| Tag | Content |
|---|
EnhancerAtlas ID | HS092-03552 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:161990620-161992250 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:161991705-161991720 | GGGGGGCAGAGGGCA | + | 6.45 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_30030 | chr1:161990610-161994606 | Fetal_Muscle |
|
Enhancer Sequence | TGTAAAAAGG AAAAGAAGAA ATTGGAGAGA TTGAAAAGTT GGTATTCAAG TTTGAAGACT 60
ACTGGCATCT CTCATTCATT TATTCAACAT TTATGGAGTG CCTACTAAGG ACTGTGAGGT 120
GCTGTGAAGG ATAAAGAGAT GGGCCAGATG GAGAGCCTGC TCTCAAGAAG CCTACAGTGC 180
AGGAGGCATA GAAATAGCAG TCACACAGAG TACAGAGTGA TAAGTGCCCC CGAAGAGGCA 240
GAGGGAAAGG GCAGTGGGAG CTAAGAGCGG CTCCAACTGG AAGCCAGGGA AGACTTCTTC 300
GAGGAGTGGC ATTTAATCTG GGCCTTGAAG GATGGGTTAG ATGTGGAGAA AGGGAATTGA 360
GAGGAAAGAG GCAGGTCCAG AAGTTAGTAA GGTTTACTCA GTCTAAGAGT TCATGCTTCT 420
GAACCTAAAC CCCAGGCCAA ACCCAGGAAA GCAAACTGGC AGCACTTGCT GCTTTTGCAA 480
TGCTAAACAT TTCCTTCTGG GCACTTGCCC CTGCCAGCCT CCCCAGGCAG GAAAACACGC 540
GACAGTAGGC TTTCTGGAGC CCCAACTCTG GGCGCTTGCT GGGAAAAGGC TCTTCTCTCC 600
CAATCCTCTC CAAAAGGCCC TACATCCCCA AAGCCAGGGC TCCCTTCCTA GGCAGGCAGA 660
AGGGTTCCCT TCATTTGATT AATGATTTCA GTGGGCAAGC ATTGAGCTTG TTTGAGTAGA 720
AATGTTCCTT GGGATGCTGT CTGGGGGAAG AAGACTTGTA ATGTTTTCCT TGCAAAGATT 780
GGGTTTCTTC TAATACTAAT ATTTGCTTTA GGGCTGTTGT CAAACACAGA ATGGATCAGT 840
GGAAGAAGGT GGTGTAGTTA AGGGTGACTT AAGCGGCTGT TCTTTACGGG CTGATAGTAA 900
ATTGTGGCTG TCTGCTCTCT GAAACTCTGC CTGGATTCCT ACATAACCCT GCTCTGAGAA 960
CCCTGGGTGG ATTCCTTCCT TACAGGAGGC TCGGGTTTCA GGAAAGTTTT TGTTGATAGT 1020
GTTCCAGAGC CCCAGTGTGA GAGATTTTTA TGTCTTTTCG ATTTAGGGGT CAGTGGGAGG 1080
TAATGGGGGG GCAGAGGGCA TACATTAGCA TCATTATTAA AGGAAGAGTG AGGAGGCTAG 1140
TGTTTGATAA ATCCCAAAGT GCAGCTGATT ATTCTCTCTA CAGGAAGGAG ACAAGGCCCA 1200
GTCCTAGGGC TTGGTGGAGG TGAAGGTACA GGCAGCCCTG GAGGATCCTT TTTCAGACAT 1260
CCCCCATTCT GAGGATTCTG GTGACACCCA CCACACGTCA TCATGCCGGC TCTGGAGAGC 1320
ACAAAATAAA CACTCCAGAG AGAACTACCC CTTACAGACA TGAGATCTGG GCTGAAGACT 1380
GTCAGACGCC CTGGCTCTAC CCATGTATCT CTTCTTTTTT TTTTTTTTTT TTTTTTTTGA 1440
GACGGAGTCT CACTCTGTCA CTCAGGATGG AGTGCAGTGG CGCGATCTCC GCTTACTGCA 1500
ACCTCCACCT CCCGGGTTCA AGCGATTCTC CTGCCTCAGC CTCCTGAGTA GCTGGGACTA 1560
CAGGTGCCTG CCACCACGCC TGGCTAATTT TGGTATTTTT AGTAGAGATG GGGTTTCATC 1620
ATATTGGCCA 1630
|
