Tag | Content |
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EnhancerAtlas ID | HS098-15393 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:31313850-31315260 |
SNPs | Number: 2 | 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 | chr13:31314365-31314380 | ATTGCTGACTCATAT | - | 6.39 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_37797 | chr13:31313747-31315477 | HSMMtube | SE_59818 | chr13:31293174-31321295 | Ly4 | SE_63988 | chr13:31313927-31315310 | HSMM |
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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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Enhancer Sequence | CATGAAACCA GCCTAGAAAT ACATACTATT ATTTATTCTT GTTTTACAGA TAAGCAAAGT 60 GAGTCATGGA GAATTTGGTT GAAAGTCCCA AGGTCAGGAG TCGTGAAGCT GGGATTAAAA 120 CCTAATCATC TGACTTTAGA GAGTAGACAC TTGCTCCATG CATATTGCCT CCAATTCATT 180 CATTCAAGCA CTCCCTGCTC AAGAAGTTCT TTCTTATGTT GAGCTGAAAT CTGCAGCCCT 240 ATGCGTTTTA CCCAGCAGTC CTGGTGCTGT TCCCTAAAAT CACTTAGACT GTGCCTGCTC 300 TTTCTGTGTT TACAGTGTCA GCTGTAATAT CCCCCTCTTC GGCCTAACGT TTCTGAAGTC 360 CCTTGCCACT GGGTCTCCTC TCCTCTTCCT GTGTTCTTTC TAAGAACACC TATGCAGATA 420 GGTGTCTTCT GTACAGGGAA GCTGTTCCTG AGATCCGGGC ATCGACTCTG TTAGAATAAT 480 CTACGTATGA GTTATTTTTT TGAGAACTAT GTGTCATTGC TGACTCATAT TAACTCTGTG 540 GTTAACTAAA ATCTCAAGAT CTCTTTATGT TTGTTGAGAA ACTTATTTAA CTTCTCTGGC 600 CCTCCGTTTC CTTCACTGAG CAGTGGAGTG ATTGATAACC TCCACCTGTG GTTGCTGAAG 660 GTCTTGCACA AGATGATATA GTTAAAGTAG CTAGCAGTGC CCACGTACGG CGGATGCCTC 720 ACAACGGTTT GCAGCCATCT CTCTATCTGT GTCTTTGTCT CTCTCTCACA CTGGTTTTGG 780 CTTACTGTTA GCAGCTAGCC GAGATAAGTG TGTTTATGGT CTTTGCATGT ATTGTTTCTG 840 TAGCATACTG GAGGATTACA AGAGGTTGGG GAGTGAGGGG GCGGTGAGGA GTAGACAAAG 900 GCAGCCAACT CTTCCAAGTT TAGCTTAGAA GGAAGGAGCG GTAAACCCTA GTTGAATGTT 960 GGACTGAAGC AGGTTTGTTT TTGTTTTGTT TAAAGGATAG GGAAGATCTG TGCGTGTTTC 1020 CAGGATAAAG AAAAGGAGAG AATATGATAT TAAAGATTCT GGAAGTGGGA GAAGGAGCAA 1080 TGAAATACAG ACTTGAAGTC AGTGGCATGG ACAGGGTCAA GATCACAGTT AGAGGATGCA 1140 GCCTTAGAGA AAAGGAAGGG GCTCGGTTCT CTGAGCAAGG AGGGAAAGAA GAGAGGCAGA 1200 TGCAGAGAAG TACGGCACAT CGTGCTGCTG GTTGTAGAAA TAACCTCTGA CTTTTAATAA 1260 AGTCATCCCT CGGTATCCCT GGGGGATTAG TTCTATGACC TCCCTCGGAT GCCAAAATTC 1320 GTGGATGCTC AAGTCCCTGA TATAAAATGG CATAGTATTT GCATTTAACC TACACACATC 1380 CTCCATATCC TTTTTTTTTT TTTTTTTTTT 1410
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