| Tag | Content |
|---|
EnhancerAtlas ID | HS055-07889 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr7:75193880-75196120 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr7:75195544-75195559 | TGAACTCCTGACCTC | - | 6.22 | | RFX2 | MA0600.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | + | 6.18 | | RFX2 | MA0600.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | - | 6.19 | | RFX5 | MA0510.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | + | 6.44 | | RFX5 | MA0510.2 | chr7:75195857-75195873 | TGTTGCCATAGCAATG | - | 6.52 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I075564 | chr7 | 75193814 | 75196122 |
|
Enhancer Sequence | AGCCAATGTG CCCTGCCTAT TTGTAAATAT TTTTTTGAGA TTGGGTCTTA GTCTGTCGCC 60
CAGGCTGGAG TATAGTGGCA AAATCATAGC TCACTGCAGC CTTGACCTCC CTGGGCCCAA 120
GGGATCCTCT CACCTCAGCC TCCAAGTAGC TGGGAGTACA GGTGTGTGCC ACCACACCTG 180
GCTAATTTTT TGTGTGTTTT TGATAAAGAT GGGGTCTCTC TATGTTGTCC AGGCTGGTCT 240
CAAACTCCTG GGCTCAAGCC ATCTACCCAC CTTGGCCTTC CAAAGTGCTG GGATTATAGG 300
TGAGAGCCAC CATGCTTGGC CTGTTTTAAT TTTTTTAGAG ACAAGGTCTT GCTGTGTCAC 360
CCAGGCTGAA GTGCAGTGGA ACGATCAAGG CTTGCTGCAA TCTCAACCTC CTGGGCTCAA 420
GCGATCCTCC CACCTCAGCC TCCTGAGTAG CTGGAGTTAA CTACATCTAT TCTGAGATGA 480
AAGGGGTACA TGGGCCTTAA ATCCTTTGGC CTGCAACAAT GAACTTTCTC CAGCTTAGTC 540
CAATAAACGA AACCCCCAGG GTCTCGTTAC AGCCTGTCAG ATCCCAAGAC TTAGGCCTGT 600
CTCTGTCTCT GTGACATCAC TGCTGCTTCC CCTGAATTCA AGGACAGTGA GGTCTCAGAC 660
AGCAGCCGTG TCTGTGTGGA ACAGCAAAGT GGCTACTCAG GGGAGATGTT TTTCTAAGCT 720
AGAAGCAAAT GAAAGGAAAT GAAATCACCT GACCACACAT CCCCATCTTG CTGGTTTGGA 780
GCCAACAGTA ACAGGCTCAA CTGCTTTCAC AAGCTACCGG AATTTGACAT TCCAGGAAAT 840
CAGCCTCAGG GCCTGTCTCC TTGGACTAAA GAAGCCATTT ATCACAGAAT ATGTACTCGG 900
CTTCTCAAAT GGAACAGGGG TACCAGGAGG TGGGTACAAC CACACACTTG TCCTTCGCTT 960
GCTCCTGGGG AACCAGGCAG AGAAGCTGAA ACTTGGCATT TGGGAGTTAT GGTCAAGGGT 1020
GAGGAAATTA ACAGGAAAAA CAAGAGAGTG CACTTTTACA CAGCTAAGTC AGGAGGCCCT 1080
TCTCAGCCCC CTCTGTCCTC CCAACTCTCA CTCTATTATC CTTCCCTTTT GCCTGGTTTC 1140
GCCTCCCCTC CCCTCCTTTC CTTTTTTTTT TTTTGGATGG AGTCTTGCTC TGTTGCCCAA 1200
GCTGTAGTGC AGTGGCATGA TCTCAGCTCA TTGCAACCTC TGCCACCTGA GTTCAAGCAA 1260
TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGG CTAATTTTTG TATTTACAGT 1320
AGAGACAGGG TTTCATCATG TTAGCCAGGC TGCTCTCAAA CTCCTGACCT CAAGCGATCC 1380
ACTTGCTTCG GCCTCCCAAA GTGCTGGGAT TACAGGTGTG AGCCACTGCA CCCAGCCTAA 1440
GTAAAGATCT TTTGTTTTTG TTTTTGTTTT GAGATGGAAT CTCATTCTGA CGCCCAGGCC 1500
TGAGTGCAGT GATGTGATCT TGGCTCACTG CAACCTCCAC CTCCTGGGTT CAAGCGATTC 1560
TTCTGCCTCA GCCTCCCGAG TAGCTGGGAT TACAGGTGTG CACCACCATG CCCTGCTAAT 1620
TTTTTAGTAG AGACGGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT CCTGACCTCA 1680
AGTGATCTGC CCACCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACTGCACC 1740
CGGCTGGTGT TAGCAACTTT TATTGAGGCG GCAGTGCACA GCCAGCAGCG GAGGTCCTGT 1800
TCCTTGCAGC GCAGGGCTAC TCCATACGCA GTGAGCCCAG AATAGCAGCT GTTACATTTA 1860
TACCCACTTT TAATTATATG TAAATTAAGG GGCAGATTAT GCAGAAATTT CTAGAAAAAA 1920
AGTGGTAAAT TCCAGATTGT CAGGTTATTG CCATGGAAAG GGGCGCTAAC TTCCGGATGT 1980
TGCCATAGCA ATGGTAAACT GTCACTGCAC ACTGGTAGGT GTGTCTTATG CAGAGGTGCT 2040
TCCGCCCTTT CCCTGTTTTA CTTGTCCTTA ATTTGGTCCG ATGCCCAAGC CCTGCCTCCA 2100
GAGTCCAGTC TCCCATCCCA CCTCAGAAGC AGGTCATATT TGTAGGGTAT CAACCAAACC 2160
TGCTAGTGGA TTGGACATGG GGGATGAGGA AAATGGTGAC TTCCAGATCT CTGGCCTAAA 2220
TGGATGATGG CAGTATTTGT 2240
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