| Tag | Content |
|---|
EnhancerAtlas ID | HS154-02093 |
Organism | Homo sapiens |
Tissue/cell | Osteoblast |
Coordinate | chr1:226098680-226099770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:226099202-226099221 | TGGCGCCCTCTGGCGGCGC | - | 6.12 | | Zfx | MA0146.2 | chr1:226099335-226099349 | GAGGCCTAGGCGGG | - | 6.24 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_11743 | chr1:226097033-226100035 | CD20 | | SE_23251 | chr1:226097612-226099209 | Colon_Crypt_1 | | SE_23870 | chr1:226098772-226099274 | Colon_Crypt_2 | | SE_25061 | chr1:226098646-226099436 | Colon_Crypt_3 | | SE_56863 | chr1:226098717-226099267 | VACO_400 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 226098696 | 226098800 | | chr1 | 226098800 | 226099124 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I225910 | chr1 | 226098568 | 226099771 |
|
Enhancer Sequence | CAACCTCTGG TTATTAGCGC TGTCCTGCCA GACACCAAGC CCAGCCTTTA TCTCATTGAA 60
TCCTCATCTC AGCCCATGAG GTGGGGATCC TTCTCACCCT CACTTGACAG ATAAGTTCTT 120
GGAGGTTGAA TAACTCACCC AAGGTCACCT GTCGTTAAAG TGACTGACTC TCTAGGCCTC 180
GTCTTGAGCA AGATGGGTGT ATTTCGATTC AGATGGCCCA CGTCAGGCTG GACACGCGGG 240
CCCCTGGTGA GGCCTGAGTC CCTGGCCGGG GAGCTCCGCT AAGCTGCCCG ACCTCCCATG 300
TGCAGAGGGC GCTGCTGGGG CCACAGGCGA GGCTGCGTGG GGAAGCGGAG CGTGGATTCC 360
AGCGCTTTCC CCTAGATCCA ACTCTGAGCT GCTTTGCTAT GTGAACTCAG GAAATGACCT 420
GCCACAACTA GCAGGTGGGC ACCCAGCCGG GGCTGGGGTT TGCACCCGGT TTCTCTCCAA 480
CCAGGCCGGG GCTGGCGGCC TGGGGAGTTC GGCTGTGGCG CCTGGCGCCC TCTGGCGGCG 540
CGGGGAGGTC CTCCTCGGCC GCGGGCGGCC GGGACCGCTT GGAGCCGCGA AGGGACGTTT 600
TTTAGGAACC ACTAGCCAGG CGCGGGGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC 660
CTAGGCGGGC GGATCACGAG GTCAAGAGAT AGAGACCATC TTGGCCAAAA TGGTGAAACC 720
CCGTCTTTAC TAAAAATACA ATGCTGTCCT CAAGGGTCTT CTTAGGAACT CTTCTGTGAG 780
CTGAGTGGGG AAAACGGGAA AGAAGACTCG AGTCTGGAGG CTGAGATTTT GACACCGGCT 840
TCCCCAGTCA TCTTGGATGG GTGCCTTGAG TTCTTCCTAT GGGGGACGGG AATGGCGATG 900
GGGACAGGGA TGGGGATGCC CCCTCCCTAC GTGCCTCCAG ATCGCCGTGG GACTCCTGCT 960
GGATGCGACG AGTGACAGCC CCTTGTCAGC CCAGAAGCGC TACTATAGAG CAAAGACTTG 1020
TGTTCATGAG AAAATAACTG ACAGTCCAGG ATGCCAAGGA CCAATGGCCC AGGAAGGAGC 1080
TGGGGAGAGA 1090
|
