| Tag | Content |
|---|
EnhancerAtlas ID | HS024-01292 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:204319730-204320860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX5 | MA0510.2 | chr1:204320203-204320219 | AGTTACCACGGCAACC | + | 6.21 | | RFX5 | MA0510.2 | chr1:204320203-204320219 | AGTTACCACGGCAACC | - | 6.28 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23313 | chr1:204319448-204321081 | Colon_Crypt_1 | | SE_24138 | chr1:204319800-204321034 | Colon_Crypt_2 | | SE_28816 | chr1:204318597-204321101 | Fetal_Intestine_Large | | SE_33663 | chr1:204319261-204321062 | H2171 | | SE_50227 | chr1:204316786-204321139 | Sigmoid_Colon | | SE_52903 | chr1:204319289-204321122 | Small_Intestine | | SE_65374 | chr1:204317203-204320948 | Pancreatic_islets |
|
| | 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 |
| GH01I204347 | chr1 | 204316837 | 204321118 |
|
Enhancer Sequence | AGGCACTGCT CCCAAACGTG TGCTCTGGAG GTCCAAGTTC TCTCCATTTT ACAGATGAAG 60
AAATCAAAGC TCAAAGAGGT AAAATTGTCT GGGAGATGGG GGCGGGGGGA GGACCAGGAC 120
TGACGTCTTG GTTTGGATGG CCCCTGGTTT TATCACTGCC AGGGTTAGCT CCTGAGCCGC 180
CCTGTCAAAT CCCCTAAACG TCCCATGAAG GCCAAGACGA CTCACACTGC AAAACATACA 240
CACAAAGGGT CGGAAACAGC ACAACATTCT TTCCTACCTG CCTTTTTCTG GCTTTCCCAG 300
TCCCACGAGG GAGAGAGGAG AGGGCTGTGC TGGGGGCATC TGGGATCTGT CTTCCTCCTT 360
GTCCAGCCCT TGTCCTTCTC TGCCTCTTTT GAGGCTGACT TCCCCCAGCT CACCACCCTC 420
CTCTCCGAAC GCCAGCTAAC CGGTTACCCG GGCAACCCAG CTGGGAGGCC GCCAGTTACC 480
ACGGCAACCC AGCATGGCCG CCAGGCTGCC TTGCTTAGGA AGGTCAGGGG ACCAGCCGGG 540
CTACCGAGCA GCTGGGATGC TGCTGGCAGG ACTGGCCCAG GCAGGGGGAG TGGGGTGTGG 600
CGGGGGGGAG GTGGCCTACG TGCCTGAGAT AACTAAGTTC CTGCTGTCAG GGGCCACCTT 660
TCCCTTTGAC ATGTTTCCCA TGAAGCAGGC TCCCCCAACT TGGGCATGAA CCACAAGCCG 720
TCCTCCCCAG TTCCATCACC CAAGCCGAAC CCGACCCCTC CCACCTTCTC TACAGAGTTC 780
CGGTCGCCTC ACCTCCAGGA AGGCTTCTCA GGCTGAGCAG CAGCCAGCTG TCATTCAGCC 840
TAACCCCAGG CCCTCTCACC CTCCGCCCTT CCTGAGCATA TCCAGGAGTC CACACATATG 900
CAACATGCGT GTGTCAGCGT GCAGATGTGG TCTCTCTGTG AAATATGGTG GTAAAAATCA 960
TAAGGAAGAG CTAATATTTT CTAGTACTTA CTATGTGCCT AGCATGTTGT AGGTGACTTG 1020
TGTGAAGTTT CTCAATTGAG CCATACAACA ATCATATTAT CCTCACTTCG CAGATAGAGT 1080
GCCTGAGACT TAGAGAAGGT GAGGGACTTA CTCAAGGCTG CACAGGTACT 1130
|
