| Tag | Content |
|---|
EnhancerAtlas ID | HS182-09233 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:25892930-25894230 |
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 | TCACGGTTTC TGGTGTAGAC CTCTAGGAGT TTTGACAGCT GAGCATCCTT TTGAAGGTTG 60
TCCCATGAGC CATCCCAGGC ATCTGCTGCA GTTCATAGGG TTCTTCCTGT TGGTCTCCAT 120
ACCACTCACC CGAAGCATGC GAGAAGCTGC AGGGGCTTGG GGGCAGTTGG AGTTCATGTG 180
GGGGTGGGGG TTCCCCAGAT GATTCACTGG AAGGAGGGAG ATGACCGTGT TCTTATTGAC 240
TCAGGTCCTA CCTTTTGGAG GGAGGTGGCA AGGCAGGGAA AACCTCTTGG TGGCCTTGCA 300
TCCTGGACAT CCTGGGTGCC TGGTCCCCAG CCCCTGCTGC AGGGCCTGCT GGAGCCTGCA 360
CATCTCCCAC CCAGCACCTG CCCCGGGAAG TATGTGCTGA CTCCCCAGCT CCCAGGCACA 420
AACTATTTTT GGCTGCAGTG ACTGTTCACT ACAGTCATGA AAACAGAAAC CCCTCTCCCT 480
GCCTCCTTCT TCCCTGGGAC ACTGCACTGG GGGCCAGGGC TGCCGGGGAC CCTGGGCTCA 540
GGCCCCCTTG TCATGAATCG CCTGTGGAGC TGGGTGACAG CCAAGGTGTC CAGGGGCACA 600
GGGCCCCCAC CTCTGGGGAT GCCAAGAGAA GCCCGAGGCG TGAGCCCACC TGGGCTGGAG 660
GATTATGAGG TAGGCACGGG GGTCTGGGCG CAGGAGGCCA TTCCACAGCT CCCTGGAGTT 720
GAGTCTGTTT GCTAGACTCT GAGTCCCTGC TTTGCTACCT GGCTGTAGAA CACGTGTGGA 780
GAAATCGCAT GTTGGGGCAG AAGGTGCTTG TTTCATGACT TCATTCGCTG TCTTCTGTGT 840
GATAAAGTCA CTGGGGATCA GTTAGAATCT TCCTGAAATA GATCCTCCCC ATCCTTCTAG 900
TGAATAGTGT TTGGTCATTT CCTGCTTTTG AGTAGGACAC ACACTTGTTC TGAGCATGCT 960
GCTTTTTTAC AGGGAGCTTA AGAACGTGGA GCTGTATAGG CTGATCCAGC TCTACCTCTC 1020
CATGCTTCTG GTTGACCAGG CCAGGGAGGC CGATGGTTAT AGAGACTGTG AGTGCTGACT 1080
TTGGGGTCAC ACAGACCAAG GTCCAAATCC AGGCCCTGTT ACTCAGGGCT TGCAGTGTCT 1140
TAAGGTGTGT AACTTAATCT CTATGAAGCT CAGTTCCTTA GCTACCAAGC AGTTGTGCCT 1200
AGGCTACTTA CACGGTGGTG ATAATACCAA TAGTTGTTAT TTTTATGATT AGACTGATTG 1260
TGAAAAGGGA AAATACTTCA AGAAGCTGTG TAAGAATCCA 1300
|
