Tag | Content |
---|
EnhancerAtlas ID | HS059-08316 | Organism | Homo sapiens | Tissue/cell | GM12878 | Coordinate | chr11:66221570-66223070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP8 | MA0747.1 | chr11:66221820-66221832 | CCCACGCCCCCT | + | 6.04 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 66221780 | 66221966 | chr11 | 66221788 | 66222095 | chr11 | 66221749 | 66222155 |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I066454 | chr11 | 66221780 | 66221966 |
| Enhancer Sequence | GAGATGTTGG CGGCGTGAAG CTCAGGAGTA TACATCAGAG AAAGCCAAAA GCCAGCTGGA 60 ATAGTTCCTG AATACAGTTT TAACCTTGCT TGCAATTATT TTGAAGGGGA GAAATCATCT 120 GGATTGGAAT TAAGATGCTC TGGTTTCAAG GAAATAGCAT GCAGCTTGCC AGATCCTCCC 180 TTGGACTCTT CTTGATAAAC TGCTCTGTCT CTAAGACAAC TCTGCCCGTG CTGACCTTAT 240 TCACAAAGGA CCCACGCCCC CTTTGTGGTG AAGCCAAGGA AGTACTCAAG CCTTATAGTA 300 ACAGGTTTAT TTTACAGGAA GTGAACGTCA CACTTCCAGA AAACTCTGCC TGGTATGAAA 360 GGTATAAATT TGACATTCCT GTCTTTCACT TGTGTGGCCA GTTTCTGATG ATGCATCAAG 420 AAAACACCTC AAAACTTGAC AAACAGCTCC TGAAACTTGA GCAGCAAAGT ACCGGAGGCT 480 GACGAATGCC CTCATGATTT TCCACCCTCT CTTCCTATAC GGCATCTTCC TAAGGAAATG 540 ACCATGGCCT GATACTCCTT TTGTCACCTA TACAGAGCCC TAAGGATATT CTGAACTCAG 600 TGGTGCCAAA TAAATGTTGA CATTCCTCTT TTGGTTGATG GGGGAAAAAA AAAGGGAGCC 660 CAGACTCCTC GCTCTCATCT GCCTTCCCCC TCCTCTGTCT GCTCTTCCCT GCTCCTCCTG 720 GGGGCTCCCC AGGTACCAAG CAAGAGGCTG ATGTTGCTTG TGTATGATAG CTACAAATCT 780 CCGGCTTGTT ATCCTTACTT GCTCATTTGG TTACCGGAGG GATTATTTTA GTGAAGTCTA 840 TCTCCTCCTT CTTGCTGCCA GAGTGTGAAG CCTCAGATGT CACTTCTCAG GGGGTACAGC 900 CTTGGGTACC CAGTCATCAT GGGTTAACAA GGGTTTTGAC AGGACTCTCT TTGACTGACT 960 CGTCCCCTGA CACACCCAGC TGTTAGGCTC CAGTAATTGC CAGCTGAGTT GTCTATTACT 1020 GTATTTTCAA CAAAGCTCTG GGGTATAAAC TCCTCCACAA ATGGATCCAG TCAAACCTGG 1080 TGATGCCTTT GAAGAAACAG TCCTGGAGGT CAGTGTCTGA GATTTGTTCT GACTCTAGCA 1140 GGATTCTCCA GTTTCCCTTT CCCCAGTTTC TCTCCAGCAA ACTAGCCAGC CTGCAATTTA 1200 ACCTGTATCT CCAAAGTCCA TCAATCTCCC CTCTATTGCT TTTCCCCATA ACCTCCAGTA 1260 TTTTGAGAGT GCTCTTGGGC TTGAACTTAA ACTTCTCTAC AACCTGTAAC AAATGTTCCT 1320 TTAGGGAAAG ATCTGGAGCT CTCTCTCTTA CTACCTACTT TTTTTTTTTT TTTTTTTTTT 1380 TCAATACTTG ATCTTGCTCT GTCACCCAGG AGGCTGGAGT GCAGTGGCAC AATCTTGGTA 1440 ACTACAACCT CTGCTTCCTG GGTTCAAGTG ATTCTCCTGC CTCAGTAGCT TGTATTACAG 1500
|
| |
|
|
|