATTA CCATTGAACT GGCTTGGTAT AGGGGTCTGG GCAGCAGTAC TTTTCAGAAG 240
CTCAATAGGT GATTCCTGTA GGCAACCAGG GTCTAGATCC ATGACCCTAA ATAAATGCTG 300
AGATCCCTGT AAGCTTTTGC ATTTAAGGAT TCTATCAAAG AGATAAAGGA GTAAGAAACA 360
GAGACTTCTA GAAGGAGAAA TTCTGATGGG TTTTGGTCTT TAAAGTATCA TCAAATTAAG 420
TTGTCTCATT GGACAGATGG GAAAATTGGG GCCCCAAACT AAGGGATGAG TTTAAAACCA 480
CATAATGAGC GGCTGGTGGC CTGGTCTAGA ACCTGTGTCA TCTGAAGCAA ACCACAAAAA 540
TGTCAGTAAT AAAAAGATCA GAGGAGGAGG AGGAGGAAGC TGAAAATAAA GAAAGAAGGA 600
AATGCAAAAA AGGGCAAATA AAAAATGAAA AAAAAAAAAC AGAAGGAAGT AAAAGAAAGG 660
AATGGGAGGT CAGGGAAGAG AAAGGGGTAA AACGTAGAGG GACAAAAAGA AATAAAAGCC 720
ACAACTGAGG CACGAGCAAC TCGGATAGTA CCCTGTGAGT CAGGGCAGCT CTGAGCCACA 780
CTTGGCTGTA CAGTTCGTAT TTGGCAATTG CAACCCGGGC AAGAGCTCTG ATCCCAGCTG 840
GGGCCCCAGG CCCAGGGCTG GAGCCTGCGT GGGGACGGTC TGACTCACAG CTGCTACTTC 900
CTCACCCTGT TTCCAGCCTC TTGCTCAATC CAGGCAGGAG GCAGGATAGA TGCTCTTTTG 960
CAAGGTGATC CCAGCCCAGA GGGCCCTGCA ACCTTTATGA AACGATTCTG GTTAGGTGTA 1020
GGAAACAAAT GGGGCAGCAG ACCCTGTACT CCCAACATGC TGAACAGCAA GATGACTCCC 1080
AAAGCGGCCA GCCCTTTCCT GCCTCCAGGC CTTTGTTTGA TGCCCATTTC CACTGGAGTG 1140
CCCTTCCCCA CAGATACCCT GCCTCACATG GCATCTGAGG CCTCCCAAGT CTGGCCCTGT 1200
AATATCTCTC TACTCATGGT TCCCCTCCAT GCTTTCTACA CTACCCATAA AGCCATTTAT 1260
TAAAAGTAAT GGCAAAAACC ACAATTACCA ACCTTAAGAC ATTTACTACT CCTCACCTTT 1320
GCTTATGATG TGCTCACTCT CCTACGCAAT GGAACCCACA GGCATCTTTC AAATCCCACA 1380
AACACACAAA AATCCCACAT GAAATGTCCC TGCTTTAATT CCATCTTTCC AAATGGCTTT 1440
CTCTTATCAC TACAGTCAAA ATCATTCTCT CTCTTCTACA ACTCCACATC AAGTGTTCAG 1500
TCTGTCCCCT GTAATACTTA GCACTCTGAC TCTTTTATCT CAGACCACAA AATTGGAAGT 1560
TCTACGTGAC CAGATTTACA TCCATATAAC GTCTCTGGGC ATAAACTGTG AACTGTGACA 1620
GATCTGGGTT TCAATCTAGC TTCCACCACC TGCTATCTGT CTGCTTCAAA GCACAGTATC 1680
TTCATCTGCA ATATAAACCT GTCAATTTTA CCCTGTATTA TAGTTTTAAG TATTACTAGC 1740
AATAATACAG GAGGAGTATC TGGAACATAG TGCCAGCTTT AAAAAACAGT TACTTTGCTG 1800
TTGTCATGAG TCACCTATGG GATTCCCTAT GGGATCCTGT GCTGGGTCTG GCCTGGAGTG 1860
GTCTTCAGAA AATGTAGCTT ACATTACTCA ACTGAAGCTC AGTTGCTCTC TGAAAACAGT 1920
GTGGGCAAGG TGGGGATTGG GAGAGGAAAA GGGAGAGAAA ATAAGAATGC GTCCAACAGT 1980
GCTGCAATAT AAGGATGTTG TTCTGCTCTT TTACTCGTGA AAGAAATGAA GGCTGGCAGA 2040
TCTACAGCAA CTTTAACACT CAAAAACTCA TTCCCTCCTC CTAATATCCC TGAGAGATAG 2100
GCAGGAATTC CTGTCCCTGA CAAATGCAGA AAGATCCAAC CTGATGCAGG TGGGTTGGGA 2160
CAAGGTAAAG TTAGGGCTTA AACTCTCCTG CCCTTTAGAG GCCTTGCTGT AAGACTCTGC 2220
TGCCTGCTAG GAGAGGAAGC AGTCTTGGCT CCCGTTATGA ATAGATGTCA GCCTTTTGGC 2280
ACAATGCAAC CCAACTGTCA GCCTAAAGGA AGCCGCATGT ACTCAGGGAA ACCCTGTCTG 2340
CTCTGCCTTT 2350
|
