Tag | Content |
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EnhancerAtlas ID | HS148-14156 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr5:52692730-52694890 |
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) |
SCRT1 | MA0743.1 | chr5:52692953-52692968 | GCCCACTTGTTGCTT | - | 6.16 | SCRT2 | MA0744.1 | chr5:52692955-52692968 | CCACTTGTTGCTT | - | 6 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_35145 | chr5:52692543-52694634 | HeLa | SE_36207 | chr5:52693831-52694516 | HMEC | SE_44571 | chr5:52692775-52694762 | NHDF-Ad | SE_44899 | chr5:52693353-52694617 | NHLF | SE_45640 | chr5:52692669-52697482 | Osteoblasts | SE_55926 | chr5:52691931-52695580 | u87 | SE_67876 | chr5:52691931-52695580 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I053396 | chr5 | 52692687 | 52694698 |
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Enhancer Sequence | TGTAGAAGAG TCTCTCCTCA TGGCTACCAC TGCCCCATTT TCATGATGAG TACTACCTGA 60 CTACTGCTGA TGTTCATTCA AGGCCCAGGG GCTTTTCAAT CAGCTTATGG AGAAGGCTGC 120 CAGGCCTGAG ACTCTCCCTT CAGGGCAGTG GGCTCCCTTC TGGCTCAGGG CAGGTCCAGA 180 AATGCTGTCC AAGAGCCAAA GCCTGGAATC AGGGACTTCA AGGGCCCACT TGTTGCTTTA 240 CCTCACTGTG GCTGAGCTGG TACCTAAGCT GCAAGACAAA GTTCCCTTTA GTCTTCCCTC 300 TCCTTTTCTC AAGCAGAAAT CCCTTCCCAT AGCCACCACA GCTGGGAATA TGCCCGGTCA 360 CATCTGAAGC ACATCTCTGA ATCTCACCAA AGGTCCACAG GGACTACTGC CTGGTACCAC 420 TACTGATTAT TCAGGGCCCA AGGGCTGTTT CGTCAGCAGT GATGAATCCT GCCAGGATTG 480 GGTCATTTCC TTCAAAGCAG TGGGTTCCCT TCTGGCCCAG GGTGTGTCTG GAAATGTCTA 540 CAAGCTAGGG CCTGGAATTG GGGATCTGAT ATGGTTAGGC TTTGTGTCCC CACCCAAATG 600 TCATTTTGAA TTTTAATCCC CCAGTGTCAA GGAAGAGATC TGGTGGGAGG TGATTAAATC 660 ACAAGGGTGG TGTCCCCCAT GCTGTTCTCG TGATAATGAG TGAGTTCTCA CGAGGTCTGG 720 TGGTTTTATA AGTGTCTGAC AGCTCCTCCT TTATGCATTC ACTGTCTTTC ACCTGCCACC 780 ACGTAAGATG TGCTTCTTCC CCTTCTGCTA TGATTTTAAA TATCCTGTGA CCTCCCCAGC 840 CATGTGGAAC TGTGAATCAA TTAAACCTCT TTTCTTTATA AATTACCCAG GCTTGGGAAG 900 CTCTTTATAG TGGTGTGAGA ATGGACTATT ATAGGGTCTC AGCTCTCTCC CTGGTGCTCT 960 ATCTTAACGT GGCTGAGCTG GTATCCAAGT TGCAAGACAG TCCTCTTTAC TCTTCCCTCT 1020 CCTTTCCTCT AGCAAAGGAA GGAGTCTCCC CCGGAGCTGC AAGCTGTATT GCCTGGGGTT 1080 GGGTGAGGAG TGACAAAAGC ACTCCCTTGG TCACTCCAAC TGGTGTCTCA CTGAGTCATG 1140 TGCCCCCAGA GTCCACTGGC TCCATGCCCA GCATAGCACT GGGACTTGCC CAGGAATTGT 1200 AGTGCTTTTG GCCTGGACTG CCTTTCAAGT TTATTTGGAG TCACAGAGCA CTTTAGCCCC 1260 TTTTAGTCAG AATTCAGTTT CCAGCTGCTG GGATGAGCAA GTCTCTTCTA GATAGGGCTG 1320 GTCTAAATGC TCACTCTGTG GGTGCTAGCT GAATTCTGCC TAAAATTGCT TTTCACAGTG 1380 TCAAGACAGC ATGGAGTTCT AAAGCAAAAT CCCACAATCA CTATGGTCTT CCTTCCCCAA 1440 GCGCACAGAT TCTCCATGCC ATGTGGCAAC TGTTGAGGGA ATGGGGAAGG GGTGGTGGCA 1500 GCAATTCAAG ACTATCTTTT CTACCCTCTT ATGCCTTTTT AATGATATGA AGTTAAAACC 1560 AGGCACTGTT CCCTTTAGTC TTGAGTTTCC TGAGGTTCAA ATTGCAATAT TTTATTGAGG 1620 ATTTTTGCAT CTGTGTTCAC AAGAGGTGTC AGTGTATATT TTTCTTGTAA TGTCTTTATC 1680 TGGTTTTGGT ATCAGGATAA TACTAGCCTC ATAAATGAGT TAGGAAGTTT TGCTCTCCTC 1740 AGATTTTCTG GAAGATATTG TAAAGCATTG GCATTATTTC TTCCTTCATG TTTGGTAGAA 1800 TTCACAAGTG AAAACATCTG GGCCTGGTGC TTTCTATTTT GTACAGTATT AATTGTTGAT 1860 TCCATTTCTT TAATGATATA CACCTATGTG AATTAGCTAT TTCTTATTGT ACAAATTTTA 1920 CTAGATTGTG TATTTTATGT AATTATTTTT TAGATTGTGT CTTTTAAGAA ATTAGTCAAT 1980 TCAATCCAAG TTAGCAACCT CATGGGTATA GAATCTCCAA ACTTTTTTAT TCCTTTCTTT 2040 ACAATCTGCC ATAGCAGTTT TTGCTTCTCT ATCTCATTTA ATGTGGACCA TGACTTTCCA 2100 TAAAGGTCCA AGAGCAATCC AGCAGTGTAC TAGAATTATC TCCAAGGGTG CTTGCCATAT 2160
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