| Tag | Content |
|---|
EnhancerAtlas ID | HS006-07146 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr11:66649320-66651490 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr11:66651427-66651438 | TGGGTGTGGCC | - | 6.62 | | PLAG1 | MA0163.1 | chr11:66650692-66650706 | GGGGACAAAGGGGG | + | 6.08 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00471 | chr11:66649578-66656547 | Adipose_Nuclei | | SE_34512 | chr11:66647482-66651643 | HCT-116 | | SE_69114 | chr11:66647380-66651074 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 66650071 | 66651451 | | chr11 | 66649347 | 66649983 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I066880 | chr11 | 66648183 | 66651850 |
|
Enhancer Sequence | GCAGGAGCTC GGACCCATCA GAGTTGGCCT ATGGACTCTT CACTCAACTA AAGGAGTAAG 60
TCACGGCTTT CATCAGGAGC ACAGTGTGAC AGGCACTTGG AAACCAAAAT ACCAAAACCA 120
AAAACCCCAC TTCTGATAAA ACTGTCACTG GCCTGGCCTC CAGCAGGGCC ACCAGTGGCA 180
CTCAGAGCTT CCCAACGAGA GCTGACGAAC AATGTCAGCA GTCACATGTC CCAGATAAGC 240
CAAGGCAGTT TCAATTTGTC TAATAAATCA TCAAAATGTC CCTGAAATCC CACTACTTCA 300
GACCTGAACT ACATCTCCCA GGATGCCTCT TGCAACCAGA AGGAGCACAG AATCCTGCTG 360
TCAGGCCATC ATCCCCCAAG TTTTGTTCCA GACAACAACG TGGCCCCAGT GCTCAGCAGC 420
CTTTCTGGGG ACCAGGGCAG GGCGCCACCT AAGAGCTGCT GCAGCTGAGG CCCCACATCG 480
CTTCGTCCTA CATATTCCTG TCCTCACAGA GCGTCTCCTG CAGCCTCAGA GGGCAGCAGT 540
GGGCAAGAGG CCGCAGAGGA AGGGAAAGAC CAGGCCCTGC TTCAGGGGCG GGTGGCCAGC 600
AAGTTGGTTC TGAAAGCCCA GCAGAGCACC TGGGTCCCTC AGCAAATCCT CAGAGGTGTG 660
CTGGAGAGCA GCAGAGGGCA GAGAAGAAAG AAGTGTGGTT CAGAAACAGG CCCCAGGAAC 720
CTCCGAACCA ACAAAGCTCC ACACACCTAC TTCCTATGGG CCCAGCTGCC CCCAGCACCA 780
GCACCCGCAC CAGGCTGTGC CCCTAGCCCC AGCTGGGCTC CACAGCTGCC AGTGAAAGCA 840
GGTCAGAACC AGAAAGAAAG AGCTCTTGGC AGAGCACTCG GGGCTGCGGC GGTGGCAGCT 900
CTGACGGATG GGGCCGCTCT CCCCAGGCGG CTCTGCTCTA AACATGTCCG ACGGGCCCCA 960
GGGCTGGCAG CCAAGAGGGA CAGATGAAAG AACGACTCCA CCTGGCTCTC AGGGCTGCCA 1020
CGGCTGATAT CAAAGCACCC AAGAGAGGAC AGACTGAGGC TGAGATTTCT GGGCAGGGGG 1080
GGCAGAAGGG AGGACGCTGG AAACAATGCA GGTGACAGAC ACAGAAGACA GGAGAGAGAC 1140
AATACCAAAG ACGGAAACAG ACACAGCACG GGTGCTCGCC GAGGCTCAGC TGTCCGGGCT 1200
CTGGGCCCCC AGGAGCGCCG GCTGCTCCAA GTGGCACTGC GGCGACGAAC AGCAGTGAAC 1260
AGTGCCAGCA GGGCTCCTCA TCGCCCTGGC AACCCTCTAT TCAAAGGAGC AGCCGAGGGG 1320
GAAAGGGTGG CACCGAGGCG ACTGGCGCCA TGGTCTCGGG ACTTGTGGAC TGGGGGACAA 1380
AGGGGGTCTC AGAGAAAGCA GAGTGAGGGG TCCCGAGGGC CTGCAGTGAG GTGGCTGCTC 1440
CATCCCAGCC TCACTGGAAA GCAGTGAGAA TTTCAGGGCC AACACTGCCC CCTGGCGCAC 1500
GAGGAGCCAG CTTCCTGCCG ACCCTGCAGC ACGGGGTGTG GGCAGGGCTC ACATGGGAAG 1560
GTCACTTGTC CCCATTCCTC CACATCCTAT AGGAGTAGGC TCAGGAATGC CTTCCCTATA 1620
TTCCCCGGGC AGCCACCTCC CTCAGCTCTG TCCTTGTCTG TGCCCCACCC ATCGTCCTGC 1680
TCAGGGGGCT CTCCATGAGG TCTCCGTGGC GTCTGTGTCC TCAGCAAAGA GCATTTAATG 1740
TTATAAAGAT TTGTTGACCC GTCTTGTCTC CTTTAATAGA CACTGTTAGG GCCCTGGGCA 1800
CAGGATCCCT GGTCTCTTTT GTCCCCACAT CTCCCTGGCA CTCTGTACAG TGCGTAAGAC 1860
CAGAACTAAA TAAATGTCTG AGGGAATGAA TCAGTGAAGA AATACTTCAG GTCACAATGA 1920
GGTTGCAGAG TGGCATGAGG CTGTTAAGAT TCACCGTGAG GCGTGGTGGC TCATGCTTGT 1980
AATCTCAGCA CTTTAAGAGG CCGAGGCAGG GGTATCACTT GAGTCTAGGA GTTTGAGATC 2040
AGCTTGGGCA ACATATTGAG ATCCTGTCTC TGCCAAAAAA TTAAAAAAAA AACTTTTTAA 2100
AATTAGCTGG GTGTGGCCTG GCACGTGGCT CACACTTGTA ATCCCAGCAC TTTGGGAGGC 2160
TGAAGCGGGT 2170
|
