Tag | Content |
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EnhancerAtlas ID | HS117-00632 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr1:205144200-205145600 |
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) |
FOSL2 | MA0478.1 | chr1:205144744-205144755 | GGATGACTCAT | + | 6.62 | JUN(var.2) | MA0489.1 | chr1:205144741-205144755 | AAGGGATGACTCAT | + | 7.38 | JUNB | MA0490.1 | chr1:205144744-205144755 | GGATGACTCAT | + | 6.62 | REST | MA0138.2 | chr1:205144924-205144945 | CTTAGCACCTAGAACAGTGCC | + | 6.02 |
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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 |
GH01I205174 | chr1 | 205143979 | 205146682 |
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Enhancer Sequence | GATATATTGG CACCCACAAA GAAGCTGCCC TTTTTTTTTT TTTTTCTGAG ACAGAGTCTC 60 GCTCTGTTGC CCAGGCTGGA GTGCAGTGGC GCAATCTTGG CTCATGCAAG CTCCGCCTCC 120 CAGGTTCACG CCATTCTCCT GCCTCAGCCT CCCATGTTGC TGGGACTACA GGCGCACGCC 180 CGGCAATTTT TTTGTATTTT TAGTGGAGTC AGGGTTTCAC CATGTTATCC AGGATGGTCT 240 CGATCTCCTG ACCTCGTGAT CCGCCTGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCG 300 TGAGCCACCG TGCCCGCCAG AAGCTGCCTA TTCCTAAATA TACCTTGTAC TAAACAAAAA 360 TGGATAGAAA ACAGGTATCA TGCTCTGTCT TCTCCCTTCC CCAGTTGACC AACATGTGCA 420 GTTGGTCTCA CTGCTCTGAG TATCATGATT GTCAGAAGAT AGGCAAAGAG CTGCTGGCAG 480 AGACCCTGGC AGCAGTACGA ATTAGGCTGG AATGTGATAT GCGATTCTGC AATACTCAGT 540 GAAGGGATGA CTCATGCTTG ACGGTTATAA ACAAAAAAGG ACGCCAACAC TGTTTCCTGG 600 AGACAGGGAG TGAAAAAATA AAAATTAATA TAAAGAGGAT GAGCCAGAGC TGTTATGGGC 660 CTTAGTATGG CCACCTGAGA GGGAAGTCTG ACCTCAGACT GTTTCATGGA TGGCTATATA 720 CCTTCTTAGC ACCTAGAACA GTGCCTGGCA CTTAGTAAGC ATCCAATAAA TAAACATGGA 780 ATGAATTAAT GAAGAAATGA TGCTCAAAGC CACTTTCAAT CGGCATATGT AAAATCTTCT 840 ATCTTTCAAC TCCCATCCCA CACATTTTAT CCCACACATT TATCTGAAAT TGCATTTGCC 900 TCTACTCCAA GAATAAAGCA ATGAGTAAGC ATTTTGCTCC TAACTCAATC AAGTAAAAAG 960 AATCTCAAGG AATCATGACA ATAACCCATA ATTCCTATAT TGAGTCATAG TGAATTCCTA 1020 AAGAGATTTC TCTTGTAGAA CGCATTCTGC ATAAATCTGT GGAGTTTACA GAAGTTGATC 1080 TGTTACCACC CATTTTCTCG GCATGATTAA GAAATGCAAT AGAGGCTGGG TGCAGTGATT 1140 CACGCCTGTA ATCCCAGCAT TTAGGGAGGC CGAGACAGGC AGATCACCTG AGGTTGGGAG 1200 TTCAAGACCA GCCTGATCAA CATGGAGAAA CCCCATCTCT GCTGAAAACA CAAAATTAGC 1260 CGGGGTGGTG GCGTATGCCT GTAATTCCAG CTACTCGGGA GGCTGAGGCA GGAGAATTGC 1320 TTGAGCCCAG GAGGCGGAGG TTGCGGTGAG CCGAGATCAT GCCATAGCAC TCCAGCCTGG 1380 GCAACAAGAG TGAAACTCCC 1400
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