Tag | Content |
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EnhancerAtlas ID | HS104-55003 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr7:75193860-75196040 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I075564 | chr7 | 75193814 | 75196122 |
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Enhancer Sequence | ATGTTGGGGT TATAGGCGTG AGCCAATGTG CCCTGCCTAT TTGTAAATAT TTTTTTGAGA 60 TTGGGTCTTA GTCTGTCGCC CAGGCTGGAG TATAGTGGCA AAATCATAGC TCACTGCAGC 120 CTTGACCTCC CTGGGCCCAA GGGATCCTCT CACCTCAGCC TCCAAGTAGC TGGGAGTACA 180 GGTGTGTGCC ACCACACCTG GCTAATTTTT TGTGTGTTTT TGATAAAGAT GGGGTCTCTC 240 TATGTTGTCC AGGCTGGTCT CAAACTCCTG GGCTCAAGCC ATCTACCCAC CTTGGCCTTC 300 CAAAGTGCTG GGATTATAGG TGAGAGCCAC CATGCTTGGC CTGTTTTAAT TTTTTTAGAG 360 ACAAGGTCTT GCTGTGTCAC CCAGGCTGAA GTGCAGTGGA ACGATCAAGG CTTGCTGCAA 420 TCTCAACCTC CTGGGCTCAA GCGATCCTCC CACCTCAGCC TCCTGAGTAG CTGGAGTTAA 480 CTACATCTAT TCTGAGATGA AAGGGGTACA TGGGCCTTAA ATCCTTTGGC CTGCAACAAT 540 GAACTTTCTC CAGCTTAGTC CAATAAACGA AACCCCCAGG GTCTCGTTAC AGCCTGTCAG 600 ATCCCAAGAC TTAGGCCTGT CTCTGTCTCT GTGACATCAC TGCTGCTTCC CCTGAATTCA 660 AGGACAGTGA GGTCTCAGAC AGCAGCCGTG TCTGTGTGGA ACAGCAAAGT GGCTACTCAG 720 GGGAGATGTT TTTCTAAGCT AGAAGCAAAT GAAAGGAAAT GAAATCACCT GACCACACAT 780 CCCCATCTTG CTGGTTTGGA GCCAACAGTA ACAGGCTCAA CTGCTTTCAC AAGCTACCGG 840 AATTTGACAT TCCAGGAAAT CAGCCTCAGG GCCTGTCTCC TTGGACTAAA GAAGCCATTT 900 ATCACAGAAT ATGTACTCGG CTTCTCAAAT GGAACAGGGG TACCAGGAGG TGGGTACAAC 960 CACACACTTG TCCTTCGCTT GCTCCTGGGG AACCAGGCAG AGAAGCTGAA ACTTGGCATT 1020 TGGGAGTTAT GGTCAAGGGT GAGGAAATTA ACAGGAAAAA CAAGAGAGTG CACTTTTACA 1080 CAGCTAAGTC AGGAGGCCCT TCTCAGCCCC CTCTGTCCTC CCAACTCTCA CTCTATTATC 1140 CTTCCCTTTT GCCTGGTTTC GCCTCCCCTC CCCTCCTTTC CTTTTTTTTT TTTTGGATGG 1200 AGTCTTGCTC TGTTGCCCAA GCTGTAGTGC AGTGGCATGA TCTCAGCTCA TTGCAACCTC 1260 TGCCACCTGA GTTCAAGCAA TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGG 1320 CTAATTTTTG TATTTACAGT AGAGACAGGG TTTCATCATG TTAGCCAGGC TGCTCTCAAA 1380 CTCCTGACCT CAAGCGATCC ACTTGCTTCG GCCTCCCAAA GTGCTGGGAT TACAGGTGTG 1440 AGCCACTGCA CCCAGCCTAA GTAAAGATCT TTTGTTTTTG TTTTTGTTTT GAGATGGAAT 1500 CTCATTCTGA CGCCCAGGCC TGAGTGCAGT GATGTGATCT TGGCTCACTG CAACCTCCAC 1560 CTCCTGGGTT CAAGCGATTC TTCTGCCTCA GCCTCCCGAG TAGCTGGGAT TACAGGTGTG 1620 CACCACCATG CCCTGCTAAT TTTTTAGTAG AGACGGGGTT TCACCATGTT GGCCAGGCTG 1680 GTCTTGAACT CCTGACCTCA AGTGATCTGC CCACCTCGGC CTCCCAAAGT GCTGGGATTA 1740 CAGGCATGAG CCACTGCACC CGGCTGGTGT TAGCAACTTT TATTGAGGCG GCAGTGCACA 1800 GCCAGCAGCG GAGGTCCTGT TCCTTGCAGC GCAGGGCTAC TCCATACGCA GTGAGCCCAG 1860 AATAGCAGCT GTTACATTTA TACCCACTTT TAATTATATG TAAATTAAGG GGCAGATTAT 1920 GCAGAAATTT CTAGAAAAAA AGTGGTAAAT TCCAGATTGT CAGGTTATTG CCATGGAAAG 1980 GGGCGCTAAC TTCCGGATGT TGCCATAGCA ATGGTAAACT GTCACTGCAC ACTGGTAGGT 2040 GTGTCTTATG CAGAGGTGCT TCCGCCCTTT CCCTGTTTTA CTTGTCCTTA ATTTGGTCCG 2100 ATGCCCAAGC CCTGCCTCCA GAGTCCAGTC TCCCATCCCA CCTCAGAAGC AGGTCATATT 2160 TGTAGGGTAT CAACCAAACC 2180
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