| Tag | Content |
|---|
EnhancerAtlas ID | HS183-14676 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr9:140157670-140158690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:140157796-140157814 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr9:140158244-140158262 | GCTTCCTCCCATCTTTCC | - | 6.12 | | EWSR1-FLI1 | MA0149.1 | chr9:140157687-140157705 | CCCTCCTTCCCCCCTACC | - | 6.18 | | EWSR1-FLI1 | MA0149.1 | chr9:140157679-140157697 | ACTGCCCTCCCTCCTTCC | - | 6.3 | | EWSR1-FLI1 | MA0149.1 | chr9:140157727-140157745 | CCCTCCCTCCTTCCCTCC | - | 6.84 | | EWSR1-FLI1 | MA0149.1 | chr9:140157723-140157741 | CCCTCCCTCCCTCCTTCC | - | 7.12 | | EWSR1-FLI1 | MA0149.1 | chr9:140157879-140157897 | CCCTCCCTCCCTCCTTCC | - | 7.12 | | ZNF263 | MA0528.1 | chr9:140157915-140157936 | CTCTCCTTCCCCCTCTGCCCC | - | 6.21 | | ZNF263 | MA0528.1 | chr9:140157840-140157861 | CCTCCCTCCTCCCCCTCCGCC | - | 6.3 | | ZNF263 | MA0528.1 | chr9:140157806-140157827 | CTCCCTCCTTCTCCCTTCTCC | - | 6.58 | | ZNF263 | MA0528.1 | chr9:140157747-140157768 | CTCCCCGGCCCTCCCTCCTTC | - | 6.61 | | ZNF263 | MA0528.1 | chr9:140157723-140157744 | CCCTCCCTCCCTCCTTCCCTC | - | 6.82 | | ZNF263 | MA0528.1 | chr9:140157809-140157830 | CCTCCTTCTCCCTTCTCCCCC | - | 6.97 | | ZNF263 | MA0528.1 | chr9:140157831-140157852 | CTCCCCGGCCCTCCCTCCTCC | - | 7.06 | | ZNF263 | MA0528.1 | chr9:140157843-140157864 | CCCTCCTCCCCCTCCGCCCTC | - | 7.25 | | ZNF263 | MA0528.1 | chr9:140157879-140157900 | CCCTCCCTCCCTCCTTCCCCC | - | 7.29 | | ZNF263 | MA0528.1 | chr9:140157799-140157820 | TCCCTCCCTCCCTCCTTCTCC | - | 7.36 | | ZNF263 | MA0528.1 | chr9:140157796-140157817 | CCCTCCCTCCCTCCCTCCTTC | - | 8.94 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41683 | chr9:140157306-140157877 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 140157967 | 140158029 | | chr9 | 140158516 | 140158656 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I137262 | chr9 | 140157307 | 140157877 |
|
Enhancer Sequence | CAAGGTAGCA CTGCCCTCCC TCCTTCCCCC CTACCCTCCT GAAGGTAGTG CTGCCCTCCC 60
TCCCTCCTTC CCTCCCACTC CCCGGCCCTC CCTCCTTCCC CCACTGCCCT CCTGAAGGTA 120
GCGCTGCCCT CCCTCCCTCC CTCCTTCTCC CTTCTCCCCC GCTCCCCGGC CCTCCCTCCT 180
CCCCCTCCGC CCTCCTGAAG GTAGCGCTGC CCTCCCTCCC TCCTTCCCCC CAACTCCCCG 240
GCCCTCTCTC CTTCCCCCTC TGCCCCTCCT GAAGGTAGCA TTGCCCTCCC TCCTTCCCCC 300
TGGCCCTCCT GGCTCCTCTC CTCTCCGTGG GTTTGGCTTG GCCCGGGACC ACCTGGGCGC 360
CCTTCTCTCC CATGCCTGTT TCCTGGGCTC TGGTCTTTCT GTCCTGTGTG CTGGCCCTTT 420
GGCTTCTCTC CAGACCCTGA TGGGGGAAGG AGGCTAGTCC CCTGCATCTG AGCCAGAGAC 480
CTGGCCGTTC CCGGGGACTC CCTTGCCCCG TCCAGCCCTT TCTGTGTTCC CGAGGGCTGT 540
ATGACCTACG GGCTGGACCT TGACCATTGC CCCAGCTTCC TCCCATCTTT CCACCTGGCC 600
TGTGGCCCTC CCCTTCCCCA GAACCCTGGG TGCTGCTTGT TGGCCAGGTA CCAAGTGCTC 660
TAGGAACGGG GTTTCCCTTC ATACGGACCC TCCAGCCCTG AGACCATCTT TCCGGGACTT 720
GGGAGTCACC CTCCGAGGCT TCCATTGCTT GGAGTGCTGC AGTGGCCACC CCCACACTCA 780
GGGTGCCATG AAGGAGTCCG TTTTTAGAAA GAAACATCAT CACTTTCTCC ACCACTGTCC 840
TGACCCTGCT GCTTTGGCCG GGAGGTGTGG GGAACACTGC ACCGTCAGGA TGACTGGTGC 900
CTGCTGCCGC CCCCCGCAGC AGCTATGATT GAACAAGAGG CCAGGGCCTG GAGCTGTGTT 960
TGGGGCCTGG GTCTCTGGTC ATCCTGGGAG GTTTGGGCTG GTCCCGACCG TGCTTCCTCC 1020
|
