| Tag | Content |
|---|
EnhancerAtlas ID | HS187-10203 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:25892890-25894220 |
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 | TGTTTTCTAC ATTTTTTTTT TCATTTGCAT GGACTCCAGT TCACGGTTTC TGGTGTAGAC 60
CTCTAGGAGT TTTGACAGCT GAGCATCCTT TTGAAGGTTG TCCCATGAGC CATCCCAGGC 120
ATCTGCTGCA GTTCATAGGG TTCTTCCTGT TGGTCTCCAT ACCACTCACC CGAAGCATGC 180
GAGAAGCTGC AGGGGCTTGG GGGCAGTTGG AGTTCATGTG GGGGTGGGGG TTCCCCAGAT 240
GATTCACTGG AAGGAGGGAG ATGACCGTGT TCTTATTGAC TCAGGTCCTA CCTTTTGGAG 300
GGAGGTGGCA AGGCAGGGAA AACCTCTTGG TGGCCTTGCA TCCTGGACAT CCTGGGTGCC 360
TGGTCCCCAG CCCCTGCTGC AGGGCCTGCT GGAGCCTGCA CATCTCCCAC CCAGCACCTG 420
CCCCGGGAAG TATGTGCTGA CTCCCCAGCT CCCAGGCACA AACTATTTTT GGCTGCAGTG 480
ACTGTTCACT ACAGTCATGA AAACAGAAAC CCCTCTCCCT GCCTCCTTCT TCCCTGGGAC 540
ACTGCACTGG GGGCCAGGGC TGCCGGGGAC CCTGGGCTCA GGCCCCCTTG TCATGAATCG 600
CCTGTGGAGC TGGGTGACAG CCAAGGTGTC CAGGGGCACA GGGCCCCCAC CTCTGGGGAT 660
GCCAAGAGAA GCCCGAGGCG TGAGCCCACC TGGGCTGGAG GATTATGAGG TAGGCACGGG 720
GGTCTGGGCG CAGGAGGCCA TTCCACAGCT CCCTGGAGTT GAGTCTGTTT GCTAGACTCT 780
GAGTCCCTGC TTTGCTACCT GGCTGTAGAA CACGTGTGGA GAAATCGCAT GTTGGGGCAG 840
AAGGTGCTTG TTTCATGACT TCATTCGCTG TCTTCTGTGT GATAAAGTCA CTGGGGATCA 900
GTTAGAATCT TCCTGAAATA GATCCTCCCC ATCCTTCTAG TGAATAGTGT TTGGTCATTT 960
CCTGCTTTTG AGTAGGACAC ACACTTGTTC TGAGCATGCT GCTTTTTTAC AGGGAGCTTA 1020
AGAACGTGGA GCTGTATAGG CTGATCCAGC TCTACCTCTC CATGCTTCTG GTTGACCAGG 1080
CCAGGGAGGC CGATGGTTAT AGAGACTGTG AGTGCTGACT TTGGGGTCAC ACAGACCAAG 1140
GTCCAAATCC AGGCCCTGTT ACTCAGGGCT TGCAGTGTCT TAAGGTGTGT AACTTAATCT 1200
CTATGAAGCT CAGTTCCTTA GCTACCAAGC AGTTGTGCCT AGGCTACTTA CACGGTGGTG 1260
ATAATACCAA TAGTTGTTAT TTTTATGATT AGACTGATTG TGAAAAGGGA AAATACTTCA 1320
AGAAGCTGTG 1330
|
