| Tag | Content |
|---|
EnhancerAtlas ID | HS105-33519 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:25892900-25894080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr17:25893398-25893419 | ACCCCTCTCCCTGCCTCCTTC | - | 6.05 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_28195 | chr17:25893411-25894524 | Fetal_Intestine | | SE_28854 | chr17:25893371-25895532 | Fetal_Intestine_Large | | SE_30131 | chr17:25892663-25894512 | Fetal_Muscle | | SE_39962 | chr17:25892902-25895479 | K562 | | SE_51370 | chr17:25892863-25902462 | Skeletal_Muscle | | SE_54042 | chr17:25892988-25898661 | Spleen | | SE_65525 | chr17:25892922-25893928 | 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 |
| GH17I027565 | chr17 | 25892921 | 25908255 |
|
Enhancer Sequence | ATTTTTTTTT TCATTTGCAT GGACTCCAGT TCACGGTTTC TGGTGTAGAC CTCTAGGAGT 60
TTTGACAGCT GAGCATCCTT TTGAAGGTTG TCCCATGAGC CATCCCAGGC ATCTGCTGCA 120
GTTCATAGGG TTCTTCCTGT TGGTCTCCAT ACCACTCACC CGAAGCATGC GAGAAGCTGC 180
AGGGGCTTGG GGGCAGTTGG AGTTCATGTG GGGGTGGGGG TTCCCCAGAT GATTCACTGG 240
AAGGAGGGAG ATGACCGTGT TCTTATTGAC TCAGGTCCTA CCTTTTGGAG GGAGGTGGCA 300
AGGCAGGGAA AACCTCTTGG TGGCCTTGCA TCCTGGACAT CCTGGGTGCC TGGTCCCCAG 360
CCCCTGCTGC AGGGCCTGCT GGAGCCTGCA CATCTCCCAC CCAGCACCTG CCCCGGGAAG 420
TATGTGCTGA CTCCCCAGCT CCCAGGCACA AACTATTTTT GGCTGCAGTG ACTGTTCACT 480
ACAGTCATGA AAACAGAAAC CCCTCTCCCT GCCTCCTTCT TCCCTGGGAC ACTGCACTGG 540
GGGCCAGGGC TGCCGGGGAC CCTGGGCTCA GGCCCCCTTG TCATGAATCG CCTGTGGAGC 600
TGGGTGACAG CCAAGGTGTC CAGGGGCACA GGGCCCCCAC CTCTGGGGAT GCCAAGAGAA 660
GCCCGAGGCG TGAGCCCACC TGGGCTGGAG GATTATGAGG TAGGCACGGG GGTCTGGGCG 720
CAGGAGGCCA TTCCACAGCT CCCTGGAGTT GAGTCTGTTT GCTAGACTCT GAGTCCCTGC 780
TTTGCTACCT GGCTGTAGAA CACGTGTGGA GAAATCGCAT GTTGGGGCAG AAGGTGCTTG 840
TTTCATGACT TCATTCGCTG TCTTCTGTGT GATAAAGTCA CTGGGGATCA GTTAGAATCT 900
TCCTGAAATA GATCCTCCCC ATCCTTCTAG TGAATAGTGT TTGGTCATTT CCTGCTTTTG 960
AGTAGGACAC ACACTTGTTC TGAGCATGCT GCTTTTTTAC AGGGAGCTTA AGAACGTGGA 1020
GCTGTATAGG CTGATCCAGC TCTACCTCTC CATGCTTCTG GTTGACCAGG CCAGGGAGGC 1080
CGATGGTTAT AGAGACTGTG AGTGCTGACT TTGGGGTCAC ACAGACCAAG GTCCAAATCC 1140
AGGCCCTGTT ACTCAGGGCT TGCAGTGTCT TAAGGTGTGT 1180
|
