| Tag | Content |
|---|
EnhancerAtlas ID | HS192-06351 |
Organism | Homo sapiens |
Tissue/cell | U2OS |
Coordinate | chr17:79080710-79082270 |
Target genes | | Number: 23 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr17:79080935-79080950 | GGGTCAGCCTGTCCC | + | 6.32 | | KLF5 | MA0599.1 | chr17:79080792-79080802 | GGGGCGGGGC | - | 6.02 | | STAT1 | MA0137.3 | chr17:79081836-79081847 | TTTCCAGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr17:79081836-79081850 | TTTCCAGGAAACTG | + | 6.5 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65309 | chr17:79081641-79082353 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I081107 | chr17 | 79081642 | 79082353 |
|
Enhancer Sequence | AGTGGGCGGG GCCGGGGCTG GGAGGGGCCC GCAGGTGGAA CAGTGGGCTC AGCCTGCAGT 60
CCCCCGTTGG AGCCTCCGCT GAGGGGCGGG GCGCCTGGGG GTCTGGGTCT TTGGACAGCC 120
CTGGGGTGAA GGCTGCATGA TTTGGGAATG TGTACACACC CCTGCTTCGG CCTCAGGCTG 180
CCCGCCTCGC CGCAGCAGGC TCCCTGTGTC GGCATGCTGG GGCTGGGGTC AGCCTGTCCC 240
TCATGGTGCC CTCAGCCAGC CACGGGCAAC TCACTGCTCT GTCCAAGGGG GCAGCGTCTG 300
GGCTGGGAAG TGGCTGGCCT AGAGGTGGGC CTGGACGCCG CCGCCTTTTG GGAGAGCCAG 360
GGGGGCAGGA TCTCTTCCGT GAGAACCACG GGGCTCCCTC AGTCACATCC ATGAGATGGG 420
AGTGCTTGCT GCTCAGCCCT GGCATGTGGC TGGACCCCTT CCAGTCAGTG TGACCCTGGA 480
TTTGGGCCAT CTGGTGCCGG GAGGCCAGAG GTGGAGGATC AGGGCCTGGG TCCTAGGCCC 540
TGGTGTGGGT TCTCGGAAAC CCGGGATCAT GGCGGTCCTG GTATCTAGGC TGGGGCAGGG 600
TGTGAGCGTG CATCTCAACT TGCCGGGTTC CAGCCCGCTC CGTCCAGGGA GGCTCCTGGG 660
GTTGGAGAGT TGGAGACCCC TGTCTGTCTG GGGCTCCTCA GCCAGAGGTC CAGTTTGTGG 720
GATATTGGCT GGGCTAGCAG CTTTGTTCCC GGGGCCGGTC TCCAGGGCTG GGCCTCAGGC 780
AGTGAGTAGA GAGAAGAAGA GAACCCACCT TTTTCCGAGA TAACAGGTAG CCTGGGTGAC 840
TACTCAGCTA TTGACCCACA AGTGAGGAGT CCCTAGATTG ACAGCCTGAG CTGAGGCCGC 900
AGGAGGCAAC CTGGAGAGGT TTGGGCTCTG GGCCGTGGGT GTTCCACAGG TCAGCCTCTG 960
GGGTGGGCTC AGTGCTGGGA GAGCCAAGGA GGGGTCTGCA TCTGCCCTAG GCCGCGGGCC 1020
AGGCCATGCT GGCAGATGAA GGGCACAGCC AGCCCCAGCG CCACACCTGG GCGCTCCTCC 1080
CAGGCAGTGT CACCCTCCCA GGGGCCGGGA TGGTACATGT GACAAGTTTC CAGGAAACTG 1140
CAGCTGGGGT CTGGGTCTGG TCCTGGGTCC TACAAGCAGG CGGAGGAGTC CCAGGGGCCC 1200
GCCCAGGCAT GGGTGAGGTG CTGCAGGTGC CCTGCGGGGG CCTCGGCTCC CTGGGGGCAG 1260
GAGGAGGGGT CTCAGGCGGC CAGTCTTGCA TCTGTTTGGG AGTGTGCAAC AAGCACACAA 1320
ATTGAGGTGG CCGCTGGCTG GAGGAGGTAT CCCCTTTAAT TTGGGCAGTC ATTACTTTAC 1380
CACTGGGACC AGGGCTCCAG GCAGGTCTCT GAGTGCTGCA GCCAGGAGAT GGGGAGCCTT 1440
CCAAAGGAAC ACGGTTTGAA CCTTGTCCAG GCAGGATCAC CATTTGTGGG TGTGTACAGG 1500
CAGCGGGTGG GGGTGACCAC AGGCCCCGTC ACCCGGCCTG ACATGTTTCT GCCTCTGCCC 1560
|
