Tag | Content |
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EnhancerAtlas ID | HS095-11056 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:16115290-16116620 |
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) |
Foxd3 | MA0041.1 | chr16:16115586-16115598 | AAACAAACAAAC | - | 6.32 | NFE2L1 | MA0089.2 | chr16:16116061-16116076 | CGTGCTGAGTCACTG | - | 6.01 | Nfe2l2 | MA0150.2 | chr16:16116063-16116078 | TGCTGAGTCACTGAG | - | 6.6 | RUNX1 | MA0002.2 | chr16:16116281-16116292 | GTCTGTGGTTT | + | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_13655 | chr16:16113960-16117852 | CD34_Primary_RO01536 | SE_26926 | chr16:16114478-16117838 | Esophagus | SE_32168 | chr16:16115386-16118019 | Gastric | SE_44900 | chr16:16115308-16116788 | NHLF | SE_47158 | chr16:16111262-16124112 | Panc1 | SE_48435 | chr16:16114024-16117178 | Psoas_Muscle |
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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 |
GH16I016018 | chr16 | 16112512 | 16117921 |
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Enhancer Sequence | AGGCCAGGTG TGGTGGCTTA CACCTATAAA CCCAGCACTT TGGGAGGCCG AGGCAGGTAG 60 ATCACCTGAG ATCAGGAGTT TGAGACCAGC CTGACCAACA TGGTGAAATC CCATCTCTAC 120 TAAAAATACA AAAATTAGCT GGGCATGGTG TTGAGCACCT GTGATCCCTG CTATTTAGGA 180 GGCAGAGGCA GGAGAATTGC TTGTGCCCGG GAGGCGGAGG TTGCAGTGAG CTGAGATCGC 240 TCCAGTCTGG GCAACAGACT GAGACCCTGT CTCAAACAAA CAACGAACAA ATGAACAAAC 300 AAACAAACAA AATAACCACA TAACTACCTA GCAACGTAGC CTAGCAATTG AGATGGGGGC 360 AAGGAAGGGT AGGAACCAGG TCCTGTGAGA ATCAGCTAGA CTTGTGGCTT TGGGCTCGGT 420 GCTCTTCCTT TGGGGACGTC AGCAGCCCCT TCTTGAAAAC GGGTTGCAAC TCGATTTGTT 480 GTTGGCTTCA CCTCCTCTCT CTGTCCCAGA CCTGAGCCCT GTGATCTGGG GAGGAGGACA 540 ACGGGACAAC CTGTTTGCTT GTTTTCCCAT CACTCTCAGG GATTGAATCA CAGTGGAGCC 600 AGGAAGATGG GGAGAGTCCA GGCTTGCTGC TCTCCCATCC TCAGAGCAGC AGCAGGCCAT 660 CCATCACCTG TCGCCTGTCC TCAGAGTGAT CAGCCAAGGC CTGGGGCGGC TGGGGTCAGG 720 TCAGGCAGGG CGTGGGTGGG AGCTGGCAGG GCTGGCTCCT CCAGGCCACT TCGTGCTGAG 780 TCACTGAGTC GGCCAATCCT CCCCAGCTGG CCCTGCTCCC ACTCCATGAC TCAGATGTCT 840 ATTCCAGCCC TGGCTGCTTG GTGGGGCTCC TCCCATCTGT CCTTCTGGCT CTGGGGCTGC 900 CGAGGCTTTT GGGAGCCTGG GCAGGGCTGA CCAAGACTGC CAGAGCTCCG GCCGGTCCCC 960 AGTCTCCTGC CTTTTTTCTC ATTGGCACTG AGTCTGTGGT TTAGGTTTGG GGGAGGAGGG 1020 TCTTGTAGAT AAGGGGATCA AGGCCAAAGG AGATCATTTA TTAGGTCCCA GCTGAAAGCA 1080 GAGGTCCTTG GACCAGTTGG AATGCTCGAC ATCCCCCGGA AGCTTGCTAG AAATGCTGGG 1140 TCTCAGGCCT CATCCCAGAC CTACCAAGTC AAACTCATTT TAACAAGATC TCCAGGTGGT 1200 TCAGGGTTGC AAATCACTGG TTTGGAACAT TCAGTGAAAG CTACTCAGCT CGTTTGCAGT 1260 AAGAGGTATT TTTAGTCCTG TCTGTATAAT ATGTAATATT TTCCCCCCAG CATTTTACTA 1320 TGAACATTCT 1330
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