| Tag | Content |
|---|
EnhancerAtlas ID | HS098-33780 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:239068300-239070030 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:239069133-239069152 | CAGCCAGCAGGTGGTGCAG | + | 6 | | JUN | MA0488.1 | chr2:239069439-239069452 | ATGACCTCATCTA | - | 6.15 | | JUND(var.2) | MA0492.1 | chr2:239069438-239069453 | CATGACCTCATCTAA | - | 6.13 | | Zfx | MA0146.2 | chr2:239068431-239068445 | GTGGCCCAGGCCTG | + | 6.15 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I238160 | chr2 | 239068713 | 239068841 |
|
Enhancer Sequence | ATGTGGCTTT GAGTCAAGTG ATCAGGTGGC TTTTGGCCGT GAGTGGGTGA TCTTGAGCTC 60
TGCCCTGCCC CCTCCTCTCC AGGGTTTTGG AGCCTGGACT GCTGAGCAGA GGGTGGTCCG 120
GTTGGGGAGG TGTGGCCCAG GCCTGAGGAG GGGAGAACTT CAGAGGAGCC CTCAGTGTGG 180
CCGGGCCTTG GGTCAGGGAG ACAGGGCTGC CCCAGGGAAG CCGGGGTGGG CGGCCGGTGC 240
TGTTTATTCT GAAGATGCTC AGGGGCAGTA GAGGGGAGAG CCAGGAACGC ATCTACTAGA 300
GAGGACAGGG GTGCAGCCAG GCCTGGGGTC CCCCAGAGTT CTCTATCCCG GCCCCATCAC 360
ACCCAGCCAC TTCCCAGGGA CTGAAGGCAC CCCCTCCCCG TGCAGTTGGC CAAACCACCC 420
AGGTGGGCAC AGCAGCCAAA TGTCAGGGCA CTGTCAGCAG GAGGCAGACG GGGCTCAGGG 480
GCTTCCAGGT GGAGTTTTGG CCTTGGACCC TGTTTGTGGG GGACACAGTG ACACCAGAGG 540
TCCTCCCAGG CTCCAAGGCT TGTTTCTGAG AGACCCCTTG TGGCTGGAAC CAGGGCAGCT 600
GCCCAATACC CACCCCCATT GCTGGGGCCG TCTCCTGGGA CGCCACCTTC TGCCTGTTAC 660
AGCTCTACCT GCAAACCACA CTGGGGTCAG GGTCCGGCCA CAGGCCACAG GTGCAGCTGG 720
GAGGGTCAGC TGGGCACACC CCTCCTGGCC GGTGTGCGGC ATCCTCGCCC CATGTTTCCA 780
CGGAGGGCAC ACAGGAAGTG GAAGAGGGTC CTGGGAGGGG GTAGAGGGGA GATCAGCCAG 840
CAGGTGGTGC AGTTGACCCT CTAAGGCACA AGGAAGCACT GAGCAGCGCT GAGGGCCCTG 900
GGCCCCTGAA CCCTTTCTCC GCCCAACCAC AGGCTCCTCG GCACCGCAGC CCCCATCTTC 960
CCACCACAAC ACCCTGGCCT GCGCATTGGT CAGCCAGCTC CCAAAAGAAG GCCCTGCATC 1020
CCCCCAGATC AGCCAGGAAC CAAAGGCAGT GACTTGGCAG CCGGCTTTGT CTCTGATAAA 1080
AGGGCCCAGT CAGCTCTAAA ATCCCAGGGT CCTTCCGTCA GCCCCCAGCG TCAGCACCCA 1140
TGACCTCATC TAAGCCCTCT TGGGCCGGTT TCCTTCCCAG CTGGCAGCCT TGCCTGGAGC 1200
CCAGATAGCC CAAGGCCTCT CCCAGGAAGG TCCCTCCCAA AACTGTGCTC AGTGTCAGCA 1260
TCAGTCAGGA TGCAGCGCGG ACAGGAATGG GAACTTCCGG AAGCATCACT GTCCATGTGT 1320
CAGTGTCTCA GAAGTGCTGA GGAAATGAAA GTCTCACACA GAGGCCTCGC GTCATGACAG 1380
CTCGCCTGGT CCTCTCCCCC ACTGGACTGT AACCCGAGGC AGCTGTGAGA GCTGAATTTG 1440
CCTCCTTAGA ACTTCTGACA CTGGGGGAGG ATGGACAGAG GAGGGTTGGC TAGTAGTTGG 1500
GCTCCCTGAT AATCACAGTT GCTTCTTCCT GAGCACCTAT GGGTGCTCCA GTGGTCGGAT 1560
CCTCCTGGTG ACTGGAGGAC GGTGTGATCA CTGCAGCTCC TCTGGAGGAA GGAGGCCCAG 1620
CAGTACGGGG ATTCACCCCG ATATCCAAGC CCTGCACCCC ATTTTCCCTC CAGGCATCTT 1680
GGGTCTGCCT CTCCCATGAG TGCCAAGTCC AGGCCGAGGT GTGGCCCGTT 1730
|
