Tag | Content |
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EnhancerAtlas ID | HS146-02435 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr11:5301820-5303190 |
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) |
NFE2L1 | MA0089.2 | chr11:5301989-5302004 | TCATGACTCAGCATT | + | 7.17 | Nfe2l2 | MA0150.2 | chr11:5301987-5302002 | CATCATGACTCAGCA | + | 7.77 | YY1 | MA0095.2 | chr11:5303079-5303091 | GCAGCCATGTTG | - | 6.14 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_12715 | chr11:5302619-5302786 | CD34_fetal | SE_12715 | chr11:5302804-5302963 | CD34_fetal | SE_40081 | chr11:5300688-5304763 | K562 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I005279 | chr11 | 5300941 | 5303569 |
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Enhancer Sequence | GGCATCCATT TTCTTTATGA TGCCGTTTGA GGTGGAGTTT TAGTCAGGTG GTCAGCTTCT 60 CCTTTTTTTT GCCATCTGCC CTGTAAGCAT CCTGCTGGGG ACCCAGATAG GAGTCATCAC 120 TCTAGGCTGA GAACATCTGG GCACACACCC TAAGCCTCAG CATGACTCAT CATGACTCAG 180 CATTGCTGTG CTTGAGCCAG AAGGTTTGCT TAGAAGGTTA CACAGAACCA GAAGGCGGGG 240 GTGGGGCACT GACCCCGACA GGGGCCTGGC CAGAACTGCT CATGCTTGGA CTATGGGAGG 300 TCACTAATGG AGACACACAG AAATGTAACA GGAACTAAGG AAAAACTGAA GCTTATTTAA 360 TCAGAGATGA GGATGCTGGA AGGGATAGAG GGAGCTGAGC TTGTAAAAAG TATAGTAATC 420 ATTCAGCAAA TGGTTTTGAA GCACCTGCTG GATGCTAAAC ACTATTTTCA GTGCTTGAAT 480 CATAAATAAG AATAAAACAT GTATCTTATT CCCCACAAGA GTCCAAGTAA AAAATAACAG 540 TTAATTATAA TGTGCTCTGT CCCCCAGGCT GGAGTGCAGT GGCACGATCT CAGCTCACTG 600 CAACCTCCGC CTCCCGGGTT CAAGCAATTC TCCTGCCTCA GCCACCCTAA TAGCTGGGAT 660 TACAGGTGCA CACCACCATG CCAGGCTAAT TTTTGTACTT TTTGTAGAGG CAGGGTATCA 720 CCATGTTGTC CAAGATGGTC TTGAACTCCT GAGCTCCAAG CAGTCCACCC ACCTCAGCCT 780 CCCAAAGTGC TGGGATTACA GGTGTGAGAC ACCATGCCCA GATTTTCCAT ATTTAATAGA 840 GGTATTTATG GGATGGGGGA AAAGAATGTT TCTCTCACTG TGGATTATTT TAGAGAGTGG 900 AGAATGGTCA AGATTTTTTT AAAAATTAAG AAAACATAAG TTGGACCTTG AGAAATGAAA 960 ATTTATTTTT TTGTTGGAGG ATACCCATTC TCTATCTCCC ATCAGGGCAA GCTGTAAGGA 1020 ACTGGCTAAG ACACAGTGAG ACAGAGTGAC TTAGTCTTAG AGGCCCCACT GGTACCCAGA 1080 TGAGAAGGCA CCTTCATCAC TCATCACAGT CAGCTCTGCC TTTCTCCTCT CTCCTTTCTC 1140 ATCAGAAATT TCATAAGTCT ACTAGGGTCA GGCAGATCAC ATAAGAAAAG AGGATGCCAG 1200 TTAAGGTCTG CAGTGAGTAT GAGCCCATCC CTGATGAATT AAGGCAATCA ACACTTTAGG 1260 CAGCCATGTT GCCATGAGAG ATTAGGAGGG GCCAAATGAG CCCAGAAATA CCACCTACTT 1320 CTTAGATGAT CTTGAGCAAG TTGCTTAACT TCTTGAAGTC TCTGAAATAT 1370
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