| Tag | Content |
|---|
EnhancerAtlas ID | HS088-48456 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr7:74105790-74107900 |
Target genes | | Number: 10 | 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) |
| Zfx | MA0146.2 | chr7:74107337-74107351 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I074692 | chr7 | 74106496 | 74107350 |
|
Enhancer Sequence | GCCTCCCAAA GTGCAGAGGG ATTATAGGCG TGGGCCACTG CGCCTGGCCA AGTTATATTT 60
TCTTCTAAAA CAGAATGAGG TTTAAACTAA AAAAGATTTT CTGAAATGTT TATGGAGACA 120
TTTCAAAATG CTCAAAAGGA ATCACTGAAA TATGTCAGGA TAGATACTGA AGAGTTAAGA 180
AAAATGGTAG TGTTTGTTGT ACGGTGTTCC TTGCTTGGCT TTACTCTGGG TTAATGAGAT 240
GCATTAGAGA GAAGGTAATG AAGGTAGAGA AATTTTGAAT AGGTTAAAAC TTTTACTCAG 300
ATAAGGAGTT ATTTTCTTTT TCTTTTTTTT TTTTGAGACA GAGTTTCACT CTTGGCCCCC 360
TGGGCTGGAG TGCAATGGCA CGATCTCGGC TCATTGCAAC CTCCACCTCC CATGTTCAAG 420
CAATTCTTCT ACCTCATCCT CCCGAGTAGC TGGGATTACA GGTGCCCACC ACCATGCCTG 480
GCTAATTTTT GTAATTTTAG TAAAGACAGG GTTTTGCCAT GTTGGCCAAG TTGGTCTCAA 540
ACTCCTGACC TCAGGTGATC TGCTTGCCTT GGCCTCCCAA AGTGCTAGGA TTTCAGGCAT 600
GAGCCACCAC TCTCGGCTTT TTTTTTTTTT TTAAGAGATG GGGTCTCGCT CCGTCACCAG 660
GCTGGAGTGC AGTGGCGCGA TCTCCGCTCA CTGCAACTTC CACCTCCTGT ATTCAAGCAA 720
TTCTTCTACC TCAGCCTCTG GAGTAGCTGG GATTACAGGT GCACACCACC ATACCTAGAT 780
AATTTTTTGT ATTTTTAGTA CAGACAGGGT TTCTCCATGT TGGCCAGGCT GGTCTTGAGC 840
TCCTGACCCG AGGAGCCCAC CTCGGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 900
CACATCCGGC CGGGAGTTCT TTTCTAGATA AAAAGTTGGT GTGTTGAAAA CCAGTGATTC 960
ACTGTGCAAG TTTGTTTAAG CATATTGCAA AATTAAACAG TTCTCCTCCA CTCCCTCACA 1020
GATACGAGTC ACCTTATCAC AGTCTTCAGT GAGTTTTGTA ATCTGCATTT AGAGCAGTGG 1080
TGAGCTTATT TGACATTGGA ACAGTGTTGA AATTTACTAT AGGGTTTTAA TACCCACAGC 1140
CTTTCACAGT ATGACCATTT TCATATCTGT GTTTAACCTA ACACTGTAGG TTTTATGTTA 1200
ACTGATTGAT ACAGCATTTT CTTAAAAACA TGGAAAGGGA ACAAAAAAAG CTAGGGTATC 1260
TATAGGCACA TATTATATAT GGGCATACCT CATTTTTTGT TGTTGTCATT TTTGTTTTTT 1320
TGAGACGGAG TTTTGCTCTT GTTGCCCAGG CTAGAGTGCA ATGGTGCGAT CTCGGCTCAC 1380
CGCAACCTCT GCCTCTTGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG 1440
ATTACAGGCA TGCACCACCA CACCCAGCTA GTTTTGTATT TTTAGTAGAG ATGGGGTTTC 1500
TCCATGTTGG TCAGGCTGGT CTCGTACTCC TGACCTCAGG TTATCTGCCC GCCTCGGCCT 1560
CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACTGTGCCCG ACCGGGCATA TCTCATTTTT 1620
TTTTTTTGTG CCTTGCAGAC ACTGCAGTTT TCACACATTG AAGATTTGTG GCAACCTTGT 1680
GTCAAGTCTA TTGGTGCCAT TTTTCCTGCA GCATGTGCTT ACTTGGTTCT CTGTGTTGCA 1740
TTTTGGTAAC TCTTGGCATA GCATTATTTG AGACTTTTTC ATGATTATTG TATCCGCTGT 1800
AGTGGAATTT TTTTTTTTTT TTTTTTTTTT TTTTTGAGAT GGAGGTTTGC TCCGTCACCC 1860
TGGCTGGAGT GCAGTGGTGC GATCTCGGCT CACTGCATCC CCTGCCTCCT TGGTTCAAGG 1920
TATTGAGATC AGTGATCTTT GATGTTACTA TTGTAATTGT ACTGGGAGTC CTCGAACGCA 1980
CACATATAAT ATGGCAAACC TAATAGGTAA ATATGTGTTC TGACTGCTTC ACCAATCGCC 2040
TGGTCCCCCA TCATTCCCTT TCCTCAGGCC TCCCTGGTCC CTGAGACACA ATATTGAAAT 2100
TAGGCCGGCC 2110
|
