Tag | Content |
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EnhancerAtlas ID | HS104-03827 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:154423300-154424630 |
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) |
Crx | MA0467.1 | chr1:154423452-154423463 | GAGAGGATTAG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:154423777-154423792 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr1:154424447-154424468 | CTTCCTCCCTACTCCTCATCC | - | 6.09 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09189 | chr1:154422671-154430649 | CD14 | SE_18405 | chr1:154422817-154423718 | CD4p_CD25-_Il17-_PMAstim_Th |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154450 | chr1 | 154422818 | 154423718 |
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Enhancer Sequence | CCTCGTTCCC CATCCCTGGG TGGATTCCTG CCTGCACTGA TGCTGGCTGC CTCTGCTACA 60 ACAGCCCAGG TACAAAGCCC TACCATGGTG CAGTGCACCT GTGGAGGACC TGCTAAATAC 120 CTGGGGCTGA GCTCTGCACA GTTGGGGACT CGGAGAGGAT TAGAGCCATC CCTGTTCTCA 180 AGGAGGCTAC AGTCCAGGCT CTGACAAAGA GTAAATTGGT AACTGTGACA AAGACCAGCA 240 TGTGAGATGG GCCAAAAGGG AGGCACAGAT AAAGCAAAGT GGAATTTAGA GATTTGAAAG 300 AGTATATCAA GCTGAGCAGT CACAGAAAGC TCATGGAGGA AGTGCCATTT GAAATGGGCT 360 TTGAATGGTA TGGGTGGGAT GCAAGAGGTT GGGTGTTCAA AGGTTGCTAT GGGCCGGGCG 420 CGGTGGCTTA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG AGGTAGGAGA ATCACCTGAG 480 GTCAGGAGTT CAAGACTAGC CTGGCCAACA TGGTGAAACC CCATCTCTAC TAAAAATACA 540 AAAATTAGCC AGGCGTGATG GCAGGTGCCT ATAATCCCAG CTACTTGGGA GGCTGAGGCA 600 AGAGAATCAC TTGAACCTGG GAGGCAGAGG TTGCAGTGAG CTGAGATCGA GCCACTGCAC 660 TCTAGCCTGG GCCACAGAGT GAGATTCCAT GTCAAAAAAA CAAAACAACA ACAACAAAAA 720 CAAAAGCTGC TATGGAGGAG GGGAACCTCC AGTCCTCTTC GTCCACCCTC ACTGATGATT 780 TTTTTTCTTT TTTTTGAGAC GGAGTCTCGT CAAGCGATTC TCCTGCCTCA GCCTCCCGAG 840 TAGCTGAGAT TACAGGCATG CACCACCACG CCTGGCTAAT TTTGTATTTT TAGTAGAAAC 900 GGGGTTTCTC CATGTTAGTC AGGCTGGACT CGAACTCCCC ACCTCAGGTG ATCTGCCTGC 960 CTCGGTCTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC CGCGCCTGGC CAGCATTCTC 1020 AAATTTAACA TGTCTAAAAG AGAACACCTG ACGCCTCCCC ACCTATTCAA CCCAGATCTG 1080 TTCTTCTCCA TCTTCCCTAT CTCAGTAACT GGTACCGCAT TTGCTCAGGT GCGGGGGATC 1140 GGGCAGGCTT CCTCCCTACT CCTCATCCTG TGTCCAGTCC CTCAGCAAGC GTTGTCCTTG 1200 TGCTTTGAGA CGTATCTAGG AATTGACCAC TCCTCACCAT CTCCAGTGCC AACACCCAGT 1260 CCAGCCCCTG CCGCCTCTCA TCCAGCAGGG CTTCCTGGGC TGCCAACTGG TCTACCAACT 1320 TCTAGTCTTA 1330
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