| Tag | Content |
|---|
EnhancerAtlas ID | HS060-05842 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:60705500-60706950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr11:60706558-60706569 | GGGCGGGAAGG | + | 6.62 | | Zfx | MA0146.2 | chr11:60705548-60705562 | CAGGCCCAGGCCCC | - | 6.73 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I060939 | chr11 | 60706618 | 60712694 |
|
Enhancer Sequence | CAGAGGGGGA GCAGAGACGA TCTCAGGGGC TGGTGCAGGC GCAGAGAACA GGCCCAGGCC 60
CCTGCTTGCT GCCCCTGACC CTGCCCCCAC CAAGCCACCC TCCAGGCTTC CCCTGGATGC 120
CTGTCCACTC AGTGGCAATG ACAGCACCCA TGCATCAATG CCGCCTTCCC CTCTGCCCTG 180
CTCACCTGCC TCCTGGCTGA ACCCCTGCAC CGGGGTACTC CATGCGCTGC CCCAATAGCT 240
CTGTCTCCCC TCCTCCCCTT CCTGCCAGGT CTATCATTTC AGTGACAGCA CCATCTTTAC 300
CTCCTCTCTC TCCCCACCCT CTCTGCCCAC CTTCAACGTC ATCGTCAAAT TGTTTTGATA 360
CAGCCTCTGA AATCTATTCT AAATATATGT CCTTCTCTCT ATTCCCTCTG CCCTGGGTCC 420
AACCCCAGCC CTGGTCACTT TCTGCAAATG CCTCTTAAAC TCCCCTGACT CCTGTCCTCC 480
TCACACAGCC AGGAGCATCA GTCTAAAGGA CCTCGGATGG GGTCCTTTCC CGGCCAAAAC 540
CCCCTGGAGA GGAGGGGCGC TGTTGCCTTC AGGAGAAATC CCAAGGTGCA GGCTCAGCGC 600
ACAAAGCCCT TCGACACTTC GGCTCCCTGC ACCTCCCATG CCTCTCCAGC CCTATCCCCC 660
ACGCTTCCCA AAGGCTTGGG CCTTTGCTTA TGCTGTTCCC TCTGCCTGTA AGACCGCTCC 720
TCCTACCCAC TCACCTGCCC GCCTCCTCTC CATGCTTAAG GGCTCCCACT GCACTCTGCC 780
CTGACTTCCA CAGCACTCCA CTGGCTCACT GTTTGCCTGA CTCTCTCCCC ATCTGAGTGA 840
GCTCCCAGGG TCAGTCTTTT CTTTATGTCT GACCCAGCCT AGCCCTGGGC CCGCAGCTGA 900
GGAAGCCCTT GCTTTTTTGC TGACTGAAGG GCCTGCCCCA GCCTTGCAGC TCTAGCTCCC 960
AGCCCGGGGA AGGGGGTTGG GAGGGTGGGG AGCGAAGGAC ATAGAAATCC ATTACTATGA 1020
CCCAGAGTAC TGTGTGCTAT GATAGAGAGA TGAACACGGG GCGGGAAGGG AGGACCCCTT 1080
CTGCCCAAGG ACCTTGGTAT TTAGGCTCAG AATTGAAGGG GATATTGGAG TTCACCTTCA 1140
GTCTAAGGTA GAGGGAACAG CAACTTCAAA GACACAGAGG GTGGAGAACC TGGCACCAGG 1200
GGAATACGTG GAGAGCTGGT GTGGGAAGTT TCTTGCTCGC CTCCAAATCC CCAGTGCCTG 1260
TCACATAGGG GCTGACTTGA ACCAGGTGCT AATTATAGAC CCCCGTTGGG TGAATGAGCC 1320
CTGGTCAGAA AACACTGCCT TCCTCCATGC AGATGGGCCC TGGGGGCTGC ATCCCTGGGG 1380
TACCTGACTT TGAGGTGCCA CCGGGCAGAG CCCATCACTG GTGCAGGAGC AGGGGAGGGG 1440
ATCCAGGGTA 1450
|
